Opiate antagonists improve spatial memory

Remembrance of places passed: Spatial memory in rats.

Olton, D. S., & Samuelson, R. J. (1976) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.2.2.97 · Cited by 1,934 · see citing works

Time-Dependent Processes in Memory Storage: Recent studies of learning and memory indicate that memory storage involves time-dependent processes.

McGaugh, J. L. (1966) · Science · doi:10.1126/science.153.3742.1351 · Cited by 1,468 · see citing works

Hippocampal place units in the freely moving rat: Why they fire where they fire

O'Keefe, J. M., & Conway, D. H. (1978) · Experimental Brain Research · doi:10.1007/bf00239813 · Cited by 1,007 · see citing works

Foot-shock induced stress increases β-endorphin levels in blood but not brain

Rossier, J., French, E., Rivier, C., Ling, N., Guillemin, R., & Bloom, F. (1977) · Nature · doi:10.1038/270618a0 · Cited by 535 · see citing works

Stimulus control of spatial behavior on the eight-arm maze in rats

Suzuki, S., Augerinos, G., & Black, A. H. (1980) · Learning and Motivation · doi:10.1016/0023-9690(80)90018-1 · Cited by 485 · see citing works

The retroactive effect of electroshock on learning.

Duncan, C. P. (1949) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0058173 · Cited by 428 · see citing works

TRAUMATIC AMNESIA

Russell, W. R., & NATHAN, P. W. (1946) · Brain · doi:10.1093/brain/69.4.280 · Cited by 305 · see citing works

Effect of naloxone and morphine on various forms of memory in the rat: Possible role of endogenous opiate mechanisms in memory consolidation

Izquierdo, I. (1979) · Psychopharmacology · doi:10.1007/bf00427631 · Cited by 268 · see citing works

Manipulation of opiate activity in the amygdala alters memory processes

Gallagher, M., & Kapp, B. S. (1978) · Life Sciences · doi:10.1016/0024-3205(78)90565-9 · Cited by 221 · see citing works

Naloxone enhancement of memory

Messing, R. B., Jensen, R. A., Martinez, J. L., Spiehler, V. R., Vásquez, B. J., Soumireu-Mourat, B., Liang, K., & McGaugh, J. L. (1979) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(79)92328-8 · Cited by 208 · see citing works

Effects of Naloxone in Senile Dementia: A Double-Blind Trial

Reisberg, ‌., Ferris, S. H., Anand, R., Mir, P., Geibel, V., de Leon, M. J., & Roberts, E. R. (1983) · New England Journal of Medicine · doi:10.1056/nejm198303243081213 · Cited by 151 · see citing works

Effects of morphine and heroin on discrimination learning and consolidation in mice

Castellano, C. (1975) · Psychopharmacology · doi:10.1007/bf00421262 · Cited by 136 · see citing works

Memory facilitation by naloxone is due to release of dopaminergic and beta-adrenergic systems from tonic inhibition

Izquierdo, I., & Graudenz, M. S. (1980) · Psychopharmacology · doi:10.1007/bf00431268 · Cited by 116 · see citing works

B-ETA-Endorphin immunoreactivity in rat and human blood: radioimmunoassay, comparative levels and physiological alterations.

Akil, H., Watson, S., Barchas, J., & Li, C.-H. (1979) · Life Science · doi:10.1016/0024-3205(79)90250-9 · Cited by 103 · see citing works

Naloxone enhancement of memory processes: Effects of other opiate antagonists

Gallagher, M. (1982) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(82)91020-2 · Cited by 99 · see citing works

Beta-endorphin causes retrograde amnesia and is released from the rat brain by various forms of training and stimulation

Izquierdo, I., Souza, D. O., Carrasco, M. A., Dias, R. D., Perry, M. L. S., Eisinger, S., Elisabetsky, E., & Vendite, D. (1980) · Psychopharmacology · doi:10.1007/bf00435310 · Cited by 95 · see citing works

Endorphins alter acquisition and consolidation of an inhibitory avoidance response in rats

Martinez, J. L., & Rigter, H. (1980) · Neuroscience Letters · doi:10.1016/0304-3940(80)90194-9 · Cited by 78 · see citing works

Retrograde amnesia caused by Met- Leu- and des-Tyr-Met-enkephalin in the rat and its reversal by naloxone

Izquierdo, I., & Dias, R. D. (1981) · Neuroscience Letters · doi:10.1016/0304-3940(81)90086-0 · Cited by 57 · see citing works

