Johnson A L, Johnson P A, van Tienhoven A
Biol Reprod. 1984 Nov;31(4):646-55. doi: 10.1095/biolreprod31.4.646.
Experiments were conducted to investigate hypophyseal and follicular competency at two distinct stages of the hen's egg laying sequence: 1) 14 h prior to the first (C1) ovulation of a sequence (27 h following the previous ovulation); and 2) 14 h prior to the second (C2) ovulation of a sequence (13 h following the previous ovulation). When a single dose of mammalian luteinizing hormone-releasing hormone (mLHRH) or chicken luteinizing hormone-releasing hormone (cLHRH) was injected 14 h prior to a C1 ovulation, premature ovulation was induced in 19 of 20 hens. In contrast, ovulation was premature in only 1 of 20 hens when mLHRH or cLHRH was injected 14 h prior to a C2 ovulation. There was no difference between the two stages of the sequence in the amount of luteinizing hormone (LH) released for up to 60 min following a single i.v. injection of 20 micrograms mLHRH. However, only prior to a C1 ovulation did LH levels further increase to reach preovulatory concentrations. By contrast, progesterone (P4) concentrations were increased within the first 60 min to a lesser extent in hens injected prior to a C2 ovulation compared to a C1 ovulation. In C2-injected birds, P4 fell to levels that were not different from vehicle-injected controls by 45 to 60 min following injection, whereas P4 secretion was maintained in hens injected prior to a C1 ovulation. We suggest that the lack of sustained LH secretion following treatment with either species of LHRH 14 h prior to a C2 ovulation is related to follicular immaturity with respect to ability to produce and secrete P4. At the dosage administered, there was no difference in the ability of mLHRH compared to cLHRH to release LH at either stage of the sequence. Finally, two successive injections of mLHRH at 14 and 13 h prior to a C2 ovulation induced premature ovulation in 6 of 11 hens. It is suggested that LH, and possibly P4, exerts a priming effect on the largest preovulatory follicle to initiate fully potentiated P4 production and secretion.
1)序列中第一次(C1)排卵前14小时(上次排卵后27小时);2)序列中第二次(C2)排卵前14小时(上次排卵后13小时)。当在C1排卵前14小时注射单剂量的哺乳动物促黄体生成激素释放激素(mLHRH)或鸡促黄体生成激素释放激素(cLHRH)时,20只母鸡中有19只诱导了过早排卵。相比之下,当在C2排卵前14小时注射mLHRH或cLHRH时,20只母鸡中只有1只过早排卵。在单次静脉注射20微克mLHRH后的60分钟内,序列的两个阶段释放的促黄体生成激素(LH)量没有差异。然而,仅在C1排卵前,LH水平进一步升高以达到排卵前浓度。相比之下,与C1排卵相比,在C2排卵前注射的母鸡中,孕酮(P4)浓度在最初60分钟内升高的程度较小。在C2注射的鸡中,注射后45至60分钟,P4降至与注射赋形剂的对照无差异的水平,而在C1排卵前注射的母鸡中P4分泌得以维持。我们认为,在C2排卵前14小时用任何一种LHRH处理后缺乏持续的LH分泌与卵泡在产生和分泌P4能力方面的不成熟有关。在所给予的剂量下,在序列的任一阶段,mLHRH与cLHRH释放LH的能力没有差异。最后,在C2排卵前14小时和13小时连续两次注射mLHRH诱导11只母鸡中的6只过早排卵。有人提出,LH,可能还有P4,对最大的排卵前卵泡发挥启动作用,以启动充分增强的P4产生和分泌。