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首页> 外文期刊>Transplantation Proceedings >Protective effect of diltiazem on hepatic ischemia-reperfusion injury in rats by improving liver tissue blood flow.
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Protective effect of diltiazem on hepatic ischemia-reperfusion injury in rats by improving liver tissue blood flow.

机译:地尔硫卓通过改善肝组织血流量对大鼠肝脏缺血再灌注损伤的保护作用。

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摘要

BACKGROUND: Cytosolic calcium ions are known to play an important role in ischemia-reperfusion (IR) injury. However, the protective effect of calcium channel blockers remains controversial in liver IR injury. Moreover, calcium channel blockers improve hepatic IR injury not due to blocking an increase in hepatic calcium concentration. Therefore, we hypothesized that calcium antagonists protected a liver from IR injury by a vasodilatory action rather than by the inhibition of an increase in Ca2+ within parenchymal cells. This study evaluated the effects of diltiazem, a calcium channel blocker, on liver energy metabolism and blood flow after IR injury. METHODS: Twenty-seven rats underwent hepatic ischemia for 30 minutes followed by 60 minutes of reperfusion. The animals were allocated into group C (without drug); group D5 (diltiazem, 5 microg/kg per min); or group D10 (diltiazem, 10 microg/kg per min). Diltiazem was infused before laparotomy and then throughout the experiment. RESULTS: After 60 minutes ofreperfusion, liver tissue blood flow and ATP concentrations were significantly higher in group D10 than the other animals (both, P < .05). Changes in ATP values strongly correlated those observed in blood flow (R = 0.80, P < .001). CONCLUSION: Diltiazem improved ATP-generating capacity during reperfusion by improving liver tissue blood flow. An improvement in hepatic tissue perfusion may be a therapeutic strategy for liver IR injury.
机译:背景:已知胞质钙离子在缺血再灌注(IR)损伤中起重要作用。但是,钙通道阻滞剂的保护作用在肝IR损伤中仍存在争议。此外,钙通道阻滞剂可改善肝IR损伤,而不是阻止肝钙浓度的升高。因此,我们假设钙拮抗剂通过血管扩张作用而不是通过抑制实质细胞内Ca2 +的增加来保护肝脏免受IR损伤。这项研究评估了地尔硫卓(一种钙通道阻滞剂)对IR损伤后肝脏能量代谢和血流的影响。方法:二十七只大鼠进行肝缺血30分钟,然后再灌注60分钟。将动物分为C组(无药物); D5组(地尔硫卓,每分钟5微克/千克);或D10组(地尔硫卓,每分钟10微克/千克)。在开腹手术之前,然后在整个实验过程中,先注入地尔硫卓。结果:再灌注60分钟后,D10组的肝组织血流量和ATP浓度显着高于其他动物(均P <.05)。 ATP值的变化与血流中观察到的那些紧密相关(R = 0.80,P <.001)。结论:地尔硫卓可通过改善肝脏组织血流量来提高再灌注过程中的ATP生成能力。肝组织灌注的改善可能是肝IR损伤的治疗策略。

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