O'Neil Meaghan M, Korthanke Curtis M, Scarpa José O, Welsh Thomas H, Cardoso Rodolfo C, Williams Gary L
Animal Reproduction Laboratory, Texas A&M AgriLife Research, Beeville, TX; Department of Animal Science, Texas A&M University, College Station, TX.
Department of Animal Science, Texas A&M University, College Station, TX.
J Equine Vet Sci. 2019 Apr;75:93-103. doi: 10.1016/j.jevs.2019.01.013. Epub 2019 Feb 6.
We tested the hypotheses that in winter anovulatory mares (1) both chronic daily injections of estradiol-17β (E2) and subcutaneous E2 implants could enhance pituitary secretion of gonadotropins in response to continuous subcutaneous infusion of native gonadotropin-releasing hormone (GnRH); and (2) the secretory pattern of follicle-stimulating hormone (FSH) in response to continuous subcutaneous infusion of native GnRH is similar to that of luteinizing hormone (LH) but differs between mares that develop or fail to develop an estrogen-active, preovulatory follicle. In Experiment 1, 20 winter anovulatory mares (n = 5 per group) in early February received twice-daily injections of corn oil (control) or 5 mg of E2 with or without continuous subcutaneous treatment with native GnRH (100 μg/hr) or received GnRH only for up to 14 days. In Experiment 2, 24 winter anovulatory mares (n = 6 per group) were treated with a full-length (high dose) or quarter-length (low dose) E2 implant (Compudose) in combination with continuous GnRH infusion (100 μg/hr) for up to 28 days or served as sham controls. Mares developing 35-mm follicles were induced to ovulate with human chorionic gonadotropin. Mares not developing a 35-mm follicle within 14 days received a replacement 14-day GnRH pump. In Experiment 1, E2 enhanced the response to GnRH beginning on Day 3, with mean LH greater (P < .001) in GnRH + E2 than in GnRH only and control mares. In Experiment 2, plasma E2 and estrone sulfate were increased in association with the development of a large (35 mm) follicle but did not increase in response to either E2 implant despite marked increases in uterine edema following their insertion. A sustained increase (P < .0001) in plasma LH was observed in all GnRH-treated mares, but this effect was not modified by implant treatment. By Day 28, six of six GnRH, five of six GnRH + low E2, two of six GnRH + high E2, and zero of six control mares developed 35-mm follicles and were induced to ovulate. A marked increase (P < .0001) in plasma FSH was observed within 24 hours in all GnRH-treated mares, returning to baseline by Day 4. In summary, twice-daily injection of 5 mg E2 enhanced pituitary secretion of LH in response to continuous administration of GnRH, but commercial E2 cattle implants failed to duplicate these effects. Continuous infusion of GnRH produced a differential but consistent pattern of FSH secretion (short-term increase) compared with LH (sustained increase). Differences in ovarian responses to GnRH treatment could not be explained by variation in gonadotropin secretion.
在冬季,处于乏情期的母马,(1)每日皮下注射雌二醇-17β(E2)以及皮下植入E2,均可增强垂体对持续皮下输注天然促性腺激素释放激素(GnRH)的促性腺激素分泌反应;(2)在持续皮下输注天然GnRH时,促卵泡素(FSH)的分泌模式与促黄体素(LH)相似,但在能发育出具有雌激素活性的排卵前卵泡的母马和未能发育出此类卵泡的母马之间存在差异。在实验1中,20匹于2月初处于冬季乏情期的母马(每组n = 5),每天接受两次玉米油注射(对照组)或5毫克E2注射,同时或不同时接受持续皮下注射天然GnRH(100微克/小时),或仅接受GnRH注射,持续14天。在实验2中,24匹冬季乏情期母马(每组n = 6)接受全长(高剂量)或四分之一长度(低剂量)的E2植入物(Compudose),同时持续输注GnRH(100微克/小时),持续28天,或作为假手术对照组。发育出直径35毫米卵泡的母马用人类绒毛膜促性腺激素诱导排卵。14天内未发育出直径35毫米卵泡的母马接受更换的14天GnRH泵。在实验1中,E2从第3天开始增强对GnRH的反应,GnRH + E2组的平均LH水平高于(P <.001)仅GnRH组和对照组母马。在实验2中,血浆E2和硫酸雌酮随着大卵泡(35毫米)的发育而增加,但尽管植入E2后子宫水肿明显增加,但对任何一种E2植入物均无反应。在所有接受GnRH治疗的母马中均观察到血浆LH持续升高(P <.0001),但这种效应未因植入治疗而改变。到第28天,6匹接受GnRH治疗的母马中有6匹、6匹GnRH + 低剂量E2组中有5匹、6匹GnRH + 高剂量E2组中有2匹以及6匹对照组母马中有0匹发育出35毫米卵泡并被诱导排卵。在所有接受GnRH治疗的母马中,24小时内血浆FSH显著升高(P <.0001),并在第4天恢复到基线水平。总之,每天两次注射5毫克E2可增强垂体对持续给予GnRH的LH分泌反应,但市售的E2牛用植入物未能重复这些效应。与LH(持续升高)相比,持续输注GnRH产生了不同但一致的FSH分泌模式(短期升高)。卵巢对GnRH治疗反应的差异无法通过促性腺激素分泌的变化来解释。