吉非齐尔药物对雄性白化大鼠胰腺组织生理和组织学影响的研究

Noor Saad Sbbar
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摘要

吉非罗齐是一种长期控制肥胖的药物,FDA通过抑制胰脂肪酶批准,它可以减少饮食中脂肪的吸收。本研究的目的是阐明吉非罗齐治疗高脂饮食引起的高脂血症大鼠胰腺疾病的潜在作用,以及这些变化如何影响脂肪酶的生理机能。选取平均12周龄的雄性白化肥胖大鼠40只,分为5组,每组8只。第一组为对照组,第二组高脂血症大鼠给予高脂饮食治疗组,第三组;诱导的高脂血症大鼠给予gimfibrozil (600 mg/kg/d)治疗,第四组诱导的高脂血症大鼠给予gimfibrozil (1200 mg/kg/d)治疗,第五组诱导的高脂血症大鼠给予gimfibrozil (1500mg/kg/d)治疗。结果表明:与其他组相比,第2组(高脂饲料)胰腺脂肪酶显著升高(P≤0.05)。高脂血症引起急性胰腺炎,胰岛β细胞和α细胞严重坏死,导致胰岛内形成空腔,空腔内充满淋巴细胞,并在第2期占据大部分胰岛病变区域。组(高脂饮食)。结论:吉非罗齐可通过降低甘油三酯水平来治疗高脂血症,甘油三酯可引起胰腺组织变性、胰管扩张、分泌物潴留和充血。胰腺腺泡内可见炎性细胞浸润,朗格汉斯岛血管充血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of some physiological and histological effects of gemfibrozil Drug in Pancreas Tissue of male Albino rats
Gemfibrozil is the medication for long-term control of obesity that the FDA has approved by inhibiting Pancreatic lipase , it decreases the absorption of dietary fat. The purpose of the current study is to provide light on potential gemfibrozil in treatment of pancreatic disorder in induced hyperlipidemic rats which caused by high fat diet and how these changes may affect the physiology of the lipase enzyme.  Used 40 male albino obese rats with mean 12 weeks .The animal divide to five Groups and all group include of these 8 animals . The first group is control , second group induced hyperlipidimic rats give high fat diet untreated group , third group  induced hyperlipidimic rats then treated by gimfibrozil (600 mg/kg/day) , fourth group induced hyperlipidimic rats then treated by gimfibrozil (1200 mg/kg/day) and fifth group induced hyperlipidimic rats then treated by gimfibrozil (1500mg/kg/day). The results showed significant increased (P≤ 0.05) pancreatic lipase in group 2(high fat diet ) in compared to other group. Hyperlipidemia caused acute pancreatitis , Severe necrosis of beta and alpha cells of Langerhans islets led to form spaces in Langerhans islet, also these spaces filled with lymphocytes  that occupied most of affected Langerhans islet area in second  group ( high fat diet). Conclusion: Gemfibrozil is recommended in the treatment hyperlipidemia by reduces triglyceride levels that caused pancreatic tissue degeneration, dilation of pancreatic duct with retained secretion and congestion. inflammatory cell infiltration observed in pancreatic acini and vascular congestion with islets of Langerhans .
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