HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Pranidipine enhances the action of nitric oxide released from endothelial cells.

Abstract
Nitric oxide (NO) synthesis in vascular endothelium of patients with hypertension is altered. Calcium antagonists have been shown to improve endothelial function in hypertensive patients. Here we report that pranidipine, one of the latest long-acting calcium antagonists in the dihydropyridine group, enhances the actions of NO released from endothelial cells (ECs). Pranidipine significantly enhanced cGMP accumulation in vascular smooth muscle cells cocultured with ECs, whereas amlodipine and nifedipine had no significant effects. In addition, pranidipine also suppressed basal and thrombin-stimulated endothelin-1 production from ECs. Pranidipine also enhanced cGMP accumulation in rat aortic segments with endothelium but not in endothelium-denuded vessels. In contrast, pranidipine had no effect in the presence of N(G)-monomethyl-L-arginine, an inhibitor of NO synthesis. Pranidipine did not affect the basal expression of endothelial NO synthase in ECs. However, pranidipine upregulated the activity of superoxide dismutase in ECs. These findings suggest that pranidipine enhances NO action through inhibition of superoxide-induced NO decomposition in the vessel wall. Thus, pranidipine may be useful in the treatment of impaired endothelial function in patients with hypertension.
AuthorsJ Yang, K Fukuo, S Morimoto, T Niinobu, T Suhara, T Ogihara
JournalHypertension (Dallas, Tex. : 1979) (Hypertension) Vol. 35 Issue 1 Pt 1 Pg. 82-5 (Jan 2000) ISSN: 0194-911X [Print] United States
PMID10642279 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Calcium Channel Blockers
  • Dihydropyridines
  • Endothelin-1
  • Amlodipine
  • Nitric Oxide
  • pranidipine
  • NOS3 protein, human
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type III
  • Nos3 protein, rat
  • Superoxide Dismutase
  • Cyclic GMP
  • Nifedipine
Topics
  • Amlodipine (pharmacology)
  • Animals
  • Aorta, Thoracic (drug effects, metabolism)
  • Calcium Channel Blockers (pharmacology)
  • Cells, Cultured
  • Coculture Techniques
  • Cyclic GMP (metabolism)
  • Dihydropyridines (pharmacology)
  • Endothelin-1 (biosynthesis)
  • Endothelium, Vascular (drug effects, metabolism)
  • Humans
  • Hypertension (drug therapy, metabolism)
  • Male
  • Muscle, Smooth, Vascular (drug effects, metabolism)
  • Nifedipine (pharmacology)
  • Nitric Oxide (biosynthesis)
  • Nitric Oxide Synthase (metabolism)
  • Nitric Oxide Synthase Type III
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: