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首页> 外文期刊>Basic & clinical pharmacology & toxicology. >Matrine Induces Apoptosis in Angiotensin II-Stimulated Hyperplasia of Cardiac Fibroblasts: Effects on Bcl-2/Bax Expression and Caspase-3 Activation.
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Matrine Induces Apoptosis in Angiotensin II-Stimulated Hyperplasia of Cardiac Fibroblasts: Effects on Bcl-2/Bax Expression and Caspase-3 Activation.

机译:苦参碱在血管紧张素II刺激的心脏成纤维细胞增生中诱导凋亡:对Bcl-2 / Bax表达和Caspase-3活化的影响。

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摘要

The present study was designed to assess the effect of matrine, an active component of Chinese traditional medicine, on angiotensin II (Ang II)-induced hyperplastic growth of cardiac fibroblasts in vitro. Cardiac fibroblasts were prepared from hearts of neonatal Kunming mice by collagenase disruption. Cultured cardiac fibroblasts were either not treated, treated with 0.1 microM Ang II, or matrine (2.0 approximately 4.0 mM) plus Ang II for 12-72 hr. Cell morphology was monitored under an inverted phase contrast microscope. Number of cells was counted with a haemocytometer. Cell apoptosis was determined by propidium iodide/Hoechst 33342 staining and flow cytometry. The cleaved caspase-3 fragment expression, anti-apoptotic Bcl-2 and pro-apoptotic Bax protein expressions were also studied. The results show that Ang II stimulation resulted in hyperplastic growth of cardiac fibroblasts. Matrine significantly, dose and time dependently inhibited Ang II-induced cell proliferation. Matrine addition to the culture medium led to most cells being arrested in the G1 phase of the cell cycle, the fraction of cells in S phase was markedly decreased compared to control and Ang II alone groups. Cell apoptosis in matrine treatment group was markedly increased, accompanied by down-regulation in Bcl-2/Bax ratio and up-regulation in cleaved caspase-3 activity. These results suggest that matrine can induce apoptosis and thereby inhibit Ang II-induced hyperplasic growth of cardiac fibroblasts. The regulations of matrine on Bcl-2/Bax expression and caspase-3 activation may be the pro-apoptotic mechanisms involved.
机译:本研究旨在评估苦参碱(中药的一种有效成分)对血管紧张素II(Ang II)诱导的体外心肌成纤维细胞增生性生长的影响。通过破坏胶原酶从新生昆明小鼠的心脏制备心脏成纤维细胞。培养的心脏成纤维细胞未处理,用0.1 microM Ang II或苦参碱(2.0约4.0 mM)加Ang II处理12-72小时。在反相显微镜下监测细胞形态。用血球计数器计数细胞数。细胞凋亡通过碘化丙啶/ Hoechst 33342染色和流式细胞术确定。还研究了裂解的caspase-3片段表达,抗凋亡Bcl-2和促凋亡Bax蛋白表达。结果表明,Ang II刺激导致心脏成纤维细胞增生。苦参碱显着地,剂量和时间依赖性地抑制了Ang II诱导的细胞增殖。向培养基中添加苦参碱导致大多数细胞停滞在细胞周期的G1期,与对照组和单独的Ang II组相比,处于S期的细胞比例明显减少。苦参碱治疗组的细胞凋亡明显增加,同时伴随着Bcl-2 / Bax比值的下调和裂解的caspase-3活性的上调。这些结果表明苦参碱可以诱导细胞凋亡,从而抑制Ang II诱导的心脏成纤维细胞的增生生长。苦参碱对Bcl-2 / Bax表达和caspase-3活化的调控可能是所涉及的促凋亡机制。

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