A systematic, updated review of Xuezhikang, a domestically developed lipid-lowering drug, in the application of cardiovascular diseases

IF 14.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY
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Abstract

Cardiovascular diseases (CVDs) are a major threat to public health globally. A large proportion of people with dyslipidaemia have poorly controlled lipid levels, emphasizing the need for alternative lipid-lowering treatments that are both effective and safe. Xuezhikang, a red yeast rice (RYR) extract, containing 13 kinds of monacolins and other bioactive components, emerges as one such promising option. Its discovery was built on a long history of RYR use as a functional food supplement and traditional Chinese medicine. Several randomized, controlled clinical trials have substantiated its lipid-lowering effects and its potential to protect against CVDs. Safety concerns with statins did not arise during decades of experience with Xuezhikang treatment in clinical practice. The approval of Xuezhikang in multiple regions of Asia marked a conceptual shift in CVD management, moving from single agents to polypills and from synthetic medicines to natural extracts. This review comprehensively addresses important topics related to this medicinal natural extract, including the ancient utilization of RYR, the development of Xuezhikang, its mechanisms of action, pleiotropic effects, clinical studies, challenges, and future perspectives to enhance our understanding regarding the role of Xuezhikang, a representative, domestic lipid-lowering drug of RYR, in prevention and treatment of CVD.

Abstract Image

Abstract Image

关于国产降脂药雪芝康在心血管疾病中应用的最新系统综述
心血管疾病(CVD)是全球公共卫生的一大威胁。很大一部分血脂异常患者的血脂水平控制不佳,因此需要既有效又安全的降脂替代疗法。红麴提取物 "雪芝康 "含有 13 种单胞菌素和其他生物活性成分,是一种很有前景的选择。它的发现是建立在红麴作为功能性食品补充剂和传统中药的悠久历史基础之上的。几项随机对照临床试验证实了它的降脂效果和预防心血管疾病的潜力。在数十年的临床实践中,雪芝康治疗过程中并未出现他汀类药物的安全性问题。学志康在亚洲多个地区获得批准,标志着心血管疾病治疗理念的转变,从单一药物到多丸剂,从合成药物到天然提取物。这篇综述全面论述了与这种药用天然提取物相关的重要课题,包括栝楼仁的古代利用、学之康的开发、作用机制、多效作用、临床研究、挑战和未来展望,以加深我们对栝楼仁中具有代表性的国产降脂药学之康在预防和治疗心血管疾病中的作用的认识。
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来源期刊
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
22.40
自引率
5.50%
发文量
1051
审稿时长
19 weeks
期刊介绍: The Journal of the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association oversees the peer review process for Acta Pharmaceutica Sinica. B (APSB). Published monthly in English, APSB is dedicated to disseminating significant original research articles, rapid communications, and high-quality reviews that highlight recent advances across various pharmaceutical sciences domains. These encompass pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis, and pharmacokinetics. A part of the Acta Pharmaceutica Sinica series, established in 1953 and indexed in prominent databases like Chemical Abstracts, Index Medicus, SciFinder Scholar, Biological Abstracts, International Pharmaceutical Abstracts, Cambridge Scientific Abstracts, and Current Bibliography on Science and Technology, APSB is sponsored by the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association. Its production and hosting are facilitated by Elsevier B.V. This collaborative effort ensures APSB's commitment to delivering valuable contributions to the pharmaceutical sciences community.
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