ВОПРОСЫ ЭВОЛЮЦИИ ЦИКЛА БОДРСТВОВАНИЕ-СОН. ЧАСТЬ 2: НЕЙРОМЕДИАТОРНЫЕ МЕХАНИЗМЫ РЕГУЛЯЦИИ

Г.А. Оганесян, Е.А. Аристакесян, И.В. Романова, С.И. Ватаев, В.В. Кузик, Д.К. Камбарова

Аннотация


Во второй части обзора по эволюции цикла бодрствование-сон рассмотрены литературные и собственные данные о нейромедиаторных и нейрогормональных механизмах его регуляции. Отмечены оригинальные работы авторов по сравнительным морфологическим и иммуногистохимическим особенностям состояния дофамин-, глутамат- и ГАМК-ергических нейромедиаторных систем в диэнцефальных и телэнцефальных отделах головного мозга в условиях сондепривационного стресса и постдепривационного сна и по морфофункциональному состоянию вазопрессин(вазотоцин)- и окситоцин(мезотоцин)-ергической систем диэнцефалона в цикле бодрствование-сон у холоднокровных и теплокровных позвоночных. По мере становления структурной дифференциации переднемозговых отделов и развития диэнцефальных и стволовых систем в филогенезе степень совместности в локализации нейромедиаторных систем заметно снижается. Происходит дифференциация нейромедиаторных систем, их разделение на тормозные и активирующие за счет формирования большого разнообразия специфических рецепторов. В конечном счете, все это способствует формированию многоуровневых систем запуска и поддержания высокоэффективных бодрствования и сна.

Ключевые слова


эволюция ЦНС, цикл бодрствование-сон, сноподобные формы покоя холоднокровных, иммуногистохимия, нейромедиаторы, нейрогормоны.

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Литература


Аристакесян Е.А. Сравнительный нейрофизиологический анализ цикла бодрствование-сон в раннем постнатальном онтогенезе крыс и морских свинок // Ж. эвол. биохим. и физиол. – 1997. – Т. 33. – C. 622–629.

Аристакесян Е.А. Эволюционные аспекты взаимодействия сна и стресса: фило-онтогенетический подход // Ж. эвол. биохим. и физиол. – 2009. – Т. 45. – С. 598–611.

Арушанян Э.Б. Ритмоорганизующие структуры мозга и фармакологический эффект // Вестник РАМН. – 2000. – № 8. – С. 17–21.

Карамян А.И. Эволюция конечного мозга позвоночных. – Л. : Наука, 1976.

Карманова И.Г. Новое об особенностях сна и организации цикла бодрствованиесон холоднокровных позвоночных // Ж. эвол. биохим. и физиол. – 1996. – Т. 32. – С. 511–535.

Карманова И.Г., Аристакесян Е.А., Шиллинг Н.В. Нейрофизиологический анализ гипоталамических механизмов регуляции первичного сна и гипобиоза // ДАН СССР. – 1987. – Т. 294. – С. 245–248.

Карманова И.Г., Хомутецкая О.Е., Шиллинг Н.В. Сравнительно-физиологический анализ эволюции сна и механизмов его регуляции // Усп. физиол. наук. – 1981. – Т. 12. – № 2. – С. 3–20.

Карманова И.Г., Шиллинг Н.В., Аристакесян Е.А., Попова Н.К. Влияние ингибитора синтеза серотонина – парахлорфенилаланина на структуру первичного сна травяной лягушки Rana temporaria // Ж. эвол. биохим. физиол. – 1984. – Т. 20. – С. 511–516.

Ковальзон В.М. Основы сомнологии: физиология и нейрохимия цикла «бодрствование – сон». – М. : Бином, 2012.

Нейродегенеративные заболевания: фундаментальные и прикладные аспекты / под ред. М.В. Угрюмова. – М. : Наука, 2010.

Оганесян Г.А., Аристакесян Е.А., Романова И.В. и др. Дофаминергическая нигростриатная система в условиях депривации сна у крыс // Рос. физиол. ж. им. И.М. Сеченова. – 2007. – Т. 93. – С. 1344–1354.

Оганесян Г.А., Аристакесян Е.А., Романова И.В. и др. Вопросы эволюции цикла бодрствование-сон. Часть 1: нейрофизиологические аспекты // Биосфера. – 2011. – Т. 3. – № 4. – С. 514–531.

Оганесян Г.А., Аристакесян Е.А., Романова И.В. О фило-онтогенетическом становлении дофаминовой регуляции цикла бодрствование-сон позвоночных // Рос. физиол. ж. им. И.М. Сеченова. – 2012. – Т. 98. C. 1213– 1227.

Оганесян Г.А., Романова И.В., Аристакесян Е.А. и др. Диэнцефало-телэнцефальные изменения тирозингидроксилазы у крыс и травяных лягушек при депривации сна // Ж. эвол. биохим. и физиол. – 2008. – Т. 44. – С. 250–257.

Оганесян Г.А., Романова И.В., Аристакесян Е.А. и др. Дофаминергическая система телэнцефало-диэнцефальных отделов головного мозга позвоночных в организации цикла бодрствование-сон // Рос. физиол. ж. им. И.М. Сеченова. – 2008. – Т. 94. – С. 1071 –1091.

Оганесян Г.А., Романова И.В., Аристакесян Е.А. Участие активирующих систем переднего мозга в организации цикла бодрствование-сон // Рос. физиол. ж. им. И.М. Сеченова. – 2011. – Т. 94. – С. 193–204.

Оганесян Г.А., Романова И.В., Глазова М.В. и др. О механизмах участия возбуждающих нейротрансмиттерных систем переднего мозга в регуляции двигательной активности позвоночных // Сб.: Актуальные проблемы интегративной деятельности и пластичности нервной системы. Ред. Казарян К.В. – Ереван : Гитутюн, 2009. – С. 231 –234.

Поленов А.Л., Кулаковский Э.Е. Происхождение и эволюция нейроэндокринных клеток и нейрогормональной регуляции у Metazoa // Основы современной физиологии (нейроэндокринология). – Кн. 1. – Ч. 1. – Л. : Наука, 1993. – C. 139–187.

