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Bromopride is a dopamine D2 receptor antagonist (Ki = 14 nM).1 It binds to bovine anterior pituitary membranes with an IC50 value of 2.13 μM.2 Bromopride inhibits cholinesterase activity in vitro in rat plasma and striatum homogenate (IC50s = 67.8 and 38.4 μM, respectively).3 It increases serum prolactin levels in rats by 100% when used at a dose of 0.02 mol/kg.2 Bromopride (2.5 mg/kg) decreases locomotion and rearing in an open field test and impairs acquistion, but not retention, of a conditioned avoidance response in a two-way active conditioned avoidance test in rats.4
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1. Clinical implications of enteric and central D2 receptor blockade by antidopaminergic gastrointestinal prokinetics. Aliment. Pharmacol. Ther. 19(4), 379-390 (2004).
2. Effects of a series of substituted benzamides on rat prolactin secretion and 3H-
3. Differential effects of bromopride and domperidone on cholinesterase activity in rat tissues. Life Sci. 56(3), 151-156 (1995).
4. A comparison of bromopride and domperidone effects on rat conditioned avoidance and motor activity. Pharmacol. Toxicol. 68(1), 46-50 (1991).