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Effect of endotoxin on cholesterol biosynthesis and distribution in serum lipoproteins in Syrian hamsters

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dc.contributor Landspitali - The National University Hospital of Iceland
dc.contributor.author Feingold, Kenneth R.
dc.contributor.author Harðardóttir, Ingibjörg
dc.contributor.author Memon, Riedel
dc.contributor.author Krul, E. J.T.
dc.contributor.author Moser, A. H.
dc.contributor.author Taylor, J. M.
dc.contributor.author Grunfeld, Carl
dc.date.accessioned 2022-11-22T01:04:15Z
dc.date.available 2022-11-22T01:04:15Z
dc.date.issued 1993
dc.identifier.citation Feingold , K R , Harðardóttir , I , Memon , R , Krul , E J T , Moser , A H , Taylor , J M & Grunfeld , C 1993 , ' Effect of endotoxin on cholesterol biosynthesis and distribution in serum lipoproteins in Syrian hamsters ' , Journal of Lipid Research , vol. 34 , no. 12 , pp. 2147-2158 . https://doi.org/10.1016/S0022-2275(20)35355-4
dc.identifier.issn 0022-2275
dc.identifier.other 59938267
dc.identifier.other afafa1a6-9086-4ef6-ab18-704a3c945e0c
dc.identifier.other 0027135157
dc.identifier.other 8301233
dc.identifier.uri https://hdl.handle.net/20.500.11815/3625
dc.description.abstract Infection and inflammation increase serum triglyceride and cholesterol levels in rodents and rabbits. Endotoxin (LPS) has been used as a model of infection and its effects on triglyceride metabolism have been previously characterized. In the present study we demonstrate that both low (100 ng/100 g body weight) and high dose (100 μg/100 g body weight) LPS increase serum cholesterol levels in hamsters. The increase in serum cholesterol is first observed 16 h after LPS and persists for at least 24 h. This increase is primarily due to an increase in low density lipoprotein (LDL) cholesterol. High density lipoprotein (HDL) cholesterol levels decrease after LPS treatment. Both low and high dose LPS increase hepatic cholesterol synthesis (low dose 85%, high dose 205%) and total HMG-CoA reductase activity (low dose 2.97-fold, high dose 9.96-fold). However, the proportion of HMG-CoA reductase in the active form is reduced by LPS treatment. Additionally, the mass of HMG-CoA reductase protein in the liver, measured by Western blotting, is increased after LPS. Moreover, LPS increases hepatic HMG-CoA reductase mRNA levels (low dose 3.1-fold, high dose 14.2-fold). The increase in hepatic HMG- CoA reductase mRNA levels is first seen 4 h after LPS and persists for at least 24 h. In contrast, LPS had only minimal effects on hepatic LDL receptor protein and mRNA levels. These results suggest that LPS increases serum cholesterol levels by increasing hepatic cholesterol synthesis. LPS administration decreases apoE mRNA levels in the liver while having no effect on apoA-I mRNA levels. These results suggest that HMG-CoA reductase is a member of a group of hepatic proteins that are positively regulated by inflammatory stimuli (acute phase proteins) while apoE can be considered a negative acute phase protein in hamsters. It is possible that increases in hepatic HMG-CoA reductase provide cholesterol that allows for the increased production of lipoproteins and elevations in serum lipid levels that may be beneficial to the body's host defense.
dc.format.extent 12
dc.format.extent 1472501
dc.format.extent 2147-2158
dc.language.iso en
dc.relation.ispartofseries Journal of Lipid Research; 34(12)
dc.rights info:eu-repo/semantics/openAccess
dc.subject acute phase response
dc.subject apoA-I
dc.subject apoE
dc.subject HMG-CoA reductase
dc.subject LDL receptor
dc.subject Biochemistry
dc.subject Endocrinology
dc.subject Cell Biology
dc.title Effect of endotoxin on cholesterol biosynthesis and distribution in serum lipoproteins in Syrian hamsters
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1016/S0022-2275(20)35355-4
dc.relation.url http://www.scopus.com/inward/record.url?scp=0027135157&partnerID=8YFLogxK
dc.contributor.department Clinical Laboratory Services, Diagnostics and Blood Bank
dc.contributor.department Faculty of Medicine


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