## Abstract Prostaglandins (PGs) and leukotrienes (LTs) derived from arachidonic acid (AA) are potent mediators of inflammation and cell proliferation. Dietary intake of eicosapentaenoic acid (EPA) appears beneficial to both inflammatory processes and cell proliferation. However, there is no clear
The biological effects of antiadhesion agents on activated RAW264.7 macrophages
β Scribed by Habara, Toshihiro ;Nakatsuka, Mikiya ;Konishi, Hideki ;Asagiri, Kazuo ;Noguchi, Soichi ;Kudohabara, Takafumi
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 220 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0021-9304
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The objective of this study is to determine the biological effects of various antiadhesion agents on macrophages, which play an essential role in wound healing and adhesion. To determine these effects, RAW264.7 macrophages were activated with lipopolysaccharide in the presence of antiadhesion agents: oxidized regenerated cellulose (oxyC), sodium hyaluronate (HA), dexamethasone (Dex), or chondroitin sulfate (CS). The release of nitric oxide (NO), vascular endothelial growth factor (VEGF), interleukinβ6 (ILβ6), or matrix metalloproteinases (MMPs) from RAW264.7 was measured. We found that oxyC reduced the release of NO, ILβ6, MMPβ2, and MMPβ9, whereas it enhanced the release of VEGF. HA reduced the release of MMPβ2, whereas it enhanced the release of VEGF and NO. HA exhibited no significant effect on the release of ILβ6 or MMPβ9. Dex reduced the release of NO, VEGF, ILβ6, MMPβ2, and MMPβ9. CS reduced the release of VEGF, ILβ6, and MMPβ2, although it had no significant effect on the release of NO and MMPβ9. Antiadhesion agents, which have been clinically used as physical barriers, modulated the functions of macrophages. Β© 2002 Wiley Periodicals, Inc. J Biomed Mater Res 61: 628β633, 2002
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