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黄芩苷对豚鼠肺中前列腺素生成及气管收缩反应的影响。

Effects of baicalein on prostanoid generation from the lung and contractile responses of the trachea in guinea pig.

作者信息

Miyamoto K, Katsuragi T, Abdu P, Furukawa T

机构信息

Department of Pharmacology, Fukuoka University School Medicine, Japan.

出版信息

Am J Chin Med. 1997;25(1):37-50. doi: 10.1142/S0192415X9700007X.

Abstract

Effects of baicalein on release of slow reacting substance of anaphylaxis (SRS-A) or leukotriene (LT) from the sensitized guinea pig lung after antigen challenge and tonus of guinea pig tracheal muscles were studied. Baicalein inhibited release of SRS-A from sensitized guinea pig lung after antigen challenge. High-performance liquid chromatography (HPLC) analysis revealed that released SRS-A consisted to LTC4 and D4. Baicalein also reduced release of LTC4 and D4 from the sensitized lung after antigen challenge. Baicalein relaxed the isolated guinea pig tracheal smooth muscle contracted by LTD4, carbachol or histamine. However, this compound produced a contraction when the tracheal muscle was contracted by prostaglandin F2 alpha(PGF2 alpha). This contraction by baicalein was abolished by pretreatment with indomethacin, a cyclooxygenase inhibitor. Baicalein elicited a relaxation in the normal non-sensitized preparation but a contraction in the tissue isolated from actively sensitized guinea pig in 4 among 7 cases. Baicalein also produced a contraction in the trachea pretreated with phorbol dibutyrate and contracted by carbachol, which was eliminated after treatment with indomethacin. The results suggest that baicalein exerts action via, at least, two different mechanisms, the inhibition of releasing SRS-A (LTs) and direct relaxing effects on the trachea. Besides, baicalein seems to produce contraction under certain conditions, which may involve stimulation of the cyclooxygenase pathway.

摘要

研究了黄芩苷对抗原攻击后致敏豚鼠肺中过敏反应慢反应物质(SRS-A)或白三烯(LT)释放以及豚鼠气管肌肉张力的影响。黄芩苷可抑制抗原攻击后致敏豚鼠肺中SRS-A的释放。高效液相色谱(HPLC)分析显示,释放的SRS-A由LTC4和D4组成。黄芩苷还可减少抗原攻击后致敏肺中LTC4和D4的释放。黄芩苷可使由LTD4、卡巴胆碱或组胺收缩的离体豚鼠气管平滑肌舒张。然而,当气管肌肉由前列腺素F2α(PGF2α)收缩时,该化合物会产生收缩。黄芩苷引起的这种收缩可被环氧化酶抑制剂吲哚美辛预处理消除。黄芩苷在正常未致敏制剂中引起舒张,但在7例中有4例在从主动致敏豚鼠分离的组织中引起收缩。黄芩苷还可使经佛波酯预处理并由卡巴胆碱收缩的气管产生收缩,吲哚美辛处理后这种收缩消失。结果表明,黄芩苷至少通过两种不同机制发挥作用,即抑制SRS-A(LTs)释放和对气管的直接舒张作用。此外,黄芩苷在某些条件下似乎会产生收缩,这可能涉及对环氧化酶途径的刺激。

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