Serveur d'exploration Chloroquine

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

A quantitative metabolic inhibition test for screening toxic compounds with cultured cells

Identifieur interne : 003645 ( Main/Exploration ); précédent : 003644; suivant : 003646

A quantitative metabolic inhibition test for screening toxic compounds with cultured cells

Auteurs : D. G. Wenzel [États-Unis] ; G. N. Cosma [États-Unis]

Source :

RBID : ISTEX:067581B9A408346BA6AA22541B6E3F5B3F76699B

Descripteurs français

English descriptors

Abstract

Abstract: The toxicity of substances for monolayer cultures of rat lung fibroblasts with phenol red as a pH indicator in the medium was measured by comparing the changes produced in medium color against 10 stable color standards. The toxicities of 6 concentrations each of actinomycin D, amphotericin B, chloroquine, 2-deoxyglucose, oligomycin, puromycin, and silicon dioxide were measured at 12 h and daily for 7 days on the same cultures throughout. Morphologic changes were monitored at the same times. The method, which simultaneously measures both concentration and time effects, was rapid, simple-to-perform, reproducible, low-in-cost, and quite sensitive. Its reproducibility depended on details of the cell culture methodology. The method is unsuitable for acidic or basic substances, or substances poorly-soluble in culture medium. Unless combined with morphologic evaluation, substances producing delayed toxicity may give misleading results.

