Suzuki Y, Yamaguchi T
Shiseido Pharmaceutical Research Laboratories, Yokohama, Japan.
Agents Actions. 1993 Jan;38(1-2):32-7. doi: 10.1007/BF02027210.
The effects of hyaluronic acid (HA) on macrophage function, in terms of the phagocytosis of latex beads and superoxide anion and hydrogen peroxide release stimulated by phorbol myristate acetate (PMA), were studied in guinea-pig peritoneal macrophages. Phagocytosis was inhibited in a dose- and molecular-weight-dependent manner by HA. The addition of PMA to the culture, at a dose of more than 10 ng ml-1, caused an increase in the release of active oxygens. The release of active oxygens was inhibited by high molecular weight HA (MW 2.02 x 10(6), HA-202) in a dose-dependent manner. In cell-free systems, HA-202 had a negligible effect in scavenging these active oxygens. Of the three molecular sizes of HA (MW: 0.28 x 10(6), 0.98 x 10(6) and 2.02 x 10(6)), HA-202 most strongly inhibited the active oxygen release. These results indicate that high-molecular-weight HA acts directly on macrophages to inhibit phagocytosis and active oxygen formation, which, in turn, ameliorates the progression of chronic inflammation.
在豚鼠腹腔巨噬细胞中,研究了透明质酸(HA)对巨噬细胞功能的影响,包括对乳胶珠的吞噬作用以及佛波酯(PMA)刺激下超氧阴离子和过氧化氢的释放。HA以剂量和分子量依赖性方式抑制吞噬作用。向培养物中添加剂量超过10 ng/ml的PMA会导致活性氧释放增加。高分子量HA(MW 2.02 x 10(6),HA - 202)以剂量依赖性方式抑制活性氧的释放。在无细胞系统中,HA - 202清除这些活性氧的作用可忽略不计。在HA的三种分子大小(MW:0.28 x 10(6)、0.98 x 10(6)和2.02 x 10(6))中,HA - 202对活性氧释放的抑制作用最强。这些结果表明,高分子量HA直接作用于巨噬细胞,抑制吞噬作用和活性氧的形成,进而改善慢性炎症的进展。