Literature DB >> 29034440

Risperidone-induced metabolic dysfunction is attenuated by Curcuma longa extract administration in mice.

Florent Auger1,2, Françoise Martin3,4,5,6, Olivier Pétrault2,7, Jennifer Samaillie3,8, Thierry Hennebelle3,8, Mohamed-Sami Trabelsi4,5,6, François Bailleul3,8, Bart Staels3,4,5,6, Régis Bordet2, Patrick Duriez9,10,11.   

Abstract

Antipsychotics, such as risperidone, increase food intake and induce alteration in glucose and lipid metabolism concomitantly with overweight and body fat increase, these biological abnormalities belong to the metabolic syndrome definition (high visceral adiposity, hypertriglyceridemia, hyperglycemia, low HDL-cholesterol and high blood pressure). Curcumin is a major component of traditional turmeric (Curcuma longa) which has been reported to improve lipid and glucose metabolism and to decrease weight in obese mice. We questioned the potential capacity of curcumin, contained in Curcuma longa extract (Biocurcuma™), to attenuate the risperidone-induced metabolic dysfunction. Two groups of mice were treated once a week, for 22 weeks, with intraperitoneal injection of risperidone (Risperdal) at a dose 12.5 mpk. Two other groups received intraperitoneal injection of the vehicle of Risperdal following the same schedule. Mice of one risperidone-treated groups and of one of vehicle-treated groups were fed a diet with 0.05% Biocurcuma™ (curcumin), while mice of the two other groups received the standard diet. Curcumin limited the capacity of risperidone to reduce spontaneous motricity, but failed to impede risperidone-induced increase in food intake. Curcumin did not reduce the capacity of risperidone to induce weight gain, but decreased visceral adiposity and decreased the risperidone-induced hepatomegaly, but not steatosis. Furthermore, curcumin repressed the capacity of risperidone to induce the hepatic over expression of enzymes involved in lipid metabolism (LXRα, FAS, ACC1, LPL, PPARγ, ACO, SREBP2) and decreased risperidone-induced glucose intolerance and hypertriglyceridemia. Curcumin decreased risperidone-induced increases in serum markers of hepatotoxicity (ALAT, ASAT), as well as of one major hepatic pro-inflammatory transcription factor (NFκB: p105 mRNA and p65 protein). These findings support that nutritional doses of curcumin contained in Curcuma longa extract are able to partially counteract the risperidone-induced metabolic dysfunction in mice, suggesting that curcumin ought to be tested to reduce the capacity of risperidone to induce the metabolic syndrome in human.

Entities:  

Keywords:  Atypical antipsychotics; Curcumin; Glucose; Lipids; Risperidone

Mesh:

Substances:

Year:  2017        PMID: 29034440     DOI: 10.1007/s11011-017-0133-y

Source DB:  PubMed          Journal:  Metab Brain Dis        ISSN: 0885-7490            Impact factor:   3.584


  85 in total

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Authors:  Hui-Jun He; Guo-Yu Wang; Yuan Gao; Wen-Hua Ling; Zhi-Wen Yu; Tian-Ru Jin
Journal:  World J Diabetes       Date:  2012-05-15

2.  Antipsychotic drug action on SREBPs-related lipogenesis and cholesterogenesis in primary rat hepatocytes.

Authors:  Emilie Lauressergues; Bart Staels; Karine Valeille; Zouher Majd; Dean W Hum; Patrick Duriez; Didier Cussac
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2010-03-24       Impact factor: 3.000

3.  Chronic antipsychotics treatment regulates MAOA, MAOB and COMT gene expression in rat frontal cortex.

Authors:  Mao-Liang Chen; Chia-Hsiang Chen
Journal:  J Psychiatr Res       Date:  2005-06-17       Impact factor: 4.791

4.  Increased Framingham 10-year risk of coronary heart disease in middle-aged and older patients with psychotic symptoms.

Authors:  Hua Jin; David Folsom; Alana Sasaki; Sunder Mudaliar; Robert Henry; Monique Torres; Shah Golshan; Danielle K Glorioso; Dilip Jeste
Journal:  Schizophr Res       Date:  2010-11-19       Impact factor: 4.939

5.  Weight gain related to treatment with atypical antipsychotics is due to activation of PKC-β.

Authors:  C Pavan; V Vindigni; L Michelotto; A Rimessi; G Abatangelo; R Cortivo; P Pinton; B Zavan
Journal:  Pharmacogenomics J       Date:  2009-12-22       Impact factor: 3.550

6.  Overweight induced by chronic risperidone exposure is correlated with overexpression of the SREBP-1c and FAS genes in mouse liver.

Authors:  Emilie Lauressergues; Françoise Martin; Audrey Helleboid; Emmanuel Bouchaert; Didier Cussac; Régis Bordet; Dean Hum; Gérald Luc; Zouher Majd; Bart Staels; Patrick Duriez
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2011-02-19       Impact factor: 3.000

7.  Structural and organizational determinants of quality of care in patients with schizophrenia in Italy.

Authors:  Paola Bollini; Sandro Pampallona; Giuseppe Tibaldi; Maurizio Bianco; Salvatore Nieddu; Carmine Munizza
Journal:  J Nerv Ment Dis       Date:  2008-12       Impact factor: 2.254

8.  Socio-economic mobility among patients with schizophrenia or major affective disorder. A 17-year retrospective follow-up.

Authors:  S Aro; H Aro; I Keskimäki
Journal:  Br J Psychiatry       Date:  1995-06       Impact factor: 9.319

9.  A multivariate approach linking reported side effects of clinical antidepressant and antipsychotic trials to in vitro binding affinities.

Authors:  Johanna Michl; Christian Scharinger; Miriam Zauner; Siegfried Kasper; Michael Freissmuth; Harald H Sitte; Gerhard F Ecker; Lukas Pezawas
Journal:  Eur Neuropsychopharmacol       Date:  2014-07-03       Impact factor: 4.600

10.  Combination of curcumin and piperine prevents formation of gallstones in C57BL6 mice fed on lithogenic diet: whether NPC1L1/SREBP2 participates in this process?

Authors:  Yongnan Li; Min Li; Shuodong Wu; Yu Tian
Journal:  Lipids Health Dis       Date:  2015-09-03       Impact factor: 3.876

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Journal:  Pharmacol Res       Date:  2019-12-23       Impact factor: 7.658

Review 2.  Influence of the use of atypical antipsychotics in metabolic syndrome.

Authors:  P Doménech-Matamoros
Journal:  Rev Esp Sanid Penit       Date:  2020-07-20

Review 3.  Antidepressants- and antipsychotics-induced hepatotoxicity.

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Review 4.  Natural Products Targeting Liver X Receptors or Farnesoid X Receptor.

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Journal:  Front Pharmacol       Date:  2022-01-05       Impact factor: 5.810

  4 in total

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