Expression of neuropeptide Y and its receptors Y1 and Y2 in the rat heart and its supplying autonomic and spinal sensory ganglia in experimentally induced diabetes
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18201831
DOI
10.1016/j.neuroscience.2007.07.069
PII: S0306-4522(07)01553-9
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- experimentální diabetes mellitus chemicky indukované patologie MeSH
- ganglion stellatum metabolismus MeSH
- krysa rodu Rattus MeSH
- myokard metabolismus MeSH
- neuropeptid Y genetika metabolismus MeSH
- potkani Wistar MeSH
- receptory neuropeptidu Y genetika metabolismus MeSH
- regulace genové exprese účinky léků fyziologie MeSH
- spinální ganglia metabolismus MeSH
- streptozocin MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- neuropeptid Y MeSH
- neuropeptide Y-Y1 receptor MeSH Prohlížeč
- neuropeptide Y2 receptor MeSH Prohlížeč
- receptory neuropeptidu Y MeSH
- streptozocin MeSH
Diabetic cardiomyopathy, involving both cardiomyocytes and the sensory and autonomic cardiac innervation, is a major life-threatening complication in diabetes mellitus. Here, we induced long-term (26-53 weeks) diabetes in rats by streptozotocin injection and analyzed the major cardiac neuropeptide signaling system, neuropeptide Y (NPY) and its receptors Y1R and Y2R. Heart compartments and ganglia supplying sympathetic (stellate ganglion) and spinal sensory fibers (upper thoracic dorsal root ganglia=DRG) were analyzed separately by real-time reverse transcription-polymerase chain reaction (RT-PCR) and immunohistochemistry. Ventricular, but not atrial innervation density by NPY-immunoreactive fibers was diminished, and preproNPY expression was transiently (26 weeks) reduced in left atria, but remained unchanged in sympathetic neurons and was not induced in DRG neurons. In all ganglia and heart compartments, Y1R expression dominated over Y2R, and Y1R-immunoreactivity was observed on cardiomyocytes and neuronal perikarya. Atrial, but not ventricular Y1R expression was up-regulated after 1 year of diabetes. Collectively, these data show that a disturbance of the cardiac NPY-Y1R/Y2R signaling system develops slowly in the course of experimentally induced diabetes and differentially affects atria and ventricles. This is in parallel with the clinically observed imbalances of the cardiac autonomic innervation in diabetic cardiac autonomic neuropathy.
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