Попова Н.К., Лобачева И.И., Карманова И.Г., Шиллинг Н.В. Изменение уровня серотонина в мозгу при различных формах покоя первичного сна у лягушки Rana temporaria // Ж. эвол. биохим. и физиол. – 1982. – Т. 18. – С. 430–432.

Попова Н.К., Науменко Е.В., Колпаков В.Г. Серотонин и поведение. – Новосибирск : Наука, 1978.

Силькис И.Г. Гипотетический механизм взаимовлияний нейромодуляторов при парадоксальном сне // Нейрохимия. – 2006. – T. 23. – № 4. – C. 299–309.

Шабанов П.Д., Лебедев А.А., Мещеров Ш.К. Дофамин и подкрепляющие системы мозга. – СПб. : Лань, 2002.

Элиава М.И., Аристакесян Е.А. Эффекты шестичасовой тотальной депривации сна на цикл бодрствование-сон крыс в разные сроки онтогенеза // Ж. эвол. биохим. и физиол. – 1998. – Т. 34. – С. 202–211.

Airaksinen M.S., Panula P. Comparative neuroanatomy of the histaminergic system in the brain of the frog Xenopus laevis // J. Comp. Neurol. – 1990. – V. 292. – № 3. – P. 412–423.

Akanmu M.A., Honda K. Selective stimulation of orexin receptor type 2 promotes wakefulness in freely behaving rats // Brain Res. – 2005. – Vol. 1048. – P. 138–145.

Argiolas A., Gessa G.L. Central functions of oxytocin // Neurosci. Biobehav. Rev. – 1991. – V. 15. – P. 217–231.

Arihara Z., Takahashi K., Murakami O. et al. Orexin-A in the human brain and tumor tissues of ganglioneuroblastoma and neuroblastoma // Peptides. – 2000. – Vol. 21. – P. 565–570.

Arrigoni E., Rainnie D.G., McCarley R.W., Greene R.W. Adenozine-mediated presynaptic modulation of glutamatergic transmission in laterodorsal tegmentum // J. Neurosci. – 2001. – Vol. 21. – P. 1076–1085. 117

Azmitia E.C., Segal M. An autoradiographic analysis of the differential ascending projections of the dorsal and median raphe nuclei in the rat // J. Comp. Neurol. – 1978. – Vol. 179. – P. 641–667.

Bannai M., Kawai N. New therapeutic strategy for amino acid medicine: glycine improves the quality of sleep // J. Pharmacol. Sci. – 2012. – Vol. 118. – P. 145–148.

Bannai M., Kawai N., Nagao K. et al. Oral administration of glycine increases extracellular serotonin but not dopamine in the prefrontal cortex of rats // Psychiatry Clin. Neurosci. – 2011. – Vol. 65. – P. 142–149.

Bayer L., Eggermann E., Saint-Mleux B. et al. Selective action of orexin (hypocretin) on nonspecific thalamocortical projection neurons // J. Neurosci. – 2002. – Vol. 22. – P. 7835–7839.

Benington J.H., Heller H.C. Restoration of brain energy metabolism as the function of sleep // Prog. Neurobiol. – 1995. – Vol. 45. – P. 347–360.

Berridge C., Waterhouse B. The locus coeruleus noradrenergic system: modulation of behavioral state and state –dependent cognitive processes // Brain Res. Rev. – 2003. – Vol. 42. – P. 33–84.

Borbely A.A. A two process model of sleep regulation // Human Neurobiol. – 1982. – № 1. – P. 195–204.

Borbely A.A. From slow waves to sleep homeostasis: new perspectives // Arch. Ital. Biol. – 2001. – Vol. 139. – P. 53–61.

Borland L.M., Michael A.C. Voltammetric study of the control of striatal dopamine release by glutamate // J. Neurochem. – 2004. – Vol. 91. – P. 220–229.

Boutrel B., Monaca C., Hen R. et al. Involvement of 5-HT1A receptors in homeostatic and stress-induced adaptive regulations of paradoxical sleep: studies in 5-HT1A knock-out mice // J. Neurosci. – 2002. – Vol. 22. – P. 4686–4692.

Broman J., Rinvik E., Sassoe-Pognetto M. et al. Glutamate // The rat nervous system / Ed. by G. Paxinos – San Diego : Elsevier, 2004. – Р. 1269– 1292.

Brooks P.L., Peever J.H. Glycinergic and GABA(A)-mediated inhibition of somatic motoneurons does not mediate rapid eye movement sleep motor atonia // J. Neurosci. – 2008. – Vol. 28. – P. 3535–3545.

Brown R.E., McCarley R.W. Neuroanatomical and neurochemical basis of wakefulness and REM sleep systems // Neurochemistry of sleep and wakefulness / Eds.: J.M. Monty, S.R. PandiPerumal, C.M. Sinton. – Cambridge University Press, 2008. – P. 23–58.

Burlet S., Cespuglio R. Voltammetric detection of nitric oxide (NO) in the rat brain: its variations throughout the sleep-wake cycle // Neurosci. Lett. – 1997. – Vol. 226. – P. 131 –135.

Cardinali D.P., Pandi-Perumal S.R., Niles L.P. Melatonin and its receptors: biological function in circadian sleep-wake regulation // Neurochemistry of sleep and wakefulness / Eds.: J.M. Monty, S.R. Pandi-Perumal, C.M. Sinton. – Cambridge University Press, 2008. – P. 283–314.

Carl V., Moroni F. General anaesthetics inhibit the responses induced by glutamate receptor agonists in the mouse cortex // Neurosci. Lett. – 1992. – Vol. 146. – P. 21–24.

Carlsson A. Perspectives on the discovery of central monoaminergic neurotransmission //Ann. Rev. Neurosci. – 1987. – Vol. 10. – P. 19–40.

Carnes K.M., Fuller T.A., Price J.L. Sources of presumptive glutamatergic/aspartatergic afferents to the magnocellular basal forebrain in the rat // J. Comp. Neurol. – 1990. – Vol. 302. – P. 824–852.

Castro S.L., Zigmond M.J. Stress-induced increase in extracellular dopamine in striatum: role of glutamatergic action via N-methyl-D-aspartate receptors in substantia nigra // Brain Res. – 2001. – Vol. 901. – P. 47 –54.