A Proposed Test Battery and Constellations of Specific Behavioral Paradigms to Investigate the Behavioral Phenotypes of Transgenic and Knockout Mice

Crawley, J. N., & Paylor, R. E. (1997) · Hormones and Behavior · doi:10.1006/hbeh.1997.1382 · Cited by 551 · see citing works

The role of interactions between the cholinergic system and other neuromodulatory systems in learing and memory

Decker, M. W., & McGaugh, J. L. (1991) · Synapse · doi:10.1002/syn.890070209 · Cited by 524 · see citing works

Addictive drugs as reinforcers: multiple partial actions on memory systems

White, N. M. (1996) · Addiction · doi:10.1046/j.1360-0443.1996.9179212.x · Cited by 436 · see citing works

Facilitation of glutamate receptors enhances memory.

Staubli, U. V., Rogers, G. A., & LYNCH, G. S. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.2.777 · Cited by 328 · see citing works

Addictive drugs as reinforcers: multiple partial actions on memory systems

WHITE, N. M. (1996) · Addiction · doi:10.1111/j.1360-0443.1996.tb03586.x · Cited by 439 · see citing works

The radial arm maze as a tool in behavioral pharmacology

Olton, D. S. (1987) · Physiology & Behavior · doi:10.1016/0031-9384(87)90286-1 · Cited by 242 · see citing works

Dissociating learning and performance: Drug and hormone enhancement of memory storage

McGaugh, J. L. (1989) · Brain Research Bulletin · doi:10.1016/0361-9230(89)90220-7 · Cited by 207 · see citing works

Animal models of normal aging: Relationship between cognitive decline and markers in hippocampal circuitry

Gallagher, M., & Nicolle, M. M. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90131-9 · Cited by 189 · see citing works

Memory-enhancing effects of posttraining naloxone: involvement of ß-noradrenergic influences in the amygdaloid complex

McGaugh, J. L., Introini-Collison, I. B., & Nagahara, A. H. (1988) · Brain Research · doi:10.1016/0006-8993(88)91294-2 · Cited by 180 · see citing works

Muscimol injections in the medial septum impair spatial learning

Brioni, J. D., Decker, M. W., Gamboa, L. P., Izquierdo, I., & McGaugh, J. L. (1990) · Brain Research · doi:10.1016/0006-8993(90)91465-s · Cited by 149 · see citing works

Naltrexone, relapse prevention, and supportive therapy with alcoholics: An analysis of patient treatment matching.

Jaffe, A. J., Rounsaville, B. J., Chang, G., Schottenfeld, R. S., Meyer, R. E., & O'Malley, S. S. (1996) · Journal of Consulting and Clinical Psychology · doi:10.1037//0022-006x.64.5.1044 · Cited by 149 · see citing works

Endogenous Opioid Regulation of Hippocampal Function

Simmons, M. L., & Chavkin, C. (1996) · International review of neurobiology · doi:10.1016/s0074-7742(08)60666-2 · Cited by 148 · see citing works

Microwave irradiation affects radial‐arm maze performance in the rat

Lai, H. C., Horita, A., & Guy, A. W. (1994) · Bioelectromagnetics · doi:10.1002/bem.2250150202 · Cited by 147 · see citing works

Sexual reinforcement is blocked by infusion of naloxone into the medial preoptic area.

Ågmo, A., & Gómez, M. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.5.812 · Cited by 125 · see citing works

Psychopharmacological effects in the radial-arm maze

Levin, E. D. (1988) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(88)80008-3 · Cited by 120 · see citing works

The Psychobiology Of Reinforcers

White, N. M., & Milner, P. M. (1992) · Annual Review of Psychology · doi:10.1146/annurev.ps.43.020192.002303 · Cited by 114 · see citing works

Age-dependent deficits in spatial memory are related to impaired hippocampal kindling.

de Toledo‐Morrell, L., Morrell, F., & Fleming, S. (1984) · Behavioral Neuroscience · doi:10.1037//0735-7044.98.5.902 · Cited by 117 · see citing works

Elevated dynorphin in the hippocampal formation of aged rats: relation to cognitive impairment on a spatial learning task.

