American Journal of Physiology-Endocrinology and Metabolism · 1989 · 28 citations · 24 references
MedicinePharmacologyPhysiologyCalcium HomeostasisPharmacodynamicsRenal PathophysiologyCalcitonin PhysiologyDiuretic TherapyRenal HemodynamicsSodium HomeostasisCalcitonin Effects On Renal Calcium ExcretionCalcitonin Gene-related Peptide PhysiologyCalcitonin PharmacologyFractional Excretion Of SodiumPlasma Renin ActivityRenal Hemodynamic EffectsRenal Phosphate Excretion
Cardiovascular and renal actions of human calcitonin gene-related peptide II (or beta) (CGRP) and of human calcitonin (CT) infused intravenously for 1 h each (79 and 263 pmol.kg-1.h-1) have been compared in normal men (n = 10 for CGRP, n = 6 for CT and vehicle alone). CGRP lowered diastolic blood pressure by 26% and increased the heart rate by 35% and raised plasma levels of norepinephrine, epinephrine, and dopamine and renin activity (P less than 0.01). The fractional excretion rates (FE) of sodium and chloride were doubled (P less than 0.05-0.01) in the presence of an unaltered glomerular filtration rate. CT, on the other hand, did not affect the diastolic blood pressure, but the stimulation of diuresis and of the FE of sodium and chloride was more pronounced with CT than with CGRP (P less than 0.01). Moreover, CT lowered serum calcium levels and stimulated urinary adenosine 3',5'-cyclic monophosphate and phosphate excretion (P less than 0.01). In conclusion, the cardiovascular effects of CGRP are contrasted by weaker renal tubular actions of the neuropeptide in relation to CT.
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Calcitonin gene-related peptide is a potent vasodilator
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P Weidmann, L Hasler, Markus Gnädinger et al. · Journal of Clinical Investigation · 1986 · 346 citations · Full text
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