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Sex Differences in Addictive Behavior of Adult Rats: Effects of Prenatal Alcohol Exposure

https://doi.org/10.33647/2074-5982-19-2-27-36

Abstract

Alcohol experienced during gestation is associated with the development of neurodevelopmental and neuropsychiatric dysfunctions, as well as addictive behavior in the offspring. However, the biological basis of these effects remains poorly understood. Taking into account that the extrahypothalamic corticotropin-releasing factor (CRF) system plays an important role in regulation of the negative emotional state produced by alcohol abuse and withdrawal, the present study was aimed at investigating: 1) the effect of prenatal alcohol exposure (PA) on voluntary alcohol drinking (free choice 24 hours/day) or intermittent (“drinking in the dark”) regimen in adult Wistar rats; 2) differences in the basal gene expression levels of CRF and CRF-R1 in amygdala of adult PA and control rats; and 3) the effect of voluntary alcohol drinking on the above mRNA levels. PA males displayed a significantly greater voluntary alcohol intake than control males as observed by both drinking paradigms. 24 hours after the first withdrawal episode, PA males demonstrated a higher level of anxiety in the light-dark box test. No differences were found between PA and control females. Basal amygdalar CRF and CRFR1 mRNA levels did not differ between PA and control rats of both sexes. No difference was observed in the amygdalar CRF and CRFR1 mRNA levels after alcohol drinking in PA and control males. Conversely, the CRF mRNA levels in amygdala of PA female rats decreased under the action of alcohol consumption, compared to control female rats. The results show that the PA effect on future alcohol-related behavior is sex-specific, but do not support the hypothesis that changes in CRF and CRFR1 mRNA levels in amygdala may be responsible for high alcohol intake in males.

About the Authors

P. K. Anokhin
National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia
Russian Federation

Petr K. Anokhin - Cand. Sci. (Biol.), National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia.

119002, Moscow, Maliy Mogiltsevskiy Lane, 3



T. V. Proskuryakova
National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia
Russian Federation

Tatyana V. Proskuryakova - Dr. Sci. (Biol.), National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia.

119002, Moscow, Maliy Mogiltsevskiy Lane, 3



V. A. Shokhonova
National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia
Russian Federation

Vera A. Shokhonova - Cand. Sci. (Biol.), National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia.

119002, Moscow, Maliy Mogiltsevskiy Lane, 3



V. S. Kokhan
National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia
Russian Federation

Victor S. Kokhan - Cand. Sci. (Biol.), National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia.

119002, Moscow, Maliy Mogiltsevskiy Lane, 3



I. E. Tarabarko
National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia
Russian Federation

Irina E. Tarabarko.

119002, Moscow, Maliy Mogiltsevskiy Lane, 3



I. Yu. Shamakina
National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia
Russian Federation

Inna Yu. Shamakina - Cand. Sci. (Biol.), National Scientific Center for Narcology — Branch of the V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Ministry of Health Care of Russia.

119002, Moscow, Maliy Mogiltsevskiy Lane, 3



References

1. Proskuryakova T.V., Shohonova V.A., Anohin P.K., Tarabarko I.E., Anohina I.P. Gendernye razlichiya v povedenii potomstva krys, upotreblyavshikh alkogol' do i vo vremya beremennosti [Gender differences in the behavior of the offspring of rats that consumed alcohol before and during pregnancy]. Voprosy narkologii [Journal of Addiction Problems]. 2018;10-11(170):40-54. (In Russian).

2. Proskuryakova T.V., Anohin P.K., Shohonova V.A., Razumkina E.V., Shamakina I.Iu. Polovye razlichiya urovnya mRNK kortikotropin-rilizing faktora, ego retseptora v mozge i kortikosterona v krovi u potomstva samok krys, up-otreblyavshikh alkogol' do i vo vremya beremennosti [Sex differences in the mRNA levels of corticotropin-releasing factor, its receptor in the brain, and corticosterone in the blood of the offspring of female rats that consumed alcohol before and during pregnancy]. Voprosy narkologii [Journal of Addiction Problems]. 2019;12(183):66-80. (In Russian). DOI: 10.47877/0234-0623_2019_12_66.

