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与牛雌性发情同期化通常使用剂量相比,更大剂量的醋酸甲羟孕酮在调节促黄体生成素和17β-雌二醇分泌方面并不能模拟内源性孕酮。

Melengestrol acetate at greater doses than typically used for estrous synchrony in bovine females does not mimic endogenous progesterone in regulation of secretion of luteinizing hormone and 17 beta-estradiol.

作者信息

Kojima F N, Chenault J R, Wehrman M E, Bergfeld E G, Cupp A S, Werth L A, Mariscal V, Sanchez T, Kittok R J, Kinder J E

机构信息

Department of Animal Science, University of Nebraska-Lincoln, 68583-0908, USA.

出版信息

Biol Reprod. 1995 Feb;52(2):455-63. doi: 10.1095/biolreprod52.2.455.

Abstract

Our working hypothesis was that doses of melengestrol acetate (MGA) greater than those typically administered in estrous synchrony regimens would regulate secretion of LH and 17 beta-estradiol (E2) as endogenous progesterone (P4) does during the midluteal phase of the estrous cycle. We also hypothesized that endogenous P4 from the CL would interact with MGA to further decrease the frequency of LH pulses and E2. Cows on Day 5 of their estrous cycle (Day 0 = estrus) were randomly assigned to an untreated control group (CONT, n = 5) or to one of six MGA treatment groups (n = 5 per group): 1) MGA administered orally each day via a gelatin capsule at a dose of 0.5 mg MGA/cow with the CL present (0.5CIL); 2) 0.5 mg MGA/cow daily in the absence of CL (0.5NO); 3) 1.0 mg MGA with CL present (1.0CL); 4) 1.0 mg MGA without CL (1.0NO); 5) 1.5 mg MGA with CL present (1.5CL); 6) 1.5 mg without CL (1.5NO). MGA was administered for 10 days (Day 5 = initiation of treatment). To regress CL, cows assigned to groups without CL received injections of prostaglandin F 2 alpha (PGF 2 alpha; 25 mg) on Days 6 and 7 of their estrous cycle. All cows were administered PGF2 alpha at the end of the 10-day treatment period. During the treatment period, daily blood samples were collected to determine concentrations of E2. Serial blood samples were collected at 15-min intervals for 24 h on Days 8, 11, and 14 to determine pattern of LH secretion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们的工作假设是,醋酸美仑孕酮(MGA)的剂量高于发情同步方案中通常使用的剂量时,会像发情周期黄体中期内源性孕酮(P4)那样调节促黄体生成素(LH)和17β-雌二醇(E2)的分泌。我们还假设,来自黄体的内源性P4会与MGA相互作用,进一步降低LH脉冲频率和E2水平。处于发情周期第5天(第0天=发情)的奶牛被随机分配到未处理的对照组(CONT,n = 5)或六个MGA处理组之一(每组n = 5):1)在黄体存在时,每天经明胶胶囊口服0.5 mg MGA/头奶牛(0.5CIL);2)在无黄体时,每天0.5 mg MGA/头奶牛(0.5NO);3)有黄体时1.0 mg MGA(1.0CL);4)无黄体时1.0 mg MGA(1.0NO);5)有黄体时1.5 mg MGA(1.5CL);6)无黄体时1.5 mg(1.5NO)。MGA给药10天(第5天=开始治疗)。为使黄体退化,分配到无黄体组的奶牛在发情周期的第6天和第7天注射前列腺素F2α(PGF2α;25 mg)。在10天治疗期结束时,所有奶牛均注射PGF2α。在治疗期间,每天采集血样以测定E2浓度。在第8、11和14天,每隔15分钟采集一次系列血样,持续24小时,以测定LH分泌模式。(摘要截短于250字)

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