Michaelis-Menten kinetics of galactose elimination by the isolated perfused pig liver
- PMID: 1275072
- DOI: 10.1152/ajplegacy.1976.230.5.1302
Michaelis-Menten kinetics of galactose elimination by the isolated perfused pig liver
Abstract
The relation between galactose elimination rates and blood concentrations in the isolated perfused pig liver was analyzed by a mathematical kinetic model. It assumes that the substrate, under steady-state conditions, is removed from the blood that flows through the sinusoids by an irreversible process which follows Michaelis-Menten (i.e., saturation) kinetics. The experiments consisted of successive periods with constant infusions of galactose. The model fitted the data to within the experimental uncertainty. The estimated maximal rate (Vmax) ranged from 0.34 to 0.57 mmol-min(-1)-kg(-1) liver, and the Michaelis constant, Km, ranged from 0.12 to 0.30 mmol-liter(-1) plasma water in nine experiments. The ratio between the galactose concentration in hepatocyte water and plasma water was not significantly different from 1.0, indicating that membrane transport is not rate limiting for the elimination of galactose. In experiments with increasing concentrations of galactose in hepatocyte water and approximately saturated elimination rates, the concentrations of galactose 1-phosphate, UDPgalactose, and UDPglucose remained essentially constant. This indicates that the phosphorylation of galactose to galactose 1-phosphate is the rate-determining process.
Similar articles
-
Hepatic galactose elimination kinetics in the intact pig.Scand J Clin Lab Invest. 1982 May;42(3):253-9. Scand J Clin Lab Invest. 1982. PMID: 7134810
-
Kinetics of ethanol inhibition of galactose elimination in perfused pig liver.Scand J Clin Lab Invest. 1977 Oct;37(6):487-94. doi: 10.3109/00365517709101836. Scand J Clin Lab Invest. 1977. PMID: 616067
-
Galactose removal kinetics during hypoxia in perfused pig liver: reduction of Vmax, but not of intrinsic clearance Vmax/Km.Eur J Clin Invest. 1990 Jun;20(3):305-9. doi: 10.1111/j.1365-2362.1990.tb01860.x. Eur J Clin Invest. 1990. PMID: 2114992
-
Defective galactosylation in galactosemia: is low cell UDPgalactose an explanation?Eur J Pediatr. 1995;154(7 Suppl 2):S65-71. doi: 10.1007/BF02143806. Eur J Pediatr. 1995. PMID: 7671968 Review.
-
[Clinical variants and basic principles of the diagnosis of galactosemia (review of the literature)].Vopr Okhr Materin Det. 1975 Aug;20(8):58-62. Vopr Okhr Materin Det. 1975. PMID: 241152 Review. Russian. No abstract available.
Cited by
-
An understanding of the role of enzyme localization of the liver on metabolite kinetics: a computer simulation.J Pharmacokinet Biopharm. 1983 Oct;11(5):451-68. doi: 10.1007/BF01062205. J Pharmacokinet Biopharm. 1983. PMID: 6668553
-
First-pass elimination. Basic concepts and clinical consequences.Clin Pharmacokinet. 1984 Jan-Feb;9(1):1-25. doi: 10.2165/00003088-198409010-00001. Clin Pharmacokinet. 1984. PMID: 6362950 Review.
-
Hepatic ethanol elimination kinetics in patients with cirrhosis.Scand J Gastroenterol. 2009;44(7):867-71. doi: 10.1080/00365520902929856. Scand J Gastroenterol. 2009. PMID: 19404864 Free PMC article.
-
Hepatic galactose metabolism quantified in humans using 2-18F-fluoro-2-deoxy-D-galactose PET/CT.J Nucl Med. 2011 Oct;52(10):1566-72. doi: 10.2967/jnumed.111.092924. Epub 2011 Aug 29. J Nucl Med. 2011. PMID: 21875925 Free PMC article.
-
Transport of D-fructose and D-galactose into isolated rat hepatocytes.Biochem J. 1980 Oct 15;192(1):373-5. doi: 10.1042/bj1920373. Biochem J. 1980. PMID: 7305908 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources