Robinson F E, Etches R J, Anderson-Langmuir C E, Burke W H, Cheng K W, Cunningham F J, Ishii S, Sharp P J, Talbot R T
Department of Animal and Poultry Science, University of Guelph, Ontario, Canada.
Gen Comp Endocrinol. 1988 Mar;69(3):455-66. doi: 10.1016/0016-6480(88)90038-x.
The effects of chicken luteinizing hormone (cLH: IRC-2 and PRC AE1-1), turkey LH (B221B and HS-5-18), bovine follicle-stimulating hormone (bFSH: HS-2-17), chicken FSH (cFSH: PRC DC3(2) and AGCQSQ113445C), and turkey FSH (B150A and HS-1-153) on steroid output were evaluated by in vitro incubation of various ovarian tissues with the gonadotrophins. Output of androstenedione and estradiol was determined by 3-hr incubations of individual whole small follicles, classified by size and color as follows: small white (SWF, less than 1 mm), large white (LWF, 2-3 mm), and small yellow follicles (SYF, 5-10 mm). The effects of gonadotrophin preparations were also evaluated in large preovulatory follicles (F1-F5). Androstenedione and estradiol output was measured in incubation media from 100,000 theca cells and progesterone content was determined in the incubation media of 100,000 granulosa cells. All incubations were conducted in 1 ml of Medium 199 at 37 degrees. Steroid output was quantitated by radioimmunoassay of incubation media. Potency estimates were derived by calculation of a peak stimulation index. The standard reference preparation was bLH (NIAMDD-LH-B4). Steroidogenesis was stimulated by three avian LH preparations. preparations. PRC AE1-1 was the most potent, with IRC-2 and B150A showing approximately 50% of the biological activity of PRC AE1-1 in most tissues. Turkey LH HS-5-18 was generally not potent. The presence of multiple isohormones of LH was implied, as various LH preparations exhibited different potency estimates in different tissues. The effects of FSH on steroidogenesis were not significant in most cases. Although the addition of cFSH AGCQSQ113445C failed to significantly increase output of estradiol from small follicles, potency estimates of this preparation were 0.15, 0.20, and 0.13 relative to NIAMDD-LH-B4 follicles was more highly stimulated by LH than by FSH, and thus it would seem that FSH does not play a significant role in steroidogenesis in the hen's ovary. The results of this study suggest that steroid biosynthesis in the hen's ovary may be regulated by multiple forms of LH.
通过将各种卵巢组织与促性腺激素进行体外孵育,评估了鸡促黄体生成素(cLH:IRC - 2和PRC AE1 - 1)、火鸡促黄体生成素(B221B和HS - 5 - 18)、牛促卵泡素(bFSH:HS - 2 - 17)、鸡促卵泡素(cFSH:PRC DC3(2)和AGCQSQ113445C)以及火鸡促卵泡素(B150A和HS - 1 - 153)对类固醇生成的影响。通过对单个完整小卵泡进行3小时孵育来测定雄烯二酮和雌二醇的生成量,这些小卵泡按大小和颜色分类如下:小白卵泡(SWF,小于1毫米)、大白卵泡(LWF, 2 - 3毫米)和小黄卵泡(SYF, 5 - 10毫米)。还评估了促性腺激素制剂对大的排卵前卵泡(F1 - F5)的影响。在来自100,000个卵泡膜细胞的孵育培养基中测量雄烯二酮和雌二醇的生成量,并在100,000个颗粒细胞的孵育培养基中测定孕酮含量。所有孵育均在37℃下于1毫升199培养基中进行。通过对孵育培养基进行放射免疫测定来定量类固醇生成量。通过计算峰值刺激指数得出效价估计值。标准参考制剂为bLH(NIAMDD - LH - B4)。三种禽类促黄体生成素制剂刺激了类固醇生成。PRC AE1 - 1活性最强,在大多数组织中,IRC - 2和B150A的生物活性约为PRC AE1 - 1的50%。火鸡促黄体生成素HS - 5 - 18通常活性不强。这暗示了促黄体生成素存在多种同工激素,因为不同的促黄体生成素制剂在不同组织中表现出不同的效价估计值。在大多数情况下,促卵泡素对类固醇生成的影响不显著。虽然添加cFSH AGCQSQ113445C未能显著增加小卵泡中雌二醇的生成量,但该制剂相对于NIAMDD - LH - B4的效价估计值分别为0.15、0.20和0.13。卵泡对促黄体生成素的反应比对促卵泡素的反应更强烈,因此似乎促卵泡素在母鸡卵巢的类固醇生成中不发挥重要作用。本研究结果表明,母鸡卵巢中的类固醇生物合成可能受多种形式的促黄体生成素调节。