Lopez-Cepero M, Friedman M, Klein T, Friedman H
J Leukoc Biol. 1986 Jun;39(6):679-86. doi: 10.1002/jlb.39.6.679.
The effects of tetrahydrocannabinol (THC) on several parameters of macrophage function in vitro were assessed. Delta 9 THC added to cultures of normal mouse peritoneal cells in vitro affected the ability of the cells to spread on glass surfaces and also had some effect on their ability to phagocytize yeast. These effects were dose related. A concentration of 20 micrograms of THC almost completely inhibited macrophage spreading, but it also decreased viability and the total number of these cells. Doses of 10 or 5 micrograms of THC also inhibited spreading but had little effect on cell viability or number. A dose of 1.0 microgram of THC had some inhibitory effect on spreading and the lowest dose affecting spreading appeared to be about 0.05 micrograms per culture. Higher doses of THC were necessary to inhibit phagocytosis of yeast particles as determined by direct microscopic examination or use of radiolabeled yeast as the test particles. These results indicate that several readily measured functions of macrophages may be suppressed by THC.
评估了四氢大麻酚(THC)对体外巨噬细胞功能若干参数的影响。体外向正常小鼠腹腔细胞培养物中添加Δ⁹ THC会影响细胞在玻璃表面铺展的能力,对其吞噬酵母的能力也有一定影响。这些影响与剂量相关。20微克THC的浓度几乎完全抑制巨噬细胞铺展,但也会降低这些细胞的活力和总数。10微克或5微克THC的剂量也会抑制铺展,但对细胞活力或数量影响较小。1.0微克THC的剂量对铺展有一定抑制作用,影响铺展的最低剂量似乎约为每培养物0.05微克。通过直接显微镜检查或使用放射性标记酵母作为测试颗粒确定,抑制酵母颗粒吞噬需要更高剂量的THC。这些结果表明,巨噬细胞的几种易于测量的功能可能会被THC抑制。