Potential of Pseudoshikonin I Isolated from Lithospermi Radix as Inhibitors of MMPs in IL-1β-Induced SW1353 Cells

Autor: Je Hun Choi, Young-Seob Lee, Jong-Gil Choi, Ye-Joo Lee, Geum-Soog Kim, Dae Young Lee, Soo-Im Choi, Se Hee Han, Seung Eun Lee
Jazyk: angličtina
Rok vydání: 2016
Předmět:
0301 basic medicine
Matrix Metalloproteinase 3
Magnetic Resonance Spectroscopy
Cell Survival
nuclear magnetic resonance (NMR)
Matrix metalloproteinase inhibitor
Chemical structure
Interleukin-1beta
Matrix Metalloproteinase Inhibitors
DEPT
Matrix metalloproteinase
Lithospermi radix
pseudoshikonin I
matrix-metalloproteinase (MMPs)
Article
Catalysis
lcsh:Chemistry
Inorganic Chemistry
03 medical and health sciences
Cell Line
Tumor

Matrix Metalloproteinase 13
Humans
Physical and Theoretical Chemistry
lcsh:QH301-705.5
Molecular Biology
Spectroscopy
Tissue Inhibitor of Metalloproteinase-2
Chromatography
Molecular Structure
Chemistry
Lithospermum
Organic Chemistry
Interleukin
General Medicine
Nuclear magnetic resonance spectroscopy
Matrix Metalloproteinases
Computer Science Applications
030104 developmental biology
lcsh:Biology (General)
lcsh:QD1-999
Matrix Metalloproteinase 9
Biochemistry
Cell culture
Matrix Metalloproteinase 1
Zdroj: International Journal of Molecular Sciences; Volume 17; Issue 8; Pages: 1350
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES(17): 8
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 17, Iss 8, p 1350 (2016)
ISSN: 1422-0067
DOI: 10.3390/ijms17081350
Popis: Pseudoshikonin I, the new bioactive constituent of Lithospermi radix, was isolated from this methanol extract by employing reverse-phase medium-pressure liquid chromatography (MPLC) using acetonitrile/water solvent system as eluents. The chemical structure was determined based on spectroscopic techniques, including 1D NMR (H-1, C-13, DEPT), 2D NMR (gCOSY, gHMBC, gHMQC), and QTOF/MS data. In this study, we demonstrated the effect of pseudoshikonin I on matrix-metalloproteinase (MMPs) activation and expression in interleukin (IL)-1 beta-induced SW1353 chondrosarcoma cells. MMPs are considered important for the maintenance of the extracellular matrix. Following treatment with PS, active MMP-1, -2, -3, -9, -13 and TIMP-2 were quantified in the SW1353 cell culture supernatants using a commercially available ELISA kit. The mRNA expression of MMPs in SW1353 cells was measured by RT-PCR. Pseudoshikonin I treatment effectively protected the activation on all tested MMPs in a dose-dependent manner. TIMP-2 mRNA expression was significantly upregulated by pseudoshikonin I treatment. Overall, we elucidated the inhibitory effect of pseudoshikonin on MMPs, and we suggest its use as a potential novel anti-osteoarthritis agent.
Databáze: OpenAIRE