Ab. Guttormsen et al., KINETICS OF PLASMA HOMOCYSTEINE IN HEALTHY-SUBJECTS AFTER PERORAL HOMOCYSTEINE LOADING, Clinical chemistry, 39(7), 1993, pp. 1390-1397
The kinetics of plasma homocysteine were determined in 13 healthy subj
ects after peroral administration and in one person after intravenous
injection. Various forms of homocysteine completely dissolved in an aq
ueous solution were rapidly absorbed after peroral administration, and
the bioavailability was estimated to be 0.53. The volume of distribut
ion was 0.66 L/kg. The area under the plasma concentration curve (AUC0
-48 h) was proportional to the administered dose (33.5-134 mumol/kg bo
dy wt), and showed small interindividual variations. Plasma homocystei
ne showed first-order elimination kinetics for at least 6 h. The half-
life (t1/2) was 223 +/- 45 min, and there was a significant correlatio
n between t1/2 values determined on two different occasions in the sam
e individual. The transient hyperhomocysteinemia was associated with a
n increase in plasma methionine, which probably reflects intracellular
remethylation of homocysteine. Less than 2% of the administered homoc
ysteine dose was recovered in the urine. These findings may form the b
asis for future studies on the regulation of plasma homocysteine in he
alth and disease, and should motivate the evaluation of a homocysteine
loading test as a diagnostic tool.