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Quantitative autoradiography on [35S]TBPS binding sites of gamma-aminobutyric acidA receptors in discrete brain regions of high-alcohol-drinking and low-alcohol-drinking rats selectively bred for high- and low-alcohol preference

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Journal of Biomedical Science

Abstract

It has been documented that ethanol can potentiate brain γ-aminobutyric acid (GABA)ergic function, and there is a close link between the GABAA receptor complex and effects of ethanol, including reinforcement of alcohol which is a fundamental element of alcohol preference. However, it is unknown in what discrete brain regions GABAA receptors might be associated with alcohol preference. In the present study, [35S]t-butylbicyclophosphorothionate ([35S]TBPS) was used to localize GABAA receptors in high-alcohol-drinking (HAD) rats and low-alcohol-drinking (LAD) rats which were selectively bred for high and low alcohol preference, respectively. Initial qualitative observations indicated that [35S]TBPS binding sites were abundant in many brain areas including the cerebral cortex, hypothalamus and amygdala of HAD and LAD rats. Furthermore, the quantitative autoradiographic analysis revealed fewer [35S]TBPS binding sites of GABAA receptors in the amygdaloid complex, central medial thalamic nucleus, lateral hypothalamic nucleus and anterior hypothalamic nucleus of HAD rats than LAD rats. Collectively, this study has indicated that HAD rats selectively bred for high alcohol preference possess lower [35S]TBPS binding in the brain. Since lower TBPS binding has been proposed to reflect enhanced GABAergic function, as evidenced in rats with seizure or under alcohol withdrawal, the results from the present study suggest that HAD rats might have an enhanced GABAergic function. It is thus likely that enhanced GABAergic function in the brain might be related to high alcohol preference which is characteristic in HAD rats. In addition, the present result showing no difference of [35S]TBPS binding in the nucleus accumbens is also in agreement with a notion that [35S]TBPS binding may represent only a small spectrum of the GABAA receptor complex which is constituted of a sophisticated subunit combination whose functional compositions are still unknown. In conclusion, the present study supports the working hypothesis that GABAA receptors are involved in alcohol preference in HAD rats.

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References

  1. Colombo G, Agabio R, Lobina C, Reali R, Zocchi A, Fadda F, Gesa GL. Sardinian alcohol-preferring rats: A genetic animal model of anxiety. Physiol Behav 57:1181–1185;1995.

    Google Scholar 

  2. Concas A, Mascia MP, Sanna E, Sautoro G, Serra M, Biggio G. ‘In vivo’ administration of valproate decreases t-[35S]butylbicyclophosphorothionate binding in the rat brain. Naunyn Schmiedebergs Arch Pharmacol 343:296–300;1991.

    Google Scholar 

  3. Concas A, Sanna E, Serra M, Mascia MP, Santoro V, Biggio G. ‘Ex vivo’ binding of [35S]TBPS as a tool to study the pharmacology of GABAA receptors. In: Biggio G, Costa E, eds. GABA and Benzodiazepine Receptor Subtypes. New York, Raven Press, 89–108;1990.

    Google Scholar 

  4. Criswell HE, Simson PE, Duncan GE, McCown TJ, Herbert JS, Morrow AL, Breese GR. Molecular basis for regionally specific action of ethanol on GABAA receptors: Generalization to other ligand-gated ion channels. J Pharmacol Exp Ther 267:522–536;1993.

    Google Scholar 

  5. Davis M, Rainnie D, Cassell M. Neurotransmission in the rat amygdala related to fear and anxiety. Trends Neurosci 17:208–214;1994.

    Google Scholar 

  6. Drugan RC, Paul SM, Crawley JN. Decreased forebrain [35S]TBPS binding and increased [3H]muscimol binding in rats that do not develop stress-induced behavioral depression. Brain Res 631:270–275;1993.

    Google Scholar 

  7. Edgar PP, Schwartz RD. Localization and characterization of35S-t-butylbicyclophosphorothionate binding in rat brain: An autoradiographic study. J Neurosci 10:603–612;1990.

    Google Scholar 

  8. Feller DJ, Harris RA, Crabbe JC. Differences in GABA activity between ethanol withdrawal seizure prone and resistant mice. Eur J Pharmacol 157:147–154;1988.

    Google Scholar 

  9. Giorgi O, Cancedda E, Lecca D, Orlandi M, Corda MG. Allosteric modulation of [35S]TBPS-binding in the cerebral cortex of the rat during postnatal development. Dev Brain Res 80:73–80;1994.

