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山柰酚诱导大鼠子宫平滑肌舒张的相关机制。

Mechanisms involved in kaempferol-induced relaxation in rat uterine smooth muscle.

作者信息

Revuelta M P, Cantabrana B, Hidalgo A

机构信息

Farmacología, Dpto Medicina, Facultad de Medicina, Universidad de Oviedo, Spain.

出版信息

Life Sci. 2000 Jun 8;67(3):251-9. doi: 10.1016/s0024-3205(00)00627-5.

Abstract

The effect of kaempferol on KCI (60 mM)-induced tonic contraction in isolated rat uterus and its modification by inhibitors of cAMP-dependent protein kinase (PKA) (Rp-cAMPS and TPCK), phosphodiesterase (papaverine), adenylyl cyclase (2',3'-dideoxyadenosine, DDA), transcription (actinomycin D), protein synthesis (cycloheximide) and ornithine decarboxylase (alpha-difluoromethyl-ornithine, DFMO), as well as a polyamine, spermine, have been assayed. Kaempferol (3 to 60 microM) induced concentration-dependent relaxation on KCl-induced tonic contraction (IC50: 10.1 +/- 1.89 microM). This relaxing effect was antagonized (p<0.05) by Rp-cAMPS (10 microM), TPCK (3 microM), DDA (100 microM), actinomycin D (4 and 12 microM), cycloheximide (100 microM), DFMO (10 mM), actinomycin D (12 microM) plus TPCK and actinomycin D (12 microM) plus spermine (1 mM). Furthermore, the displacement obtained with actinomycin D plus DFMO was not statistically significant. Our results suggest that kaempferol through cAMP produces transcriptional events and polyamines are, at least partially, involved in the relaxant effect of kaempferol.

摘要

已检测山奈酚对氯化钾(60 mM)诱导的离体大鼠子宫强直性收缩的作用,以及环磷酸腺苷依赖性蛋白激酶(PKA)抑制剂(Rp-cAMPS和TPCK)、磷酸二酯酶抑制剂(罂粟碱)、腺苷酸环化酶抑制剂(2',3'-二脱氧腺苷,DDA)、转录抑制剂(放线菌素D)、蛋白质合成抑制剂(环己酰亚胺)、鸟氨酸脱羧酶抑制剂(α-二氟甲基鸟氨酸,DFMO)以及一种多胺精胺对其作用的影响。山奈酚(3至60 microM)对氯化钾诱导的强直性收缩产生浓度依赖性舒张作用(IC50:10.1±1.89 microM)。Rp-cAMPS(10 microM)、TPCK(3 microM)、DDA(100 microM)、放线菌素D(4和12 microM)、环己酰亚胺(100 microM)、DFMO(10 mM)、放线菌素D(12 microM)加TPCK以及放线菌素D(12 microM)加精胺(1 mM)可拮抗这种舒张作用(p<0.05)。此外,放线菌素D加DFMO产生的位移无统计学意义。我们的结果表明,山奈酚通过环磷酸腺苷产生转录事件,多胺至少部分参与了山奈酚的舒张作用。

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