Заключение

Глава посвящена анализу основных звеньев систем регуляции моторного поведения: сенсомоторная кора, мозжечок, красное ядро и стриатум. Приведены работы последних лет. Описывается строение и связи этих структур, их участие в процессах обучения и памяти.

Литература

Аршавский Ю.И., Гельфанд И.М, Орловский, Г.Н. Мозжечок и управление ритмическими движениями. М.: Наука, 1984. 165 с.

Базян А.С. Нейромодуляторные интегративные механизмы формирования эмоционально-мотивационных состояний // Нейрохимия. 1999. Т 16. № 2. С. 88-103.

Базян А.С. Взаимодействие медиаторных и модуляторных систем головного мозга и их возможная роль в формировании психофизиологических и психопатологических состояний // Усп. физиол. наук. 2001. Т 32. № 3. С. 3-22.

Базян А.С., Григорьян Г.А. Молекулярно-химические основы эмоциональных состояний и подкрепления // Успехи физиол. наук. 2006.

Базян А.С., Сегал О.Л. Индуцируемый гиперполяризацией Ih пейсмекерный канал в головном мозге млекопитающих // Нейрохимия. 2010. Т 27. № 4. С. 269-279.

Базян А.С., Хашаев З.Х. Аллостерическая пластичность ГАМКА рецептора и внутринейрональная интеграция на уровне трансдукционного сигнала // Успехи физиол. наук. 2010. Т 41. № 1. С. 3-25.

Базян А.С., Григорьян ГА., Иоффе М.Е. Регуляция моторного поведения // Успехи физиол. наук. 2011. Т 42. № 3. С. 65-80.

Балезина Н.П. Нарушение выработанной двигательной координации после повреждения ядер мозжечка у собак // Сравнительная физиология высшей нервной деятельности человека и животных. М.: МГУ, 1988. ч. 1.

Балезина Н.П., Варга М.Е., Васильева О.Н., Иванова Н.Г., Иоффе М.Е., Павлова О.Г., Фролов А.Г. Исследование механизмов реорганизации двигательных координаций при обучении // Мозг и поведение. М.: Наука, 1990. С. 108-119.

Николлс Дж.Г., Мартин А.Р., Валлас Б.Дж., Фукс П.А. От нейрона к мозгу. М.: УРСС, 2003. 671 с.

Иоффе М.Е. Механизмы двигательного обучения. М.: Наука, 1991. 135 с.

Шаповалова К.Б. Современные представления о нейроморфологии и нейрохимии холинергической системы стриатума и ее роли в регуляции движений // ЖВНД. 1996. Т 46. № 4. С. 656-673.

Шаповалова К.Б. Мускариновые рецепторы неостриатума - участие в регуляции оперантного поведения у собак // Росс. физиол. журнал. 2000. Т 86. №. 11. С. 1404-1417.

Шаповалова К.Б., Камкина Ю.В. Сравнение эффектов системного (внутримышечного) и внутристриарного введения селективного блокатора Д1 дофаминовых рецепторов на двигательное поведение и перестройку позы у собак // ЖВНД. 2009. Т 59. № 2. С. 221-227.

Шепард Г. Нейробиология. М.: Мир, 1987. Т 1-2. 454 с.

Abercrombie E., De Boer P. Substantia nigra D1 receptors and stimulation of striatal cholinergic intemeurons by dopamine: A proposed circuit mechanism // J. Neurosci. 1997. Vol. 17. № 21. P. 8498-8505.

Aflado T.S., Graciano M.S.A. Relationship between unconstrained arm movements and single-neuron firing in the macaque motor cortex // J.

Albus J.S. A theory of cerebellar function // Math. Biosci. 1971. Vol. 10. P. 25-61.

Alexander G.E., DeLong M.R., Strick P.L. Parallel organization of functionally segregated circuits linking basal ganglia and cortex // Ann. Rev. Neurosci. 1986. Vol. 9. P. 357-381.

Alexander S.P.H., Mathie A., Peters J.A. Guide to Receptors and Channels (GRAC), 5th edition // Brit. J. Pharmacol. 2011. Vol. 164. Supl. 1. P. S1-S324.

