Involvement of progesterone and estrogen receptors in the ram sperm acrosome reaction.
Acrosome Reaction
/ drug effects
Animals
Antioxidants
/ administration & dosage
Cell Survival
Cells, Cultured
Estradiol
/ pharmacology
Estrogens
/ pharmacology
Male
Progesterone
/ pharmacology
Receptors, Estrogen
/ antagonists & inhibitors
Receptors, Progesterone
/ physiology
Resveratrol
/ pharmacology
Sheep
Sperm Capacitation
/ drug effects
Sperm Motility
Spermatozoa
/ physiology
Tamoxifen
/ pharmacology
Acrosome reaction
Mifepristone
Ram spermatozoa
Resveratrol
Tamoxifen
Tanaproget
Journal
Domestic animal endocrinology
ISSN: 1879-0054
Titre abrégé: Domest Anim Endocrinol
Pays: United States
ID NLM: 8505191
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
31
03
2020
revised:
01
07
2020
accepted:
17
07
2020
pubmed:
18
8
2020
medline:
15
12
2021
entrez:
18
8
2020
Statut:
ppublish
Résumé
The steroid hormones 17-β estradiol (E2) and progesterone (P4) can regulate capacitation, hyperactive motility, and the acrosome reaction (AR) during the sperm transit through the female tract. Moreover, exogenous P4 and E2 can induce the AR in ovine spermatozoa, and progesterone receptor (PR) and estrogen receptors (ERα and ERβ) are present in these cells. Thus, to investigate whether the effects both steroid hormones in ram sperm capacitation and AR are receptor-mediated, we incubated them with receptor agonists (tanaproget 1 μM and 5 μM for PR or resveratrol 5 μM and 10 μM for ER) or antagonists (mifepristone 4 μM and 40 μM for PR or tamoxifen 5 μM and 10 μM for ER) in capacitating conditions. The addition of receptor modulators did not affect sperm viability or total motility, although changes in progressive motility were detected. The incubation with both receptor agonists increased the percentage of acrosome-reacted spermatozoa, evaluated by chlortetracycline staining, when compared with the capacitated nontreated sample (Cap-C, P < 0.001). Moreover, the ER agonist resveratrol 10 μM provoked a greater AR than E2 (P < 0.01). Furthermore, the incubation with the receptor antagonists prevented the induction of the AR by P4 or E2, as the antagonists-treated spermatozoa presented a similar CTC pattern to that of Cap-C. In conclusion, these results confirm that P4 and E2 can induce the AR in ram spermatozoa and that this effect is receptor-mediated.
Identifiants
pubmed: 32799038
pii: S0739-7240(20)30094-1
doi: 10.1016/j.domaniend.2020.106527
pii:
doi:
Substances chimiques
Antioxidants
0
Estrogens
0
Receptors, Estrogen
0
Receptors, Progesterone
0
Tamoxifen
094ZI81Y45
Progesterone
4G7DS2Q64Y
Estradiol
4TI98Z838E
Resveratrol
Q369O8926L
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
106527Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.