» Articles » PMID: 8453956

Comparative Effects of Felodipine, Nitrendipine and Nifedipine in Healthy Subjects: Concentration-effect Relationships of Racemic Drugs and Enantiomers

Overview
Specialty Pharmacology
Date 1993 Jan 1
PMID 8453956
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

The effects of racemic (rac) felodipine, rac-nitrendipine and nifedipine (all 20 mg solution p.o.) on non-invasively measured blood pressure and heart rate were investigated in a randomised, double-blind, cross-over study in 12 normotensive, young, healthy males. Compared to baseline values, heart rate increased more after rac-felodipine treatment (+47% at maximum) than rac-nitrendipine (+40%) and nifedipine (+38%); only small and variable changes in blood pressure were observed with any of the drugs. The baseline-corrected area under the heart rate-time curve up to 4 h after the administration of rac-felodipine was 197% and 180% larger than after nifedipine and rac-nitrendipine treatment, respectively. The effects on heart rate could be fitted individually to a sigmoidal Emax-model without hysteresis for all drugs under investigation. The relative potencies of the unbound drugs for their indirect effects on heart rate were 1:7:43 for nifedipine, rac-nitrendipine and rac-felodipine, respectively. The active (S)-enantiomers of felodipine and nitrendipine appeared to be 9- and 60-times as potent as nifedipine in this respect, assuming no (inter)activity of the (R)-enantiomers. Individual and mean changes in blood pressure were small, they were not related to plasma concentrations, and did not differ between treatments.

Citing Articles

Enantioselectivity in Drug Pharmacokinetics and Toxicity: Pharmacological Relevance and Analytical Methods.

Coelho M, Fernandes C, Remiao F, Tiritan M Molecules. 2021; 26(11).

PMID: 34070985 PMC: 8197169. DOI: 10.3390/molecules26113113.


1,4-dihydropyridines: the multiple personalities of a blockbuster drug family.

Cataldi M, Bruno F Transl Med UniSa. 2013; 4:12-26.

PMID: 23905059 PMC: 3728803.


Clinical and pharmacokinetic results with a new ultrashort-acting calcium antagonist, clevidipine, following gradually increasing intravenous doses to healthy volunteers.

ERICSSON H, Fakt C, Jolin-Mellgard A, NORDLANDER M, Sohtell L, Sunzel M Br J Clin Pharmacol. 1999; 47(5):531-8.

PMID: 10336577 PMC: 2014189. DOI: 10.1046/j.1365-2125.1999.00933.x.


Determination of (+)- and (-)-nicardipine concentrations in human serum and their correlation with the antihypertensive effect after oral administration of racemic nicardipine.

Iwaoka T, Inotsume N, Inoue J, Naomi S, Okamoto Y, Higuchi S Eur J Clin Pharmacol. 1995; 48(5):345-9.

PMID: 8641321 DOI: 10.1007/BF00194949.


Effects of acute febrile infectious diseases on the oral pharmacokinetics and effects of nitrendipine enantiomers and of bisoprolol.

Soons P, Grib C, Breimer D, Kirch W Clin Pharmacokinet. 1992; 23(3):238-48.

PMID: 1355019 DOI: 10.2165/00003088-199223030-00006.

References
1.
Edgar B, Regardh C, Attman P, Aurell M, Herlitz H, Johnsson G . Pharmacokinetics of felodipine in patients with impaired renal function. Br J Clin Pharmacol. 1989; 27(1):67-74. PMC: 1379706. DOI: 10.1111/j.1365-2125.1989.tb05336.x. View

2.
Triggle D, Langs D, Janis R . Ca2+ channel ligands: structure-function relationships of the 1,4-dihydropyridines. Med Res Rev. 1989; 9(2):123-80. DOI: 10.1002/med.2610090203. View

3.
Bellemann P, Schade A, Towart R . Dihydropyridine receptor in rat brain labeled with [3H]nimodipine. Proc Natl Acad Sci U S A. 1983; 80(8):2356-60. PMC: 393819. DOI: 10.1073/pnas.80.8.2356. View

4.
FLECKENSTEIN A . Historical overview. The calcium channel of the heart. Ann N Y Acad Sci. 1988; 522:1-15. DOI: 10.1111/j.1749-6632.1988.tb33337.x. View

5.
Blychert E, Hedner T, Dahlof C, Elmfeldt D . Plasma concentration-effect relationships of intravenous and extended-release oral felodipine in hypertensive patients. J Cardiovasc Pharmacol. 1990; 15(3):428-35. DOI: 10.1097/00005344-199003000-00013. View