Glycogen synthase kinase-3 beta inhibitors protectagainst the acute lung injuries resulting from acute necrotizing pancreatitis 1

Hongzhong Jin, Xiaojiao Yang, Kailiang Zhao, Liang Zhao, Chen Chen, Jia Yu
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引用次数: 7

Abstract

Abstract Purpose The research is intended for clarification of the efficacy as well as the underlying mechanism of GSK-3β inhibitors on the advancement of acute lung injuries in acute necrotizing pancreatitis (ANP) in rats. Methods Seventy-two rats were randomly divided into 6 groups: (1)ANP-vehicle; (2)ANP-TDZD-8;(3)ANP-SB216763;(4)Sham-vehicle;(5)Sham-TDZD-8;(6)Sham-SB216763; Blood biochemical test, histopathological examination and immunohistochemical analysis of rats pancreas and lung tissues were performed. The protein expression of GSK-3β, phospho-GSK-3β (Ser9), iNOS, ICAM-1, TNF-α, and IL-10 were detected in lung tissues by Western-blot. Results The outcomes revealed that the intervention of GSK-3β inhibitors alleviated the pathological damage of pancreas and lung (P<0.01), reduced serum amylase, lipase, hydrothorax and lung Wet-to-Dry Ratio, attenuated serum concentrations of IL-1β and IL-6 (P<0.01), inhibited the activation of NF-κB, and abated expression of iNOS, ICAM-1 and TNF-α protein, but up-regulated IL-10 expression in lung of ANP rats (P<0.01). The inflammatory response and various indicators in ANP-TDZD-8 groups were lower than those in ANP-SB216763 groups. Conclusions Inhibition of GSK-3β weakens acute lung injury related to ANP via the inhibitory function of NF-κB signaling pathway. Different kinds of GSK-3β inhibitors have different effects to ANP acute lung injury.
糖原合成酶激酶-3 β抑制剂对急性坏死性胰腺炎引起的急性肺损伤有保护作用
目的探讨GSK-3β抑制剂对急性坏死性胰腺炎(ANP)大鼠急性肺损伤进展的影响及其机制。方法72只大鼠随机分为6组:(1)ANP-vehicle;(2) ANP-TDZD-8; (3) ANP-SB216763; (4) Sham-vehicle; (5) Sham-TDZD-8; (6) Sham-SB216763;对大鼠胰腺和肺组织进行血液生化、组织病理学检查和免疫组织化学分析。Western-blot检测肺组织中GSK-3β、磷酸化GSK-3β (Ser9)、iNOS、ICAM-1、TNF-α、IL-10蛋白的表达。结果GSK-3β抑制剂干预可减轻ANP大鼠胰腺和肺的病理损伤(P<0.01),降低血清淀粉酶、脂肪酶、胸水和肺湿干比,降低血清IL-1β和IL-6浓度(P<0.01),抑制NF-κB的活化,降低iNOS、ICAM-1和TNF-α蛋白的表达,上调肺组织IL-10的表达(P<0.01)。ANP-TDZD-8组炎症反应及各项指标均低于ANP-SB216763组。结论抑制GSK-3β可通过抑制NF-κB信号通路减弱ANP相关急性肺损伤。不同类型GSK-3β抑制剂对ANP急性肺损伤的作用不同。
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