ABSORPTION, TISSUE DISTRIBUTION AND EXCRETION OF RADIOLABELED COMPOUNDS IN RATS AFTER ADMINISTRATION OF [C-14] L-ALPHA-GLYCERYLPHOSPHORYLCHOLINE

Citation
G. Abbiati et al., ABSORPTION, TISSUE DISTRIBUTION AND EXCRETION OF RADIOLABELED COMPOUNDS IN RATS AFTER ADMINISTRATION OF [C-14] L-ALPHA-GLYCERYLPHOSPHORYLCHOLINE, European journal of drug metabolism and pharmacokinetics, 18(2), 1993, pp. 173-180
Citations number
7
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
03787966
Volume
18
Issue
2
Year of publication
1993
Pages
173 - 180
Database
ISI
SICI code
0378-7966(1993)18:2<173:ATDAEO>2.0.ZU;2-V
Abstract
The kinetics and metabolism of L-alpha-glycerylphosphoryl-choline (alp ha-GPC) were investigated in male and female rats after i.v. (10 mg/kg ) and oral doses (100-300 mg/kg). Alpha-GPC was labelled with [C-14]-g lycerol ([14G]-GPC) or [C-14]-choline [C-14]-choline ([C-14]-GPC). Dif ferent kinetic and metabolic profiles were observed after i.v. and ora l administration. It is assumed that alpha-GPC is hydrolyzed by phosph odiesterases in the gut mucosa. The different labelled metabolites hav e different kinetic properties of absorption, distribution and clearan ce, leading to different blood concentration-time curves of total radi oactivity. Both labelled compounds save a wide distribution of radioac tivity, particularly concentrated in the liver, kidney, lung and splee n compared to blood. Brain concentrations of [C-14]-GPC were comparabl e to ([14G]-GPC) or lower than ([C-14]-GPC) total blood radioactivity. The metabolite profile in the perfused brain showed a small amount of choline and two unknown metabolites, probably the same as in blood. I n addition, choline was incorporated into brain phospholipids increasi ng amounts within 24 h of dosing. In all caws renal and fecal excretio n of radioactivity was low and comparable for [14G]-GPC and [C-14]-GPC . Mostly the administered radioactivity was exhaled as (CO2)-C-14, thi s degradation being faster and more pronounced for the glycerol-labell ed metabolites than for the choline-labelled metabolites for both rout es of administration. In all cases the results were the same for male and female rats.