Licht P, Porter D, Millar R P
Gen Comp Endocrinol. 1987 May;66(2):248-55. doi: 10.1016/0016-6480(87)90274-7.
In vitro perifusion was employed to compare the potencies of mammalian, avian, salmon, and lamprey gonadotropin-releasing hormones (GnRHs) on the release of luteinizing hormone (LH) from the pituitaries of an amphibian (Rana pipiens) and a reptile (Chrysemys picta). The chicken-I and salmon GnRH variants were equipotent with mammalian GnRH in both the frog and the turtle glands. By contrast, the lamprey GnRH was inactive (less than 1% as potent as the others). Lamprey GnRH also failed to stimulate LH release or to induce GnRH priming when administered chronically to the frog gland. These results support the hypothesis that the GnRH receptors on nonmammalian pituitary cells are much less specific than those of the mammal with regard to the amino acid at position 8 of the GnRH molecule. These data suggest that the native GnRH variant or the one most like that found in the brain of a species is not necessarily the most potent biologically in that species. However, the nonmammalian pituitary does show some specificity with regard to the structure of natural GnRHs in that none of the tetrapod species studied is responsive to lamprey GnRH.
采用体外灌流法比较哺乳动物、鸟类、鲑鱼和七鳃鳗促性腺激素释放激素(GnRH)对两栖动物(豹蛙)和爬行动物(彩龟)垂体释放促黄体生成素(LH)的作用强度。鸡-I型和鲑鱼GnRH变体在青蛙和乌龟腺体中与哺乳动物GnRH的效力相当。相比之下,七鳃鳗GnRH无活性(效力不到其他GnRH的1%)。长期给青蛙腺体注射七鳃鳗GnRH时,它也无法刺激LH释放或诱导GnRH引发效应。这些结果支持以下假说:就GnRH分子第8位氨基酸而言,非哺乳动物垂体细胞上的GnRH受体比哺乳动物的GnRH受体特异性低得多。这些数据表明,天然GnRH变体或在某一物种大脑中发现的最相似的变体在该物种中不一定具有最强的生物学活性。然而,非哺乳动物垂体对天然GnRH的结构确实表现出一定的特异性,因为所研究的四足动物物种对七鳃鳗GnRH均无反应。