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水乙醇叶和树皮提取物的细胞毒性、抗脂肪生成、低密度脂蛋白氧化抑制活性及急性毒性研究

Cytotoxicity, Antiadipogenic, Low-Density Lipoprotein Oxidation Inhibitory Activities, and Acute Toxicity Study of Hydroethanolic Leaf and Bark Extracts.

作者信息

Mba Jean Romuald, Zouheira Djamila, Guetchueng Stephanie Tamdem, Daïrou Hadidjatou, Djouonzo Paul Toukam, Ayong Lawrence, Kuiate Jules-Roger, Agbor Gabriel A

机构信息

Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies, P.O. Box 13033, Yaoundé, Cameroon.

Department of Biochemistry, Faculty of Sciences, University of Dschang, P.O. Box 67, Dschang, Cameroon.

出版信息

ScientificWorldJournal. 2024 Dec 17;2024:1732653. doi: 10.1155/tswj/1732653. eCollection 2024.

DOI:10.1155/tswj/1732653
PMID:39720344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11668551/
Abstract

Obesity is increasingly taking an important stage as a cause of death worldwide, and interventions with a good cost-effectiveness ratio are needed. is one of these natural products with health benefits. Objective. The present study evaluated the cytotoxicity, antiadipogenic, low-density lipoprotein (LDL), oxidation inhibitory activities, and acute toxicity of hydroethanolic leaf and bark extracts. The cytotoxicity evaluation of the extracts (62.5, 125, 250, and 500 μg/mL) using the MTT assay and the antiadipogenic activity (25, 50, 100, and 200 μg/mL) using oleic acid were carried out in SW-872 cells. Copper sulfate (CuSO)-induced oxidation was used in the evaluation of the effect of extracts (0.25, 0.5, and 1 mg/mL) against LDL oxidation. The oral acute toxicity evaluation of a single dose of 2000 mg/kg of the extracts was performed in Wistar albino rats weighing 127 ± 2 g. The leaf and bark extracts did not show any sign of cytotoxicity at the tested concentrations. The best antiadipogenic activity was observed by the standard orlistat (38.45 ± 1.70 μg/mL), followed by the leaf extract (IC: 41.47 ± 0.50 μg/mL) and the least the bark extract (IC: 107.50 ± 0.90 μg/mL). At a concentration of 1 mg/mL, the leaf extract presented an oxidation lag time of 130 min, which was higher and better than that of the bark extract (120 min). Quercetin (standard) presented an oxidation lag time longer than 3 h. The oral acute toxicity evaluation did not show any signs of toxicity indicating that the LD was greater than 2000 mg/kg. Based on the results obtained, the hydroethanolic leaf extract possesses a better antioxidant and antiadipogenic activities than the bark extract.

摘要

肥胖作为全球范围内的一个死亡原因,正日益占据重要地位,因此需要具有良好成本效益比的干预措施。[具体物质名称]是一种具有健康益处的天然产物之一。目的。本研究评估了[具体物质名称]水乙醇叶和树皮提取物的细胞毒性、抗脂肪生成、低密度脂蛋白(LDL)氧化抑制活性以及急性毒性。使用MTT法对提取物(62.5、125、250和500μg/mL)进行细胞毒性评估,并在SW - 872细胞中使用油酸对提取物(25、50、100和200μg/mL)进行抗脂肪生成活性评估。使用硫酸铜(CuSO)诱导的氧化来评估提取物(0.25、0.5和1mg/mL)对LDL氧化的影响。在体重为127±2g的Wistar白化大鼠中进行单剂量2000mg/kg提取物的口服急性毒性评估。叶和树皮提取物在测试浓度下未显示出任何细胞毒性迹象。标准奥利司他(38.45±1.70μg/mL)观察到最佳抗脂肪生成活性,其次是叶提取物(IC:41.47±0.50μg/mL),树皮提取物最低(IC:107.50±0.90μg/mL)。在1mg/mL浓度下,叶提取物的氧化滞后时间为130分钟,高于且优于树皮提取物(120分钟)。槲皮素(标准品)的氧化滞后时间超过3小时。口服急性毒性评估未显示任何毒性迹象,表明LD大于2000mg/kg。基于所得结果,[具体物质名称]水乙醇叶提取物比树皮提取物具有更好的抗氧化和抗脂肪生成活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/e6d00b4f8864/TSWJ2024-1732653.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/000534687190/TSWJ2024-1732653.001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/f9426d1d39f1/TSWJ2024-1732653.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/fe25d3d5638e/TSWJ2024-1732653.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/e6d00b4f8864/TSWJ2024-1732653.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/000534687190/TSWJ2024-1732653.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/f87d34b2c5f7/TSWJ2024-1732653.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/7ea34b287be6/TSWJ2024-1732653.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/43d0bead8917/TSWJ2024-1732653.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/5858392694dc/TSWJ2024-1732653.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/f9426d1d39f1/TSWJ2024-1732653.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/fe25d3d5638e/TSWJ2024-1732653.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f3/11668551/e6d00b4f8864/TSWJ2024-1732653.008.jpg

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