Acute Phase Responses After Acute Liver Injury by Parital Hepatectomy in Rats As Indicators of Cytokine Release
Open Access
- 1 June 1990
- journal article
- research article
- Published by Wolters Kluwer Health in Hepatology
- Vol. 11 (6) , 923-931
- https://doi.org/10.1002/hep.1840110604
Abstract
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 backterial lipopolysaccharide translocated by acute liver injury. Time courses of fever, neutrophilia and low blood–zinc levels generally attributed to cytokines were quantified after partial (37%) 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. This complements the conclusion of this study that unspecified cytokines are released after partial hepatectomy of rats.(HEPATOLOGY 1990;11:923–931.).This publication has 63 references indexed in Scilit:
- Activation of a Cl-dependent K flux by cAMP in pig red cellsAmerican Journal of Physiology-Cell Physiology, 1989
- Tumor necrosis factor stimulates DNA synthesis in the liver of intact ratsBiochemical and Biophysical Research Communications, 1988
- Intestinal endotoxemiaGastroenterology, 1988
- Endotoxin levels measured by a chromogenic assay in portal, hepatic and peripheral venous blood in patients with cirrhosisHepatology, 1988
- Activation of polyamine biosynthetic decarboxylases during the acute phase response of rat liverBiochemical and Biophysical Research Communications, 1987
- Induction of β2-interferon by tumor necrosis factor: A homeostatic mechanism in the control of cell proliferationCell, 1986
- Essential role of polyamine metabolism in hepatic regenerationGastroenterology, 1986
- Induction of ornithine decarboxylase in the liver and spleen of mice by interleukin 1-like factors produced from a macrophage cell lineBiochimica et Biophysica Acta (BBA) - General Subjects, 1985
- Bacterial lipopolysaccharide induction of ornithine decarboxylase in the macrophage-like cell line RAW264: Requirement of an inducible soluble factorJournal of Cellular Physiology, 1985
- Ornithine decarboxylase activity and the onset of deoxyribonucleic acid synthesis in regenerating liverBiochemical Journal, 1978