Targeting matrix metalloproteases: A promising strategy for herbal medicines to treat rheumatoid arthritis

被引:22
作者
Li, Ruo-Lan [1 ]
Duan, Hu-Xinyue [1 ]
Liang, Qi [1 ]
Huang, Yong-Liang [2 ]
Wang, Ling-Yu [1 ]
Zhang, Qing [1 ]
Wu, Chun-Jie [1 ]
Liu, Shu-Qin [2 ]
Peng, Wei [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Pharm, State Key Lab Southwestern Chinese Med Resources, Chengdu, Peoples R China
[2] Hosp Chengdu Univ Tradit Chinese Med, Chengdu, Peoples R China
关键词
matrix metalloproteinases; rheumatoid arthritis; herbal medicines; therapeutic; strategy; COLLAGEN-INDUCED ARTHRITIS; FIBROBLAST-LIKE SYNOVIOCYTES; WILFORDII HOOK-F; NF-KAPPA-B; INFLAMMATORY ARTHRITIS; DOWN-REGULATION; GENE-EXPRESSION; EXTRACT; MIGRATION; TISSUE;
D O I
10.3389/fimmu.2022.1046810
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As a type of metalloproteinase, matrix metalloproteinases (MMPs) can be divided into collagenase, gelatinase, stromelysins, membrane-type (MT)-MMPs and heterogeneous subgroups according to their structure and function. MMP contents in the human body are strictly regulated, and their synthesis, activation and inhibition processes should be kept in a certain balance; otherwise, this would result in the occurrence of various diseases. Rheumatoid arthritis (RA) is a known immune-mediated systemic inflammatory disease that is affected by a variety of endogenous and exogenous factors. In RA development, MMPs act as important mediators of inflammation and participate in the degradation of extracellular matrix substrates and digestion of fibrillar collagens, leading to the destruction of joint structures. Interestingly, increasing evidence has suggested that herbal medicines have many advantages in RA due to their multitarget properties. In this paper, literature was obtained through electronic databases, including the Web of Science, PubMed, Google Scholar, Springer, and CNKI (Chinese). After classification and analysis, herbal medicines were found to inhibit the inflammatory process of RA by regulating MMPs and protecting joint structures. However, further preclinical and clinical studies are needed to support this view before these herbal medicines can be developed into drugs with actual application to the disease.
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页数:17
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共 101 条
[31]   Systems pharmacology-based dissection of mechanisms of Tibetan medicinal compound Ruteng as an effective treatment for collagen-induced arthritis rats [J].
Huang, Xian-Ju ;
Wang, Jing ;
Muhammad, Azhar ;
Tong, Hai-Ying ;
Wang, Da-Gui ;
Li, Jun ;
Ihsan, Awais ;
Yang, Guang-Zhong .
JOURNAL OF ETHNOPHARMACOLOGY, 2021, 272
[32]   Metalloproteinases in Rheumatoid Arthritis: Potential Therapeutic Targets to Improve Current Therapies [J].
Itoh, Yoshifumi .
MATRIX METALLOPROTEINASES AND TISSUE REMODELING IN HEALTH AND DISEASE: TARGET TISSUES AND THERAPY, 2017, 148 :327-338
[33]   Polyoxypregnane glycoside from Dregea volubilis extract inhibits IL-1β-induced expression of matrix metalloproteinase via activation of NF-κB in human chondrocytes [J].
Itthiarbha, Akanit ;
Phitak, Thanyaluck ;
Sanyacharernkul, Saksri ;
Pothacharoen, Peraphan ;
Pompimon, Wilart ;
Kongtawelert, Prachya .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2012, 48 (01) :43-53
[34]   Matrix metalloproteinases (MMPs), the main extracellular matrix (ECM) enzymes in collagen degradation, as a target for anticancer drugs [J].
Jablonska-Trypuc, Agata ;
Matejczyk, Marzena ;
Rosochacki, Stanislaw .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2016, 31 :177-183
[35]   Effect of the oral application of a highly selective MMP-13 inhibitor in three different animal models of rheumatoid arthritis [J].
Juengel, Astrid ;
Ospelt, Caroline ;
Lesch, Mark ;
Thiel, Melissa ;
Sunyer, Teresa ;
Schorr, Olivier ;
Michel, Beat A. ;
Gay, Renate E. ;
Kolling, Christoph ;
Flory, Craig ;
Gay, Steffen ;
Neidhart, Michel .
ANNALS OF THE RHEUMATIC DISEASES, 2010, 69 (05) :898-902
[36]   Selective Inhibition of Membrane Type 1 Matrix Metalloproteinase Abrogates Progression of Experimental Inflammatory Arthritis: Synergy With Tumor Necrosis Factor Blockade [J].
Kaneko, Kazuyo ;
Williams, Richard O. ;
Dransfield, Daniel T. ;
Nixon, Andrew E. ;
Sandison, Ann ;
Itoh, Yoshifumi .
ARTHRITIS & RHEUMATOLOGY, 2016, 68 (02) :521-531
[37]   Metastasis and MAPK Pathways [J].
Kciuk, Mateusz ;
Gielecinska, Adrianna ;
Budzinska, Adrianna ;
Mojzych, Mariusz ;
Kontek, Renata .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (07)
[38]   Matrix Metalloproteinases: Regulators of the Tumor Microenvironment [J].
Kessenbrock, Kai ;
Plaks, Vicki ;
Werb, Zena .
CELL, 2010, 141 (01) :52-67
[39]   Cinnamomulactone, a new butyrolactone from the twigs of Cinnamomum cassia and its inhibitory activity of matrix metalloproteinases [J].
Kim, Geum Jin ;
Lee, Jong Yeong ;
Choi, Hyun Gyu ;
Kim, So Young ;
Kim, Eonmi ;
Shim, Sang Hee ;
Nam, Joo-Won ;
Kim, Sang-Hyun ;
Choi, Hyukjae .
ARCHIVES OF PHARMACAL RESEARCH, 2017, 40 (03) :304-310
[40]   Tissue Inhibitor of Metalloproteinase-3 Promotes Schwann Cell Myelination [J].
Kim, Jihyun ;
Elias, Anthony ;
Lee, Taeweon ;
Maurel, Patrice ;
Kim, Haesun A. .
ASN NEURO, 2017, 9 (06)