Allen G.I, Tsukahara N. Cerebrocerebellar communication systems // Physiol. Rev. 1974. Vol. 54. P. 9571006.

Al Tajir G., Starr M.S. Anticonvulsant effect of striatal dopamine D2 receptor stimulation: dependence on cortical circuits? // Neurosci. 1991. Vol. 43. P. 51-57.

Amabeoku G., Chikuni O. GABAergic and dopaminergic systems may be involved in seizures induced by pyrimethamine in mice // Gen. Pharmacol. 1994. Vol. 25. P. 1269-1277.

AmalricM., OuagazzalA., Baunez C., Nieoullon A. Functional interactions between glutamate and dopamine in the rat striatum // Neurochem. Int. 1994. Vol. 25. P 123-131.

Ballion B., Mallet N., Bezard E. et al. Intratelencephalic corticostriatal neurons equally excite striatonigral and striatopallidal neurons and their discharge activity is selectively reduced in experimental parkinsonism // Eur. J. Neurosci. 2008. Vol. 27. P 2313-2321.

Baunez C., Nieoullon A., Amalric M. N-methyl-D-aspartate receptor blockade impairs behavioural performance of rats in a reaction time task: new evidence for glutamatergic-dopaminergic interactions in the striatum // Neurosci. 1994. Vol. 61. P. 521-531.

Bayazitov I. T., Kleshchevnikov A.M. Afferent high strength tetanizations favours potentiation of the NMDA vs AMPA receptor-mediated components of field EPSP in CA1 hippocampal slices of rats // Brain Res.

2000. Vol. 866. P. 15-23.

Bazyan A.S. Two types of epilepsy models and processes of cognition: Pentylenetetrazole kindling and absence epilepsy of WAG/Rij rats strain // Underlying Mechanisms of Epilepsy.

Bazyan A.S., van Luijtelaar G. Review Article. Neurochemical and Behavioral Features in Genetic Absence Epilepsy and in Acutely Induced Absence Seizures // ISRN Neurology. 2013, Article ID 875834, 48 pages. http://dx.doi.org/10.1155/2013/875834.

Bazyan A.S., Zhulin V.V., Karpova M.N., Klishina N.Y., Glebov R.N. Long-term reduction of benzodiazepine receptor density in the rat cerebellum by acute seizures and kindling and its recovery six months later by a pentylenetetrazole challenge // Brain Res. 2001. Vol. 888. № 2. P. 212-220.

Beloozerova I.N., Sirota M.G., Orlovsky G.N., Deliagina T.G. Activity of pyramidal tract neurons in the cat during postural correction // J. Neurophysiol. 2005. Vol. 93. P. 1831-1844.

Bevan M.D., Wilson C.J. Mechanisms underlying spontaneous oscillation and rhythmic firing in rat subthalamic neurons // J. Neurosci. 1999. Vol. 19. № 17. P. 7617-7628.

Biewenga J.E., Schrama L.H., Gispen W.H. Presynaptic phosphoprotein B-50/GAP-43 in neuronal and synaptic plasticity // Acta. Biochim. Pol. 1996. Vol. 43. P. 327-338.

Black J.E., Isaacs K.R., Anderson B.J., et al. Learning causes synaptogenesis, whereas motor activity causes angiogenesis, in cerebellar cortex of adult rats // Proc. Natl. Acad. Sci. USA. 1990. Vol. 87. P. 55685572.

Brindley G.S. The use made by the cerebellum of the information that it receives from sense organs // Int. Brain Res. Org. Bull. 1964. Vol. 3. P. 80.

Brooks-Kayal, M.R., Shumate, M.D., Jin, H., Rikhter, T.Y., Coulter, D.A. Selective changes in single cell GABAA receptors subunit expression and function in temporal lobe epilepsy // Nature Med. 1998. Vol. 4. P. 1166-1172.

Buhmann C., Gorsler A., Baumer T. et al. Abnormal excitability of premotor-motor connections in de novo Parkinson’s disease // Brain. 2004. Vol. 127. Pt 12. P. 2732-2746.

Buzsaki G., Smith A., Berger S., et al. Petit mal epilepsy and parkinsonian tremor: hypothesis of a common pacemaker // Neurosci.

