Rhodes F M, Entwistle K W, Kinder J E
Department of Biomedical and Tropical Veterinary Sciences, James Cook University of North Queensland, Townsville, Australia.
Biol Reprod. 1996 Dec;55(6):1437-43. doi: 10.1095/biolreprod55.6.1437.
The aim of this study was to monitor endocrine and ovarian changes immediately preceding the onset of nutritionally induced anestrus. Daily blood samples were obtained from 14 postpubertal heifers for one estrous cycle (initial estrous cycle). Subsequently, heifers designated "restricted" were given a limited diet (n = 9), and daily blood samples were obtained for approximately 21 days preceding onset of anestrus (anovulatory cycle). Controls were allowed ad libitum dietary intake (n = 5), and daily blood samples were collected for a complete estrous cycle during a time period that coincided with that preceding onset of anestrus in restricted heifers. Plasma samples were assayed for LH, FSH, progesterone, and estradiol-17 beta. The ovaries of all heifers were examined daily using transrectal ultrasonography from the initial until the final or anovulatory estrous cycles to determine changes in growth of follicles and corpora lutea. Anestrus was defined as failure of ovulation of the dominant follicle following luteolysis. When anovulatory and initial estrous cycles in restricted heifers were compared, mean concentrations of LH were lower (p < 0.01), and diameters of dominant follicles were smaller (p < 0.01); mean concentrations of estradiol-17 beta were also lower in the three days following luteolysis (p = 0.06), but concentrations of FSH appeared to be higher (p = 0.003); maximum diameters of corpora lutea were smaller (p < 0.001), but duration of luteal phases and concentrations of progesterone preceding luteolysis were similar (p > 0.10). In controls, no differences were found between estrous cycles for any of these variables. It is concluded that failure of ovulation, following reduced dietary intake, resulted from insufficient circulating LH to stimulate maturation of the ovulatory follicle.
本研究的目的是监测营养诱导的发情周期开始前紧挨着的内分泌和卵巢变化。从14头青春期后小母牛获取每日血样,为期一个发情周期(初始发情周期)。随后,将指定为“限饲”的小母牛给予限量饮食(n = 9),并在发情周期开始前约21天(无排卵周期)获取每日血样。对照组小母牛自由采食(n = 5),并在与限饲小母牛发情周期开始前的时间段一致的时间内,为一个完整的发情周期采集每日血样。检测血浆样本中的促黄体生成素(LH)、促卵泡生成素(FSH)、孕酮和雌二醇-17β。从初始发情周期到最终或无排卵发情周期,每天使用经直肠超声检查所有小母牛的卵巢,以确定卵泡和黄体生长的变化。发情周期停止被定义为黄体溶解后优势卵泡排卵失败。当比较限饲小母牛的无排卵发情周期和初始发情周期时,LH的平均浓度较低(p < 0.01),优势卵泡直径较小(p < 0.01);黄体溶解后的三天内,雌二醇-17β的平均浓度也较低(p = 0.06),但FSH的浓度似乎较高(p = 0.003);黄体的最大直径较小(p < 0.001),但黄体期持续时间和黄体溶解前孕酮浓度相似(p > 0.10)。在对照组中,这些变量在发情周期之间未发现差异。得出的结论是,饮食摄入量减少后排卵失败是由于循环LH不足以刺激排卵卵泡成熟所致。