n -乙酰半胱氨酸在门脉高压性胃病中的协同抗氧化和抗炎作用。

IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Hepatology Forum Pub Date : 2022-04-26 eCollection Date: 2022-05-01 DOI:10.14744/hf.2021.2021.0034
Francielli Licks, Renata Minuzzo Hartmann, Elizângela Schemitt, Josieli Raskopf Colares, Camila Marques, Henrique Fillmann, Norma Possa Marroni
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引用次数: 0

摘要

背景和目的:门脉高压(PH)是一种与肝硬化相关的综合征,其特征是门脉压力进行性增加,随之而来的代偿性血管扩张。与氧化和亚硝化应激相关的胃血管改变是门静脉高压性胃病(PHG)的临床表现特征。此外,炎症过程被认为是导致胃组织损伤的加重因素。研究n -乙酰半胱氨酸(NAC)对ph大鼠胃的协同抗炎和抗氧化作用。材料和方法:选用Wistar雄性大鼠18只,分为假手术组(SO)、部分门静脉结扎组(PPVL)和PPVL + NAC组(每组6只)。术后第8天开始用NAC治疗,剂量为10mg /kg (i.p),持续7天。Western blot法检测大鼠胃组织中iNOS、NQO-1、HSP-90、SOD的表达,免疫组化法检测核因子-κB (NF-κB)和肿瘤坏死因子(TNF)-α的表达。结果:PPVL组与对照组相比,HSP-90、iNOS、SOD、NQO-1表达增加。NAC降低了所有研究蛋白的表达。同样,PPVL动物的NF-κB和TNF-α染色分别高于对照组,PPVL + NAC动物的NF-κB和TNF-α染色低于PPVL动物。结论:NAC对实验性门静脉部分结扎性PHG具有抗炎和抗氧化双重作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synergistic antioxidant and anti-inflammatory action of N-acetylcysteine in portal hypertensive gastropathy in rats.

Background and aim: Portal hypertension (PH) is a syndrome associated with cirrhosis and characterized by a progressive increase in portal pressure, with consequent compensatory vascular dilation. Gastric vascular changes associated with oxidative and nitrosative stress characterize the clinical presentation of portal hypertensive gastropathy (PHG). In addition, the inflammatory process is considered an aggravating factor for severity by contributing to gastric tissue injury. The aim of this study was to investigate the synergistic anti-inflammatory and antioxidant action of N-acetylcysteine (NAC) in the stomach of rats with PH.

Materials and methods: Eighteen Wistar male rats were used in this experimental protocol and were divided into three groups with six in each group: sham-operated (SO), partial portal vein ligation (PPVL), and PPVL + NAC. Treatment with NAC at a dose of 10 mg/kg (i.p.) was initiated on day 8 after surgery and continued for 7 days. We evaluated the expression of iNOS, NQO-1, HSP-90, and SOD by Western blot, as well as nuclear factor-kappa B (NF-κB) and tumor necrosis factor (TNF)-α staining by immunohistochemistry, in the rat stomach.

Results: The PPVL group exhibited increased expression of HSP-90, iNOS, SOD, and NQO-1 when compared with controls. NAC reduced the expression of all studied proteins. Similarly, NF-κB and TNF-α staining was increased in PPVL animals versus controls and reduced in PPVL + NAC versus PPVL animals, respectively.

Conclusion: These results suggest the effectiveness of NAC as a dual anti-inflammatory and antioxidant in animals with experimental PHG induced by partial ligation of the portal vein.

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