Calabresi P., Picconi B., Tozzi A., Di Filippo. M. Dopamine-mediated regulation of corticostriatal synaptic plasticity // Trends in Neurosci. 2007. Vol. 30. P. 211-219.

Carmichael S. T., Chesselet M.-F. Synchronous Neuronal Activity Is a Signal for Axonal Sprouting after Cortical Lesions in the Adult // J. Neurosci. 2002. Vol. 22. P. 6062-6070.

Chen Z., Ito K., Fujii S., Miura M., Furuse H., Sasaki H., Kaneko K., Kato H., Miyakawa H. Roles of dopamine receptors in long-term depression: enhancement via D1 receptors and inhibition via D2 receptors // Receptors Channels. 1996. Vol. 4. P. 1-8.

Chen S., Wang J., Siegelbaum, S.A. Properties of hyperpolarization-activated pacemaker current defined by coassembly of HCN1 and HCN2 subunits and basal modulation by cyclic nucleotide // J. Gen. Physiol.

2001. Vol. 117. № 5. P. 491-504.

Civelli O., Bunzow J.R., Grandy D.K. Molecular diversity of the dopamine receptors // Ann. Rev. Pharmacol. Toxicol. 1993. Vol. 32. P. 281-307.

Clapham D.E. Not So Funny Anymore: Pacing Channels Are Cloned // Neuron. 1998. Vol. 21. № 1. P. 5-7.

Corda M.G., Orlandi M., Lecca D., Giorgi O. Decrease in GABAergic function induced by pentylenetetrazole kindling in rats: antagonism by MK-801 // J. Pharmacol. Exptl. Therap. 1992. Vol. 262. P. 792-800.

Damsma G., Robertson G.S., Tham C.S, Fibiger H.C. Dopamine regulation of striatal acetylcholine release: importance of D1and N-Methyl-D-aspartate receptors // J. Pharmacol. Exp. Ther. 1991. Vol. 259. № 3. P. 1064-1072.

Deadwyler S.A., Dunwiddie T., Lynch G. A critical level of protein synthesis is required long-term potentiation // Synapse. 1987. Vol. 1. P. 90-95.

De Boer P., Damsma G., Schram Q. et al. The effect of intrastriatal application of directly and indirectly acting dopamine agonists and antagonists on the in vivo release of acetylcholine measured by brain microdialysis. The importance of the post-surgery interval // Naun. Schmied. Arch.

DeLong M.R., Crutcher M.D, Georgopoulos A.P. Primate globus pallidus andsubthalamic nucleus: functional organization // J. Neurophysiol. 1985. Vol. 53. № 2. P. 530-543.

Diedrichsen J., Verstynen T., Lehman S.L., Ivry R.B. Cerebellar involvement in anticipating the consequences of self-produced actions during bimanual movements // J. Neurophysiol. 2005. Vol. 93. P. 801-812.

Diener H.C., Dichgans J., Guschlbauer B. et al. Associated postural adjustments with body movement in normal subjects and patients with parkinsonism and cerebellar disease // Rev. Neurol. (Paris). 1990. Vol. 146. P. 555-563.

DiFrancesco D. The cardiac hyperpolarizing-activated current If. Origins and developments // Prog. Bio- phys. Mol. Biol. 1985. Vol. 16. № 3. P. 163-183.

Doya K. What are the computations of the cerebellum, of the basal ganglia, and cerebral cortex // J. Neural Networks. 1999. Vol. 12. P. 961-974.

Doya K. Complementary roles of basal ganglia and cerebellum in learning and motor control // Curr. Opin. Neurobiol. 2000. Vol. 10. P. 732-739.

Evans M.S., Viola-McCabe K.E. Midazolam inhibits long-term potentiation through modulation of GABAA receptors // Neuropharmacol. 1996. Vol. 35. P. 347-357.

Evarts E.V Relation of pyramidal tract activity to force exerted during voluntary movement // J. Neurophysiol. 1968. Vol. 31. P 14-27.

