The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Acetylcholine Activates an α-Bungarotoxin-Sensitive Nicotinic Current in Rat Hippocampal Interneurons, But Not Pyramidal Cells
Open accessAbstract
The effects of acetylcholine on both pyramidal neurons and interneurons in the area CA1 of the rat hippocampus were examined, using intracellular recording techniques in an in vitro slice preparation. In current-clamp mode, fast local application of acetylcholine (ACh) to the soma of inhibitory interneurons in stratum radiatum resulted in depolarization and rapid firing of action potentials. Under voltage-clamp, ACh produced fast, rapidly desensitizing inward currents that were insensitive to atropine but that were blocked by nanomolar concentrations of the nicotinic α7 receptor-selective antagonists α-bungarotoxin (αBgTx) and methyllycaconitine. Nicotinic receptor antagonists that are not selective for α7-containing receptors had little (mecamylamine) or no effect (dihydro-β-erythroidine) on the ACh-induced currents. Glutamate receptor antagonists had no effect on the ACh-evoked response, indicating that the current was not mediated by presynaptic facilitation of glutamate release. However, the current could be desensitized almost completely by bath superfusion with 100 n m nicotine. In contrast to those actions on interneurons, application of ACh to the soma of CA1 pyramidal cells did not produce a detectable current. Radioligand-binding experiments with [125 I]-αBgTx demonstrated that stratum radiatum interneurons express α7-containing nAChRs, and in situ hybridization revealed significant amounts of α7 mRNA. CA1 pyramidal cells did not show specific binding of [125 I]-αBgTx and only low levels of α7 mRNA. These results suggest that, in addition to their proposed presynaptic role in modulating transmitter release, α7-containing nAChRs also may play a postsynaptic role in the excitation of hippocampal interneurons. By desensitizing these receptors, nicotine may disrupt this action and indirectly excite pyramidal neurons by reducing GABAergic inhibition.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The α7-nicotinic receptor is found presynaptically on glutamate nerve terminals and postsynaptically on inhibitory interneurons (Figure 2B), particularly in the hippocampus and nucleus reticularis thalamis (9).”
From Sensory Processing Dysfunction in the Personal Experience and Neuronal Machinery of Schizophrenia (2015) · cites this paper as [9]
In the citing paper
“For both PPI and P50 gating, despite the origin of the effect in reticular brain stem neurons, the response engages an entire network of brain circuits, the dopaminergic circuits of the basal ganglia for PPI and the basal cholinergic nuclei and cortex for P50 gating (8, 9).”
From Sensory Processing Dysfunction in the Personal Experience and Neuronal Machinery of Schizophrenia (2015) · cites this paper as [9]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,478
Séguéla, P., Wadiche, J. I., Dineley‐Miller, K., Dani, J., & Jw, P. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-02-00596.1993 · Cited by 1,471
Nicotine enhancement of fast excitatory synaptic transmission in CNS by presynaptic receptors
McGehee, D. S., Heath, M. J. S., Gelber, S., Devay, P., & Role, L. W. (1995) · Science · doi:10.1126/science.7569895 · Cited by 1,070
The Diversity of Neuronal Nicotinic Acetylcholine Receptors
Sargent, P. B. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.002155 · Cited by 1,052
Clarke, P. B. S., Schwartz, R., Paul, S. M., Cb, P., & Pert, A. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-05-01307.1985 · Cited by 1,037
Physiological Diversity of Nicotinic Acetylcholine Receptors Expressed by Vertebrate Neurons
McGehee, D. S., & Role, L. W. (1995) · Annual Review of Physiology · doi:10.1146/annurev.ph.57.030195.002513 · Cited by 1,022
Cholinergic systems in mammalian brain and spinal cord
WOOLF, N. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90006-m · Cited by 948
Hippocampal synaptic transmission enhanced by low concentrations of nicotine
Gray, R. G. F., Rajan, A. S., Radcliffe, K. A., Yakehiro, M., & Dani, J. A. (1996) · Nature · doi:10.1038/383713a0 · Cited by 947
Couturier, S., Bertrand, D., Matter, J., Hernandez, M., Bertrand, S., Millar, N. S., Valera, S., BARKAS, T., & Ballivet, M. (1990) · Neuron · doi:10.1016/0896-6273(90)90344-f · Cited by 941
Nicotinic Receptors in the Development and Modulation of CNS Synapses
