Opioid-induced hyperalgesia: abnormal or normal pain?

Enduring changes in brain and behavior produced by chronic amphetamine administration: A review and evaluation of animal models of amphetamine psychosis

Robinson, T. G., & BECKER, J. (1986) · Brain Research · doi:10.1016/s0006-8993(86)80193-7 · Cited by 2,110 · see citing works

Cellular and molecular mechanisms of drug dependence

Koob, G. F., & Bloom, F. E. (1988) · Science · doi:10.1126/science.2903550 · Cited by 2,070 · see citing works

Contribution of central neuroplasticity to pathological pain: review of clinical and experimental evidence

Coderre, T. J., Katz, J., Vaccarino, A. L., & Melzack, R. (1993) · Pain · doi:10.1016/0304-3959(93)90161-h · Cited by 1,966 · see citing works

Enduring changes in brain and behavior produced by chronic amphetamine administration: A review and evaluation of animal models of amphetamine psychosis

Robinson, T. E., & Becker, J. B. (1986) · Brain Research Reviews · doi:10.1016/0165-0173(86)90002-0 · Cited by 1,796 · see citing works

An opponent-process theory of motivation. I. Temporal dynamics of affect

Solomon, R. L., & Corbit, J. D. (1974) · Psychological Review · doi:10.1037/h0036128 · Cited by 1,704 · see citing works

Inhibition of Morphine Tolerance and Dependence by the NMDA Receptor Antagonist MK-801

Trujillo, K. A., & Akil, H. (1991) · Science · doi:10.1126/science.1824728 · Cited by 1,217 · see citing works

The opponent-process theory of acquired motivation: The costs of pleasure and the benefits of pain.

Solomon, R. L. (1980) · American Psychologist · doi:10.1037//0003-066x.35.8.691 · Cited by 1,196 · see citing works

The opponent-process theory of acquired motivation: the costs of pleasure and the benefits of pain

Solomon, R. L. (1980) · American Psychologist · doi:10.1037/0003-066x.35.8.691 · Cited by 1,194 · see citing works

Protein kinase C reduces Mg2+ block of NMDA-receptor channels as a mechanism of modulation

Chen, L., & Huang, L.-Y. M. (1992) · Nature · doi:10.1038/356521a0 · Cited by 964 · see citing works

μ-Opioid receptor desensitization by β-arrestin-2 determines morphine tolerance but not dependence

Bohn, L., Gainetdinov, R. R., Lin, F., Lefkowitz, R. J., & Caron, M. G. (2000) · Nature · doi:10.1038/35047086 · Cited by 930 · see citing works

Activity-dependent neuronal plasticity following tissue injury and inflammation

Dubner, R. A., & Ruda, M. A. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90019-5 · Cited by 926 · see citing works

Acute Opioid Tolerance

Guignard, B., Bossard, A. E., Coste, C., Sessler, D. I., Lebrault, C., Alfonsi, P., Fletcher, D., & CHAUVIN, M. (2000) · Anesthesiology · doi:10.1097/00000542-200008000-00019 · Cited by 885 · see citing works

Mechanisms of hyperalgesian and morphine tolerance: a current view of their possible interactions

Mao, J., Price, D. D., & Mayer, D. J. (1995) · Pain · doi:10.1016/0304-3959(95)00073-2 · Cited by 817 · see citing works

Dual regulation of adenylate cyclase accounts for narcotic dependence and tolerance.

Sharma, S. K., Klee, W. A., & Nirenberg, M. W. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.8.3092 · Cited by 671 · see citing works

Evidence from rats that morphine tolerance is a learned response

Siegel, S. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077058 · Cited by 657 · see citing works

Isolation, sequencing, synthesis, and pharmacological characterization of two brain neuropeptides that modulate the action of morphine.

Yang, H., Fratta, W., Majane, E. A., & Costa, E. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.22.7757 · Cited by 608 · see citing works

Tolerance and sensitization to the behavioral effects of drugs

Stewart, J., & Badiani, A. (1993) · Behavioural Pharmacology · doi:10.1097/00008877-199308000-00003 · Cited by 594 · see citing works

Long-lasting Hyperalgesia Induced by Fentanyl in Rats: Preventive Effect of Ketamine

Célèrier, E., Rivat, C., Jun, Y., Laulin, J.-P., Larcher, A., Reynier, P., & Simonnet, G. (2000) · Anesthesiology · doi:10.1097/00000542-200002000-00029 · Cited by 584 · see citing works

The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury

Coderre, T. J., & Melzack, R. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-09-03665.1992 · Cited by 567 · see citing works

Morphine receptors as regulators of adenylate cyclase activity.

Sharma, S. K., Nirenberg, M. W., & Klee, W. A. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.2.590 · Cited by 533 · see citing works

Opioid therapy for chronic nonmalignant pain: a review of the critical issues

Portenoy, R. K. (1996) · Journal of Pain and Symptom Management · doi:10.1016/0885-3924(95)00187-5 · Cited by 532 · see citing works

The activity of neurons in the rostral medulla of the rat during withdrawal from noxious heat

Fields, H. L., Bry, J., Hentall, I. D., & Zorman, G. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-12-02545.1983 · Cited by 518 · see citing works

Supraspinal contributions to hyperalgesia

Urban, M. O., & Gebhart, G. F. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.14.7687 · Cited by 518 · see citing works

Evidence for spinal N-methyl-d-aspartate receptor involvement in prolonged chemical nociception in the rat

Haley, J. E., & Dickenson, A. H. (2016) · Brain Research · doi:10.1016/j.brainres.2016.02.001 · Cited by 511 · see citing works

Role for G protein-coupled receptor kinase in agonist-specific regulation of μ-opioid receptor responsiveness

Zhang, J., Ferguson, S. S. G., Barak, L. S., Bodduluri, S. R., Laporte, S. A., Law, P., & Caron, M. G. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.7157 · Cited by 505 · see citing works

Evidence for spinalN-methyl-d-aspartate receptor involvement in prolonged chemical nociception in the rat

Haley, J. E., Sullivan, A. F., & Dickenson, A. H. (1990) · Brain Research · doi:10.1016/0006-8993(90)90975-h · Cited by 463 · see citing works

Thermal hyperalgesia in association with the development of morphine tolerance in rats: roles of excitatory amino acid receptors and protein kinase C

Mao, J., Price, D. D., & Mayer, D. J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-04-02301.1994 · Cited by 458 · see citing works

Sustained potentiation of NMDA receptor-mediated glutamate responses through activation of protein kinase C by a μ opioid

Chen, L., & Marine, L.-Y. M. H. (1991) · Neuron · doi:10.1016/0896-6273(91)90270-a · Cited by 445 · see citing works

The effects of a non-competitive NMDA receptor antagonist, MK-801, on behavioral hyperalgesia and dorsal horn neuronal activity in rats with unilateral inflammation

Ren, K., Hylden, J. L. K., Williams, G. M., Ruda, M. A., & Dubner, R. A. (1992) · Pain · doi:10.1016/0304-3959(92)90039-e · Cited by 412 · see citing works

Intermittent versus continuous stimulation: Effect of time interval on the development of sensitization or tolerance

Post, R. M. (1980) · Life Sciences · doi:10.1016/0024-3205(80)90085-5 · Cited by 387 · see citing works

Nociceptive action of excitatory amino acids in the mouse: effects of spinally administered opioids, phencyclidine and sigma agonists.

Aanonsen, L. M., & Wilcox, G. L. (1987) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)39258-x · Cited by 377 · see citing works

Morphine-activated opioid receptors elude desensitization by β-arrestin

Whistler, J. L., & von Zastrow, M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.17.9914 · Cited by 370 · see citing works

Drug Addiction: The Yin and Yang of Hedonic Homeostasis

Koob, G. F. (1996) · Neuron · doi:10.1016/s0896-6273(00)80109-9 · Cited by 347 · see citing works

Dynorphin Promotes Abnormal Pain and Spinal Opioid Antinociceptive Tolerance

Vanderah, T. W., Gardell, L. R., Burgess, S. E., Ibrahim, M. M., Dogrul, A. B., Zhong, C.-M., Zhang, E.-T., Malan, T. P., Ossipov, M. H., Lai, J. Y., et al. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-07074.2000 · Cited by 344 · see citing works

Tonic Descending Facilitation from the Rostral Ventromedial Medulla Mediates Opioid-Induced Abnormal Pain and Antinociceptive Tolerance

Vanderah, T. W., Suenaga, N. M. H., Ossipov, M. H., Malan, T. P., Lai, J. Y., & Porreca, F. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00279.2001 · Cited by 335 · see citing works

Rapid Development of Tolerance to Analgesia During Remifentanil Infusion in Humans

Vinik, H. R., & Kissin, I. (1998) · Anesthesia & Analgesia · doi:10.1097/00000539-199806000-00033 · Cited by 325 · see citing works

