Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2002-6-13
pubmed:abstractText
The orphan nuclear hormone receptor SHP has been proposed to have a key role in the negative feedback regulation of bile acid production. Consistent with this, mice lacking the SHP gene exhibit mild defects in bile acid homeostasis and fail to repress cholesterol 7-alpha-hydroxylase expression in response to a specific agonist for the bile acid receptor FXR. However, this repression is retained in SHP null mice fed bile acids, demonstrating the existence of compensatory repression pathways of bile acid signaling. We provide evidence for two such pathways, based on activation of the xenobiotic receptor PXR or the c-Jun N-terminal kinase JNK. We conclude that redundant mechanisms regulate this critical aspect of cholesterol homeostasis.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Anticholesteremic Agents, http://linkedlifedata.com/resource/pubmed/chemical/Bile Acids and Salts, http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol 7-alpha-Hydroxylase, http://linkedlifedata.com/resource/pubmed/chemical/Cholic Acid, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/GW 4064, http://linkedlifedata.com/resource/pubmed/chemical/Isoxazoles, http://linkedlifedata.com/resource/pubmed/chemical/JNK Mitogen-Activated Protein..., http://linkedlifedata.com/resource/pubmed/chemical/LG 100268, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Nicotinic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytoplasmic and Nuclear, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Retinoic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Steroid, http://linkedlifedata.com/resource/pubmed/chemical/Retinoid X Receptors, http://linkedlifedata.com/resource/pubmed/chemical/Tetrahydronaphthalenes, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/farnesoid X-activated receptor, http://linkedlifedata.com/resource/pubmed/chemical/nuclear receptor subfamily 0..., http://linkedlifedata.com/resource/pubmed/chemical/pregnane X receptor
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1534-5807
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
721-31
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12062085-Animals, pubmed-meshheading:12062085-Anticholesteremic Agents, pubmed-meshheading:12062085-Bile Acids and Salts, pubmed-meshheading:12062085-Cholesterol 7-alpha-Hydroxylase, pubmed-meshheading:12062085-Cholic Acid, pubmed-meshheading:12062085-DNA-Binding Proteins, pubmed-meshheading:12062085-Feedback, pubmed-meshheading:12062085-Homeostasis, pubmed-meshheading:12062085-Isoxazoles, pubmed-meshheading:12062085-JNK Mitogen-Activated Protein Kinases, pubmed-meshheading:12062085-Mice, pubmed-meshheading:12062085-Mice, Knockout, pubmed-meshheading:12062085-Mitogen-Activated Protein Kinases, pubmed-meshheading:12062085-Nicotinic Acids, pubmed-meshheading:12062085-Nuclear Proteins, pubmed-meshheading:12062085-RNA, Messenger, pubmed-meshheading:12062085-Receptors, Cytoplasmic and Nuclear, pubmed-meshheading:12062085-Receptors, Retinoic Acid, pubmed-meshheading:12062085-Receptors, Steroid, pubmed-meshheading:12062085-Retinoid X Receptors, pubmed-meshheading:12062085-Stem Cells, pubmed-meshheading:12062085-Tetrahydronaphthalenes, pubmed-meshheading:12062085-Transcription Factors
pubmed:year
2002
pubmed:articleTitle
Redundant pathways for negative feedback regulation of bile acid production.
pubmed:affiliation
Department of Molecular and Cellular Biology, Houston, TX 77030, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S.