Role, L. W., & Berg, D. K. (1996) · Neuron · doi:10.1016/s0896-6273(00)80134-8 · Cited by 762
Cited by
Sorted by citations
Items 101–200 of 374
α7 Nicotinic acetylcholine receptors and their role in cognition
Lendvai, B., Kassai, F., Szájli, Á., & Némethy, Z. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.11.003 · Cited by 99
Albuquerque, E. X., Pereira, E. F. R., Mike, Á., Eisenberg, H. M., Maelicke, A., & Alkondon, M. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00208-4 · Cited by 95
Cognitive dysfunction in schizophrenia: unifying basic research and clinical aspects
McCarley, R. W., Niznikiewicz, M. A., Salisbury, D. F., Nestor, P. G., O’Donnell, B. F., Hirayasu, Y., Grunze, H., Greene, R. W., & Shenton, M. E. (1999) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/pl00014188 · Cited by 94
Svoboda, K. R., Adams, C. E., & Lupica, C. R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00085.1999 · Cited by 99
Fujii, S., Jia, Y., Yang, A., & Sumikawa, K. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02119-3 · Cited by 93
Regulation of GABA release by nicotinic acetylcholine receptors in the neonatal rat hippocampus
Maggi, L., Sher, E., & Cherubini, E. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00089.x · Cited by 91
Nicotinic acetylcholine receptors during prenatal development and brain pathology in human aging
Hellström‐Lindahl, E., & COURT, J. A. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00210-2 · Cited by 92
Song, C., Murray, T. A., Kimura, R., Wakui, M., Ellsworth, K. R., Javedan, S. P., Marxer-Miller, S., Lukas, R. J., & Wu, J. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.01.003 · Cited by 88
Levy, R. B., & Aoki, C. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-05001.2002 · Cited by 86
Giovannini, M. G., Lana, D., & Pepeu, G. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.12.014 · Cited by 93
Modulation of Hippocampal Circuits by Muscarinic and Nicotinic Receptors
Dannenberg, H., Young, K., & Hasselmo, M. E. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00102 · Cited by 89
Alpha7 Nicotinic Receptors as Therapeutic Targets in Schizophrenia
Tregellas, J. R., & Wylie, K. P. (2018) · Nicotine & Tobacco Research · doi:10.1093/ntr/nty034 · Cited by 95
Rapid Upregulation of α7 Nicotinic Acetylcholine Receptors by Tyrosine Dephosphorylation
Cho, C.-H., Song, W., Leitzell, K., Teo, E., Meleth, A. D., Quick, M. W., & Lester, R. A. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5389-03.2005 · Cited by 87
Allosteric Modulators of the α7 Nicotinic Acetylcholine Receptor
Faghih, R., Gopalakrishnan, M., & Briggs, C. A. (2008) · Journal of Medicinal Chemistry · doi:10.1021/jm070256g · Cited by 89
Yang, K., Buhlman, L. M., Khan, G. M., Nichols, R. A., Jin, G.-Z., McIntosh, J. M., Whiteaker, P., Lukas, R. J., & Wu, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3003-10.2011 · Cited by 87
Nakauchi, S., Brennan, R. J., Boulter, J., & Sumikawa, K. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05513.x · Cited by 84
Nicotinic receptors in circuit excitability and epilepsy
Raggenbass, M., & Bertrand, D. (2002) · Journal of Neurobiology · doi:10.1002/neu.10152 · Cited by 85
Nicotinic Mechanisms in the Treatment of Psychotic Disorders: A Focus on the α7 Nicotinic Receptor
D, A. O. M., & Freedman, R. (2012) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-25758-2_8 · Cited by 80
Self-citationMuscarinic Blockade Slows and Degrades the Location-Specific Firing of Hippocampal Pyramidal Cells
Brazhnik, E. S., Muller, R. U., & Fox, S. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00611.2003 · Cited by 78
Fuhrer, C., & Huh, K.-H. (2002) · Molecular Neurobiology · doi:10.1385/mn:25:1:079 · Cited by 82
Frazier, C. J., Strowbridge, B. W., & Papke, R. L. (2003) · Journal of Neurophysiology · doi:10.1152/jn.01036.2002 · Cited by 80
Self-citationFedele, E., Varnier, G., Ansaldo, M. A., & Raiteri, M. (1998) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0702130 · Cited by 79
Mann, E. O., & Greenfield, S. A. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.045492 · Cited by 79
Davis, J. A., & Gould, T. J. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0047-y · Cited by 78
Rousseau, S., Jones, I. W., Pullar, I. A., & Wonnacott, S. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.01.030 · Cited by 77
Zhang, L., & Warren, R. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.01025.2001 · Cited by 75