Progressive enhancement of delayed hyperalgesia induced by repeated heroin administration: a sensitization process

Célèrier, E., Laulin, J.-P., Corcuff, J.-B., Le Moal, M., & Simonnet, G. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-11-04074.2001 · Cited by 315 · see citing works

Response of chronic neuropathic pain syndromes to ketamine: a preliminary study

Bačkonja, M., Arndt, G. A., Gombar, K. A., Check, B., & Zimmermann, M. E. (1994) · Pain · doi:10.1016/0304-3959(94)90149-x · Cited by 312 · see citing works

Pronociceptive actions of dynorphin maintain chronic neuropathic pain

Wang, Z., Gardell, L. R., Ossipov, M. H., Vanderah, T. W., Brennan, M. B., Hochgeschwender, U., Hruby, V. J., Malan, T. P., Lai, J., & Porreca, F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01779.2001 · Cited by 301 · see citing works

Excitatory amino acid antagonists (kynurenic acid and MK-801) attenuate the development of morphine tolerance in the rat

Marek, P., Ben‐Eliyahu, S., Gold, M. S., & Liebeskind, J. C. (1991) · Brain Research · doi:10.1016/0006-8993(91)90576-h · Cited by 298 · see citing works

Spinal pharmacology of thermal hyperesthesia induced by constriction injury of sciatic nerve. Excitatory amino acid antagonists

Yamamoto, T., & Yaksh, T. L. (1992) · Pain · doi:10.1016/0304-3959(92)90198-k · Cited by 296 · see citing works

Intraoperative high dose fentanyl induces postoperative fentanyl tolerance

Chia, Y., Liu, K., Wang, J.-J., Kuo, M.-C., & Ho, S.-T. (1999) · Canadian Journal of Anesthesia/Journal canadien d anesthésie · doi:10.1007/bf03012978 · Cited by 296 · see citing works

Intrathecal MK-801 and local nerve anesthesia synergistically reduce nociceptive behaviors in rats with experimental peripheral mononeuropathy

Mao, J., Price, D. D., Mayer, D. J., Lü, J., & Hayes, R. L. (1992) · Brain Research · doi:10.1016/0006-8993(92)90688-6 · Cited by 283 · see citing works

The NMDA Receptor antagonists, LY274614 and MK-801, and the nitric oxide synthase inhibitor, NG-nitro-L-arginine, attenuate analgesic tolerance to the mu-opioid morphine but not to kappa opioids

Elliott, K. J., Minami, N., Kolesnikov, Y. A., Pasternak, G. W., & Inturrisi, C. E. (1994) · Pain · doi:10.1016/0304-3959(94)90151-1 · Cited by 279 · see citing works

Blockade of tolerance to morphine but not to kappa opioids by a nitric oxide synthase inhibitor.

Kolesnikov, Y. A., Pick, C. G., Ciszewska, G. R., & Pasternak, G. W. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.11.5162 · Cited by 275 · see citing works

MK-801 blocks the development of thermal hyperalgesia in a rat model of experimental painful neuropathy

Davar, G., Hama, A. T., Deykin, A., Vos, B. P., & Maciewicz, R. J. (1991) · Brain Research · doi:10.1016/0006-8993(91)90844-l · Cited by 271 · see citing works

Mechanisms of opioid-induced pain and antinociceptive tolerance: descending facilitation and spinal dynorphin

Vanderah, T. W., Ossipov, M. H., Lai, J. Y., Malan, P. T., & Porreca, F. (2001) · Pain · doi:10.1016/s0304-3959(01)00311-6 · Cited by 271 · see citing works

Cellular mechanisms of opioid tolerance: studies in single brain neurons.

Christie, M. J., Williams, J. T., & NORTH, R. A. (1987) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)13048-4 · Cited by 264 · see citing works

Potentiation of Opiate Analgesia and Apparent Reversal of Morphine Tolerance by Proglumide

Watkins, L. R., Kinscheck, I. B., & Mayer, D. J. (1984) · Science · doi:10.1126/science.6546809 · Cited by 259 · see citing works

Continuous subcutaneous administration of the N -methyl-D-aspartic acid (NMDA) receptor antagonist ketamine in the treatment of post-herpetic neuralgia

Eide, P. K., Stubhaug, A., Øye, I., & Breivik, H. (1995) · Pain · doi:10.1016/0304-3959(94)00182-e · Cited by 257 · see citing works

The role of CCK, caerulein, and CCK antagonists in nociception

Baber, N. S., Dourish, C. T., & Hill, D. R. (1989) · Pain · doi:10.1016/0304-3959(89)90045-6 · Cited by 249 · see citing works

Intrathecal treatment with dextrorphan or ketamine potently reduces pain-related behaviors in a rat model of peripheral mononeuropathy

Mao, J., Price, D. D., Hayes, R. L., Lü, J., Mayer, D. J., & Frenk, H. (1993) · Brain Research · doi:10.1016/0006-8993(93)91368-3 · Cited by 238 · see citing works

Differential roles of NMDA and non-NMDA receptor activation in induction and maintenance of thermal hyperalgesia in rats with painful peripheral mononeuropathy

Mao, J., Price, D. D., Hayes, R. L., Lü, J., & Mayer, D. J. (1992) · Brain Research · doi:10.1016/0006-8993(92)90193-d · Cited by 237 · see citing works

Novel opiate binding sites selective for benzomorphan drugs.

Chang, K. J., Hazum, E., & Cuatrecasas, P. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.7.4141 · Cited by 226 · see citing works

Morphine tolerance as habituation.

Baker, T. B., & Tiffany, S. T. (1985) · Psychological Review · doi:10.1037/0033-295x.92.1.78 · Cited by 223 · see citing works

Homeostatic theory of drug tolerance: a general model of physiological adaptation

Poulos, C. X., & Cappell, H. (1991) · Psychological Review · doi:10.1037/0033-295x.98.3.390 · Cited by 221 · see citing works

Opiate receptor down-regulation and desensitization in neuroblastoma X glioma NG108-15 hybrid cells are two separate cellular adaptation processes.

Law, P., Hom, D. S., & Loh, H. H. (1983) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)14452-0 · Cited by 216 · see citing works

The development of morphine tolerance and dependence is associated with translocation of protein kinase C

Mayer, D. J., Mao, J., & Price, D. D. (1995) · Pain · doi:10.1016/0304-3959(95)00023-l · Cited by 214 · see citing works

Isolation, sequencing, synthesis, and pharmacological characterization of two brain neuropeptides that modulate the action of morphine

Yang (1985) · Medical Entomology and Zoology · Cited by 201 · see citing works

Opiate tolerance and dependence: receptors, G-proteins, and antiopiates

Harrison, L. M., Kastin, A. J., & Zadina, J. E. (1998) · Peptides · doi:10.1016/s0196-9781(98)00126-0 · Cited by 200 · see citing works

Characterization of [Nphe1]nociceptin(1‐13)NH2, a new selective nociceptin receptor antagonist

Calò, G., Guerrini, R., Bigoni, R., Rizzi, A., Marzola, G., Okawa, H., Bianchi, C., Lambert, D. G., Salvadori, S., & Regoli, D. C. (2000) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0703169 · Cited by 190 · see citing works

Glutamate participates in the peripheral modulation of thermal hyperalgesia in rats

Jackson, D. L., Graff, C. B., Richardson, J. D., & Hargreaves, K. (1995) · European Journal of Pharmacology · doi:10.1016/0014-2999(95)00449-u · Cited by 188 · see citing works

Differential effects of morphine on responses of dorsal horn lamina V type cells elicited by A and C fibre stimulation in the spinal cat

Bars, D. L., Guilbaud, G., Jurna, I., & Besson, J. (1976) · Brain Research · doi:10.1016/0006-8993(76)90370-x · Cited by 188 · see citing works

Dynorphin increases in the dorsal spinal cord in rats with a painful peripheral neuropathy

Kajander, K. C., Sahara, Y., Iadarola, M. J., & Bennett, G. J. (1990) · Peptides · doi:10.1016/0196-9781(90)90187-a · Cited by 188 · see citing works

Clinical experience of long–term treatment with epidural and intrathecal opioids – a nationwide survey

Arnér, S., Rawal, N., & Gustafsson, L. L. (1988) · Acta Anaesthesiologica Scandinavica · doi:10.1111/j.1399-6576.1988.tb02725.x · Cited by 184 · see citing works

Acute tolerance associated with a single opiate administration: involvement of N-methyl-d-aspartate-dependent pain facilitatory systems

Larcher, A., Laulin, J., Célèrier, E., Moal, M. L., & Simonnet, G. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00556-3 · Cited by 183 · see citing works

Hyperalgesia during Naloxone-Precipitated Withdrawal from Morphine Is Associated with Increased On-Cell Activity in the Rostral Ventromedial Medulla

