Manikkam M, Calder M D, Salfen B E, Youngquist R S, Keisler D H, Garverick H A
Department of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211-5300, USA.
Anim Reprod Sci. 2001 Sep 15;67(3-4):189-203. doi: 10.1016/s0378-4320(01)00120-8.
The objectives were to compare expression of mRNA for cytochrome P450 cholesterol side-chain cleavage (P450scc), cytochrome P450 17alpha-hydroxylase (P450c17), cytochrome P450 aromatase (P450arom), 3beta-hydroxysteroid dehydrogenase Delta(4), Delta(5) isomerase (3beta-HSD), FSH receptor (FSHr) and LH receptor (LHr) in bovine ovarian follicles of the first and second waves of the bovine oestrous cycle and to determine if LH infusion changes growth, steroidogenesis and gene expression in second wave follicles. Transrectal ultrasonography was used to examine follicular size changes during the oestrous cycle in non-lactating Holstein cows (n=31). Saline or purified bovine LH was infused intravenously into cows at emergence of follicular waves for 2 or 4 days using a computer-controlled syringe pump (n=5-6 per treatment). Treatments were: wave 1, saline (W1S); wave 2, saline (W2S) or LH (25 microg/h; W2LH). During infusion, blood samples were collected at 12min intervals for 8h via i.v. catheters for measurement of serum LH concentrations. Ovaries were removed from cows on days 2 or 4 after emergence of follicular waves. Follicles were frozen and stored at -80 degrees C. Follicular fluid (FF, 50 microl) was collected for determination of progesterone (P4), oestradiol-17beta (E2) and androstenedione (A4) concentrations. Frozen sections (14 microm) were used for in situ hybridization to measure expression of mRNA (% pixel intensity) for P450scc, P450c17, P450arom, 3beta-HSD, FSHr, and LHr. LH infusion resulted in a serum LH pattern (high frequency) similar to the early luteal phase. There were no significant differences in size of follicles among the three treatment groups. Follicular fluid concentrations of E2 and A4 in W2S were lower than those of W1S on day 2 of a follicular wave. LH infusion into cows during the midluteal phase increased follicular fluid E2 and A4 concentrations in second wave follicles on day 2 of a follicular wave (W2LH) compared to those of W2S. The increase in follicular fluid E2 on day 2 in wave 2 follicles after LH infusion occurred possibly through an increase in mRNA expression of P450c17 and 3beta-HSD. In conclusion, follicular fluid concentrations of E2 and A4 were lower in W2S than in W1S and E2 and A4 concentrations were restored by infusion of LH in W2LH with an increase in mRNA expression of P450c17 and 3beta-HSD.
目的是比较牛发情周期第一波和第二波的卵巢卵泡中细胞色素P450胆固醇侧链裂解酶(P450scc)、细胞色素P450 17α-羟化酶(P450c17)、细胞色素P450芳香化酶(P450arom)、3β-羟基类固醇脱氢酶Δ⁴,Δ⁵异构酶(3β-HSD)、促卵泡激素受体(FSHr)和促黄体生成素受体(LHr)的mRNA表达,并确定促黄体生成素(LH)输注是否会改变第二波卵泡的生长、类固醇生成和基因表达。使用经直肠超声检查非泌乳荷斯坦奶牛(n = 31)发情周期中的卵泡大小变化。在卵泡波出现时,使用计算机控制的注射泵将生理盐水或纯化的牛LH静脉内注入奶牛体内,持续2或4天(每个处理n = 5 - 6)。处理方式如下:第1波,生理盐水(W1S);第2波,生理盐水(W2S)或LH(25微克/小时;W2LH)。在输注过程中,通过静脉导管每隔12分钟采集一次血样,共采集8小时,用于测定血清LH浓度。在卵泡波出现后第2天或第4天从奶牛体内取出卵巢。将卵泡冷冻并储存在-80℃。收集卵泡液(FF,50微升)用于测定孕酮(P4)、雌二醇-17β(E2)和雄烯二酮(A4)的浓度。使用冰冻切片(14微米)进行原位杂交,以测量P450scc、P450c17、P450arom、3β-HSD、FSHr和LHr的mRNA表达(%像素强度)。LH输注导致血清LH模式(高频)类似于黄体早期。三个处理组之间卵泡大小没有显著差异。在卵泡波第2天,W2S组卵泡液中E2和A4的浓度低于W1S组。与W2S组相比,在黄体中期向奶牛输注LH可使卵泡波第2天第二波卵泡的卵泡液中E2和A4浓度增加(W2LH)。LH输注后第2天第二波卵泡中卵泡液E2的增加可能是通过P450c17和3β-HSD的mRNA表达增加实现的。总之,W2S组卵泡液中E2和A4的浓度低于W1S组,而W2LH组通过输注LH恢复了E2和A4的浓度,同时P450c17和3β-HSD的mRNA表达增加。