Evoked slow muscarinic acetylcholinergic synaptic potentials in rat hippocampal interneurons
Widmer, H., Ferrigan, L., Davies, C. H., & Cobb, S. (2006) · Hippocampus · doi:10.1002/hipo.20191 · Cited by 77
Timofeeva, O. A., & Levin, E. D. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.038 · Cited by 74
Bell, K. A., Shim, H., Chen, C.-K., & McQuiston, A. R. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.08.024 · Cited by 74
Buhler, A. V., & Dunwiddie, T. V. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00316.2001 · Cited by 72
Self-citationCermak, J. M., Blusztajn, J. K., Meck, W. H., Williams, C. L., Fitzgerald, C. M., Rosene, D. L., & Loy, R. (1999) · Developmental Neuroscience · doi:10.1159/000017371 · Cited by 75
Ca2+ Dyshomeostasis Disrupts Neuronal and Synaptic Function in Alzheimer’s Disease
McDaid, J., Mustaly-Kalimi, S., & Stutzmann, G. E. (2020) · Cells · doi:10.3390/cells9122655 · Cited by 73
Wanaverbecq, N., Semyanov, A. V., Pavlov, I., Walker, M. C., & Kullmann, D. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1732-07.2007 · Cited by 74
Potier, B., Jouvenceau, A., Epelbaum, J., & Dutar, P. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.06.040 · Cited by 72
Albuquerque, E. X., Pereira, E. F. R., Braga, M. F. M., & Alkondon, M. (1998) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(98)80039-9 · Cited by 70
Liu, Q., Huang, Y., Shen, J., Steffensen, S. C., & Wu, J. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-155 · Cited by 71
Huang, H., Xu, Y., & van den Pol, A. N. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00740.2010 · Cited by 70
Arnáiz‐Cot, J. J., Gonzalez, J., Sobrado, M., Baldelli, P., Carbone, E., Gandı́a, L., Garcı́a, A. G., & Hernández-Guijo, J. M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06077.x · Cited by 69
Activation of nicotinic acetylcholine receptors patterns network activity in the rodent hippocampus
Cobb, S. R., Bulters, D. O., Suchak, S. K., Riedel, G., Morris, R., & Davies, C. H. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0131r.x · Cited by 68
Cholinergic Modulation of Spindle Bursts in the Neonatal Rat Visual Cortex In Vivo
Hanganu, I. L., Staiger, J. F., Ben-Ari, Y., & Khazipov, R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5233-06.2007 · Cited by 67
Functional α7‐containing nicotinic receptors of NG2‐expressing cells in the hippocampus
Vélez-Fort, M., Audinat, E., & Angulo, M. C. (2009) · Glia · doi:10.1002/glia.20834 · Cited by 69
Functional connectivity and cholinergic modulation in auditory cortex
Metherate, R. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.11.010 · Cited by 66
Zaninetti, M., Tribollet, E., Bertrand, D., & Raggenbass, M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00689.x · Cited by 66
Houlihan, L. M., Slater, Y., Guerra, D. L., Peng, J., Kuo, Y., Lukas, R. J., Cassels, B. K., & Bermúdez, I. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00481.x · Cited by 64
Nicotinic ACh Receptors in the Hippocampus: Role in Excitability and Plasticity
Yakel, J. L. (2012) · Nicotine & Tobacco Research · doi:10.1093/ntr/nts091 · Cited by 65
Hashimoto, K., Iyo, M., Freedman, R., & Stevens, K. E. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0142-0 · Cited by 63
Self-citationMagueresse, C. L., Safiulina, V. F., Changeux, J., & Cherubini, E. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.117572 · Cited by 59
Yamazaki, Y., Jia, Y., Hamaue, N., & Sumikawa, K. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04259.x · Cited by 63
Fisher, J. L., & Dani, J. A. (2000) · Neuropharmacology · doi:10.1016/s0028-3908(00)00102-7 · Cited by 62
Bowers, B. J., McClure‐Begley, T. D., Keller, J. J., Paylor, R. E., Collins, A. C., & Wehner, J. M. (2005) · Alcoholism Clinical and Experimental Research · doi:10.1097/01.alc.0000156116.40817.a2 · Cited by 61
Roberts, J. P., Stokoe, S. A., Sathler, M. F., Nichols, R. A., & Kim, S. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100402 · Cited by 64
Fujii, S., & Sumikawa, K. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02058-3 · Cited by 60
Liotta, A., Çalışkan, G., Haq, R. U., Hollnagel, J., Rösler, A., Heinemann, U., & Behrens, C. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00186.2010 · Cited by 59
Son, J., & Winzer‐Serhan, U. H. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21828 · Cited by 58
GABAergic Systems Modulate Nicotinic Receptor-Mediated Seizures in Mice
Dobelis, P., Hutton, S. R., Lü, Y., & Collins, A. C. (2003) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.103.053066 · Cited by 58
