Related Experiment Video
Updated: Aug 14, 2026

Measurement of Cyclic Guanosine Monophosphate (cGMP) in Solid Tissues using Competitive Enzyme-Linked Immunosorbent Assay (ELISA)
Published on: July 3, 2025
Validation of an electrometric blood cholinesterase measurement in goats
M M H Al-Jobory1, F K Mohammad
1Department of Physiology, Division of Pharmacology and Toxicology, College of Veterinary Medicine, University of Mosul, Mosul, P. O. Box 11136, Iraq.
Abstract:
A modified electrometric method was described and validated for measurement of plasma and erythrocyte cholinesterase activities in 6-18 months old goats. The enzymatic reaction mixture contained 3 ml distilled water, 3 ml barbital-phosphate buffer (pH 8.1), 0.2 ml plasma or erythrocytes and 0.1 ml acetylthiocholine iodide (7.5%) as a substrate. The mixture was incubated at 37 degrees C for 40 minutes. The pH of the reaction mixture was determined by a pH meter before and after the incubation. The initial pH was measured before the substrate addition. The enzyme activity was expressed as DeltapH/40 min. The coefficients of variation of the described method in measuring plasma and erythrocyte cholinesterase activities were 4 and 2%, respectively. Preliminary reference values (n = 14) of the mean cholinesterase activity (DeltapH/40 min) and 95% confidence interval in the plasma were 0.194 and 0.184-0.204, respectively, and those of the erythrocytes were 0.416 and 0.396-0.436, respectively. The pseudocholinesterase activity of the plasma cholinesterase was 63.5% as determined by quinidine sulfate inhibition. The organophosphorus insecticides dichlorvos and diazinon at 0.5-4 microM and the carbamate insecticide carbaryl at 5-20 microM in the reaction mixture significantly inhibited plasma (13.7-85.5%) and erythrocyte (16.4-71.9%) cholinesterases in vitro in a concentration-dependent manner. The results suggest that the described electrometric method is simple, precise and efficient in measuring blood cholinesterase activity in goats.
