Abstract
We evaluated G-proteins that are components of adenylyl cyclase (AC) signal transduction in erythrocyte and lymphocyte membranes from 26 family history positive (FHP) non-alcoholic and 26 family history negative (FHN) nonalcoholic subjects. Subjects were classified as FHP if their father met criteria for alcohol dependence; as FHN, if there was no history of alcoholism in any first or second degree relatives. Immunoblot analysis indicated that levels of erythrocyte membrane Gs alpha from FHP subjects were greater than levels in FHN subjects (171 +/- 11 vs 100 +/- 6, P < 0.001). To confirm the results of the immunoblot analysis, Gs alpha was quantitated by cholera toxin-dependent [32P]ADP-ribosylation. Levels of erythrocyte [32P]ADP-ribose-Gs alpha from FHP subjects were greater than levels in FHN subjects (236 +/- 28 vs 100 +/- 14, P < 0.001). Gs alpha levels did not correlate with age or alcohol consumption. By contrast to differences in Gs alpha, immunoblot analysis showed similar levels of Gi(2)alpha and Gi(3)alpha in erythrocyte membranes of FHP and FHN subjects. Pertussis toxin-catalyzed [32P]ADP-ribosylation of Gi-like G-proteins confirmed the immunoblot observations. Lastly, compared to FHN subjects, FHP subjects had enhanced Gs alpha expression in lymphocyte membranes as well (138 +/- 11 vs 100 +/- 5.5; P < 0.02). In summary, compared to FHN nonalcoholic men, FHP nonalcoholic men had greater levels of the stimulatory G-protein, Gs alpha, in erythrocyte and lymphocyte membranes. Enhanced expression of Gs alpha may be a marker of increased risk for the future development of alcoholism.
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- Andreasen N. C., Endicott J., Spitzer R. L., Winokur G. The family history method using diagnostic criteria. Reliability and validity. Arch Gen Psychiatry. 1977 Oct;34(10):1229–1235. doi: 10.1001/archpsyc.1977.01770220111013. [DOI] [PubMed] [Google Scholar]
- Chang F. H., Bourne H. R. Dexamethasone increases adenylyl cyclase activity and expression of the alpha-subunit of Gs in GH3 cells. Endocrinology. 1987 Nov;121(5):1711–1715. doi: 10.1210/endo-121-5-1711. [DOI] [PubMed] [Google Scholar]
- Cloninger C. R., Bohman M., Sigvardsson S. Inheritance of alcohol abuse. Cross-fostering analysis of adopted men. Arch Gen Psychiatry. 1981 Aug;38(8):861–868. doi: 10.1001/archpsyc.1981.01780330019001. [DOI] [PubMed] [Google Scholar]
- Cotton N. S. The familial incidence of alcoholism: a review. J Stud Alcohol. 1979;40(1):89–116. doi: 10.15288/jsa.1979.40.89. [DOI] [PubMed] [Google Scholar]
- Crabb D. W. Biological markers for increased risk of alcoholism and for quantitation of alcohol consumption. J Clin Invest. 1990 Feb;85(2):311–315. doi: 10.1172/JCI114439. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Devor E. J., Cloninger C. R. Genetics of alcoholism. Annu Rev Genet. 1989;23:19–36. doi: 10.1146/annurev.ge.23.120189.000315. [DOI] [PubMed] [Google Scholar]
- Diamond I., Wrubel B., Estrin W., Gordon A. Basal and adenosine receptor-stimulated levels of cAMP are reduced in lymphocytes from alcoholic patients. Proc Natl Acad Sci U S A. 1987 Mar;84(5):1413–1416. doi: 10.1073/pnas.84.5.1413. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Froehlich J. C., Li T. K. Animal models for the study of alcoholism: utility of selected lines. J Addict Dis. 1991;10(1-2):61–71. doi: 10.1300/J069v10n01_05. [DOI] [PubMed] [Google Scholar]
