Laboratory of Veterinary Physiology, School of Veterinary Medicine, Kitasato University, Aomori 034-8628, Japan.
Clinic for Small Domestic Animals and Radiology, Faculty of Veterinary Medicine, Mahanakorn University of Technology, Bangkok 10530, Thailand.
J Reprod Dev. 2021 Jun 21;67(3):217-221. doi: 10.1262/jrd.2021-029. Epub 2021 Apr 10.
Functional relationship between nuclear receptor subfamily 4 group A member 3 (Nr4a3) and annexin A5 (Anxa5), which are two gonadotropin-releasing hormone (GnRH)-inducible genes, has been established while evaluating pituitary gonadotropes in relation to follicle-stimulating hormone beta (Fshb) expression. However, the physiological variations that arise due to the differential expression of these genes in the pituitary gland during rat estrous cycle remain unknown. This study aimed to evaluate the Nr4a3 and Anxa5 mRNA expression during the estrous cycle in rats in comparison with the expression of the gonadotropin subunit genes, luteinizing hormone beta (Lhb) and Fshb. Nr4a3 mRNA expression showed a single peak at 1400 h of proestrus during the 4-d estrous cycle. Anxa5 mRNA level was elevated along with increased Fshb mRNA expression after the decline of Nr4a3 mRNA until 2300 h. Lhb mRNA expression levels were not significantly changed during the estrous cycle. Notably, addition of a GnRH antagonist at 1100 h completely eradicated luteinizing hormone secretion at 1400 h and 1700 h of proestrus, and significantly reduced the Nr4a3 mRNA expression level at both the time points. These results suggest that GnRH is, at least partly, responsible for the increase in pituitary Nr4a3, and that the interaction between NR4A3 and ANXA5 is required to regulate Fshb expression during the preovulatory gonadotropin surge.
核受体亚家族 4 组 A 成员 3(Nr4a3)和膜联蛋白 A5(Anxa5)是两种促性腺激素释放激素(GnRH)诱导基因,它们之间的功能关系在评估与卵泡刺激素β(Fshb)表达相关的垂体促性腺激素细胞时已经建立。然而,由于这些基因在大鼠发情周期中垂体的差异表达而产生的生理变化尚不清楚。本研究旨在评估 Nr4a3 和 Anxa5 在大鼠发情周期中的表达,与促性腺激素亚基基因黄体生成素β(Lhb)和 Fshb 的表达进行比较。Nr4a3 mRNA 的表达在发情周期的 4 天中,于发情前期的 1400 小时出现单峰。随着 Nr4a3 mRNA 表达的下降,Anxa5 mRNA 水平与 Fshb mRNA 表达一起升高,直到 2300 小时。发情周期中 Lhb mRNA 表达水平没有明显变化。值得注意的是,在 1100 小时添加 GnRH 拮抗剂完全消除了发情前期 1400 小时和 1700 小时的黄体生成素分泌,并显著降低了这两个时间点的 Nr4a3 mRNA 表达水平。这些结果表明,GnRH 至少部分负责增加垂体 Nr4a3,并且 NR4A3 和 ANXA5 之间的相互作用是调节发情前促性腺激素激增期间 Fshb 表达所必需的。