Abstract
In women, a relative hyperandrogenicity is statistically associated with insulin resistance and centralization of body fat, which are predictors for the development of non-insulin-dependent diabetes mellitus. The aim of this study was to evaluate the effect of androgenization of newborn female rats on insulin sensitivity at adult age. To mimic the neonatal androgen peak normally observed in male rats, female pups were administered one high dose of testosterone (T) subcutaneously within 3 h after birth. They were then given back to their mothers and followed to adult age. At the end of the week 9, tail samples were taken, showing no differences in fasting plasma concentrations of glucose, lactate, insulin, or free fatty acids between T-treated rats and controls. Plasma concentrations of T and progesterone were significantly lower in the T-treated rats, whereas no differences were found in the levels of corticosterone, estradiol, insulin-like growth factor I, or ACTH. After 10 wk, insulin sensitivity was studied with hyperglycemic and euglycemic hyperinsulinemic (5 mU insulin/kg/min) clamp techniques. The T-treated rats showed insulin resistance with both techniques, which was overcome with time and increasing insulin concentrations during the clamp measurements. The T-treated rats were also heavier and had increased relative weights of skeletal muscles and the spleen. Parametrial, retroperitoneal, and inguinal adipose tissues decreased in weight while mesenteric adipose tissue tended to increase, resulting in an approximately 30-50% larger mesenteric than other adipose tissues. It is concluded that neonatal T imprinting of female rats is followed by insulin resistance, changes in adipose tissue distribution, and an enlarged lean mass, without elevation of circulating T. Similar changes are seen in adult female rats or women receiving T.
Full Text
The Full Text of this article is available as a PDF (160.1 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BARRACLOUGH C. A. Production of anovulatory, sterile rats by single injections of testosterone propionate. Endocrinology. 1961 Jan;68:62–67. doi: 10.1210/endo-68-1-62. [DOI] [PubMed] [Google Scholar]
- Bain J. Sexual development, maturation, and behavior. Compr Ther. 1983 Jun;9(6):21–31. [PubMed] [Google Scholar]
- Batuman O. A., Sajewski D., Ottenweller J. E., Pitman D. L., Natelson B. H. Effects of repeated stress on T cell numbers and function in rats. Brain Behav Immun. 1990 Jun;4(2):105–117. doi: 10.1016/0889-1591(90)90013-g. [DOI] [PubMed] [Google Scholar]
- Baucom D. H., Besch P. K., Callahan S. Relation between testosterone concentration, sex role identity, and personality among females. J Pers Soc Psychol. 1985 May;48(5):1218–1226. doi: 10.1037//0022-3514.48.5.1218. [DOI] [PubMed] [Google Scholar]
- Björntorp P. Regional obesity and NIDDM. Adv Exp Med Biol. 1993;334:279–285. doi: 10.1007/978-1-4615-2910-1_21. [DOI] [PubMed] [Google Scholar]
- Blanchard D. C., Spencer R. L., Weiss S. M., Blanchard R. J., McEwen B., Sakai R. R. Visible burrow system as a model of chronic social stress: behavioral and neuroendocrine correlates. Psychoneuroendocrinology. 1995;20(2):117–134. doi: 10.1016/0306-4530(94)e0045-b. [DOI] [PubMed] [Google Scholar]
- Chowen J. A., García-Segura L. M., González-Parra S., Argente J. Sex steroid effects on the development and functioning of the growth hormone axis. Cell Mol Neurobiol. 1996 Jun;16(3):297–310. doi: 10.1007/BF02088097. [DOI] [PubMed] [Google Scholar]
- Collaer M. L., Hines M. Human behavioral sex differences: a role for gonadal hormones during early development? Psychol Bull. 1995 Jul;118(1):55–107. doi: 10.1037/0033-2909.118.1.55. [DOI] [PubMed] [Google Scholar]
- De Pergola G., Xu X. F., Yang S. M., Giorgino R., Bjorntorp P. Up-regulation of androgen receptor binding in male rat fat pad adipose precursor cells exposed to testosterone: study in a whole cell assay system. J Steroid Biochem Mol Biol. 1990 Nov 30;37(4):553–558. doi: 10.1016/0960-0760(90)90400-f. [DOI] [PubMed] [Google Scholar]
