首页> 美国卫生研究院文献>The Korean Journal of Physiology Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology >Effects of Local Pancreatic Renin-Angiotensin System on the Microcirculation of Rat with Severe Acute Pancreatitis
【2h】

Effects of Local Pancreatic Renin-Angiotensin System on the Microcirculation of Rat with Severe Acute Pancreatitis

机译:局部胰肾素-血管紧张素系统对重症急性胰腺炎大鼠微循环的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Severe acute pancreatitis (SAP) is normally related to multiorgan dysfunction and local complications. Studies have found that local pancreatic renin-angiotensin system (RAS) was significantly upregulated in drug-induced SAP. The present study aimed to investigate the effects of angiotensin II receptors inhibitor valsartan on dual role of RAS in SAP in a rat model and to elucidate the underlying mechanisms. 3.8% sodium taurocholate (1 ml/kg) was injected to the pancreatic capsule in order for pancreatitis induction. Rats in the sham group were injected with normal saline in identical locations. We also investigated the regulation of experimentally induced SAP on local RAS expression in the pancreas through determination of the activities of serum amylase, lipase and myeloperoxidase, histological and biochemical analysis, radioimmunoassay, fluorescence quantitative PCR and Western blot analysis. The results indicated that valsartan could effectively suppress the local RAS to protect against experimental acute pancreatitis through inhibition of microcirculation disturbances and inflammation. The results suggest that pancreatic RAS plays a critical role in the regulation of pancreatic functions and demonstrates application potential as AT1 receptor antagonists. Moreover, other RAS inhibitors could be a new therapeutic target in acute pancreatitis.
机译:重症急性胰腺炎(SAP)通常与多器官功能障碍和局部并发症有关。研究发现,局部胰腺肾素-血管紧张素系统(RAS)在药物诱导的SAP中明显上调。本研究旨在探讨血管紧张素II受体抑制剂缬沙坦对大鼠模型中RAS在SAP中的双重作用的影响,并阐明其潜在机制。将3.8%的牛磺胆酸钠(1 ml / kg)注射到胰腺囊中以诱导胰腺炎。假手术组在相同部位注射生理盐水。我们还通过测定血清淀粉酶,脂肪酶和髓过氧化物酶的活性,组织学和生化分析,放射免疫分析,荧光定量PCR和Western印迹分析研究了实验诱导的SAP对胰腺局部RAS表达的调节。结果表明,缬沙坦可通过抑制微循环障碍和炎症来有效抑制局部RAS,从而预防实验性急性胰腺炎。结果表明,胰腺RAS在调节胰腺功能中起关键作用,并显示出作为AT1受体拮抗剂的应用潜力。此外,其他RAS抑制剂可能成为急性胰腺炎的新治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号