Cardiomyopathy in streptozotocin-induced diabetes involves intra-axonal accumulation of calcitonin gene-related peptide and altered expression of its receptor in rats
Language English Country United States Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
15951122
DOI
10.1016/j.neuroscience.2005.03.058
PII: S0306-4522(05)00392-1
Knihovny.cz E-resources
- MeSH
- Analysis of Variance MeSH
- Axons metabolism MeSH
- Time Factors MeSH
- Diabetes Mellitus, Experimental complications metabolism MeSH
- Functional Laterality MeSH
- Immunohistochemistry methods MeSH
- Cardiomyopathies etiology metabolism MeSH
- Rats MeSH
- RNA, Messenger metabolism MeSH
- Calcitonin Gene-Related Peptide metabolism MeSH
- Reverse Transcriptase Polymerase Chain Reaction methods MeSH
- Rats, Wistar MeSH
- Radioimmunoassay methods MeSH
- Receptors, Calcitonin Gene-Related Peptide metabolism MeSH
- Gene Expression Regulation drug effects physiology MeSH
- Heart Ventricles metabolism MeSH
- Heart Atria metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- RNA, Messenger MeSH
- Calcitonin Gene-Related Peptide MeSH
- Receptors, Calcitonin Gene-Related Peptide MeSH
Calcitonin gene-related peptide (CGRP) is a vasorelaxant and positive inotropic and chronotropic peptide that binds to the calcitonin receptor-like receptor. In the heart, upon stimulation CGRP is released from sensory nerve terminals and improves cardiac perfusion and function. In the present study, we investigated alterations in the components of the CGRP signaling system during development of diabetic cardiomyopathy. Rats received a single injection of streptozotocin. Four, 8, and 16 weeks thereafter cardiac CGRP content (radioimmunoassay), calcitonin receptor-like receptor expression (by real-time RT-PCR), and CGRP and calcitonin receptor-like receptor tissue distribution (immunohistochemistry) were assessed. CGRP content of atria and ventricles progressively increased during the 4 months following streptozotocin-treatment, while the distribution of CGRP-immunoreactive fibers was not visibly altered. Conversely, cardiac expression of calcitonin receptor-like receptor initially (4 weeks after treatment) increased but then gradually declined to 47% of control levels in both atria after 16 weeks. These quantitative changes were not associated with altered cellular distribution patterns (primarily in venous and capillary endothelium). Since sensory neurons have been reported to decrease expression of the CGRP precursor in the course of diabetes, the intra-axonal accumulation of CGRP observed here reflects impaired release, which, coupled with the down-regulation of its cognate receptor, calcitonin receptor-like receptor, may contribute to the well-documented impairment of cardioprotective functions in diabetes.
References provided by Crossref.org
Substance P Receptor in the Rat Heart and Regulation of Its Expression in Long-Term Diabetes