Jiang, H. K., Owyang, V., Hong, J., & Gallagher, M. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.8.2948 · Cited by 112 · see citing works

G Protein-Coupled Receptors (GPCRs) in Alzheimer’s Disease: A Focus on BACE1 Related GPCRs

Zhao, J., Deng, Y., Jiang, Z., & Qing, H. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00058 · Cited by 108 · see citing works

A review of the relation between dissociation, memory, executive functioning and social cognition in military members and civilians with neuropsychiatric conditions

McKinnon, M. C., Boyd, J. E., Frewen, P. A., Lanius, U. F., Jetly, R., Richardson, J. D., & Lanius, R. A. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.07.017 · Cited by 94 · see citing works

Associative regulation of Pavlovian fear conditioning: Unconditioned stimulus intensity, incentive shifts, and latent inhibition.

Young, S. L., & Fanselow, M. S. (1992) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037//0097-7403.18.4.400 · Cited by 93 · see citing works

Chronic opioids impair acquisition of both radial maze and Y-maze choice escape

Spain, J. W., & Newsom, G. C. (1991) · Psychopharmacology · doi:10.1007/bf02316870 · Cited by 116 · see citing works

A GPCR/secretase complex regulates β- and γ-secretase specificity for Aβ production and contributes to AD pathogenesis

Teng, L., Zhao, J., Wang, F., Ma, L., & Pei, G. (2010) · Cell Research · doi:10.1038/cr.2010.3 · Cited by 91 · see citing works

Opioid Receptors Regulate the Extinction of Pavlovian Fear Conditioning.

McNally, G. P., & Westbrook, R. F. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.6.1292 · Cited by 91 · see citing works

Dopamine antagonists during parturition disrupt maternal care and the retention of maternal behavior in rats

Byrnes, E. M., Rigero, B. A., & Bridges, R. S. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(02)00941-3 · Cited by 90 · see citing works

Spatial learning in deer mice: sex differences and the effects of endogenous opioids and 60 Hz magnetic fields

Kavaliers, M., Ossenkopp, K., Prato, F. S., Innes, D. G. L., Galea, L. A. M., Kinsella, D. M., & Perrot-Sinal, T. S. (1996) · Journal of Comparative Physiology A · doi:10.1007/bf00216135 · Cited by 86 · see citing works

Kappa opioids inhibit induction of long-term potentiation in the dentate gyrus of the guinea pig hippocampus

Terman, G. W., Wagner, J. J., & Chavkin, C. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-08-04740.1994 · Cited by 85 · see citing works

Selective changes in μ, δ and ϰ opioid receptor binding in certain limbic regions of the brain in Alzheimer's disease patients

Hiller, J. M., Itzhak, Y., & Simon, E. J. (1987) · Brain Research · doi:10.1016/0006-8993(87)90764-5 · Cited by 85 · see citing works

Enkephalin Elevations Contribute to Neuronal and Behavioral Impairments in a Transgenic Mouse Model of Alzheimer's Disease

Meilandt, W. J., Yu, G.-Q., Chin, J., Roberson, E. D., Palop, J. J., Wu, T. Z., Scearce-Levie, K. A., & Mucke, L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0590-08.2008 · Cited by 84 · see citing works

Hormonal Modulation of Memory

McGaugh, J. L., & Gold, P. E. (1989) · Elsevier eBooks · doi:10.1016/b978-0-12-137952-0.50011-2 · Cited by 84 · see citing works

A role for hippocampal opioids in long-term functional plasticity

MORRIS, B. J., & Johnston, H. M. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93927-p · Cited by 80 · see citing works

Radial-arm maze deficits produced by colchicine administered into the area of the nucleus basalis are ameliorated by cholinergic agents

Tilson, H. A., McLamb, R. L., Shaw, S., Rogers, B. C., Pediaditakis, P., & Cook, L. L. (1988) · Brain Research · doi:10.1016/0006-8993(88)91326-1 · Cited by 80 · see citing works

Pharmacological evidence of a central effect of naltrexone, morphine, and β-endorphin and a peripheral effect of met- and leu-enkephalin on retention of an inhibitory response in mice

Introini-Collison, I. B., McGaugh, J. L., & Baratti, C. M. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)90832-5 · Cited by 79 · see citing works

Differential effect of posttraining naloxone, β-endorphin, leu-enkephalin and electroconvulsive shock administration upon memory of an open-field habituation and of a water-finding task

Netto, C. A., Dias, R. D., & Izquierdo, I. (1986) · Psychoneuroendocrinology · doi:10.1016/0306-4530(86)90005-3 · Cited by 77 · see citing works

