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在泊洛沙姆-407诱导的急性高脂血症大鼠模型中,树叶可预防血脂异常和氧化应激。

leaves prevent dyslipidemia and oxidative stress in a rat model of poloxamer-407-induced acute hyperlipidemia.

作者信息

Abduh Maisa Siddiq, Saghir Sultan A M, Al Hroob Amir M, Bin-Ammar Albandari, Al-Tarawni Ayat H, Murugaiyah Vikneswaran, Mahmoud Ayman M

机构信息

Immune Responses in Different Diseases Research Group, Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.

Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Front Pharmacol. 2023 Feb 6;14:1134812. doi: 10.3389/fphar.2023.1134812. eCollection 2023.

Abstract

The star fruit [ L (Oxalidaceae)] is traditionally used in the treatment of many ailments in many countries. It possesses several pharmacological activities, including antioxidant and anti-inflammatory effects. However, it contains the neurotoxic caramboxin and its high content of oxalic acid limits its consumption by individuals with compromised kidney function. This study assessed the anti-hyperlipidemic and antioxidant activities of different fractions of the methanolic extract of leaves (MEACL). The antioxidant activity was investigated using FRAP, and ABTS and DPPH radical-scavenging assays and the inhibitory activity toward pancreatic lipase (PL) and HMG-CoA reductase was assayed . Acute hyperlipidemia was induced by poloxamer-407 (P-407) in rats and different fractions of MEACL (-hexane, chloroform, -butanol, ethyl acetate (EA), water, and chloroform) were orally administered. Cholesterol and triglycerides were determined at 0, 12, 24, and 48 h and LDL-C, vLDL-C, HDL-C, lipid peroxidation (LPO) and antioxidants were assayed after 48 h. The expression of ABCA1, ABCG5, ABCG8, LDL-R, SREBP-1, and SREBP-2 and the activity of HMG-CoA reductase were assayed in the liver of P-407-administered rats treated with the EA fraction. The data revealed potent radical-scavenging activities of MEACL fractions with the most potent effect showed by the EA fraction that also suppressed the activities of HMG-CoA reductase and PL. In P-407-induced hyperlipidemic rats, all fractions prevented dyslipidemia as shown by the decrease in total cholesterol, triglycerides, LDL-C, vLDL-C and atherogenic index. MEACL and its fractions prevented LPO and boosted GSH, superoxide dismutase, glutathione peroxidase, and catalase in P-407-administered rats. The EA fraction showed more effective anti-hyperlipidemic and antioxidant effects than other fractions and downregulated SREBP-2 while upregulated ABCA1 and LDL-R and ameliorated LPL and HMG-CoA reductase in hyperlipidemic rats. MEACL showed and antioxidant activity and the EA fraction significantly ameliorated dyslipidemia in a rat model of P-407-induced acute hyperlipidemia by modulating LPL, PL, HMG-CoA reductase, and cholesterolgenesis-related factors. Therefore, the leaves of represent a safe alternative for the star fruit particularly in kidney disease patients, and the EA is the most effective anti-hyperlipidemic and antioxidant fraction.

摘要

杨桃[酢浆草科(Oxalidaceae)]在许多国家传统上用于治疗多种疾病。它具有多种药理活性,包括抗氧化和抗炎作用。然而,它含有神经毒性的杨桃毒素,并且其高含量的草酸限制了肾功能受损个体对其的食用。本研究评估了杨桃叶甲醇提取物(MEACL)不同馏分的抗高血脂和抗氧化活性。使用铁还原抗氧化能力(FRAP)、ABTS和二苯基苦味酰基自由基(DPPH)清除试验研究抗氧化活性,并测定对胰脂肪酶(PL)和3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶的抑制活性。用泊洛沙姆-407(P-407)诱导大鼠急性高血脂,并口服给予MEACL的不同馏分(正己烷、氯仿、正丁醇、乙酸乙酯(EA)、水和氯仿)。在0、12、24和48小时测定胆固醇和甘油三酯,并在48小时后测定低密度脂蛋白胆固醇(LDL-C)、极低密度脂蛋白胆固醇(vLDL-C)、高密度脂蛋白胆固醇(HDL-C)、脂质过氧化(LPO)和抗氧化剂。在给予P-407并用EA馏分处理的大鼠肝脏中测定ATP结合盒转运体A1(ABCA1))、ATP结合盒转运体G5(ABCG5)、ATP结合盒转运体G8(ABCG8)、低密度脂蛋白受体(LDL-R)、固醇调节元件结合蛋白-1(SREBP-1)和固醇调节元件结合蛋白-2(SREBP-2)的表达以及HMG-CoA还原酶的活性。数据显示MEACL馏分具有强大的自由基清除活性,其中EA馏分的效果最强,它还抑制了HMG-CoA还原酶和PL的活性。在P-407诱导的高血脂大鼠中,所有馏分都预防了血脂异常,总胆固醇、甘油三酯、LDL-C、vLDL-C和动脉粥样硬化指数降低。MEACL及其馏分在给予P-407的大鼠中预防了LPO并提高了谷胱甘肽(GSH)、超氧化物歧化酶、谷胱甘肽过氧化物酶和过氧化氢酶的水平。EA馏分显示出比其他馏分更有效的抗高血脂和抗氧化作用,下调了SREBP-2,同时上调了ABCA1和LDL-R,并改善了高血脂大鼠的脂蛋白脂肪酶(LPL)和HMG-CoA还原酶。MEACL显示出抗氧化活性,并且EA馏分通过调节LPL、PL、HMG-CoA还原酶和胆固醇生成相关因子,在P-407诱导的急性高血脂大鼠模型中显著改善了血脂异常。因此,杨桃叶是杨桃的一种安全替代品,尤其适用于肾病患者,而EA是最有效的抗高血脂和抗氧化馏分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e37/9939629/bcca77c7195c/fphar-14-1134812-g001.jpg

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