- DeFronzo R. A. Lilly lecture 1987. The triumvirate: beta-cell, muscle, liver. A collusion responsible for NIDDM. Diabetes. 1988 Jun;37(6):667–687. doi: 10.2337/diab.37.6.667. [DOI] [PubMed] [Google Scholar]
- Dunaif A., Segal K. R., Futterweit W., Dobrjansky A. Profound peripheral insulin resistance, independent of obesity, in polycystic ovary syndrome. Diabetes. 1989 Sep;38(9):1165–1174. doi: 10.2337/diab.38.9.1165. [DOI] [PubMed] [Google Scholar]
- Elbers J. M., Asscheman H., Seidell J. C., Megens J. A., Gooren L. J. Long-term testosterone administration increases visceral fat in female to male transsexuals. J Clin Endocrinol Metab. 1997 Jul;82(7):2044–2047. doi: 10.1210/jcem.82.7.4078. [DOI] [PubMed] [Google Scholar]
- Evans D. J., Hoffmann R. G., Kalkhoff R. K., Kissebah A. H. Relationship of androgenic activity to body fat topography, fat cell morphology, and metabolic aberrations in premenopausal women. J Clin Endocrinol Metab. 1983 Aug;57(2):304–310. doi: 10.1210/jcem-57-2-304. [DOI] [PubMed] [Google Scholar]
- Haffner S. M. Sex hormone-binding protein, hyperinsulinemia, insulin resistance and noninsulin-dependent diabetes. Horm Res. 1996;45(3-5):233–237. doi: 10.1159/000184794. [DOI] [PubMed] [Google Scholar]
- Hamilton W., Chapman P. H. Biochemical determinants in Gender identity. Padiatr Padol Suppl. 1977;(5):69–81. doi: 10.1007/978-3-7091-8491-2_9. [DOI] [PubMed] [Google Scholar]
- Hines M., Sandberg E. C. Sexual differentiation of cognitive abilities in women exposed to diethylstilbestrol (DES) prenatally. Horm Behav. 1996 Dec;30(4):354–363. doi: 10.1006/hbeh.1996.0041. [DOI] [PubMed] [Google Scholar]
- Holmäng A., Larsson B. M., Brzezinska Z., Björntorp P. Effects of short-term testosterone exposure on insulin sensitivity of muscles in female rats. Am J Physiol. 1992 Jun;262(6 Pt 1):E851–E855. doi: 10.1152/ajpendo.1992.262.6.E851. [DOI] [PubMed] [Google Scholar]
- Holmäng A., Svedberg J., Jennische E., Björntorp P. Effects of testosterone on muscle insulin sensitivity and morphology in female rats. Am J Physiol. 1990 Oct;259(4 Pt 1):E555–E560. doi: 10.1152/ajpendo.1990.259.4.E555. [DOI] [PubMed] [Google Scholar]
- Jermendy G. Hyperandrogenicity as a prediabetic condition in women. J Intern Med. 1994 Jul;236(1):101–101. doi: 10.1111/j.1365-2796.1994.tb01128.x. [DOI] [PubMed] [Google Scholar]
- Kraegen E. W., James D. E., Bennett S. P., Chisholm D. J. In vivo insulin sensitivity in the rat determined by euglycemic clamp. Am J Physiol. 1983 Jul;245(1):E1–E7. doi: 10.1152/ajpendo.1983.245.1.E1. [DOI] [PubMed] [Google Scholar]
- Krotkiewski M., Björntorp P. Muscle tissue in obesity with different distribution of adipose tissue. Effects of physical training. Int J Obes. 1986;10(4):331–341. [PubMed] [Google Scholar]
- Kumagai S., Holmäng A., Björntorp P. The effects of oestrogen and progesterone on insulin sensitivity in female rats. Acta Physiol Scand. 1993 Sep;149(1):91–97. doi: 10.1111/j.1748-1716.1993.tb09596.x. [DOI] [PubMed] [Google Scholar]
- Lacasa D., Agli B., Mur B., Dieudonné M. N., Giudicelli Y. Protein kinase in rat adipocytes: influence of androgenic status and regional fat distribution. J Endocrinol. 1993 Sep;138(3):493–501. doi: 10.1677/joe.0.1380493. [DOI] [PubMed] [Google Scholar]
- Lindstedt G., Lundberg P. A., Lapidus L., Lundgren H., Bengtsson C., Björntorp P. Low sex-hormone-binding globulin concentration as independent risk factor for development of NIDDM. 12-yr follow-up of population study of women in Gothenburg, Sweden. Diabetes. 1991 Jan;40(1):123–128. doi: 10.2337/diab.40.1.123. [DOI] [PubMed] [Google Scholar]
- Lovejoy J. C., Bray G. A., Bourgeois M. O., Macchiavelli R., Rood J. C., Greeson C., Partington C. Exogenous androgens influence body composition and regional body fat distribution in obese postmenopausal women--a clinical research center study. J Clin Endocrinol Metab. 1996 Jun;81(6):2198–2203. doi: 10.1210/jcem.81.6.8964851. [DOI] [PubMed] [Google Scholar]
- Martin R. J., Jeanrenaud B. Growth hormone in obesity and diabetes: inappropriate hypothalamic control of secretion. Int J Obes. 1985;9 (Suppl 1):99–104. [PubMed] [Google Scholar]
