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首页> 外文期刊>World Journal of Gastroenterology >N-acetylcysteine modulates angiogenesis and vasodilation in stomach such as DNA damage in blood of portal hypertensive rats
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N-acetylcysteine modulates angiogenesis and vasodilation in stomach such as DNA damage in blood of portal hypertensive rats

机译:N-乙酰半胱氨酸调节胃血管生成和血管舒张,例如门脉高压大鼠血液中的DNA损伤

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AIM: To evaluate the antioxidant effect of N-acetylcysteine (NAC) on the stomach of rats with portal hypertension. METHODS: Twenty-four male Wistar rats weighing ± 250 g were divided into four experimental groups (n = 6 each): Sham-operated (SO), SO + NAC, partial portal vein ligation (PPVL), and PPVL + NAC. Treatment with NAC in a dose of 10 mg/kg (i.p.) diluted in 0.6 mL of saline solution was administered daily for 7 d starting 8 d after the surgery. Animals from the PPVL and SO group received saline solution (0.6 mL) for the same period of time as the PPVL + NAC and SO + NAC group. On the 15th day the animals were anesthetized and we evaluated portal pressure by cannulating mesenteric artery. After, we removed the stomach for further analysis. We performed immunohistochemical analysis for endothelial nitric oxide synthase (eNOS), vascular endothelial growth factor (VEGF), and nitrotirosine (NTT) proteins in stomach. We also evaluated eNOS and VEGF by Western blot analysis and assessed DNA damage in blood samples by the comet assay. RESULTS: The portal hypertension group exhibited increases in portal pressure when compared to SO group (29.8 ± 1.8 vs 12.0 ± 0.3 mmHg) (P 0.001). The same was observed when we compared the eNOS (56.8 ± 3.7 vs 13.46 ± 2.8 pixels) (P 0.001), VEGF (34.9 ± 4.7 vs 17.46 ± 2.6 pixels) (P 0.05), and NTT (39.01 ± 4.0 vs 12.77 ± 2.3 pixels) (P 0.05) expression by immunohistochemistry of the PPVL animals with the SO group. The expression of eNOS (0.39 ± 0.03 vs 0.25 ± 0.03 a.μ) (P 0.01) and VEGF (0.38 ± 0.04 vs 0.26 ± 0.04 a.μ) (P 0.01) were also evaluated by Western blot analysis, and we observed an increase of both proteins on PPVL animals. We also evaluated the DNA damage by comet assay, and observed an increase on damage index and damage frequency on those animals. NAC decreased portal pressure values in PPVL + NAC animals (16.46 ± 2 vs 29.8 ± 1.8 mmHg) (P 0.001) when compared to PPVL. The expression of eNOS (14.60 ± 4.1 vs 56.8 ± 3.7 pixels) (P 0.001), VEGF (19.53 ± 3.2 vs 34.9 ± 4.7 pixels) (P 0.05) and NTT (21.84 ± 0.7 vs 39.01 ± 4.0 pixels) (P 0.05) evaluated by immunohistochemistry were also reduced in PPVL + NAC animals. Also, when evaluated by Western blot eNOS expression (0.32 ± 0.03 vs 0.39 ± 0.03 a.μ) (P 0.05) and VEGF expression (0.31 ± 0.09 vs 0.38 ± 0.04 a.μ) (P 0.01). Furthermore, NAC modulated DNA damage in PPVL + NAC animals. CONCLUSION: In view of these results, we believe NAC is able to protect the stomach from the alterations induced by the PPVL procedure.
机译:目的:评估N-乙酰半胱氨酸(NAC)对门脉高压大鼠胃的抗氧化作用。方法:将二十四只体重为±250 g的雄性Wistar大鼠分为四个实验组(每组6只):假手术(SO),SO + NAC,部分门静脉结扎(PPVL)和PPVL + NAC。手术后8天开始,每天以10 mg / kg(i.p.)的NAC溶液(在0.6 mL盐溶液中稀释)进行治疗,持续7天。 PPVL和SO组的动物在与PPVL + NAC和SO + NAC组相同的时间内接受盐溶液(0.6 mL)。在第15天,将动物麻醉,并通过插管肠系膜动脉评估门静脉压力。之后,我们移开胃进行进一步分析。我们对胃中的内皮一氧化氮合酶(eNOS),血管内皮生长因子(VEGF)和硝氮酪氨酸(NTT)蛋白进行了免疫组织化学分析。我们还通过蛋白质印迹分析评估了eNOS和VEGF,并通过彗星分析评估了血液样本中的DNA损伤。结果:与SO组相比,门脉高压组的门脉压力升高(29.8±1.8 vs 12.0±0.3 mmHg)(P 0.001)。当我们比较eNOS(56.8±3.7 vs 13.46±2.8像素)(P 0.001),VEGF(34.9±4.7 vs 17.46±2.6像素)(P 0.05)和NTT(39.01±4.0 vs 12.77±2.3)时,观察到的结果相同SO组的PPVL动物的免疫组织化学表达(P = 0.05)(P 0.05)。还通过蛋白质印迹分析评估了eNOS(0.39±0.03 vs 0.25±0.03a.μ)(P 0.01)和VEGF(0.38±0.04 vs 0.26±0.04a.μ)(P 0.01)的表达,我们观察到两种蛋白质对PPVL动物的增加。我们还通过彗星试验评估了DNA损伤,并观察到这些动物的损伤指数和损伤频率增加。与PPVL相比,NAC降低了PPVL + NAC动物的门静脉压力值(16.46±2 vs 29.8±1.8 mmHg)(P 0.001)。 eNOS(14.60±4.1 vs 56.8±3.7像素)(P 0.001),VEGF(19.53±3.2 vs 34.9±4.7像素)(P 0.05)和NTT(21.84±0.7 vs 39.01±4.0像素)(P 0.05)的表达在PPVL + NAC动物中,通过免疫组织化学评估的结果也降低了。同样,通过Western印迹评估eNOS表达(0.32±0.03 vs 0.39±0.03a.μ)(P 0.05)和VEGF表达(0.31±0.09 vs 0.38±0.04a.μ)(P 0.01)。此外,NAC调节了PPVL + NAC动物的DNA损伤。结论:鉴于这些结果,我们认为NAC能够保护胃免受PPVL程序引起的改变。

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