Effects of nocistatin on nociceptin-induced impairment of learning and memory in mice

Hiramatsu, M., & Inoue, K. (1999) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00003-5 · Cited by 77 · see citing works

Antagonism of endogenous opioids modulates memory processing

Flood, J. F., Cherkin, A., & Morley, J. E. (1987) · Brain Research · doi:10.1016/0006-8993(87)90929-2 · Cited by 72 · see citing works

Opioid receptor dependent long-term potentiation: Peptidergic regulation of synaptic plasticity in the hippocampus

Bramham, C. R. (1992) · Neurochemistry International · doi:10.1016/0197-0186(92)90021-i · Cited by 72 · see citing works

Role of β‐Endorphin in Behavioral Regulationa

Izquierdo, I., & Netto, C. A. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb37587.x · Cited by 67 · see citing works

Effects of opiate antagonists on spatial memory in young and aged rats

Gallagher, M., Bostock, E., & King, R. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)90688-0 · Cited by 66 · see citing works

The impairment of retention induced by β-endorphin in mice may be mediated by a reduction of central cholinergic activity

Introini-Collison, I. B., & Baratti, C. M. (1984) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(84)90527-2 · Cited by 66 · see citing works

Enkephalins and learning and memory: a review of evidence for a site of action outside the blood-brain barrier.

Martinez, J. L., Weinberger, S., & Schulteis, G. (1988) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(88)90517-1 · Cited by 61 · see citing works

Irreversible Effects in Rats of Toluene (Inhalation) Exposure for Six Months

Ladefoged, O., Strange, P., Møller, A., Lam, H. R., Østergaard, G., Larsen, J., & Arlien-Søborg, P. (1991) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.1991.tb01257.x · Cited by 60 · see citing works

Separable roles of hippocampal granule cells in forgetting and pyramidal cells in remembering spatial information

Collier, T. J., Quirk, G. J., & Routtenberg, A. (1987) · Brain Research · doi:10.1016/0006-8993(87)90717-7 · Cited by 57 · see citing works

Naloxone in the Prevention of the Adverse Cognitive Effects of ECT A Within-Subject, Placebo Controlled Study

Prudic, J. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00015-9 · Cited by 56 · see citing works

Endogenous opiates: 1983

Olson, G. A., Olson, R. D., & Kastin, A. J. (1984) · Peptides · doi:10.1016/0196-9781(84)90125-6 · Cited by 56 · see citing works

Opioid peptidergic systems modulate the activity of β-adrenergic mechanisms during memory consolidation processes

Introini-Collison, I. B., & Baratti, C. M. (1986) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(86)90710-7 · Cited by 55 · see citing works

Applications of Transcutaneous Electrical Nerve Stimulation in the Management of Patients with Pain

Gersh, M. R., & Wolf, S. L. (1985) · Physical Therapy · doi:10.1093/ptj/65.3.314 · Cited by 53 · see citing works

Opiate antagonists enhance the working memory of rats in the radial maze

Canli, T., Cook, R. G., & Miczek, K. A. (1990) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(90)90250-l · Cited by 62 · see citing works

Age-related changes in hippocampal drug facilitation of memory processing in SAMP 8 Mice

Flood, J. F., Harris, F. J., & Morley, J. E. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(95)02007-1 · Cited by 49 · see citing works

Brief exposure to 60 Hz magnetic fields improves sexually dimorphic spatial learning performance in the meadow vole, Microtus pennsylvanicus

Kavaliers, M., Eckel, L. A., & Ossenkopp, K. (1993) · Journal of Comparative Physiology A · doi:10.1007/bf00192983 · Cited by 48 · see citing works

Opiate antagonist facilitation of time-dependent memory processes: Dependence upon intact norepinephrine function

Gallagher, M., Rapp, P. R., & Fanelli, R. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90188-x · Cited by 48 · see citing works

Opioid modulation of social play reward in juvenile rats

Achterberg, E. J. M., van Swieten, M. M. H., Houwing, D. J., Trezza, V., & Vanderschuren, L. J. M. J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.09.007 · Cited by 52 · see citing works

Effects of acute and chronic methylphenidate administration on beta-endorphin, growth hormone, prolactin and cortisol in children with attention deficit disorder and hyperactivity.

