| Autor: |
Ridger, V. C., Greenacre, S. A. B., Handy, R. L. C., Halliwell, B., Moore, P. K., Whiteman, M., Brain, S. D. |
| Zdroj: |
British Journal of Pharmacology; November 1997, Vol. 122 Issue: 6 p1083-1088, 6p |
| Abstrakt: |
1Peroxynitrite (ONOO−) is a cytotoxic species, formed by the reaction between nitric oxide and superoxide free radicals, that may be involved in inflammation. In this study we have investigated the effect of peroxynitrite on plasma extravasation and microvascular blood flow in the dorsal skin and on nociceptive responses in the hind paw of the rat.2Male Wistar rats were anaesthetized and their dorsal skin shaved. Plasma extravasation was measured by the extravascular accumulation of 125I‐labelled albumin over 0–45 min and 0–240 min. Blood flow was measured by laser‐Doppler flowmetry over 0–240 min. Studies in the hind paw were carried out in the conscious rat. Hind paw weight changes were determined by volume displacement and nociception by a mechanical hyperalgesia technique.3Intradermal (i.d.) peroxynitrite (100–200 nmol site−1) produced a significant (P<0.01) dose‐dependent increase in plasma extravasation in dorsal skin over 0–45 min which was not increased over 45–240 min. Plasma extravasation was significantly (P<0.001) decreased in rats pretreated with the anti‐inflammatory steroid dexamethasone (1 mg kg−1, i.v.; −180 min), but not modulated by treatment with the hydrogen peroxide deactivator catalase (2200 u site−1), or the superoxide scavenger superoxide dismutase (500 u site−1), effective doses of the tachykinin NK1antagonist SR140333 (1 nmol site−1), the cyclo‐oxygenase inhibitor indomethacin (358 μmol site−1), or combined pretreatment with mepyramine (histamine H1‐receptor antagonist; 2.8 nmol site−1) and methysergide (5‐HT antagonist; 1.9 nmol site−1).4Microvascular blood flow was significantly (P<0.05) increased 30 and 120 min after i.d. peroxynitrite (100 nmol site−1) in dorsal skin and remained raised until the end of the recording period (240 min). The increase in blood flow was unaffected by dexamethasone (1 mg kg−1, i.v.; −180 min) or indomethacin (10 mg kg−1, s.c.; −30 min).5Hind paw volume was significantly (P<0.001) increased 30 min after intraplantar peroxynitrite (87.5 and 175 nmol paw−1) and remained raised for the duration of the experiment (360 min). By comparison, nociception was not altered by intraplantar peroxynitrite.6These data indicate that peroxynitrite can cause an increase in both plasma extravasation and blood flow, suggesting that peroxynitrite could be of biological relevance to microvascular responses. These findings may be of importance in the pathology of inflammatory diseases in which peroxynitrite formation occurs. |
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