Fujii, S., & Sumikawa, K. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02057-1 · Cited by 58
Keller, J. J., Keller, A. B., Bowers, B. J., & Wehner, J. M. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.03.004 · Cited by 57
Yamazaki, Y., Jia, Y., Niu, R., & Sumikawa, K. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04714.x · Cited by 57
Maggi, L., Sola, E., Minneci, F., Magueresse, C. L., Changeux, J., & Cherubini, E. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.067041 · Cited by 56
Acetylcholine release and inhibitory interneuron activity in hippocampal CA1
McQuiston, A. R. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00020 · Cited by 60
Prenatal Primary Prevention of Mental Illness by Micronutrient Supplements in Pregnancy
Freedman, R., Hunter, S. K., & Hoffman, M. C. (2018) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2018.17070836 · Cited by 59
Self-citationfMRI of Response to Nicotine During a Smooth Pursuit Eye Movement Task in Schizophrenia
Tregellas, J. R., Tanabe, J., Martín, L., & Freedman, R. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.2.391 · Cited by 55
Self-citationFisher, J. L., Pidoplichko, V. I., & Dani, J. A. (1998) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(98)80012-0 · Cited by 55
Buhler, A. V., & Dunwiddie, T. V. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00257-3 · Cited by 54
Self-citationNicotinic receptors and hippocampal synaptic plasticity…it’s all in the timing
McGehee, D. S. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)02127-5 · Cited by 53
Khiroug, S. S., Khiroug, L. S., & Yakel, J. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.01.017 · Cited by 53
Jia, Y., Yamazaki, Y., Nakauchi, S., Ito, K., & Sumikawa, K. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07058.x · Cited by 51
Klein, R. C., & Yakel, J. L. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.118232 · Cited by 51
McMahon, L. L., Williams, J. H. P., & Kauer, J. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-15-05640.1998 · Cited by 52
Prefrontal neuromodulation by nicotinic receptors for cognitive processes
Coura, R., & Granon, S. (2012) · Psychopharmacology · doi:10.1007/s00213-011-2596-6 · Cited by 57
Alexander, J. K., Sagher, D., Krivoshein, A. V., Criado, M., Jefford, G., & Green, W. N. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6344-09.2010 · Cited by 51
Potentiation and inhibition of neuronal α4β4 nicotinic acetylcholine receptors by choline
Zwart, R., & Vijverberg, H. P. M. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00002-9 · Cited by 51
Functional Magnetic Resonance Imaging of Effects of a Nicotinic Agonist in Schizophrenia
Tregellas, J. R., D, A. O. M., Johnson, L. L., Tanabe, J., Shatti, S., Martín, L., Singel, D., Du, Y. P., Soti, F. S., Kem, W. R., et al. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.196 · Cited by 50
Self-citationAlkondon, M., Pereira, E. F. R., & Albuquerque, E. X. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00214.2003 · Cited by 50
Higher Gestational Choline Levels in Maternal Infection Are Protective for Infant Brain Development
Freedman, R., Hunter, S. K., Law, A. J., Wagner, B. D., D’Alessandro, A., Christians, U., Noonan, K., Wyrwa, A., & Hoffman, M. C. (2019) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2018.12.010 · Cited by 48
Self-citationShao, Z., & Yakel, J. L. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00507.x · Cited by 49
Dobelis, P., Staley, K. J., & Cooper, D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041108 · Cited by 48
Cholinergic Circuits and Signaling in the Pathophysiology of Schizophrenia
Berman, J. A., Talmage, D. A., & Role, L. W. (2007) · International Review of Neurobiology · doi:10.1016/s0074-7742(06)78007-2 · Cited by 47
Ferencz, I., Leanza, G., Nanobashvili, A., Kokaia, Z., Kokaia, M., & Lindvall, O. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00499-1 · Cited by 47
Spinal mechanisms underlying A-85380-induced effects on acute thermal pain
Rueter, L. E., Meyer, M. D., & Decker, M. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02472-0 · Cited by 47
Regulation of hippocampal inhibitory circuits by nicotinic acetylcholine receptors
Griguoli, M., & Cherubini, E. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.220095 · Cited by 46
Nakauchi, S., & Sumikawa, K. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08056.x · Cited by 45
