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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Effect of tongxinluo on vasoconstriction induced by the chronic injury of the adventitia in the rat carotid artery.
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Effect of tongxinluo on vasoconstriction induced by the chronic injury of the adventitia in the rat carotid artery.

机译:通心络对大鼠颈动脉外膜慢性损伤所致血管收缩的影响。

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OBJECTIVE: Tongxinluo (TXL) is a traditional Chinese medicine that is developed on the meridian theory of traditional Chinese medicine, with the function of alleviating the angina. The present study was undertaken to explore the molecular mechanism of TXL in treating the pectoris angina through observing the effectiveness of TXL superfine powder on the vasoconstriction and the activation of RhoA/Rho-kinase pathway induced by the injury of the adventitia. METHODS: 36 male Wistar Kyoto rats were assigned to 3 treatments (n=12): vehicle, TXL (400 mg kg(-1) day(-1)) and fasudil (15 mg kg(-1) day(-1)). After 1 week of treatment, adventitia injury was induced by positioning a silicone collar around the right carotid artery for 1 week. Blood flow and vascular reactivity to serotonin were determined 1 week after injurying, the both sides of carotids were harvested for morphometry, Western blotting analysis and RT-PCR analysis. RESULTS: Adventitia injury leaded to histological changes of vasoconstriction with the lumen cross-sectional area of 44.7% (p<0.001) decreasing and the media diameter of 62.31% (p<0.001) increasing, accompanying by the reduction of the blood flow and the increase of vascular reactivity sensitivity to serotonin. Treatment with both TXL superfine powder and fasudil can prevent the development of vasoconstriction, improve the carotid blood flow and normalize the vascular hypersensitivity to serotonin. Adventitia injuring of the rat carotid increased the expression of Rho-kinase mRNA and p-MYPT1(Thr696) protein by 1.78-fold (p<0.05) and >2-fold respectively (p<0.05). TXL reduced the expression of Rho-kinase mRNA and p-MYPT1(Thr696) protein by 54.2% (p<0.05) and 57.1% (p<0.05) respectively in collared arteries. Fasudil restrained the p-MYPT1(Thr696) protein expression by 63.8% (p<0.05) in collared arteries, did not affect the collar-induced the increase of Rho-kinase mRNA expression (p>0.05). CONCLUSIONS: Treatment with TXL, similar to that with fasudil, can effectively prevent collar-induced vasoconstriction and vascular hyperreactivity to serotonin through inhibiting the RhoA/Rho-kinase pathway.
机译:目的:通心络(TXL)是在中医经络理论基础上发展起来的具有缓解心绞痛功能的中药。本研究旨在通过观察TXL超细粉对血管收缩和外膜损伤诱导的RhoA / Rho激酶途径激活的有效性,探索TXL治疗胸大肌绞痛的分子机制。方法:将36只雄性Wistar Kyoto大鼠分为3种治疗方法(n = 12):媒介物,TXL(400 mg kg(-1)天(-1))和法舒地尔(15 mg kg(-1)天(-1)) )。治疗1周后,通过在右颈动脉周围放置一个硅胶套环1周来诱导外膜损伤。损伤后1周测定血流和对5-羟色胺的血管反应性,收集颈动脉的两侧进行形态测定,Western印迹分析和RT-PCR分析。结果:外膜损伤导致血管收缩的组织学改变,管腔横截面积减少44.7%(p <0.001),而介质直径增加62.31%(p <0.001),伴有血流减少和血管收缩。增强对5-羟色胺的血管反应性敏感性。 TXL超细粉和法舒地尔的治疗均可以预防血管收缩的发展,改善颈动脉血流,并使血管对血清素的超敏反应正常化。大鼠颈动脉外膜损伤使Rho激酶mRNA和p-MYPT1(Thr696)蛋白的表达分别增加1.78倍(p <0.05)和> 2倍(p <0.05)。 TXL减少颈动脉Rho激酶mRNA和p-MYPT1(Thr696)蛋白的表达分别降低54.2%(p <0.05)和57.1%(p <0.05)。 Fasudil抑制颈动脉中p-MYPT1(Thr696)蛋白的表达达63.8%(p <0.05),不影响颈圈诱导的Rho激酶mRNA表达的增加(p> 0.05)。结论:类似于法舒地尔的TXL治疗,可通过抑制RhoA / Rho激酶途径,有效预防衣领引起的血管收缩和血管对血清素的过度反应。

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