The aim of the present work was to study the morphology of the brain and to analyze the behavior of the offspring of female rats with chronic alcohol intoxication. Experiments were performed using 60-day-old animals born to mothers with chronic alcoholic hepatobiliary system disease. Over a period of 1.5 months, one group of animals was reared in standard conditions, the other in an enriched environment. Behavior was analyzed in an open field test. The thicknesses of the cortex and its molecular layer were also studied. The offspring of mothers with chronic hepatobiliary system disease were characterized by decreased movement and exploratory activity and increased emotional reactivity, which were accompanied by changes in the structure of the cortex. Prolonged placing of “alcoholic” rats in the enriched environment for 1.5 months promoted increases in movement and exploratory activity and emotional reactivity, and produced changes in the structure of the cortex.
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G. V. Bryukhin and M. L. Sizonenko, “The role of experimental liver damage in mothers in the development of physiological immaturity in offspring,” Byull. Eksperim. Biol. Med., 154, No. 11, 544–547 (2012).
G. V. Bryukhin, “Morphofunctional characteristics of the thyroid in the offspring of female rats with chronic experimental liver disease of different etiologies,” Morfologiya, 128, No. 5, 56–69 (2005).
T. Buresh, O. Bureshova, and D. P. Houston, Methods and Basic experiments for Studies of Brain and Behavior, Vysshaya Shkola, (1991).
Yu. V. Burov, N. N. Vedernikova, V. Ya. Ivanov, and T. I. Ivanenko, “Changes in the gonadotropic function of the hypophysis in rats on development of experimental alcoholism,” Byull. Eksperim. Biol. Med., 12, No. 6, 675–676 (1986).
V. A. Vakhnin and G. B. Bryukhin, “Characteristics of the formation of spatial orientation in the offspring of female rats with experimental liver disease in the Morris water maze,” Ros. Fiziol. Zh., 99, No. 4, 464–470 (2013).
I. As. Volchegorskii, I. I. Dolgushin, O. L. Kolesnikova, and V. E. Tseilikman, Experimental Modeling and the Laboratory Evaluation of Body Reactions, Chelyabinsk State Medical Academy, Chelyabinsk (2000).
M. N. Zaichenko, G. L. Vanetsian, and G. Kh. Merzhanova, “Differences in the behavior of impulsive and self-controlled rats on testing in the open field and light-dark boxes,” Zh. Vyssh. Nerv. Deyat., 61, No. 3, 340–350 (2011).
E. V. Koplik, R. M. Salieva, and A. V. Gorbunova, “The open field test as a prognostic criterion for resistance to emotional stress in Wistar rats,” Zh. Vyssh. Nerv. Deyat., 45, No. 4, 775–781 (1995).
A. B. Kuznetsova and G. V. Bryukhin, “Characteristics of neurosecretory hypothalamic cells in the offspring of female rats with chronic alcohol intoxication at different stages of postnatal ontogeny,” in: Current Directions in Theoretical and Applied Research, Chernomor’e, Odessa (2006), pp. 40–41.
A. B. Kuznetsova and G. V. Bryukhin, “The influence of chronic alcoholic disease in female rats on the structural-functional establishment of neurosecretory cells in the supraoptic nucleus of their offspring,” Vestn. YurGU, 4, No. 104, 29–30 (2008).
A. L. Markel’, “Evaluation of major behavioral characteristics in rats in the open field test,” Zh. Vyssh. Nerv. Deyat., 31, No. 2, 301–307 (1981).
G. I. Mikhailova, G. V. Bryukhin, and E. N. Pashnina, “Comparative characteristics of structural-functional changes in the spleen in the offspring of female rats with experimental chronic liver disease of different etiologies,” Morfologiya, 3, 48–51 (2005).
O. V. Perepelkina, N. V. Markina, and I. I. Poletaeva, “The ability to extrapolate movement direction in mice selected for large and small brain weight: effects of being kept in an ‘enriched’ environment,” Zh. Vyssh. Nerv. Deyat., 56, No. 2, 282–286 (2006).
D. S. Sarkisov and Yu. L. Perov, Techniques in Microscopy, Meditsina, Moscow (1996).
K. Yu. Sarkisova, M. A. Kulikov, and I. A. Kolomeitseva, “Effects of substance P on behavioral measures in the open field and forced swimming tests in rats with different types of behavior,” Byull. Eksperim. Biol. Med., 3, 244–247 (1996).
