Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-1-13
pubmed:abstractText
Interstitial fibrosis plays a causal role in the development of heart failure after chronic myocardial infarction (MI), and anti-fibrotic therapy represents a promising strategy to mitigate this pathological process. The purpose of this study was to investigate the effect of long-term administration of scutellarin (Scu) on cardiac interstitial fibrosis of myocardial infarct rats and the underlying mechanisms.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1476-5381
pubmed:author
pubmed:copyrightInfo
© 2011 The Authors. British Journal of Pharmacology © 2011 The British Pharmacological Society.
pubmed:issnType
Electronic
pubmed:volume
162
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
688-700
pubmed:meshHeading
pubmed-meshheading:20942814-Animals, pubmed-meshheading:20942814-Apigenin, pubmed-meshheading:20942814-Collagen, pubmed-meshheading:20942814-Cytokines, pubmed-meshheading:20942814-Drugs, Chinese Herbal, pubmed-meshheading:20942814-Echocardiography, pubmed-meshheading:20942814-Erigeron, pubmed-meshheading:20942814-Fibrosis, pubmed-meshheading:20942814-Glucuronic Acids, pubmed-meshheading:20942814-Heart Failure, pubmed-meshheading:20942814-Hemodynamics, pubmed-meshheading:20942814-Male, pubmed-meshheading:20942814-Mitogen-Activated Protein Kinase 1, pubmed-meshheading:20942814-Myocardial Infarction, pubmed-meshheading:20942814-Phytotherapy, pubmed-meshheading:20942814-Rats, pubmed-meshheading:20942814-Rats, Wistar, pubmed-meshheading:20942814-Transforming Growth Factor beta1, pubmed-meshheading:20942814-Ventricular Dysfunction, Left, pubmed-meshheading:20942814-Ventricular Remodeling, pubmed-meshheading:20942814-p38 Mitogen-Activated Protein Kinases
pubmed:year
2011
pubmed:articleTitle
Scutellarin alleviates interstitial fibrosis and cardiac dysfunction of infarct rats by inhibiting TGF?1 expression and activation of p38-MAPK and ERK1/2.
pubmed:affiliation
Department of Pharmacology, Harbin Medical University, Harbin, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't