分析Omega-369在预防对乙酰氨基酚所致肝损伤中的潜在抗氧化作用

Yousif Hashim Mohammed, A. Hassan
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引用次数: 0

摘要

背景:随着对乙酰氨基酚(APAP)毒性在许多国家变得越来越普遍,相关中毒病例,无论是有意还是无意,已被确定为急性肝衰竭的关键因素。目的:发现omega-369脂肪酸是否能保护雄性小鼠的肝脏免受对乙酰氨基酚的影响。方法:将35只雄性白化小鼠随机分为5组。第1组为“阴性对照”,在连续10天以10 ml/kg的剂量口服石蜡液后,于试验第11天腹腔注射生理盐水(10 ml/kg)。2组为阳性对照,取液体石蜡。3组给予Omega 369 (50 mg/kg/80 ml)。4组给予Omega 369 (100 mg/kg/35 ml)。5组给予n -乙酰半胱氨酸(100 mg/kg/10 ml)。小鼠分别灌胃Omega-369、n -乙酰半胱氨酸和液体石蜡10天。结果:2组血清谷胱甘肽过氧化物酶(GP-X)和超氧化物歧化酶(SOD)水平显著低于1组,丙二醛(MDA)水平显著高于1组。在给予对乙酰氨基酚之前,给予omega-369和n -乙酰半胱氨酸剂量的小鼠的GP-X和SOD水平显著升高,而与2组相比,3、4和5组的MDA水平显著降低。结论:口服Omega-369脂肪酸具有抗氧化作用,可降低对乙酰氨基酚所致肝损伤的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analyzing the Potential Antioxidative Effects of Omega-369 in Preventing Acetaminophen-Induced Liver Damage
Background: As acetaminophen (APAP) toxicity has become more common in many countries, related cases of poisoning, whether deliberate or unintentional, have been identified as a key contributor to acute liver failure. Aime: To discover if omega-369 fatty acids could protect the liver of male mice from the effects of acetamiophen. Methods: Thirty-five albino male mice were allocated to one of five groups at random. Group 1 served as the "negative control" and received a single intraperitoneal injection (10 ml/kg) of normal saline on the eleventh day of the test following ten days of receiving liquid paraffin orally at a dose of 10 ml/kg. The liquid paraffin was given to group 2 "positive control". Group 3 received Omega 369 (50 mg/kg/80 ml). Group 4 received Omega 369 (100 mg/kg/35 ml). Group 5 received N-acetylcysteine (100 mg/kg/10 ml). The mice were given Omega-369, N-acetylcysteine, and liquid paraffin via oral gavage for 10 days. Results: Group 2 had significantly lower levels of glutathione peroxidase (GP-X) and superoxide dismutase (SOD) than group 1, but significantly greater levels of malondialdehyde (MDA). GP-X and SOD levels were significantly higher in mice given the doses of omega-369, and N-acetylcysteine prior to acetaminophen administration, whereas MDA levels were significantly lower in groups 3, 4, and 5 when compared with group 2. Conclusion: Omega-369 fatty acids, when taken orally, exhibit antioxidative effects and may reduce the risk of acetaminophen-induced liver injury.
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