    Google Scholar 

  10. Hawkinson JE, Kimbrough CL, Belelli D, Lambert JJ, Purdy RH, Lan NC. Correlation of neuroactive steroid modulation of [35S]-t-butylbicyclophosphorothionate and [3H]-flunitrazepam binding and γ-aminobutyric acidA receptor function. Mol Pharmacol 46:977–985;1994.

    Google Scholar 

  11. Hodge CW, Chappelle AM, Samson HH. GABAergic transmission in the nucleus accumbens is involved in the termination of ethanol self-administration in rats. Alcoholism: Clin Exp Res 19:1486–1493;1995.

    Google Scholar 

  12. Hwang BH, Kunkler PE, Lumeng L, Li T. Calcitonin gene-related peptide (CGRP) content and CGRP receptor binding sites in discrete forebrain regions of alcohol-preferring vs. nonpreferring rats and high alcohol-drinking vs. low alcohol-drinking rats. Brain Res 690:249–253;1995.

    Google Scholar 

  13. Hwang BH, Lumeng L, Wu JY, Li TK. Increased number of GABAergic terminals in the nucleus accumbens is associated with alcohol preference in rats. Alcohol Clin Exp Res 14:503–507;1990.

    Google Scholar 

  14. Hyytia P, Koob GF. GABAA receptor antagonism in the extended amygdala decreases ethanol self-administration in rats. Eur J Pharmacol 283:151–159;1995.

    Google Scholar 

  15. Ishihara S, Hiramatsu M, Kameyama T, Nabeshima T. Development of tolerance to anxiolytic effects of chlordiazepoxide in elevated plusmaze test and decrease of GABAA receptors. J Neural Transm 91:27–37;1993.

    Google Scholar 

  16. Ito Y, Ho IK. Studies on picrotoxin binding sites of GABAA receptors in rat cortical synaptoneurosomes. Brain Res 33:373–378;1994.

    Google Scholar 

  17. June HL, Murphy JM, Heywitt RL, Greene TL, Lin M, Mellor-Burke JJ, Lumeng L, Li TK. Benzodiazepine receptor ligands with different intrinsic efficacies alter ethanol intake in alcohol-nonpreferring (NP) rats. Neuropsychopharmacology 14:55–66;1996.

    Google Scholar 

  18. June HL, Murphy JM, Mellor-Burke JJ, Lumeng L, Li TK. The benzodiazepine inverse agonist Ro19-4603 exerts prolonged and selective suppression of ethanol intake in alcohol-preferring (P) rats. Psychopharmacology 115:325–331;1994.

    Google Scholar 

  19. Keir WJ, Morrow AL. Differential expression of GABAA receptor subunit mRNAs in ethanol-naive withdrawal seizure resistant (WSR) vs. withdrawal seizure prone (WSP) mouse brain. Mol Brain Res 25:200–208;1994.

    Google Scholar 

  20. Korpi ER. Role of GABAA receptors in the actions of ethanol and in alcoholism: Recent advances. Alcohol Alcohol 29:115–129;1994.

    Google Scholar 

  21. Kunkler PE, Hwang BH. Lower GABAA receptor binding in the amygdala and hypothalamus of spontaneously hypertensive rats. Brain Res Bull 36:57–61;1195.

    Google Scholar 

  22. Lankford MF, Myers RD. Genetics of alcoholism: Simultaneous presentation of a chocolate drink diminishes alcohol preference in high drinking HAD rats. Pharmacol Biochem Behav 49:417–425;1194.

    Google Scholar 

  23. Lankford MF, Roscoe AK, Pennington SN, Myers RD. Drinking of high concentrations of ethanol versus palatable fluids in alcohol-preferring (P) rats: Valid animal model of alcoholism. Alcohol 8:293–299;1991.

    Google Scholar 

  24. Li TK, Lumeng L, Doolittle DP. Selective breeding for alcohol preference and associated responses. Behav Genet 23:163–170;1993.

    Google Scholar 

  25. Li TK, Lumeng L, Froehlich JC, Murphy JM, McBride WJ. Genetic influence on response to the reinforcing properties of ethanol in rats. In: Kuriyama K, Takada A, Ishii H, eds. Biomedical and social aspects of alcohol and alcoholism. New York, Elsevier, 487–490;1988.

    Google Scholar 

  26. Liljequist S, Engel J. Effect of GABAergic agonists and antagonists on ethanol-induced behavioral changes. Psychopharmacology 78:71–75;1982.

