富勒烯c60衍生物对兔胸主动脉内皮源性舒张的抑制作用

M. Satoh, T. Mashino, T. Nagano, M. Hirobe, I. Takayanagi, K. Koike
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引用次数: 4

摘要

研究了新合成的富勒烯C60衍生物1 (C60-二(N,N-二甲基吡咯吡啶碘化))、2 (C60-脯氨酸-N-乙酸)和3 (C60-乙二胺-N, N ' -二乙酸)对乙酰胆碱诱导的经苯肾上腺素(10−6 M)预收缩的完整内皮兔胸主动脉松弛的抑制作用。富勒烯C60衍生物1 (3 × 10−6 M)、2(10−5 M)和3(10−5 M)降低了乙酰胆碱诱导弛豫的最大振幅,但浓度-响应曲线的pD2值没有显著变化。在富勒烯C60衍生物1(10−5 M)的存在下,乙酰胆碱诱导的松弛被消除,乙酰胆碱诱导的收缩被观察到。提示富勒烯C60衍生物1对内皮(一氧化氮)依赖性乙酰胆碱所致兔胸主动脉舒张有较强的抑制作用。
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INHIBITORY EFFECTS OF FULLERENE C60 DERIVATIVES ON ENDOTHELIUM-DERIVED RELAXATION IN RABBIT THORACIC AORTA
Inhibitory effects of newly synthesized fullerene C60 derivatives 1 (C60-bis(N,N-dimethylpyrrolidinium iodide)), 2 (C60-proline-N-acetic acid) and 3 (C60-ethylenediamine-N, N′-diacetic acid) on acetylcholine-induced relaxation in endothelium-intact rabbit thoracic aorta precontracted by phenylephrine (10−6 M) were studied. Fullerene C60 derivative 1 (3 × 10−6 M), 2 (10−5 M) and 3 (10−5 M) reduced the maximum amplitude of the acetylcholine-induced relaxation without significantly changing the pD2 values obtained from the concentration - response curves. In the presence of fullerene C60 derivative 1 (10−5 M) the acetylcholine-induced relaxation was eliminated and an acetylcholine-induced contraction was observed. These results suggest that fullerene C60 derivative 1 strongly inhibits endothelium (nitric oxide)-dependent acetylcholine-induced relaxation in thoracic aorta of rabbit.
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