Obesity exacerbates the acute metabolic side effects of olanzapine

• Published in: Psychoneuroendocrinology Vol. 88; pp. 121 - 128
• Main Authors: Townsend, Logan K., Peppler, Willem T., Bush, Natasha D., Wright, David C.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.02.2018
• Subjects: Animals; Blood Glucose - metabolism; Diet, High-Fat - adverse effects; Glucose; Hyperglycemia - metabolism; Insulin - blood; Insulin resistance; Insulin Resistance - physiology; Liver - metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Obese; Muscle, Skeletal - metabolism; Obesity; Obesity - complications; Obesity - metabolism; Olanzapine; Olanzapine - metabolism; Olanzapine - pharmacology; Schizophrenia; Schizophrenia; Obesity; Insulin resistance; Olanzapine; Glucose
• ISSN: 0306-4530; 1873-3360
• DOI: 10.1016/j.psyneuen.2017.12.004

•Olanzapine-induced hyperglycemia and systemic insulin resistance were exacerbated in high-fat diet-induced obese mice.•Olanzapine also profoundly inhibited insulin signalling in skeletal muscle and liver, which appears to be exacerbated by obesity.•The greater olanzapine-induced hyperglycemia may also result from increased hepatic glucose output in obese mice. Olanzapine is a second-generation antipsychotic used in the management of schizophrenia and various off-label conditions. The acute metabolic responses of olanzapine recapitulate many of the side effects associated with obesity. Obesity rates are high in the schizophrenic population, but it is unknown whether pre-existing obesity-associated metabolic dysfunction augments the acute side effects of olanzapine. To address this question, we compared the responses to olanzapine in lean and high-fat diet-induced (HFD) obese mice. Four weeks of HFD (60% kcal from fat) led to obese, hyperglycemic, and insulin resistant mice. Olanzapine-induced hyperglycemia and systemic insulin resistance were exacerbated in HFD-induced obese mice. Olanzapine also profoundly inhibited insulin signalling in skeletal muscle and liver, which appears to be exacerbated by obesity. The greater olanzapine-induced hyperglycemia may also result from increased hepatic glucose output in obese mice as pyruvate challenge led to significantly higher blood glucose concentrations, with associated increases in hepatic content of gluconeogenic enzymes. Olanzapine also suppressed RER while acutely increasing oxygen consumption in obese mice. A single olanzapine treatment reduced physical activity for up to 24 h, regardless of obesity. Considering obesity is very common in the schizophrenic population, these data suggest that previous research may be under-estimating the severity of olanzapine’s acute side effects.