Secretion of tumor necrosis factor by endotoxin-treated equine mammary exudate macrophages: effect of dexamethasone and pentoxifylline.

The Cornell veterinarian Pub Date : 1992-10-01
S B Milam, R J Mackay, L A Skelley
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Abstract

Secretion of tumor necrosis factor (TNF) by equine mammary exudate macrophages (MEM phi) exposed to bacterial lipopolysaccharide (LPS) was dose-dependent and was maximal (216.5 +/- 51.9 U/ml) at 100 micrograms LPS/ml, the highest concentration tested. All concentrations of dexamethasone tested (10(-8) to 10(-4) M) significantly (P less than or equal to 0.05) inhibited TNF production by MEM phi when the agent was added 1 hour before LPS. Pretreatment with pentoxifylline at concentrations greater than 3 micrograms/ml also significantly (P less than or equal to 0.05) reduced secretion of TNF by MEM phi. The inhibitory effect of dexamethasone (10(-4) M) was observed when the agent was added to MEM phi from 30 minutes before until 4 hours after LPS. Pentoxifylline (100 micrograms/ml) significantly (P less than or equal to 0.05) suppressed TNF when added from 2 hours before until 2 hours after LPS; however, when pentoxifylline addition was delayed until 8 hours post-LPS, TNF production was enhanced. These apparent inhibitory effects of dexamethasone and pentoxifylline were not due to reduced macrophage viability or to interfering effects of the agents at the level of the TNF bioassay.

内毒素处理的马乳腺渗出巨噬细胞分泌肿瘤坏死因子:地塞米松和己酮茶碱的影响。
马乳腺渗出性巨噬细胞(MEM phi)在细菌脂多糖(LPS)作用下分泌肿瘤坏死因子(TNF)呈剂量依赖性,在100微克LPS/ml时达到最大值(216.5 +/- 51.9 U/ml)。所有地塞米松浓度(10(-8)至10(-4)M)均显著(P <或等于0.05)在LPS前1小时加入地塞米松,通过MEM phi抑制TNF生成。预处理浓度大于3微克/毫升的己酮茶碱也显著(P小于或等于0.05)降低MEM phi分泌TNF。地塞米松(10(-4)M)于LPS前30分钟至LPS后4小时加入MEM phi,观察其抑制作用。自LPS前2小时至LPS后2小时,添加己酮茶碱(100微克/ml)显著(P小于或等于0.05)抑制TNF;然而,当己酮茶碱添加延迟至lps后8小时时,TNF的产生增强。地塞米松和己酮茶碱的这些明显抑制作用不是由于巨噬细胞活力降低或药物在TNF生物测定水平上的干扰作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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