TY - JOUR
T1 - Effects of cortisol on prostaglandin F2α secretion and expression of genes involved in the arachidonic acid metabolic pathway in equine endometrium - In vitro study
T2 - Cortisol regulation of endometrial prostaglandin F2α in mare
AU - Szóstek-Mioduchowska, Anna Z.
AU - Shiotani, Haruki
AU - Yamamoto, Yuki
AU - Sadowska, Agnieszka
AU - Wójtowicz, Anna
AU - Kozai, Keisuke
AU - Hojo, Takuo
AU - Kimura, Koji
AU - Skarzynski, Dariusz J.
AU - Okuda, Kiyoshi
N1 - Funding Information:
A.Sz-M was supported by a Japan Society for the Promotion of Science (JSPS) post-doctoral fellow (P-14082). We would like to thank Dr. Naoki Takenouchi and Dr. Miki Sakatani (Livestock and Grassland Research Division, Kyushu Okinawa Agricultural Research Center, NARO, Kumamoto, Japan) for their technical supports; to Senko Farm CO. Ltd (Kumamoto, Japan) for providing equine samples. We thank Dr. M. Bogacki and Dr. K. Witek (Institute of Animal Reproduction and Food Research, Polish Academy of Science) for technical support.
Funding Information:
A.Sz-M was supported by a Japan Society for the Promotion of Science (JSPS) post-doctoral fellow ( P-14082 ). We would like to thank Dr. Naoki Takenouchi and Dr. Miki Sakatani ( Livestock and Grassland Research Division , Kyushu Okinawa Agricultural Research Center , NARO , Kumamoto, Japan) for their technical supports; to Senko Farm CO., Ltd (Kumamoto, Japan) for providing equine samples. We thank Dr. M. Bogacki and Dr. K. Witek ( Institute of Animal Reproduction and Food Research , Polish Academy of Science) for technical support.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Glucocorticoids (GCs) are known to play an important role in maintaining basal and stress-related homeostasis by interacting with endocrine mediators and prostaglandins (PGs). Although a growing body of evidence shows that GCs exert their regulatory action at a multitude of sites in the reproductive axis through corticosteroid receptors, little is known about the direct role of cortisol, an active form of GCs, in the equine endometrium. Thus, the study aimed to determine the effect of cortisol on PGF2α synthesis in the endometrial tissue and cells in vitro. In Exp.1, the immunolocalization and the expression of the glucocorticoid receptor (GCR) in the endometrium throughout the estrous cycle were established. In Exp. 2 and 3, the effects of cortisol on PGF2α secretion and transcripts associated with the arachidonic acid (AA) cascade in endometrial tissues, and cells were defined. Endometrial tissues obtained from the early, mid, and late luteal phases and the follicular phase of the estrous cycle were exposed to cortisol (100, 200, and 400 nM) for 24 h. Endometrial epithelial and stromal cells (early phase of estrous cycle) were exposed to cortisol (100 nM) for 24 h. Then, PGF2α secretion and transcripts associated with the AA cascade (PLA2G2A, PLA2G4A, PTGS2, and PGFS) were assessed. GCR was expressed in the cytoplasm and the nucleus in the luminal and glandular epithelium as well as in the stroma. Endometrial GCR protein abundance was up-regulated at the late luteal phase compared to the mid-luteal phase of the estrous cycle. Cortisol dose-dependently decreased PGF2α secretion, PLA2G2A and PLA2G4A transcripts in endometrial tissues. Additionally, cortisol treatment decreased PGF2α secretion from endometrial epithelial and stromal cells. Moreover, it affected PLA2G2A, PLA2G4A, and PTGS2 transcripts in endometrial stromal cells. These findings suggest that cortisol suppresses the synthesis of PGF2α by affecting the AA cascade in the equine endometrium during the estrous cycle.
AB - Glucocorticoids (GCs) are known to play an important role in maintaining basal and stress-related homeostasis by interacting with endocrine mediators and prostaglandins (PGs). Although a growing body of evidence shows that GCs exert their regulatory action at a multitude of sites in the reproductive axis through corticosteroid receptors, little is known about the direct role of cortisol, an active form of GCs, in the equine endometrium. Thus, the study aimed to determine the effect of cortisol on PGF2α synthesis in the endometrial tissue and cells in vitro. In Exp.1, the immunolocalization and the expression of the glucocorticoid receptor (GCR) in the endometrium throughout the estrous cycle were established. In Exp. 2 and 3, the effects of cortisol on PGF2α secretion and transcripts associated with the arachidonic acid (AA) cascade in endometrial tissues, and cells were defined. Endometrial tissues obtained from the early, mid, and late luteal phases and the follicular phase of the estrous cycle were exposed to cortisol (100, 200, and 400 nM) for 24 h. Endometrial epithelial and stromal cells (early phase of estrous cycle) were exposed to cortisol (100 nM) for 24 h. Then, PGF2α secretion and transcripts associated with the AA cascade (PLA2G2A, PLA2G4A, PTGS2, and PGFS) were assessed. GCR was expressed in the cytoplasm and the nucleus in the luminal and glandular epithelium as well as in the stroma. Endometrial GCR protein abundance was up-regulated at the late luteal phase compared to the mid-luteal phase of the estrous cycle. Cortisol dose-dependently decreased PGF2α secretion, PLA2G2A and PLA2G4A transcripts in endometrial tissues. Additionally, cortisol treatment decreased PGF2α secretion from endometrial epithelial and stromal cells. Moreover, it affected PLA2G2A, PLA2G4A, and PTGS2 transcripts in endometrial stromal cells. These findings suggest that cortisol suppresses the synthesis of PGF2α by affecting the AA cascade in the equine endometrium during the estrous cycle.
KW - Cortisol
KW - Endometrium
KW - Mare
KW - Phospholipase a
KW - Prostaglandin
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UR - http://www.scopus.com/inward/citedby.url?scp=85112365842&partnerID=8YFLogxK
U2 - 10.1016/j.theriogenology.2021.08.009
DO - 10.1016/j.theriogenology.2021.08.009
M3 - Article
C2 - 34399386
AN - SCOPUS:85112365842
SN - 0093-691X
VL - 173
SP - 221
EP - 229
JO - Theriogenology
JF - Theriogenology
ER -