Bederson, J. B., Fields, H. L., & Barbaro, N. M. (1990) · Somatosensory & Motor Research · doi:10.3109/08990229009144706 · Cited by 182 · see citing works

Evidence for opiate-activated NMDA processes masking opiate analgesia in rats

Célèrier, E., Laulin, J.-P., Larcher, A., Le Moal, M., & Simonnet, G. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01998-8 · Cited by 182 · see citing works

Fentanyl Enhancement of Carrageenan-induced Long-lasting Hyperalgesia in Rats

Rivat, C., Laulin, J., Corcuff, J., Célèrier, E., Pain, L., & Simonnet, G. (2002) · Anesthesiology · doi:10.1097/00000542-200202000-00025 · Cited by 181 · see citing works

NG-Nitro-L-arginine prevents morphine tolerance

Kolesnikov, Y. A., Pick, C. G., & Pasternak, G. W. (1992) · European Journal of Pharmacology · doi:10.1016/0014-2999(92)90732-j · Cited by 180 · see citing works

Opiate tolerance to daily heroin administration: an apparent phenomenon associated with enhanced pain sensitivity

Laulin, J. P., Célèrier, E., Larcher, A., Le Moal, M., & Simonnet, G. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00652-6 · Cited by 179 · see citing works

Hyperalgesia and myoclonus with intrathecal infusion of high-dose morphine

Conno, F. D., Caraceni, A. T., Martini, C., Spoldi, E., Salvetti, M., & Ventafridda, V. (1991) · Pain · doi:10.1016/0304-3959(91)90225-m · Cited by 175 · see citing works

A review of the role of anti‐opioid peptides in morphine tolerance and dependence

Rothman, R. B. (1992) · Synapse · doi:10.1002/syn.890120206 · Cited by 167 · see citing works

Up-regulation of opioid gene expression in spinal cord evoked by experimental nerve injuries and inflammation

Draisci, G., Kajander, K. C., Dubner, R. A., Bennett, G. J., & Iadarola, M. J. (1991) · Brain Research · doi:10.1016/0006-8993(91)91231-o · Cited by 164 · see citing works

The role of excitatory amino acid receptors and intracellular messengers in persistent nociception after tissue injury in rats

Coderre, T. J. (1993) · Molecular Neurobiology · doi:10.1007/bf02769177 · Cited by 161 · see citing works

Noxious stimuli induce an N -methyl-D-aspartate receptor-dependent hypersensitivity of the flexion withdrawal reflex to touch: implications for the treatment of mechanical allodynia

Ma, Q., & Woolf, C. J. (1995) · Pain · doi:10.1016/0304-3959(94)00195-k · Cited by 159 · see citing works

Long-lasting increased pain sensitivity in rat following exposure to heroin for the first time

Laulin, J., Larcher, A., Célèrier, E., Moal, M. L., & Simonnet, G. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00083.x · Cited by 156 · see citing works

A murine model of opioid-induced hyperalgesia

Li, X., Angst, M. S., & Clark, J. D. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00260-6 · Cited by 155 · see citing works

The NMDA receptor antagonist MK-801 prevents long-lasting non-associative morphine tolerance in the rat

Ben‐Eliyahu, S., Marek, P., Vaccarino, A. L., Mogil, J. S., Sternberg, W. F., & Liebeskind, J. C. (1992) · Brain Research · doi:10.1016/0006-8993(92)90094-p · Cited by 153 · see citing works

Central neural mediators of secondary hyperalgesia following heat injury in rats: Neuropeptides and excitatory amino acids

Coderre, T. J., & Melzack, R. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90339-u · Cited by 149 · see citing works

The spinal loop dialysis catheter: characterization of use in the unanesthetized rat

Maršala, M., Malmberg, A. B., & Yaksh, T. L. (1995) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(95)00053-4 · Cited by 146 · see citing works

Hyperalgesia and myoclonus in terminal cancer patients treated with continuous intravenous morphine

Sjøgren, P., Jonsson, T., Jensen, N., Drenck, N.-E., & Jensen, T. S. (1993) · Pain · doi:10.1016/0304-3959(93)90188-u · Cited by 143 · see citing works

Dynorphin: A possible modulatory peptide on morphine or β-endorphin analgesia in mouse

Friedman, H. J., Jen, M.-F., Chang, J. K., Lee, N. M., & Loh, H. H. (1981) · European Journal of Pharmacology · doi:10.1016/0014-2999(81)90483-0 · Cited by 143 · see citing works

Opioid and anti‐opioid peptides

Cesselin, F. (1995) · Fundamental and Clinical Pharmacology · doi:10.1111/j.1472-8206.1995.tb00517.x · Cited by 142 · see citing works

Continuous co-administration of dextromethorphan or MK-801 with morphine: attenuation of morphine dependence and naloxone-reversible attenuation of morphine tolerance

Manning, B. H., Mao, J., Frenk, H., Price, D. D., & Mayer, D. J. (1996) · Pain · doi:10.1016/0304-3959(96)81972-5 · Cited by 141 · see citing works

Delayed application of MK-801 attenuates development of morphine tolerance in rats

Marek, P., Ben‐Eliyahu, S., Vaccarino, A. L., & Liebeskind, J. C. (1991) · Brain Research · doi:10.1016/0006-8993(91)90736-f · Cited by 141 · see citing works

Inhibition of nitric oxide synthase attenuates the development of morphine tolerance and dependence in mice

Majeed, N. H., Przewłocka, B., Machelska, H., & Przewłocki, R. (1994) · Neuropharmacology · doi:10.1016/0028-3908(94)90006-x · Cited by 140 · see citing works

Increases in protein kinase C gamma immunoreactivity in the spinal cord of rats associated with tolerance to the analgesic effects of morphine

Mao, J., Price, D. D., Phillips, L. L., Lü, J., & Mayer, D. J. (1995) · Brain Research · doi:10.1016/0006-8993(95)00161-i · Cited by 137 · see citing works

Cholecystokinin antagonists selectively potentiate analgesia induced by endogenous opiates

Watkins, L. R., Kinscheck, I. B., Kaufman, E. F. S., Miller, J. W., Frenk, H., & Mayer, D. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)91512-4 · Cited by 136 · see citing works

Opioid-Induced Hyperalgesia and Incisional Pain

Li, X., Angst, M. S., & Clark, J. D. (2001) · Anesthesia & Analgesia · doi:10.1097/00000539-200107000-00040 · Cited by 133 · see citing works

Phencyclidine selectively blocks a spinal action of N-methyl-d-aspartate in mice

Aanonsen, L. M., & Wilcox, G. L. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90396-4 · Cited by 131 · see citing works

Loss of opiate receptor activity in neuroblastoma X glioma NG108-15 hybrid cells after chronic opiate treatment. A multiple-step process.

Law, P., Hom, D. S., & Loh, H. H. (1982) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)14943-2 · Cited by 126 · see citing works

Antagonism at the glycine site on the NMDA receptor reduces spinal nociception in the rat

Dickenson, A. H., & Aydar, E. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90700-4 · Cited by 124 · see citing works

Effects of chronic morphine exposure on opioid inhibition of adenylyl cyclase in 7315c cell membranes: a useful model for the study of tolerance at mu opioid receptors.

Puttfarcken, P. S., Werling, L. L., & Cox, B. M. (1988) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)13363-4 · Cited by 118 · see citing works

Glutamate antagonists prevent morphine withdrawal in mice and guinea pigs

Tanganelli, S., Antonelli, T., Morari, M., Bianchi, C., & Beani, L. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90875-t · Cited by 117 · see citing works

Reduced development of tolerance to the analgesic effects of morphine and clonidine in PKCγ mutant mice

Zeitz, K. P., Malmberg, A. B., Gilbert, H., & Basbaum, A. I. (2001) · Pain · doi:10.1016/s0304-3959(01)00353-0 · Cited by 116 · see citing works

Acute Tolerance in Morphine Analgesia

Kissin, I., Brown, P. T., Robinson, C. A., & Bradley, E. L. (1991) · Anesthesiology · doi:10.1097/00000542-199101000-00025 · Cited by 116 · see citing works

Antinociceptive Potentiation and Attenuation of Tolerance by Intrathecal Co-Infusion of Magnesium Sulfate and Morphine in Rats

McCarthy, R. J., Kroin, J. S., Tuman, K. J., Penn, R. D., & Ivankovich, A. D. (1998) · Anesthesia & Analgesia · doi:10.1097/00000539-199804000-00028 · Cited by 116 · see citing works

Nitric Oxide Synthase Inhibitors Preclinical Studies of Potential Use for Treatment of Opioid Withdrawal

Vaupel, D. B. (1995) · Neuropsychopharmacology · doi:10.1016/0893-133x(95)00138-4 · Cited by 115 · see citing works

Nitric oxide and opioid tolerance

Babey, A., Kolesnikov, Y. A., Cheng, J., Inturrisi, C. E., Trifiletti, R. R., & Pasternak, G. W. (1994) · Neuropharmacology · doi:10.1016/0028-3908(94)90050-7 · Cited by 114 · see citing works

IgG from neuropeptide FF antiserum reverses morphine tolerance in the rat

Lake, J. R., Hammond, M. V., Shaddox, R. C., Hunsicker, L. M., Yang, H.-Y. T., & Malin, D. H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90425-s · Cited by 108 · see citing works

Effects of naloxone and D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 and the protein kinase inhibitors H7 and H8 on acute morphine dependence and antinociceptive tolerance in mice.

