Morris D D, Henry M M, Moore J N, Fischer J K
Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens 30602.
Am J Vet Res. 1991 Apr;52(4):528-32.
A study was conducted to determine whether dietary supplements with alpha-linolenic acid altered the ability of equine peritoneal macrophages to produce tumor necrosis factor (TNF) in response to endotoxin. Peritoneal macrophages were harvested from 6 healthy adult horses before and after the horses were fed a nutritionally balanced ration that contained 8% linseed oil as a source of alpha-linolenic acid. The macrophages were cultured in media containing no additives (control), endotoxin (0.5 to 50 ng/ml), or the calcium ionophore, A23187. Macrophage supernatants were collected after 6 and 24 hours' incubation and stored at -70 C. Tumor necrosis factor activity was estimated by a modified in vitro cytotoxicity bioassay, using the murine fibrosarcoma cell line, WEHI 164 clone 13. The TNF activity after 6 and 24 hours' incubation was greater in culture media of macrophages exposed to endotoxin than in media from control macrophages. For macrophages cultured in media that contained endotoxin, neither the concentration of endotoxin nor incubation time had any effect on TNF activity. Endotoxin-induced macrophage production of TNF, as determined by measurement of TNF activity, was significantly less after horses were fed the alpha-linolenic acid-rich ration for 8 weeks.
进行了一项研究,以确定补充富含α-亚麻酸的膳食是否会改变马腹膜巨噬细胞对内毒素产生肿瘤坏死因子(TNF)的能力。从6匹健康成年马身上采集腹膜巨噬细胞,在马饲喂含有8%亚麻籽油作为α-亚麻酸来源的营养均衡日粮之前和之后进行采集。将巨噬细胞培养在不含添加剂(对照)、内毒素(0.5至50 ng/ml)或钙离子载体A23187的培养基中。孵育6小时和24小时后收集巨噬细胞上清液,并储存在-70℃。使用鼠纤维肉瘤细胞系WEHI 164克隆13,通过改良的体外细胞毒性生物测定法估计肿瘤坏死因子活性。暴露于内毒素的巨噬细胞培养基中孵育6小时和24小时后的TNF活性高于对照巨噬细胞培养基中的活性。对于在内毒素培养基中培养的巨噬细胞,内毒素浓度和孵育时间对TNF活性均无影响。通过测量TNF活性确定,在马饲喂富含α-亚麻酸的日粮8周后,内毒素诱导的巨噬细胞产生TNF的量显著减少。