Two models for weight gain and hyperphagia as side effects of atypical antipsychotics in male rats: Validation with olanzapine and ziprasidone

• Published in: Behavioural brain research 2011-01, Vol.216 (2), p.561-568
• Main Authors: Shobo, Miwako, Yamada, Hiroshi, Mihara, Takuma, Kondo, Yuji, Irie, Megumi, Harada, Katsuya, Ni, Keni, Matsuoka, Nobuya, Kayama, Yukihiko
• Format: Article
• Language: English
• Subjects: Adult and adolescent clinical studies; Animal models; Animals; Antipsychotic Agents - administration & dosage; Antipsychotic Agents - adverse effects; Antipsychotics; Appetite; Behavioral psychophysiology; Benzodiazepines - administration & dosage; Benzodiazepines - adverse effects; Biological and medical sciences; Body weight gain; Diets; Disease Models, Animal; Dose-Response Relationship, Drug; Feeding behavior; Feeding Behavior - drug effects; Food intake; Fundamental and applied biological sciences. Psychology; Hyperphagia; Hyperphagia - chemically induced; Male; Male SD rat; Medical sciences; Metabolic diseases; Neuroleptics; Neuropharmacology; Obesity; olanzapine; Pharmacology. Drug treatments; Piperazines - administration & dosage; Piperazines - adverse effects; Psycholeptics: tranquillizer, neuroleptic; Psychology. Psychoanalysis. Psychiatry; Psychology. Psychophysiology; Psychopathology. Psychiatry; Psychopharmacology; Psychoses; Rats; Rats, Sprague-Dawley; Schizophrenia; Side effects; Thiazoles - administration & dosage; Thiazoles - adverse effects; Weight Gain - drug effects; ziprasidone
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2010.08.046

▶ Six-week chronic treatment with olanzapine in male rats increased weight gain and fatty tissues. ▶ Plasma concentration of olanzapine in the rats was comparable to clinical setting. ▶ Food intake and duration were significantly increased in acute olanzapine treated male rats. ▶ Ziprasidone administration caused no observable adverse effects. Body weight gain is one of the most serious side effects associated with clinical use of antipsychotics. However, the mechanisms by which antipsychotics induce body weight gain are unknown, and no reliable animal models of antipsychotics-induced weight gain have been established. The present studies were designed to establish male rat models of weight gain induced by chronic and acute treatment with antipsychotics. Six-week chronic treatment with olanzapine (5, 7.5, and 10 mg/kg/day) in male Sprague-Dawley rats fed a daily diet resembling a human macronutrient diet, significantly increased body weight gain and weight of fatty tissues. In contrast, ziprasidone (1.25, 2.5, and 5 mg/kg/day) administration caused no observable adverse effects. We then investigated feeding behavior with acute antipsychotic treatment in male rats using an automated food measurement apparatus. Rats were allowed restricted access to normal laboratory chow (4 h/day). With acute olanzapine (0.5, 1, and 2 mg/kg, i.p.) treatment in the light phase, food intake volume and duration were significantly increased, while treatment with ziprasidone (0.3, 1, and 3 mg/kg, i.p.) did not increase food intake volume or meal time duration. Findings from the present studies showed that chronic treatment with olanzapine in male rats induced body weight gain, and acute injection induced hyperphagia, suggesting that hyperphagia may be involved in the weight gain and obesity-inducing properties of chronically administered olanzapine. These animal models may provide useful experimental platforms for analysis of the mechanism of hyperphagia and evaluating the potential risk of novel antipsychotics to induce weight gain in humans.