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姜黄素衍生物防治肥胖及其相关代谢并发症的治疗作用:体外和体内研究综述。

Therapeutic Effects of Curcumin Derivatives against Obesity and Associated Metabolic Complications: A Review of In Vitro and In Vivo Studies.

机构信息

Biomedical Research and Innovation Platform, South African Medical Research Council, Cape Town 7505, South Africa.

Department of Biochemistry, North-West University, Mmabatho 2745, South Africa.

出版信息

Int J Mol Sci. 2023 Sep 21;24(18):14366. doi: 10.3390/ijms241814366.


DOI:10.3390/ijms241814366
PMID:37762669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10531575/
Abstract

Obesity is a major cause of morbidity and mortality globally, increasing the risk for chronic diseases. Thus, the need to identify more effective anti-obesity agents has spurred significant interest in the health-promoting properties of natural compounds. Of these, curcumin, the most abundant and bioactive constituent of turmeric, possesses a variety of health benefits including anti-obesity effects. However, despite its anti-obesity potential, curcumin has demonstrated poor bioavailability, which limits its clinical applicability. Synthesizing curcumin derivatives, which are structurally modified analogs of curcumin, has been postulated to improve bioavailability while maintaining therapeutic efficacy. This review summarizes in vitro and in vivo studies that assessed the effects of curcumin derivatives against obesity and its associated metabolic complications. We identified eight synthetic curcumin derivatives that were shown to ameliorate obesity and metabolic dysfunction in diet-induced obese animal models, while five of these derivatives also attenuated obesity and associated metabolic complications in cell culture models. These curcumin derivatives modulated adipogenesis, lipid metabolism, insulin resistance, steatosis, lipotoxicity, inflammation, oxidative stress, endoplasmic reticulum stress, apoptosis, autophagy, fibrosis, and dyslipidemia to a greater extent than curcumin. In conclusion, the findings from this review show that compared to curcumin, synthetic curcumin derivatives present potential candidates for further development as therapeutic agents to modulate obesity and obesity-associated metabolic complications.

摘要

肥胖是全球发病率和死亡率的主要原因,增加了患慢性病的风险。因此,需要识别更有效的抗肥胖药物,这促使人们对天然化合物的健康促进特性产生了浓厚的兴趣。在这些化合物中,姜黄素是姜黄中最丰富和最具生物活性的成分,具有多种健康益处,包括抗肥胖作用。然而,尽管姜黄素具有抗肥胖的潜力,但它的生物利用度很差,这限制了它的临床应用。合成姜黄素衍生物,即姜黄素的结构修饰类似物,被认为可以提高生物利用度,同时保持治疗效果。这篇综述总结了评估姜黄素衍生物对肥胖及其相关代谢并发症的影响的体外和体内研究。我们确定了八种合成姜黄素衍生物,这些衍生物在饮食诱导的肥胖动物模型中显示出改善肥胖和代谢功能障碍的作用,而其中五种衍生物在细胞培养模型中也能减轻肥胖和相关代谢并发症。这些姜黄素衍生物在调节脂肪生成、脂质代谢、胰岛素抵抗、脂肪变性、脂毒性、炎症、氧化应激、内质网应激、细胞凋亡、自噬、纤维化和血脂异常方面的作用比姜黄素更为显著。总之,本综述的研究结果表明,与姜黄素相比,合成姜黄素衍生物作为治疗肥胖及其相关代谢并发症的药物具有更大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/8247a4a86404/ijms-24-14366-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/b3756ead7232/ijms-24-14366-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/4f17e6a636c4/ijms-24-14366-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/97878455eb2d/ijms-24-14366-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/8247a4a86404/ijms-24-14366-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/b3756ead7232/ijms-24-14366-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/4f17e6a636c4/ijms-24-14366-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/97878455eb2d/ijms-24-14366-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c7/10531575/8247a4a86404/ijms-24-14366-g004.jpg

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Int J Mol Sci. 2025-7-17

[2]
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J Nanobiotechnology. 2025-5-7

[3]
Research progress on the mechanism of curcumin anti-oxidative stress based on signaling pathway.

Front Pharmacol. 2025-4-7

[4]
RNA Modification in Metabolism.

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[5]
Exploring the role of curcumin in mitigating oxidative stress to alleviate lipid metabolism disorders.

Front Pharmacol. 2025-1-30

[6]
The PI3K/Akt pathway: a target for curcumin's therapeutic effects.

J Diabetes Metab Disord. 2025-1-17

[7]
Targeting STAT3 signaling pathway by curcumin and its analogues for breast cancer: A narrative review.

Animal Model Exp Med. 2024-12

[8]
Obesity-Associated Colorectal Cancer.

Int J Mol Sci. 2024-8-14

[9]
Modulatory Effects of -Fermented Turmeric on Metabolic Dysregulation and Gut Microbiota in High-Fat Diet-Induced Obesity in Mice.

J Agric Food Chem. 2024-8-14

[10]
Targeted Screening of Curcumin Derivatives as Pancreatic Lipase Inhibitors Using Computer-Aided Drug Design.

ACS Omega. 2024-6-13

本文引用的文献

[1]
Strategies for Improving Bioavailability, Bioactivity, and Physical-Chemical Behavior of Curcumin.

Molecules. 2022-10-13

[2]
Keto-enol tautomerism of curcumin in the preparation of nanobiocomposites with fumed silica.

Spectrochim Acta A Mol Biomol Spectrosc. 2022-9-5

[3]
Curcumin and Derivatives in Nanoformulations with Therapeutic Potential on Colorectal Cancer.

AAPS PharmSciTech. 2022-4-19

[4]
In Vitro and In Vivo Cardioprotective Effects of Curcumin against Doxorubicin-Induced Cardiotoxicity: A Systematic Review.

J Oncol. 2022-2-21

[5]
Curcumin and Weight Loss: Does It Work?

Int J Mol Sci. 2022-1-7

[6]
Curcumin supplementation improves biomarkers of oxidative stress and inflammation in conditions of obesity, type 2 diabetes and NAFLD: updating the status of clinical evidence.

Food Funct. 2021-12-13

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Anti-obesity drug discovery: advances and challenges.

Nat Rev Drug Discov. 2022-3

[8]
Ameliorative effect of curcumin and zinc oxide nanoparticles on multiple mechanisms in obese rats with induced type 2 diabetes.

Sci Rep. 2021-10-19

[9]
Curc-mPEG454, a PEGylated curcumin derivative, as a multi-target anti-fibrotic prodrug.

Int Immunopharmacol. 2021-12

[10]
Curcumin analogue C66 attenuates obesity-induced myocardial injury by inhibiting JNK-mediated inflammation.

Biomed Pharmacother. 2021-11

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