肉桂醛是一种有希望防治代谢综合征的膳食植物化学物质:系统综述。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-01-01 DOI:10.2174/1389557523666230725113446
Mohaddeseh Khaafi, Zahra Tayarani-Najaran, Behjat Javadi
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引用次数: 0

摘要

背景:代谢综合征(METS代谢综合征(METS)是一系列不健康的病症,被认为是当今必不可少的健康问题。肉桂醛(Cinnamaldehyde,CA)是肉桂精油中的主要植物化学物质,具有抗氧化、抗炎、降血糖和降血脂活性。此外,我们还调查了 CA 的细胞和分子作用机制、药代动力学特征以及潜在的结构-活性关系(SAR):方法:检索PubMed、Science Direct、Scopus和Google Scholar上的相关论文:结果:CA具有多种抗METS活性,包括抗炎、抗氧化、抗糖尿病、抗血脂异常、抗肥胖和抗高血压特性。这些活性涉及多种分子机制,如刺激胰岛素释放,发挥促胰岛素作用;降低脂质过氧化以及胰岛氧化和炎症毒性;提高胰岛抗氧化酶的活性;抑制促炎细胞因子的产生;调节前脂肪细胞中 PPAR-γ 和 AMPK 的分子信号通路;防止脂肪细胞分化和脂肪生成等:结论:CA 可有效阻止 METS,但目前还没有可靠的临床数据支持其在人体中的作用。因此,开展临床试验以评估 CA 在人体中的疗效、安全剂量、药代动力学特征以及可能出现的不良反应具有重要意义。
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Cinnamaldehyde as a Promising Dietary Phytochemical Against Metabolic Syndrome: A Systematic Review.

Background: Metabolic syndrome (METS) is a set of unhealthy medical conditions considered essential health problems today. Cinnamaldehyde (CA) is the major phytochemical present in the essential oil of cinnamon and possesses antioxidant, anti-inflammatory, hypoglycemic, and antihyperlipidemic activities.

Aim: We aim to systematically review the effects of CA in preventing and attenuating METS components. Moreover, the cellular and molecular mechanisms of actions of CA, its pharmacokinetics features, and potential structure-activity relationship (SAR) were also surveyed.

Methods: PubMed, Science Direct, Scopus, and Google Scholar were searched to retrieve the relevant papers.

Results: CA possesses various anti-METS activities, including anti-inflammatory, antioxidant, antidiabetic, antidyslipidemia, antiobesity, and antihypertensive properties. Various molecular mechanisms such as stimulating pancreatic insulin release, exerting an insulinotropic effect, lowering lipid peroxidation as well as pancreatic islet oxidant and inflammatory toxicity, increasing the activities of pancreatic antioxidant enzymes, suppressing pro-inflammatory cytokines production, regulating the molecular signaling pathways of the PPAR-γ and AMPK in preadipocytes and preventing adipocyte differentiation and adipogenesis are involved in these activities.

Conclusions: CA would effectively hinder METS; however, no robust clinical data supporting these effects in humans is currently available. Accordingly, conducting clinical trials to evaluate the efficacy, safe dosage, pharmacokinetics characteristics, and possible unwanted effects of CA in humans would be of great importance.

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4.30%
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