Cespuglio R., Walker E., Gomez M.E., Musolino R. Cooling of the nucleus raphe dorsalis induces sleep in the cat // Neurosci. Lett. – 1976. – Vol. 3. – № 4. – P. 221–227.

Chase M.H., Soja P.J., Morales F.R. Evidence that glycine mediates the postsynaptic potentials that inhibit lumbar motoneurons during the atonia of active sleep // J. Neurosci. – 1989. – Vol. 9. – P. 743–751.

Chemelli R.M., Willie J.T., Sinton C.M. et al. Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation // Cell. – 1999. – Vol. 98. – P. 437–451.

Chu J., Wilczynski W., Wilcox E. Pharmacological characterization of the D1- and D2-like dopamine receptors from the brain of the leopard frog, Rana pipiens // Brain Behav. Evol. – 2001. – Vol. 57. – P. 328–342.

Clinton J.M., Davis C.J., Zielinski M.R. et al. Biochemical regulation of sleep and sleep biomarker // J. Clin. Sleep Med. – 2011. – Vol. 7. – № 5 (Suppl). – P. S38–S42.

Cunha R.A. Adenosine as a neuromodulator and as a homeostatic regulator in the nervous system: different roles, different sources and different receptors // J. Neurochem. – 2001. – Vol. 74. – P. 334–338.

Curtis D.R., Hosli L., Johnston G.A. Inhibition of motoneurones by iontophoresis of glycine // Nature. – 1967. – Vol. 215. – P. 1502–1503.

Datta S., Patterson E.H., Spoley E.E. Excitation of the pedunculopontine tegmental NMDA receptors induces wakefulness and cortical activation in the rat // J. Neurosci. Res. – 2001. – Vol. 66. – P. 109–116.

Datta S., Spoley E.E., Patterson E.H. Microinjection of glutamate into the pedunculopontine tegmentum induces REM sleep and wakefulness in the rat // Am. J. Physiol. Regul. Integr. Comp. Physiol. – 2001. – Vol. 280. – P. R752 –R759.

Duck U., Roth G. Evolution of the amphibian nervous system // Evolution of nervous systems: a comprehensive reference / Eds. J.H. Kaas, T.H. Bullock. – Vol. 2. – Amsterdam, Boston etc. : Acad. Press., 2007. – P. 64–123.

Economo C. Encephalitis lethargica // Wien Med. Wochenschr. – 1923. – Vol. 73. – P. 777–782.

Elazar Z., Berchanski A. Glutamatergic-cholinergic synergistic interaction in the pontine reticular formation. Effects on catalepsy // NaunynSchemiedbergs Arch. Pharmacol. – 2001. – Vol. 363. – P. 569 –576.

Endepols H., Roden K., Luksch H. et al. Dorsal striato-pallidal system in anurans // J. Comp. Neurol. – 2004. – Vol. 468. – P. 299–310.

Feinberg I., Cambell I.G. Glutamate neurotransmission and sleep // Neurochemistry of sleep and wakefulness / Eds.: J.M. Monty, S.R. PandiPerumal, C.M. Sinton. – Cambridge University Press, 2008. – P. 224–243.

Fink G. Neuroendocrine system // Stress Science: Neuroendocrinology / Ed. by G. Fink. – Amsterdam, Boston etc. : Acad. Press., 2010. – P. 45–58.

Ford B., Holmes C.J., Mainville L., Jones B.E. GABAergic neurons in the rat pontomesencephalic tegmentum: codistribution with cholinergic and other tegmental neurons projecting to the posterior lateral hypothalamus // J. Comp. Neurol. – 1995. – Vol. 363. – P. 177–196.

Frank M.G., Stryker M.P., Tecott L.H. Sleep and sleep homeostasis in mice lacking the 5-HT2c receptor // Neuropsychopharmacol. – 2002. – Vol. 27. – P. 869–873.

Fredholm B.B., Arslan G., Halldner L. et al. Structure and function of adenosine receptors and their genes // Naunyn Schmiedebergs Arch. Pharmacol. – 2000. – Vol. 362. – P. 364–374.

Galas L., Vaudry H., Braun B. et al. Immunohistochemical localization and biochemical characterization of hypocretin/orexin-related peptides in the central nervous system of the frog Rana ridibunda // J. Comp. Neurol. – 2001. – Vol. 429. – P. 242–252.

Gallopin T., Luppi P.H., Cauli B. et al. The endogenous somnogen adenosine excites a subset of sleep promoting neurons via A2A receptors in the ventrolateral preoptic nucleus // Neurosci. – 2005. – Vol. 134. – P. 1377–1390.

Gerashchenko D., Kohls M.D., Greco M. et al. Hypocretin-2-saporin lesions of the lateral hypothalamus produce narcoleptic-like sleep behavior in the rat // J. Neurosci. – 2001. – Vol. 21. – P. 7273–7283.

Gervasoni D., Peyron D., Rampon C. et al. Role and origin of the GABAergic innervation of dorsal raphe serotoninergic neurons // J. Neurosci. – 2000. – Vol. 20. – P. 4217–4225.

Glagow M., Ewert J.-P. Dopaminergic modulation of visual responses in toads. 1 Apomorphine-induced effects on visually directed appetitive and consummatory prey-catching behavior // J. Comp. Physiol. – 1997. – Vol. 380. – P. 1–9.

Glendenning K.K. Distribution of muscimol, QNB and 5HT binding in the vertebrate diencephalon: a comparative study of eight mammals and three non-mammals // Microsc. Res. Tech. – 2003. – Vol. 62. – P. 247–261.

Gonzalez A., Smeets W.J.A.J. Comparative analysis of dopamine and tyrosine hydroxylase immunoreactivities in the brain of two amphibians, the anauran Rana ridibunda and the urodele Pleurodeles waltlii // J. Comp. Neurol. – 1991. – Vol. 303. – P. 457–477.

Goodson J.L., Bass A.H. Social behavior function and related characteristics of vasotocin/ vasopressin in systems in vertebrates // Brain Res. Rev. – 2001. – Vol. 35. – P. 246–265.

