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中国临床药理学与治疗学 ›› 2009, Vol. 14 ›› Issue (6): 637-641.

• 基础研究 • 上一篇    下一篇

肾缺血再灌注损伤时血栓素/前列环素的动态变化及川芎嗪的调控作用

毛朝鸣1, 陈辉乐1, 王万铁2, 金可可2, 邱晓晓2, 谢克俭3   

  1. 1温州医学院附属第二医院肾内科,2病理生理学教研室,3检验医学与公共卫生学院放免中心, 温州 325035, 浙江
  • 收稿日期:2009-03-04 修回日期:2009-05-25 出版日期:2009-06-26 发布日期:2020-10-27
  • 作者简介:毛朝鸣,男,副主任医师,主要从事肾脏缺血再灌注损伤基础研究及肾脏病临床诊治。 E-mail:maochaoming@126.com
  • 基金资助:
    浙江省教育厅科研基金资助项目(19990444)

Regulatory effect of ligustrazine on the dynamic change of thromboxane/prostacyclin in renal ischemia reperfusion injury rabbits

MAO Chao-ming1, CHEN Hui-le1, WANG Wan-tie2, JIN Ke-ke2, QIU Xiao-xiao2, XIE Ke-jian3   

  1. 1Department of Nephrology, the Second Affiliated Hospital of Wenzhou Medical College;
    2Department of Morbid Physiology;
    3Radioimmune Center of Laboratory Medical Science & Public Health, Wenzhou 325035, Zhejiang, China
  • Received:2009-03-04 Revised:2009-05-25 Online:2009-06-26 Published:2020-10-27

摘要: 目的: 观察兔肾缺血再灌注损伤时血栓素/前列环素体系的动态变化, 探讨中药川芎嗪注射液的调控作用及机制。方法: 日本大耳白兔30只, 随机均分为3 组:假手术组、再灌注组、川芎嗪组。复制在体兔肾缺血再灌注损伤动物模型, 在缺血前、缺血1 h、再灌注1、3、5 h 分别经颈总动脉抽血检测血栓素B2 (TXB2) 和6-酮-前列腺素F(6-keto-PGF) 含量, 计算其比值;实验结束时取肾组织检测TXB2 和6-keto-PGF含量与比值。结果: 再灌注组血浆TXB2 含量随缺血和再灌注时间的延长呈阶梯性升高, 与假手术组各时点相比均明显升高(均P<0.01);川芎嗪组血浆TXB2 含量与再灌注组及假手术组同时相点比较, 均明显下降(均P<0.01) 。川芎嗪组血浆TXB2 6-keto-PGF在缺血和再灌注各时点与假手术组相比差异均无统计学意义(均P>0.05), 但均显著低于再灌注组(均P<0.01) 。川芎嗪组与再灌注组比较肾组织TXB2、TXB2 6-keto-PGF下降非常明显(均P<0.01), 6-keto-PGF差异无统计学意义(P>0.05) 。结论: 川芎嗪能抑制血小板释放TXA2,调控TXA2/PGI2 的平衡, 遏制无复流现象, 故可减轻肾缺血再灌注损伤。

关键词: 川芎嗪, 肾, 缺血再灌注损伤, 血栓素A2, 前列环素

Abstract: AIM: To investigate the dynamic change of thromboxane prostacyclin in renal ischemia reperfusion injury rabbits, and approach the regulatory effects of ligustrazine injection on renal ischemia reperfusion injury and its mechanisms. METHODS: Thirty rabbits were divided into three groups randomly:sham operation group (group S), ischemia reperfusion injury group (group IR) and ischemia reperfusion injury plus ligustrazine injection group (group LZ), each group had ten rabbits.The renal ischemia reperfusion injury model of rabbit was established in vivo.The content of thromboxane B2 (TXB2), 6-keto-prostaglandin F(6-keto-PGF) were detected in the blood plasma gathered from common carotid artery at times:pre-ischemia, ischemia 1 h, reperfusion 1, 3 and 5 h, the ratio of TXB2 and 6-keto-PGFwere calculated.The content and the ratio of TXB2 and 6-keto-PGF in kidney tissue were detected at the end of the experiment. RESULTS: The content of TXB2 in plasma showed a time-dependent ascensus in group IR during ischemia reperfusion, it was significant higher than that in group S at all time points (all P<0.01).Compared withgroup IR and with group S, the content of TXB2 in plasma was decreased significantly in group LZ at each time point during ischemia reperfusion (all P<0.01). Compared with group S, there was not different significance for the TXB2 6-keto-PGF in group LZ(all P> 0.05).Compared with group IR, it was significant lower in group LZ at each of time point (all P<0.01). Compared with group IR, in group LZ, the TXB2 level and TXB2 6-keto-PGF in kidney tissue were decreased remarkably (all P<0.01), there was no different significances in 6-keto-PGF (P>0.05). CONCLUSION: Ligustrazine could inhibit platelet to release TXA2, regulate the balance of TXA2/PGI2, restrain no reflow phenomenon, so it could prevent renal ischemia reperfusion injury.

Key words: ligustrazine, kidney, ischemia reperfusion injury, thromboxane A2, prostacyclin

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