- Froehlich J. C., Zweifel M., Harts J., Lumeng L., Li T. K. Importance of delta opioid receptors in maintaining high alcohol drinking. Psychopharmacology (Berl) 1991;103(4):467–472. doi: 10.1007/BF02244246. [DOI] [PubMed] [Google Scholar]
- Gianoulakis C., Béliveau D., Angelogianni P., Meaney M., Thavundayil J., Tawar V., Dumas M. Different pituitary beta-endorphin and adrenal cortisol response to ethanol in individuals with high and low risk for future development of alcoholism. Life Sci. 1989;45(12):1097–1109. doi: 10.1016/0024-3205(89)90167-7. [DOI] [PubMed] [Google Scholar]
- Gianoulakis C., Béliveau D., Angelogianni P., Meaney M., Thavundayil J., Tawar V., Dumas M. Different pituitary beta-endorphin and adrenal cortisol response to ethanol in individuals with high and low risk for future development of alcoholism. Life Sci. 1989;45(12):1097–1109. doi: 10.1016/0024-3205(89)90167-7. [DOI] [PubMed] [Google Scholar]
- Goodwin D. W., Schulsinger F., Hermansen L., Guze S. B., Winokur G. Alcohol problems in adoptees raised apart from alcoholic biological parents. Arch Gen Psychiatry. 1973 Feb;28(2):238–243. doi: 10.1001/archpsyc.1973.01750320068011. [DOI] [PubMed] [Google Scholar]
- Gordon A. S., Collier K., Diamond I. Ethanol regulation of adenosine receptor-stimulated cAMP levels in a clonal neural cell line: an in vitro model of cellular tolerance to ethanol. Proc Natl Acad Sci U S A. 1986 Apr;83(7):2105–2108. doi: 10.1073/pnas.83.7.2105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hellevuo K., Yoshimura M., Kao M., Hoffman P. L., Cooper D. M., Tabakoff B. A novel adenylyl cyclase sequence cloned from the human erythroleukemia cell line. Biochem Biophys Res Commun. 1993 Apr 15;192(1):311–318. doi: 10.1006/bbrc.1993.1415. [DOI] [PubMed] [Google Scholar]
- Hoffman P. L., Tabakoff B. Ethanol and guanine nucleotide binding proteins: a selective interaction. FASEB J. 1990 Jun;4(9):2612–2622. doi: 10.1096/fasebj.4.9.2161371. [DOI] [PubMed] [Google Scholar]
- Kendler K. S., Heath A. C., Neale M. C., Kessler R. C., Eaves L. J. A population-based twin study of alcoholism in women. JAMA. 1992 Oct 14;268(14):1877–1882. [PubMed] [Google Scholar]
- Kuchler K., Dohlman H. G., Thorner J. The a-factor transporter (STE6 gene product) and cell polarity in the yeast Saccharomyces cerevisiae. J Cell Biol. 1993 Mar;120(5):1203–1215. doi: 10.1083/jcb.120.5.1203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levine M. A., Ahn T. G., Klupt S. F., Kaufman K. D., Smallwood P. M., Bourne H. R., Sullivan K. A., Van Dop C. Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy. Proc Natl Acad Sci U S A. 1988 Jan;85(2):617–621. doi: 10.1073/pnas.85.2.617. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levine M. A., Downs R. W., Jr, Singer M., Marx S. J., Aurbach G. D., Spiegel A. M. Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism. Biochem Biophys Res Commun. 1980 Jun 30;94(4):1319–1324. doi: 10.1016/0006-291x(80)90563-x. [DOI] [PubMed] [Google Scholar]
