Turzillo A M, Juengel J L, Nett T M
Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins 80523, USA.
Biol Reprod. 1995 Aug;53(2):418-23. doi: 10.1095/biolreprod53.2.418.
As circulating concentrations of progesterone decrease during the early preovulatory period, concentrations of mRNA encoding ovine GnRH receptor in the anterior pituitary gland increase. The purpose of this study was to determine whether removal of progesterone affects amounts of GnRH receptor mRNA directly or whether withdrawal of progesterone affects GnRH receptor gene expression indirectly by permitting secretion of GnRH to increase. Ovulation was induced in seasonally anestrous ewes, and luteolysis was initiated with prostaglandin F2 alpha (PGF2 alpha) 11 or 12 days later. Anterior pituitary glands were collected 0 h, 4 h, 12 h, or 24 h after treatment with PGF2 alpha, and 24 h after injection of saline (n = 3 or 4 animals/group). Two groups of ewes (n = 3) received infusions of GnRH (250 ng infused over 6 min) hourly for 12 h; luteolysis was induced in one of these groups at the time that treatment with GnRH was initiated, and anterior pituitary glands were collected at the end of the 12-h infusion period. Blood samples were collected at 15-min intervals for 12 h from all ewes treated with GnRH and from animals administered PGF2 alpha and killed 12 h later. No differences in concentrations of GnRH receptor mRNA, numbers of GnRH receptors, or circulating concentrations of progesterone or estradiol were detected between groups of animals at 0 h and 24 h after treatment with saline; therefore, data from these control groups were combined. Concentrations of progesterone in serum decreased in PGF2 alpha-treated ewes and were lower (p < 0.05) than those in controls 24 h after treatment with PGF2 alpha.(ABSTRACT TRUNCATED AT 250 WORDS)
在排卵前期早期,随着循环中的孕酮浓度下降,垂体前叶中编码绵羊促性腺激素释放激素(GnRH)受体的mRNA浓度会升高。本研究的目的是确定孕酮的去除是直接影响GnRH受体mRNA的量,还是孕酮的撤离通过允许GnRH分泌增加而间接影响GnRH受体基因表达。对季节性发情期母羊诱导排卵,并在11或12天后用前列腺素F2α(PGF2α)启动黄体溶解。在PGF2α处理后0小时、4小时、12小时或24小时,以及注射生理盐水后24小时采集垂体前叶(每组n = 3或4只动物)。两组母羊(n = 3)每小时接受一次GnRH输注(6分钟内输注250 ng),持续12小时;其中一组在开始GnRH治疗时诱导黄体溶解,并在12小时输注期结束时采集垂体前叶。对所有接受GnRH治疗的母羊以及接受PGF2α治疗并在12小时后处死的动物,每隔15分钟采集一次血样,共采集12小时。在注射生理盐水处理后0小时和24小时,各动物组之间未检测到GnRH受体mRNA浓度、GnRH受体数量或孕酮和雌二醇循环浓度的差异;因此,将这些对照组的数据合并。PGF2α处理的母羊血清中孕酮浓度下降,且在PGF2α处理后24小时低于对照组(p < 0.05)。(摘要截断于250字)