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Baicalein inhibits IL-1ß-induced extracellular matrix degradation with decreased MCP-1 expression in primary rat chondrocytes.
Cho, InA; Chung, Ki-Ho; Kim, Young; Choi, Choong-Ho; Koh, Jeong-Tae.
Afiliación
  • Cho I; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186 Republic of Korea.
  • Chung KH; Hard-Tissue Biointerface Research Center, School of Dentistry, Chonnam National University, Gwangju, 61186 Republic of Korea.
  • Kim Y; Department of Preventive and Public Health Dentistry, School of Dentistry, Chonnam National University, Gwangju, 61186 Republic of Korea.
  • Choi CH; Hard-Tissue Biointerface Research Center, School of Dentistry, Chonnam National University, Gwangju, 61186 Republic of Korea.
  • Koh JT; Department of Oral Pathology, School of Dentistry, Chonnam National University, Gwangju, 61186 Republic of Korea.
Toxicol Res ; 40(2): 237-246, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38525128
ABSTRACT
Baicalein is a flavonoid extracted from the roots of Scutellaria baicalensis and Scutellaria lateriflora. This compound exerts various biochemical activities, including antioxidant and anti-inflammatory effects. The study aimed to investigate the effect of baicalein on articular cartilage cells and elucidate its underlying mechanism. In primary rat chondrocyte cultures, treatment with baicalein demonstrated a reduction in the loss of proteoglycan and extracellular matrix degradation induced by interleukin (IL)-1ß. Baicalein suppressed IL-1ß-induced catabolic responses, including the expression and activation of matrix metalloproteinase (MMP)-13, MMP-3, and MMP-1. In addition, baicalein effectively reduced nitric oxide and prostaglandin E2 production, and it downregulated the expression of inducible nitric oxide synthase and cyclooxygenase-2 in primary rat chondrocytes. Furthermore, baicalein downregulated IL-1ß-induced inflammatory chemokines and cytokines, such as GM-CSF and MCP-1. These findings suggest that baicalein could potentially mitigate the catabolic responses of IL-1ß in chondrocytes, making it a promising candidate for both the prevention and treatment of osteoarthritis. Supplementary Information The online version contains supplementary material available at 10.1007/s43188-024-00225-4.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Toxicol Res Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Toxicol Res Año: 2024 Tipo del documento: Article
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