Molecular forms of butyrylcholinesterase and obesity

This study compared obese (N = 134) and unobese (N = 92) male blood donors, regarding the relative intensity (RI) and activity of different molecular forms (G1, G2, G4 and G1-ALB) of butyrylcholinesterase (BChE, EC 3.1.1.8) found in plasma, thereby searching for an association between these variables with obesity and SNPs of exons 1 and 4 of the BCHE gene. It was shown that obese and unobese individuals do not differ in the RI of each BChE band, even when classifying the sample into three genotypes of exons 1 and 4 of the BCHE gene (-116GG/539AA, -116GG/539AT, -116GA/539AT). Although the mean BChE activity of each band was significantly higher in obese than in unobese blood donors, the proportions of BChE bands were maintained, even under the metabolic stress associated to obesity, thereby leading to infer that this proportion is somehow regulated, and may therefore be important for BChE functions

Effects of physical exercise on butyrylcholinesterase in obese adolescents

Abstract The aim of the present study was to evaluate the effect of a 12 week program of physical exercise (PE) on butyrylcholinesterase (BChE) in obese adolescents. This study compared obese adolescents (N = 54) before and after PE, regarding the relative intensity (RI) and activity of different molecular forms (G1, G2, G4 and G1-ALB) of BChE found in plasma. Waist circumference (WC) and lipid profile were also assessed before and after PE. It was shown that before PE, mean plasma BChE activity was significantly higher in obese than in non-obese adolescents and that it was significantly reduced after PE, becoming similar to that found in non-obese adolescents. Lipid profile and WC also changed in response to PE. These results are consistent with studies that found a correlation between BChE and lipid metabolism and suggest that PE may have led to a physiological regularization of plasma BChE activity. Although mean BChE activity of each isoform was significantly reduced by PE, their RI did not change. This is in accordance with a previous suggestion that this proportion is maintained under factors such as obesity, and may therefore be important for BChE functions. Key words: BChE activity; physical exercise, obesity. Butyrylcholinesterase (BChE; EC 3.1.1.8) is coded by BCHE gene (3q26.1-q26.2), synthesized in the liver and distributed to several parts of the organism. Plasmatic BChE is found in four possible homomeric forms (G1 monomers, G2 dimmers, G3 trimers and G4 tetramers) or heteromeric forms formed in association with other proteins, such as albumin, G1-Alb (Masson, 1989). Several studies verified that BChE has a role in lipid metabolism The aim of this study was to compare the relative intensity (RI) of BChE isoforms revealed as bands (G1, G1-Alb, G2 and G4) in obese adolescents before and after 12 weeks of physical exercise (PE), and to search for a correlation between RI of BChE isoform bands, plasma BChE activity and PE. The sample comprised 54 obese adolescents (BMI above percentile 95 and mean age 12.6 ± 2.01), these being participants of a 12 week program of physical exercise. Aerobic exercise consisted of 50 to 100 min activity during the first four weeks. Intensity was set at 35%-55% of VO 2 peak, and was increased to 55%-75% during the next eight weeks. Plasma was sampled at baseline and after terminating the program. A sample of non-obese adolescents (N = 45; mean age 13.3 ± 2.15) was used to measure plasma BChE activity. The detection and analysis of BChE bands in plasma was made according to Mean plasma BChE activity was significantly reduced after the 12 weeks program (before: 7.66 ± 2.64 KU/L, after: 5.89 ± 2.34 KU/L; t = 2.96, p = 0.008). Accompanying BChE activity, waist circumference (WC; before: 97.41 ± 11.20 cm, after: 94.62 ± 10.51 cm, t = 3.6 and p = 0.03), LDL-cholesterol (LDL-C; before: 94.45 ± 20.83 mg/dL, after: 86.00 ± 16.37 mg/dL, t = 2.77 and p = 0.012) and triglycerides (TG; before: 114.30 ± 57.14 mg/dL, after: 82.75 ± 42.66 mg/dL, t = 3.1 and p = 0.006) also showed significant reduction with PE

Biochemical and genetic analysis of butyrylcholinesterase (BChE) in a family, due to prolonged neuromuscular blockade after the use of succinylcholine

Butyrylcholinesterase (BChE) is a plasma enzyme that catalyzes the hydrolysis of choline esters, including the muscle-relaxant succinylcholine and mivacurium. Patients who present sustained neuromuscular blockade after using succinylcholine usually carry BChE variants with reduced enzyme activity or an acquired BChE deficiency. We report here the molecular basis of the BCHE gene underlying the slow catabolism of succinylcholine in a patient who underwent endoscopic nasal surgery. We measured the enzyme activity of BChE and extracted genomic DNA in order to study the promoter region and all exons of the BCHE gene of the patient, her parents and siblings. PCR products were sequenced and compared with reference sequences from GenBank. We detected that the patient and one of her brothers have two homozygous mutations: nt1615 GCA > ACA (Ala539Thr), responsible for the K variant, and nt209 GAT > GGT (Asp70Gly), which produces the atypical variant A. Her parents and two of her brothers were found to be heterozygous for the AK allele, and another brother is homozygous for the normal allele. Sequence analysis of exon 1 including 5′UTR showed that the proband and her brother are homozygous for –116GG. The AK/AK genotype is considered the most frequent in hereditary hypocholinesterasemia (44%). This work demonstrates the importance of defining the phenotype and genotype of the BCHE gene in patients who are subjected to neuromuscular block by succinylcholine, because of the risk of prolonged neuromuscular paralysis

Kuri: A Simulator of Ecological Genetics for Tree Populations

This paper presents Kuri, a software package developed to simulate the temporal and spatial dynamics of genetic variability in populations and multispecies communities of trees, as well as their interactions with environmental factors. A conceptual model using agents inspired on Echo models is used to define the environment, the hierarchical structures, and the low-level rules of the system. At the individual agent (tree) level a genetic algorithm is used to model the genotypic structure and the genetic processes, from a small set of simple rules, complex higher-order population, and environmental interactions emerge. The program was written in Delphi for the Windows environment, and was designed to be used for educational and research purposes