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Zinc tetrakis(N-methyl-4′-pyridyl) porphyrinato is an effective inhibitor of stimulant-induced activation of RAW 264.7 cells

Title
Zinc tetrakis(N-methyl-4′-pyridyl) porphyrinato is an effective inhibitor of stimulant-induced activation of RAW 264.7 cells
Authors
Kang J.L.Pack I.S.Hong S.M.Lee H.S.Hah J.S.Nam W.Leonard S.Castranova V.
Ewha Authors
남원우하종식이지희
SCOPUS Author ID
남원우scopus; 하종식scopus; 이지희scopus
Issue Date
2001
Journal Title
Toxicology and Applied Pharmacology
ISSN
0041-008XJCR Link
Citation
vol. 172, no. 2, pp. 140 - 149
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
One proposed mechanism for the development of silica-induced fibrosis is prolonged pulmonary inflammation and lung damage resulting from the secretion of reactive mediators from alveolar macrophages. Metalloporphyrins have antioxidative and antiinflammatory activities. However, the molecular basis for the antiinflammatory action of zinc tetrakis(N-methyl-4′-pyridyl) porphyrinato (ZnTMPyP) has not been elucidated. The objective of this study was to determine whether ZnTMPyP exhibited the ability to inhibit the production of reactive oxygen species (ROS), the activation of NF-κB, or the secretion of IL-1 in RAW 264.7 cells, and whether such inhibitory activity was related to the ROS-scavenging ability of ZnTMPyP. The results indicate that, although ZnT-MPyP is not cytotoxic to RAW 264.7 cells, it is a potent inhibitor in ROS production by RAW 264.7 cells in response to various stimulants, such as silica, zymosan, or phorbol myristate acetate. ZnTMPyP is also effective in reducing stimulant-induced DNA-binding activity of NF-κB and silica-induced tyrosine phosphorylation of IκB-α. ZnTMPyP also inhibits LPS-induced IL-1 production. However, ZnTMPyP exhibits relatively weak ability to directly scavenge hyroxyl or superoxide radicals. On the basis of effective concentrations of ZnTMPyP, these results suggest that ZnTMPyP directly acts as an inhibitor of cellular activation in addition to exhibiting an antioxidant effect. Therefore, it is suggested that further studies concerning the effects of ZnTMPyP using in vivo oxidative stress models or its effects on the cytotoxic process of human diseases associated with lung inflammation and injury are warranted. In addition, ZnTMPyP may be a useful tool to investigate the molecular mechanisms involved in stimulant-induced signal pathways. © 2001 Academic Press.
DOI
10.1006/taap.2001.9144
Appears in Collections:
자연과학대학 > 화학·나노과학전공 > Journal papers
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