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原儿茶酸可预防呋喃暴露大鼠的肝肾毒性。

Protocatechuic acid protects against hepatorenal toxicities in rats exposed to Furan.

机构信息

Cancer Research and Molecular Biology Laboratories, Department of Biochemistry, University of Ibadan, Ibadan, Nigeria.

Nutrition and Industrial Biochemistry Laboratories, Department of Biochemistry, University of Ibadan, Ibadan, Nigeria.

出版信息

Drug Chem Toxicol. 2022 Jul;45(4):1840-1850. doi: 10.1080/01480545.2021.1890109. Epub 2021 Feb 28.

Abstract

Furan formed in processed food is hepatotoxic and likely carcinogenic in humans. We investigated protocatechuic acid (PCA) protective role in rats' hepatorenal function treated with furan. Rats were grouped and treated as follows: Control, PCA (50 mg/kg), furan alone (8 mg/kg), furan + PCA1 (25 + 8 mg/kg), and furan + PCA2 (50 + 8 mg/kg). Upon sacrifice, evaluation of hepatorenal function, oxidative stress status, reactive oxygen and nitrogen species (RONS), lipid peroxidation (LPO), myeloperoxidase (MPO) activity, among nitric oxide (NO) levels were performed. Cytokine levels (IL-10, IL-1ß, TNF-alpha), Caspase 3 and 9 activities, and histopathological examination were also assessed. We found that the final body and relative liver weights changed significantly  0.05) in treated groups. Hepatic transaminases, urea, and creatinine increased  0.05) in furan only treated group, and reduced in PCA co-treated groups. The furan-induced decrease in antioxidant status increased RONS, and LPO levels were alleviated  0.05) by PCA co-treatment. Furthermore, furan-mediated increase in NO, IL-1ß, TNF-alpha levels, MPO, Cas-3, and 9 activities and suppressed IL-10 levels was reversed accordingly in rats' kidney and liver co-treated with PCA. The extent of furan-mediated hepatorenal lesions was lessened in PCA co-treated rats. Our findings suggest that PCA protects against oxido-inflammatory pathways, enhanced caspases 3 and 9 activations induced by furan in rat hepatorenal system.

摘要

呋喃在加工食品中形成,对人类具有肝毒性,可能致癌。我们研究了原儿茶酸(PCA)对呋喃处理大鼠肝肾功能的保护作用。将大鼠分组并进行如下处理:对照组、PCA(50mg/kg)、单独呋喃(8mg/kg)、呋喃+PCA1(25+8mg/kg)和呋喃+PCA2(50+8mg/kg)。处死时,评估肝肾功能、氧化应激状态、活性氧和氮物种(RONS)、脂质过氧化(LPO)、髓过氧化物酶(MPO)活性以及一氧化氮(NO)水平。还评估了细胞因子水平(IL-10、IL-1β、TNF-α)、Caspase 3 和 9 活性以及组织病理学检查。我们发现,处理组的最终体重和相对肝重均有显著变化(P<0.05)。仅用呋喃处理的大鼠肝转氨酶、尿素和肌酐升高(P<0.05),而 PCA 共同处理组则降低。PCA 共同处理减轻了呋喃诱导的抗氧化状态下降,缓解了 RONS 和 LPO 水平(P<0.05)。此外,PCA 共同处理还逆转了呋喃介导的 NO、IL-1β、TNF-α水平、MPO、Caspase-3 和 9 活性以及抑制的 IL-10 水平升高,减轻了呋喃对大鼠肝肾的损伤。

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