Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2011-1-20
pubmed:abstractText
Peroxisome proliferator-activated receptor-? (PPAR?) is a nuclear receptor for the antidiabetic agent thiazolidinedione, which exerts various physiological activities, independent of lowering blood glucose. However, the role of PPAR? in aldosterone production has not been clarified. The objective of this study was to investigate the effect of PPAR? on aldosterone synthase gene (CYP11B2) expression and aldosterone production. Localization of PPAR? expression in normal adrenal cortex was determined by immunohistochemistry. Aldosterone production and CYP11B2 expression levels were determined using human adrenocortical carcinoma H295R cells. Pioglitazone suppressed angiotensin II-induced aldosterone secretion and CYP11B2 expression. PPAR? was expressed in zona glomerulosa in human normal adrenal gland. PPAR? overexpression enhanced pioglitazone-mediated CYP11B2 transrepression. The pioglitazone-mediated suppression of aldosterone secretion and CYP11B2 expression were canceled by PPAR? L466A/E469A mutant. Pioglitazone also suppressed potassium-mediated CYP11B2 induction, but not N6-2'-O-dibutyladenosine-3',5'-cyclic monophosphate stimulation. Rosiglitazone and GW1929 also suppressed CYP11B2 transactivation. Mutation analysis revealed that the Ad1/CRE element in CYP11B2 5'-flanking region was responsible for the pioglitazone-mediated transrepression. Pioglitazone suppressed ionomycin and a truncated constitutively active form Ca(2+)/calmodulin-dependent kinase I (CaMKI)-mediated CYP11B2 transcriptional activation. A CaMK inhibitor KN-93 attenuated pioglitazone-mediated CYP11B2 transrepression. PPAR? suppresses CYP11B2 expression and aldosterone secretion.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aldosterone, http://linkedlifedata.com/resource/pubmed/chemical/Aldosterone Synthase, http://linkedlifedata.com/resource/pubmed/chemical/Benzophenones, http://linkedlifedata.com/resource/pubmed/chemical/Benzylamines, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent..., http://linkedlifedata.com/resource/pubmed/chemical/GW 1929, http://linkedlifedata.com/resource/pubmed/chemical/Ionomycin, http://linkedlifedata.com/resource/pubmed/chemical/KN 93, http://linkedlifedata.com/resource/pubmed/chemical/PPAR gamma, http://linkedlifedata.com/resource/pubmed/chemical/Sulfonamides, http://linkedlifedata.com/resource/pubmed/chemical/Thiazolidinediones, http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine, http://linkedlifedata.com/resource/pubmed/chemical/pioglitazone, http://linkedlifedata.com/resource/pubmed/chemical/rosiglitazone
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1479-6813
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
46
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
37-49
pubmed:meshHeading
pubmed-meshheading:21106862-Adrenal Cortex, pubmed-meshheading:21106862-Aldosterone, pubmed-meshheading:21106862-Aldosterone Synthase, pubmed-meshheading:21106862-Benzophenones, pubmed-meshheading:21106862-Benzylamines, pubmed-meshheading:21106862-Blotting, Western, pubmed-meshheading:21106862-Calcium-Calmodulin-Dependent Protein Kinase Type 1, pubmed-meshheading:21106862-Cell Line, pubmed-meshheading:21106862-Gene Expression, pubmed-meshheading:21106862-Gene Expression Regulation, Enzymologic, pubmed-meshheading:21106862-Humans, pubmed-meshheading:21106862-Ionomycin, pubmed-meshheading:21106862-Mutation, pubmed-meshheading:21106862-PPAR gamma, pubmed-meshheading:21106862-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:21106862-Sulfonamides, pubmed-meshheading:21106862-Thiazolidinediones, pubmed-meshheading:21106862-Transcription, Genetic, pubmed-meshheading:21106862-Tyrosine, pubmed-meshheading:21106862-Zona Glomerulosa
pubmed:year
2011
pubmed:articleTitle
Peroxisome proliferator-activated receptor-{gamma} suppresses CYP11B2 expression and aldosterone production.
pubmed:affiliation
Department of Advanced Biological Sciences for Regeneration, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't