TY - JOUR
T1 - Chaenomeles Fructus (CF), the Fruit of Chaenomeles sinensis Alleviates IL‐1β Induced Cartilage Degradation in Rat Articular Chondrocytes
AU - Yeo, Changhwan
AU - Ahn, Chae Ryeong
AU - Kim, Jai Eun
AU - Kim, Young Woo
AU - Park, Jinbong
AU - Ahn, Kwang Seok
AU - Ha, In Jin
AU - Lee, Yoon Jae
AU - Baek, Seung Ho
AU - Ha, In Hyuk
N1 - Funding Information:
Funding: This work was supported by the Dongguk University Research Program and National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (NRF‐ 2020R1I1A3063625).
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Osteoarthritis (OA) causes persistent pain, joint dysfunction, and physical disability. It is the most prevalent type of degenerative arthritis, affecting millions of people worldwide. OA is currently treated with a focus on pain relief, inflammation control, and artificial joint surgery. Hence, a therapeutic agent capable of preventing or delaying the progression of OA is needed. OA is strongly associated with the degeneration of the articular cartilage and changes in the ECM, which are primarily associated with a decrease in proteoglycan and collagen. In the progress of articular cartilage degradation, catabolic enzymes, such as matrix metalloproteinases (MMPs), are activated by IL‐1β stimulation. Given the tight relationship between IL‐1β and ECM (extra‐cellular matrix) degradation, this study examined the effects of Chaenomeles Fructus (CF) on IL‐1β‐induced OA in rat chondrocytes. The CF treatment reduced IL‐1β‐induced MMP3/13 and ADAMTS‐5 production at the mRNA and protein levels. Similarly, CF enhanced col2a and aggrecan accumulation and chondrocyte proliferation. CF inhibited NF‐κB (nuclear factor kappa B) activation, nuclear translocation induced by IL‐1β, reactive oxygen species (ROS) production, and ERK phosphorylation. CF demonstrated anti‐OA and articular regeneration effects on rat chondrocytes, thus, suggesting that CF is a viable and fundamental therapeutic option for OA.
AB - Osteoarthritis (OA) causes persistent pain, joint dysfunction, and physical disability. It is the most prevalent type of degenerative arthritis, affecting millions of people worldwide. OA is currently treated with a focus on pain relief, inflammation control, and artificial joint surgery. Hence, a therapeutic agent capable of preventing or delaying the progression of OA is needed. OA is strongly associated with the degeneration of the articular cartilage and changes in the ECM, which are primarily associated with a decrease in proteoglycan and collagen. In the progress of articular cartilage degradation, catabolic enzymes, such as matrix metalloproteinases (MMPs), are activated by IL‐1β stimulation. Given the tight relationship between IL‐1β and ECM (extra‐cellular matrix) degradation, this study examined the effects of Chaenomeles Fructus (CF) on IL‐1β‐induced OA in rat chondrocytes. The CF treatment reduced IL‐1β‐induced MMP3/13 and ADAMTS‐5 production at the mRNA and protein levels. Similarly, CF enhanced col2a and aggrecan accumulation and chondrocyte proliferation. CF inhibited NF‐κB (nuclear factor kappa B) activation, nuclear translocation induced by IL‐1β, reactive oxygen species (ROS) production, and ERK phosphorylation. CF demonstrated anti‐OA and articular regeneration effects on rat chondrocytes, thus, suggesting that CF is a viable and fundamental therapeutic option for OA.
KW - Chaenomeles Fructus
KW - Chaenomeles sinensis
KW - cartilage degradation
KW - natural product
KW - osteoarthritis
UR - http://www.scopus.com/inward/record.url?scp=85128113674&partnerID=8YFLogxK
U2 - 10.3390/ijms23084360
DO - 10.3390/ijms23084360
M3 - Article
C2 - 35457176
AN - SCOPUS:85128113674
VL - 23
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
SN - 1661-6596
IS - 8
M1 - 4360
ER -