Literature DB >> 8126345

The Brown Norway rat as a model of male reproductive aging: evidence for both primary and secondary testicular failure.

D A Gruenewald1, M A Naai, D L Hess, A M Matsumoto.   

Abstract

In man, aging is associated with both primary and secondary testicular dysfunction. In contrast, most studies in male rat models of aging have demonstrated only secondary testicular failure. We previously reported that testes from aging male F344 rats secrete excessive progesterone (P), which may suppress gonadotropin secretion and confound aging studies. To determine whether the male Brown Norway (BN) rat is a more suitable aging model, trunk blood was collected from intact (sham-operated) and orchidectomized young (3 mo), middle-aged (13 mo), old (23 mo), and senescent (28-30 mo) animals. Testosterone (T), estradiol (E2), P, prolactin (PRL), luteinizing hormone (LH), and follicle-stimulating hormone (FSH) were measured by RIA. In intact rats, T levels declined with aging, while LH was unchanged, and FSH increased progressively with aging. In contrast to F344 rats, no age-related increases in P or E2 occurred, nor did PRL or other steroid hormones increase. In the absence of testicular feedback (orchidectomized rats), FSH and LH declined progressively with aging. These findings suggest that, as in men, aging male BN rats manifest both primary and secondary testicular failure, and do not exhibit decreased gonadotropin levels secondary to excessive steroid or PRL secretion. Therefore, the BN rat appears to be the best available rat model for studies of male reproductive aging.

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Year:  1994        PMID: 8126345     DOI: 10.1093/geronj/49.2.b42

Source DB:  PubMed          Journal:  J Gerontol        ISSN: 0022-1422


  17 in total

1.  Analytical construct of reversible desensitization of pituitary-testicular signaling: illustrative application in aging.

Authors:  Daniel M Keenan; Ali Iranmanesh; Johannes D Veldhuis
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-11-17       Impact factor: 3.619

2.  Short-term aromatase-enzyme blockade unmasks impaired feedback adaptations in luteinizing hormone and testosterone secretion in older men.

Authors:  Johannes D Veldhuis; Ali Iranmanesh
Journal:  J Clin Endocrinol Metab       Date:  2004-10-13       Impact factor: 5.958

3.  Testosterone's short-term positive effect on luteinizing-hormone secretory-burst mass and its negative effect on secretory-burst frequency are attenuated in middle-aged men.

Authors:  Peter Y Liu; Paul Y Takahashi; Pamela D Roebuck; Joy N Bailey; Daniel M Keenan; Johannes D Veldhuis
Journal:  J Clin Endocrinol Metab       Date:  2009-07-07       Impact factor: 5.958

4.  Long-term suppression of Leydig cell steroidogenesis prevents Leydig cell aging.

Authors:  H Chen; B R Zirkin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

5.  Localization of gonadotropin-releasing hormone (GnRH), gonadotropin-inhibitory hormone (GnIH), kisspeptin and GnRH receptor and their possible roles in testicular activities from birth to senescence in mice.

Authors:  Shabana Anjum; Amitabh Krishna; Rajagopala Sridaran; Kazuyoshi Tsutsui
Journal:  J Exp Zool A Ecol Genet Physiol       Date:  2012-10-01

6.  Aging and estradiol effects on gene expression in the medial preoptic area, bed nucleus of the stria terminalis, and posterodorsal medial amygdala of male rats.

Authors:  Victoria L Nutsch; Margaret R Bell; Ryan G Will; Weiling Yin; Andrew Wolfe; Ross Gillette; Juan M Dominguez; Andrea C Gore
Journal:  Mol Cell Endocrinol       Date:  2016-12-20       Impact factor: 4.102

7.  Effects of aging, high-fat diet, and testosterone treatment on neural and metabolic outcomes in male brown Norway rats.

Authors:  V Alexandra Moser; Amy Christensen; Jiahui Liu; Amanda Zhou; Shunya Yagi; Christopher R Beam; Liisa Galea; Christian J Pike
Journal:  Neurobiol Aging       Date:  2018-09-22       Impact factor: 4.673

8.  Aging results in hypermethylation of ribosomal DNA in sperm and liver of male rats.

Authors:  Christopher C Oakes; Dominic J Smiraglia; Christoph Plass; Jacquetta M Trasler; Bernard Robaire
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-06       Impact factor: 11.205

9.  Drug ligand-induced activation of translocator protein (TSPO) stimulates steroid production by aged brown Norway rat Leydig cells.

Authors:  J Y Chung; H Chen; A Midzak; A L Burnett; V Papadopoulos; B R Zirkin
Journal:  Endocrinology       Date:  2013-03-22       Impact factor: 4.736

10.  Steroidogenic fate of the Leydig cells that repopulate the testes of young and aged Brown Norway rats after elimination of the preexisting Leydig cells.

Authors:  Haolin Chen; Jingjing Guo; Renshan Ge; Qingquan Lian; Vassilios Papadopoulos; Barry R Zirkin
Journal:  Exp Gerontol       Date:  2015-09-01       Impact factor: 4.032

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