    Google Scholar 

  27. Luddens H, Korpi ER. GABA antagonists differentiate between recombinant GABAA/benzodiazepine receptor subtypes. J Neurosci 15:6957–6962;1995.

    Google Scholar 

  28. McBride WJ, Murphy JM, Lumeng L, Li TK. Effects of Ro 15-45 13, fluoxetine and desipramine on the intake of ethanol, water and food by the alcohol-preferring (P) and nonpreferring (NP) lines of rats. Pharmacol Biochem Behav 30:1045–1050;1988.

    Google Scholar 

  29. McBride WJ, Murphy JM, Lumeng L, Li TK. Serotonin, dopamine and GABA involvement in alcohol drinking of selectively bred rats. Alcohol 7:199–205;1990.

    Google Scholar 

  30. Mhatre MC, Pena G, Sieghart W, Ticku MK. Antibodies specific for GABAA receptora subunits reveal that chronic alcohol treament down-regulatesa-subunit expression in rat brain regions. J Neurochem 61:1620–1625;1993.

    Google Scholar 

  31. Mhatre M, Ticku MK. Chronic ethanol treatment upregulates the GABA receptor beta subunit expression. Mol Brain Res 23:246–252;1994.

    Google Scholar 

  32. Montpied P, Morrow AL, Karanian JW, Ginns EI, Martin BM, Paul SM. Prolonged ethanol inhalation decreases gamma-aminobutyric acidA receptor subunit mRNAs in the rat cerebral cortex. Mol Pharmacol 39:157–163;1991.

    Google Scholar 

  33. Morrow AL, Montpied P, Lingford-Hughes A, Paul SM. Chronic ethanol and pentobarbital administration in the rat: Effects on GABAA receptor function and expression in brain. Alcohol 7:237–244;1990.

    Google Scholar 

  34. Morrow AL, Suzdak PD, Karanian JW, Paul SM. Chronic ethanol administration alters gamma-aminobutyric acid, pentabarbital and ethanol-mediated36Cl uptake in cerebral cortical synapto-neurosomes. Pharmacol Exp Ther 246:158–164;1988.

    Google Scholar 

  35. Nestoro JN. Ethanol specifically potentiates GABA-mediated neurotransmission in feline cerebral cortex. Science 209:708–710;1980.

    Google Scholar 

  36. Paxinos G, Watson C. The rat brain in stereotaxic coordinates. Sydney, Academic Press, 1986.

    Google Scholar 

  37. Rassnick S, D'Amico E, Riley E, Koob GF. GABA antagonist and benzodiazepine partial inverse agonist reduce motivational responding for ethanol. Alcohol Clin Exp Res 17:124–130;1993.

    Google Scholar 

  38. Rassnick S, Krechman J, Koob GF. Chronic ethanol produces a decreased sensitivity to the response-disruptive effects of GABA receptor complex antagonists. Pharmacol Biochem Behav 44:943–950;1993.

    Google Scholar 

  39. Rastogi SK, Thyagarajan R, Clothier J, Ticku MK. Effect of chronic treatment of ethanol on benzodiazepine and picrotoxin sites on the GABA receptor complex in regions of the brain of the rat. Neuropharmacology 25:1179–1184;1986.

    Google Scholar 

  40. Rastogi SK, Ticku MK. Involvement of a GABAergic mechanism in the anticonvulsant effect of pentobarbital agonist maximal electroshock-induced seizures in rats. Pharmacol Biochem Behav 22:141–146;1981.

    Google Scholar 

  41. Ritz MC, Garcia JM, Protz D, George FR. Operant ethanol-reinforced behavior in PP, NP, HAD and LAD rats bred for high versus low ethanol preference. Alcohol Clin Exp Res 198:1406–1415;1994.

    Google Scholar 

  42. Ritz MC, Garcia JM, Protz D, Rael AM, George FR. Ethanol-reinforced behavior in P, NP, HAD and LAD rats: Differential genetic regulation of reinforcement and motivation. Behav Pharmacol 5:521–531;1994.

    Google Scholar 

  43. Samson HH, Tolliver GA, Pfeffer AO, Sadeghi KG, Mills FG. Oral ethanol reinforcement in the rat: Effect of the partial inverse benzodiazepine agonist Ro 15-4513. Pharmacol Biochem Behav 27:517–519;1987.

