Linked Life Data

11711031

Source:http://linkedlifedata.com/resource/pubmed/id/11711031

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2-3
pubmed:dateCreated
2001-11-16
pubmed:databankReference
pubmed:abstractText
Although it is well established that fish possess corticotropin-releasing factor (CRF) and a CRF-like peptide, urotensin I, comparatively little is known about the pharmacology of their cognate receptors. Here we report the isolation and functional expression of two complementary DNAs (cDNAs), from the chum salmon Oncorhynchus keta, which encode orthologues of the mammalian and amphibian CRF type 1 (CRF(1)) and type 2 (CRF(2)) receptors. Radioligand competition binding experiments have revealed that the salmon CRF(1) and CRF(2) receptors bind urotensin I with approximately 8-fold higher affinity than rat/human CRF. These two peptides together with two related CRF-like peptides, namely, sauvagine and urocortin, were also tested in cAMP assays; for cells expressing the salmon CRF(1) receptor, EC(50) values for the stimulation of cAMP production were between 4.5+/-1.8 and 15.3+/-3.1 nM. For the salmon CRF(2) receptor, the corresponding values were: rat/human CRF, 9.4+/-0.4 nM; urotensin I, 21.2+/-2.1 nM; sauvagine, 0.7+/-0.1 nM; and urocortin, 2.2+/-0.7 nM. We have also functionally coupled the O. keta CRF(1) receptor, in Xenopus laevis oocytes, to the endogenous Ca(2+)-activated chloride conductance by co-expression with the G-protein alpha subunit, G(alpha16). The EC(50) value for channel activation by rat/human CRF (11.2+/-2.6 nM) agrees well with that obtained in cAMP assays (15.3+/-3.1 nM). We conclude that although sauvagine is 13- and 30-fold more potent than rat/human CRF and urotensin I, respectively, in activating the salmon CRF(2) receptor, neither receptor appears able to discriminate between the native ligands CRF and urotensin I.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0014-2999
pubmed:author
pubmed:issnType
Print
pubmed:day
2
pubmed:volume
430
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
193-202
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11711031-Amino Acid Sequence, pubmed-meshheading:11711031-Animals, pubmed-meshheading:11711031-Binding, Competitive, pubmed-meshheading:11711031-Cell Line, pubmed-meshheading:11711031-Cloning, Molecular, pubmed-meshheading:11711031-Corticotropin-Releasing Hormone, pubmed-meshheading:11711031-Cyclic AMP, pubmed-meshheading:11711031-DNA, Complementary, pubmed-meshheading:11711031-Dose-Response Relationship, Drug, pubmed-meshheading:11711031-Female, pubmed-meshheading:11711031-Gene Expression, pubmed-meshheading:11711031-Humans, pubmed-meshheading:11711031-Male, pubmed-meshheading:11711031-Membrane Potentials, pubmed-meshheading:11711031-Molecular Sequence Data, pubmed-meshheading:11711031-Oncorhynchus keta, pubmed-meshheading:11711031-Oocytes, pubmed-meshheading:11711031-Phylogeny, pubmed-meshheading:11711031-RNA, pubmed-meshheading:11711031-Rats, pubmed-meshheading:11711031-Receptors, Corticotropin-Releasing Hormone, pubmed-meshheading:11711031-Sequence Alignment, pubmed-meshheading:11711031-Sequence Analysis, DNA, pubmed-meshheading:11711031-Sequence Homology, Amino Acid, pubmed-meshheading:11711031-Tissue Distribution, pubmed-meshheading:11711031-Urotensins, pubmed-meshheading:11711031-Xenopus laevis
pubmed:year
2001
pubmed:articleTitle
Cloning and functional pharmacology of two corticotropin-releasing factor receptors from a teleost fish.
pubmed:affiliation
Institut für Zellbiochemie und Klinische Neurobiologie, Universitätsklinikum Hamburg-Eppendorf, Universität Hamburg, Martinistrasse 52, 20246, Hamburg, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't