Guzeloglu A, Ambrose J D, Kassa T, Diaz T, Thatcher M J, Thatcher W W
Department of Animal Sciences, University of Florida, Gainesville 32611-0920, USA.
Anim Reprod Sci. 2001 Apr 30;66(1-2):15-34. doi: 10.1016/s0378-4320(01)00082-3.
The objective of this study was to examine the quality of successive dominant follicles (DFs) after induced heat stress. Non-lactating dairy cows expressing estrus at normal intervals were allocated randomly to heat stress (HS; n=8) and control (C; n=8) groups. Cows received GnRH (100 microg, i.m.) on Day 0, a progesterone CIDR-B device on Day 4 and prostaglandin (PGF(2alpha); 25mg, i.m.) on Day 7 upon removal of the CIDR device. The DF and follicles >5mm were aspirated on Day 8, and GnRH (100 microg) injected following aspiration, to initiate a new follicular wave. In this manner, a DF was aspirated every 8 days (one "follicular cycle") for 10 cycles. After the first follicular cycle, HS cows were placed in environmental chambers for 7 days during the second follicular cycle (8h per day at 43.3 degrees C set point and 16h per day at 24 degrees C for 4 days, and 8h per day at 43.3 degrees C set point and 16h per day at 32.2 degrees C set point for 3 days; relative humidity, 40%) and thereafter maintained outdoors with control cows at a mean ambient temperature (18.5 degrees C; range 12.7-26 degrees C). Rectal temperature increased (P<0.001) in HS as compared with C cows (39.28+/-0.01 degrees C versus 38.78+/-0.01 degrees C). Concentrations of estradiol (E(2); 1662+/-189 versus 1493+/-188ng/ml) and progesterone (P(4); 44.7+/-5 versus 54.1+/-5.1ng/ml) in follicular fluid (FF) of DF did not differ between C and HS treatments, respectively. Total FF protein concentration was greater (P<0.05) in HS (99.7+/-2.3mg/ml) than in C (92.7+/-2.3mg/ml). Heat shock protein 90 (Hsp 90) in FF was not altered by heat stress. IGF-II ligand blots were conducted with FF samples (n=79) from four HS and four C cows. There was a predominance of IGFBP-3 in 76 of 79 FF samples, indicating healthy follicular status, and only three FF samples had the lower molecular weight IGFBP-2 indicative of a poor quality follicle. Plasma P(4) and E(2) concentrations did not differ between C and HS groups. The number of class 1 and 3 follicles increased during and just after heat stress, but the number of class 2 follicles did not differ between C and HS cows. Heat stress appeared to induce a decrease in follicular dominance, but GnRH-induced follicular cycles resulted in development of healthy preovulatory follicles in both groups.
本研究的目的是检测诱导热应激后连续优势卵泡(DFs)的质量。将正常间隔发情的非泌乳奶牛随机分为热应激组(HS;n = 8)和对照组(C;n = 8)。奶牛在第0天接受促性腺激素释放激素(GnRH,100μg,肌肉注射),在第4天放置孕酮控释阴道装置(CIDR - B),在第7天取出CIDR装置后注射前列腺素(PGF₂α;25mg,肌肉注射)。在第8天抽吸DF和直径>5mm的卵泡,抽吸后注射GnRH(100μg)以启动新的卵泡波。通过这种方式,每8天(一个“卵泡周期”)抽吸一个DF,共进行10个周期。在第一个卵泡周期后,HS组奶牛在第二个卵泡周期期间置于环境舱中7天(设定温度43.3℃每天8小时,24℃每天16小时,持续4天;设定温度43.3℃每天8小时,32.2℃每天16小时,持续3天;相对湿度40%),之后与对照组奶牛一起在户外饲养,平均环境温度为18.5℃(范围12.7 - 26℃)。与C组奶牛相比,HS组奶牛的直肠温度升高(P<0.001)(39.28±0.01℃对38.78±0.01℃)。DF卵泡液(FF)中雌二醇(E₂;1662±189对1493±188ng/ml)和孕酮(P₄;44.7±5对54.1±5.1ng/ml)的浓度在C组和HS组之间无差异。HS组FF总蛋白浓度(99.7±2.3mg/ml)高于C组(92.7±2.3mg/ml)(P<0.05)。热应激未改变FF中的热休克蛋白90(Hsp 90)。对来自4头HS组和4头C组奶牛的FF样本(n = 79)进行了胰岛素样生长因子II(IGF - II)配体印迹分析。79个FF样本中有76个以胰岛素样生长因子结合蛋白3(IGFBP - 3)为主,表明卵泡状态良好,只有3个FF样本具有较低分子量的IGFBP - 2,表明卵泡质量较差。C组和HS组血浆P₄和E₂浓度无差异。在热应激期间及刚结束时,1级和3级卵泡数量增加,但C组和HS组奶牛的2级卵泡数量无差异。热应激似乎导致卵泡优势度下降,但GnRH诱导的卵泡周期使两组均发育出健康的排卵前卵泡。