Gottesmann C. The neurochemistry of waking and sleeping mental activity: the disinhibitiondopamine hypothesis // Psychiatry Clin. Neurosci. – 2002. – Vol. 56. – P. 345–354.

Haas H.L., Konnerth A. Histamine and noradrenaline decrease calcium-activated potassium conductance in hippocampal pyramidal cells // Nature. – 1983. – Vol. 302. – P. 432–434.

Hayaishi O. Molecular genetic studies on sleep-wake regulation, with special emphasis on the prostaglandin D2 system // J. Appl. Physiol. – 2002. – Vol. 92. – P. 863–868.

Hess W.R. Das Schlafsyndrom als Folge diencephaler Reizung // Helv. Physiol. Acta. – 1944 – Vol. 2. – P. 305–344.

Hilakivi I., Leppavuori A., Putkonen P.T. Prazosin increases paradoxical sheep // Eur. J. Pharmacol. – 1980. – Vol. 65. – P. 417–420.

Hobson J.A., McCarley R.W., Wyzinski P.W. Sleep cycle oscillation: reciprocal discharge by two brainstem neuronal groups // Science. – 1975. – Vol. 189. – P. 55–58.

Hollis D.M., Boyd S.K. Distribution of GABA-like immunoreactive cell bodies in the brains of two amphibians, Rana catesbeiana and Xenopus laevis // Brain Behav. Evol. – 2005. – Vol. 65. – P. 127–142.

Holmes C.J., Jones B.E. Importance of cholinergic, GABAergic, serotonergic and other neurons in the medial medullary reticular formation for sleep-wake states studied by cytotoxic lesions in the cat // Neurosci. – 1994. – Vol. 62. P. 1179– 2000.

Horner R.L., Kubin L. Pontine carbachol elicits multiple rapid eye movement sleep-like neural events in urethane-anaesthetized rats // Neurosci. – 1999. – Vol. 93. – P. 215–226.

Huang Z.L., Qu W.M., Eguchi N. et al. Adenosine A2A, but not A1, receptors mediate the arousal effect of caffeine // Nat. Neurosci. – 2005. – Vol. 8. – P. 858–859.

Isaak S.O., Berridge C.W. Wake-promoting actions of dopamine D1 and D2 receptor stimulation // J. Pharmacol. Exp. Ther. – 2003. – Vol. 307. – P. 386–394.

Jones B.E. Cytoarchitecture, transmitters and projections // The Rat Nervous System. / Ed.: G. Paxinos. – San Diego : Acad. Press, 1995. – P. 155–171.

Jones B.E. Arousal systems // Front. Biosci. – 2003. – Vol. 8. – P. 438–451.

Jones B.E. From waking to sleeping neuronal and chemical substrates // Trends Pharmacol. Sci. – 2005. – Vol. 26. –P. 578–586.

Jouvet M. Mechanisms of the state of sleep: a neuropharmacological approach // Sleep and Altered States of Consciousness / Eds.: S.S. Kety, V. Evarts, H.L. Williams. – Baltimore : Williams and Wilkins, 1967. – P. 86–126.

Jouvet M. Role of monoamines and acetylcholine containing neurons in the regulation of the sleep-waking cycle // Ergeb. Physiol. – 1972. – Vol. 4. – P. 166–307.

Kim U., Sanchez-Vives M.V., McCormick D.A. Functional dynamics of GABAergic inhibition in the thalamus // Science. – 1997. – Vol. 278. – P. 130–134. 119

Kloet de E.R. From vasotocin to stress and cognition // Eur. J. Pharmacol. – 2010. – Vol. 626. – P. 18–26.

Korotkova T.M., Eriksson K.S., Haas H.L., Brown R.E. Selective excitation of GABAergic neurons in the substantia nigra of the rat by orexin/hypocretin in vitro // Regul. Pept. – 2002. – Vol. 104. – P. 83–89.

Krueger J.M., Obal F.J., Fang J. et al. The role of cytokines in physiological sleep regulation // Ann. N.Y. Acad. Sci. – 2001. – Vol. 933. – P. 211–221.

Krystal A.D., Goforth H.W., Roth T. Effects of antipsychotic medications on sleep in schizophrenia // Int. Clin. Psychopharmacol. – 2008. – Vol. 23. – P. 150–160.

Lai Y.Y., Siegel J.M. Pontomedullary glutamate receptors mediating locomotion and muscle tone suppression // J. Neurosci. – 1991. – Vol. 11. – P. 2931–2937.

Lancel M., Kromer S., Neumann I.D. Intracerebral oxytocin modulates sleep –wake behaviour in male rats // Regulatory Peptides. – 2003. – Vol. 114. – P. 145–152.

Landgraf R. Intracerebrally released vasopressin and oxytocin: measurement, mechanisms and behavioural consequences // J. Neuroendocrinol. – 1995. – P. 243–253.

Le Crom S., Kapsimali M, Barome P.-O. Vernier P. Dopamine receptors for every species: gene duplications and functional diversification in craniates // J. Structural and Functional Genomics. – 2003. – Vol. 3. – P. 161–176.

Lee M.G., Hassani O.K., Jones B.E. Discharge of identified orexin/hypocretin neurons across the sleep-waking cycle // J. Eurosci. – 2005. – Vol. 25. – P. 6716–6720.

Leppavuori A., Putkonen, P.T. Alpha-adrenoceptive influences on the control of the sleepwaking cycle in the cat // Brain Res. – 1980. – Vol. 193. – P. 95–115.

Lin J.S., Hou Y., Sakai K., Jouvet M. Histaminergic descening inputs to mesopontine tegmentum and their role in the control of cortical activation and wakefulness in the cat // J. Neurosci. – 1996. – Vol. 16. – P 1523–1537.

Liu R.J., van den Pol A.N., Aghajanian G.K. Hypocretins (orexins) regulate serotonin neurons in the dorsal raphe nucleus by excitatory direct and inhibitory indirect actions // J. Neurosci. – 2002. – Vol. 22. – P. 9453–9464.

Lu J., Bjorkum A.A., Xu M. et al. Selective activation of the extended ventrolateral preoptic nucleus during rapid eye movement sleep // J. Neurosci. – 2002. – Vol. 22. – P. 4568–4576.

