I just found the answer to this question:
Citicoline is a water-soluble compound with greater than 90-percent bioavailability. (3) Pharmacokinetic studies on healthy adults have shown oral doses of citicoline are
rapidly absorbed, with less than one percent excreted in feces.
Plasma levels peak in a biphasic manner, at one hour after ingestion followed by a second larger peak at 24 hours post-dosing. Citicoline is metabolized in the gut wall and liver. The byproducts of exogenous citicoline formed by hydrolysis in the intestinal wall are choline and cytidine. Following absorption, choline and cytidine are dispersed throughout the body, enter systemic circulation for utilization in various biosynthetic pathways, and cross the blood-brain barrier for re-synthesis into citicoline in the brain. (4)
Pharmacokinetic studies using [sup.14]C citicoline show citicoline elimination occurs mainly via respiratory C[O.sub.2], and urinary excretion, in two phases mirroring the biphasic plasma peaks. The initial peak in plasma concentration is followed by a sharp decline, which then
slows over the next 4-10 hours. In the second phase, an initially
rapid decline after the 24-hour plasma peak is similarly followed by a slower elimination rate.
The elimination half-life is 56 hours for C[O.sub.2] and 71 hours for urinary excretion. (5)Oral administration of citicoline raises plasma levels of cytidine and choline in rats within six to eight hours. Prolonged administration for 42 and 90 days increases brain concentrations of phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine--the three major phospholipids in brain cell membranes. Evidence for the role of these metabolites as substrates for phosphatidylcholine synthesis was found in a study giving rats daily oral doses of citicoline for 90 days. At a dose of 500 mg/kg per day phosphatidylcholine levels increased by 25 percent, phosphatidylethanolamine by 17 percent, and phosphatidylserine by 42 percent. (8)
From
http://findarticles....1_9/ai_n5990648Since choline is water soluble and is never stored in the body, then I guess the effect of CDP-Choline will be instant, not cumulative. Am I correct?