Inhibin secretion in the stallion.
Abstract: To examine the physiological role of inhibin in the stallion, a heterologous radioimmunoassay (RIA) based on a bovine RIA was validated and used to measure immunoreactive (ir)-inhibin concentrations in plasma and testicular homogenates. The bioactivity of equine testicular inhibin was also examined using an assay for suppression of FSH secretion from rat anterior pituitary cells. In addition, to identify the cell responsible for secreting testicular inhibin, the localisation of inhibin in the testis was investigated by an immunohistochemical method using a polyclonal antibody against (Tyr30)-porcine inhibin alpha(1-30) NH2. In the RIA, parallel dose response curves were obtained for the bovine inhibin standard and serial dilutions of stallion plasma and equine testicular homogenates. Parallel FSH inhibition curves were also observed for the bovine inhibin standard and serial dilutions of equine testicular homogenates in the bioassay. The inhibition of FSH secretion from rat pituitary cells by equine testicular homogenates was neutralised by an antiserum against bovine inhibin in vitro. Plasma concentrations of ir-inhibin, testosterone and oestradiol-17beta in stallions decreased abruptly after bilateral gonadectomy and FSH and LH concentrations in the plasma subsequently increased. Therefore, circulating inhibin in the stallion appeared to be largely of testicular origin. The histochemical results showed for the first time that strong immunopositive staining for inhibin occurred in the Leydig cells of the testes. Sertoli cells were also stained by the inhibin antibody but the reaction was weaker than that in Leydig cells. These results indicate clearly that both Leydig and Sertoli cells are potential sources of testicular inhibin in the stallion. A clear increase in plasma ir-inhibin concentrations was observed during the natural breeding season. Similar seasonal changes in the plasma concentrations of testicular steroid hormones and pituitary gonadotrophins occurred throughout the year. In conclusion, the testes appear to be the main source of inhibin, and testicular inhibin is secreted by Leydig and Sertoli cells in stallions. The positive correlations between plasma ir-inhibin and testicular activity during both the breeding and nonbreeding seasons indicate that plasma ir-inhibin is a useful indicator of reproductive activity in the stallion.
Publication Date: 1998-04-16 PubMed ID: 9535064DOI: 10.1111/j.2042-3306.1998.tb04467.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research study investigates the secretion of the hormone inhibin in stallions, which plays an important role in their reproductive system. The study concludes that inhibin, produced mainly by Leydig and Sertoli cells in the testes of a stallion, is a valuable indicator of reproductive activity, changing with the breeding seasons.
Study Methodology
- The study utilized a heterologous radioimmunoassay (RIA) for detecting immunoreactive-inhibin levels in the plasma and testicular homogenates of stallions. This RIA was based on a bovine one and thereby validated.
- The biocapacity of the equine testicular inhibin was also analysed by conducting an assay to gauge the suppression of Follicle-Stimulating Hormone (FSH) secretion from rat anterior pituitary cells.
- Moreover, to trace the testicular cell responsible for the secretion of inhibin, the researchers performed localisation of inhibin in the testis by applying an immunohistochemical method. This method employed a polyclonal antibody against (Tyr30)-porcine inhibin alpha(1-30) NH2.
Findings and Observations
- The RIA showed reliable dose-response curves for both the bovine inhibin standard and the diluted samples of stallion plasma and equine testicular homogenates.
- The findings from the bioassay conducting FSH inhibition also matched the RIA results. The response of stallion plasma and equine testicular homogenates against the bovine inhibin standard was found to be analogous.
- The histological examination revealed that significant immunopositive staining for inhibin was present in the Leydig cells of the testes. Although Sertoli cells also stained positively, the reaction was weaker compared to the Leydig cells. Thus, both Leydig and Sertoli cells in stallions were recognized as potential sources of testicular inhibin.
- The plasma concentrations of inhibin, testosterone, and oestradiol-17beta in stallions precipitously decreased following bilateral gonadectomy. Following this decrease, there was an increase in FSH and LH (luteinizing hormone) concentrations in the plasma. This indicates that the majority of circulating inhibin observed in stallions originates from the testes.
Conclusions
- The study concludes that the main source of inhibin in stallions is the testes, specifically the Leydig and Sertoli cells.
- There was a clear rise in plasma inhibin concentrations detected during the natural breeding season. Similar seasonal fluctuations were noticed in plasma concentrations for testicular steroid hormones and pituitary gonadotrophins, demonstrating a clear correlation with inhibin.
- Overall, the study suggests that plasma inhibin levels could serve as an effective gauge of reproductive activity in stallions, considering these levels fluctuate in unison with their breeding seasons.
Cite This Article
APA
Nagata S, Miyake YI, Nambo Y, Nagamine N, Watanabe G, Tsunoda N, Taniyama H, Hondo E, Yamada J, Taya K.
(1998).
Inhibin secretion in the stallion.
Equine Vet J, 30(2), 98-103.
https://doi.org/10.1111/j.2042-3306.1998.tb04467.x Publication
Researcher Affiliations
- Laboratory of Racing Chemistry, Tokyo, Japan.
MeSH Terms
- Animals
- Breeding
- Cattle
- Dose-Response Relationship, Immunologic
- Estradiol / analysis
- Follicle Stimulating Hormone / analysis
- Horses / metabolism
- Immune Sera / immunology
- Immunohistochemistry
- Inhibins / blood
- Inhibins / metabolism
- Inhibins / physiology
- Leydig Cells / metabolism
- Luteinizing Hormone / analysis
- Male
- Rabbits
- Radioimmunoassay / veterinary
- Rats
- Sertoli Cells / metabolism
- Testis / cytology
- Testis / metabolism
- Testosterone / analysis
Citations
This article has been cited 5 times.- Yu C, Jiang F, Zhang M, Luo D, Shao S, Zhao J, Gao L, Zuo C, Guan Q. HC diet inhibited testosterone synthesis by activating endoplasmic reticulum stress in testicular Leydig cells.. J Cell Mol Med 2019 May;23(5):3140-3150.
- Suzuki T, Mizukami H, Nambo Y, Ishimaru M, Miyata K, Akiyama K, Korosue K, Naito H, Nagaoka K, Watanabe G, Taya K. Different effects of an extended photoperiod treatment on growth, gonadal function, and condition of hair coats in Thoroughbred yearlings reared under different climate conditions.. J Equine Sci 2015;26(4):113-24.
- Kunii H, Nambo Y, Okano A, Matsui A, Ishimaru M, Asai Y, Sato F, Fujii K, Nagaoka K, Watanabe G, Taya K. Effects of an extended photoperiod on gonadal function and condition of hair coats in Thoroughbred colts and fillies.. J Equine Sci 2015;26(2):57-66.
- Dhakal P, Tsunoda N, Nakai R, Kitaura T, Harada T, Ito M, Nagaoka K, Toishi Y, Taniyama H, Gen W, Taya K. Annual Changes in Day-length, Temperature, and Circulating Reproductive Hormones in Thoroughbred Stallions and Geldings.. J Equine Sci 2011;22(2):29-36.
- Weng Q, Medan MS, Okano T, Murase T, Tsubota T, Xu M, Watanabe G, Taya K. Changes in serum inhibin levels and immunolocalization of inhibin/activin subunits during the breeding season in the wild male Japanese black bear (Ursus thibetanus japonicus).. Endocrine 2006 Apr;29(2):345-50.
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