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Original Research Article | OPEN ACCESS

3-O-Caffeoylquinic acid in Periploca forrestii Schltr extract ameliorates collagen-induced arthritis by inducing IL17/IL23 cells in rats

Qiaoyi Ning1,2, Xueming Yao2, Ying Huang2, Lei Hou2, Daomin Lu2, Yutao Yang3, Yamei Zhan4, Yiting He5, Wukai Ma2

1The 2nd Clinical School, Guangzhou University of Chinese Medicine, Guangzhou 510120, China; 2Rheumatology and Immunology Department, The 2nd Hospital Affiliated with Guizhou university of Traditional Chinese Medicine, Guiyang 550003, China; 3Physical Examination Center, The 2nd Hospital Affiliated With Guizhou University of Traditional Chinese Medicine, Guiyang 550003, China; 4Department of Pharmacy, Guizhou Provincial People’s Hospital, Guiyang 550002, China; 5Intellectual Property Management and Transformation Center, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510120, China.

For correspondence:-  Wukai Ma   Email: w7n3kx@163.com   Tel:+8685185556970

Accepted: 19 June 2022        Published: 31 July 2022

Citation: Ning Q, Yao X, Huang Y, Hou L, Lu D, Yang Y, et al. 3-O-Caffeoylquinic acid in Periploca forrestii Schltr extract ameliorates collagen-induced arthritis by inducing IL17/IL23 cells in rats. Trop J Pharm Res 2022; 21(7):1445-1452 doi: 10.4314/tjpr.v21i7.13

© 2022 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To study the therapeutic effect of 3-O-caffeoylquinic acid (3-O-CQA) from Periploca forrestii extract (PFE) on collagen-mediated arthritis (CIA) in rats, as well as the potential underlying mechanism of action.
Methods: PFE and 3-O-CQA were successively and intragastrically administered to CIA rats. Paw swelling, arthritic scores and H & E staining were used to evaluate the therapeutic effect of 3-O-CQA. Moreover, to determine the effects of PFE and 3-O-CQA on fibroblast-resembling synoviocytes obtained from arthritic subjects (RAFLS), the viability of RAFLS cultured in vitro was measured with MMT, while apoptotic lesions were analyzed by flow cytometry. The levels of IL-6 in CIA and RAFLS were determined by enzyme-linked immunosorbent assay (ELISA), while quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunoblotting were used to assess their mRNA and polypeptide levels, respectively.  
Results: PFE in 3-O-CQA ameliorated swelling and reduced arthritic scores in CIA rat model, and also decreased cytokine levels (p < 0.05). By decreasing mRNA and protein expressions, 3-O-CQA repressed the phosphorylation of STAT3 and JAK2 as well as the protein levels of IL-23 and RORγt (p < 0.05).
Conclusion: The results of this study show that CIA and RAFLS are ameliorated in rats by 3-O-CQA in PFE through regulation of IL17/ IL23 and Th17 cells. Thus, 3-O-CQA affords a therapeutic strategy for the management of collagen-induced arthritis.

Keywords: Arthritis, Periploca forrestii Schltr extract, 3-O-Caffeoylquinic acid, Interleukin (IL)-17, IL-23, Th17 cells

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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