Weizman, R., Dick, J., Gil-Ad, I., Weitz, R., Tyano, S., & Laron, Z. (1987) · Life Science · doi:10.1016/0024-3205(87)90060-9 · Cited by 43 · see citing works

Animal Behavioral Models in the Discovery of Compounds To Treat Memory Dysfunction

Gamzu, E. R. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb37602.x · Cited by 45 · see citing works

Inhibition of Neprilysin by Infusion of Thiorphan into the Hippocampus Causes an Accumulation of Amyloid β and Impairment of Learning and Memory

Zou, L.-B., Mouri, A., Iwata, N., Saido, T. C., Wang, D., Wang, M., Mizoguchi, H., Noda, Y., & Nabeshima, T. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.095687 · Cited by 44 · see citing works

Naltrexone reduces self-injury and improves learning.

Sandman, C. A., Hetrick, W. P., Taylor, D. V., Barron, J. L., Touchette, P. E., Lott, I. T., Crinella, F. M., & Martinazzi, V. P. (1993) · Experimental and Clinical Psychopharmacology · doi:10.1037/1064-1297.1.1-4.242 · Cited by 43 · see citing works

Naloxone and ?-endorphin alter the effects of post-training epinephrine on memory

Introini-Collison, I. B., & McGaugh, J. L. (1987) · Psychopharmacology · doi:10.1007/bf00177921 · Cited by 43 · see citing works

Reversal of scopolamine-induced amnesia of passive avoidance by pre- and post-training naloxone

Rush, D. K. (1986) · Psychopharmacology · doi:10.1007/bf00174363 · Cited by 43 · see citing works

Depletion of brain norepinephrine with DSP-4 does not alter acquisition or performance of a radial-arm maze task

Chrobak, J. J., DeHaven, D. L., & Walsh, T. J. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)91316-0 · Cited by 41 · see citing works

Neuropeptides and Memory

Koob, G. F. (1987) · Springer eBooks · doi:10.1007/978-1-4613-1819-4_9 · Cited by 40 · see citing works

Memory: Neural Organization and Behavior

Squire, L. R. (1987) · Comprehensive physiology · doi:10.1002/cphy.cp010508 · Cited by 43 · see citing works

Maze performance: A direct comparison of food vs. water mazes

Kant, G. J., Yen, M. H., D'Angelo, P. C., Brown, A. J., & Eggleston, T. (1988) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(88)90378-4 · Cited by 38 · see citing works

Functional changes after prenatal opiate exposure related to opiate receptors' regulated alterations in cholinergic innervation

Yanai, J., Huleihel, R., Izrael, M., Metsuyanim, S., Shahak, H., Vatury, O. M., & Yaniv, S. P. (2003) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145703003523 · Cited by 37 · see citing works

Effects of naloxone and naltrexone on memory consolidation in CD1 mice: Involvement of GABAergic mechanisms

Castellano, C., Introini-Collison, I. B., Pavone, F., & McGaugh, J. L. (1989) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(89)90197-4 · Cited by 37 · see citing works

Evidence that cholecystokinin-enhanced retention is mediated by changes in opioid activity in the amygdala

Flood, J. F., Garland, J. S., & Morley, J. E. (1992) · Brain Research · doi:10.1016/0006-8993(92)91194-j · Cited by 37 · see citing works

Pentoxifylline reverses age-related deficits in spatial memory

de Toledo‐Morrell, L., Morrell, F., Fleming, S., & Cohen, M. M. (1984) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(84)90364-9 · Cited by 37 · see citing works

Isolation reduces contextual but not auditory-cue fear conditioning: A role for endogenous opioids.

Rudy, J. W., Kuwagama, K., & Pugh, C. R. (1999) · Behavioral Neuroscience · doi:10.1037//0735-7044.113.2.316 · Cited by 36 · see citing works

Influence of naloxone on brain and behavior of a self-injurious woman

Sandman, C. A., Barron, J. L., Crinella, F. M., & Donnelly, J. F. (1987) · Biological Psychiatry · doi:10.1016/0006-3223(87)90088-6 · Cited by 35 · see citing works

Differential effects of methionine5 enkephalin on hippocampal pyramidal cells and interneurons

Pang, K. C. H. (1989) · Neuropharmacology · doi:10.1016/0028-3908(89)90208-6 · Cited by 34 · see citing works

Effects of naloxone on Morris water maze learning in the rat: Enhanced acquisition with pretraining but not posttraining administration

