The anticonvulsant, gabapentin is transported across biological membra
nes via the L-amino acid transport system (System-L). Absorption of ga
bapentin is saturable, and in-vitro data have previously demonstrated
that both L-leucine and L-phenylalanine may compete with the intestina
l transport of gabapentin. The purpose of this study therefore was to
determine whether a high-protein meal would interfere with gabapentin
absorption. Ten healthy volunteers received in a randomized, cross-ove
r design, a single 600-mg dose of gabapentin in the fasting state and
after a high-protein meal consisting of 80 gm total protein (4.1 g phe
nylalanine, 8.2 g leucine and 4.2 g isoleucine), 52 g carbohydrate, an
d 9 g fat. Plasma gabapentin concentrations were measured by HPLC at b
aseline, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24,
30 h. Calculated pharmacokinetic parameters included C-max, T-max, AUC
and T-1/2. In addition, a pharmacodynamic assessment (using visual an
alog scales) of gabapentin-related adverse effects was performed at 2
h post drug ingestion and was compared between study phases. Statistic
al analysis included Student's t-test for paired data, with significan
ce assigned at P < 0.05. C-max was significantly increased by 36% (3.8
7 +/- 1.15 vs 5.28 +/- .97 mu g/ml, P = 0.002), and T-max tended to be
shorter (3.9 +/- 1.8 vs 2.8 +/- .35 h, P = 0.10), after the high-prot
ein meal. Although AUC was increased by 11%, this did not achieve stat
istical significance. Despite significantly higher plasma concentratio
ns at 2 h, subjects reported significantly fewer adverse effects after
the high-protein meal. Potential mechanisms to explain these unexpect
ed findings may be that the large amino acid load delivered with the h
igh-protein meal enhanced gabapentin absorption via trans-stimulation,
the process by which acutely increased intestinal luminal amino acid
concentrations result in an acute up regulation in System-L activity.
Conversely, the decrease in perceived adverse CNS effects of gabapenti
n following the high-protein meal may reflect CNS competition for Syst
em-L transport.