Inhibition of agonist-induced vasocontraction and impairment of endothelium-dependent vasorelaxation by extract of motorcycle exhaust particles in vitro

Citation
Yw. Cheng et Jj. Kang, Inhibition of agonist-induced vasocontraction and impairment of endothelium-dependent vasorelaxation by extract of motorcycle exhaust particles in vitro, J TOX E H A, 57(2), 1999, pp. 75-87
Citations number
41
Categorie Soggetti
Environment/Ecology,"Pharmacology & Toxicology
Journal title
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
ISSN journal
15287394 → ACNP
Volume
57
Issue
2
Year of publication
1999
Pages
75 - 87
Database
ISI
SICI code
1528-7394(19990528)57:2<75:IOAVAI>2.0.ZU;2-M
Abstract
The in vitro effects of motorcycle exhaust particulate extract (MEPE) on bl ood vessels were studied in thoracic aorta isolated from Wistar rat. The ME PE relaxed the phenylephrine-precontracted aorta with an EC50 value or 0.05 +/- 0.004 mg/ml. This relaxing effect of MEPE persisted in endothelium-den uded aorta, suggesting that the relaxation induced by MEPE is endothelium-i ndependent. The phenylephrine-induced vasocontraction and inositol 1,4,5-tr iphosphate formation were inhibited concentration dependently in aorta pret reated with MEPE. However, the high-K+-induced vasocontraction and the Ca2 sensitivity of the contractile proteins were not significantly affected by MEPE. In addition to the inhibitory effects on agonist-induced contraction , the vasorelaxing effects both of acetylcholine and of sodium nitroprussid e were impaired by MEPE. The inhibitory effects of MEPE on acetylcholine an d sodium nitroprusside, bur not phenylephrine, were reversed by cotreatment with superoxide dismutase. These results showed that the MEPE, added in vi tro, inhibited the phenylephrine-induced, but nor depolarization-induced, v asocontraction of aorta. The MEPE also impaired the vasorelaxation induced by acetylcholine in a superoxide anion-dependent manner.