4.6 Article

Psoralen downregulates osteoarthritis chondrocyte inflammation via an estrogen-like effect and attenuates osteoarthritis

期刊

AGING-US
卷 14, 期 16, 页码 6716-6726

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/aging.204245

关键词

psoralen; estrogen receptor; estrogen-like effects; osteoarthritis

资金

  1. Natural Science Foundation of Hubei Province [2020CFB687]

向作者/读者索取更多资源

This study confirmed the inhibitory effect of psoralen on osteoarthritis (OA) through estrogen-like activity. Psoralen showed similar effects to estrogen, promoting the expression of estrogen target genes and reducing the expression of inflammation-related genes in chondrocytes. Animal experiments demonstrated that psoralen attenuated cartilage tissue destruction, improved subchondral bone mineral density, and decreased OA severity.
Estrogen and its receptor play a positive role in the development of osteoarthritis (OA). Psoralen is a plant-derived estrogen analog. This study aimed to verify whether psoralen inhibits OA through an estrogen-like effect. First, human primary chondrocytes in the late stage of OA were extracted to complete collagen type II immunofluorescence staining and cell proliferation experiments. Subsequently, estrogen, psoralen and estrogen receptor antagonists were co-cultured with OA chondrocytes, and RT-PCR was performed to detect the gene expression. A rabbit OA model was subsequently made by anterior cruciate ligament transection (ACLT). They were set as Sham group, OA group and Psoralen group, respectively. The articular cartilage samples were taken after 5 weeks of treatment, and the effect was observed by gross observation, histological staining, micro-CT scanning of subchondral bone. The results of cellular experiments displayed that the cultured cells were positive for collagen II fluorescence staining and 12 mu g/mL psoralen was selected as the optimal concentration. In addition, psoralen had effects similar to estrogen, promoting the expression of estrogen tar-get genes CTSD, PGR and TFF1 and decreasing the expression of the inflammation-related gene TNF-alpha, IL-1 beta and IL-6. The effect of psoralen was blocked after the use of an estrogen receptor antagonist. Further animal experiments indicated that the psoralen group showed less destruction of cartilage tissue and decreased OASRI scores compared with the OA group. A subchondral bone CT scan demonstrated that psoralen significantly increased subchondral bone mineral density (BMD), trabecular thickness and trabecular number and decreased trabecular separation. In summary, psoralen inhibits the inflammatory production of chondrocytes, which is related to estrogen-like effect, and can be used to attenuate the progression of OA.

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