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双内啡肽在体内的镇痛活性。

Analgesic activity of double endorphins in vivo.

作者信息

Dorociak A, Misterek K, Rewerski W, Ciupak S

出版信息

Acta Physiol Pol. 1984 Jul-Aug;35(4):310-6.

PMID:6545925
Abstract

The effects of double endorphins DALA2, DYNO2, CASO2 on pain threshold in the rats were compared with those of DALA (D-Ala2-Met5-enkephalinamide). Marked differences in the analgesic potency of the investigated peptides were noted. The most potent analgesic effect was exerted by DALA2. DYNO2 was weaker than DALA and DALA2 due to lack of glycine residue in position 3, probably responsible for the receptor affinity and analgesic activity in vivo. The weak analgesic activity of CASO2 in vivo corresponds with the weak opiate agonistic action of this peptide in vitro [see 7]. All investigated peptides induced changes in animal behaviour when injected i.c.v. The results indicated that among peptides in the novel group of double endorphins, DALA2 is of special interest because of a potent and long lasting analgesic action.

摘要

将双内啡肽DALA2、DYNO2、CASO2对大鼠痛阈的影响与DALA(D-丙氨酸2-甲硫氨酸5-脑啡肽酰胺)进行了比较。结果发现,所研究的肽类在镇痛效力上存在显著差异。DALA2的镇痛效果最为显著。由于3位缺乏甘氨酸残基,DYNO2比DALA和DALA2弱,而甘氨酸残基可能与体内的受体亲和力和镇痛活性有关。CASO2在体内的弱镇痛活性与其在体外的弱阿片激动作用相一致[见7]。当通过脑室内注射时,所有研究的肽都引起了动物行为的变化。结果表明,在新型双内啡肽组的肽中,DALA2因其强大而持久的镇痛作用而特别值得关注。

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