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Regulation of CP-25 on P-glycoprotein in synoviocytes of rats with adjuvant arthritis.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2019 Nov; Vol. 119, pp. 109432. Date of Electronic Publication: 2019 Sep 12. - Publication Year :
- 2019
-
Abstract
- Objective: Methotrexate (MTX) is a commonly used drug for the treatment of rheumatoid arthritis (RA) and it has been studied in RA resistance recently. P-glycoprotein (P-gp) is one of the important transporters that mediate MTX resistance. This study investigated the effect of Paeoniflorin-6'-O-benzene sulfonate (code: CP-25) in the resistance of P-gp-mediated MTX to RA.<br />Methods: Adjuvant arthritis (AA) was induced in rats via complete Freund's adjuvant. The experimental groups were divided into normal group; AA model group; monotherapy groups, including CP-25, MTX and dexamethasone; and CP-25 combined with MTX group. The expression of P-gp in synovial tissue was measured by western blot and histochemistry. Besides, P-gp high expression of human hepatoma cell line Bel7402/5-FU and Bel7402 were chose to study in MTX resistance and the function of P-gp was detected by Flow cytometry.<br />Results: CP-25 had a good therapeutic effect on AA rats, significantly improved manifestations and reduced the expression of P-gp in synovial tissue, spleen medulla and small intestinal epithelial cells in the apical tissues of AA rats. In addition, CP-25 significantly inhibited the up-regulation of P-gp induced by TNF-α stimulation in synoviocytes. Furthermore, according to the accumulation and efflux of rhodamine 123 in Bel7402/5-FU resistant cells and Bel7402 sensitive cells, CP-25 could reverse the resistance of MTX in Bel7402/5-FU cells compared with Bel7402 cells, which was reflected by the reduced IC50 values of MTX. Further study indicated that CP-25 could decrease P-gp expression and inhibit P-gp function in Bel7402/5-FU cells.<br />Conclusion: CP-25 regulates the expression of P-gp and inhibits the function of P-gp, thereby improving the resistance of MTX.<br /> (Copyright © 2019 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
- Subjects :
- Animals
Arthritis, Experimental pathology
Cell Line, Tumor
Drug Resistance drug effects
Glucosides pharmacology
Inflammation drug therapy
Inflammation pathology
Intestine, Small drug effects
Intestine, Small pathology
Joints drug effects
Joints pathology
Male
Methotrexate pharmacology
Methotrexate therapeutic use
Monoterpenes pharmacology
Rats, Sprague-Dawley
Rhodamine 123 metabolism
Spleen drug effects
Spleen pathology
Synoviocytes drug effects
Synoviocytes pathology
Tumor Necrosis Factor-alpha pharmacology
ATP Binding Cassette Transporter, Subfamily B, Member 1 metabolism
Arthritis, Experimental drug therapy
Arthritis, Experimental metabolism
Glucosides therapeutic use
Monoterpenes therapeutic use
Synoviocytes metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 119
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 31521892
- Full Text :
- https://doi.org/10.1016/j.biopha.2019.109432