- Levine M. A., Eil C., Downs R. W., Jr, Spiegel A. M. Deficient guanine nucleotide regulatory unit activity in cultured fibroblast membranes from patients with pseudohypoparathyroidism type I. a cause of impaired synthesis of 3',5'-cyclic AMP by intact and broken cells. J Clin Invest. 1983 Jul;72(1):316–324. doi: 10.1172/JCI110971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lex B. W., Ellingboe J. E., Teoh S. K., Mendelson J. H., Rhoades E. Prolactin and cortisol levels following acute alcohol challenges in women with and without a family history of alcoholism. Alcohol. 1991 Sep-Oct;8(5):383–387. doi: 10.1016/0741-8329(91)90618-7. [DOI] [PubMed] [Google Scholar]
- Mochly-Rosen D., Chang F. H., Cheever L., Kim M., Diamond I., Gordon A. S. Chronic ethanol causes heterologous desensitization of receptors by reducing alpha s messenger RNA. Nature. 1988 Jun 30;333(6176):848–850. doi: 10.1038/333848a0. [DOI] [PubMed] [Google Scholar]
- Morrill A. C., Wolfgang D., Levine M. A., Wand G. S. Stress alters adenylyl cyclase activity in the pituitary and frontal cortex of the rat. Life Sci. 1993;53(23):1719–1727. doi: 10.1016/0024-3205(93)90158-y. [DOI] [PubMed] [Google Scholar]
- Nagy L. E., Diamond I., Gordon A. Cultured lymphocytes from alcoholic subjects have altered cAMP signal transduction. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6973–6976. doi: 10.1073/pnas.85.18.6973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newlin D. B., Thomson J. B. Alcohol challenge with sons of alcoholics: a critical review and analysis. Psychol Bull. 1990 Nov;108(3):383–402. doi: 10.1037/0033-2909.108.3.383. [DOI] [PubMed] [Google Scholar]
- Patten J. L., Johns D. R., Valle D., Eil C., Gruppuso P. A., Steele G., Smallwood P. M., Levine M. A. Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy. N Engl J Med. 1990 May 17;322(20):1412–1419. doi: 10.1056/NEJM199005173222002. [DOI] [PubMed] [Google Scholar]
- Patten J. L., Levine M. A. Immunochemical analysis of the alpha-subunit of the stimulatory G-protein of adenylyl cyclase in patients with Albright's hereditary osteodystrophy. J Clin Endocrinol Metab. 1990 Nov;71(5):1208–1214. doi: 10.1210/jcem-71-5-1208. [DOI] [PubMed] [Google Scholar]
- Pickens R. W., Svikis D. S., McGue M., Lykken D. T., Heston L. L., Clayton P. J. Heterogeneity in the inheritance of alcoholism. A study of male and female twins. Arch Gen Psychiatry. 1991 Jan;48(1):19–28. doi: 10.1001/archpsyc.1991.01810250021002. [DOI] [PubMed] [Google Scholar]
- Rabin R. A. Chronic ethanol exposure has a dual effect on adenylate cyclase activity and cyclic AMP content. Ann N Y Acad Sci. 1991;625:441–443. doi: 10.1111/j.1749-6632.1991.tb33874.x. [DOI] [PubMed] [Google Scholar]
- Rabin R. A. Chronic ethanol exposure of PC 12 cells alters adenylate cyclase activity and intracellular cyclic AMP content. J Pharmacol Exp Ther. 1990 Mar;252(3):1021–1027. [PubMed] [Google Scholar]
- Rabin R. A. Direct effects of chronic ethanol exposure on beta-adrenergic and adenosine-sensitive adenylate cyclase activities and cyclic AMP content in primary cerebellar cultures. J Neurochem. 1990 Jul;55(1):122–128. doi: 10.1111/j.1471-4159.1990.tb08829.x. [DOI] [PubMed] [Google Scholar]
