Autor: |
Shiang Suo Huang, Mabayoje A., Mashino, Tadahiko, Mochizuki, Masataka, Long Y. Chiang, Masataka, Lan Hui Chih, Masataka, Hung Ming Hsieh, Masataka, Chen Ming Teng, Masataka, Okuda, Kensuke, Hirota, Takasi, Ming Cheng Tsai, Takasi |
Předmět: |
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Zdroj: |
Pharmacology; Feb2002, Vol. 64 Issue 2, p91-97, 7p, 3 Diagrams, 2 Graphs |
Abstrakt: |
The effects of hexasulfobutylated C[sub 60] (FC[sub 4] S) and monomalonic acid C[sub 60] (MMA C[sub 60] ), the fullerene C[sub 60] derivatives, on isolated endothelium-containing or endothelium-denuded aorta of guinea pig were studied pharmacologically in vitro. In the endothelium-containing preparation of the aortic rings, phenylephrine (PHE) elicited contracture and acetylcholine (ACh) elicited a relaxing effect on the PHE-precontracted preparation. In the PHE-precontracted preparation, MMA C[sub 60] (10 μmol/l) did not elicit a relaxing effect on the PHE-precontracted preparation. However, MMA C[sub 60] (10 μmol/l) significantly reduced the maximum response of the relaxation elicited by ACh. FC[sub 4] S itself significantly relaxed the PHE-precontracted aortic rings. ACh-induced relaxation in PHE-precontracted endothelium-containing strips of the aortic rings was significantly potentiated if pretreated with FC[sub 4] S (10 μmol/l). In the denuded aortic rings, FC[sub 4] S did not elicit the relaxing effect in the PHE-precontracted preparation. The relaxing effect of FC[sub 4] S on the PHE-precontracted preparation was not altered when superoxide dismutase (250 units/ml) was pretreated. However, the relaxing effect was reduced when N(G)-nitro-L-arginine methyl ester (L-NAME, 1 mmol/l) or methylene blue (1 μmol/l) was pretreated. These results demonstrated that the vasorelaxation effect of FC[sub 4] S on the PHE-precontracted aortic ring is partly dependent on the release of nitric oxide (NO) or an NO-derived substance from the vascular endothelium.Copyright © 2002 S. Karger AG, Basel [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
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