Url:
DOI: 10.1016/0300-483X(83)90049-5


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title>A quantitative metabolic inhibition test for screening toxic compounds with cultured cells</title>
<author>
<name sortKey="Wenzel, D G" sort="Wenzel, D G" uniqKey="Wenzel D" first="D. G." last="Wenzel">D. G. Wenzel</name>
</author>
<author>
<name sortKey="Cosma, G N" sort="Cosma, G N" uniqKey="Cosma G" first="G. N." last="Cosma">G. N. Cosma</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:067581B9A408346BA6AA22541B6E3F5B3F76699B</idno>
<date when="1983" year="1983">1983</date>
<idno type="doi">10.1016/0300-483X(83)90049-5</idno>
<idno type="url">https://api.istex.fr/ark:/67375/6H6-TPW44BLH-F/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001009</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001009</idno>
<idno type="wicri:Area/Istex/Curation">001009</idno>
<idno type="wicri:Area/Istex/Checkpoint">002405</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">002405</idno>
<idno type="wicri:doubleKey">0300-483X:1983:Wenzel D:a:quantitative:metabolic</idno>
<idno type="wicri:Area/Main/Merge">003722</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:84-0227374</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000103</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000067</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000103</idno>
<idno type="wicri:explorRef" wicri:stream="PascalFrancis" wicri:step="Checkpoint">000103</idno>
<idno type="wicri:doubleKey">0300-483X:1983:Wenzel D:a:quantitative:metabolic</idno>
<idno type="wicri:Area/Main/Merge">003760</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:6658799</idno>
<idno type="wicri:Area/PubMed/Corpus">000600</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000600</idno>
<idno type="wicri:Area/PubMed/Curation">000600</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000600</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000574</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000574</idno>
<idno type="wicri:Area/Ncbi/Merge">001128</idno>
<idno type="wicri:Area/Ncbi/Curation">001128</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">001128</idno>
<idno type="wicri:doubleKey">0300-483X:1983:Wenzel D:a:quantitative:metabolic</idno>
<idno type="wicri:Area/Main/Merge">003696</idno>
<idno type="wicri:Area/Main/Curation">003645</idno>
<idno type="wicri:Area/Main/Exploration">003645</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a">A quantitative metabolic inhibition test for screening toxic compounds with cultured cells</title>
<author>
<name sortKey="Wenzel, D G" sort="Wenzel, D G" uniqKey="Wenzel D" first="D. G." last="Wenzel">D. G. Wenzel</name>
<affiliation wicri:level="4">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pharmacology and Toxicology, School of Pharmacy, University of Kansas, Lawrence, Kansas 66045-2505</wicri:regionArea>
<orgName type="university">Université du Kansas</orgName>
<placeName>
<settlement type="city">Lawrence (Kansas)</settlement>
<region type="state">Kansas</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Cosma, G N" sort="Cosma, G N" uniqKey="Cosma G" first="G. N." last="Cosma">G. N. Cosma</name>
<affiliation wicri:level="4">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pharmacology and Toxicology, School of Pharmacy, University of Kansas, Lawrence, Kansas 66045-2505</wicri:regionArea>
<orgName type="university">Université du Kansas</orgName>
<placeName>
<settlement type="city">Lawrence (Kansas)</settlement>
<region type="state">Kansas</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Toxicology</title>
<title level="j" type="abbrev">TOX</title>
<idno type="ISSN">0300-483X</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1983">1983</date>
<biblScope unit="volume">29</biblScope>
<biblScope unit="issue">1–2</biblScope>
<biblScope unit="page" from="173">173</biblScope>
<biblScope unit="page" to="182">182</biblScope>
</imprint>
<idno type="ISSN">0300-483X</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0300-483X</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Animal</term>
<term>Animals</term>
<term>Cells, Cultured</term>
<term>Drug Evaluation, Preclinical (methods)</term>
<term>Fibroblast</term>
<term>Fibroblasts (drug effects)</term>
<term>Fibroblasts (metabolism)</term>
<term>Hydrogen-Ion Concentration</term>
<term>Investigation method</term>
<term>Lung</term>
<term>Lung (drug effects)</term>
<term>Metabolism inhibition test</term>
<term>Monolayer culture</term>
<term>Rat</term>
<term>Rats</term>
<term>Respiratory system</term>
<term>Toxicity</term>
<term>Toxicology</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Cellules cultivées</term>
<term>Concentration en ions d'hydrogène</term>
<term>Fibroblastes ()</term>
<term>Fibroblastes (métabolisme)</term>
<term>Poumon ()</term>
<term>Rats</term>
<term>Toxicologie</term>
<term>Évaluation préclinique de médicament ()</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Fibroblasts</term>
<term>Lung</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Fibroblasts</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Drug Evaluation, Preclinical</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Fibroblastes</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Cells, Cultured</term>
<term>Hydrogen-Ion Concentration</term>
<term>Rats</term>
<term>Toxicology</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Animal</term>
<term>Animaux</term>
<term>Appareil respiratoire</term>
<term>Cellules cultivées</term>
<term>Concentration en ions d'hydrogène</term>
<term>Culture monocouche</term>
<term>Fibroblaste</term>
<term>Fibroblastes</term>
<term>Méthode étude</term>
<term>Poumon</term>
<term>Rat</term>
<term>Rats</term>
<term>Test inhibition métabolisme</term>
<term>Toxicité</term>
<term>Toxicologie</term>
<term>Évaluation préclinique de médicament</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en">
<term>Anaerobic environment</term>
<term>Bacto trypsin</term>
<term>Chloroquine</term>
<term>Color change</term>
<term>Color changes</term>
<term>Color standards</term>
<term>Culture dishes</term>
<term>Culture medium</term>
<term>Cultured cells</term>
<term>Difco trypsin</term>
<term>Dioxide</term>
<term>Drug pairs</term>
<term>Drug toxicity</term>
<term>Ekwall</term>
<term>Hela</term>
<term>Hela cells</term>
<term>Inhibition test</term>
<term>Initial period</term>
<term>Lung fibroblasts</term>
<term>Metabolic inhibition test</term>
<term>Preliminary studies</term>
<term>Publishers ireland</term>
<term>Qmit</term>
<term>Qmit color grades</term>
<term>Qmit grades</term>
<term>Second subculture</term>
<term>Silicon</term>
<term>Silicon dioxide</term>
<term>Subculture</term>
<term>Test agent</term>
<term>Test agents</term>
<term>Toxicity</term>
<term>Toxicology</term>
<term>Uniform results</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Toxicologie</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: The toxicity of substances for monolayer cultures of rat lung fibroblasts with phenol red as a pH indicator in the medium was measured by comparing the changes produced in medium color against 10 stable color standards. The toxicities of 6 concentrations each of actinomycin D, amphotericin B, chloroquine, 2-deoxyglucose, oligomycin, puromycin, and silicon dioxide were measured at 12 h and daily for 7 days on the same cultures throughout. Morphologic changes were monitored at the same times. The method, which simultaneously measures both concentration and time effects, was rapid, simple-to-perform, reproducible, low-in-cost, and quite sensitive. Its reproducibility depended on details of the cell culture methodology. The method is unsuitable for acidic or basic substances, or substances poorly-soluble in culture medium. Unless combined with morphologic evaluation, substances producing delayed toxicity may give misleading results.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Kansas</li>
</region>
<settlement>
<li>Lawrence (Kansas)</li>
</settlement>
<orgName>
<li>Université du Kansas</li>
</orgName>
</list>
<tree>
<country name="États-Unis">
<region name="Kansas">
<name sortKey="Wenzel, D G" sort="Wenzel, D G" uniqKey="Wenzel D" first="D. G." last="Wenzel">D. G. Wenzel</name>
</region>
<name sortKey="Cosma, G N" sort="Cosma, G N" uniqKey="Cosma G" first="G. N." last="Cosma">G. N. Cosma</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003645 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003645 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:067581B9A408346BA6AA22541B6E3F5B3F76699B
   |texte=   A quantitative metabolic inhibition test for screening toxic compounds with cultured cells
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021