Linked Life Data

12770550

Source:http://linkedlifedata.com/resource/pubmed/id/12770550

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2003-5-28
pubmed:abstractText
This work addresses the presence, pharmacological properties, and anatomical localization of calcitonin gene-related peptide-alpha (CGRPalpha) binding sites and the receptor's accessory proteins in endplate-enriched and non-endplate muscle membrane samples from adult rat gracilis muscles. We examined the binding of (125)I-[Tyr(0)]-CGRPalpha, the competitive binding of CGRPalpha analogs, the immunohistochemical localization of the receptor's accessory proteins, and Western blots of the receptor component protein. Results show that: (a). (125)I-[Tyr(0)]-CGRPalpha binding is saturable, specific, and consistent with the presence of a homogeneous population of binding sites (Hill coefficients=1.0) in endplate and non-endplate samples exhibiting dissociation constants of 0.39 nM and 0.38 nM, respectively; (b). the density of binding sites in the endplate samples (71.0 fmoles/mg protein) is considerably higher than that in their non-endplate counterparts (34.6 fmoles/mg protein); (c). unlabeled CGRPalpha, hCGRP8-37 and calcitonin compete with the radioligand with the same order of potency in the endplate and non-endplate samples; and (d). the localization of the receptor accessory proteins, including the receptor activity-modifying protein (RAMP1) and the receptor component protein (RCP), for the most part matches that of the motor end-plates. Thus, gracilis muscles express CGRPalpha-specific binding sites which are predominantly localized in the muscle's motor endplate regions where RAMP1, RCP, CGRPalpha, acetylcholine receptors, and acetylcholinesterase are detected in high concentrations. These findings imply that the CGRPalpha binding sites reflect the presence of physiologically functional receptors with a pharmacological profile consistent with that of the CGRPalpha receptor type 1 (CGRP1). When considered together with earlier studies on the same neuromuscular preparation, the present work further suggests that the motoneuron-dependent trophic control of acetylcholine receptors and acetylcholinesterase in skeletal muscle endplates is partly mediated by nerve-derived CGRPalpha activating specific receptors which are highly sensitive to the truncated peptide hCGRP8-37.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0306-4522
pubmed:author
pubmed:issnType
Print
pubmed:volume
119
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
335-45
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12770550-Animals, pubmed-meshheading:12770550-Binding, Competitive, pubmed-meshheading:12770550-Blotting, Western, pubmed-meshheading:12770550-Bungarotoxins, pubmed-meshheading:12770550-Calcitonin, pubmed-meshheading:12770550-Calcitonin Gene-Related Peptide, pubmed-meshheading:12770550-Cell Membrane, pubmed-meshheading:12770550-Immunohistochemistry, pubmed-meshheading:12770550-Kinetics, pubmed-meshheading:12770550-Male, pubmed-meshheading:12770550-Motor Endplate, pubmed-meshheading:12770550-Muscle, Skeletal, pubmed-meshheading:12770550-Peptide Fragments, pubmed-meshheading:12770550-Radioligand Assay, pubmed-meshheading:12770550-Rats, pubmed-meshheading:12770550-Rats, Sprague-Dawley, pubmed-meshheading:12770550-Receptors, Calcitonin Gene-Related Peptide, pubmed-meshheading:12770550-Time Factors
pubmed:year
2003
pubmed:articleTitle
Calcitonin gene-related peptides: their binding sites and receptor accessory proteins in adult mammalian skeletal muscles.
pubmed:affiliation
Research and Development Service (151), Department of Veterans Affairs Medical Center, PO Box 4125, Bay Pines, FL 33744, USA. hugo.fernandez@med.va.gov
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, Non-P.H.S.