Antioxidants prevent ethanol-induced contractions of canine cerebral vascular smooth muscle: relation to alcohol-induced brain injury

Citation
Wy. Li et al., Antioxidants prevent ethanol-induced contractions of canine cerebral vascular smooth muscle: relation to alcohol-induced brain injury, NEUROSCI L, 301(2), 2001, pp. 91-94
Citations number
25
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROSCIENCE LETTERS
ISSN journal
03043940 → ACNP
Volume
301
Issue
2
Year of publication
2001
Pages
91 - 94
Database
ISI
SICI code
0304-3940(20010330)301:2<91:APECOC>2.0.ZU;2-B
Abstract
The present study was designed to test the hypothesis that alpha -tocophero l (Vit. E) and pyrrolidine dithiocarbamate (PDTC) might exert direct effect s on alcohol-induced contractions of canine basilar cerebral arteries. Afte r precontraction of arterial ring segments with ethanol, PDTC (10(-8)-10(-6 ) M) and Vit. E (10(-6)-10(-4) M) induced concentration-dependent relaxatio ns of cerebral arteries, compared to untreated controls. The effective conc entrations producing approximately 50% of the maximal relaxation responses (EC50 values) were about 2.48 +/- 0.09 x 10(-7) M for PDTC, and 1.87 +/- 0. 10 x 10(-5) mM for Vit. E, respectively. Preincubation of these arterial ri ngs with EC50's of PDTC or Vit. E for 40 min attenuate markedly the contrac tions produced by alcohol, at concentrations of 1-400 mM. However, both PDT C and Vit. E do not relax equi-potent precontractions induced by either KCI or prostaglandin F-2u (PGF(2 alpha)) or inhibit their contractions. These data suggest that alcohol-induced contractions of cerebral arteries are med iated via excitation-contraction coupling pathways different from those use d by KCI or receptor-mediated agonists such as PGF(2 alpha). The present re sults, when viewed in light of other recently published data, suggest that antioxidants may prove useful in the amelioration and treatment of alcohol- induced brain damage and strokes. (C) 2001 Elsevier Science Ireland Ltd. Al l rights reserved.