Lu J., Greco M.A., Shiromani P.J., Saper C.B. Effect of lesions of the ventrolateral preoptic nucleus on NREM and REM sleep // J. Neurosci. – 2000. – Vol. 20. – P. 3830–3842.

Luppi P.H. Neurochemical aspects of sleep regulation with specific focus on slow-wave sleep // World J. Biol. Psychiatry. – 2010. – Vol. 11 (Suppl.1). – P. 4–8.

Luppi P.H., Charlety P.J., Fort P. et al. Anatomical and electrophysiological evidence for a glycinergic inhibitory innervation of the rat locus coeruleus // Neurosci. Lett. – 1991. – Vol. 128. – P. 33–36.

Luppi P.H., Clement O., Sapin E. et al. Brainstem mechanisms of paradoxical (REM) sleep generation // Pflugers Arch. – 2012. – Vol. 463. – P. 43 –52.

Luppi Р.H., Gervasoni D., Verret L. et al. Paradoxical (REM) sleep genesis: The switch from an aminergic-cholinergic to a GABAergicglutamatergic hypothesis // J. Physiol. (Paris). – 2006. – Vol. 100. – P. 271–283.

Luppi P.H., Sakai K., Fort P. et al. The nuclei of origin of monoaminergic, peptidergic, and cholinergic afferents to the cat nucleus reticularis magnocellularis: a double-labeling study with cholera toxin as a retrograde tracer // J. Comp. Neurol. – 1988. – Vol. 277. – P. 1–20.

Lydic R, Baghdoyan H.A. Acetylcholine modulates sleep and wakefulness: a synaptic perspective // Neurochemistry of Sleep and Wakefulness / Eds.: J.M. Monty, Pandi S.R. -Perumal, C.M. Sinton. – Cambridge University Press, 2008. – P. 109–143.

Lydic R., Baghdoyan H.A. Pedunculopontine stimulation alters respiration and increases ACh release in the pontine reticular formation // Am. J. Physiol. – 1993. – Vol. 264. – P. R544– R554.

Lynch J.W. Native glycine receptor subtypes and their physiological roles // Neuropharmacol. – 2009. – Vol. 56. – P. 303–309.

Maggini C., Guazzelli M., Pieri M. et al. REM latency in psychiatric disorders: polygraphic study on major depression, bipolar disorder-manic, and schizophrenic disorder // New Trends Exp. Clin. Psychiatry. – 1986. – Vol. 2. – P. 93–101.

Marn O., Gonzlez A., Smeets W.J. Basal ganglia organization in amphibians: efferent connections of the striatum and the nucleus accumbens // J. Comp. Neurol. – 1997. – Vol. 380. – P. 23– 50.

Marn O., Gonzlez A., Smeets W.J. Basal ganglia organization in amphibians: afferent connections of the striatum and the nucleus accumbens // J. Comp. Neurol. – 1997. – Vol. 378. – P. 16– 90.

Marn O., Smeets W.J., Gonzlez A. Basal ganglia organization in amphibians: evidence for a common pattern in tetrapods // Prog. Neurobiol. – 1998. – Vol. 55. – P. 363–397.

Matsumura H., Nakajima T., Osaka T. et al. Prostaglandin D2-sensitive, sleep promoting zone defined in the ventral surface of the rostral basal forebrain // Proc. Natl. Acad. Sci. USA. – 1994. – Vol. 91. – P. 11998–12002.

McCarley R.W., Hobson J.A. Neuronal excitability modulation over the sleep cycle: a structural and mathematical model // Science. – 1975. – Vol. 189. – P. 58–60.

McGinty D., Alam N., Gong H. et al. Neurochemistry of the preoptic hypothalamic hypnogenic mechanism // Neurochemistry of Sleep and Wakefulness / Eds.: J.M. Monti, S.R. PandiPerumal, Ch.M. Sinton. – Cambridge University Press, 2008. P. 3–23.

Minacate H. Oxitocin/vasopressin and gonadotropin hormone from cephalopods to vertebrates // Ann. N.-Y. Acad. Sci. – 2010. – Vol. 1200. – P. 33–42.

Monti J.M. Catecholamines and the sleepwake cycle. II. REM sleep // Life Sci. – 1983. – Vol. 32. – P. 1401–1415.

Monti J.M. Involvement of histamine in the control of the waking state // Life Sci. – 1993. – Vol. 53. – P. 1331–1338.

Monti J.M. Serotonin control of sleep-wake behavior // Sleep Med. Rev. – 2011. – Vol. 15. – P. 269 –281.

Monti J.M., Jantos H. Effects of the serotonin 5HT1A receptor ligands flesinoxan and WAY 100635 given оr microinjected into the laterodorsal tegmental nucleus on REM sleep in the rat // Behav. Brain Res. – 2004. – Vol. 151. – P. 159–166.

Monti J.M., Jantos H. Microinjection of the nitric oxide synthase inhibitor L-NAME into the lateral basal forebrain alters the sleep/wake cycle of the rat // Prog. Neuropsychopharmacol. Biol. Psychiatry. – 2004. – Vol. 28. – P. 239–247.

Monti J.M., Jantos H. Effects of the serotonin 5-HT 2A/2C receptor agonist DOI and of the selective 5-HT2A or 5-HT2C receptor antagonists EMD 281014 and SB-243213, respectively, on sleep and waking in the rat // Eur. J. Pharmacol. – 2006. – Vol. 553. – P. 163–170.

Monti J.M., Jantos H. The roles of dopamine and serotonin, and of their receptors, in regulating sleep and waking // Prog. Brain Res. – 2008. – Vol. 17. – P. 625–646.

Monti J.M., Jantos H., Monti D. Serotonin and sleep-wake regulation // Neurochemistry of Sleep and Wakefulness / Eds.: J.M. Monti, S.R. Pandi-Perumal, C.M. Sinton. – Cambridge University Press, 2008. – P. 244–283.

Monti J.M., Jantos H., Ponzoni A. et al. Role of nitric oxide in sleep regulation: effects of L-NAME, an inhibitor of nitric oxide synthase, on sleep in rats // Behav. Brain Res. – 1999. – Vol. 100. – P. 197–205.

