首页> 外文学位 >The protective effects of aliskiren on lung histopathology after triolein-induced fat embolism in rats.
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The protective effects of aliskiren on lung histopathology after triolein-induced fat embolism in rats.

机译:阿利吉仑对三油精诱导的脂肪栓塞后大鼠肺组织病理学的保护作用。

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摘要

Background: Fat embolization (FE) and the consequent fat embolism syndrome (FES) remain poorly understood complications of skeletal and other major trauma. While FE and FES can lead to major pulmonary damage including ARDS and death, current treatment of FES is limited to supportive therapy. The renin angiotensin system (RAS) plays a significant role in the pathophysiology of FE, and drugs interfering with the RAS, captopril and losartan, have reduced histopathologic pulmonary damage in a rat model of FE. In this study, we examine the potential therapeutic effects of aliskiren, a direct renin inhibitor, on lung histopathology following FE.;Methods: A model of FE was created in unanesthetized rats using intravenous injection of the neutral fat triolein. Intraperitoneal injections of aliskiren at either 50 mg/kg or 100 mg/kg were performed one hour after FE induction via triolein. Rats were euthanized at 48 hours, and various pathology stains and methods were used to study and compare the lungs of these animals.;Results: The lungs of the triolein only treated animals showed severe gross and histopathologic damage which was mitigated by aliskiren. (1) Fibrosis: Rats treated with triolein alone showed significant fibrotic changes with increased collagen and myofibroblast activation (p < 0.01). Aliskiren blocked this inflammatory and profibrotic process to a level indistinguishable from the controls (p < 0.01). (2) Fat: Rats treated with triolein alone showed a statistically significant increase in fat (p < 0.01) with subsequent aliskiren administration at both doses reducing the size, distribution, and amount of fat droplets (p<0.01). (3) Vasculitis: There was a trend in reduced lumen patency in the triolein only treated animals which improved after aliskiren treatment.;Conclusions: Aliskiren protected the lungs of these rats from FE-induced pulmonary damage at 48 hours. Clinical implications include the use of aliskiren both prophylactically (before certain orthopedic procedures) and therapeutically (after severe trauma) to prevent the consequent severe pulmonary fibrosis of FE.
机译:背景:脂肪栓塞(FE)和随之而来的脂肪栓塞综合征(FES)仍然是人们对骨骼和其他主要外伤的并发症知之甚少。尽管FE和FES可能导致严重的肺损伤,包括ARDS和死亡,但目前FES的治疗仅限于支持疗法。肾素血管紧张素系统(RAS)在FE的病理生理中起重要作用,在FE的大鼠模型中,干扰RAS的药物,卡托普利和氯沙坦已减少了组织病理学上的肺损伤。在这项研究中,我们研究了直接肾素抑制剂阿利吉仑对FE后肺组织病理学的潜在治疗作用。方法:通过静脉注射中性脂肪三油精在未麻醉的大鼠中建立FE模型。在通过三油精诱导FE后1小时腹腔注射阿利吉仑,剂量为50 mg / kg或100 mg / kg。 48小时对大鼠实施安乐死,并使用各种病理学染色和方法研究和比较这些动物的肺部。结果:仅用油精处理的动物的肺部表现出严重的肉眼和组织病理学损害,阿利吉仑可减轻这种损害。 (1)纤维化:仅用三油精治疗的大鼠显示出明显的纤维化变化,胶原蛋白和成肌纤维细胞活化增加(p <0.01)。阿利吉仑将这种炎症和纤维化过程阻断至与对照组无可区别的水平(p <0.01)。 (2)脂肪:单独用三油精治疗的大鼠显示出统计学上显着的脂肪增加(p <0.01),随后以两种剂量阿利吉仑给药均降低了脂肪滴的大小,分布和数量(p <0.01)。 (3)血管炎:仅用三油精处理的动物的管腔通畅性降低的趋势在阿利吉仑治疗后有所改善。结论:阿利吉仑在48小时时保护了这些大鼠的肺免受FE诱导的肺损伤。临床意义包括预防性使用(在某些整形外科手术之前)和治疗性使用(在严重创伤之后)使用阿利吉仑,以预防随后发生的严重FE肺纤维化。

著录项

  • 作者

    Fletcher, Amanda.;

  • 作者单位

    University of Kansas.;

  • 授予单位 University of Kansas.;
  • 学科 Pathology.;Histology.
  • 学位 M.S.
  • 年度 2016
  • 页码 37 p.
  • 总页数 37
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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