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2000
Volume 12, Issue 4
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

[Tic4]EM1 and [Tic4]EM2, new endomorphins (EMs) analogues, caused relaxation of rat aorta rings precontracted with phenylphrine in a concentration-dependent manner and were 240- to 370-fold more potent than EMs. This effect was inhibited by endothelium removal or by incubation with NO synthase inhibitor L-NNA or opioid receptor antagonist naloxone. The results demonstrate that [Tic4]EMs have NO- and endothelium-dependent vasorelaxant effects which are mediated by the opioid receptor.

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/content/journals/ppl/10.2174/0929866053765743
2005-05-01
2025-10-15
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/content/journals/ppl/10.2174/0929866053765743
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  • Article Type:
    Review Article
Keyword(s): endomorphins; opioid; rat aorta rings; tic; vasorelaxant response
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