Bilsky, E. J., Bernstein, R. N., Wang, Z. J., Sadée, W., & Porreca, F. (1996) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)12847-4 · Cited by 105 · see citing works

Chronic morphine increases μ-opiate receptor binding in rat brain: a quantitative autoradiographic study

Brady, L. S., Herkenham, M. A., Long, J. B., & Rothman, R. B. (1989) · Brain Research · doi:10.1016/0006-8993(89)91432-7 · Cited by 97 · see citing works

NMDA receptor antagonists, MK-801 and ACEA-1011, prevent the development of tonic pain following subcutaneous formalin

Vaccarino, A. L., Marek, P., Kest, B., Weber, E., Keana, J. F. W., & Liebeskind, J. C. (1993) · Brain Research · doi:10.1016/0006-8993(93)90045-o · Cited by 97 · see citing works

The role of cholecystokinin in nociception, neuropathic pain and opiate tolerance

Wiesenfeld‐Hallin, Z., & Xu, X. (1996) · Regulatory Peptides · doi:10.1016/0167-0115(96)00068-7 · Cited by 97 · see citing works

Aids for Easy Venous Cannulation

Jarvis, A. (1986) · Anesthesiology · doi:10.1097/00000542-198610000-00028 · Cited by 96 · see citing works

A novel interaction between dynorphin(1–13) and an N-methyl-d-aspartate site

Caudle, R. M., & Isaac, L. (1988) · Brain Research · doi:10.1016/0006-8993(88)91628-9 · Cited by 94 · see citing works

Morphine tolerance increases μ-noncompetative δ binding sites

Rothman, R. B., Danks, J. A., Jacobson, A. E., Burke, T. R., Rice, K. C., Tortella, F. C., & Holaday, J. W. (1986) · European Journal of Pharmacology · doi:10.1016/0014-2999(86)90130-5 · Cited by 89 · see citing works

Inhibitory influences of mammalian FMRFamide (Phe-Met-Arg-Phe-amide)-related peptides on nociception and morphine- and stress-induced analgesia in mice

Kavaliers, M. (1990) · Neuroscience Letters · doi:10.1016/0304-3940(90)90473-m · Cited by 87 · see citing works

Perspectives on the N-Methyl-?-Aspartate/Nitric Oxide Cascade and Opioid Tolerance

Pasternak, G. W. (1995) · Neuropsychopharmacology · doi:10.1016/0893-133x(95)00084-q · Cited by 87 · see citing works

Opioid antagonists and antisera to endogenous opioids increase the nociceptive response to formalin: demonstration of an opioid kappa and delta inhibitory tone.

Ossipov, M. H., Kovelowski, C. J., Wheeler-Aceto, H., Cowan, A., Hunter, J. C., Lai, J., Malan, T. P., & Porreca, F. (1996) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)12935-2 · Cited by 86 · see citing works

Hyperalgesia Induced by High-Dose Intrathecal Sufentanil in Neuropathic Pain

Devulder, J. (1997) · Journal of Neurosurgical Anesthesiology · doi:10.1097/00008506-199704000-00007 · Cited by 85 · see citing works

Pain facilitatory circuits in the mammalian central nervous system: their behavioral significance and role in morphine analgesic tolerance

McNally, G. P. (1999) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00040-8 · Cited by 84 · see citing works

Chronic administration of morphine and naltrexone up-regulate μ-opioid binding sites labeled by [3H][D-Ala2, MePhe4, Gly-ol5]enkephalin: further evidence for two μ-binding sites

Rothman, R. B., Bykov, V., Long, J. B., Brady, L. S., Jacobson, A. E., Rice, K. C., & Holaday, J. W. (1989) · European Journal of Pharmacology · doi:10.1016/0014-2999(89)90655-9 · Cited by 84 · see citing works

Acute Tolerance to Continuously Infused Alfentanil: The Role of Cholecystokinin and N-Methyl-d-Aspartate-Nitric Oxide Systems

Kissin, I., Bright, C. A., & Bradley, E. L. (2000) · Anesthesia & Analgesia · doi:10.1213/00000539-200007000-00021 · Cited by 82 · see citing works

Biphasic effect on nociception and antiopiate activity of the neuropeptide FF (FLFQPQRFamide) in the rat

Oberling, P., Stinus, L., Moal, M. L., & Simonnet, G. (1993) · Peptides · doi:10.1016/0196-9781(93)90067-q · Cited by 79 · see citing works

Preemptive Hyperalgesia, Not Analgesia?

Eisenach, J. C. (2000) · Anesthesiology · doi:10.1097/00000542-200002000-00009 · Cited by 78 · see citing works

Morphine analgesia and acute physical dependence: rapid onset of two opposing, dose-related processes

Kim, D., Fields, H. L., & Barbaro, N. M. (1990) · Brain Research · doi:10.1016/0006-8993(90)90894-h · Cited by 75 · see citing works

Spinal dynorphin A (1–17): Possible mediator of antianalgesic action

Fujimoto, J. M., Arts, K. S., Rady, J. J., & Tseng, L. F. (1990) · Neuropharmacology · doi:10.1016/0028-3908(90)90021-i · Cited by 72 · see citing works

N‐methyl‐ d ‐aspartate receptor antagonists potentiate morphine's antinociceptive effect in the rat

Grass, S. V., Hoffmann, O. I., Xu, X., & Wiesenfeld‐Hallin, Z. (1996) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1996.566309000.x · Cited by 71 · see citing works

Differential regulation of mu and delta opiate receptors by morphine, selective agonists and antagonists and differentiating agents in SH-SY5Y human neuroblastoma cells.

Zadina, J. E., Harrison, L. M., Ge, L.-J., Kastin, A. J., & Chang, S. L. (1994) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)22512-5 · Cited by 68 · see citing works

Accelerated release and production of orphanin FQ in brain of chronic morphine tolerant rats

Li, Y., Zhou, H., Chang, J.-K., & Han, J.-S. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01337-2 · Cited by 67 · see citing works

The effects of the clinically tested NMDA receptor antagonist memantine on carrageenan-induced thermal hyperalgesia in rats

Eisenberg, E., LaCross, S., & Strassman, A. M. (1994) · European Journal of Pharmacology · doi:10.1016/0014-2999(94)90090-6 · Cited by 67 · see citing works

Spinal opioid systems in inflammation

Stanfa, L. C., & Dickenson, A. H. (1995) · Inflammation Research · doi:10.1007/bf01782974 · Cited by 64 · see citing works

Ultrastructural analysis of dynorphin B–immunoreactive cells and terminals in the superficial dorsal horn of the deafferented spinal cord of the rat

Cho, H. J., & Basbaum, A. I. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902810204 · Cited by 60 · see citing works

Attenuation of tolerance to, and physical dependence on, morphine in the rat by inhibition of nitric oxide synthase

Bhargava, H. N. (1995) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(94)00271-n · Cited by 59 · see citing works

Time Course Characteristics of Acute Tolerance Development to Continuously Infused Alfentanil in Rats

Kissin, I., Lee, S. S., Arthur, G. R., & Bradley, E. L. (1996) · Anesthesia & Analgesia · doi:10.1097/00000539-199609000-00029 · Cited by 58 · see citing works

Differential inhibitory/stimulatory modulation of spinal CCK release by μ and δ opioid agonists, and selective blockade of μ-dependent inhibition by κ receptor stimulation

Benoliel, J. J., Bourgoin, S., Mauborgne, A., Legrand, J. C., Hamon, M., & Cesselin, F. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90094-a · Cited by 57 · see citing works

Simultaneous activation of spinal antiopioid system (neuropeptide FF) and pain facilitatory circuitry by stimulation of opioid receptors in rats

Devillers, J.-P., Boisserie, F., Laulin, J., Larcher, A., & Simonnet, G. (1995) · Brain Research · doi:10.1016/0006-8993(95)00948-p · Cited by 54 · see citing works

Great Expectations

Maren, T. H. (1982) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.22.040182.000245 · Cited by 52 · see citing works

Potentiation of morphine-induced antinociception in acute spinal rats by the NMDA antagonist dextrorphan

Advokat, C. D., & Rhein, F. Q. (1995) · Brain Research · doi:10.1016/0006-8993(95)01023-o · Cited by 50 · see citing works

