Kiyma Z, Alexander B M, Van Kirk E A, Murdoch W J, Hallford D M, Moss G E
Department of Animal Science, University of Wyoming, Laramie 82071, USA.
J Anim Sci. 2004 Sep;82(9):2548-57. doi: 10.2527/2004.8292548x.
The goal of this study was to determine the effects of short-term feed withdrawal on reproductive and metabolic hormones during the luteal phase of the estrous cycle in mature ewes. Mature ewes observed in estrus were assigned randomly to control and fasted groups (n = 10 per group Trials 1 and 2). For Trials 1 and 2, control ewes had ad libitum access to feed, whereas fasted ewes were not fed from d 7 through 11 of their estrous cycle; on d 12, all ewes were treated with 10 mg of PGF2alpha, and fasted ewes were gvien ad libitum access to feed. For Trial 1, blood samples were collected daily through fasting and at 2-h intervals following PGF2alpha for 72 h. Serum concentrations of insulin (P < or = 0.002) and IGF-I (P < or = 0.01), but not GH (P > or = 0.60), were decreased during fasting compared with fed ewes. Serum concentrations of 29 (P = 0.02) and 34 kDa (P = 0.04) IGFBP were greater in fasted ewes at 96 h after initiation of fasting than in control ewes. Two control and four fasted ewes in Trial 1 did not exhibit a preovulatory surge release of LH by 72 h. Therefore, Trial 2 was conducted so that the timing of the LH surge could be predicted following the collection of blood samples at 2-h intervals for 112 h and then at 6-h intervals until 178 h following PGF2alpha administration and realimentation. The magnitude of the preovulatory LH surge in Trial 2 was decreased (P = 0.009) and delayed (P = 0.04), and serum concentrations of estradiol were diminished (P < or = 0.03) 12 h before the LH surge in fasted ewes. Ovulation rates were not influenced (P > or = 0.32) by fasting in Trials 1 and 2. Serum concentrations of progesterone in both Trials 1 and 2 were, however, greater (P < 0.001) in fasted than in control ewes. A third trial with ovariectomized ewes was conducted to determine whether the increased serum concentrations of progesterone observed in fasted ewes during Trials 1 and 2 were ovarian-derived. Ovariectomized ewes were implanted with progesterone-containing intravaginal implants and allotted to control (n = 5) or fasted (n = 5) treatment groups and fed as described for Trials 1 and 2. Similar to intact ewes, serum concentrations of progesterone were approximately twofold greater (P < 0.001) in fasted than in control implanted ovariectomized ewes. In summary, feed withdrawal for 5 d during the luteal phase of the estrous cycle increased serum concentrations of progesterone and evoked endocrine changes that could perturb the subsequent estrous cycle.
本研究的目的是确定短期禁食对成熟母羊发情周期黄体期生殖激素和代谢激素的影响。观察到发情的成熟母羊被随机分为对照组和禁食组(试验1和试验2每组n = 10)。对于试验1和试验2,对照母羊可自由采食,而禁食母羊在发情周期的第7至11天不喂食;在第12天,所有母羊均用10 mg的前列腺素F2α进行处理,禁食母羊可自由采食。对于试验1,在禁食期间每天采集血样,并在注射前列腺素F2α后每隔2小时采集一次血样,共采集72小时。与采食母羊相比,禁食期间胰岛素(P≤0.002)和胰岛素样生长因子-I(IGF-I,P≤0.01)的血清浓度降低,但生长激素(GH,P≥0.60)未降低。禁食开始后96小时,禁食母羊中29 kDa(P = 0.02)和34 kDa(P = 0.04)胰岛素样生长因子结合蛋白(IGFBP)的血清浓度高于对照母羊。试验1中的2只对照母羊和4只禁食母羊在72小时内未出现促排卵前促黄体生成素(LH)峰。因此,进行试验2,以便在每隔2小时采集血样112小时,然后每隔6小时采集血样直至注射前列腺素F2α和恢复采食后178小时后,预测LH峰的时间。试验2中促排卵前LH峰的幅度降低(P = 0.009)且延迟(P = 0.04),禁食母羊在LH峰前12小时雌二醇的血清浓度降低(P≤0.03)。试验1和试验2中,禁食对排卵率无影响(P≥0.32)。然而,试验1和试验2中禁食母羊的孕酮血清浓度均高于对照母羊(P < 0.001)。进行了第三项试验,对去卵巢母羊进行研究,以确定试验1和试验2中禁食母羊观察到的孕酮血清浓度升高是否来源于卵巢。给去卵巢母羊植入含孕酮的阴道植入物,并分配到对照(n = 5)或禁食(n = 5)处理组,并按试验1和试验2所述进行饲养。与完整母羊相似,禁食的去卵巢植入母羊的孕酮血清浓度比对照母羊高约两倍(P < 0.001)。总之,发情周期黄体期禁食5天会增加孕酮血清浓度,并引起内分泌变化,可能扰乱随后的发情周期。