Literature DB >> 8145130

Pharmacokinetics and pharmacodynamics of nitroglycerin and its dinitrate metabolites in conscious dogs: intravenous infusion studies.

F W Lee1, T Salmonson, L Z Benet.   

Abstract

Intravenous infusions of nitroglycerin (GTN), 1,2-glyceryl dinitrate (1,2-GDN), and 1,3-glyceryl dinitrate (1,3-GDN) were given to four conscious dogs at 10 micrograms/min, 30 micrograms/min, 50 micrograms/min, and 70 micrograms/min of GTN and 20 micrograms/min and 100 micrograms/min of GDNs. The steady state plasma concentrations (Css) of GTN were reached after about 60 min whereas for 1,2-GDN and 1,3-GDN the Css were reached at about 150 min after the infusion began. Except for one dog, the Css of GTN were not proportional to infusion rate, however, all dogs together showed a good linear relationship between Css of GTN and infusion rates with an average correlation coefficient of 0.917 +/- 0.102. Large variability in GTN clearance after various infusion rates was observed in all dogs. The Css ratios of 1,2-GDN/GTN and 1,3-GDN/GTN yield overall averages of 31.5 +/- 17.2 and 5.47 +/- 3.19, respectively. Average Css ratios of metabolites 1,2-GDN/1,3-GDN were 5.78 +/- 1.23. This ratio is different from those obtained after iv bolus and oral dosing indicating that the biotransformation of GTN to 1,2-GDN and 1,3-GDN differs for each dosing route. The clearances for 1,2-GDN and 1,3-GDN were not changed over the dose range of 20 micrograms/min to 100 micrograms/min. Terminal half-lives of 1,2-GDN and 1,3-GDN postinfusion were similar to those values obtained after a single bolus dose (45 min). It appears that all the GTN dose at steady state can be accounted for by the formation of measurable 1,2-GDN and 1,3-GDN. Large intra- and interdog variations in systolic blood pressure decrease (SPD) following infusions of GTN were observed, however, all dogs showed a clear systolic blood pressure decrease when the highest infusion rate (70 micrograms/min) was given. No significant systolic blood pressure drop was detected following 20 micrograms/min infusions of 1,2-GDN or 1,3-GDN. It was clear that systolic blood pressure in all dogs decreased following 100 microgram/min infusions of 1,2-GDN or 1,3-GDN. When SPD values were plotted vs. log GTN concentrations following the infusion of 70 micrograms/min of GTN in all four dogs, a counterclockwise hysteresis was observed indicating the significant contribution of the active dinitrate metabolites to GTN pharmacodynamics.

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Year:  1993        PMID: 8145130     DOI: 10.1007/bf01059113

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  14 in total

1.  Cardiac output is an apparent determinant of nitroglycerin pharmacokinetics in rats.

Authors:  H L Fung; A Blei; S Chong
Journal:  J Pharmacol Exp Ther       Date:  1986-12       Impact factor: 4.030

2.  Pharmacological activity of the dinitrate metabolites of nitroglycerin following their oral administration to healthy volunteers.

Authors:  M Gumbleton; L Z Benet
Journal:  Br J Clin Pharmacol       Date:  1991-02       Impact factor: 4.335

3.  Distribution and metabolism of nitroglycerin and its metabolites in vascular beds of sheep.

Authors:  P A Cossum; M S Roberts; A C Yong; D Kilpatrick
Journal:  J Pharmacol Exp Ther       Date:  1986-06       Impact factor: 4.030

4.  Pharmacokinetics and pharmacodynamics of glyceryl trinitrate and its two dinitrate metabolites in conscious dogs.

Authors:  F W Lee; T Salmonson; C H Metzler; L Z Benet
Journal:  J Pharmacol Exp Ther       Date:  1990-12       Impact factor: 4.030

5.  Blood vessel uptake and metabolism of organic nitrates in the rat.

Authors:  H L Fung; S C Sutton; A Kamiya
Journal:  J Pharmacol Exp Ther       Date:  1984-02       Impact factor: 4.030

6.  Transdermal isosorbide dinitrate in angina pectoris: effect of acute and sustained therapy.

Authors:  J O Parker; K A VanKoughnett; H L Fung
Journal:  Am J Cardiol       Date:  1984-07-01       Impact factor: 2.778

7.  Simultaneous determination of nitroglycerin and its dinitrate metabolites by capillary gas chromatography with electron-capture detection.

Authors:  F W Lee; N Watari; J Rigod; L Z Benet
Journal:  J Chromatogr       Date:  1988-04-29

8.  Nitroglycerin compatibility with intravenous fluid filters, containers, and administration sets.

Authors:  D M Baaske; A H Amann; D M Wagenknecht; M Mooers; J E Carter; H J Hoyt; R G Stoll
Journal:  Am J Hosp Pharm       Date:  1980-02

9.  Comparison of vasodilatory responses to nitroglycerin and its dinitrate metabolites in human veins.

Authors:  W E Haefeli; M Gumbleton; L Z Benet; B B Hoffman; T F Blaschke
Journal:  Clin Pharmacol Ther       Date:  1992-12       Impact factor: 6.875

10.  Nitroglycerin disposition in human blood.

Authors:  P A Cossum; M S Roberts
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

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  2 in total

1.  Understanding the hysteresis loop conundrum in pharmacokinetic/pharmacodynamic relationships.

Authors:  Christopher Louizos; Jaime A Yáñez; M Laird Forrest; Neal M Davies
Journal:  J Pharm Pharm Sci       Date:  2014       Impact factor: 2.327

2.  Nitroglycerin dinitrate metabolites do not affect the pharmacokinetics and pharmacodynamics of nitroglycerin in the dog: a preliminary report.

Authors:  F W Lee; J Hu; C H Metzler; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1993-04
  2 in total

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