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- W2130213534 abstract "Annals of the New York Academy of SciencesVolume 774, Issue 1 p. 29-46 Biosynthesis of DHEAS by the Human Adrenal Cortex and Its Age-Related Decline PETER J. HORNSBY, PETER J. HORNSBY Huffington Center on Aging Baylor College of Medicine 1 Baylor Plaza M320 Houston, Texas 77030Search for more papers by this author PETER J. HORNSBY, PETER J. HORNSBY Huffington Center on Aging Baylor College of Medicine 1 Baylor Plaza M320 Houston, Texas 77030Search for more papers by this author First published: December 1995 https://doi.org/10.1111/j.1749-6632.1995.tb17370.xCitations: 93AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat REFERENCES 1 Neville, A. M. & M. J. Očhare. 1982. The Human Adrenal Cortex. Pathology and Biology—An Integrated Approach. Springer-Verlag. Berlin . 2 Kime, D. E., G. P. Vinson, P. W. Major & R. Kilpatrick. 1980. Adrenal-gonad relationships. In General, Comparative and Clinical Endocrinology, Vol. 3. I. C. Jones & I. W. Henderson, Eds.: 183–200. Academic Press. London . 3 Parker, L. N. & W. D. Odell. 1980. Control of adrenal androgen secretion. Endocrinol. Rev. 1: 392–410. 4 Bachmann, R. 1954. Die Nebenniere. In Handbuch der mikroskopischen Anatomie des Menschen, Vol. 6. Blutgefass- und Lymphgefassapparat. Innersekretorische Drusen, Part 5. W. Bargmann, Ed.: 1–952. Springer-Verlag. Berlin . 5 Shire, J. G. M. 1979. Corticosteroids and adrenocortical function in animals. In Genetic Variation in Hormone Systems, Vol. 1. J. G. M. Shire, Ed.: 43–70. CRC Press. Boca Raton . 6 Haning, R. V., Jr., M. Chabot, C. A. Flood, R. Hackett & C. Longcope. 1989. Metabolic clearance rate (MCR) of dehydroepiandrosterone sulfate (DS), its metabolism to dehydroepiandrosterone, androstenedione, testosterone, and dihydrotestosterone, and the effect of increased plasma DS concentration on DS MCR in normal women. J. Clin. Endocrinol. Metab. 69: 1047–1052. 7 Parrini, D. C. Guidoni, C. Massafra & A. R. Genazzani. 1980. Spontaneous fluctuations, circadian variations, and pattern of DHAS during the last 20 weeks of pregnancy. In Adrenal Androgens. A. R. Genazzani, J. H. H. Thijssen & P. K. Siiteri, Eds.: 199–206. Raven Press, New York . 8 Dewis, P. & D. C. Anderson. 1985. The adrenarche and adrenal hirsutism. In Adrenal Cortex. D. C. Anderson & J. S. D. Winter, Eds.: 96–116. Butterworth. London . 9 Brigell, D. F., V. S. Fang & R. L. Rosenfield. 1992. Recovery of responses to ovine corticotropin-releasing hormone after withdrawal of a short course of glucocorticoid. J. Clin. Endocrinol. Metab. 74: 1036–1039. 10 Kleiber, H., F. Rey, E. Temler & F. Gomez. 1991. Dissociated recovery of cortisol and dehydroepiandrosterone sulphate after treatment for Cushingčs syndrome. J. Endocrinol. Invest. 14: 489–492. 11 Winterer, J., H. E. Gwirtsman, T. George, W. H. Kaye, D. L. Loriaux & G. B. Cutler, Jr. 1985. Adrenocorticotropin-stimulated adrenal androgen secretion in anorexia nervosa: Impaired secretion at low weight with normalization after long term weight recovery. J. Clin. Endocrinol. 61: 693–697. 12 Lindh, A., K. Carlstrom, J. Eklund & N. Wilking. 1992. Serum steroids and prolactin during and after major surgical trauma. Acta Anaesthesiol. Scand. 36: 119–124. 13 Parker, C. R., Jr. & C. R. Banter. 1985. Divergence in adrenal steroid secretory pattern after thermal injury in adult patients. J. Trauma 25: 508–510. 14 Semple, C. G., C. E. Gray & G. H. Beastall. 1987. Adrenal androgens and illness. Acta Endocrinol. (Copenh.) 116: 155–160. 15 Rudman, D., K. R. Shetty & D. E. Mattson. 1990. Plasma dehydroepiandrosterone sulfate in nursing home men. J. Am. Geriatr. Soc. 38: 421–427. 16 Christeff, N., S. Gharakhanian, N. Thobie, W. Rozenbaum & E. A. Nunez. 1992. Evidence for changes in adrenal and testicular steroids during HIV βiNfection. J. Acquired Immune Defic. Syndr. 5: 841–846. 