Linked Life Data

11981752

Source:http://linkedlifedata.com/resource/pubmed/id/11981752

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2002-4-30
pubmed:abstractText
Transforming growth factor (TGF) beta isoforms (in particular, TGF-beta1) play a central role in the fibrogenic response to injury in many organs, including the liver. Although TGF-beta is clearly important in fibrogenesis, a number of issues related to therapeutic antagonism have emerged. For example, the long-term effect of TGF-beta antagonism is unknown; furthermore, controversy exists as to appropriate levels of TGF-beta inhibition. Therefore, we aimed to examine TGF-beta in models of chronic liver injury and to determine whether an in vivo dose-response relationship exists for inhibition of TGF-beta. Liver injury was induced in BALB/c mice by administering carbon tetrachloride for 4 or 8 weeks. TGF-beta binding was inhibited with a soluble TGF-beta type II receptor (STR) construct, administered intraperitoneally over a dose range of 4.0, 1.0, 0.4, or 0.1 mg/kg twice weekly during fibrogenesis. Fibrogenesis was assessed by measurement of type I collagen messenger RNA (mRNA) expression and by quantitative morphometric analysis. In the 4-week study, STR at concentrations of 4.0, 1.0, and 0.1 mg/kg reduced type I collagen mRNA expression by 31%, 49%, and 60% compared with immunoglobulin (Ig) G controls, respectively. In the 8-week study, lower concentrations of STR (0.1 mg/kg) also had the greatest effect on type I collagen mRNA expression. Quantitative morphometrics similarly showed that lower concentrations of STR were the most antifibrogenic. In conclusion, the results confirm the antifibrotic effect of inhibiting TGF-beta in chronic hepatic wounding and, moreover, show that its in vivo effect in the mouse is dose dependent. Such findings have major translational implications for therapeutic strategies aimed at TGF-beta.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0270-9139
pubmed:author
pubmed:issnType
Print
pubmed:volume
35
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1022-30
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:11981752-Acute Disease, pubmed-meshheading:11981752-Alanine Transaminase, pubmed-meshheading:11981752-Animals, pubmed-meshheading:11981752-Chronic Disease, pubmed-meshheading:11981752-Collagen Type I, pubmed-meshheading:11981752-Dose-Response Relationship, Drug, pubmed-meshheading:11981752-Extracellular Matrix, pubmed-meshheading:11981752-Gene Expression, pubmed-meshheading:11981752-Hepatocytes, pubmed-meshheading:11981752-Liver Cirrhosis, pubmed-meshheading:11981752-Mice, pubmed-meshheading:11981752-Mice, Inbred BALB C, pubmed-meshheading:11981752-Protein-Serine-Threonine Kinases, pubmed-meshheading:11981752-RNA, Messenger, pubmed-meshheading:11981752-Receptors, Transforming Growth Factor beta, pubmed-meshheading:11981752-Recombinant Fusion Proteins, pubmed-meshheading:11981752-Solubility, pubmed-meshheading:11981752-Wound Healing
pubmed:year
2002
pubmed:articleTitle
Dose-dependent inhibition of hepatic fibrosis in mice by a TGF-beta soluble receptor: implications for antifibrotic therapy.
pubmed:affiliation
Liver Center and Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't