Effects of S-nitroso- N-acetylcysteine on contractile function of reperfused skeletal muscle.


Journal Article

The ultimate goal of replantation and microsurgical reconstructive operations is to regain or improve impaired function of the tissue. However, the data related to the influence of NO on tissue function are limited. This study evaluated the effects of the NO donor S-nitroso- N-acetylcysteine (SNAC) on contractile function of skeletal muscle during reperfusion. Forty-nine rats were divided into six groups. The extensor digitorum longus (EDL) muscles in groups I and II were not subjected to ischemia-reperfusion but were treated with a low (100 nmol/min) or high (1 μmol/min) dose of SNAC. In groups III- V, the EDL underwent 3 h of ischemia and 3 h of reperfusion and was also treated with low (100 nmol/min) or high doses (1 or 5 μmol/min) of SNAC. Group VI was a phosphate-buffered saline (PBS)-treated control group. Twenty additional animals were used to document systemic effects of SNAC and PBS only. SNAC or PBS was infused for 6.5 h, beginning 30 min before ischemia and continuing throughout the duration of reperfusion. Contractile testing compared the maximal twitch force, isometric tetanic contractile forces, fatigue, and fatigue half time of the experimental EDL and the contralateral nontreated EDL. The findings indicate that 1) SNAC does not influence contractile function of EDL muscle not subjected to ischemia-reperfusion, 2) SNAC significantly protects the contractile function of ischemic skeletal muscle against reperfusion injury in the early reperfusion period, and 3) the protective role of SNAC is critically dosage dependent; protection is lost at higher doses. The conclusion from this study is that supplementation with exogenous NO exerts a protective effect on the tissue against reperfusion injury.

Full Text

Duke Authors

Cited Authors

  • Chen, L-E; Seaber, AV; Nasser, RM; Stamler, JS; Urbaniak, JR

Published Date

  • March 1, 1998

Published In

Volume / Issue

  • 274 / 3

Start / End Page

  • R822 - R829

PubMed ID

  • 29586921

Pubmed Central ID

  • 29586921

Electronic International Standard Serial Number (EISSN)

  • 1522-1490

Digital Object Identifier (DOI)

  • 10.1152/ajpregu.1998.274.3.R822


  • eng

Conference Location

  • United States