    Google Scholar 

  44. Samna E, Concas A, Serra M, Santoro G, Bigio G. Ex vivo binding of t-[35S]butylbicocylophos-phorothionate: A biochemical tool to study the pharmacology of ethanol at the gamma-aminobutyric acid-coupled chloride channel. J Pharmacol Exp Ther 256:922–928;1991.

    Google Scholar 

  45. Sanna E, Cuccheddu T, Serra M, Conca A, Biggio G. Carbon dioxide inhalation reduces the function of GABAA receptors in the rat brain. Eur J Pharmacol 216:457–458;1992.

    Google Scholar 

  46. Sanna E, Serra M, Cossu A, Colombo G, Follesa P, Cuccheddu T, Concas A, Biggio G. Chronic ethanol intoxication induces differential effects on GABAA and NMDA receptor function in the rat brain. Alcohol Clin Exp Res 17:115–122;1993.

    Google Scholar 

  47. Sieghart W. Structure and pharmacology of γ-aminobutyric acidA receptor subtypes. Pharmacol Rev 47:181–234;1995.

    Google Scholar 

  48. Slany A, Zezula J, Tretler V, Sieghart W. Rat β3 subunit expressed in human embryonic kidney 293 cells form high affinity [35S]-butylbicyclophosphorothionate binding sites modulated by several allosteric ligands of γ-aminobutyric acid type A receptors. Mol Pharmacol 48:385–391;1995.

    Google Scholar 

  49. Smith BR, Robidoux J, Amit Z. GABAergic involvement in the acquisition of voluntary ethanol intake in laboratory rats. Alcohol Alcohol 27:227–231;1992.

    Google Scholar 

  50. Sola C, Martinez E, Camon L, Pazos A, Rodriguez-Farre E. Lindane administration to the rat induces modifications in the regional cerebral binding of [35S]-butylbicyclophosphorothionate: An autoradiographic study. J Neurochem 60:1821–1834;1993.

    Google Scholar 

  51. Spanagel R, Montkowski A, Allingham K, Stohr T, Shoaib M, Holsboer F, Landgraf R. Anxiety: A potential predictor of vulnerability to the initiation of ethanol self-administration in rats. Psychopharmacology 122:369–373;1995.

    Google Scholar 

  52. Stewart RB, Gatto GJ, Lumeng L, Li TK, Murphy JM. Comparison of alcohol-preferring (P) and nonpreferring (NP) rats on tests of anxiety and for the anxiolytic effects of ethanol. Alocohol 10:1–10;1993.

    Google Scholar 

  53. Stewart RB, Perlanski E, Grupp LA. Ethanol as a reinforcer for rats: Factors of facilitation and constraint. Alcohol Clin Exp Res 12:599–608;1988.

    Google Scholar 

  54. Suzdak PD, Glowa JR, Crawley JN, Schwartz RD, Skolnick P, Paul SM. A selecting imidazobenzodiazepine antagonist of ethanol in the rat. Science 234:1243–1246;1986.

    Google Scholar 

  55. Suzdak PD, Schwartz RD, Skolnick P, Paul SM. Alcohols stimulate gamma-aminobutyric acid receptor-mediated chloride uptake in brain vesicles: Correlation with intoxication potency. Brain Res 444:340–345;1988.

    Google Scholar 

  56. Thyagarajan R, Ticku MK. The effect of in vitro and in vivo ethanol administration on [35S]t-butylbicyclophosphorothionate binding in C57 mice. Brain Res Bull 15:343–345;1985.

    Google Scholar 

  57. Ticku MK, Mhatre M, Mehta AK. Modulation of GABAergic transmission by ethanol. In: Biggio G, Concas A, Costa E, eds. GABAergic Synaptic Transmission. New York, Raven Press, 255–268;1992.

    Google Scholar 

  58. Vincens M, Dartois E, Moyse E, Haour F, Fillion G. An autoradiographic study comparing the interactions of 3a-OH-5a-prognan-20-one pregnenolone sulfate and pentobarbital with [35S]-TBPS binding sites and their modulation by GABA in different structures of the rat brain. Naunyn Schmidebergs Arch Pharmacol 351:356–361;1995.

    Google Scholar 

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Hwang, B.H., Kunkler, P.E. & Lumeng, L. Quantitative autoradiography on [35S]TBPS binding sites of gamma-aminobutyric acidA receptors in discrete brain regions of high-alcohol-drinking and low-alcohol-drinking rats selectively bred for high- and low-alcohol preference. J Biomed Sci 4, 308–314 (1997). https://doi.org/10.1007/BF02258355

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