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Effects of Nifedipine on Renal and Cardiovascular Responses to Neuropeptide Y in Anesthetized Rats
Neuropeptide Y (NPY) acts via multiple receptor subtypes termed Y(1), Y(2) and Y(5). While Y(1) receptor-mediated effects, e.g., in the vasculature, are often sensitive to inhibitors of L-type Ca(2+) channels such as nifedipine, little is known about the role of such channels in Y(5)-mediated effect...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347858/ https://www.ncbi.nlm.nih.gov/pubmed/34361613 http://dx.doi.org/10.3390/molecules26154460 |
Sumario: | Neuropeptide Y (NPY) acts via multiple receptor subtypes termed Y(1), Y(2) and Y(5). While Y(1) receptor-mediated effects, e.g., in the vasculature, are often sensitive to inhibitors of L-type Ca(2+) channels such as nifedipine, little is known about the role of such channels in Y(5)-mediated effects such as diuresis and natriuresis. Therefore, we explored whether nifedipine affects NPY-induced diuresis and natriuresis. After pre-treatment with nifedipine or vehicle, anesthetized rats received infusions or bolus injections of NPY. Infusion NPY (1 µg/kg/min) increased diuresis and natriuresis, and this was attenuated by intraperitoneal injection of nifedipine (3 µg/kg). Concomitant decreases in heart rate and reductions of renal blood flow were not attenuated by nifedipine. Bolus injections of NPY (0.3, 1, 3, 10 and 30 μg/kg) dose-dependently increased mean arterial pressure and renovascular vascular resistance; only the higher dose of nifedipine (100 μg/kg/min i.v.) moderately inhibited these effects. We conclude that Y(5)-mediated diuresis and natriuresis are more sensitive to inhibition by nifedipine than Y(1)-mediated renovascular effects. Whether this reflects a general sensitivity of Y(5) receptor-mediated responses or is specific for diuresis and natriuresis remains to be investigated. |
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