Relaxant Effect of Oxygen Free Radicals on Rabbit Tracheal Smooth Muscle

We investigated the effect of exogenously generated superoxide anions (O2−), hydrogen peroxide (H2O2) and hydroxyl radicals (•OH) on isolated rabbit tracheal smooth muscle suspended in Krebs–Ringer solution. The ability of oxygen free radicals (OFRs) to affect acetyicholine (Ach)-induced contraction...

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Veröffentlicht in:Pulmonary pharmacology & therapeutics 2002-01, Vol.15 (4), p.375-384
Hauptverfasser: Prasad, Kailash, Gupta, Jang B.
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Sprache:eng
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Zusammenfassung:We investigated the effect of exogenously generated superoxide anions (O2−), hydrogen peroxide (H2O2) and hydroxyl radicals (•OH) on isolated rabbit tracheal smooth muscle suspended in Krebs–Ringer solution. The ability of oxygen free radicals (OFRs) to affect acetyicholine (Ach)-induced contraction in these muscles was also investigated. OFRs, in general, produced a concentration-dependent relaxation of the tracheal smooth muscle in the doses used. However, in large concentrations, O2− and H2O2 produced effects which were smaller than those obtained with lower concentrations. The relaxant effects of these oxyradicals were progressive and lasted throughout the 20min observation period. At all concentrations used, the OFRs tended to abolish or reduce Ach-induced contraction in a concentration-dependent manner. O2− was more potent than H2O2 or DHF in relaxing the Ach-precontracted muscle and in inhibiting the response of the muscle to Ach. OFR-induced relaxation of the Ach-contracted muscle was not due to inactivation of the Ach by OFRs. Relaxation produced by OFRs was greater in preparations with intact epithelium than in those denuded of epithelium. The relaxant effects were blocked by indomethacin, a cyclooxygenase inhibitor. OFRs in the presence of indomethacin produced contraction only in the preparations with intact epithelium, suggesting a release of contractile factor(s) from epithelium. These results suggest that OFRs relax rabbit tracheal smooth muscle. The relaxation appears to be mediated through the synthesis and release of prostaglandins from the epithelium and smooth muscles.
ISSN:1094-5539
1522-9629
DOI:10.1006/pupt.2002.0370