The antinociceptive effect of combined systemic administration of morphine and the glycine/NMDA receptor antagonist, (+)‐HA966 in a rat model of peripheral neuropathy

Christensen, D., Idänpään-Heikkilä, J. J., Guilbaud, G., & Kayser, V. (1998) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0702240 · Cited by 47 · see citing works

Opioidergic control of the spinal release of neuropeptides. Possible significance for the analgesic effects of opioids

Bourgoin, S., Benoliel, J. J., Collin, E., Mauborgne, A., Pohl, M., Hamon, M., & Cesselin, F. (1994) · Fundamental and Clinical Pharmacology · doi:10.1111/j.1472-8206.1994.tb00809.x · Cited by 47 · see citing works

Dextromethorphan potentiates morphine antinociception, but does not reverse tolerance in rats

Hoffmann, O. I., & Wiesenfeld‐Hallin, Z. (1996) · Neuroreport · doi:10.1097/00001756-199602290-00037 · Cited by 40 · see citing works

The development of pain-related behaviour and opioid tolerance after neuropathy-inducing surgery and sham surgery

Christensen, D., & Kayser, V. (2000) · Pain · doi:10.1016/s0304-3959(00)00334-1 · Cited by 40 · see citing works

Spinal cord nitric oxide synthase and heme oxygenase limit morphine induced analgesia

Li, X., & Clark, J. D. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00251-0 · Cited by 40 · see citing works

The difference between methadone and morphine in regulation of δ-opioid receptors underlies the antagonistic effect of methadone on morphine-mediated cellular actions

Liu, J., Liao, X.-P., Gong, Z., & Qin, B.-Y. (1999) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00270-8 · Cited by 37 · see citing works

The nociceptin/orphanin FQ receptor antagonist, [Nphe1]NC(1-13)NH2, potentiates morphine analgesia

Rizzi, A., Bigoni, R., Marzola, G., Guerrini, R., Salvadori, S., Regoli, D. C., & Calò, G. (2000) · Neuroreport · doi:10.1097/00001756-200008030-00007 · Cited by 35 · see citing works

ACEA-1328, A NMDA RECEPTOR/GLYCINE SITE ANTAGONIST, ACUTELY POTENTIATES ANTINOCICEPTION AND CHRONICALLY ATTENUATES TOLERANCE INDUCED BY MORPHINE

Lutfy, K., DOAN, P., & Weber, E. (1999) · Pharmacological Research · doi:10.1006/phrs.1999.0538 · Cited by 34 · see citing works

Prolongation of morphine analgesia by competitive NMDA receptor antagonist d-CPPene (SDZ EAA 494) in rats

Bespalov, A., Kudryashova, M. F., & Zvartau, E. E. (1998) · European Journal of Pharmacology · doi:10.1016/s0014-2999(98)00324-0 · Cited by 32 · see citing works

Methadone-induced desensitization of the δ-opioid receptor is mediated by uncoupling of receptor from G protein

Liu, J., Liao, X.-P., Gong, Z., & Qin, B.-Y. (1999) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00322-2 · Cited by 32 · see citing works

Demonstration of dynorphin A 1–8 immunoreactive axons contacting spinal cord projection neurons in a rat model of peripheral inflammation and hyperalgesia

Nahin, R. L., Hylden, J. L. K., & Humphrey, E. (1992) · Pain · doi:10.1016/0304-3959(92)90254-9 · Cited by 32 · see citing works

Nociceptin receptors in the rat spinal cord during morphine tolerance

Gouardères, C., Tafani, J. A. M., Meunier, J., Jhamandas, K. H., & Zajac, J. ‐. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01713-8 · Cited by 31 · see citing works

Effect of 7-Nitroindazole on Tolerance to Morphine, U-50,488H and [ d -Pen 2 , d -Pen 5 ]Enkephalin in Mice

Bhargava, H. N., Cao, Y., & Zhao, G. (1997) · Peptides · doi:10.1016/s0196-9781(97)00021-1 · Cited by 31 · see citing works

Interaction of morphine and naloxone in acute spinal cats

Goldfarb, J., KAPLAN, E., & Jenkins, H. R. (1978) · Neuropharmacology · doi:10.1016/0028-3908(78)90150-8 · Cited by 29 · see citing works

Antinociceptive activity of combination of morphine and NMDA receptor antagonists depends on the inter-injection interval

Владимировна, Б. И., Драволина, О. А., Neznanova, O., Danysz, W., & Bespalov, A. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00184-9 · Cited by 29 · see citing works

N-Methyl-d-Aspartate Receptor Antagonists Potentiate the Antinociceptive Effects of Morphine in Squirrel Monkeys

Allen, R. M., & Dykstra, L. (2001) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)29380-0 · Cited by 29 · see citing works

Enhancement of morphine actions in morphine-naive and morphine-tolerant mice by LY 235959, a competitive antagonist of the NMDA receptor

Bhargava, H. N. (1997) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(96)00163-2 · Cited by 28 · see citing works

Nitric oxide synthase inhibition attenuates tolerance to morphine but not to [d-Ala2,Glu4]deltorphin II, a δ2-Opioid receptor agonist in mice

Zhao, G., & Bhargava, H. N. (1996) · Peptides · doi:10.1016/0196-9781(96)00073-3 · Cited by 28 · see citing works

The Effects of Midazolam in Propofol-Induced Anesthesia

Vinik, H. R. (1998) · Anesthesia & Analgesia · doi:10.1097/00000539-199805000-00055 · Cited by 28 · see citing works

Functional studies using antibodies against orphanin FQ/nociceptin

Tian, J., & Han, J. (2000) · Peptides · doi:10.1016/s0196-9781(00)00242-4 · Cited by 27 · see citing works

Release of Neuropeptide FF, an Anti‐Opioid Peptide, in Rat Spinal Cord Slices Is Voltage‐ and Ca2+‐Sensitive: Possible Involvement of P‐Type Ca2+ Channels

Devillers, J.-P., Labrouche, S., Castes, E., & Simonnet, G. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.64041567.x · Cited by 27 · see citing works

Dextromethorphan Potentiates the Antinociceptive Effects of Morphine and the δ-Opioid Agonist SNC80 in Squirrel Monkeys

Allen, R. M., Granger, A. L., & Dykstra, L. (2002) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.300.2.435 · Cited by 20 · see citing works

A single injection of diazepam induces long-lasting sensitization.

Antelman, S. M., Kocan, D. J., Dj, E., & Knopf, S. (1987) · PubMed · Cited by 19 · see citing works

Modulation of neuropeptide FF release from rat spinal cord slices by glutamate. Involvement of NMDA receptors

Devillers, J.-P., & Simonnet, G. (1994) · European Journal of Pharmacology · doi:10.1016/0014-2999(94)90279-8 · Cited by 18 · see citing works

The Potentiation of Morphine‐induced Inhibition of Spinal Transmission by Proglumide, a Putative Cholecystokinin Antagonista

Suberg, S. N., Culhane, E. S., Carstens, E., & Watkins, L. R. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb29980.x · Cited by 18 · see citing works

Acute Tolerance to the Hypnotic Effect of Morphine in Rats

Kissin, I., Brown, P. T., Robinson, C. A., & Bradley, E. L. (1991) · Anesthesia & Analgesia · doi:10.1213/00000539-199111000-00018 · Cited by 5 · see citing works

Opioid-induced Hyperalgesia: A Qualitative Systematic Review

Angst, M. S., & Clark, J. D. (2006) · Anesthesiology · doi:10.1097/00000542-200603000-00025 · Cited by 1,188 · see citing works

Opioid use disorder

Strang, J., Volkow, N. D., Degenhardt, L., Hickman, M., Johnson, K., Koob, G. F., Marshall, B. D. L., Tyndall, M., & Walsh, S. L. (2020) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0137-5 · Cited by 639 · see citing works

Opioid-induced Hyperalgesia in Humans

Chu, L. F., Angst, M. S., & Clark, J. D. (2008) · Clinical Journal of Pain · doi:10.1097/ajp.0b013e31816b2f43 · Cited by 572 · see citing works

Neurobiology of opioid addiction: Opponent process, hyperkatifeia, and negative reinforcement

Koob, G. F. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.05.023 · Cited by 477 · see citing works

Alcohol dependence as a chronic pain disorder

Egli, M., Koob, G. F., & Edwards, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.07.010 · Cited by 347 · see citing works

Drug Addiction: Hyperkatifeia/Negative Reinforcement as a Framework for Medications Development

Koob, G. F. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000083 · Cited by 337 · see citing works

Five days at outdoor education camp without screens improves preteen skills with nonverbal emotion cues

Uhls, Y. T., Michikyan, M., Morris, J., Garcia, D., Small, G. W., Zgourou, E., & Greenfield, P. M. (2014) · Computers in Human Behavior · doi:10.1016/j.chb.2014.05.036 · Cited by 257 · see citing works

Long-Term Potentiation in Spinal Nociceptive Pathways as a Novel Target for Pain Therapy

Ruscheweyh, R., Wilder‐Smith, O. H. G., Drdla-Schutting, R., Liu, X., & Sandkühler, J. (2011) · Molecular Pain · doi:10.1186/1744-8069-7-20 · Cited by 236 · see citing works

RF9, a potent and selective neuropeptide FF receptor antagonist, prevents opioid-induced tolerance associated with hyperalgesia

Simonin, F., Schmitt, M., Laulin, J., Laboureyras, E., Jhamandas, J. H., MacTavish, D., Matifas, A., Mollereau, C., Laurent, P., Parmentier, M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502090103 · Cited by 232 · see citing works

Different profiles of buprenorphine-induced analgesia and antihyperalgesia in a human pain model

Koppert, W., Ihmsen, H., Körber, N., Wehrfritz, A., Sittl, R., Schmelz, M., & Schüttler, J. (2005) · Pain · doi:10.1016/j.pain.2005.06.030 · Cited by 226 · see citing works

Remifentanil tolerance and hyperalgesia: short‐term gain, long‐term pain?

