Cornell R P
Division of Science, Northeast Missouri State University, Kirksville 63501.
Hepatology. 1990 Jun;11(6):923-31. doi: 10.1002/hep.1840110604.
The purpose of this study was to support the hypothesis that cytokines such as interleukin-1, tumor necrosis factor and interleukin-6 are released by macrophages or monocytes within 1 to 2 hr of phagocytosis of circulating, gut-derived bacterial lipopolysaccharide translocated by acute liver injury. Time courses of fever, neutrophilia and low blood-zinc levels generally attributed to cytokines were quantified after partial (67%) hepatectomy of rats under ether anesthesia. These acute phase responses in hepatectomized rats were compared with those after intravenous injection of exogenous endotoxin and human natural interleukin-1. Fever commenced 30 min after interleukin-1 injection, 4 hr after exogenous lipopolysaccharide injection and 6 hr after 67% liver resection. Similarly, rectal temperatures were significantly elevated in recipient rats 30 min after intravenous administration of donor plasma from hepatectomized animals, indicating that cytokines, not lipopolysaccharide, elicited the febrile response. Neutrophilia was present 1, 2, and 4 hr after interleukin-1 injection, lipopolysaccharide injection and hepatectomy, respectively. Furthermore, the reduction in plasma zinc, which depends on cellular metallothionein synthesis, occurred 4 hr after interleukin-1 administration and 6 hr after lipopolysaccharide injection or partial hepatectomy. Donor plasma from hepatectomized rats also elicited neutrophilia at 1 hr and low blood-zinc levels 4 hr after injection in recipient animals. The timing of these responses, just as for the fever, implies that cytokines and not lipopolysaccharide in the donated plasma elicited the neutrophilia and hypozincemia. Evidence was reviewed that interleukin-1, tumor necrosis factor and interleukin-6 function as hepatotrophic factors and have been identified in the circulation of humans with liver damage.(ABSTRACT TRUNCATED AT 250 WORDS)
诸如白细胞介素-1、肿瘤坏死因子和白细胞介素-6等细胞因子是由巨噬细胞或单核细胞在吞噬循环中、肠道来源的、因急性肝损伤而移位的细菌脂多糖后1至2小时内释放的。在乙醚麻醉下对大鼠进行部分(67%)肝切除术后,对通常归因于细胞因子的发热、中性粒细胞增多和低血锌水平的时间进程进行了量化。将肝切除大鼠的这些急性期反应与静脉注射外源性内毒素和人天然白细胞介素-1后的反应进行了比较。白细胞介素-1注射后30分钟开始发热,外源性脂多糖注射后4小时发热,67%肝切除后6小时发热。同样,在静脉注射来自肝切除动物的供体血浆30分钟后,受体大鼠的直肠温度显著升高,表明引起发热反应的是细胞因子而非脂多糖。白细胞介素-1注射后1小时、脂多糖注射后2小时和肝切除后4小时出现中性粒细胞增多。此外,依赖细胞金属硫蛋白合成的血浆锌减少分别在白细胞介素-1给药后4小时、脂多糖注射后6小时或部分肝切除后6小时出现。肝切除大鼠的供体血浆在受体动物注射后1小时也引起中性粒细胞增多,4小时后引起低血锌水平。这些反应的时间,就像发热一样,意味着供体血浆中的细胞因子而非脂多糖引起了中性粒细胞增多和低锌血症。有证据表明白细胞介素-1、肿瘤坏死因子和白细胞介素-6作为肝营养因子发挥作用,并且已在肝损伤患者的循环中被鉴定出来。(摘要截断于250字)