Testing of serum atherogenicity in cell cultures: questionable data published

In a large series of studies was reported that culturing of smooth muscle cells with serum from atherosclerosis patients caused intracellular lipid accumulation, while serum from healthy controls had no such effect. Cultures were used for evaluation of antiatherogenic drugs. Numerous substances were...

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Main Author: Sergei V. Jargin
Format: Article
Language:deu
Published: German Medical Science GMS Publishing House 2012-01-01
Series:GMS German Medical Science
Subjects:
Online Access:http://www.egms.de/static/en/journals/gms/2012-10/000153.shtml
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spelling doaj-0183dfc3f82646d58296f2cfc3d714432020-11-25T02:37:39ZdeuGerman Medical Science GMS Publishing HouseGMS German Medical Science1612-31742012-01-0110Doc02Testing of serum atherogenicity in cell cultures: questionable data publishedSergei V. JarginIn a large series of studies was reported that culturing of smooth muscle cells with serum from atherosclerosis patients caused intracellular lipid accumulation, while serum from healthy controls had no such effect. Cultures were used for evaluation of antiatherogenic drugs. Numerous substances were reported to lower serum atherogenicity: statins, trapidil, calcium antagonists, garlic derivatives etc. On the contrary, beta-blockers, phenothiazines and oral hypoglycemics were reported to be pro-atherogenic. Known antiatherogenic agents can influence lipid metabolism and cholesterol synthesis, intestinal absorption or endothelium-related mechanisms. All these targets are absent in cell monocultures. Inflammatory factors, addressed by some antiatherogenic drugs, are also not reproduced. In vivo, relationship between cholesterol uptake by cells and atherogenesis must be inverse rather than direct: in familial hypercholesterolemia, inefficient clearance of LDL-cholesterol by cells predisposes to atherosclerosis. Accordingly, if a pharmacological agent reduces cholesterol uptake by cells in vitro, it should be expected to elevate cholesterol in vivo. Validity of clinical recommendations, based on serum atherogenicity testing in cell monocultures, is therefore questionable. These considerations pertain also to the drugs developed on the basis of the cell culture experiments. http://www.egms.de/static/en/journals/gms/2012-10/000153.shtmlatherosclerosisserumcell culturecholesterol
collection DOAJ
language deu
format Article
sources DOAJ
author Sergei V. Jargin
spellingShingle Sergei V. Jargin
Testing of serum atherogenicity in cell cultures: questionable data published
GMS German Medical Science
atherosclerosis
serum
cell culture
cholesterol
author_facet Sergei V. Jargin
author_sort Sergei V. Jargin
title Testing of serum atherogenicity in cell cultures: questionable data published
title_short Testing of serum atherogenicity in cell cultures: questionable data published
title_full Testing of serum atherogenicity in cell cultures: questionable data published
title_fullStr Testing of serum atherogenicity in cell cultures: questionable data published
title_full_unstemmed Testing of serum atherogenicity in cell cultures: questionable data published
title_sort testing of serum atherogenicity in cell cultures: questionable data published
publisher German Medical Science GMS Publishing House
series GMS German Medical Science
issn 1612-3174
publishDate 2012-01-01
description In a large series of studies was reported that culturing of smooth muscle cells with serum from atherosclerosis patients caused intracellular lipid accumulation, while serum from healthy controls had no such effect. Cultures were used for evaluation of antiatherogenic drugs. Numerous substances were reported to lower serum atherogenicity: statins, trapidil, calcium antagonists, garlic derivatives etc. On the contrary, beta-blockers, phenothiazines and oral hypoglycemics were reported to be pro-atherogenic. Known antiatherogenic agents can influence lipid metabolism and cholesterol synthesis, intestinal absorption or endothelium-related mechanisms. All these targets are absent in cell monocultures. Inflammatory factors, addressed by some antiatherogenic drugs, are also not reproduced. In vivo, relationship between cholesterol uptake by cells and atherogenesis must be inverse rather than direct: in familial hypercholesterolemia, inefficient clearance of LDL-cholesterol by cells predisposes to atherosclerosis. Accordingly, if a pharmacological agent reduces cholesterol uptake by cells in vitro, it should be expected to elevate cholesterol in vivo. Validity of clinical recommendations, based on serum atherogenicity testing in cell monocultures, is therefore questionable. These considerations pertain also to the drugs developed on the basis of the cell culture experiments.
topic atherosclerosis
serum
cell culture
cholesterol
url http://www.egms.de/static/en/journals/gms/2012-10/000153.shtml
work_keys_str_mv AT sergeivjargin testingofserumatherogenicityincellculturesquestionabledatapublished
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