Yu, H., Tran, D. H. D., Lam, S. W., & Irwin, M. G. (2016) · Anaesthesia · doi:10.1111/anae.13602 · Cited by 225 · see citing works

Postoperative Hyperalgesia

Wilder‐Smith, O. H. G., & Arendt‐Nielsen, L. (2006) · Anesthesiology · doi:10.1097/00000542-200603000-00028 · Cited by 219 · see citing works

What Do Mirror Neurons Contribute to Human Social Cognition?

Jacob, P. (2008) · Mind & Language · doi:10.1111/j.1468-0017.2007.00337.x · Cited by 215 · see citing works

Spatial frequencies or emotional effects?

Delplanque, S., N’Diaye, K., Scherer, K. R., & Grandjean, D. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.05.030 · Cited by 209 · see citing works

Understanding endorphins and their importance in pain management.

Sprouse‐Blum, A. S., Smith, G., Sugai, D. Y., & Parsa, F. D. (2010) · Europe PMC (PubMed Central) · Cited by 193 · see citing works

Arousal and valence effects on event-related P3a and P3b during emotional categorization

Delplanque, S., Silvert, L., Hot, P., Rigoulot, S., & Sequeira, H. (2005) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.06.006 · Cited by 187 · see citing works

Do Opioids Induce Hyperalgesia in Humans? An Evidence-Based Structured Review

Fishbain, D. A., Cole, B., Lewis, J. E., Gao, J., & Rosomoff, R. S. (2009) · Pain Medicine · doi:10.1111/j.1526-4637.2009.00653.x · Cited by 167 · see citing works

The dark side of opioids in pain management: basic science explains clinical observation

Rivat, C., & Ballantyne, J. (2016) · PAIN Reports · doi:10.1097/pr9.0000000000000570 · Cited by 160 · see citing works

Opioid-free anesthesia opioid side effects: Tolerance and hyperalgesia

Lavand'homme, P. M., & Steyaert, A. (2017) · Best practice & research. Clinical anaesthesiology · doi:10.1016/j.bpa.2017.05.003 · Cited by 166 · see citing works

The Physiology of Pain Mechanisms: From the Periphery to the Brain

Marchand, S. (2008) · Rheumatic Disease Clinics of North America · doi:10.1016/j.rdc.2008.04.003 · Cited by 165 · see citing works

Preoperative Chronic Opioid Therapy

Jain, N. K., Phillips, F. M., Weaver, T. E., & Khan, S. N. (2018) · Spine · doi:10.1097/brs.0000000000002609 · Cited by 163 · see citing works

Sciatic nerve cuffing in mice: A model of sustained neuropathic pain

Benbouzid, M., Pallage, V., Rajalu, M., Waltisperger, E., Doridot, S., Poisbeau, P., Freund‐Mercier, M. J., & Barrot, M. (2007) · European Journal of Pain · doi:10.1016/j.ejpain.2007.10.002 · Cited by 164 · see citing works

Development of mechanical hypersensitivity in rats during heroin and ethanol dependence: Alleviation by CRF1 receptor antagonism

Edwards, S., Vendruscolo, L. F., Schlosburg, J. E., Misra, K., Wee, S., Park, P. E., Schulteis, G., & Koob, G. F. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.006 · Cited by 158 · see citing works

Neural Basis for the Hyperalgesic Action of Cholecystokinin in the Rostral Ventromedial Medulla

Heinricher, M. M., & Neubert, M. J. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00411.2004 · Cited by 158 · see citing works

The impact of opioid-induced hyperalgesia for postoperative pain

Koppert, W., & Schmelz, M. (2007) · Best Practice & Research Clinical Anaesthesiology · doi:10.1016/j.bpa.2006.12.004 · Cited by 154 · see citing works

Intraoperative use of remifentanil and opioid induced hyperalgesia/acute opioid tolerance: systematic review

Kim, S. H., Stoicea, N., Soghomonyan, S., & Bergese, S. D. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00108 · Cited by 147 · see citing works

Therapeutic manipulation of peroxynitrite attenuates the development of opiate-induced antinociceptive tolerance in mice

Muscoli, C., Cuzzocrea, S., Ndengele, M. M., Mollace, V., Porreca, F., Fabrizi, F., Esposito, E., Masini, E., Matuschak, G. M., & Salvemini, D. (2007) · Journal of Clinical Investigation · doi:10.1172/jci32420 · Cited by 145 · see citing works

Non-Nociceptive Environmental Stress Induces Hyperalgesia, Not Analgesia, in Pain and Opioid-Experienced Rats

Rivat, C., Laboureyras, E., Laulin, J., Roy, C. L., Richebé, P., & Simonnet, G. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301340 · Cited by 145 · see citing works

Ketamine Improves the Management of Exaggerated Postoperative Pain Observed in Perioperative Fentanyl-treated Rats

Richebé, P., Rivat, C., Laulin, J., Maurette, P., & Simonnet, G. (2005) · Anesthesiology · doi:10.1097/00000542-200502000-00028 · Cited by 138 · see citing works

Opioid-induced Hyperalgesia in a Murine Model of Postoperative Pain

Célèrier, E., González, J. R., Maldonado, R. J., Cabañero, D., & Puig, M. M. (2006) · Anesthesiology · doi:10.1097/00000542-200603000-00023 · Cited by 137 · see citing works

Increased pain sensitivity in alcohol withdrawal syndrome

Jochum, T., Boettger, M. K., Burkhardt, C., Juckel, G., & Bär, K. (2010) · European Journal of Pain · doi:10.1016/j.ejpain.2009.11.008 · Cited by 128 · see citing works

Maturational effects on newborn ERPs measured in the mismatch negativity paradigm

Leppänen, P. H. T., Guttorm, T. K., Pihko, E., Takkinen, S., Eklund, K., & Lyytinen, H. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.06.002 · Cited by 126 · see citing works

Modulation of Remifentanil-induced Analgesia and Postinfusion Hyperalgesia by Parecoxib in Humans

Tröster, A., Sittl, R., Singler, B., Schmelz, M., Schüttler, J., & Koppert, W. (2006) · Anesthesiology · doi:10.1097/00000542-200611000-00024 · Cited by 124 · see citing works

Nitrous Oxide Revisited

Richebé, P., Rivat, C., Creton, C., Laulin, J., Maurette, P., Lemaire, M., & Simonnet, G. (2005) · Anesthesiology · doi:10.1097/00000542-200510000-00024 · Cited by 123 · see citing works

Psychophysiology of developmental dyslexia: a review of findings including studies of children at risk for dyslexia

Lyytinen, H., Guttorm, T. K., Huttunen-Scott, T., Hämäläinen, J. A., Leppänen, P. H. T., & Vesterinen, M. (2005) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2004.11.001 · Cited by 115 · see citing works

The clinical role of NMDA receptor antagonists for the treatment of postoperative pain

Kock, M. F. D., & Lavand'homme, P. M. (2007) · Best practice & research. Clinical anaesthesiology · doi:10.1016/j.bpa.2006.12.006 · Cited by 116 · see citing works

Modulation of Remifentanil-Induced Postinfusion Hyperalgesia by Propofol

Singler, B., Tröster, A., Manering, N. A., Schüttler, J., & Koppert, W. (2007) · Anesthesia & Analgesia · doi:10.1213/01.ane.0000261305.22324.f3 · Cited by 115 · see citing works

Homing in on consciousness in the nervous system: An action-based synthesis

Morsella, E., Godwin, C. A., Jantz, T. K., Krieger, S. C., & Gazzaley, A. H. (2015) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15000643 · Cited by 116 · see citing works