Decker, M. W., Introini-Collison, I. B., & McGaugh, J. L. (1989) · Psychobiology · doi:10.1007/bf03337778 · Cited by 34 · see citing works

Induction of cognitive impairment by scopolamine and noncholinergic agents in rhesus monkeys

Rupniak, N. M. J., Samson, N. A., Steventon, M. J., & Iversen, S. D. (1991) · Life Sciences · doi:10.1016/0024-3205(91)90036-b · Cited by 33 · see citing works

Convergent Effects on Cell Signaling Mechanisms Mediate the Actions of Different Neurobehavioral Teratogens: Alterations in Cholinergic Regulation of Protein Kinase C in Chick and Avian Models

Yanai, J., Beer, A., Huleihel, R., Izrael, M., KATZ, S., LEVI, Y., ROZENBOIM, I., Yaniv, S. P., & Slotkin, T. A. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1316.074 · Cited by 33 · see citing works

Leu-enkephalin impairs memory of an appetitive maze response in mice.

Linden, D. J., & Martinez, J. L. (1986) · Behavioral Neuroscience · doi:10.1037//0735-7044.100.1.33 · Cited by 33 · see citing works

Pretraining morphine impairs acquisition and performance in the Morris water maze: Motivation reduction rather than anmesia

McNamara, R. K., & Skelton, R. W. (1991) · Psychobiology · doi:10.3758/bf03332085 · Cited by 32 · see citing works

The brain β-endorphin system and behavior: The modulation of consecutively and simultaneously processed memories

Izquierdo, I., & Netto, C. A. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)90268-7 · Cited by 32 · see citing works

Neuropeptides, Behavior, and Aging

Morley, J. E. (1986) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1986.tb06340.x · Cited by 32 · see citing works

Effect of naltrexone upon self-injurious behavior, learning and activity: a case study

Taylor, D. V., Hetrick, W. P., Neri, C. L., Touchette, P. E., Barron, J. L., & Sandman, C. A. (1991) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(91)90324-u · Cited by 31 · see citing works

Reduced ethanol response in the alcohol‐preferring RHA rats and neuropeptide mRNAs in relevant structures

Guitart‐Masip, M., Giménez‐Llort, L., Fernández‐Teruel, A., Cañete, T., Tobeña, A., Ögren, S. O., Terenius, L. Y., & Johansson, B. A. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04556.x · Cited by 30 · see citing works

Divergent short- and long-term effects of acute stress in object recognition memory are mediated by endogenous opioid system activation

Nava-Mesa, M. O., Lamprea, M. R., & Múnera, A. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.09.002 · Cited by 31 · see citing works

The opioid system in neurologic and psychiatric disorders and in their experimental models

Gulya, K. (1990) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(90)90026-x · Cited by 29 · see citing works

High-dose naloxone in tardive dyskinesia

Lindenmayer, J., Gardner, E. L., Goldberg, E., Opler, L. A., Kay, S. R., van Praag, H. M., Weiner, M., & Zukin, S. R. (1988) · Psychiatry Research · doi:10.1016/0165-1781(88)90083-2 · Cited by 28 · see citing works

Modulation of acetylcholine release in human cortical slices: Possible implications for Alzheimer's disease

Feuerstein, T. J., & Seeger, W. (1997) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(97)00006-5 · Cited by 28 · see citing works

Role of noradrenergic function in the opiate antagonist facilitation of spatial memory.

Fanelli, R. J., Rosenberg, R. A., & Gallagher, M. (1985) · Behavioral Neuroscience · doi:10.1037//0735-7044.99.4.751 · Cited by 28 · see citing works

The effect of phobic anxiety on plasma β-endorphin: a single-subject experiment

Thyer, B. A., & Matthews, J. (1986) · Behaviour Research and Therapy · doi:10.1016/0005-7967(86)90099-9 · Cited by 27 · see citing works

Effects of phencyclidine, N-allyl-N-normetazocine (SKF-10,047), and verapamil on performance in a radial maze

McCann, D. J., & Winter, J. C. (1986) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(86)90336-9 · Cited by 25 · see citing works

Naloxone facilitates spatial learning in a water-maze task in female, but not male, adult nonbreeding meadow voles

Galea, L. A. M., Saksida, L. M., Kavaliers, M., & Ossenkopp, K. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90009-4 · Cited by 24 · see citing works

Differentially expressed gene (DEG) based protein-protein interaction (PPI) network identifies a spectrum of gene interactome, transcriptome and correlated miRNA in nondisjunction Down syndrome