17 Mulder, J. W., P. H. Frissen, P. Krijnen, E. Endert, F. De Wolf, J. Goudsmit, J. G. Masterson & J. M. Lange. 1992. Dehydroepiandrosterone as predictor for progression to AIDS in asymptomatic human immunodeficiency virus-infected men. J. Infect. Dis. 165: 413–418. 18 Parker, L. N., E. T. Lifrak & W. D. Odell. 1983. A 60,000 molecular weight human pituitary glycopeptide stimulates adrenal androgen secretion. Endocrinology 113: 2092–2100. 19 Mellon, S. H., J. E. Shively & W. L. Miller. 1991. Human proopiomelanocortin-(79–96), a proposed androgen stimulatory hormone, does not affect steroidogenesis in cultured human fetal adrenal cells. J. Clin. Endocrinol. Metab. 72: 19–22. 20 Penhoat, A., P. Sanchez, C. Jaillard, D. Langlois, M. Begeot & J. M. Saez. 1991. Human proopiomelanocortin-(79–96), a proposed cortical androgen-stimulating hormone, does not affect steroidogenesis in cultured human adult adrenal cells. J. Clin. Endocrinol. Metab. 72: 23–26. 21 Hornsby, P. J. & K. A. Aldern. 1984. Steroidogenic enzyme activities in cultured human definitive zone adrenocortical cells: Comparison with bovine adrenocortical cells and resultant differences in adrenal androgen synthesis. J. Clin. Endocrinol. Metab. 58: 121–130. 22 Hyatt, P. J., K. Bhatt & J. F. Tait. 1983. Steroid biosynthesis by zona fasciculata and zona reticularis cells purified from the mammalian adrenal cortex. J. Steroid Biochem. 19: 953–960. 23 Jones, T., M. Groom & K. Griffiths. 1970. Steroid biosynthesis by cultures of normal human adrenal tissue. Biochem. Biophys. Res. Commun. 38: 355–361. 24 Očhare, M. J., E. C. Nice & A. M. Neville. 1980. Regulation of androgen secretion and sulfoconjugation in the adult human adrenal cortex: Studies with primary monolayer cell cultures. In Adrenal Androgens. A. R. Genazzani, J. H. H. Thijssen & P. K. Siiteri, Eds.: 7–25. Raven Press. New York . 25 Endoh, A., S. Kristiansen, P. Casson, J. E. Buster & P. J. Hornsby. 1995. Submitted for publication. 26 Baird, A. C., G. Brisson, K. W. Kan, W. C. Duguid & S. Solomon. 1978. Control of steroid synthesis in human fetal adrenals in monolayer culture. Can. J. Biochem. 56: 577–584. 27 Voutilainen, R. & A. I. Kahri. 1980. Placental origin of the suppression of 3β-hydroxysteroid dehydrogenase in the fetal zone cells of human fetal adrenals. J. Steroid Biochem. 13: 39–43. 28 Winter, J. S. D., K. Fujieda, C. Faiman, F. I. Reyes & J. Thliveris. 1980. Control of steroidogenesis by human fetal adrenal cells in tissue culture. In Adrenal Androgens. A. R. Genazzani, J. H. H. Thijssen & P. K. Siiteri, Eds.: 55–62. Raven Press. New York . 29 Crickard, K., C. R. Ill & R. B. Jaffe. 1981. Control of proliferation of human fetal adrenal cells in vitro. J. Clin. Endocrinol. Metab. 53: 790–796. 30 Simonian, M. H. & M. W. Capp. 1984. Characterization of steroidogenesis in cell cultures of the human fetal adrenal cortex: Comparison of definitive zone and fetal zone cells. J. Clin. Endocrinol. Metab. 59: 643–651. 31 Hornsby, P. J., M. J. Očhare & A. M. Neville. 1974. Functional and morphological observations on rat adrenal zona glomerulosa cells in monolayer culture. Endocrinology 95: 1240–1251. 32 Crivello, J. F. & G. N. Gill. 1983. Induction of cultured bovine adrenocortical zona glomerulosa cell 17-hydroxylase activity by ACTH. Mol. Cell. Endocrinol. 30: 97–107. 33 Hornsby, P. J. 1985. The regulation of adrenocortical function by control of growth and structure. In Adrenal Cortex. D. C. Anderson & J. S. D. Winter, Eds.: 1–31. Butter-worth. London . 34 Cheng, C. Y., M. V. Flasch & P. J. Hornsby. 1992. Expression of 17α-hydroxylase and 3β-hydroxysteroid dehydrogenase in fetal human adrenocortical cells transfected with SV40 T antigen. J. Mol. Endocrinol. 9: 7–17. 35 Kristiansen, S., A. Endoh, P. Casson, J. E. Buster & P. J. Hornsby. 1995. Submitted for publication. 36 Cameron, E. H. D., T. Jones, D. Jones, A. B. M. Anderson & K. Griffiths. 