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催产素四种合成类似物的一些药理作用。

Some pharmacological actions of four synthetic analogues of oxytocin.

作者信息

BERDE B, DOEPFNER W, KONZETT H

出版信息

Br J Pharmacol Chemother. 1957 Jun;12(2):209-14. doi: 10.1111/j.1476-5381.1957.tb00121.x.

Abstract

Four structural analogues of oxytocin were investigated with regard to their oxytocic, milk-ejecting, pressor and diuretic/antidiuretic effects. In three of them the isoleucyl group of oxytocin was replaced by a phenylalanyl, leucyl, or valyl residue; in the fourth the asparaginyl group was replaced by a glutaminyl residue. Synthetic oxytocin and the international standard pituitary (posterior lobe) powder were used for comparison. Although the analogues showed marked differences in their oxytocic effects, there was a fairly good agreement between the results obtained on the isolated rat uterus and the blood pressure of the chicken for each polypeptide. The milk-ejection pressure test gave much higher values throughout. The pressor and antidiuretic activities of the four analogues showed no obvious correlation with the values obtained in the other tests. The valyl and the leucyl analogues also had a diuretic effect. The phenylalanyl analogue was remarkable for the close correspondence between its oxytocic and antidiuretic effects: practically identical values were obtained for the potency, whether measured on the rat uterus in vitro, the blood pressure in the chicken, the cat uterus in situ or water diuresis in the rat. The leucyl analogue showed an oxytocic activity on the cat uterus in situ or the rabbit mammary gland roughly 7 to 9 times as high as that measured by means of the conventional bioassay methods, such as the blood pressure of the chicken or the rat uterus in vitro. The glutaminyl analogue, the weakest of the whole series, had only a modest effect on the mammary gland. The valyl analogue was the most interesting of the new polypeptides. Its oxytocic action on the cat uterus in situ and its milk-ejecting effect were greater than that of synthetic oxytocin, whereas its antidiuretic and pressor effects were less. In cats and rats, the uterine effect was stronger in situ than in vitro. There were also distinct species differences between cats, rabbits, and rats in their sensitivity to valyl-oxytocin.

摘要

对催产素的四种结构类似物进行了研究,观察它们的催产、排乳、升压和利尿/抗利尿作用。其中三种类似物中,催产素的异亮氨酰基被苯丙氨酰基、亮氨酰基或缬氨酰基取代;在第四种类似物中,天冬氨酰基被谷氨酰胺基取代。使用合成催产素和国际标准垂体(后叶)粉作为对照。尽管这些类似物在催产作用上表现出显著差异,但对于每种多肽,在离体大鼠子宫上得到的结果与鸡的血压之间存在相当好的一致性。整个排乳压力试验得到的值要高得多。这四种类似物的升压和抗利尿活性与在其他试验中得到的值没有明显的相关性。缬氨酰基和亮氨酰基类似物也有利尿作用。苯丙氨酰基类似物的显著特点是其催产和抗利尿作用之间有密切的对应关系:无论在体外大鼠子宫上、鸡的血压上、原位猫子宫上还是大鼠的水利尿上进行测定,其效价得到的数值实际上是相同的。亮氨酰基类似物对原位猫子宫或兔乳腺的催产活性比通过传统生物测定方法(如鸡的血压或体外大鼠子宫)测得的活性大约高7至9倍。谷氨酰胺基类似物是整个系列中最弱的,对乳腺只有适度的作用。缬氨酰基类似物是这些新多肽中最有趣的。它对原位猫子宫的催产作用及其排乳作用比合成催产素的作用更强,而其抗利尿和升压作用则较弱。在猫和大鼠中,子宫作用原位比体外更强。猫、兔和大鼠对缬氨酰催产素的敏感性也存在明显的种属差异。

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