Targeting metabolic diseases with celastrol: A comprehensive review of anti-inflammatory mechanisms and therapeutic potential

被引:4
作者
Wang, Xiaojuan [1 ,2 ]
Bakar, Mohamad Hafizi Abu [1 ]
Liqun, Song [2 ]
Kassim, Mohd Asyraf [1 ]
Shariff, Khairul Anuar [3 ]
Karunakaran, Thiruventhan [4 ]
机构
[1] Univ Sains Malaysia, Sch Ind Technol, Bioproc Technol Div, Gelugor 11800, Penang, Malaysia
[2] Taishan Vocat Coll Nursing, Dept Pharm, Tai An 271099, Shandong, Peoples R China
[3] Univ Sains Malaysia, Sch Mat & Mineral Resources Engn, Nibong Tebal 14300, Penang, Malaysia
[4] Univ Sains Malaysia, Ctr Drug Res, Gelugor 11800, Penang, Malaysia
关键词
Celastrol; Low-grade chronic inflammation; Diabetes; Obesity; Therapeutic potential; HEPATIC INSULIN-RESISTANCE; GLUCOSE-INDUCED MIGRATION; FATTY LIVER-DISEASE; KAPPA-B; OXIDATIVE STRESS; MITOCHONDRIAL DYSFUNCTION; INDUCED INFLAMMATION; TISSUE INFLAMMATION; ENDOTHELIAL-CELLS; PODOCYTE INJURY;
D O I
10.1016/j.jep.2025.119560
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Tripterygium wilfordii is a traditional Chinese medicine used to treat rheumatic diseases, with properties such as clearing heat, detoxifying, dispelling wind, and relieving pain. In recent years, its active compound, celastrol, garnered significant attention for its potential therapeutic effects on metabolic diseases. Celastrol exhibits bioactivities such as regulating metabolic functions and anti-inflammatory effects, positioning it as a promising candidate for the treatment of obesity, diabetes, atherosclerosis (AS), and nonalcoholic fatty liver disease (NAFLD). Aim of the review: This review aims to explore the pharmacological mechanisms of celastrol in metabolic diseases, focusing on its anti-inflammatory mechanisms and metabolic regulation effects, providing theoretical support for further investigation of its therapeutic potential in metabolic diseases. Methods: Literature was retrieved from PubMed, Web of Science, Scopus, Cochrane, and Google Scholar. This review primarily focuses on anti-inflammatory mechanisms of celastrol, its metabolic regulation, and toxicity studies, by systematically analyzing its effects in obesity, diabetes, AS, and NAFLD, providing scientific evidence for its potential clinical applications. Results: Celastrol regulates multiple signaling pathways, particularly inhibiting NF-kappa B and activating AMPK, reducing the production of pro-inflammatory cytokines and improving insulin sensitivity, enhancing its therapeutic potential in metabolic diseases. Additionally, celastrol regulates adipogenesis and energy metabolism by influencing key transcription factors such as PPAR gamma and SREBP-1c. Numerous studies highlight its role in alleviating oxidative stress and improving mitochondrial function, further enhancing its metabolic benefits. Conclusion: In summary, celastrol holds great promise as a multi-target therapeutic agent for metabolic diseases, offering anti-inflammatory, metabolic regulatory, and antioxidative benefits. Despite these, challenges remain for the clinical application of celastrol due to its poor bioavailability and potential toxicity. Advanced formulation strategies and targeted delivery systems are urgently needed to overcome challenges related to bioavailability and clinical translation.
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页数:17
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共 192 条
[1]   Celastrol alleviates high-fat diet-induced obesity via enhanced muscle glucose utilization and mitochondrial oxidative metabolism-mediated upregulation of pyruvate dehydrogenase complex [J].
Abu Bakar, Mohamad Hafizi ;
Shahril, Nor Shafiqah Nor ;
Khalid, Mohamad Shamil Faris Mohamad ;
Mohammad, Sharifah ;
Shariff, Khairul Anuar ;
Karunakaran, Thiruventhan ;
Salleh, Rabeta Mohd ;
Rosdi, Mohamad Norisham Mohamad .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2022, 449
[2]   Celastrol attenuates high-fructose diet-induced inflammation and insulin resistance via inhibition of 11β-hydroxysteroid dehydrogenase type 1 activity in rat adipose tissues [J].
Abu Bakar, Mohamad Hafizi ;
Mohamad Khalid, Mohamad Shamil Faris ;
Nor Shahril, Nor Shafiqah ;
Shariff, Khairul Anuar ;
Karunakaran, Thiruventhan .
BIOFACTORS, 2022, 48 (01) :111-134
[3]   Celastrol attenuates inflammatory responses in adipose tissues and improves skeletal muscle mitochondrial functions in high fat diet-induced obese rats via upregulation of AMPK/SIRT1 signaling pathways [J].
Abu Bakar, Mohamad Hafizi ;
Shariff, Khairul Anuar ;
Tan, Joo Shun ;
Lee, Lai Kuan .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2020, 883
[4]   Improvement of mitochondrial function by celastrol in palmitate-treated C2C12 myotubes via activation of PI3K-Akt signaling pathway [J].
Abu Bakar, Mohamad Hafizi ;
Tan, Joo Shun .
BIOMEDICINE & PHARMACOTHERAPY, 2017, 93 :903-912
[5]   Celastrol attenuates mitochondrial dysfunction and inflammation in palmitate-mediated insulin resistance in C3A hepatocytes [J].
Abu Bakar, Mohamad Hafizi ;
Sarmidi, Mohamad Roji ;
Tan, Joo Shun ;
Rosdi, Mohamad Norisham Mohamad .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2017, 799 :73-83
[6]   Mitochondrial dysfunction as a central event for mechanisms underlying insulin resistance: the roles of long chain fatty acids [J].
Abu Bakar, Mohamad Hafizi ;
Kai, Cheng Kian ;
Hassan, Wan Najihah Wan ;
Sarmidi, Mohamad Roji ;
Yaakob, Harisun ;
Huri, Hasniza Zaman .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2015, 31 (05) :453-475
[7]   Metabolomics - the complementary field in systems biology: a review on obesity and type 2 diabetes [J].
Abu Bakar, Mohamad Hafizi ;
Sarmidi, Mohamad Roji ;
Cheng, Kian-Kai ;
Khan, Abid Ali ;
Suan, Chua Lee ;
Huri, Hasniza Zaman ;
Yaakob, Harisun .
MOLECULAR BIOSYSTEMS, 2015, 11 (07) :1742-1774
[8]   Celastrol Protects against Antimycin A-Induced Insulin Resistance in Human Skeletal Muscle Cells [J].
Abu Bakar, Mohamad Hafizi ;
Cheng, Kian-Kai ;
Sarmidi, Mohamad Roji ;
Yaakob, Harisun ;
Huri, Hasniza Zaman .
MOLECULES, 2015, 20 (05) :8242-8269
[9]   Amelioration of Mitochondrial Dysfunction-Induced Insulin Resistance in Differentiated 3T3-L1 Adipocytes via Inhibition of NF-κB Pathways [J].
Abu Bakar, Mohamad Hafizi ;
Sarmidi, Mohamad Roji ;
Kai, Cheng Kian ;
Huri, Hasniza Zaman ;
Yaakob, Harisun .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (12) :22227-22257
[10]   PGC-1a Is a Master Regulator of Mitochondrial Lifecycle and ROS Stress Response [J].
Abu Shelbayeh, Othman ;
Arroum, Tasnim ;
Morris, Silke ;
Busch, Karin B. .
ANTIOXIDANTS, 2023, 12 (05)