3. Proskuryakova T.V., Shohonova V.A., Shamakina I.Iu. Eksperimental'nye modeli formirovaniya fizicheskoy zavisimosti ot alkogolya [Experimental models of the formation of physical dependence on alcohol]. Rossiyskiy psikhiatricheskiy zhurnal [Russian Journal of Psychiatry]. 2021;4:80-92. (In Russian). DOI: 10.47877/1560-957X-2021-10409.

4. Shabanov P.D., Lebedev A.A. [Gormonal'nye mekhanizmy zavisimosti. Kontseptsiya gipertsirkulyatsii v amigdalo-gipotalamo-gipofizarno-nadpochechnikovoy sisteme [Hormonal mechanisms of dependence. The concept of hypercirculation in the amygdala-hypothalamic-pituitary-adrenal system]. Ehkologiya cheloveka [Human ecology]. 2009;8:19-24. (In Russian).

5. Alati R., Al Mamun A., Williams G.M., O'Callaghan M., Najman J.M., Bor W. In utero alcohol exposure and prediction of alcohol disorders in early adulthood: A birth cohort study. Arch. Gen. Psychiatry. 2006;63(9):1009-1016. DOI: 10.1001/archpsyc.63.9.1009.

6. Baer J.S., Sampson P.D., Barr H.M., Connor P.D., Streissguth A.P. A 21-year longitudinal analysis of the effects of prenatal alcohol exposure on young adult drinking. Arch. Gen. Psychiatry. 2003;60(4):377-385. DOI: 10.1001/archpsyc.60.4.377.

7. Breese G.R., Overstreet D.H., Knapp D.J., Navarro M. Prior multiple ethanol withdrawals enhance stress-induced anxiety-like behavior: Inhibition by CRF1-and benzodiazepine-receptor antagonists and a 5-HT1a-receptor agonist. Neuropsychopharmacology. 2005;30(9):1662-1669. DOI: 10.1038/sj.npp.1300706.

8. Breese G.R., Overstreet D.H., Knapp D.J. Conceptual framework for the etiology of alcoholism: A “kin-dling”/stress hypothesis. Psychopharmacology (Berl.). 2005;178(4):367-380. DOI: 10.1007/s00213-004-2016-2.

9. Brunton P.J., Donadio M.V., Russell J.A. Sex differences in prenatally programmed anxiety behaviour in rats: Differential corticotropin-releasing hormone receptor mRNA expression in the amygdaloid complex. Stress. 2011;14(6):634-643. DOI: 10.3109/10253890.2011.604750.

10. Heilig M., Koob G.F. A key role for corticotropin-releasing factor in alcohol dependence. Trends Neurosci. 2007;30(8):399-406. DOI: 10.1016/j.tins.2007.06.006.

11. Honey P.L., Galef B.G. Jr. Ethanol consumption by rat dams during gestation, lactation and weaning increases ethanol consumption by their adolescent young. Dev. Psychobiol. 2003;42(3):252-260. DOI: 10.1002/dev.10098.

12. Kirson D., Khom S., Rodriguez L., Wolfe S.A., Varodayan F.P., Gandhi P.J., Patel R.R., Vlkolinsky R., Bajo M., Roberto M. Sex differences in acute alcohol sensitivity of naive and alcohol dependent central amygdala GABA synapses. Alcohol Alcohol. 2021;56(5):581-588. DOI: 10.1093/alcalc/agab034.

13. Kirson D., Steinman M.Q., Wolfe S.A., Spierling Bagsic S.R., Bajo M., Sureshchandra S., Oleata C.S., Messaoudi I., Zorrilla E.P., Roberto M. Sex and context differences in the effects of trauma on comorbid alcohol use and post-traumatic stress phenotypes in actively drinking rats. J. Neurosci. Res. 2021;99(12):3354-3372. DOI: 10.1002/jnr.24972.