Monti J.M., Monti D. Role of dorsal raphe nucleus serotonin 5-HT1A receptor in the regulation of REM sleep // Life Sci. – 2000. – Vol. 66. – P. 1999–2012.

Monti J.M., Monti D. The involvement of dopamine in the modulation of sleep and waking // Sleep Med. – 2007. – Vol. 11. – P. 113–133.

Moore R., Bloom F. Central catecholamine neuron systems: anatomy and physiology of the norepinephrine and epinephrine systems // Ann. Rev. Neurosci. – 1979. – P. 113–168.

Morales F.R., Sampogna S., Rampon C. et al. Brainstem glycinergic neurons and their activation during active (rapid eye movement) sleep in the cat // Neurosci. – 2006. – Vol. 142. – P. 37–47.

Moruzzi G., Magoun H.W. Brainstem reticular formation and activation of the EEG // Electroencephalogr. Clin. Neurophysiol. – 1949. – Vol. 1. – P. 455–473.

Nadal M. Secretory rhythm of vasopressin in healthy subjects with inversed sleep-wake cycle: evidence for the existence of an intrinsic regulation // Eur. J. Endocrinol. – 1996. – Vol. 134. – P. 174–176.

Nathan C., Xie Q. Nitric oxide synthases: roles, tolls and controls // Cell. – 1994. – Vol. 78. – P. 915–918.

Neary N.J., Norcutt G. Nuclear organization of the bullfrog diencephalon // J. Comp. Neurol. – 1983. – Vol. 213. – P. 262–278.

Neumann I.D., Wigger A., Torner L. et al. Brain oxytocin inhibits basal and stress-induced activity of the hypothalamo-pituitary-adrenal axis in male and female rats: partial action within the paraventricular nucleus // J. Neuroendocrinol. – 2000. – P. 235–244.

Nishino S., Shelton J., Renaud A. et al. Effect of 5-HT1A receptor agonists and antagonists on canine cataplexy // J. Pharmacol. Exp. Ther. – 1995. – Vol. 272. – P. 1170–1175.

Nitz D., Siegel J. GABA release in the dorsal raphe nucleus: role in the control of REM sleep // Am. J. Physiol. – 1997. – Vol. 273. – P. R451–R455. 141. Novak С.M., Nunez A.A. Daily rhythms in Fos activity in the at ventrolateral preoptic area and midline thalamic nuclei // Am. J. Physiol. – 1998. – Vol. 275. – № 5 (Pt 2). – P. R1620–R1626.

Obal F. Jr., Alfoldi P., Cady A.B. et al. Growth hormone-releasing factor enhances sleep in rats and rabbits // Am. J. Physiol. Regul. Integr. Comp. Physiol. – 1988. – Vol. 255. – P. R310– R316.

Obal F. Jr., Krueger J.M. GHRH and sleep // Sleep Med. Rev. – 2004. – P. 367–377.

O’Brien L.M., Ivanenko A., Crabtree V.M. et al. Sleep disturbances in children with attention deficit hyperactivity disorder // Pediatr. Res. – 2003. – Vol. 54. – P. 237–243.

Okuno A., Fukuwatari T., Shibata K. High tryptophan diet reduces extracellular dopamine release via kynurenic acid production in rat striatum // J. Neurochem. – 2011. – Vol. 118. – P. 796– 805.

Onoe H., Sakai K. Kainate receptors: a novel mechanism in paradoxical (REM) sleep generation // Neuroreport. – 1995. – P. 353–356.

Panula P., Pirvola U., Auvinen S., Airaksinen M.S. Histamine-immunoreactive nerve fibers in the rat brain // Neurosci. – 1989. – Vol. 28. – P. 585 –610.

Parga J., Rodriguez-Pallares J., Munoz A. et al. Serotonin decreases generation of dopaminergic neurons from mesencephalic precursors via serotonin type 7 and type 4 receptors // Dev. Neurobiol. – 2007. – Vol. 67. – P. 10–22.

Parmentier R., Ohtsu H., Djebbara-Hannas Z. et al. Anatomical, physiological, and pharmacological characteristics of histidine decarboxylase knock-out mice: evidence for the role of brain histamine in behavioral and sleep-wake control // J. Neurosci. – 2002. – Vol. 22. – P. 7695–7711.

Pavel S., Adrien J. Vasotocin increases quite sleep and suppresses active sleep in newborn cats. Opposite effects after vasotocin immunoneutralization // Brain Res. Bull. – 1989. – Vol. 23. – P.463–466.

Perras B., Wagner U., Born J., Fehm H.L. Improvement of sleep and pituitary-adrenal inhibition after subchronic intranasal vasopressin treatment in elderly humans // J. Clin. Psychopharmacol. – 2003. – Vol. 23. – P. 35–44.

Peterfi Z., McGinty D., Sarai E., Szymusiak R. Growth hormone-releasing hormone activates sleep regulatory neurons of the rat preoptic hypothalamus // Am. J. Physiol. Regul. Integr. Comp. Physiol. – 2010. – Vol. 298. – P. R147–R156. 121

Peyron C., Tighe D.K., van den Pol A.N. et al. Neurons containing hypocretin (orexin) project to multiple neuronal systems // J. Neurosci. – 1998. – Vol. 18. – P. 9996–10015.

Pompeiano M., Cirelli C., Tononi G. Effects of sleep deprivation on fos-like immunoreactivity in the rat brain // Arch. Ital. Biol. – 1992. – Vol. 130. – P. 325–335.

Porkka-Heiskanen T., Strecker R.E., Bjorkum A.A. et al. Adenosine: a mediator of the sleepinducing effects of prolonged wakefulness // Science. – 1997. – Vol. 276. – P. 1265–1268.

Porkka-Heiskanen T., Alanko L., Stenberg D. Neurochemistry of sleep // Cell. Mol. Life Sci. – 2007. – Vol. 64. – P. 1187–1204.

Porkka-Heiskanen T., Kalinchuk A.V. Adenosine, energy metabolism and sleep homeostasis // Sleep Med. – 2011. – Vol. 15. – P. 123 –135.

Pulles L., Milan F.J., de la Torre M. A segmental map of subdivisions in the diencephalons of the Rana perezi: Acetilcholinesterase-histochemical observations // Brain Behav. Evol. – 1996. – Vol. 7. – P. 279–310.