FlahertyA.W., GraybielA.M. Corticostriatal transformations in the primate somatosensory system. Projections from physiologically mapped body-part representations // J. Neurophysiol. 1991. Vol. 66. P. 1249-1263.

Georgopoulos A.P., Kalaska J.F, Caminiti R, Massey J.T. On the relations between the direction of twodimensional arm movements and cell discharge in primate motor cortex // J. Neurosci. 1982. Vol. 2. P. 1527-1537.

Georgopoulos A.P, Ashe J., Smyrnis N., Taira M. The motor cortex and the coding of force // Science. 1992. Vol. 256. P. 1692-1695.

Gomi H., Kawato M. Equilibrium-point control hypothesis examined by measured arm stiffness during multijoint movement // Science. 1996. Vol. 272. P. 117-120.

Gradano M.S.A., Taylor C.S.R., Moore T. Complex movements evoked by microstimulation of precentral cortex // Neuron. 2002. Vol. 34. P. 841-851.

Greengard P., Allen P.B., Nairn A.C. Beyond the dopamine receptor: the DARPP-32/protein phosphatase-1 cascade // Neuron. 1999. Vol. 23. N 3. P 435-447.

Hagiwara N., Irisawa H., Kameyama M. Contribution of two types of calcium currents to the pacemaker potentials of rabbit sino-atrial node cells // J. Physiol. Lond. 1988. Vol. 395. P. 233-253.

HallettM. Plasticity of the human motor cortex and recovery from stroke // Brain Res. Rev. 2001. Vol. 36. P 169-174.

Higashima M., Kinoshita H., Koshino Y. Differences in the effects of zolpidem and diazepam on recurrent inhibition and long-term potentiation in rat hippocampal slices // Neurosci. Lett. 1998. Vol. 245. P. 77-80.

Hicks A., Davis S., Rodger J., Helme-Guizon A., Laroche S., Mallet J. Synapsin I and syntaxin 1B: key elements in the control of neurotransmitter release are regulated by neuronal activation and long-term potentiation in vivo // Neurosci. 1997. Vol. 79. P 329-340.

Hikosaka O. Basal ganglia mechanisms of reward-oriented eye movement // Ann. N. Y. Acad. Sci. 2007. Vol. 1104. P 229-249.

Hikosaka O., Tarikawa Y., Kawagoe R. Role of the basal ganglia in the control of purposive saccadic eye movements // Physiol. Rev. 2000. Vol. 80. P. 953-978.

Houk J.C. Neurophysiology of frontal-subcortical loops // Frontal-Subcortical Circuits. Psychiatry and Neurology. Ed. D.G. Lichter. NY: Cummings Guilford Publications, 2001. Ch. 4. P 92-113.

Houk J.C, Buckingham J.T, Barto A.G. Models of the cerebellum and motor learning // Behav. Brain Sci. 1996. Vol. 19. P 368-383.

Imamizu H., Miyauchi S., Tamada T. et al. Human cerebellar activity reflecting an acquired internal model of a new tool // Nature. 2000. Vol. 403. P. 192-195.

Imperato A., ObinuM.C., CasuM.A., MasciaM.S., DazziL., Gessa G.L. Evidence that neuroleptics increase striatal acetylcholine releasethrough stimulation of dopamine D1 receptors // J. Pharmacol. Exp. Ther. 1993. Vol. 266. № 2. P. 557-562.

Ioffe M.E, Ivanova N.G, Frolov A.A. et al. On the role of motor cortex in the learned rearrangement of postural coordinations // Stance and Motion. Facts and Concepts. Eds VS. Gurfinkel, M.E. Ioffe, J. Mas- sion, J.P. Roll. NY: Plenum Press, 1988. P. 213-226.

Ioffe M.E., Ustinova K.I., Chernikova L.A., Kulikov M.A. Supervised learning of postural tasks in patients with poststroke hemiparesis, Parkinson’s disease or cerebellar ataxia // Exp. Brain. Res. 2006. Vol. 168. P. 384-394.

Irisawa H., Brown H.F., Giles W. Cardiac pacemaking in the sinoatrial node // Physiol. Rev. 1993. Vol. 73. № 1. P. 197-227.

