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首页> 外文期刊>Japanese Journal of Pharmacology >INHIBITORY EFFECT OF BASSIANOLIDE, A CYCLODEPSIPEPTIDE, ON DRUG-INDUCED CONTRACTIONS OF ISOLATED SMOOTH MUSCLE PREPARATIONS
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INHIBITORY EFFECT OF BASSIANOLIDE, A CYCLODEPSIPEPTIDE, ON DRUG-INDUCED CONTRACTIONS OF ISOLATED SMOOTH MUSCLE PREPARATIONS

机译:环肽BASSIANOLIDE对药物诱导的分离的平滑肌制剂的抑制作用

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References(30) Cited-By(3) Bassianol1de (BASS) is a cyclodepsipeptide isolated from cultured mycelia of Beauveria bassiana and is pathogenic to insects. In a longitudinal muscle preparation from guinea pig ileum, 10-6 M BASS almost irreversibly inhibited an isotonic contraction induced by acetylcholine (ACH) and made the dose-response curve shift in parallel to the right (pA2: 7.6). It also inhibited the contractions induced by carbachol, pilocarpine, histamine, 5-hydroxytriptamine (5-HT) and prostaglandin E2, but did not inhibit the contraction induced by barium or a high concentration (40-60 mM) of potassium (high K). When applied to the guinea pig vas deferens, 10-8-10-7 M BASS inhibited an isometric contraction induced by norepinephrine (NE) (3×10-6-10-5 M), phenylephrine (3×10-6-10-5 M) or ACH (10-6-10--5M). When the contractions of the three agonists exceeded the concentrations mentioned above, BASS failed to exert an inhibitory effect upon any of these agonists. It also inhibited the contraction caused by carbachol and histamine, but did not inhibit that induced by barium or high K. BASS itself failed to cause the contraction or relaxation of both muscle preparations. From these results, it is suggested that BASS inhibits the contraction induced by an agonist which acts upon selective sites of smooth muscle cells, but which does not inhibit a contraction induced by an agonist that has an effect on non-selective sites of cells.
机译:参考文献(30)Cited-By(3)Bassianol1de(BASS)是从球孢白僵菌培养的菌丝体中分离出来的环二肽,对昆虫致病。在豚鼠回肠的纵向肌肉制剂中,10-6 M BASS几乎不可逆地抑制了乙酰胆碱(ACH)诱导的等张收缩,并使剂量反应曲线平行于右侧移动(pA2:7.6)。它也抑制了卡巴胆碱,毛果芸香碱,组胺,5-羟基三乙胺(5-HT)和前列腺素E2引起的收缩,但没有抑制钡或高浓度(40-60 mM)钾(高K)引起的收缩。 。当将10-8-10-7 M BASS用于豚鼠输精管时,可抑制去甲肾上腺素(NE)(3×10-6-10-5 M),去氧肾上腺素(3×10-6-10)引起的等轴收缩-5 M)或ACH(10-6-10--5M)。当三种激动剂的收缩超过上述浓度时,BASS不能对这些激动剂中的任何一种施加抑制作用。它还抑制了由卡巴胆碱和组胺引起的收缩,但没有抑制由钡或高K引起的收缩。BASS本身未能引起两种肌肉制剂的收缩或松弛。从这些结果表明,BASS抑制由激动剂诱导的收缩,该激动剂作用于平滑肌细胞的选择性位点,但不抑制由激动剂诱导的对细胞的非选择性位点有影响的收缩。

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