Intravenous morphine titration to treat severe pain in the ED

Lvovschi, V.-E., Aubrun, F., Bonnet, P., Bouchara, A., Bendahou, M., Humbert, B., Hausfater, P., & Riou, B. (2008) · The American Journal of Emergency Medicine · doi:10.1016/j.ajem.2007.10.025 · Cited by 112 · see citing works

Local Anesthetic-like Inhibition of Voltage-gated Na+Channels by the Partial μ-opioid Receptor Agonist Buprenorphine

Leffler, A., Frank, G., Kistner, K., Niedermirtl, F., Koppert, W., Reeh, P. W., & Nau, C. (2012) · Anesthesiology · doi:10.1097/aln.0b013e3182557917 · Cited by 109 · see citing works

Computational correlates of consciousness

Cleeremans, A. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(05)50007-4 · Cited by 108 · see citing works

Chronic preoperative opioid use is a risk factor for increased complications, resource use, and costs after cervical fusion

Jain, N. K., Brock, J. L., Phillips, F. M., Weaver, T. E., & Khan, S. N. (2018) · The Spine Journal · doi:10.1016/j.spinee.2018.03.015 · Cited by 108 · see citing works

Predictive Factors of Severe Postoperative Pain in the Postanesthesia Care Unit

Aubrun, F., Valade, N., Coriat, P., & Riou, B. (2008) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e318168b2ce · Cited by 108 · see citing works

Naloxone provokes similar pain facilitation as observed after short-term infusion of remifentanil in humans

Koppert, W., Angst, M. S., Alsheimer, M., Sittl, R., Albrecht, S., Schüttler, J., & Schmelz, M. (2003) · Pain · doi:10.1016/s0304-3959(03)00294-x · Cited by 106 · see citing works

Management of chronic pain in the elderly: focus on transdermal buprenorphine

Vadivelu, N., & Hines, R. L. (2008) · Clinical Interventions in Aging · doi:10.2147/cia.s1880 · Cited by 103 · see citing works

Opioid-Induced Hyperalgesia and Tolerance

Bekhit, M. H. (2010) · American Journal of Therapeutics · doi:10.1097/mjt.0b013e3181ed83a0 · Cited by 99 · see citing works

The cerebellum, internal models and prediction in ‘non-motor’ aspects of language: A critical review

Argyropoulos, G. P. D. (2015) · Brain and Language · doi:10.1016/j.bandl.2015.08.003 · Cited by 103 · see citing works

Supra-additive effects of tramadol and acetaminophen in a human pain model ☆

Filitz, J., Ihmsen, H., Günther, W., Tröster, A., Schwilden, H., Schüttler, J., & Koppert, W. (2007) · Pain · doi:10.1016/j.pain.2007.06.036 · Cited by 94 · see citing works

Counter-Regulation of Opioid Analgesia by Glial-Derived Bioactive Sphingolipids

Muscoli, C., Doyle, T. M., Dagostino, C., Bryant, L., Chen, Z., Watkins, L. R., Ryerse, J. S., Bieberich, E., Neumman, W., & Salvemini, D. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2391-10.2010 · Cited by 92 · see citing works

Opioid-free anesthesia

Lavand'homme, P. M., & Estèbe, J.-P. (2018) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0000000000000632 · Cited by 91 · see citing works

Involvement of neuropeptide FF receptors in neuroadaptive responses to acute and chronic opiate treatments

Elhabazi, K., Trigo, J., Mollereau, C., Moulédous, L., Zajac, J., Bihel, F. J. ‐., Schmitt, M., Bourguignon, J., Méziane, H., Petit‐Demoulière, B., et al. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01563.x · Cited by 87 · see citing works

Refractory dependence on opioid analgesics

Ballantyne, J. C., Sullivan, M. D., & Koob, G. F. (2019) · Pain · doi:10.1097/j.pain.0000000000001680 · Cited by 81 · see citing works

The Use of Very-Low-Dose Methadone for Palliative Pain Control and the Prevention of Opioid Hyperalgesia

Salpeter, S. R., Buckley, J. S., & Bruera, E. D. (2013) · Journal of Palliative Medicine · doi:10.1089/jpm.2012.0612 · Cited by 80 · see citing works

A Qualitative Systematic Review

Angst, M. S., & Clark, J. D. (2006) · Cited by 79 · see citing works

RF-amide neuropeptides and their receptors in Mammals: Pharmacological properties, drug development and main physiological functions

Quillet, R., Ayachi, S., Bihel, F. J. ‐., Elhabazi, K., Ilien, B., & Simonin, F. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.02.005 · Cited by 80 · see citing works

Characterization of morphine-induced hyperalgesia in male and female rats

Holtman, J. R., & Wala, E. P. (2005) · Pain · doi:10.1016/j.pain.2004.11.014 · Cited by 78 · see citing works

Polyamine deficient diet to relieve pain hypersensitivity

Rivat, C., Richebé, P., Laboureyras, E., Laulin, J., Havouis, R., Noble, F., Moulinoux, J.-P., & Simonnet, G. (2007) · Pain · doi:10.1016/j.pain.2007.08.021 · Cited by 77 · see citing works

Opioid-induced hyperalgesia in a mice model of orthopaedic pain: preventive effect of ketamine

Minville, V., Fourcade, O., Girolami, J., & Tack, I. (2009) · British Journal of Anaesthesia · doi:10.1093/bja/aep363 · Cited by 77 · see citing works

Nociception increases during opioid infusion in opioid receptor triple knock-out mice

Juni, A., Klein, G. E., Pintar, J. E., & Kest, B. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.04.030 · Cited by 75 · see citing works

Oxycodone Plus Ultra-Low-Dose Naltrexone Attenuates Neuropathic Pain and Associated μ-Opioid Receptor–Gs Coupling

Largent‐Milnes, T. M., Guo, W., Wang, H.-Y., Burns, L. H., & Vanderah, T. W. (2008) · Journal of Pain · doi:10.1016/j.jpain.2008.03.005 · Cited by 74 · see citing works

The striatum and probabilistic implicit sequence learning

Wilkinson, L., & Jahanshahi, M. (2006) · Brain Research · doi:10.1016/j.brainres.2006.12.051 · Cited by 75 · see citing works

Is Altered Central Pain Processing Related to Disease Stage in Chronic Pancreatitis Patients with Pain? An Exploratory Study

Bouwense, S. A. W., Olesen, S. S., Drewes, A. M., Frøkjær, J. B., van Goor, H., & Wilder‐Smith, O. H. G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055460 · Cited by 74 · see citing works

Targeting Opioid-Induced Hyperalgesia in Clinical Treatment: Neurobiological Considerations

Arout, C. A., Edens, E., Petrakis, I. L., & Sofuoglu, M. (2015) · CNS Drugs · doi:10.1007/s40263-015-0255-x · Cited by 80 · see citing works

NMDA receptor antagonism disrupts the development of morphine analgesic tolerance in male, but not female C57BL/6J mice

Bryant, C. D., Eitan, S., Sinchak, K., Fanselow, M. S., & Evans, C. J. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00831.2005 · Cited by 72 · see citing works

Chronic<scp>CRF</scp>₁receptor blockade reduces heroin intake escalation and dependence‐induced hyperalgesia

Park, P. E., Schlosburg, J. E., Vendruscolo, L. F., Schulteis, G., Edwards, S., & Koob, G. F. (2015) · Addiction Biology · doi:10.1111/adb.12120 · Cited by 69 · see citing works

Why mu‐opioid agonists have less analgesic efficacy in neuropathic pain?

Martínez‐Navarro, M., Maldonado, R. J., & Baños, J.-E. (2018) · European Journal of Pain · doi:10.1002/ejp.1328 · Cited by 65 · see citing works

Spinal NK‐1 receptor‐expressing neurons and descending pathways support fentanyl‐induced pain hypersensitivity in a rat model of postoperative pain

Rivat, C., Vera–Portocarrero, L. P., Ibrahim, M. M., Mata, H. P., Stagg, N. J., Felice, M. D., Porreca, F., & Malan, T. P. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06616.x · Cited by 65 · see citing works

Sex-specific Mediation of Opioid-induced Hyperalgesia by the Melanocortin-1 Receptor

Juni, A., Cai, M., Staňková, M., Waxman, A. R., Arout, C. A., Klein, G. E., Dahan, A., Hruby, V. J., Mogil, J. S., & Kest, B. (2009) · Anesthesiology · doi:10.1097/aln.0b013e3181c53849 · Cited by 64 · see citing works

The importance of communication in the management of postoperative pain.

