Cargando…

Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats

INTRODUCTION: Thyroid hormones play a major role in the regulation of testicular maturation and growth and in the control of Sertoli and Leydig cell functions in adulthood. When naturally occurring, hypothyroidism causes male hypogonadotropic hypogonadism and Sertoli cell function disorders, but whe...

Descripción completa

Detalles Bibliográficos
Autores principales: Gołyński, Marcin, Metyk, Michał, Szkodziak, Piotr, Lutnicki, Krzysztof, Kalisz, Grzegorz, Szczepanik, Marcin, Wilkołek, Piotr, Dobrowolski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458557/
https://www.ncbi.nlm.nih.gov/pubmed/30989148
http://dx.doi.org/10.2478/jvetres-2019-0008
_version_ 1783410030694891520
author Gołyński, Marcin
Metyk, Michał
Szkodziak, Piotr
Lutnicki, Krzysztof
Kalisz, Grzegorz
Szczepanik, Marcin
Wilkołek, Piotr
Dobrowolski, Piotr
author_facet Gołyński, Marcin
Metyk, Michał
Szkodziak, Piotr
Lutnicki, Krzysztof
Kalisz, Grzegorz
Szczepanik, Marcin
Wilkołek, Piotr
Dobrowolski, Piotr
author_sort Gołyński, Marcin
collection PubMed
description INTRODUCTION: Thyroid hormones play a major role in the regulation of testicular maturation and growth and in the control of Sertoli and Leydig cell functions in adulthood. When naturally occurring, hypothyroidism causes male hypogonadotropic hypogonadism and Sertoli cell function disorders, but when iatrogenic and methimazole-induced its influence on the pituitary-testicular axis function with respect to Sertoli cells is poorly known. MATERIAL AND METHODS: Male adult Wistar rats (n = 14) were divided into two groups: E – taking methimazole orally for 60 days, and C – control animals. After 60 d, the concentrations in serum of testosterone, follicle-stimulating and luteinising hormones, and inhibins A and B were measured. Testicles were examined morphologically: the apoptotic Sertoli cell percentage (ASC%) and number of these cells functional per tubular mm(2) (FSCN/Tmm(2)) were calculated. RESULTS: In group E, inhibin A was higher while inhibin B was lower than in group C. ASC% was higher and FSCN/Tmm(2) lower in group E than in group C. CONCLUSION: A specific modulation of Sertoli cell function in the course of methimazole-induced hypothyroidism leads to a simultaneous concentration increase in inhibin A and decrease in B. Inhibin A might share responsibility for pituitary-testicular axis dysfunction and hypogonadotropic hypogonadism in this model of hypothyroidism.
format Online
Article
Text
id pubmed-6458557
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Sciendo
record_format MEDLINE/PubMed
spelling pubmed-64585572019-04-15 Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats Gołyński, Marcin Metyk, Michał Szkodziak, Piotr Lutnicki, Krzysztof Kalisz, Grzegorz Szczepanik, Marcin Wilkołek, Piotr Dobrowolski, Piotr J Vet Res Research Article INTRODUCTION: Thyroid hormones play a major role in the regulation of testicular maturation and growth and in the control of Sertoli and Leydig cell functions in adulthood. When naturally occurring, hypothyroidism causes male hypogonadotropic hypogonadism and Sertoli cell function disorders, but when iatrogenic and methimazole-induced its influence on the pituitary-testicular axis function with respect to Sertoli cells is poorly known. MATERIAL AND METHODS: Male adult Wistar rats (n = 14) were divided into two groups: E – taking methimazole orally for 60 days, and C – control animals. After 60 d, the concentrations in serum of testosterone, follicle-stimulating and luteinising hormones, and inhibins A and B were measured. Testicles were examined morphologically: the apoptotic Sertoli cell percentage (ASC%) and number of these cells functional per tubular mm(2) (FSCN/Tmm(2)) were calculated. RESULTS: In group E, inhibin A was higher while inhibin B was lower than in group C. ASC% was higher and FSCN/Tmm(2) lower in group E than in group C. CONCLUSION: A specific modulation of Sertoli cell function in the course of methimazole-induced hypothyroidism leads to a simultaneous concentration increase in inhibin A and decrease in B. Inhibin A might share responsibility for pituitary-testicular axis dysfunction and hypogonadotropic hypogonadism in this model of hypothyroidism. Sciendo 2019-03-22 /pmc/articles/PMC6458557/ /pubmed/30989148 http://dx.doi.org/10.2478/jvetres-2019-0008 Text en © 2019 M. Gołyński et al. published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Research Article
Gołyński, Marcin
Metyk, Michał
Szkodziak, Piotr
Lutnicki, Krzysztof
Kalisz, Grzegorz
Szczepanik, Marcin
Wilkołek, Piotr
Dobrowolski, Piotr
Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats
title Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats
title_full Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats
title_fullStr Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats
title_full_unstemmed Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats
title_short Pituitary-testicular Axis Dysfunction in Methimazole-induced Hypothyroidism in Rats
title_sort pituitary-testicular axis dysfunction in methimazole-induced hypothyroidism in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458557/
https://www.ncbi.nlm.nih.gov/pubmed/30989148
http://dx.doi.org/10.2478/jvetres-2019-0008
work_keys_str_mv AT gołynskimarcin pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT metykmichał pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT szkodziakpiotr pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT lutnickikrzysztof pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT kaliszgrzegorz pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT szczepanikmarcin pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT wilkołekpiotr pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats
AT dobrowolskipiotr pituitarytesticularaxisdysfunctioninmethimazoleinducedhypothyroidisminrats