Ito M. Recent advances in cerebellar physiology and pathology // Adv. Neurol. 1978. Vol. 21. P. 59-84.

Ito M. The cerebellum and neural control. NY: Raven Press, 1984.

Ito M. Long-term depression // Annu. Rev. Neurosci. 1989. Vol. 12. P. 85-102.

Ito M. Movement and thought: identical control mechanisms by the cerebellum // Trends Neurosci. 1993. Vol. 16. P 448-450.

ItoM. Mechanisms of motor learning in the cerebellum // Brain Res. 2000. Vol. 886. P. 237-245.

Ito M., KarachotL. Protein kinases and phosphatase inhibitors mediating long-term desensitization of glutamate receptors in cerebellar Purkinje cells // Neurosci. Res. 1992. Vol. 14. P. 27-38.

Joel D., Weiner I. The connections of the primate subthalamic nucleus: indirect pathways and the open- interconnected scheme of basal gangliathalamocortical circuitry // Brain. Res. Rev. 1997. Vol. 23. № 1. P. 62-78.

Johnston J.D., Price S.A. and Bristow D.R. Flunitrazepam rapidly reduces GABA(A) receptor subunit protein expression via a protein kinase C-dependent mechanism // Br. J. Pharmacol. 1998. Vol. 124. P. 1338-1340.

Kawato M., WolpertD. Internal models for motor control // Novartis Found Symp. 1998. Vol. 218. P. 291304.

Kokaia M., Pratt G.D., Elmer E., Bengzon J., Fritschy J.M., Kokaia Z., Lindvall O., Mohler H. Biphasic differential changes of GABAA receptor subunit mRNA levels in dentate gyrus granule cells following recurrent kindling-induced seizures // Mol. Brain Res. 1994. Vol. 23. P. 323-332.

Koff J.M., Pritchard, G.A., Greenblatt, D.J., Miller, L.G. The NMDA receptor competitive antagonist CPP modulates benzodiazepine tolerance and discontinuation // Pharmacol. 1997. Vol. 55. P. 217-227.

KotterR. Postsynaptic integration of glutamatergic and dopaminergic signals in the striatum // Prog. Neuro- biol. 1994. Vol. 44. P. 163-196.

Kornhuber H.H. Cerebral cortex, cerebellum and basal ganglia: an introduction to their motor functions // The Neurosci.: 3rd Study Progr. Eds. F.O. Schmidt, F.G. Worden. Cambridge: MIT Press, 1974. P. 267-280.

KrishekB.J., XieX., Blackston C., HuganirR.L., MossS.J., Smart T.G. Regulation of GABAA receptor function by protein kinase C phosphorylation // Neuron. 1994. Vol. 12. P. 1081-1095.

Lehmann O., Jeltsch H., Lehnardt O., Pain L., Lazarus C., Cassel J.C. Combined lesions of cholinergic and serotonergic neurons in the rat brain using 192 IgG-saporin and 5,7-dihydroxytryptamine: neurochemical and behavioural characterization // Eur. J. Neurosci. 2000. Vol. 12. № 1. P. 67-79.

LlinasR., Welsh J.P. On the cerebellum and motor learning // Curr. Opin. Neurobiol. 1993. Vol. 3. P. 958-965.

MacdonaldR.L., OlsenR.W. GABAA receptor channels // Annu. Rev. Neurosci. 1994. Vol. 17. P. 569-602.

Marr D. A theory of cerebellar cortex // J. Physiol. 1969. Vol. 202. P. 437-470.

Martin J.P. The basal ganglia and posture. Putman, 1967.

Matsumura M., Kojima J., Gardiner T. W., Hikosaka O. Visual and oculomotor functions of monkey subthalamic nucleus // J. Neurophysiol. 1992. Vol. 67. № 6. P. 1615-1632.

MayfordM., Abel T., KandelE.R. Transgenic approaches to cognition // Cur. Opin. Neurobiol. 1995. Vol. 5. P. 141-148.

Mayse J.F., De Vietti T.L. A comparison of state-dependent learning induced by electroconvulsive shock and pentobarbital // Physiol. Behav. 1971. Vol. 7. P. 717-721.

