Rónai A Z, Berzétei I P, Székely J I, Miglécz E, Kurgyis J, Bajusz S
Eur J Pharmacol. 1981 Jan 29;69(3):263-71. doi: 10.1016/0014-2999(81)90472-6.
The opioid activities of enkephalin analogues bearing D- or L-aminopentane-sulfonic/phosphonic acid at position 5 were studied in vitro, in electrically stimulated longitudinal muscle strip of guinea-pig ileum and mouse vas deferens preparations and in vivo in the rat tail-flick test. Using their in vitro effects Met-enkephalin-like, beta-endorphin-like, (nor)morphine-like and derivatives of intermediate character could be differentiated. Correlating the in vitro activities with the analgesic activity in vivo it is concluded that the enkephalin-like character in a pentapetide may hinder the expression of analgesic activity, when the compounds are given into the cerebroventricular system.
研究了在第5位带有D-或L-氨基戊烷磺酸/膦酸的脑啡肽类似物的阿片样活性,采用豚鼠回肠和小鼠输精管的电刺激纵肌条进行体外研究,并在大鼠甩尾试验中进行体内研究。根据它们的体外效应,可以区分出甲硫氨酸脑啡肽样、β-内啡肽样、(去甲)吗啡样以及具有中间特性的衍生物。将体外活性与体内镇痛活性相关联后得出结论,当将这些化合物注入脑室系统时,五肽中的脑啡肽样特性可能会阻碍镇痛活性的表达。