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Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid

It has been recently shown that mammalian spermatozoa were hyperactivated by steroids, amines and amino acids. In the present study, we investigated whether hyperactivation of hamster sperm is regulated by progesterone (P) and γ-aminobutyric acid (GABA). Although sperm hyperactivation was enhanced b...

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Autores principales: KON, Hiroe, TAKEI, Gen L., FUJINOKI, Masakatsu, SHINODA, Motoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085384/
https://www.ncbi.nlm.nih.gov/pubmed/24614320
http://dx.doi.org/10.1262/jrd.2013-076
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author KON, Hiroe
TAKEI, Gen L.
FUJINOKI, Masakatsu
SHINODA, Motoo
author_facet KON, Hiroe
TAKEI, Gen L.
FUJINOKI, Masakatsu
SHINODA, Motoo
author_sort KON, Hiroe
collection PubMed
description It has been recently shown that mammalian spermatozoa were hyperactivated by steroids, amines and amino acids. In the present study, we investigated whether hyperactivation of hamster sperm is regulated by progesterone (P) and γ-aminobutyric acid (GABA). Although sperm hyperactivation was enhanced by P, GABA significantly suppressed P-enhanced hyperactivation in a dose-dependent manner. Suppression of P-enhanced hyperactivation by GABA was significantly inhibited by an antagonist of the GABA(A) receptor (bicuculline). Moreover, P bound to the sperm head, and this binding was decreased by GABA. Because the concentrations of GABA and P change in association with the estrous cycle, these results suggest that GABA and P competitively regulate the enhancement of hyperactivation through the GABA(A) receptor.
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spelling pubmed-40853842014-07-08 Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid KON, Hiroe TAKEI, Gen L. FUJINOKI, Masakatsu SHINODA, Motoo J Reprod Dev Original Article It has been recently shown that mammalian spermatozoa were hyperactivated by steroids, amines and amino acids. In the present study, we investigated whether hyperactivation of hamster sperm is regulated by progesterone (P) and γ-aminobutyric acid (GABA). Although sperm hyperactivation was enhanced by P, GABA significantly suppressed P-enhanced hyperactivation in a dose-dependent manner. Suppression of P-enhanced hyperactivation by GABA was significantly inhibited by an antagonist of the GABA(A) receptor (bicuculline). Moreover, P bound to the sperm head, and this binding was decreased by GABA. Because the concentrations of GABA and P change in association with the estrous cycle, these results suggest that GABA and P competitively regulate the enhancement of hyperactivation through the GABA(A) receptor. The Society for Reproduction and Development 2014-03-10 2014-06 /pmc/articles/PMC4085384/ /pubmed/24614320 http://dx.doi.org/10.1262/jrd.2013-076 Text en ©2014 Society for Reproduction and Development http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original Article
KON, Hiroe
TAKEI, Gen L.
FUJINOKI, Masakatsu
SHINODA, Motoo
Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid
title Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid
title_full Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid
title_fullStr Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid
title_full_unstemmed Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid
title_short Suppression of Progesterone-enhanced Hyperactivation in Hamster Spermatozoa by γ-aminobutyric Acid
title_sort suppression of progesterone-enhanced hyperactivation in hamster spermatozoa by γ-aminobutyric acid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085384/
https://www.ncbi.nlm.nih.gov/pubmed/24614320
http://dx.doi.org/10.1262/jrd.2013-076
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