Mink J.W. The basal ganglia // Fundamental Neuroscience. 2nd edition. Eds. L.R. Squire, F.T. Bloom, S.C. McConnell S.C. et al. Elsevier Science, Academic Press, 2003. P. 815-839.

Miyachi S. Cortico-basal ganglia circuits--parallel closed loops and convergent/divergent connections // Brain Nerve. 2009. Vol. 61. P. 351-359.

NicollR.A., MalenkaR.C., Kauer J.A. Functional comparison of neurotransmitter receptor subtypes in mammalian central nervous system // Physiol. Rev. 1990. Vol. 70. № 2. P 513-565.

NilesL.P., Smith L.J., Tenn C.C. Modulation of c-fos expression in the rat striatum by diazepam // Neurosci. Lett. 1997. Vol. 236. P 5-8.

Nudo R.J., Milliken G.W., Jenkins W.M., Merzenich M.M. Use-dependent alterations of movement representations in primary motor cortex of adult squirrel monkeys // J. Neurosci. 1996. Vol. 16. P 785-807.

Nudo R.J., Plautz E.J., Frost S.B. Role of adaptive plasticity in recovery of function after damage to motor cortex // Muscle Nerve. 2001. Vol. 24. P 1000-1019.

Olsen R.W., Yang J., King R.G., Dilber A., Stauber G.B., Ransom R.W. Barbiturate and benzodiazepine modulation of GABA receptor binding and function // Life Sci. 1986. Vol. 39. P 1969-1976.

Ogren S.O., Pakh B. Effects of dopamine D1 and D2 receptor agonists and antagonists on seizures induced by chemoconvulsants in mice // Pharmacol. Toxicol. 1993. Vol. 72. P 213-220.

Parent A., Hazrati L.N. Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidum in basal ganglia circuitry // Brain Res. Rev. 1995. Vol. 20. № 1. P. 128-154.

Pasqualotto B.A., Lanius R.A., Shaw C.A. Regulation of GABAA and AMPA receptors by agonist and depolarizing stimulation requires phosphatase or kinase activity // Neuroreport. 1993. Vol. 4. P. 447-450.

Phillips C.G., Porter R. Corticospinal neurones. Their role in movement. Monogr. Physiol. Soc. 1977. Vol. 34. 450 p.

Pisani A., Bonsi P., Picconi B. et al. Role of tonically-active neurons in the control of striatal function: cellular mechanisms and behavioral correlates // Prog. Neuropsychopharm. Biol. Psychiatry. 2001. Vol. 25. P. 211-230.

Plautz E.J., Milliken G.W., Nudo R.J. Effects of repetitive motor training on movement representations in adult squirrel monkey: Role of use vs. learning // Neurobiology of Learning and Memory. 2000. Vol. 74. P. 27-55.

Porter R., Lemon R.N. Corticospinal Function and Voluntary Movement. Oxford: Clarendon Press. 1993. 421 p

Pratt G.D., Kokaia M., Bengzon J., Kokaia Z., Fritschy J. M., Mohler H., Lindvall O. Differential regulation of N-methyl-D-aspartate receptor subunit messenger RNAs in kindling-induced epileptogenesis // Neurosci. 1993. Vol. 57. P 307-318.

Qin Z. H., Weiss B. Dopamine receptor blockade increases dopamine D2 receptor and glutamic acid decarboxylase mRNAs in mouse substantia nigra // Eur. J. Pharmacol. 1994. Vol. 269. P 25-33.

Redgrave P., Prescott T.J., Gurney K. The basal ganglia: a vertebrate solution to the selection problem? // Neuroscience. 1999. Vol. 89. P 1009-1023.

Roth R.H., Wolf M.E., Deutch A.Y. Neurochemisry of midbrain dopamine system // Psychopharmacology: The Third Generation of Progress. Ed. H.Y. Meltzer. NY: Raven Press, 1987. Ch. 9. P 81-98.

Roth R.H., Wolf M.E., DeutchA.Y. Biochemical pharmacology of midbrain dopamine system // Psychopharmacology: The Fourth Generation of Progress. Eds. F.E. Bloom, D.J. Kupfer. NY: Raven Press, 1995. Ch. 21. P 227-243.

