Norepinephrine turnover in the left ventricle of subtotally nephrectomized rats
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
31928041
DOI
10.33549/physiolres.934354
PII: 934354
Knihovny.cz E-resources
- MeSH
- Renal Insufficiency, Chronic complications metabolism physiopathology MeSH
- Cardiovascular Diseases etiology MeSH
- Kidney metabolism MeSH
- Disease Models, Animal MeSH
- Nephrectomy MeSH
- Neuropeptide Y metabolism MeSH
- Norepinephrine blood MeSH
- Calcitonin Gene-Related Peptide metabolism MeSH
- Rats, Wistar MeSH
- Heart Rate MeSH
- Heart Ventricles metabolism physiopathology MeSH
- Sympathetic Nervous System physiopathology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Neuropeptide Y MeSH
- Norepinephrine MeSH
- Calcitonin Gene-Related Peptide MeSH
Increased activity of the sympathetic nervous system (SNS) has been proposed as a risk factor for increased cardiovascular mortality in patients with chronic kidney disease (CKD). Information on the activity of cardiac sympathetic innervation is non-homogeneous and incomplete. The aim of our study was to evaluate the tonic effect of SNS on heart rate, norepinephrine turnover and direct and indirect effects of norepinephrine in left ventricles of subtotally nephrectomized rats (SNX) in comparison with sham-operated animals (SHAM). Renal failure was verified by measuring serum creatinine and urea levels. SNX rats developed increased heart rates and blood pressure (BP). The increase in heart rate was not caused by sympathetic overactivity as the negative chronotropic effect of metipranolol did not differ between the SNX and SHAM animals. The positive inotropic effects of norepinephrine and tyramine on papillary muscle were not significantly different. Norepinephrine turnover was measured after the administration of tyrosine hydroxylase inhibitor, pargyline, tyramine, desipramine, and KCl induced depolarization. The absolute amount of released norepinephrine was comparable in both groups despite a significantly decreased norepinephrine concentration in the cardiac tissue of the SNX rats. We conclude that CKD associated with renal denervation in rats led to adaptive changes characterized by an increased reuptake and intracellular norepinephrine turnover which maintained normal reactivity of the heart to sympathetic stimulation.
References provided by Crossref.org
Mitochondrial dysfunction in kidney cortex and medulla of subtotally nephrectomized rats