Effects of the mammalian lignan, 2,3-dibenzyl-butane-1,4-diol, on contraction and Ca2+ mobilization induced by noradrenaline in rat aorta.

M Abe, M Morikawa, M Inoue, M Tsuboi, Y Aoyagi, A Ohta
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引用次数: 3

Abstract

1. In rat aorta, 2,3-dibenzylbutane-1,4-diol (DBB) inhibited noradrenaline (NA)-induced contraction in a concentration-dependent manner. The inhibitory effect of DBB was observed in verapamil-pretreated muscle, and did not differ from that in the high K+ solution containing verapamil (1.0 microM). 2. DBB inhibited not only contraction, but [Ca2+]i elevation induced by NA (10 microM) with the same potency. 3. The inhibitory effect of DBB on NA-induced contraction was reversed by methylene blue (3.2 microM) and enhanced by M&B 22,948 (10 microM). 4. DBB (100 microM) alone increased cyclic GMP levels. This effect was attenuated by methylene blue (3.2 microM) and augmented by M&B 22,948 (10 microM). 5. From these results, the inhibitory effects of DBB on NA-induced contraction in rat aorta may be caused by an increase of cyclic GMP levels.

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哺乳动物木脂素2,3-二苄基-丁烷-1,4-二醇对去甲肾上腺素诱导大鼠主动脉收缩和Ca2+动员的影响。
1. 在大鼠主动脉中,2,3-二苄基丁烷-1,4-二醇(DBB)以浓度依赖的方式抑制去甲肾上腺素(NA)诱导的收缩。在维拉帕米预处理的肌肉中观察到DBB的抑制作用,与含有维拉帕米的高K+溶液(1.0 microM)中的抑制作用没有区别。2. DBB不仅能抑制NA (10 μ m)诱导的心肌收缩,还能以相同的效价抑制[Ca2+]i升高。3.亚甲基蓝(3.2 μ m)可逆转DBB对na诱导收缩的抑制作用,而M&B 22,948 (10 μ m)可增强DBB对na诱导收缩的抑制作用。4. 单独使用DBB(100微米)可增加环GMP水平。亚甲基蓝(3.2微米)减弱了这种效应,而M&B 22,948(10微米)增强了这种效应。5. 由此可见,DBB对na诱导的大鼠主动脉收缩的抑制作用可能是通过提高环GMP水平引起的。
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