4.2 Article

Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin

期刊

BMC PHARMACOLOGY & TOXICOLOGY
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40360-020-00427-0

关键词

Simvastatin; Olanzapine; Brown adipose tissue; Body weight gain; Dyslipidemia

资金

  1. Key Program of Chongqing Science and Technology Research Project [cstc2016shmsxm80102]
  2. Venture & Innovation Support Program for Chongqing Overseas Returnees [cx2018089]
  3. Fundamental Research Funds for the Central Universities, P. R. China [XDJK2018B037, XDJK2018D027]
  4. Scientific and Technological Cooperation Fund of Nanchong Government [18SXHZ0443]
  5. NHMRC (National Health and Medical Research Council) [APP1104184]

向作者/读者索取更多资源

Background: Prescription of second-generation antipsychotic drugs (SGAs) to childhood/adolescent has exponentially increased in recent years, which was associated with the greater risk of significant weight gain and dyslipidemia. Statin is considered a potential preventive and treatment approach for reducing SGA-induced weight gain and dyslipidemia in schizophrenia patients. However, the effect of statin treatment in children and adolescents with SGA-induced dyslipidemia is not clearly demonstrated. Methods: To investigate the efficacy of statin interventions for reversing SGA-induced dyslipidemia, young Sprague Dawley rats were treated orally with either olanzapine (1.0 mg/kg, t.i.d.), simvastatin (3.0 mg/kg, t.i.d.), olanzapine plus simvastatin (O + S), or vehicle (control) for 5 weeks. Results: Olanzapine treatment increased weight gain, food intake and feeding efficiency compared to the control, while O + S co-treatment significantly reversed body weight gain but without significant effects on food intake. Moreover, olanzapine treatment induced a slight but significant reduction in body temperature, with a decrease in locomotor activity. Fasting plasma glucose, triglycerides (TG), and total cholesterol (TC) levels were markedly elevated in the olanzapine-only group, whereas O + S co-treatment significantly ameliorated these changes. Pronounced activation of lipogenic gene expression in the liver and down-regulated expression of uncoupling protein-1 (UCP1) and peroxisome-proliferator-activated receptor-gamma co-activator-1 alpha (PGC-1 alpha) in brown adipose tissue (BAT) was observed in the olanzapine-only group. Interestingly, these protein changes could be reversed by co-treatment with O + B. Conclusions: Simvastatin is effective in ameliorating TC and TG elevated by olanzapine. Modulation of BAT activity by statins could be a partial mechanism in reducing metabolic side effects caused by SGAs in child and adolescent patients.

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