Sugai, D. Y., Deptula, P. L., Parsa, A. A., & Parsa, F. D. (2013) · Europe PMC (PubMed Central) · Cited by 64 · see citing works

Morphine hyperalgesia in mice is unrelated to opioid activity, analgesia, or tolerance: Evidence for multiple diverse hyperalgesic systems

Juni, A., Klein, G. E., & Kest, B. (2006) · Brain Research · doi:10.1016/j.brainres.2005.11.054 · Cited by 64 · see citing works

Genetic variants of the P-glycoprotein gene Abcb1b modulate opioid-induced hyperalgesia, tolerance and dependence

Liang, D., Liao, G., Lighthall, G., Peltz, G., & Clark, J. D. (2006) · Pharmacogenetics and Genomics · doi:10.1097/01.fpc.0000236321.94271.f8 · Cited by 62 · see citing works

Long-term Potentiation at Spinal C-fiber Synapses: A Target for Pathological Pain

Liu, X., & Zhou, L. (2014) · Current Pharmaceutical Design · doi:10.2174/1381612820666141027115949 · Cited by 61 · see citing works

Buprenorphine-induced hyperalgesia in the rat

Wala, E. P., & Holtman, J. R. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.10.083 · Cited by 59 · see citing works

Involvement of Mammalian RF-Amide Peptides and Their Receptors in the Modulation of Nociception in Rodents

Ayachi, S., & Simonin, F. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00158 · Cited by 58 · see citing works

Low dose of S(+)-ketamine prevents long-term potentiation in pain pathways under strong opioid analgesia in the rat spinal cord in vivo

Benrath, J., Brechtel, C., Stark, J., & Sandkühler, J. (2005) · British Journal of Anaesthesia · doi:10.1093/bja/aei215 · Cited by 58 · see citing works

Kétamine à faibles doses : antihyperalgésique, non analgésique

Richebé, P., Rivat, C., Rivalan, B., Maurette, P., & Simonnet, G. (2005) · Annales Françaises d Anesthésie et de Réanimation · doi:10.1016/j.annfar.2005.07.069 · Cited by 59 · see citing works

Imaging opioid analgesia in the human brain and its potential relevance for understanding opioid use in chronic pain.

Lee, M. C., Wanigasekera, V., & Tracey, I. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.06.035 · Cited by 56 · see citing works

Sex differences in hyperalgesia during morphine infusion: Effect of gonadectomy and estrogen treatment

Juni, A., KLEIN, G., Kowalczyk, W. J., Ragnauth, A. K., & Kest, B. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.04.004 · Cited by 56 · see citing works

Low-dose ketamine infusion reduces postoperative hydromorphone requirements in opioid-tolerant patients following spinal fusion: A randomised controlled trial

Boenigk, K., Echevarria, G. C., Nisimov, E., von Bergen Granell, A. E., Cuff, G. E., Wang, J., & Atchabahian, A. (2019) · European Journal of Anaesthesiology · doi:10.1097/eja.0000000000000877 · Cited by 55 · see citing works

Long-Term Pain Vulnerability After Surgery in Rats: Prevention by Nefopam, an Analgesic with Antihyperalgesic Properties

Laboureyras, E., Chateauraynaud, J., Richebé, P., & Simonnet, G. (2009) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e3181aa956b · Cited by 55 · see citing works

Opioid-induced hyperalgesia: a review of epidemiology, mechanisms and management.

Low, Y., Clarke, C. F. M., & Huh, B. (2012) · PubMed · Cited by 55 · see citing works

Prediction based on preoperative opioid use of clinical outcomes after transforaminal lumbar interbody fusions

Villavicencio, A. T., Nelson, E. L., Kantha, V., & Burneikienė, S. (2016) · Journal of Neurosurgery Spine · doi:10.3171/2016.7.spine16284 · Cited by 55 · see citing works

Perioperative pain

Lavand'homme, P. M. (2006) · Current Opinion in Anaesthesiology · doi:10.1097/01.aco.0000245284.53152.1f · Cited by 55 · see citing works

Characterization of the antinociceptive effect of oxycodone in male and female rats

Holtman, J. R., & Wala, E. P. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2005.12.013 · Cited by 54 · see citing works

Opioid-induzierte Hyperalgesie

Koppert, W. (2004) · Der Anaesthesist · doi:10.1007/s00101-004-0669-1 · Cited by 51 · see citing works

Opioids: From analgesia to anti-hyperalgesia?

Simonnet, G. (2005) · Pain · doi:10.1016/j.pain.2005.07.021 · Cited by 54 · see citing works

Auditory frequency-following response: A neurophysiological measure for studying the “cocktail-party problem”

Du, Y., Kong, L. Z., Wang, Q., Wu, X. H., & Li, L. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.05.008 · Cited by 53 · see citing works

Negative affect heightens opiate withdrawal-induced hyperalgesia in heroin dependent individuals

Carcoba, L. M., Contreras, A. E., Cepeda-Benito, A., & Meagher, M. W. (2011) · Journal of Addictive Diseases · doi:10.1080/10550887.2011.581985 · Cited by 52 · see citing works

Pharmacological management of pain in chronic pancreatitis

VANESCH, A., Wilder‐Smith, O. H. G., Jansen, J. B. �. �., VANGOOR, H., & Drenth, J. P. H. (2006) · Digestive and Liver Disease · doi:10.1016/j.dld.2006.02.002 · Cited by 52 · see citing works

Opioid hyperalgesia and tolerance versus 5-HT1A receptor-mediated inverse tolerance

Xu, X., Colpaert, F. C., & Wiesenfeld‐Hallin, Z. (2003) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2003.10.005 · Cited by 51 · see citing works

Characterization of the Antinociceptive and Pronociceptive Effects of Methadone in Rats

Holtman, J. R., & Wala, E. P. (2007) · Anesthesiology · doi:10.1097/00000542-200703000-00022 · Cited by 49 · see citing works

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities

Elhabazi, K., Ayachi, S., Ilien, B., & Simonin, F. (2014) · Journal of Visualized Experiments · doi:10.3791/51264 · Cited by 46 · see citing works

Predictors of pain relief and adverse events in patients receiving opioids in a prehospital setting

Bounes, V., Barniol, C., Minville, V., Houze‐Cerfon, C., & Ducassé, J.-L. (2010) · The American Journal of Emergency Medicine · doi:10.1016/j.ajem.2009.12.005 · Cited by 46 · see citing works

The brain on opioids

Ballantyne, J. C. (2018) · Pain · doi:10.1097/j.pain.0000000000001270 · Cited by 44 · see citing works

Surgery in Chronic Pancreatitis: Indication, Timing and Procedures

Bouwense, S. A. W., Kempeneers, M. A., van Santvoort, H. C., Boermeester, M. A., van Goor, H., Besselink, M. G., & Dutch Pancreatitis Study Group (2019) · Visceral Medicine · doi:10.1159/000499612 · Cited by 44 · see citing works

Buprenorphine in Postoperative Pain Management

Vadivelu, N., & Anwar, M. A. F. (2010) · Anesthesiology Clinics · doi:10.1016/j.anclin.2010.08.015 · Cited by 44 · see citing works

Opioid-induced hyperalgesia—Pathophysiology and clinical relevance

Koppert, W. (2007) · Acute Pain · doi:10.1016/j.acpain.2006.11.001 · Cited by 41 · see citing works

Systemic Lidocaine Inhibits Remifentanil-induced Hyperalgesia via the Inhibition of cPKCgamma Membrane Translocation in Spinal Dorsal Horn of Rats

Cui, W., Li, Y., Li, S., Yang, W.-W., Jiang, J., Han, S., & Li, J. (2009) · Journal of Neurosurgical Anesthesiology · doi:10.1097/ana.0b013e3181abbde5 · Cited by 41 · see citing works

Opioid-Induced Hyperalgesia: Is It Clinically Relevant for the Treatment of Pain Patients?

Raffa, R. B., & Pergolizzi, J. V. (2011) · Pain Management Nursing · doi:10.1016/j.pmn.2011.04.002 · Cited by 40 · see citing works

Nitrous oxide (N2O) prevents latent pain sensitization and long-term anxiety-like behavior in pain and opioid-experienced rats

Bessière, B., Richebé, P., Laboureyras, E., Laulin, J., Contarino, A., & Simonnet, G. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.08.003 · Cited by 40 · see citing works

Opioids: From analgesia to anti-hyperalgesia?

Simonnet, G. (2005) · Pain · doi:10.1016/j.pain.2005.07.021 · Cited by 54 · see citing works

Opioid-Induced Hyperalgesia in Patients After Surgery

Fletcher, D., & Martinez, V. (2015) · Survey of Anesthesiology · doi:10.1097/01.sa.0000461277.28956.5d · Cited by 11 · see citing works

Paroxysmal opioid-induced pain and hyperalgesia.

Ackerman, W. E. (2006) · PubMed · Cited by 13 · see citing works

Opioid-induced hyperalgesia

Bannister, K. (2018) · Oxford University Press eBooks · doi:10.1093/med/9780198834359.003.0061

Opioid-induced hyperalgesia: fact or fiction?

Fallon, M., & Colvin, L. (2008) · Palliative Medicine · doi:10.1177/0269216307086857 · Cited by 11 · see citing works