Ramireddy, S., Sajeed, R., Raghuraman, P., & Sudandiradoss, C. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.09.056 · Cited by 24 · see citing works

Effects of Undernutrition during Suckling on Footshock Escape Behavior and on Related Neurochemical Parameters in Rats

Vendite, D., Wofchuk, S. T., & Souza, D. O. (1985) · Journal of Nutrition · doi:10.1093/jn/115.11.1418 · Cited by 24 · see citing works

Effect of naltrexone on mood and cognitive functioning among overweight men

Hatsukami, D. K., Mitchell, J. E., Morley, J. E., Morgan, S. F., & Levine, A. S. (1986) · Biological Psychiatry · doi:10.1016/0006-3223(86)90050-8 · Cited by 23 · see citing works

Prenatal heroin exposure alters cholinergic receptor stimulated activation of the PKCβII and PKCγ isoforms

Yaniv, S. P., Naor, Z., & Yanai, J. (2004) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2004.04.006 · Cited by 22 · see citing works

Factors that influence test session performance measured 0, 3, or 6 h after inhibitory avoidance training

Izquierdo, I., & Netto, C. A. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)91606-1 · Cited by 21 · see citing works

Involvement of Opioid Peptides in Learning and Memory

McGaugh, J. L., Introini-Collison, I. B., & Castellano, C. (1993) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-77540-6_17 · Cited by 21 · see citing works

The importance of behavioural bioassays in neuroscience

Brown, R. E., & Bolivar, S. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.05.022 · Cited by 20 · see citing works

Cognitive enhancers: Potential strategies and experimental results

Wenk, G. L., & Olton, D. S. (1989) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(89)90115-2 · Cited by 20 · see citing works

Reduced cerebrospinal fluid dynorphin A1–8 in Alzheimer's disease

Sunderland, T., Berrettini, W. H., Molchan, S. E., LAWLOR, B. A., Martínez, R. A., Vitiello, B., Tariot, P. N., & Cohen, R. M. (1991) · Biological Psychiatry · doi:10.1016/0006-3223(91)90073-u · Cited by 20 · see citing works

Naloxone and [Met5]enkephalin effects on retention: attenuation by adrenal denervation

Zhang, S.-Y., McGaugh, J. L., Juler, R. G., & Introini-Collison, I. B. (1987) · European Journal of Pharmacology · doi:10.1016/0014-2999(87)90334-7 · Cited by 20 · see citing works

Opioid receptor regulation of muscarinic acetylcholine receptor-mediated synaptic responses in the hippocampus

Kearns, I. R., Morton, R. A., Bulters, D. O., & Davies, C. H. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00108-3 · Cited by 19 · see citing works

The antagonistic effects of naloxone on cycloheximide and anisomicin-induced amnesia

Kameyama, T., Nabeshima, T., & Kozawa, T. (1986) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(86)90142-5 · Cited by 19 · see citing works

Reversal of heroin neurobehavioral teratogenicity by grafting of neural progenitors

Katz, S., Ben‐Hur, T., Ben-Shaanan, T. L., & Yanai, J. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05004.x · Cited by 18 · see citing works

The pattern of neurotransmitter alterations in LP-BM5 infected mice is consistent with glutamatergic hyperactivation

Kustova, Y., Ha, J., Espey, M. G., Sei, Y., Morse, D., & Basile, A. S. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00167-x · Cited by 18 · see citing works

Opiate antagonists enhance the working memory of rats in the radial maze

Canli, T., Cook, R. G., & Miczek, K. A. (1990) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(90)90250-l · Cited by 62 · see citing works

Effects of opiate antagonists on spatial memory in young and aged rats

Gallagher, M., Bostock, E., & King, R. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)90688-0 · Cited by 66 · see citing works

Role of noradrenergic function in the opiate antagonist facilitation of spatial memory.

Fanelli, R. J., Rosenberg, R. A., & Gallagher, M. (1985) · Behavioral Neuroscience · doi:10.1037//0735-7044.99.4.751 · Cited by 28 · see citing works

Opiate antagonists, morphine and spatial memory in rats

Beatty, W. W. (1983) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(83)90108-9 · Cited by 34 · see citing works

Naloxone enhancement of memory processes: Effects of other opiate antagonists

Gallagher, M. (1982) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(82)91020-2 · Cited by 99 · see citing works