1969. Further studies on the relationship between C19- and C21-steroid synthesis in the human adrenal gland. J. Endocrinol. 45: 215–230. 37 Dawson, I. M. P., J. Pryse-Davies & I. M. Snape. 1961. The distribution of six enzyme systems and of lipid in the human and rat adrenal cortex before and after administration of steroid and ACTH, with comments on the distribution in human foetuses and in some natural disease conditions. J. Pathol. Bacteriol. 81: 181–190. 38 Cavallero, C. & G. Chiappino. 1962. Histochemistry of steroid-3β-o1 dehydrogenase in the human adrenal cortex. Experientia 18: 119–120. 39 Kennerson, A. R., D. A. McDonald & J. B. Adams. 1983. Dehydroepiandrosterone sulfotransferase localization in human adrenal glands: A light and electron microscopic study. J. Clin. Endocrinol. Metab. 56: 786–790. 40 Zuber, M. X., E. R. Simpson & M. R. Waterman. 1986. Expression of bovine 17α-hydroxylase cytochrome P-450 cDNA in nonsteroidogenic (COS 1) cells. Science 234: 1258–1261. 41 Swart, P., R. W. Estabrook, J. I. Mason & M. R. Waterman. 1989. Catalytic activity of human and bovine adrenal cytochromes P-450 17α, lyase expressed in Cos 1 cells. Biochem. Soc. Trans. 17: 1025–1026. 42 Yamazaki, T., K. Nawa, S. Kominami & S. Takemori. 1992. Cytochrome P-450 (17α, lyase)-mediating pathway of androgen synthesis in bovine adrenocortical cultured cells. Biochim. Biophys. Acta 1134: 143–148. 43 White, P. C. & M. I. New. 1992. Genetic basis of endocrine disease 2: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J. Clin. Endocrinol. Metab. 74: 6–11. 44 Weliky, I. & L. L. Engel. 1963. Metabolism of progesterone-4-C14 and pregnenolone-7α-H3 by human adrenal tissue. Formation of 16α-hydroxyprogesterone-C14, corticosterone-C14, and cortisol-C14-H3. J. Biol. Chem. 238: 1302–1307. 45 Whitehouse, B. J. & G. P. Vinson. 1968. Corticosteroid biosynthesis from pregnenolone and progesterone by human adrenal tissue in vitro. A kinetic study. Steroids. 11: 245–264. 46 Rich, B. H., R. L. Rosenfield, A. W. Lucky, J. C. Helke & P. Otto. 1981. Adrenarche: Changing adrenal response to adrenocorticotropin. J. Clin. Endocrinol. Metab. 52: 1129–1136. 47 Kelnar, C. J. H. & C. G. D. Brook. 1983. A mixed longitudinal study of adrenal steroid excretion in childhood and the mechanism of adrenarche. Clin. Endocrinol. 19: 117–129. 48 Mcallister, J. M. & P. J. Hornsby. 1988. Dual regulation of 3β-hydroxysteroid dehydrogenase, 17α-hydroxylase, and dehydroepiandrosterone sulfotransferase by adenosine 3č,5č-monophosphate and activators of protein kinase C in cultured human adrenocortical cells. Endocrinology 122: 2012–2018. 49 Voutilainen, R., V. Ilvesmaki & P. J. Miettinen. 1991. Low expression of 3β-hydroxy-5-ene steroid dehydrogenase gene in human fetal adrenals in vivo; adrenocorticotropin and protein kinase C-dependent regulation in adrenocortical cultures. J. Clin. Endocrinol. Metab. 72: 761–767. 50 Doody, K. M., B. R. Carr, W. E. Rainey, W. Byrd, B. A. Murry, R. C. Strickler, J. L. Thomas & J. I. MASON. 1990. 3β-Hydroxysteroid dehydrogenase/isomerase in the fetal zone and neocortex of the human fetal adrenal gland. Endocrinology 126: 2487–2492. 51 Hornsby, P. J. 1987. Cytochrome P-450/pseudosubstrate interactions in the adrenal cortex and their possible role in adrenocortical pathology. In Corticosteroids and Peptide Hormones in Hypertension. F. Mantero & P. Vecsei, Eds.: 11–25. Raven Press. New York . 52 Anderson, D. C. 1980. Hypothesis: The adrenal androgen-stimulating hormone does not exist. Lancet 2: 454–456. 53 Rezvani, I., L. R. Garibaldi, A. M. Digeorge & H. G. Artman. 1983. Disproportionate suppression of dehydroepiandrosterone sulfate (DHEAS) in treated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatr. Res. 17: 131–134. 54 Conway, D. I., D. C. Anderson & D. E. BUčlOCK. 1982. The steroid response to controlled adrenal stimulation in congenital adrenal hyperplasia. Clin. Endocrinol. (Oxf.) 16: 215–226. 