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Time-Dependent Effects of Metformin and Olanzapine on the Metabolic System
Gizem Kurt1, Seyda T Durhan2, Mehmet Ak3
1Middle East Technical University, Department of Biological Sciences, Ankara, Turkey.
Abstract:
Second-generation antipsychotic drugs, such as olanzapine, have been associated with metabolic side effects including significant weight gain. Recent evidence suggests that this adverse effect may be attenuated by metformin.Male Wistar rats were chronically treated with olanzapine, together with or without metformin, for 7 and 14 weeks. Feeding behavior, food intake, and weight gain were recorded, as well as plasma leptin and triglyceride levels were measured. The expression of hypothalamic candidate genes, Pomc and Npy, involved in appetite and energy balance expressions' was assessed by quantitative real-time polymerase chain reaction.Olanzapine alone caused significant body weight gain, and the co-administration of metformin for 14 weeks lowered body weight and food intake compared with both the 7-week and control groups. Plasma triglyceride levels did not differ among groups. Leptin levels were significantly higher in the olanzapine-only group and were lower in both metformin-olanzapine groups, more promising in the early co-treatment with metformin. Compared to the control group, the hypothalamus of the olanzapine treatment group exhibited downregulated Pomc expression and upregulated Npy expression.Early co-treatment with metformin significantly mitigated olanzapine-induced weight gain and food intake, demonstrating its potential in preventing metabolic side effects when initiated at the beginning of antipsychotic therapy.
Insights
Metformin may reduce weight gain caused by olanzapine, a second-generation antipsychotic. Early metformin treatment shows promise in preventing these metabolic side effects.
Area of Science:
- Pharmacology
- Neuroscience
- Metabolic Research
Background:
- Second-generation antipsychotics like olanzapine are linked to significant weight gain.
- Metformin is being investigated for its potential to mitigate these metabolic side effects.
Purpose of the Study:
- To investigate the efficacy of metformin in preventing olanzapine-induced weight gain and metabolic changes in a rat model.
- To assess the impact of metformin on feeding behavior, gene expression, and metabolic markers.
Main Methods:
- Male Wistar rats were treated with olanzapine, with or without metformin, for 7 and 14 weeks.
- Measurements included feeding behavior, food intake, weight gain, plasma leptin and triglyceride levels.
- Hypothalamic gene expression (Pomc, Npy) was analyzed using quantitative real-time polymerase chain reaction.
Main Results:
- Olanzapine induced significant weight gain; metformin co-administration for 14 weeks lowered body weight and food intake.
- Leptin levels were elevated with olanzapine alone but reduced with metformin co-treatment.
- Olanzapine altered hypothalamic gene expression, downregulating Pomc and upregulating Npy, effects partially reversed by metformin.
Conclusions:
- Early co-treatment with metformin significantly mitigated olanzapine-induced weight gain and reduced food intake.
- Metformin demonstrates potential in preventing metabolic side effects associated with antipsychotic therapy when initiated early.
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