Raggenbuss M. Vasopressin- and oxytocin-induced activity in the central nervous system: electrophysiological studies using in vitro system // Prog. Neurobiol. – 2001. – Vol. 64. – P. 307 –326.

Rainnie D.G., Grunze H.C., McCarley R.W., Greene R.W. Adenosine inhibition of mesopontine cholinergic neurons: implications for EEG arousal // Science. – 1994. – Vol. 263. – P. 689–692.

Ramanathan G., Cilz N.I., Kurada L. et al. Vasopressin facilitates GABAergic transmission in rat hippocampus via activation of V(1A) receptors // Neuropharmacol. – 2012. – Vol. 63. – P. 1218–1226.

Renaud L.P., Bourque C.W. Neurophysiology and neuropharmacology of hypothalamic magnocellular neurons secreting vasopressin and oxytocin // Prog. Neurobiol. – 1991. – Vol. 36. – P. 131–169.

Sakai K., Crochet S. Serotonergic dorsal raphe neurons cease firing by disfacilitation during paradoxical sleep // Neuroreport. – 2000. – P. 3237–3241.

Sakai K., Crochet S., Onoe H. Pontine structures and mechanisms involved in the generation of paradoxical (REM) sleep // Arch. Ital. Biol. – 2001. – Vol. 139. – P. 93–107.

Sakurai T. The neural circuit of orexin (hypocretin) maintaining sleep and wakefulness // Nat. Rev. Neurosci. – 2007. – P. 171–181.

Sakurai T., Amemiya A., Ishii M. et al. Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior // Cell. – 1998. – Vol. 92. – P. 1696.

Sakurai T., Nagata R., Yamanaka A. et al. Input of orexin/hypocretin neurons revealed by a genetically encoded tracer in mice // Neuron. – 2005. – Vol. 46. – N 2. – P. 297–308.

Saper C.B., Cano G., Scammell T.E. Homeostatic, circadian and emotional regulation of sleep // J. Comp. Neurol. – 2005. – Vol. 493. – P. 92–98.

Satoh S., Matsamura H., Hayaishi O. Involvement of adenosine A2A receptor in sleep promotion // Eur. J. Pharmacol. – 1998. – Vol. 351. – P. 155–162.

Scammell T.E., Gerashcenko D., Mochizuki T. et al. An adenosine A2a agonist increases sleep and induces Fos in ventrolateral peroptic neurons // Neurosci. – 2001. – Vol. 107. – P. 653– 663.

Seifritz E., Moore P., Trachsel L. et al. The 5-HT1A agonist ipsapirone enhances EEG slow wave activity in human sleep and produces a power spectrum similar to 5-HT2 blockade // Neurosci. Lett. – 1996. – Vol. 209. – P. 41–44.

Sherin J.E., Elmqiust J.K., Torrealba F., Saper C.B. Innervation of histaminergic tuberomammillary neurons by GABAergic and galaninergic neurons in the ventrolateral preoptic nucleus of the rat // J. Neurosci. – 1996. – Vol. 18. – P. 4705– 4721.

Sherin J.E., Shiromani P.J., McCarley R.W., Saper C.B. Activation of ventrolateral preoptic neurons during sleep // Science. – 1996. – Vol. 271. – P. 216–219.

Siegel J.M. Hypocretin (orexin): role in normal behavior and neuropathology // Ann. Rev. Psychol. – 2004. – Vol. 55. – P. 125–148.

Sleep: Neurotransmitters and Neuromodulators / Ed.: A.N. Wauquier. – New York : Raven Press, 1985.

Smeets W.J., Gonzlez A. Catecholamine systems in the brain of vertebrates: new perspectives through a comparative approach // Brain Res. Rev. – 2000. – Vol. 33. – P. 308–379.

Smeet W.J.A.J., Marin O., Gonzalez A. Evolution of basal ganglia: new perspectives through a comparative approach // J. Anat. – 2000. – Vol. 196. – P. 501–517.

Smeet W.J.A.J., Reiner A. Catecholamines in the CNS of vertebrates: current concepts of evolution and functional significance // Phylogeny and Development of Catecholamine Systems in the CNS of Vertebrates / Eds.: W.J.A.J. Smeet, A. Reiner. – Cambridge University Press, 1994. – Р. 463–481.

Sofroniew M.V., Eckenstein F., Thoenen H., Cuello A.C. Topography of choline acetyltransferase-containing neurons in the forebrain of the rat // Neurosci. Lett. – 1982. – Vol. 33. – P. 7–12.

Sorensen E., Bjorvatn B., Ursin R. Sleepwake effects following the selective 5-HT(1A) receptor antagonist p-MPPI in the freely moving rat // Behav. Brain Res. – 2000. – Vol. 114. – P. 31–38.

Stanford S.C. 5-Hydoxytriptamine // Neurotransmitters, Drugs, and Brain Function / Еd.: R.A. Webster. – Chichester : John Wiley & Sons, 2001. – P. 187–209.

Steinberg D. Neuroanatomy and neurochemistry of sleep // Cell. Mol. Life Sci. – 2007. – Vol. 64. – P.1187 –1204.

Steinberg D., Litonius E.E., Halldner L. et al. Sleep and its homeostatic regulation in mice lacking the adenosine A1 receptor // Sleep Res. – 2003. – Vol. 12. – N 4. – P. 283 –290.

Steinberg D., Porka-Heiskanen T. Adenozine and sleep-wake regulation // Neurochemistry of Sleep and Wakefulness / Eds.: J.M. Monti, S.R. Pandi-Perumal, Ch.M. Sinton. – Cambridge University Press. – 2008. – P. 337–564.

Steininger T.L., Alam M.N., Gong H. et al. Sleep-waking discharge of neurons in posterior lateral hypothalamus of the albino rat // Brain Res. – 1999. – Vol.840. – P. 138–147.

Steriade M., Glenn L.L. Neocortical and caudate projections of intralaminar thalamic neurons and their synaptic excitation from midbrain reticular core // J. Neurophysiol. – 1982. – Vol. 48. – P. 352–371.

Steriade M., McCarley R. Brain Control of Wakefulness and Sleep. – New York: Kluwer Plenum, 2005.

