Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4-5
pubmed:dateCreated
2010-6-23
pubmed:abstractText
Hypertension is a common complication of type 2 diabetes mellitus (T2DM), and is the main cause for T2DM-associated mortality. Although the stringent control of blood pressure is known to be beneficial in reducing the cardiovascular mortality of T2DM patients, drugs with both anti-hypertensive and anti-hyperglycemic effects are seldom reported. The traditional Chinese medicine danshen has long been used for lowering both blood pressure and blood glucose in T2DM patients, shedding lights on the development of such medication. However, the molecular mechanism and active component remain unclear. Here, we report that the lipophilic component, 15,16-dihydrotanshinone I (DHTH) from danshen potently antagonized both mineralocorticoid and glucocorticoid receptors, and efficiently inhibited the expression of their target genes like Na(+)/K(+) ATPase, glucose 6-phosphatase (G6Pase), and phosphoenolpyruvate carboxykinase (PEPCK). In addition, DHTH increased AMPKalpha phosphorylation and regulated its downstream pathways, including increasing acetyl-CoA carboxylase (ACC) phosphorylation, inhibiting transducer of regulated CREB activity 2 (TORC2) translocation and promoting glucose uptake. Such discovered multi-target effects of DHTH are expected to have provided additional understandings on the molecular basis of the therapeutic effects of danshen against the metabolic syndrome.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/15,16-dihydrotanshinone I, http://linkedlifedata.com/resource/pubmed/chemical/AMP-Activated Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Acetyl-CoA Carboxylase, http://linkedlifedata.com/resource/pubmed/chemical/CRTC2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent..., http://linkedlifedata.com/resource/pubmed/chemical/Carboxy-Lyases, http://linkedlifedata.com/resource/pubmed/chemical/Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Glucose-6-Phosphatase, http://linkedlifedata.com/resource/pubmed/chemical/Phenanthrenes, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Glucocorticoid, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Mineralocorticoid, http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1879-1220
pubmed:author
pubmed:copyrightInfo
Copyright 2010 Elsevier Ltd. All rights reserved.
pubmed:issnType
Electronic
pubmed:volume
120
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
155-63
pubmed:meshHeading
pubmed-meshheading:20380878-3T3 Cells, pubmed-meshheading:20380878-AMP-Activated Protein Kinases, pubmed-meshheading:20380878-Acetyl-CoA Carboxylase, pubmed-meshheading:20380878-Animals, pubmed-meshheading:20380878-Calcium-Calmodulin-Dependent Protein Kinase Kinase, pubmed-meshheading:20380878-Carboxy-Lyases, pubmed-meshheading:20380878-Cell Line, pubmed-meshheading:20380878-Gene Expression, pubmed-meshheading:20380878-Glucose, pubmed-meshheading:20380878-Glucose-6-Phosphatase, pubmed-meshheading:20380878-Humans, pubmed-meshheading:20380878-Mice, pubmed-meshheading:20380878-Phenanthrenes, pubmed-meshheading:20380878-Receptors, Glucocorticoid, pubmed-meshheading:20380878-Receptors, Mineralocorticoid, pubmed-meshheading:20380878-Salvia miltiorrhiza, pubmed-meshheading:20380878-Signal Transduction, pubmed-meshheading:20380878-Sodium-Potassium-Exchanging ATPase, pubmed-meshheading:20380878-Transcription Factors
pubmed:year
2010
pubmed:articleTitle
Danshen extract 15,16-dihydrotanshinone I functions as a potential modulator against metabolic syndrome through multi-target pathways.
pubmed:affiliation
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't