“…Given that L-type calcium channel blockers have been shown to attenuate naloxone-precipitated withdrawal in nonhumans (Barrios & Baeyens, 1991; Bongianni, Carla, Moroni, & Pellegrini-Giampietro, 1986; Seth, Upadhyaya, Moghe, & Ahmad, 2011) and humans (Oliveto, Poling, Kosten, & Gonsai, 2004), as well as attenuate withdrawal during opioid detoxification (Jimenez-Lerma et al, 2002; Shulman, Jagoda, Laycock, & Kelly, 1998), this pilot study examined the tolerability and initial efficacy of gabapentin, an N-type calcium channel blocker (Eroglu et al, 2009; e.g., Maneuf et al, 2003; Snutch, Sutton, & Zamponi, 2001) and GABA analogue that promotes release of GABA (Bertrand, Morin, & Lacaille, 2003; Kuzniecky et al, 2002), to attenuate withdrawal and illicit opioid use in opioid dependent volunteers undergoing a buprenorphine detoxification protocol. Gabapentin is indicated for the treatment of post herpetic neuralgia and as adjunct therapy for epilepsy (Pfizer, 2012a).…”