Soy isoflavone effects on the adrenal glands of orchidectomized adult male rats: a comprehensive histological and hormonal study.

Genistein (G) and related soy phytoestrogens have been studied for potential usefulness in different chronic diseases, and may ameliorate signs of aging. They have a profound influence on the hypothalamo-pituitary-adrenal (HPA) axis. The present study utilized the rat model of mild andropause to thoroughly evaluate the effects of G and soy extract on the adrenal gland and related blood hormones. Adult male rats were orchidectomized (Orx) or sham operated (SO). Orx rats received daily subcutaneous injections for 3 weeks of solvent, or G (Orx+G, 30 mg/kg), or commercial soy extract (Orx+Soy, 30 mg/kg). Adrenal glands and blood were harvested at the end of the treatment for hormone analyses, histology and design-based stereology. Compared to SO rats Orx evoked significant (P<0.05) changes including: the replicating cell number in the 3 adrenocortical zones; vascularity and cortical volume and blood levels of adrenocorticotropic hormone (ACTH), aldosterone and dehydroepiandrosterone (DHEA). When comparing Orx vs. Orx+G groups the following significant (P<0.05) changes were observed: a further increase in number of replicating cells in zonas glomerulosa and reticularis, vasculature network presence, cortical and zona reticularis volumes, ACTH and corticosterone concentrations, and lower DHEA levels. Comparing Orx vs. Orx+Soy resulted in elevated (P<0.05) ACTH and corticosterone levels. Structural integrity of the adrenal gland was unchanged vs. SO rats. Overall, G and soy extract treatments resulted in proliferative activity and/or vasculature support in the adrenal cortex. The data and current literature support the impression of a beneficial effect of soy components on the homeostatic response to stress.

[1]  V. Milošević,et al.  The Morpho-Functional Parameters of Rat Pituitary Hormone Producing Cells After Genistein Treatment , 2018 .

[2]  I. Jarić,et al.  Functional morphology of pituitary -thyroid and -adrenocortical axes in middle-aged male rats treated with Vitex agnus castus essential oil. , 2016, Acta histochemica.

[3]  I. Jarić,et al.  Histological parameters of the adrenal cortex after testosterone application in a rat model of the andropause. , 2016, Histology and histopathology.

[4]  I. Jarić,et al.  Testosterone application decreases the capacity for ACTH and corticosterone secretion in a rat model of the andropause. , 2015, Acta histochemica.

[5]  V. Ajdžanovic,et al.  Soy extract-dependent changes in morphofunctional parameters of the pituitary corticotropes in adult rats. , 2014, Acta histochemica.

[6]  V. Ajdžanovic,et al.  Immuno-histomorphometric and -fluorescent characteristics of GH cells after treatment with genistein or daidzein in an animal model of andropause , 2014 .

[7]  Wancai Yang,et al.  Soy isoflavones and prostate cancer: A review of molecular mechanisms , 2014, The Journal of Steroid Biochemistry and Molecular Biology.

[8]  I. Spasojević,et al.  Glucocorticoid excess and disturbed hemodynamics in advanced age: the extent to which soy isoflavones may be beneficial. , 2012, General physiology and biophysics.

[9]  V. Ajdžanovic,et al.  Genistein stimulates the hypothalamo-pituitary-adrenal axis in adult rats: morphological and hormonal study. , 2012, Histology and histopathology.

[10]  V. Ajdžanovic,et al.  Daidzein effects on ACTH cells: immunohistomorphometric and hormonal study in an animal model of the andropause. , 2011, Histology and histopathology.

[11]  E. Ho,et al.  Differential effects of whole soy extract and soy isoflavones on apoptosis in prostate cancer cells , 2006, Experimental biology and medicine.

[12]  D. Brkic,et al.  Daidzein administration positively affects thyroid C cells and bone structure in orchidectomized middle-aged rats , 2010, Osteoporosis International.

[13]  V. Ajdžanovic,et al.  Genistein-Induced Histomorphometric and Hormone Secreting Changes in the Adrenal Cortex in Middle-Aged Rats , 2009, Experimental biology and medicine.

[14]  A. Hoeflich,et al.  Mechanisms of adrenal gland growth: signal integration by extracellular signal regulated kinases1/2. , 2008, Journal of molecular endocrinology.

[15]  D. Brkic,et al.  Genistein affects the morphology of pituitary ACTH cells and decreases circulating levels of ACTH and corticosterone in middle-aged male rats. , 2009, Biological research.

[16]  D. Brkic,et al.  Subcutaneously administrated genistein and daidzein decrease serum cholesterol and increase triglyceride levels in male middle-aged rats. , 2007, Experimental biology and medicine.