55 Vermeulen, A. 1980. Adrenal androgens and aging. In Adrenal Androgens. A. R. Genazzani, J. H. H. Thijssen & P. K. Siiteri, Eds.: 207–215. Raven Press. New York . 56 Adams, J. B. 1985. Control of secretion and the function of C19-Δ5-steroids of the human adrenal gland. Mol. Cell. Endocrinol. 41: 1–17. 57 Orentreich, N., J. L. Brind, J. H. Vogelman, R. Andres & H. Baldwin. 1992. Long-term longitudinal measurements of plasma dehydroepiandrosterone sulfate in normal men. J. Clin. Endocrinol. Metab. 75: 1002–1004. 58 Wolfsen, A. R. 1982. Aging and the adrenals. In Endocrine Aspects of Aging. S. G. Korenman, Ed.: 55–74. Elsevier. New York . 59 Vermeulen, A., J. P. Deslypere, W. Schelfhout, L. Verdonck & R. Rubens. 1982. Adrenocortical function in old age: Response to acute adrenocorticotropin stimulation. J. Clin. Endocrinol. Metab. 54: 187–195. 60 Liu, C. H., G. A. Laughlin, U. G. Fischer & S. S. Yen. 1990. Marked attenuation of ultradian and circadian rhythms of dehydroepiandrosterone in postmenopausal women: Evidence for a reduced 17,20-desmolase enzymatic activity. J. Clin. Endocrinol. Metab. 71: 900–910. 61 Blichert-Toft, M. 1978. The adrenal glands in old age. In Geriatric Endocrinology. R. B. Greenblatt, Ed.: 81–102. Raven Press. New York . 62 Kreiner, E. & G. Dhom. 1979. Altersveranderungen der menschlichen Nebenniere. Zbl. Allg. Pathol. Pathol. Anat. 123: 351–356. 63 Hornsby, P. J., C. Y. Cheng, D. S. Lala, S. S. Maghsoudlou, S. G. Raju & L. Yang. 1992. Changes in gene expression during senescence of adrenocortical cells in culture. J. Steroid Biochem. Mol. Biol. 43: 385–395. 64 Hornsby, P. J. 1995. Genes, hormones, and aging. In Advances in Cell Aging and Senescence. P.S. Timiras, Ed. JAI Press. CT . Citing Literature Volume774, Issue1Dehydroepiandrosterone (DHEA) and AgingDecember 1995Pages 29-46 ReferencesRelatedInformation" @default.
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- W2130213534 cites W1970737941 @default.
- W2130213534 cites W1971539282 @default.
- W2130213534 cites W1978275195 @default.
- W2130213534 cites W1978635521 @default.
- W2130213534 cites W1983482072 @default.
- W2130213534 cites W1987860847 @default.
- W2130213534 cites W1999817116 @default.
- W2130213534 cites W2001485520 @default.
- W2130213534 cites W2011818863 @default.
- W2130213534 cites W2012047091 @default.
- W2130213534 cites W2022883373 @default.
- W2130213534 cites W2031634506 @default.
- W2130213534 cites W2031672945 @default.
- W2130213534 cites W2032616737 @default.
- W2130213534 cites W2032825940 @default.
- W2130213534 cites W2035886683 @default.
- W2130213534 cites W2044268853 @default.
- W2130213534 cites W2054185347 @default.
- W2130213534 cites W2056291672 @default.
- W2130213534 cites W2056533698 @default.
- W2130213534 cites W2057813894 @default.
- W2130213534 cites W2059120710 @default.
- W2130213534 cites W2060400167 @default.
- W2130213534 cites W2060998559 @default.
- W2130213534 cites W2062452627 @default.
- W2130213534 cites W2066489153 @default.
- W2130213534 cites W2068709470 @default.
- W2130213534 cites W2070041561 @default.
- W2130213534 cites W2071297057 @default.
- W2130213534 cites W2074377130 @default.
- W2130213534 cites W2081447857 @default.
- W2130213534 cites W2082288584 @default.
- W2130213534 cites W2088590108 @default.
- W2130213534 cites W2091444720 @default.
- W2130213534 cites W2091905341 @default.
- W2130213534 cites W2093233584 @default.
- W2130213534 cites W2121674861 @default.
- W2130213534 cites W2127844234 @default.
- W2130213534 cites W2132573157 @default.
- W2130213534 cites W2152836400 @default.
- W2130213534 cites W2403880021 @default.
- W2130213534 cites W2479518716 @default.
- W2130213534 cites W32225221 @default.
- W2130213534 cites W4245980189 @default.
- W2130213534 cites W4247285826 @default.
- W2130213534 cites W4253004535 @default.
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