Article

Influence of lipid imbalance on butyrylcholinesterase activity and biotransformation efficiency.

Department of Cell and Molecular Biology of Drugs, Faculty of Pharmacy, Comenius University, Bratislava, Slovak Republic.
Pharmazie (impact factor: 1.01). 04/2012; 67(4):345-50.
Source: PubMed

ABSTRACT Butyrylcholinesterase (EC 3.1.1.8, BChE) is highly active in plasma, skin and lung, the tissues that first contact xenobiotics, supporting a role for BChE in detoxication of xenobiotics including medicaments. A possible involvement of BChE in lipid metabolism has been suggested. Elevated BChE activity in obese individuals correlates with some parameters of lipid metabolism including increased levels of triacylglycerols (TAG) and cholesterol. The aim of this study was to estimate the BChE activity in rats on subcellular and inter-organ levels under the conditions of untreated and treated primary hypertriacylglycerolemia with the TAG lowering agent fenofibrate. No changes in BChE activity were observed in obese animals. However fenofibrate administration led to significant increase of BChE activity in all examined tissues (plasma, liver, white adipose tissue). The impact of lipid metabolic imbalance on BChE biotransformation ability was tested by measuring the rate of hydrolysis of 0,1 to 8 mM concentrations of the antimicrobial agent N-(2-benzoyloxyethyl)-ethyldimethylammonium bromide (BCH2). The results revealed a complete shift in the BChE kinetics in all studied models. In animals with hypertriacylglycerolemia the Km value of liver BChE rised 4,6-fold, but the total enzyme efficiency expressed as Vmax/Km dropped 40% comparing to control. In contrast, in animals treated with fenofibrate the BChE efficiency increased in liver 1,6-fold. We conclude here that BChE detoxification capacity is essentially altered under conditions of disturbed lipid metabolism. Clinically, this knowledge could be important in a view of xenobiotic elimination, especially when routinely prescribed medicaments are concerned.

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Keywords

antimicrobial agent N-(2-benzoyloxyethyl)-ethyldimethylammonium bromide
 
BChE activity
 
BChE biotransformation ability
 
BChE detoxification capacity
 
BChE efficiency
 
BChE kinetics
 
Elevated BChE activity
 
fenofibrate administration
 
first contact xenobiotics
 
inter-organ levels
 
lipid metabolic imbalance
 
lipid metabolism
 
liver 1,6-fold
 
liver BChE rised 4,6-fold
 
obese individuals correlates
 
possible involvement
 
primary hypertriacylglycerolemia
 
total enzyme efficiency
 
white adipose tissue
 
xenobiotic elimination
 

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