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从独活中分离出的蛇床子素对豚鼠气管的松弛作用。

The relaxant action of osthole isolated from Angelica pubescens in guinea-pig trachea.

作者信息

Teng C M, Lin C H, Ko F N, Wu T S, Huang T F

机构信息

Pharmacological Institute, College of Medicine, National Taiwan University, Taipei.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1994 Feb;349(2):202-8. doi: 10.1007/BF00169838.

Abstract

The effect of osthole, isolated from Angelica pubescens, on the contraction of guinea-pig trachea was studied. Osthole (25-100 mumol/l), theophylline (10-1000 mumol/l) and higher concentrations of nifedipine (0.1-100 mumol/l) suppressed the contraction response curves of tracheal smooth muscle caused by carbachol, prostaglandin F2 alpha (PGF2 alpha), U46619 (thromboxane A2 analogue) and leukotriene C4 (LTC4) in a concentration-dependent manner. The contraction caused by high K+ (120 mmol/l) and cumulative concentrations of CaCl2 (0.03-3 mmol/l) was also inhibited concentration-dependently by osthole (25-100 mumol/l), theophylline (10-1000 mumol/l) and lower concentrations of nifedipine (0.01-0.1 mumol/l). The relaxant actions of osthole were not affected by propranolol (1 mumol/l), glibenclamide (10 mumol/l) or removal of tracheal epithelium. Osthole (100 mumol/l) was still effective in causing tracheal relaxation in the presence of nifedipine (1 mumol/l). In Ca(2+)-free- and EGTA (0.2 mmol/l)-containing medium, the relaxing effect of osthole was more potent than in normal Krebs solution. Osthole (25 and 50 mumol/l) caused 2.9 and 6.5, or 3.0 and 5.6 fold, respectively, increase in potency of forskolin or sodium nitroprusside in causing tracheal relaxation but did not affect that by cromakalim. Osthole (50 mumol/l) enhanced the increase in tissue cAMP and cGMP levels induced by forskolin and sodium nitroprusside, respectively, and in higher concentrations (100 and 250 mumol/l), itself increased markedly tissue cAMP and cGMP contents. Osthole (10-250 mol/l) inhibited the activity of cAMP and cGMP phosphodiesterases in a concentration-dependent manner. It is concluded that osthole exerts a non-specific relaxant effect on the trachealis by inhibiting the cAMP and cGMP phosphodiesterases.

摘要

研究了从独活中分离得到的蛇床子素对豚鼠气管收缩的影响。蛇床子素(25 - 100 μmol/l)、茶碱(10 - 1000 μmol/l)以及较高浓度的硝苯地平(0.1 - 100 μmol/l)能浓度依赖性地抑制由卡巴胆碱、前列腺素F2α(PGF2α)、U46619(血栓素A2类似物)和白三烯C4(LTC4)引起的气管平滑肌收缩反应曲线。由高钾(120 mmol/l)和累积浓度的氯化钙(0.03 - 3 mmol/l)引起的收缩也能被蛇床子素(25 - 100 μmol/l)、茶碱(10 - 1000 μmol/l)和较低浓度的硝苯地平(0.01 - 0.1 μmol/l)浓度依赖性地抑制。蛇床子素的舒张作用不受普萘洛尔(1 μmol/l)、格列本脲(10 μmol/l)或去除气管上皮的影响。在存在硝苯地平(1 μmol/l)的情况下,蛇床子素(100 μmol/l)仍能有效引起气管舒张。在无钙和含乙二醇双乙醚二胺四乙酸(EGTA,0.2 mmol/l)的培养基中,蛇床子素的舒张作用比在正常的克雷布斯溶液中更强。蛇床子素(25和50 μmol/l)分别使福斯可林或硝普钠引起气管舒张的效力增加2.9倍和6.5倍,或3.0倍和5.6倍,但不影响克罗卡林的作用。蛇床子素(50 μmol/l)分别增强了福斯可林和硝普钠诱导的组织环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)水平的升高,并且在较高浓度(100和250 μmol/l)时,其自身能显著增加组织cAMP和cGMP的含量。蛇床子素(10 - 250 μmol/l)能浓度依赖性地抑制cAMP和cGMP磷酸二酯酶的活性。结论是蛇床子素通过抑制cAMP和cGMP磷酸二酯酶对气管产生非特异性舒张作用。

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