Baolier Capsule's Secret Weapon: Piperine Boosts Cholesterol Excretion to Combat Atherosclerosis.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2024-12-28 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S499598
Mengqiu Wei, Ping LYu, Peng Li, Jing Hu, Ruozhuo Wu, Qingqing Ouyang, Kai Guo
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Abstract

Purpose: The Baolier capsule (BLEC) is a proprietary Mongolian medicine administered for treating hypercholesterolemia and atherosclerosis (AS). However, the therapeutic effects, primary bioactive ingredients, and potential mechanisms underlying hypercholesterolemia and AS remain unclear. This study aimed to investigate the pharmacological effects, principal active ingredients, and mechanisms of BLEC against hypercholesterolemia and AS.

Methods: Adeno-associated virus tail vein injection was utilized to construct liver-specific LXRα knockout ApoE-/- mice. A high-fat diet was utilized to feed ApoE-/- mice to build hyperlipidemia and AS mouse models. The aorta or liver stained with Oil Red O was used to assess the effect of the drugs on AS or fatty liver formation after the oral administration of BLEC, piperine, statins, or ezetimibe to the mice following the experimental protocol. Biochemical assays were utilized to evaluate the effect of the drugs on serum lipid levels and cholesterol efflux indicators. Transcriptomics was employed to investigate the effect of BLEC on liver gene expression levels. HPLC-MS/MS was used to determine BLEC and its major components in the liver. Western blotting or quantitative reverse transcription polymerase chain reaction was conducted to detect LXRα, ABCA1, ABCG5, ABCG8, and CYP7A1 expression.

Results: Here, we revealed that BLEC decreases lipid levels in the serum and liver, as well as decelerates AS by promoting cholesterol excretion. BLEC and piperine, which are the main components exposed in the target liver tissue, activate LXRα to upregulate ABCA1, ABCG5, ABCG8, and CYP7A1, which promotes cholesterol transport to high-density lipoprotein and excretion to bile and feces. Notably, piperines demonstrated synergistic beneficial effects with atorvastatin or ezetimibe, which are two widely used hypocholesterolemic and anti-atherosclerotic drugs.

Conclusion: BLEC and its main active ingredient, piperine, promote cholesterol excretion, reduce serum cholesterol levels, inhibit AS, and exhibit good clinical application value and prospects.

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宝利尔胶囊的秘密武器:胡椒碱促进胆固醇排泄以对抗动脉粥样硬化。
目的:宝力尔胶囊(BLEC)是一种治疗高胆固醇血症和动脉粥样硬化(AS)的蒙药。然而,高胆固醇血症和AS的治疗效果、主要生物活性成分和潜在机制尚不清楚。本研究旨在探讨BLEC抗高胆固醇血症和AS的药理作用、主要活性成分及作用机制。方法:采用腺相关病毒尾静脉注射法构建肝脏特异性LXRα敲除ApoE-/-小鼠。采用高脂饲料喂养ApoE-/-小鼠,建立高脂血症和AS小鼠模型。按照实验方案,对小鼠口服BLEC、胡椒碱、他汀类药物或依折替米贝后,用油红O染色的主动脉或肝脏评估药物对AS或脂肪肝形成的影响。采用生化法评价药物对血脂水平和胆固醇外排指标的影响。采用转录组学方法研究BLEC对肝脏基因表达水平的影响。采用HPLC-MS/MS法测定肝脏中BLEC及其主要成分。Western blotting或定量逆转录聚合酶链反应检测LXRα、ABCA1、ABCG5、ABCG8和CYP7A1的表达。结果:在这里,我们发现BLEC降低了血清和肝脏中的脂质水平,并通过促进胆固醇排泄来减缓as。暴露于靶肝组织的主要成分BLEC和胡椒碱激活LXRα上调ABCA1、ABCG5、ABCG8和CYP7A1,促进胆固醇转运为高密度脂蛋白并排泄到胆汁和粪便中。值得注意的是,胡椒碱与阿托伐他汀或依折替米贝这两种广泛使用的降胆固醇和抗动脉粥样硬化药物具有协同有益作用。结论:BLEC及其主要活性成分胡椒碱具有促进胆固醇排泄、降低血清胆固醇水平、抑制AS的作用,具有良好的临床应用价值和前景。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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