14. Merlo Pich E., Lorang M., Yeganeh M., Rodriguez de Fonseca F., Raber J., Koob G.F., Weiss F. Increase of extracellular corticotropin-releasing factor-like immunoreactivity levels in the amygdala of awake rats during restraint stress and ethanol withdrawal as measured by microdialysis. J. Neurosci. 1995;15(8):5439-5447. DOI: 10.1523/JNEUROSCI.15-08-05439.1995.

15. Mineur Y.S., Garcia-Rivas V., Thomas M.A., Soares A.R., McKee S.A., Picciotto M.R. Sex differences in stress-induced alcohol intake: A review of preclinical studies focused on amygdala and inflammatory pathways. Psychopharmacology (Berl.). 2022;239(7):2041-2061. DOI: 10.1007/s00213-022-06120-w.

16. Roberto M., Kirson D., Khom S. The role of the central amygdala in alcohol dependence. Cold Spring Harb. Perspect. Med. 2021;11(2):a039339. DOI: 10.1101/cshperspect.a039339.

17. Rodriguez L., Kirson D., Wolfe S.A., Patel R.R., Varodayan F.P., Snyder A.E., Gandhi P.J., Khom S., Vlkolinsky R., Bajo M., Roberto M. Alcohol dependence induces CRF sensitivity in female central amygdala GABA synapses. Int. J. Mol. Sci. 2022;23(14):7842. DOI: 10.3390/ijms23147842.

18. Spear N.E., Molina J.C. Fetal or infantile exposure to ethanol promotes ethanol ingestion in adolescence and adulthood: A theoretical review. Alcohol. Clin. Exp. Res. 2005;29(6):909-929. DOI: 10.1097/01.alc.0000171046.78556.66.

19. Streissguth A.P., Bookstein F.L., Barr H.M., Sampson P.D., O'Malley K., Young J.K. Risk factors for adverse life outcomes in fetal alcohol syndrome and fetal alcohol effects. J. Dev. Behav. Pediatr. 2004;25(4):228-238. DOI: 10.1097/00004703-200408000-00002.

20. Varodayan F.P., Patel R.R., Matzeu A., Wolfe S.A., Curley D.E., Khom S., Gandhi P.J., Rodriguez L., Bajo M., D'Ambrosio S., Sun H., Kerr T.M., Gonzales R.A., Leggio L., Natividad L.A., Haass-Koffler C.L., Martin-Fardon R., Roberto M. The amygdala noradrenergic system is compromised with alcohol use disorder. Biol. Psychiatry. 2022;91(12):1008-1018. DOI: 10.1016/j.biopsych.2022.02.006.

21. Wozniak J.R., Riley E.P., Charness M.E. Clinical presentation, diagnosis, and management of fetal alcohol spectrum disorder. Lancet Neurol. 2019;18(8):760-770. DOI: 10.1016/S1474-4422(19)30150-4.

22. Youngentob S.L., Molina J.C., Spear N.E., Youngentob L.M. The effect of gestational ethanol exposure on voluntary ethanol intake in early postnatal and adult rats. Behav. Neurosci. 2007;121(6):1306-1315. DOI: 10.1037/0735-7044.121.6.1293.

23. Youngentob S.L., Glendinning J.I. Fetal ethanol exposure increases ethanol intake by making it smell and taste better. Proc. Natl Acad. Sci. USA. 2009;106(13):5359-5364. DOI: 10.1073/pnas.0809804106.

24. Zhou Y., Colombo G., Gessa G.L., Kreek M.J. Effects of voluntary alcohol drinking on corticotropinreleasing factor and preprodynorphin mRNA levels in the central amygdala of Sardinian alcohol-preferring rats. Neurosci. Lett. 2013;554:110-114. DOI: 10.1016/j.neulet.2013.08.071.


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For citations:


Anokhin P.K., Proskuryakova T.V., Shokhonova V.A., Kokhan V.S., Tarabarko I.E., Shamakina I.Yu. Sex Differences in Addictive Behavior of Adult Rats: Effects of Prenatal Alcohol Exposure. Journal Biomed. 2023;19(2):27-36. (In Russ.) https://doi.org/10.33647/2074-5982-19-2-27-36

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ISSN 2074-5982 (Print)
ISSN 2713-0428 (Online)