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
Cited by
3 articles.
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