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一种阿片肽DPDPE的眼部作用。

Ocular action of an opioid peptide, DPDPE.

作者信息

Wang D, Potter D E

机构信息

Department of Pharmacology and Toxicology, Morehouse School of Medicine, Atlanta, Georgia, USA.

出版信息

J Ocul Pharmacol Ther. 1996 Summer;12(2):131-9. doi: 10.1089/jop.1996.12.131.

Abstract

This study was performed to examine some ocular actions of an opioid agonist. Experiments were performed to evaluate the effects of a delta opioid agonist, DPDPE ([D-pen2, D-pen5]enkephalin (where pen = penicillamine)), on: 1) intraocular pressure (IOP) in rabbits; 2) cAMP accumulation in rabbit iris ciliary bodies (ICBs). Unilateral, topical administration of DPDPE caused bilateral depression of IOP. Intravitreal injection of DPDPE caused a greater IOP decrease than intravitreal injection of NaH2PO4 (vehicle). Topical administration of naloxone partially inhibited the effect of DPDPE on IOP in normal rabbits. In other experiments, DPDPE suppressed both basal and isoproterenol (ISO)-stimulated cAMP accumulation in ICBs. The presence of naltrindole (NTI), a delta receptor antagonist, did not prevent the suppression of cAMP levels by DPDPE. The conclusions drawn from the findings suggest that the lowering of IOP by DPDPE is mediated, in part, by actions at postjunctional (ciliary body) sites and may involve an atypical opioid receptor.

摘要

本研究旨在检测一种阿片类激动剂的眼部作用。进行实验以评估δ阿片类激动剂DPDPE([D-青霉胺2,D-青霉胺5]脑啡肽(其中青霉胺=青霉胺))对以下方面的影响:1)兔眼内压(IOP);2)兔虹膜睫状体(ICB)中cAMP的积累。单侧局部应用DPDPE可导致双侧IOP降低。玻璃体内注射DPDPE比玻璃体内注射NaH2PO4(溶媒)引起的IOP降低幅度更大。局部应用纳洛酮可部分抑制DPDPE对正常兔IOP的作用。在其他实验中,DPDPE可抑制ICB中基础和异丙肾上腺素(ISO)刺激的cAMP积累。δ受体拮抗剂纳曲吲哚(NTI)的存在并不能阻止DPDPE对cAMP水平的抑制作用。从这些发现得出的结论表明,DPDPE降低IOP部分是通过对节后(睫状体)部位的作用介导的,并且可能涉及一种非典型阿片受体。

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