Article ID Journal Published Year Pages File Type
6259988 Behavioural Brain Research 2011 10 Pages PDF
Abstract

Second generation antipsychotics are commonly prescribed for the treatment of schizophrenia, however some can induce metabolic dysfunction side-effects such as weight gain, obesity and diabetes. Clinical reports suggest olanzapine alters satiety signals, although findings appear conflicting. Previous animal model studies have utilised a range of olanzapine dosages, however the dosage that better mimics the human scenario of olanzapine-induced weight gain is unclear. Female Sprague-Dawley rats were treated orally, three times daily with olanzapine (0.25 mg/kg, 0.5 mg/kg, 1.0 mg/kg, 2.0 mg/kg), self-administered in a sweet cookie dough pellet at eight-hourly intervals) or vehicle (n = 12/group) for 14-days. Olanzapine orally self-administered in multiple doses (eight-hourly intervals) may circumvent a drop in plasma drug concentration and ensure the maintenance of a consistently high olanzapine level in the rat. Olanzapine increased body weight (0.5 mg/kg, 1.0 mg/kg, 2.0 mg/kg), food intake (2.0 mg/kg) and feeding efficiency (0.5-2.0 mg/kg), with no effect on water intake. Subcutaneous inguinal (1.0 mg/kg, 2.0 mg/kg) and intra-abdominal perirenal fat were increased (2.0 mg/kg), but not interscapula brown adipose tissue. Olanzapine increased circulating ghrelin and cholecystokinin, but had no effect on peptide YY(3-36). Olanzapine decreased insulin (0.25-2.0 mg/kg) and locomotor activity in the open field arena (0.5-2.0 mg/kg). A low dosage of 0.25 mg/kg olanzapine had no effect on most parameters measured. Olanzapine-induced weight gain is associated with hyperphagia, enhanced feeding efficiency and adiposity, decreased locomotor activity and altered satiety signaling. The animal model used in the present study of self-administered oral olanzapine treatment (t.i.d.) at a dosage range of 0.5-2.0 mg/kg (but not 0.25 mg/kg) mimics aspects of the clinic.

Research highlights▶ An animal model of olanzapine-induced obesity by oral self-administration (three times/day). ▶ Self-administration of olanzapine mixed with food, given at eight-hourly intervals may better mimic the clinic. ▶ Olanzapine increased ghrelin and CCK levels, and decreased insulin and locomotor activity. ▶ 0.5-2.0 mg/kg (three times/day) olanzapine in the rat replicates aspects of human metabolic dysfunction. ▶ A low dosage of 0.25 mg/kg (three times/day) olanzapine had no significant effect on body weight.

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