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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German Medical Science GMS Publishing House
2012-01-01
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Online Access: | http://www.egms.de/static/en/journals/gms/2012-10/000153.shtml |
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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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1724794192458153984 |