红酵母大米还是洛瓦斯塔丁? 通过多方面的方法对安全性和有效性的比较评估
Giovanna Rigillo1, Giulia Baini2, Renato Bruni3
1Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Phytotherapy research : PTR
|November 8, 2024
概括
红酵母大米 (RYR) 显示出作为一种安全的降胆固醇替代药物的潜力. 它的植物复合物提供优越的HMG-CoA减少酶抑制和减少肌肉细胞的影响相比lovastatin.
科学领域:
- 药理学 药理学是指药理学的学科.
- 自然产品 化学 化学
- 生物化学 生物化学
背景情况:
- 红酵米 (RYR) 是一种流行的天然补充剂,用于控制胆固醇.
- 它的有效性归因于莫纳科林K (MK),与洛瓦斯塔丁 (LOV) 完全相同.
- 与纯化他类药物相比,对RYR的安全性和有效性存在担忧.
研究的目的:
- 评估RYR样本与LOV的植物化学成分,药理作用和安全性.
- 为了比较HMG-CoA减少酶抑制活性和RYR和LOV的细胞毒性.
- 为了研究RYR对肌肉细胞基因表达与损伤有关的影响.
主要方法:
- HPLC-DAD用于量化RYR中的莫纳科林和其他生物活性化合物.
- 对HMG-CoA减少酶抑制的酶定量.
- 在体外模拟消化,在模型制造药理动力学.
- 在各种细胞模型中进行体外细胞毒性测定.
- 对肌肉损伤相关的基因表达进行qRT-PCR.
主要成果:
- 在RYR植物化学成分的显著变化,包括二次莫纳可林,三烯和多.
- RYR植物复合物表现出优越的HMG-CoA减少酶抑制与孤立的LOV相比,表明了协同效应.
- 与LOV相比,RYR样本的细胞毒性和对肌肉细胞的影响较低.
- 转录分析表明,对RYR.的肌肉损伤途径的影响减少了.
结论:
- RYR植物复合物可能提供协同降胆固醇效应.
- RYR提供了一个潜在的更安全的替代品,以减少肌肉毒性净化他类药物.
- 需要进一步的研究来证实临床疗效和阐明协同作用机制.
相关概念视频
Lipid-Lowering Drugs: Statins and Miscellaneous Agents
538
Hyperlipidemia, a medical condition often referred to as high cholesterol, is characterized by abnormally elevated levels of lipids in the bloodstream. When present in excess, these lipids, specifically cholesterol and triglycerides, can lead to serious health complications, often involving cardiovascular diseases. Illnesses like atherosclerosis, heart attacks, and pancreatitis have all been linked to untreated hyperlipidemia. This means controlling and regulating cholesterol and triglyceride...
538
Pharmacovigilance
774
Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
774
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
121
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
121
Bioequivalence: Overview
926
Pharmaceutical equivalents, by definition, are drug products with the same active ingredient in the same quantities, encapsulated in identical dosage forms, and intended for the same administration routes. These pharmaceutical equivalents are deemed bioequivalent if the bioavailability of the active entity in the drug preparations is similar. Moreover, pharmaceutical equivalents demonstrating bioequivalence are also regarded as therapeutically equivalent. This means that when used as directed,...
926


