Resveratrol and inflammatory bowel disease

被引:75
作者
Shi, Yaning [1 ,2 ]
Zhou, Jie [1 ]
Jiang, Bo [2 ]
Miao, Ming [2 ]
机构
[1] Nanjing Agr Univ, Coll Food Sci & Technol, Nanjing, Jiangsu, Peoples R China
[2] Jiangnan Univ, State Key Lab Food Sci & Technol, 1800 Lihu Ave, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
inflammatory bowel disease; resveratrol; mechanism; bioavailability; metabolites; NF-KAPPA-B; ULCERATIVE-COLITIS; OXIDATIVE STRESS; TRANS-RESVERATROL; CROHNS-DISEASE; DOUBLE-BLIND; PPAR-GAMMA; MICE; METABOLISM; CELLS;
D O I
10.1111/nyas.13426
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Inflammatory bowel disease (IBD) is a chronic inflammatory disease of the gastrointestinal tract, comprising ulcerative colitis (UC) and Crohn's disease (CD). Progression of IBD leads to long-term impairment of intestinal structure and function. The pathogenesis of IBD is complex, involving environmental, immunological, genetic, microbial, and psychological factors. The conventional therapies and many existing biopharmaceuticals for IBD have limited efficacy or adverse effects. As a promising safe and effective therapy for IBD, resveratrol has been studied widely, as it has shown anti-inflammatory and antioxidant activity. Resveratrol's mechanism of action involves multiple immune responses and signaling pathways; it is absorbed quickly and metabolized into various derivatives. However, the poor water solubility and low bioavailability of resveratrol limit its clinical applications. Further research should attempt to improve the stability and oral bioavailability of resveratrol by modification and various delivery systems.
引用
收藏
页码:38 / 47
页数:10
相关论文
共 66 条
[2]
Role of microRNAs in Resveratrol-Mediated Mitigation of Colitis-Associated Tumorigenesis in ApcMin/+ Mice [J].
Altamemi, Ibrahim ;
Murphy, E. Angela ;
Catroppo, James F. ;
Zumbrun, Elizabeth E. ;
Zhang, Jiajia ;
McClellan, Jamie L. ;
Singh, Udai P. ;
Nagarkatti, Prakash S. ;
Nagarkatti, Mitzi .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2014, 350 (01) :99-109
[3]
Comparison of the fecal microbiota profiles between ulcerative colitis and Crohn's disease using terminal restriction fragment length polymorphism analysis [J].
Andoh, Akira ;
Imaeda, Hirotsugu ;
Aomatsu, Tomoki ;
Inatomi, Osamu ;
Bamba, Shigeki ;
Sasaki, Masaya ;
Saito, Yasuharu ;
Tsujikawa, Tomoyuki ;
Fujiyama, Yoshihide .
JOURNAL OF GASTROENTEROLOGY, 2011, 46 (04) :479-486
[4]
Arslan A, 2015, INT J CLIN EXP MED, V8, P10491
[5]
Inflammatory bowel disease: the role of inflammatory cytokine gene polymorphisms [J].
Balding, J ;
Livingstone, WJ ;
Conroy, J ;
Mynett-Johnson, L ;
Weir, DG ;
Mahmud, N ;
Smith, OP .
MEDIATORS OF INFLAMMATION, 2004, 13 (03) :181-187
[6]
Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[7]
Pathogenesis of Intestinal Fibrosis in Inflammatory Bowel Disease and Perspectives for Therapeutic Implication [J].
Bettenworth, Dominik ;
Rieder, Florian .
DIGESTIVE DISEASES, 2017, 35 (1-2) :25-31
[8]
OXIDATIVE STRESS: AN ESSENTIAL FACTOR IN THE PATHOGENESIS OF GASTROINTESTINAL MUCOSAL DISEASES [J].
Bhattacharyya, Asima ;
Chattopadhyay, Ranajoy ;
Mitra, Sankar ;
Crowe, Sheila E. .
PHYSIOLOGICAL REVIEWS, 2014, 94 (02) :329-354
[9]
Fibrogenesis in Crohn's disease [J].
Burke, John P. ;
Mulsow, Jurgen J. ;
O'Keane, Conor ;
Docherty, Neil G. ;
Watson, R. William G. ;
O'Connell, P. Ronan .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (02) :439-448
[10]
Mood and Nonmood Components of Perceived Stress and Exacerbation of Crohn's Disease [J].
Camara, Rafael J. A. ;
Schoepfer, Alain M. ;
Pittet, Valerie ;
Begre, Stefan ;
von Kaenel, Roland .
INFLAMMATORY BOWEL DISEASES, 2011, 17 (11) :2358-2365