Chloroquine differentially modulates coronary vasodilation in control and diabetic mice.
Identifieur interne : 000037 ( PubMed/Curation ); précédent : 000036; suivant : 000038Chloroquine differentially modulates coronary vasodilation in control and diabetic mice.
Auteurs : Qian Zhang [États-Unis] ; Atsumi Tsuji-Hosokawa [États-Unis] ; Conor Willson [États-Unis] ; Makiko Watanabe [États-Unis] ; Rui Si [États-Unis] ; Ning Lai [États-Unis] ; Ziyi Wang [États-Unis] ; Jason X-J Yuan [États-Unis] ; Jian Wang [États-Unis] ; Ayako Makino [États-Unis]Source :
- British journal of pharmacology [ 1476-5381 ] ; 2020.
Abstract
Chloroquine is a traditional medicine to treat malaria. There is increasing evidence that chloroquine not only induces phagocytosis but regulates vascular tone. Few reports investigating the effect of chloroquine on vascular responsiveness of coronary arteries have been made. In this study, we examined how chloroquine affected endothelium-dependent relaxation in coronary arteries under normal and diabetic conditions.
DOI: 10.1111/bph.14864
PubMed: 31503328
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<front><div type="abstract" xml:lang="en">Chloroquine is a traditional medicine to treat malaria. There is increasing evidence that chloroquine not only induces phagocytosis but regulates vascular tone. Few reports investigating the effect of chloroquine on vascular responsiveness of coronary arteries have been made. In this study, we examined how chloroquine affected endothelium-dependent relaxation in coronary arteries under normal and diabetic conditions.</div>
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<pubmed><MedlineCitation Status="In-Data-Review" Owner="NLM"><PMID Version="1">31503328</PMID>
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<Title>British journal of pharmacology</Title>
<ISOAbbreviation>Br. J. Pharmacol.</ISOAbbreviation>
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<ArticleTitle>Chloroquine differentially modulates coronary vasodilation in control and diabetic mice.</ArticleTitle>
<Pagination><MedlinePgn>314-327</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/bph.14864</ELocationID>
<Abstract><AbstractText Label="BACKGROUND AND PURPOSE" NlmCategory="OBJECTIVE">Chloroquine is a traditional medicine to treat malaria. There is increasing evidence that chloroquine not only induces phagocytosis but regulates vascular tone. Few reports investigating the effect of chloroquine on vascular responsiveness of coronary arteries have been made. In this study, we examined how chloroquine affected endothelium-dependent relaxation in coronary arteries under normal and diabetic conditions.</AbstractText>
<AbstractText Label="EXPERIMENTAL APPROACH" NlmCategory="METHODS">We isolated coronary arteries from mice and examined endothelium-dependent relaxation (EDR). Human coronary endothelial cells and mouse coronary endothelial cells isolated from control and diabetic mouse (TALLYHO/Jng [TH] mice, a spontaneous type 2 diabetic mouse model) were used for the molecular biological or cytosolic NO and Ca<sup>2+</sup>
measurements.</AbstractText>
<AbstractText Label="KEY RESULTS" NlmCategory="RESULTS">Chloroquine inhibited endothelium-derived NO-dependent relaxation but had negligible effect on endothelium-derived hyperpolarization (EDH)-dependent relaxation in coronary arteries of control mice. Chloroquine significantly decreased NO production in control human coronary endothelial cells partly by phosphorylating eNOS<sup>Thr495</sup>
(an inhibitory phosphorylation site of eNOS) and attenuating the rise of cytosolic Ca<sup>2+</sup>
concentration after stimulation. EDR was significantly inhibited in diabetic mice in comparison to control mice. Interestingly, chloroquine enhanced EDR in diabetic coronary arteries by, specifically, increasing EDH-dependent relaxation due partly to its augmenting effect on gap junction activity in diabetic mouse coronary endothelial cells.</AbstractText>
<AbstractText Label="CONCLUSIONS AND IMPLICATIONS" NlmCategory="CONCLUSIONS">These data indicate that chloroquine affects vascular relaxation differently under normal and diabetic conditions. Therefore, the patients' health condition such as coronary macrovascular or microvascular disease, with or without diabetes, must be taken account into the consideration when selecting chloroquine for the treatment of malaria.</AbstractText>
<CopyrightInformation>© 2019 The British Pharmacological Society.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zhang</LastName>
<ForeName>Qian</ForeName>
<Initials>Q</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, University of California, San Diego, La Jolla, California.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Physiology, The University of Arizona, Tucson, Arizona.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Tsuji-Hosokawa</LastName>
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<AffiliationInfo><Affiliation>Department of Physiology, The University of Arizona, Tucson, Arizona.</Affiliation>
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<AffiliationInfo><Affiliation>State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.</Affiliation>
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<AffiliationInfo><Affiliation>State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.</Affiliation>
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