TY - JOUR
T1 - Piperine ameliorates oxidative stress, inflammation and histological outcome in collagen induced arthritis
AU - Umar, Sadiq
AU - Golam Sarwar, Abu Hasnath Md
AU - Umar, Khalid
AU - Ahmad, Niyaz
AU - Sajad, Mir
AU - Ahmad, Sayeed
AU - Katiyar, Chandra Kant
AU - Khan, Haider A.
N1 - Funding Information:
Author is grateful to Indian Council of Medical Research, Government of India for providing the financial support in the form of Research Associateship (RA).
PY - 2013/7
Y1 - 2013/7
N2 - Objectives: Piperine, a main component of Piper species, is a plant alkaloid with a long history of medical use in a variety of inflammatory disorders like rheumatoid arthritis. Due to side effects in current treatment modalities of rheumatoid arthritis, the interest in alternative, well tolerated anti-inflammatory remedies has re-emerged. The aim of this work was to evaluate the anti-inflammatory and antiarthritic effects of piperine. Methods: Arthritis was induced in male Wistar rats by collagen induced arthritis (CIA) method. Piperine was administered at a dose of 100mgkg-1 and indomethacin at 1mgkg-1 body weight once daily for 21days. The effects of treatment in the rats were assessed by biochemical (articular elastase, MPO, LPO, GSH, Catalase, SOD and NO), inflammatory mediators (IL-1β, TNF-α, IL-10 and PGE2) and histological studies in joints. Results: Piperine was effective in bringing significant changes on all the parameters (articular elastase, MPO, LPO, GSH, Catalase, SOD and NO) studied. Oral administration of piperine resulted in significantly reduced the levels of pro-inflammatory mediators (IL-1β, TNF-α and PGE2) and increased level of IL-10. The protective effects of piperine against RA were also evident from the decrease in arthritis scoring and bone histology. Conclusions: In conclusion, the fact that piperine alter a number of factors known to be involved in RA pathogenesis indicates that piperine can be used similar to indomethacin as a safe and effective therapy for CIA and may be useful in the treatment of rheumatoid arthritis.
AB - Objectives: Piperine, a main component of Piper species, is a plant alkaloid with a long history of medical use in a variety of inflammatory disorders like rheumatoid arthritis. Due to side effects in current treatment modalities of rheumatoid arthritis, the interest in alternative, well tolerated anti-inflammatory remedies has re-emerged. The aim of this work was to evaluate the anti-inflammatory and antiarthritic effects of piperine. Methods: Arthritis was induced in male Wistar rats by collagen induced arthritis (CIA) method. Piperine was administered at a dose of 100mgkg-1 and indomethacin at 1mgkg-1 body weight once daily for 21days. The effects of treatment in the rats were assessed by biochemical (articular elastase, MPO, LPO, GSH, Catalase, SOD and NO), inflammatory mediators (IL-1β, TNF-α, IL-10 and PGE2) and histological studies in joints. Results: Piperine was effective in bringing significant changes on all the parameters (articular elastase, MPO, LPO, GSH, Catalase, SOD and NO) studied. Oral administration of piperine resulted in significantly reduced the levels of pro-inflammatory mediators (IL-1β, TNF-α and PGE2) and increased level of IL-10. The protective effects of piperine against RA were also evident from the decrease in arthritis scoring and bone histology. Conclusions: In conclusion, the fact that piperine alter a number of factors known to be involved in RA pathogenesis indicates that piperine can be used similar to indomethacin as a safe and effective therapy for CIA and may be useful in the treatment of rheumatoid arthritis.
KW - Articular elastase
KW - Collagen induced arthritis
KW - Cytokines
KW - Myeloperoxidase
KW - PGE
KW - Piperine
UR - https://www.scopus.com/pages/publications/84881219770
UR - https://www.scopus.com/inward/citedby.url?scp=84881219770&partnerID=8YFLogxK
U2 - 10.1016/j.cellimm.2013.07.004
DO - 10.1016/j.cellimm.2013.07.004
M3 - Article
C2 - 23921080
AN - SCOPUS:84881219770
SN - 0008-8749
VL - 284
SP - 51
EP - 59
JO - Cellular Immunology
JF - Cellular Immunology
IS - 1-2
ER -