Effects of metabolic inhibitors and incubation temperature on the saturable uptake of propranolol by isolated rat lung tissue

Author:

Iwamoto Kikuo1,Watanabe Jun2,Yonekawa Hina2

Affiliation:

1. Department of Pharmacy, Shimane Medical University Hospital, Izumo 693

2. Department of Biopharmaceutics, Faculty of Pharmaceutical Sciences, Nagoya City University, Nagoya 467, Japan

Abstract

Abstract The effects of several metabolic inhibitors (50 μM) on the initial uptake rate of propranolol (0·5 to 500 #mUg mL−1) by the minced lungs (0·4g) isolated from 7-week-old rats has been investigated in oxygenated, pH 7·4 Krebs-Ringer bicarbonate buffer solution (20 mL) containing 3% BSA at 37°C for 5 min. The effect of the incubation temperature was also examined. Metabolism of propranolol was almost insignificant (i.e. less than 1·3% of the initial load). The overall initial uptake rate was considered to be a combination of apparent linear transport and saturable processes. For the control uptake rate, the linear transport rate constant was 1·26 ± 0·16 g−1 mL−1 min−1, while Vmax and Km' of the capacity limited uptake process were estimated as 0·727 ± 0·074 mg g−1 min−1 and 24·8 ± 2·71 μg mL−1, respectively. No metabolic inhibitor tested had an effect on the linear transport rate of propranolol but 2,4-dinitrophenol and potassium cyanide inhibited saturable uptake rate (i.e. Vmax) of propranolol significantly (P<0·01) while ouabain, phloridine and iodoacetic acid did not do so significantly. Reduction of the incubation temperature to 15°C decreased and at 25°C tended to decrease, both linear transport and saturable uptake rates.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference10 articles.

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2. Studies on the absorption, distribution and excretion of propranolol in rat, dog and monkey;Hayes;J. Pharm. Exp. Ther.,1971

3. Avoidance of first-pass metabolism of propranolol after rectal administration as a function of the absorption site;Iwamoto;Pharm. Res.,1985

4. Age-dependence in capacity-limited uptake kinetics of propranolol by isolated rat hepatocytes;Iwamoto;Biochem. Pharmacol.,1986

5. High capacity for pulmonary first-pass elimination of propranolol in rats;Iwamoto;J. Pharm. Pharmacol.,1987

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