Actions of octocoral and tobacco cembranoids on nicotinic receptors
Ferchmin, P. A., Pagán, O. R., Ulrich, H., Szeto, A. C., Hann, R. M., & Eterović, V. A. (2009) · Toxicon · doi:10.1016/j.toxicon.2009.02.033 · Cited by 44
Acute synaptic modulation by nicotinic agonists in developing cerebellar Purkinje cells of the rat
Kawa, K. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.012885 · Cited by 43
Nicotinic acetylcholine receptor-mediated synaptic potentials in rat neocortex
Chu, Z., Zhou, F., & Hablitz, J. J. (2000) · Brain Research · doi:10.1016/s0006-8993(00)03076-6 · Cited by 40
Stoker, A. K., Olivier, B., & Markou, A. (2012) · Behavior Genetics · doi:10.1007/s10519-011-9511-0 · Cited by 40
Chang, Q., & Fischbach, G. D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1794-06.2006 · Cited by 40
Jia, Y., Yamazaki, Y., Nakauchi, S., & Sumikawa, K. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06706.x · Cited by 39
Sudweeks, S. N., van Hooft, J. A., & Yakel, J. L. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.029736 · Cited by 39
Morales, M., Hein, K., & Vogel, Z. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.12.019 · Cited by 40
Yamazaki, Y., Hamaue, N., & Sumikawa, K. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02935-9 · Cited by 39
Hunter, S. K., Kisley, M. A., McCarthy, L., Freedman, R., & Ross, R. G. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq036 · Cited by 38
Self-citationKalappa, B. I., Gusev, A. G., & Uteshev, V. V. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013964 · Cited by 39
Altered hippocampal circuit function in C3H α7 null mutant heterozygous mice
Adams, C. E., Yonchek, J. C., Zheng, L., Collins, A. C., & Stevens, K. E. (2008) · Brain Research · doi:10.1016/j.brainres.2007.12.007 · Cited by 35
Choline, folic acid, Vitamin D, and fetal brain development in the psychosis spectrum
Freedman, R., Hunter, S. K., Law, A. J., Clark, A. M., Roberts, A., & Hoffman, M. C. (2021) · Schizophrenia Research · doi:10.1016/j.schres.2021.03.008 · Cited by 36
Self-citationOndrejčák, T., Wang, Q., Kew, J. N. C., Virley, D. J., Upton, N., Anwyl, R., & Rowan, M. J. (2011) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2011.12.008 · Cited by 36
Ultrastructural Immunolocalization of the α7 nAChR Subunit in Guinea Pig Medial Prefrontal Cortex
Lubin, M., Erişir, A., & Aoki, C. J. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb11337.x · Cited by 35
Stevens, K. E., Kem, W. R., & Freedman, R. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00200-0 · Cited by 35
Self-citationCharacterization of a Nicotine-Sensitive Neuronal Population in Rat Entorhinal Cortex
Tu, B., Gu, Z., Shen, J., Lamb, P. W., & Yakel, J. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2580-09.2009 · Cited by 34
Nicotine induction of theta frequency oscillations in rodent hippocampus in vitro
Lu, C., & Henderson, Z. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.072 · Cited by 35
Metadata
- Authors
- Frazier, C. J., Rollins, Y. D., Breese, C. R., Leonard, S., Freedman, R., & Dunwiddie, T. V.
- Affiliations
- University of Colorado Health (US)
- United States Department of Veterans Affairs (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1998-02-15
- Volume
- 18
- Issue
- 4
- Pages
- 1187-1195
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6792737
- OpenAlex
- W2112157534
- Cited by
- 374
- References
- 48
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 1 · 2023: 3 · 2022: 1 · 2021: 9 · 2020: 6 · 2019: 6 · 2018: 9 · 2017: 6 · 2016: 8 · 2015: 18 · 2014: 13 · 2013: 10 · 2012: 15
- FWCI
- 10.12
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r29aa011164-05)
- National Institute on Alcohol Abuse and Alcoholism (AA11164)
- National Institute on Aging (R01AG010755)
- National Institute of Mental Health (MH-44212, P50MH044212)
- National Institute on Drug Abuse (DA 03194, R01DA003194, R01DA009457)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Keywords
- acetylcholine, alpha7 nicotinic acetylcholine receptor, alpha-bungarotoxin, hippocampal interneurons, CA1 pyramidal neurons, postsynaptic excitation, GABAergic inhibition, stratum radiatum, nicotinic antagonists
- MeSH terms
- Acetylcholine, Animals, Bungarotoxins, Electric Conductivity, gamma-Aminobutyric Acid, Hippocampus, Interneurons, Male, Nicotine, Receptors, Nicotinic, RNA, Messenger, Rats, Sprague-Dawley, Receptors, Presynaptic, Pyramidal Cells, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review