Improvement of hemodynamics in mesenteric microcirculation in septic shock rats by anisodamine and anisodine

Jian Zhong, Zhi Ouyang, Junyi Shen, Ye Zeng
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引用次数: 1

Abstract

Anisodamine and anisodine have been used in treatment of septic shock, but the underlying mechanism are still unclear. In the present study, the effects of anisodamine hydrobromide (Ani HBr) and anisodine hydrobromide (AT3) on the mesenteric hemodynamics in septic shock rats were performed. The rat model of septic shock was established by intravenous tail vein injection of 5 ​mg/kg lipopolysaccharide (LPS), and then treated with Ani HBr, AT3, racemic anisodine (Race Ani) or atropine (ATP). The mesenteric microcirculation was observed using the intravital microscopy. Then, the flow pattern of the microcirculation, leukocytes dynamics and the plasma levels of cytokines tumor necrosis factor (TNF)-α and interleukin-6 (IL-6) were analyzed. Compared with the control rats, reduced mean arterial pressure, increased heart rate, and slow microcirculatory blood flow was found in septic shock rats. The main abnormal flow patterns were intermittent and reciprocating motions. Ani HBr, AT3, Race Ani and ATP elevated the mean arterial pressure and reduced heart rate in septic shock rats. Ani HBr and AT3 not only restored the velocity of microcirculatory blood flow and improved the microcirculatory flow patterns, but also suppressed the LPS-induced leukocyte-endothelium interaction and releases of TNF-α and IL-6. Therefore, Ani HBr and AT3 improves hemodynamics in both macro- and microcirculation, which provide a novel experimental basis for exploring the mechanobiological mechanisms in septic shock.

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山莨菪碱与山莨菪碱对感染性休克大鼠肠系膜微循环血流动力学的影响
山莨菪碱和山莨菪碱已被用于治疗感染性休克,但其作用机制尚不清楚。本研究观察了氢溴山莨菪碱(Ani HBr)和氢溴山莨菪碱(AT3)对脓毒性休克大鼠肠系膜血流动力学的影响。采用尾静脉注射5 mg/kg脂多糖(LPS)建立脓毒性休克大鼠模型,然后用阿尼HBr、AT3、外消旋山莨菪碱(阿尼种)或阿托品(ATP)处理。采用活体显微镜观察肠系膜微循环。然后分析微循环血流模式、白细胞动力学及血浆细胞因子肿瘤坏死因子(TNF)-α、白细胞介素-6 (IL-6)水平。与对照组相比,感染性休克大鼠平均动脉压降低,心率升高,微循环血流减慢。异常流型主要为间歇运动和往复运动。HBr、AT3、Race Ani和ATP升高脓毒性休克大鼠平均动脉压,降低心率。HBr和AT3不仅恢复了微循环血流速度,改善了微循环血流模式,而且抑制了lps诱导的白细胞-内皮相互作用和TNF-α和IL-6的释放。因此,Ani HBr和AT3改善了大循环和微循环的血流动力学,为探索脓毒性休克的机械生物学机制提供了新的实验基础。
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