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[白藜芦醇对重症急性胰腺炎所致急性肺损伤作用的研究]

[The study in resveratrol function to acute lung injury sourced from severe acute pancreatitis].

作者信息

Wang Zheng, Ma Oing-Yong, Ren Lei, Li Zhen-Dong, Li Li

机构信息

Department of Hepatobillary Surgery, First Affiliated Hospital of Medical College of Xi'an Jiaotong University, Xi'an 710061, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2006 Nov;37(6):904-7.

Abstract

OBJECTIVE

To study the effect of resveratrol to the onset and progress of acute lung injury in rat model of severe acute pancreatitis (SAP).

METHODS

The SAP model was made by injecting 4% sodium taurocholate, a dosage of 0.1 mL/100 g, into the biliopancreatic duct. The control group is formed by injecting the equal amount of N. S into the biliopancreatic duct. For treatment group, after induction of the SAP model, the resveratrol was used to injection at a dosage of 0.3 mL/100 g through the penis vein; at solvent group, after induction of the SAP model, injecting the same amount of tween 80 through the penis vein. All rats were sacrificed at 3, 6, 12 hours. The injuries of lung were checked by pulmonary morphology change, the change of protein in bronchi alveolar lung fluid (BALF). The changes of iNOS were analyzed with special method. PECAM-1, TGF-beta1 was also detected by immunohistochemistry.

RESULTS

For pulmonary morphology change, there were more inflammation cells, more pulmonary edema in experimental group than in treatment group. And in experimental group, with the postponement, the amount of iNOS is increasing (P < 0.05). However, in treatment group, the amout of iNOS was significantly less than in experimental group. The same case was that PECAM-1 and TGF-beta1 of experimental group were higher expression than that of treatment group (P < 0.05).

CONCLUSION

Resveratrol can inhibit the expression of iNOS, PECAM-1, TGF-beta1, and reduce the adhesion between inflammatory cells and endothelium cells, so it may reduce the severity of acute lung injury complicated with severe acute pancreatitis.

摘要

目的

研究白藜芦醇对重症急性胰腺炎(SAP)大鼠模型急性肺损伤发生及进展的影响。

方法

通过向胆胰管注射4%牛磺胆酸钠(剂量为0.1 mL/100 g)制备SAP模型。对照组通过向胆胰管注射等量生理盐水形成。治疗组在诱导SAP模型后,经阴茎静脉以0.3 mL/100 g的剂量注射白藜芦醇;溶剂组在诱导SAP模型后,经阴茎静脉注射等量吐温80。所有大鼠在3、6、12小时处死。通过肺形态学改变、支气管肺泡灌洗液(BALF)中蛋白质变化检查肺损伤情况。用特殊方法分析诱导型一氧化氮合酶(iNOS)的变化。通过免疫组织化学检测血小板内皮细胞黏附分子-1(PECAM-1)、转化生长因子-β1(TGF-β1)。

结果

对于肺形态学改变,实验组炎症细胞更多,肺水肿比治疗组更严重。并且在实验组中,随着时间推迟,iNOS量增加(P < 0.05)。然而,治疗组中iNOS量明显少于实验组。同样情况是,实验组的PECAM-1和TGF-β1表达高于治疗组(P < 0.05)。

结论

白藜芦醇可抑制iNOS、PECAM-1、TGF-β1的表达,减少炎症细胞与内皮细胞之间黏附,因此可能减轻重症急性胰腺炎并发急性肺损伤的严重程度。

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