Sanes J.N., Donoghue J.P. Plasticity and primary motor cortex // Ann. Rev. Neurosci. 2000. Vol. 23. P 393415.

Sasaki K, Gemba H. Learning of fast and stable hand movement and cerebro-cerbellar interactions in the monkey // Brain Res. 1983. Vol. 277. P 41-46.

Schugens M.M., Breitenstein C., Ackermann H., Daum I. Role of the striatum and the cerebellum in motor skill acquisition // Behav. Neurol. 1998. Vol. 11. P 149-157.

Schultz W. Predictive reward signal of dopamine neurons // J. Neurophysiol. 1998. Vol. 80. P 1-27.

Schultz W., Dayan P., Montague P.R. A neural substrate of prediction and reward // Science. 1997. Vol. 275. P 1593-1599.

Seabrook G.R., Easter A., Dawson G.R., Bowery B.J. Modulation of long-term potentiation in CA1 region of mouse hippocampal brain slices by GABAA receptor benzodiazepine site ligands // Neuropharmacol. 1997. Vol. 36. P 823-830.

See R.E., Aravagiri M., Ellison G.D. Chronic neuroleptic treatment in rats produces persisting changes in GABAA and dopamine D-2, but not dopamine D-1 receptors // Life. Sci. 1989. Vol. 44. P. 229-236.

See R.E., Toga A.W., Ellison G. Autoradiographic analysis of regional alterations in brain receptors following chronic administration and withdrawal of typical and atypical neuroleptics in rats // J. Neural. Transm. Gen. Sect. 1990. Vol 82. P. 93-109.

Sigma-RBI Handbook of Receptor Classification and Signal Transduction, 5th ed. Ed. K. Watling. Sigma- RBI, 2006. 384 p.

Smirnova T., Laroche S., Errington M.L., Hicks A.A., Bliss T.V., Mallet J. Transsynaptic expression of a presynaptic glutamate receptor during hippocampal long-term potentiation // Science. 1993. Vol. 262. P. 433-436.

Stackman R.W., Walsh T.J., Brucato F.H., Swartzwelder H.S. Medial septal benzodiazepine receptors modulate hippocampal evoked responses and long-term potentiation // Brain Res. 1996. Vol. 717. P. 12-21. Stanton P.K., Sarvey J.M. Blockade of norepinephrine-induced long-lasting potentiattion in the hippocampal dentate gyrus by an inhibitor of protein synthesis // Brain Res. 1985. Vol. 361. P. 276-283.

Stephens D.N., Turski L. Kindling to the benzodiazepine receptor inverse agonist, FG 7142: evidence for involvement of NMDA, but not non-NMDA, glutamatergic receptors // Neuropharmacol. 1993. Vol. 132. P. 1011-1817.

Stoof J.C., DrukarchB., DeBoerP., WesterinkB.H.C., GroenewegenH.J. Regulation of the activity of striatal cholinergic neurons by dopamine // Neurosci. 1992. Vol. 47. № 4. P. 755-770.

Suri R.E. TD Models of reward predictive responses in dopamine neurons // Neural. Networks. 2002. Vol. 15. P. 523-533.

Thach W.T. On the specific role of the cerebellum in motor learning and cognition: clues from PET activation and lesion studies in man // Behav. Brain Sci. 1996. Vol. 19. P. 411-431.

Timmerman W., Abercrombie E.D. Amphetamine-induced release of dendritic dopamine in substantia nigra pars reticulata: D1-mediated behavioral and electrophysiological effects // Synapse. 1996. Vol. 23. № 4. P. 280-291.

Tobler P.N., Fiorillo C.D., Schultz W. Adaptive coding of reward value by dopamine neurons // Science. 2005. Vol. 307. P. 1642-1645.

Todorov E., Jordon M.I. Optimal feedback control as a theory of motor coordination // Nat. Neurosci. 2002. P. 1226-1235.

Zackheim J., Abercrombie E.D. Thalamic regulation of striatal acetylcholine efflux is both direct and indirect and qualitatively altered in the dopamine-depleted striatum // Neurosci. 2005. Vol. 131. № 2. P. 423-436.