Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1986-6-2
pubmed:abstractText
In the urinary bladder of the toad Bufo marinus, the basal rate of synthesis of a number of proteins was modulated in a bidirectional way (i.e., induced or repressed) by aldosterone and by triiodothyronine (T3). Each hormone was therefore characterized by a distinct domain of response. When both hormones were added simultaneously, the two domains consistently overlapped at least for one protein, termed AIP-1, or aldosterone-induced protein 1 (Mr approximately 65 kilodaltons, pi = 6.7, as analyzed by two-dimension gel electrophoresis). The physiological role of AIP-1 is unknown, but could be related to the late mineralocorticoid response. In five experiments, T3 (60 nM, 18-hr incubation) consistently repressed AIP-1, while aldosterone-dependent sodium transport (late response) was significantly inhibited, as previously described. The repression of AIP-1 was also observed as early as 6 hr after aldosterone addition. In addition, sodium butyrate (3 mM), which was previously shown to also selectively inhibit the late mineralocorticoid response, was also able to repress AIP-1. Our results suggest that AIP-1 is one of the proteins involved in the mediation of the late mineralocorticoid response.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0022-2631
pubmed:author
pubmed:issnType
Print
pubmed:volume
89
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
173-83
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1986
pubmed:articleTitle
Thyroid hormone antagonizes an aldosterone-induced protein: a candidate mediator for the late mineralocorticoid response.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't