Moumou Mohammadine, Tayebi Amani, Hadini Abderrahmane, Noman Omar M, Alhalmi Abdulsalam, Ahmoda Hamza, Amrani Souliman, Harnafi Hicham
Laboratory of Bioresources, Biotechnologies, Ethnopharmacology and Health, Faculty of Sciences, University Mohammed First, Oujda 60000, Morocco.
Department of Pharmacognosy, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Metabolites. 2025 Jan 10;15(1):36. doi: 10.3390/metabo15010036.
BACKGROUND/OBJECTIVES: Hyperlipidemia is a serious risk factor for cardiovascular diseases and liver steatosis. In this work, we explored the effect of an herbal formula (CBF) containing immature pods and extracts on lipid metabolism disorders and lipoprotein-rich plasma (LRP) oxidation in mice.
The phenolic composition was determined using HPLC-DAD analysis. The antioxidant activity was studied using various in vitro methods. Acute toxicity was evaluated in mice. Importantly, the effect of the CBF on lipid metabolism disorders was investigated in a high-fat diet (HFD) hyperlipidemia mouse model. An in silico study was carried out to predict underlying mechanisms.
The HPLC analysis revealed gallic acid, cinnamic acid, and naringenin as major phenolics of the carob pod aqueous extract. Concerning the basil hydro-ethanolic extract, rosmarinic, chicoric, caftaric, and caffeic acids were the main phenolics. Accordingly, the CBF prevented LRP oxidation in a concentration-dependent manner. This formula is not toxic in mice (LD > 2000 mg/kg body weight). Moreover, animals administered the CBF at 200 mg/kg/day presented a significant decline in their body weight gain, adipose tissue weight, plasma total cholesterol, low-density lipoprotein cholesterol (LDL-C) level, and glycaemia after 10 weeks' treatment. Accordingly, the CBF decreased the plasma atherogenic index and the LDL-C to HDL-C ratio and reduced the level of fats accumulated in the liver. The molecular docking study revealed that chicoric, rosmarinic, and caftaric acids, and naringenin bound particularly strongly to many proteins involved in the regulation of lipid and cholesterol metabolism. This includes the HMG-CoA reductase, PPARα/γ, PCSK9, Cyp7a1, and ATP-citrate lyase.
The CBF could be a good source of natural supplements, functional foods, and pharmaceuticals effective in managing hyperlipidemia and oxidative stress and preventing their related cardiovascular disorders.
背景/目的:高脂血症是心血管疾病和肝脂肪变性的严重危险因素。在本研究中,我们探讨了一种含有未成熟豆荚和提取物的草药配方(CBF)对小鼠脂质代谢紊乱和富含脂蛋白血浆(LRP)氧化的影响。
采用HPLC-DAD分析测定酚类成分。使用各种体外方法研究抗氧化活性。在小鼠中评估急性毒性。重要的是,在高脂饮食(HFD)高脂血症小鼠模型中研究了CBF对脂质代谢紊乱的影响。进行了计算机模拟研究以预测潜在机制。
HPLC分析显示,没食子酸、肉桂酸和柚皮素是角豆荚水提取物的主要酚类物质。关于罗勒水乙醇提取物,迷迭香酸、菊苣酸、咖啡酰酒石酸和咖啡酸是主要酚类物质。因此,CBF以浓度依赖性方式阻止LRP氧化。该配方对小鼠无毒(LD>2000mg/kg体重)。此外,以200mg/kg/天的剂量给予CBF的动物在治疗10周后体重增加、脂肪组织重量、血浆总胆固醇、低密度脂蛋白胆固醇(LDL-C)水平和血糖均显著下降。因此,CBF降低了血浆动脉粥样硬化指数和LDL-C与HDL-C的比值,并减少了肝脏中积累的脂肪水平。分子对接研究表明,菊苣酸、迷迭香酸和咖啡酰酒石酸以及柚皮素与许多参与脂质和胆固醇代谢调节的蛋白质结合特别紧密。这包括HMG-CoA还原酶、PPARα/γ、PCSK9、Cyp7a1和ATP-柠檬酸裂解酶。
CBF可能是天然补充剂、功能性食品和药物的良好来源,对控制高脂血症和氧化应激以及预防其相关的心血管疾病有效。