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肿瘤坏死因子、白细胞介素-1以及这两种细胞因子的组合对叙利亚仓鼠胆固醇代谢的影响。

Effects of TNF, IL-1, and the combination of both cytokines on cholesterol metabolism in Syrian hamsters.

作者信息

Hardardóttir I, Moser A H, Memon R, Grünfeld C, Feingold K R

机构信息

Department of Medicine, University of California San Francisco UCSF.

出版信息

Lymphokine Cytokine Res. 1994 Jun;13(3):161-6.

PMID:7948424
Abstract

Infection and inflammation are associated with alterations in lipid metabolism that may be mediated by cytokines such as TNF and IL-1. This study determined the effects of TNF and IL-1 on certain aspects of cholesterol metabolism. TNF or IL-1 administration to Syrian hamsters increased serum cholesterol levels by 17 and 21%, respectively, and decreased HDL cholesterol levels by 20 and 15%, respectively. TNF + IL-1 increased serum cholesterol levels by 58% and decreased HDL cholesterol levels by 58%. TNF or IL-1 increased hepatic HMG CoA reductase mRNA levels by 3.5- and 3-fold, respectively. TNF + IL-1 increased HMG CoA reductase mRNA levels by 7-fold. IL-1 increased hepatic LDL receptor mRNA levels by 2-fold while TNF and a combination of TNF + IL-1 had minimal effects. TNF or IL-1 did not affect hepatic apo E or apo A-I mRNA levels while a combination of TNF + IL-1 decreased both mRNA levels by 50%. Our results demonstrate that TNF and IL-1 similarly affect the parameters of cholesterol metabolism studied. Furthermore, the combination of TNF + IL-1 was, in most cases, more effective than either cytokine alone, and reproduced many of the effects of LPS.

摘要

感染和炎症与脂质代谢改变相关,这种改变可能由细胞因子如肿瘤坏死因子(TNF)和白细胞介素 -1(IL -1)介导。本研究确定了TNF和IL -1对胆固醇代谢某些方面的影响。给叙利亚仓鼠注射TNF或IL -1后,血清胆固醇水平分别升高了17%和21%,高密度脂蛋白胆固醇(HDL胆固醇)水平分别降低了20%和15%。TNF + IL -1使血清胆固醇水平升高了58%,HDL胆固醇水平降低了58%。TNF或IL -1分别使肝脏3 -羟基 -3 -甲基戊二酰辅酶A(HMG CoA)还原酶mRNA水平升高了3.5倍和3倍。TNF + IL -1使HMG CoA还原酶mRNA水平升高了7倍。IL -1使肝脏低密度脂蛋白受体(LDL受体)mRNA水平升高了2倍,而TNF以及TNF + IL -1组合的影响极小。TNF或IL -1不影响肝脏载脂蛋白E(apo E)或载脂蛋白A -I(apo A -I)mRNA水平,而TNF + IL -1组合使两种mRNA水平均降低了50%。我们的结果表明,TNF和IL -1对所研究的胆固醇代谢参数有相似影响。此外,在大多数情况下,TNF + IL -1组合比单独使用任何一种细胞因子更有效,并且重现了脂多糖(LPS)的许多作用。

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