- Rabin R. A., Edelman A. M., Wagner J. A. Activation of protein kinase A is necessary but not sufficient for ethanol-induced desensitization of cyclic AMP production. J Pharmacol Exp Ther. 1992 Jul;262(1):257–262. [PubMed] [Google Scholar]
- Rabin R. A. Ethanol-induced desensitization of adenylate cyclase: role of the adenosine receptor and GTP-binding proteins. J Pharmacol Exp Ther. 1993 Feb;264(2):977–983. [PubMed] [Google Scholar]
- Richelson E., Stenstrom S., Forray C., Enloe L., Pfenning M. Effects of chronic exposure to ethanol on the prostaglandin E1 receptor-mediated response and binding in a murine neuroblastoma clone (N1E-115). J Pharmacol Exp Ther. 1986 Dec;239(3):687–692. [PubMed] [Google Scholar]
- Saito N., Guitart X., Hayward M., Tallman J. F., Duman R. S., Nestler E. J. Corticosterone differentially regulates the expression of Gs alpha and Gi alpha messenger RNA and protein in rat cerebral cortex. Proc Natl Acad Sci U S A. 1989 May;86(10):3906–3910. doi: 10.1073/pnas.86.10.3906. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schuckit M. A. Differences in plasma cortisol after ingestion of ethanol in relatives of alcoholics and controls: preliminary results. J Clin Psychiatry. 1984 Sep;45(9):374–376. [PubMed] [Google Scholar]
- Schuckit M. A., Gold E., Risch C. Serum prolactin levels in sons of alcoholics and control subjects. Am J Psychiatry. 1987 Jul;144(7):854–859. doi: 10.1176/ajp.144.7.854. [DOI] [PubMed] [Google Scholar]
- Schuckit M. A., Li T. K., Cloninger C. R., Deitrich R. A. Genetics of alcoholism. Alcohol Clin Exp Res. 1985 Dec;9(6):475–492. doi: 10.1111/j.1530-0277.1985.tb05588.x. [DOI] [PubMed] [Google Scholar]
- Schuckit M. A., Risch S. C., Gold E. O. Alcohol consumption, ACTH level, and family history of alcoholism. Am J Psychiatry. 1988 Nov;145(11):1391–1395. doi: 10.1176/ajp.145.11.1391. [DOI] [PubMed] [Google Scholar]
- Tabakoff B., Hoffman P. L., Lee J. M., Saito T., Willard B., De Leon-Jones F. Differences in platelet enzyme activity between alcoholics and nonalcoholics. N Engl J Med. 1988 Jan 21;318(3):134–139. doi: 10.1056/NEJM198801213180302. [DOI] [PubMed] [Google Scholar]
- Uhl G. R., Persico A. M., Smith S. S. Current excitement with D2 dopamine receptor gene alleles in substance abuse. Arch Gen Psychiatry. 1992 Feb;49(2):157–160. doi: 10.1001/archpsyc.1992.01820020068010. [DOI] [PubMed] [Google Scholar]
- Waltman C., Levine M. A., McCaul M. E., Svikis D. S., Wand G. S. Enhanced expression of the inhibitory protein Gi2 alpha and decreased activity of adenylyl cyclase in lymphocytes of abstinent alcoholics. Alcohol Clin Exp Res. 1993 Apr;17(2):315–320. doi: 10.1111/j.1530-0277.1993.tb00769.x. [DOI] [PubMed] [Google Scholar]
- Wand G. S., Diehl A. M., Levine M. A., Wolfgang D., Samy S. Chronic ethanol treatment increases expression of inhibitory G-proteins and reduces adenylylcyclase activity in the central nervous system of two lines of ethanol-sensitive mice. J Biol Chem. 1993 Feb 5;268(4):2595–2601. [PubMed] [Google Scholar]
- Wand G. S., Levine M. A. Hormonal tolerance to ethanol is associated with decreased expression of the GTP-binding protein, Gs alpha, and adenylyl cyclase activity in ethanol-treated LS mice. Alcohol Clin Exp Res. 1991 Aug;15(4):705–710. doi: 10.1111/j.1530-0277.1991.tb00583.x. [DOI] [PubMed] [Google Scholar]



