Serveur d'exploration Chloroquine

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Chloroquine prevents progression of experimental pulmonary hypertension via inhibition of autophagy and lysosomal bone morphogenetic protein type II receptor degradation.

Identifieur interne : 001118 ( Main/Exploration ); précédent : 001117; suivant : 001119

Chloroquine prevents progression of experimental pulmonary hypertension via inhibition of autophagy and lysosomal bone morphogenetic protein type II receptor degradation.

Auteurs : Lu Long [Royaume-Uni] ; Xudong Yang ; Mark Southwood ; Junyu Lu ; Stefan J. Marciniak ; Benjamin J. Dunmore ; Nicholas W. Morrell

Source :

RBID : pubmed:23446737

Descripteurs français

English descriptors

Abstract

Pulmonary arterial hypertension (PAH) is characterized by excessive proliferation and apoptosis resistance in pulmonary artery smooth muscle cells (PASMCs).

DOI: 10.1161/CIRCRESAHA.111.300483
PubMed: 23446737


Affiliations:


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Le document en format XML

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<term>Animals</term>
<term>Autophagy (physiology)</term>
<term>Bone Morphogenetic Protein Receptors, Type II (antagonists & inhibitors)</term>
<term>Bone Morphogenetic Protein Receptors, Type II (metabolism)</term>
<term>Cells, Cultured</term>
<term>Chloroquine (therapeutic use)</term>
<term>Disease Models, Animal</term>
<term>Disease Progression</term>
<term>Hypertension, Pulmonary (metabolism)</term>
<term>Hypertension, Pulmonary (pathology)</term>
<term>Hypertension, Pulmonary (prevention & control)</term>
<term>Lysosomes (metabolism)</term>
<term>Lysosomes (pathology)</term>
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<term>Hypertension pulmonaire (anatomopathologie)</term>
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<term>Modèles animaux de maladie humaine</term>
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<term>Rat Sprague-Dawley</term>
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<term>Récepteurs de la protéine morphogénique osseuse de type II (antagonistes et inhibiteurs)</term>
<term>Récepteurs de la protéine morphogénique osseuse de type II (métabolisme)</term>
<term>Transduction du signal ()</term>
<term>Transduction du signal (physiologie)</term>
<term>Évolution de la maladie</term>
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<div type="abstract" xml:lang="en">Pulmonary arterial hypertension (PAH) is characterized by excessive proliferation and apoptosis resistance in pulmonary artery smooth muscle cells (PASMCs).</div>
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