A. F. Semiokhina and M. G. Pleskacheva, “Nonspecific grooming in rats during solution of an extrapolation task,” Zh. Vyssh. Nerv. Deyat., 39, No. 2, 284–291 (1989).
M. L. Sizonenko, G. V. Bryukhin, and D. S. Las’kov, “Morphological characteristics of spermatogenesis in the offspring of female rats with chronic alcohol intoxication,” Morfologiya, 143, No. 1, 59–62 (2013).
L. N. Trup and P. M. Borodin, “Formation of behavior in some laboratory rodents exposed to environments at the early stages of ontogeny,” Usp. Sovrem. Biol., 82, No. 4, 143–155 (1976).
M. M. Shekhtman, Handbook of Extragenital Pathology in Pregnancy, Triada, Moscow (2005).
M. Day, R. Langston, and R. G. M. Morris, “Glutamate-receptormediated encoding and retrieval of paired-associate learning,” Nature, 424, No. 7, 205–209 (2003).
R. G. Bechara, and A. M. Kelly, “Exercise improves object recognition memory and induces BDNF expression and cell proliferation in cognitively enriched rats,” Behav. Brain Res., 245, 96–100 (2013).
A. M. Birch, N. B. McGarry, and A. M. Kelly, “Short-term environmental enrichment, in the absence of exercise, improves memory and increases NGF concentration, early neuronal survival and synaptogenesis in the dentate gyrus in a time-dependent manner,” Hippocampus, 23, No. 6, 437–450 (2013).
M. C. Diamond, D. Krech, and M. R. Rosenzweig, “The effects of an enriched environment on the histology of the rat cerebral cortex,” J. Comp. Neurol., 123, 111–120 (1964).
T. D. Gould, Mood and Anxiety Related Phenotypes in Mice, Humana Press (2009).
K. M. Hutchinson, K. J. McLaughlin, R. L. Wright, et al., “Environmental enrichment protects against the effects of chronic stress on cognitive and morphological measures of hippocampal integrity,” Neurobiol. Learn. Mem., 97, No. 2, 250–260 (2012).
H. B. Katz and C. A. Davies, “Effects of differential environments on the cerebral anatomy of rats as a function of previous and subsequent housing conditions,” Exp. Neurol., 83, 274–287 (1984).
G. Kempermann, H. G. Kuhn, and F. H. Gage, “Experience-induced neurogenesis in the senescent dentate gyrus,” J. Neurosci., 18, 3206–3212 (1998).
G. Kempermann, D. Gast, and F. H. Gage, “Neuroplasticity in old age: sustained five-fold induction of hippocampal neurogenesis by longterm environmental enrichment,” Ann. Neurol., 52, 135–143 (2002).
J. Nithianantharajah, H. Levis, and M. Murphy, “Environmental enrichment results in cortical and subcortical changes in levels of synaptophysin and PSD-95 proteins,” Neurobiol. Learn. Mem., 81, No. 3, 200–210 (2004).
C. Nyakas, B. Buwaldan, and P. Luiten, “Hypoxia and brain development,” Prog. Neurobiol., 49, 1–51 (1996).
G. D. Rosen and R. W. Williams, “Complex trait analysis of the mouse striatum: independent QTLs modulate volume and neuron number,” BVC Neurosci., 2, No. 1, 5–17 (2001).
M. R. Rosenzweig and E. L. Bennett, “Psychobiology of plasticity: effects of training and experience on brain and behavior,” Behav. Brain Res., 78, 57–65 (1996).
H. van Praag, G. Kempermann, and F. H. Gage, “Running increases cell proliferation and neurogenesis in the adult mouse dentate gyms,” Nat. Neurosci., 2, No. 3, 266–270 (1999).
S. W. Zhu, A. Codita, N. Bogdanovic, et al., “Influence of environmental manipulation on exploratory behaviour in male BDNF knockout mice,” Behav. Brain Res., 197, No. 2, 339–346 (2009).
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Translated from Rossiiskii Fiziologicheskii Zhurnal imeni I. M. Sechenova, Vol. 100, No. 4, pp. 406–417, April, 2014.
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Vakhnin, V.A., Bryukhin, G.V. Effects of Environmental Conditions on Behavior in an Open Field Test in Rats Born to Females with Chronic Alcoholization. Neurosci Behav Physi 45, 1003–1009 (2015). https://doi.org/10.1007/s11055-015-0179-4
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DOI: https://doi.org/10.1007/s11055-015-0179-4