[17]  R. Newbold,et al.  Disruption of the female reproductive system by the phytoestrogen genistein. , 2007, Reproductive toxicology.

[18]  So Yeong Lee,et al.  Organotypic slice culture of the hypothalamic paraventricular nucleus of rat , 2007, Journal of veterinary science.

[19]  W. Drake,et al.  The endocrine system and ageing , 2007, The Journal of pathology.

[20]  J. Herman,et al.  Chronic stress induces adrenal hyperplasia and hypertrophy in a subregion-specific manner. , 2006, American journal of physiology. Endocrinology and metabolism.

[21]  M. Saint-Geniez,et al.  Vascular endothelial growth factor localization in the adult. , 2006, The American journal of pathology.

[22]  V. Viau,et al.  Central organization of androgen-sensitive pathways to the hypothalamic-pituitary-adrenal axis: Implications for individual differences in responses to homeostatic threat and predisposition to disease , 2005, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

[23]  A. Morales,et al.  Andropause (or symptomatic late-onset hypogonadism): facts, fiction and controversies , 2004, The aging male : the official journal of the International Society for the Study of the Aging Male.

[24]  K. Setchell,et al.  Behavioral effects of endocrine-disrupting substances: phytoestrogens. , 2004, ILAR journal.

[25]  L. Malendowicz Sex differences in adrenocortical structure and function , 2004, Cell and Tissue Research.

[26]  G. Vinson Adrenocortical zonation and ACTH , 2003, Microscopy research and technique.

[27]  M. Kéramidas,et al.  Role of adrenocorticotropic hormone in the development and maintenance of the adrenal cortical vasculature , 2003, Microscopy research and technique.

[28]  E. Wespes,et al.  Male andropause: myth, reality, and treatment , 2002, International Journal of Impotence Research.

[29]  F. Peale,et al.  Identification of an angiogenic mitogen selective for endocrine gland endothelium , 2001, Nature.

[30]  P. Shughrue,et al.  Distribution of estrogen receptor β immunoreactivity in the rat central nervous system , 2001 .

[31]  V. Coxam,et al.  Daidzein is more efficient than genistein in preventing ovariectomy-induced bone loss in rats. , 2000, The Journal of nutrition.

[32]  W. Mazur,et al.  Overview of naturally occurring endocrine-active substances in the human diet in relation to human health. , 2000, Nutrition.

[33]  D. Thompson,et al.  Lasofoxifene (CP-336,156), a selective estrogen receptor modulator, prevents bone loss induced by aging and orchidectomy in the adult rat. , 2000, Endocrinology.

[34]  F. Holsboer,et al.  Endogenous vasopressin contributes to hypothalamic-pituitary-adrenocortical alterations in aged rats. , 2000, The Journal of endocrinology.

[35]  宮本 浩邦 Studies on cytogenesis in adult rat adrenal cortex : circadian and zonal variations and their modulation by adrenocorticotropic hormone , 2000 .

[36]  L. Yaswen,et al.  Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin , 1999, Nature Medicine.

[37]  M. Suematsu,et al.  Development of functional zonation in the rat adrenal cortex. , 1999, Endocrinology.

[38]  K. Setchell,et al.  Phytoestrogens: the biochemistry, physiology, and implications for human health of soy isoflavones. , 1998, The American journal of clinical nutrition.

[39]  C Labrie,et al.  Expression and neuropeptidergic characterization of estrogen receptors (ERalpha and ERbeta) throughout the rat brain: anatomical evidence of distinct roles of each subtype. , 1998, Journal of neurobiology.

[40]  S. Bornstein,et al.  Tissue remodelling in the adrenal gland. , 1998, Biochemical pharmacology.

[41]  L. Terzuoli,et al.  Effect of estradiol on serum triglyceride lipoprotein levels and fatty acid composition in castrated rats. , 1997, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[42]  C. Kenyon,et al.  Control of cell proliferation in the rat adrenal gland in vivo by the renin-angiotensin system. , 1996, The American journal of physiology.

[43]  R. Brudieux,et al.  Age-related changes in plasma corticosterone and aldosterone responses to exogenous ACTH in the rat. , 1995, Hormone research.

[44]  E. B. VEDEL JENSEN,et al.  The rotator , 1993 .

[45]  H J Gundersen,et al.  The efficiency of systematic sampling in stereology and its prediction * , 1987, Journal of microscopy.

[46]  H. G. Swann THE PITUITARY-ADRENOCORTICAL RELATIONSHIP , 1940 .