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Antispasmodic effects of a new kaurene diterpene isolated from Croton argyrophylloides on rat airway smooth muscle

机译:从巴豆类植物中提取的一种新的贝壳杉烯二萜对大鼠气道平滑肌的解痉作用

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Objectives The effects of rel-(1S,4aS,7S,8aS)-7-(1-vinyl)-tetradecahydro-1, 4a-dimethylphenanthrene-7,8a-carbolactone-1-carboxylic acid (TCCA), a new ent-kaurene diterpene isolated from Croton argyrophylloides, on rat tracheal preparations were investigated. Methods Tracheae were removed and cut into two-cartilage segments that were mounted in organ baths containing Tyrode's solution. Results TCCA reduced the contractions induced by electrical field stimulation, relaxed K +-induced contractions, and inhibited both phasic and tonic components of the K +- and ACh-induced contractions. TCCA reduced the serotonin-induced contraction, abolished that evoked by K + in the presence of epinephrine, and also reduced the ACh-induced contractions under Ca 2+-free conditions. TCCA blocked contractions that depend on divalent cation inflow through voltage-operated Ca 2+ channels (VOCCs) and receptor-operated Ca 2+ channels (ROCCs), but had greater potency to block VOCC- than ROCC-dependent contractions or contractions induced by ACh in Ca 2+-free conditions. TCCA relaxed the phorbol 12,13 dibutyrate (1 μm) induced contraction, but with slight potency. Conclusions TCCA induces an antispasmodic effect through several mechanisms including blockade of either VOCCs (with greater potency) or ROCCs, blockade of IP 3-induced Ca 2+ release from sarcoplasmic reticulum (with intermediate potency) and reduction of the sensitivity of contractile proteins to Ca 2+.
机译:目的rel-(1S,4aS,7S,8aS)-7-(1-乙烯基)-十四氢-1,4a-二甲基菲-7,8a-carbolactone-1-羧酸(TCCA)的作用从巴豆类固醇类植物中分离出的牛黄烯二萜对大鼠气管制剂进行了研究。方法将气管切开,切成两节,装在装有蒂罗德溶液的器官浴中。结果TCCA减少了电场刺激引起的收缩,放松了K +诱导的收缩,并抑制了K +和ACh诱导的收缩的相位和张力成分。 TCCA减少了5-羟色胺诱导的收缩,取消了肾上腺素存在下由K +引起的收缩,并且在无Ca 2+的条件下也降低了ACh诱导的收缩。 TCCA阻止了依赖于二价阳离子通过电压控制的Ca 2+通道(VOCC)和受体操纵的Ca 2+通道(ROCC)流入的收缩,但与依赖ROCC的收缩或ACh引起的收缩相比,其阻断VOCC-的效力更高在不含Ca 2+的条件下。 TCCA放松了佛波醇12,13二丁酸酯(1μm)引起的收缩,但有轻微效力。结论TCCA通过多种机制诱导解痉作用,包括阻断VOCC(效力更高)或ROCC,阻断IP 3诱导的肌浆网释放Ca 2+(具有中等效力)以及降低收缩蛋白对Ca的敏感性。 2+。

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