“…Just as in humans, in whom only 20–30% of an ingested dose of oral cocaine reaches the bloodstream intact (Wilkinson, Van Dyke, Jatlow, Barash, & Byck, 1980), in the rat, hepatic metabolism may inactivate a considerable quantity of the cocaine consumed orally (Bouis & Boelsterli, 1990; El-Maghrabi, Calligaro, & Eldefrawi, 1988). Nevertheless, ingested cocaine has been found to be behaviorally active in rats in that it functions as a positive reinforcer (Falk, Vigorito, Tang, & Lau, 1990; Jentsch, Henry, Mason, Merritt, & Ziriax, 1998; Meert & Janssen, 1992; Seidman, Lau, Chen, & Falk, 1992; Suzuki, Masukawa, Yoshii, Kawai, & Yanaura, 1990; for an exception, see Bell, Macenski, Silverman, & Meisch, 1993), increases locomotor activity (Falk, Ma, & Lau, 1991; Lau, Iman, Ma, & Falk, 1991), and induces indications of a withdrawal syndrome during forced abstinence (Barros & Miczek, 1996). Specifically, Jentsch et al (1998) trained rats to respond for small aliquots of a cocaine-saccharin solution following home-cage preexposure to the solution.…”