Repetition priming is a basic form of learning associated with decreased neuronal responses following stimulus repetition. In this experiment, we address cholinergic and GABAergic modulation of repetition priming in a face recognition paradigm. In experiment 1, we used eventrelated functional magnetic resonance imaging (fMRI) inRepetition priming is a basic form of learning defined behaviorally as facilitated or biased processing of previously encountered stimuli. One possible neuronal signature of this form of learning is "response suppression," a decrement in the neuronal response to repeated stimulation that has been shown in monkeys (Desimone 1996). Measures of repetition priming in humans include pattern completion, object identification, or word-stem completion tasks (Schacter 1994). When using such tasks in conjunction with neuroimaging methods, studies have consistently found decreased hemodynamic responses in posterior cortical regions when items are repeated (Squire et al. 1992;Buckner et al. 1998;Buckner et al. 2000;Badgaiyan 2000;van Turennout et al. 2000 successfully demonstrated a human analog to the decreased neural firing observed in monkey cortex, which is referred to as "repetition suppression." Using a word-stem completion task, we have previously shown that "repetition suppression" is modulated by GABAergic and cholinergic neurotransmitter systems (Thiel et al. 2001). Both lorazepam and scopolamine decreased the size of repetition suppression effect in posterior and frontal cortical regions. Both drugs also impaired the behavioral index of repetition priming, suggesting that GABAergic and cholinergic systems modulate neuronal plasticity necessary for priming in this paradigm. The behavioral impairments with lorazepam were consistent with prior studies using picture-fragment completion, word-fragment completion, or wordstem completion tasks Vidailhet et al. 1994;Vidailhet et al. 1999;Danion et al. 1992;Brown et al. 1989). Behavioral impairments of repetition priming with scopolamine, on the other hand, were not in line with the majority of prior studies (Knopman 1991;Danion et al. 1990;Schifano and Curran 1994), and we suggested that these differences could be caused by a lower active dose used in these previous studies (see Thiel et al. 2001 for discussion).The rationale for the present study was to further investigate GABAergic and cholinergic modulation of repetition priming, using a paradigm involving face recognition (Ellis et al. 1990). This paradigm investigates priming of faces and its modulation by familiarity (i.e., famous vs. unfamous faces). Whereas the paradigm has been used in several psychological and neuroimaging studies (Ellis et al. 1990;Brunas-Wagstaff et al. 1992;Henson et al. 2000;Henson et al. 2002), its pharmacological modulation has not previously been investigated. Functional magnetic resonance imaging (fMRI) studies using repeated, intermixed presentations of famous and unfamous faces in implicit face priming paradigms have shown greater responses to famous than unfam...