Surendran S., Rady P.L., Szucs S. et al. High level of orexin A observed in the phenylketonuria mouse brain is due to the abnormal expression of prepro-orexin // Biochem. Biophys. Res. Com. – 2004. – Vol.317. – P. 522 –526.

Szymusiak R., Gvilia I., McGinty D. Hypothalamic control of sleep // Sleep Med. – 2007. – Vol. 8. – P. 291–301.

Szymusiak R., McGinty D. Hypothalamic regulation of sleep and arousal // Ann. N.-Y. Acad. Sci. – 2008. – Vol. 1129. – P. 275–286.

Takahashi Y., Kipnis D.M., Daughaday W.H. Growth hormone secretion during sleep // J. Clin. Invest. – 1968. – Vol. 47. – P. 2079–2090.

Thakkar M.M., McCarley R.W. Histamine in the control of sleep-wakefulness // Neurochemistry of Sleep and Wakefulness / Eds.: J.M. Monti, S.R. Pandi-Perumal, Ch.M. Sinton. – Cambridge University Press. – 2008. – P. 14–178.

Thorppe A.J., Cleary J.P., Levine A.S., Kotz S.M. Centrally administered orexin A increases motivation for sweet pellets in rats // Psychopharmacol. – 2005. – Vol.182. – P. 75–83.

Thorpy M.J., Adler C.H. Parkinson’s disease and sleep // Neurol. Clin. – 2005. – P. 1187– 1208.

Tobler I., Borbelly A. Sleep regulation after reduction of brain serotonin: effect of p-chlorphenylalanine combined with sleep deprivation in the rat // Sleep. – 1982. – Vol. 5. – P. 145–153.

Toppila J., Alanko L., Asikainen M. et al. Sleep deprivation increases somatostatin and growth hormone -releasing hormone messenger RNA in the rat hypothalamus // J. Sleep Res. – 1997. – P. 171–178.

Trbovic S.M. Schizophrenia as a possible dysfunction of the suprachiasmatic nucleus // Med. Hypotheses. – 2010. – Vol. 74. – P. 127–131.

Trulson M.E., Jacobs B.L. Raphe unit activity in freely moving cats: correlation with level of behavioral arousal // Brain Res. – 1979. – Vol.163. – P. 135–150.

Urade Y., Eguchi N., Qu W.M. et al. Sleep regulation in adenosine A2A receptor-deficient mice // Neurology. – 2003. – Vol. 61. – N 11 (Supp. 6). – P. S94–S96.

Uschakov A., Gong H., McGinty D., Szymusiak R. Sleep-active neurons in the preoptic area project to the hypothalamic paraventricular nucleus and perifornical lateral hypothalamus // Eur. J. Neurosci. – 2006. – Vol. 23. – P. 3284–3296.

Van Cauter E., Plat L., Copinschi G. Interrelations between sleep and the somatotropic axis // J. Neurophysiol. – 1998. – Vol. 21. – P. 553–566.

Vanni-Mercier G., Gigout S., Debilly G., Lin J.S. Waking selective neurons in the posterior hypothalamus and their response to histamine H3- receptor ligands: an electrophysiological study in freely moving cats // Behav. Brain Res. – 2003. – Vol.144. – P. 227–241.

Villar-Cerviño V., Barreiro-Iglesias A., Anadón R., Rodicio M.C. Distribution of glycine immunoreactivity in the brain of adult sea lamprey (Petromyzon marinus). Comparison with gammaaminobutyric acid // J. Comp. Neurol. – 2008. – Vol.507. – P. 1441–1463.

Vincent J.D. From phylogenesis to physiology: dopamine receptors // Bull. Mem. Acad. R. Med. Belg. – 1996. – Vol.151. – P. 417–427.

Watson С.О., Helen A., Baghdoyan Н.А., Lydic R. Neuropharmacology of sleep and wakefulness // Sleep Med. Clin. – 2010. – Vol. 5. – P. 513–528.

Welsh J.H. Distribution of serotonin in the nervous system of various animal species // Advances in Pharmacology. Vol. 6. Pt A. – N.-Y.; London : Acad. Press, 1968. – P. 171–190.

Westhoff G., Roth G. Morphology and projection pattern of medial and dorsal pallial neurons in the frog Discoglossus pictus and the salamander Plethodon jordani // J. Comp. Neurol. – 2002. – Vol.445. – P. 97–121.

Wied de D., Diamant M., Fodor M. Central nervous system effects of the neurohypophyseal hormones and related peptides // Front. Neuroendocrinol. – 1993. – Vol. 14. – P. 251–302.

Williams J.A., Reiner P.B. Noradrenaline hyperpolarizes identified rat mesopontine cholinergic neurons in vitro // J. Neurosci. – 1993. – Vol. 13. – P. 3878–3883.

Wu M., Zhang Z., Leranth C. et al. Hypocretin increases impulse flow in the septohippocampal GABAergic pathway: implications for arousal via a mechanism of hippocampal disinhibition // J. Neurosci. – 2002. – Vol. 22. – P. 7754–7765.

Yamamoto K., Vernier P. The evolution of dopamine systems in chordates // Front. Neuroanat. – 2011. – Vol. 5. – P. 21.

Yamamura T., Harada K., Okamura A., Kemmotsu O. Is the site of action of ketamine anesthesia the N-methyl-D-aspartate receptor? // Anesthesiology. – 1990. – Vol. 72. – P. 704–710.

Yon L., Feuilloley M., Charnay Y., Vaudry H. Immunohistochemical localization of delta sleep-inducing peptide-like immunoreactivity in the central nervous system and pituitary of the frog Rana ridibunda // Neurosci. – 1992. – Vol. 47. – P. 221–240.

Zhdanova I.V. Sleep in zebrafish // Zebrafish. – 2006. – Vol. 3. – P. 215–226.

Zhdanova I.V., Wurtman R.J. The pineal hormone – melatonin // Endocrinology: Basic and Clinical Principles / Eds.: P.M. Conn, S. Melmed. – Totowa, N.J. : Humana Press. – 1998. – P. 279–290.




DOI: http://dx.doi.org/10.24855/biosfera.v5i1.315

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