- Meaney M. J., McEwen B. S. Testosterone implants into the amygdala during the neonatal period masculinize the social play of juvenile female rats. Brain Res. 1986 Nov 29;398(2):324–328. doi: 10.1016/0006-8993(86)91492-7. [DOI] [PubMed] [Google Scholar]
- Mooradian A. D., Morley J. E., Korenman S. G. Biological actions of androgens. Endocr Rev. 1987 Feb;8(1):1–28. doi: 10.1210/edrv-8-1-1. [DOI] [PubMed] [Google Scholar]
- Ohta Y. Sterility in neonatally androgenized female rats and the decidual cell reaction. Int Rev Cytol. 1995;160:1–52. doi: 10.1016/s0074-7696(08)61552-1. [DOI] [PubMed] [Google Scholar]
- Pecquery R., Dieudonne M. N., Leneveu M. C., Giudicelli Y. Evidence that testosterone modulates in vivo the adenylate cyclase activity in fat cells. Endocrinology. 1990 Jan;126(1):241–245. doi: 10.1210/endo-126-1-241. [DOI] [PubMed] [Google Scholar]
- Polderman K. H., Gooren L. J., Asscheman H., Bakker A., Heine R. J. Induction of insulin resistance by androgens and estrogens. J Clin Endocrinol Metab. 1994 Jul;79(1):265–271. doi: 10.1210/jcem.79.1.8027240. [DOI] [PubMed] [Google Scholar]
- Poretsky L. On the paradox of insulin-induced hyperandrogenism in insulin-resistant states. Endocr Rev. 1991 Feb;12(1):3–13. doi: 10.1210/edrv-12-1-3. [DOI] [PubMed] [Google Scholar]
- Rebuffé-Scrive M., Cullberg G., Lundberg P. A., Lindstedt G., Björntorp P. Anthropometric variables and metabolism in polycystic ovarian disease. Horm Metab Res. 1989 Jul;21(7):391–397. doi: 10.1055/s-2007-1009245. [DOI] [PubMed] [Google Scholar]
- Rebuffé-Scrive M., Mårin P., Björntorp P. Effect of testosterone on abdominal adipose tissue in men. Int J Obes. 1991 Nov;15(11):791–795. [PubMed] [Google Scholar]
- Redmond G. P. Androgenic disorders of women: diagnostic and therapeutic decision making. Am J Med. 1995 Jan 16;98(1A):120S–129S. doi: 10.1016/s0002-9343(99)80070-9. [DOI] [PubMed] [Google Scholar]
- Rincon J., Holmäng A., Wahlström E. O., Lönnroth P., Björntorp P., Zierath J. R., Wallberg-Henriksson H. Mechanisms behind insulin resistance in rat skeletal muscle after oophorectomy and additional testosterone treatment. Diabetes. 1996 May;45(5):615–621. doi: 10.2337/diab.45.5.615. [DOI] [PubMed] [Google Scholar]
- Rittmaster R. S. Clinical relevance of testosterone and dihydrotestosterone metabolism in women. Am J Med. 1995 Jan 16;98(1A):17S–21S. doi: 10.1016/s0002-9343(99)80054-0. [DOI] [PubMed] [Google Scholar]
- Rubin R. T., Reinisch J. M., Haskett R. F. Postnatal gonadal steroid effects on human behavior. Science. 1981 Mar 20;211(4488):1318–1324. doi: 10.1126/science.7209511. [DOI] [PubMed] [Google Scholar]
- Simon N. G., Whalen R. E. Sexual differentiation of androgen-sensitive and estrogen-sensitive regulatory systems for aggressive behavior. Horm Behav. 1987 Dec;21(4):493–500. doi: 10.1016/0018-506x(87)90007-9. [DOI] [PubMed] [Google Scholar]
- Sjögren J., Li M., Björntorp P. Androgen hormone binding to adipose tissue in rats. Biochim Biophys Acta. 1995 May 11;1244(1):117–120. doi: 10.1016/0304-4165(94)00208-f. [DOI] [PubMed] [Google Scholar]
- Spelsberg T. C., Graham M. L., 2nd, Berg N. J., Umehara T., Riehl E., Coulam C. B., Ingle J. N. A nuclear binding assay to assess the biological activity of steroid receptors in isolated animal and human tissues. Endocrinology. 1987 Aug;121(2):631–644. doi: 10.1210/endo-121-2-631. [DOI] [PubMed] [Google Scholar]
- Terrettaz J., Jeanrenaud B. In vivo hepatic and peripheral insulin resistance in genetically obese (fa/fa) rats. Endocrinology. 1983 Apr;112(4):1346–1351. doi: 10.1210/endo-112-4-1346. [DOI] [PubMed] [Google Scholar]
- Xu X. F., De Pergola G., Björntorp P. Testosterone increases lipolysis and the number of beta-adrenoceptors in male rat adipocytes. Endocrinology. 1991 Jan;128(1):379–382. doi: 10.1210/endo-128-1-379. [DOI] [PubMed] [Google Scholar]
- Xu X., De Pergola G., Eriksson P. S., Fu L., Carlsson B., Yang S., Edén S., Björntorp P. Postreceptor events involved in the up-regulation of beta-adrenergic receptor mediated lipolysis by testosterone in rat white adipocytes. Endocrinology. 1993 Apr;132(4):1651–1657. doi: 10.1210/endo.132.4.8384992. [DOI] [PubMed] [Google Scholar]