罗景慧, 杨迎暴, 林永成, 姜广策, 陈志良. 海洋真菌Halorosellinia oceanicum323的两种代谢产物对离体豚鼠回肠收缩的影响J. 药学学报, 2004, 39(8): 586-590.
引用本文: 罗景慧, 杨迎暴, 林永成, 姜广策, 陈志良. 海洋真菌Halorosellinia oceanicum323的两种代谢产物对离体豚鼠回肠收缩的影响J. 药学学报, 2004, 39(8): 586-590.
LUO Jing-hui, YANG Ying-bao, LIN Yong-cheng, JIANG Guang-ce, CHEN Zhi-liang. Effects of two metabolites of cultured marine fungus, Halorosellinia oceanicum323, on the contraction of isolated guinea-pig ileumJ. Acta Pharmaceutica Sinica, 2004, 39(8): 586-590.
Citation: LUO Jing-hui, YANG Ying-bao, LIN Yong-cheng, JIANG Guang-ce, CHEN Zhi-liang. Effects of two metabolites of cultured marine fungus, Halorosellinia oceanicum323, on the contraction of isolated guinea-pig ileumJ. Acta Pharmaceutica Sinica, 2004, 39(8): 586-590.

海洋真菌Halorosellinia oceanicum323的两种代谢产物对离体豚鼠回肠收缩的影响

Effects of two metabolites of cultured marine fungus, Halorosellinia oceanicum323, on the contraction of isolated guinea-pig ileum

  • 摘要: 目的探讨海洋真菌Halorosellinia oceanicum 323的两种代谢产物323-A和323-B对豚鼠离体回肠收缩的影响及其与Ca2+的关系。方法建立组胺(Hist)、乙酰胆碱(ACh)、氯化钾(KCl) 致豚鼠回肠收缩的量效曲线,分别观察323-A和323-B对收缩的作用,并通过分析受试物对由ACh引起的两种收缩成分的影响,对其作用机制进行探讨。结果323-A和323-B均可剂量依赖性的抑制Hist,ACh及KCl所引起的回肠条收缩,pD2′分别为5.13,4.97,5.36 和5.51,5.56,5.62。此外,323-A和323-B对ACh诱导的两种收缩成分的影响与钙拮抗剂维拉帕米 (Ver)的作用相似,均可显著降低在外界无钙离子存在时由细胞内钙释放所产生的第一时相收缩反应,但对通过细胞外钙离子内流所引起的第二时相收缩无明显影响。结论323-A和323-B均具有钙拮抗作用,其作用机制可能与Ver类似,提示二者在该方面的药理学活性具有深入研究的价值和潜在的开发前景。

     

    Abstract: AimTo investigate the effects of 323-A and 323-B, two isomers extracted from the metabolites of cultured marine fungus, Halorosellinia oceanicum323, on the contraction of isolated guinea pig ileum (GPI). MethodsThe GPI contractions were recorded with a two-channel-physiological recorder with tension transducers. Cumulative dose-response curves of contractions of isolated GPI induced by histamine (Hist), acetylcholine (ACh) and potassium chloride (KCl) were constructed, then the influences of 323-A and 323-B on each curve were observed. Furthermore, possible mechanisms underlying effects of the two compounds were explored by analyzing their influences on the biphasic contractile response to ACh, with comparison of a calcium antagonist, verapamil (Ver). ResultsThe data indicated that both 323-A and 323-B inhibited the contractile actions of GPI triggered by Hist, ACh and KCl in a concentration-dependent manner, with pD2′ values of 5.13, 4.97, 5.36 and 5.51, 5.56, 5.62, respectively. The initial phase component of the ACh-elicited contractions, in the absence of external Ca2+, was significantly reduced by 323-A, 323-B, as well as Ver, whereas the subsequent sustained tonic contractions induced by adding Ca2+ to the bath solution were almost unaffected. ConclusionThese results suggest that 323-A and 323-B have calcium antagonistic effects similar to that of Ver in mechanisms, and they might have potential to be developed as calcium antagonists.

     

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