Literature DB >> 22423586

Effect of orlistat on lipid peroxidation, Na+, K+ ATPase, glutathione and serotonin in rat brain.

D Calderón Guzmán1, E Hernández García, A Juárez Jacobo, L Segura Abarca, G Barragán Mejía, R Rodríguez Pérez, H Juárez Olguín.   

Abstract

The aim of this study was to evaluate the effect of orlistat, a drug used in weight loss, on 5-HT and indicators of oxidative stress in rat brain. Orlistat, 12 mg/kg was administered to Wistar rats as single dose or successive doses on 3 consecutive days. Blood glucose and oxidative stress indicators were detected by measurement of lipid peroxidation, Na+, K+ ATPase, glutathione and serotonin levels using previous validated methods. The levels of glucose decreased in rats receiving successive doses. The activity of Na+, K+ ATPase and total ATPase was reduced in rats receiving successive doses, while the level of lipid peroxidation increased slightly in both groups. Glutathione underwent significant reduction in the successive doses group (p < 0.05). 5-HT increased significantly after single dose treatment (p < 0.05). Orlistat can induce pro-oxidant effects in the brain due to alteration of serotonergic metabolism and the reduction of glutathione.

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Year:  2011        PMID: 22423586

Source DB:  PubMed          Journal:  Proc West Pharmacol Soc        ISSN: 0083-8969


  2 in total

1.  Orlistat induces ferroptosis-like cell death of lung cancer cells.

Authors:  Wenjing Zhou; Jing Zhang; Mingkun Yan; Jin Wu; Shuo Lian; Kang Sun; Baiqing Li; Jia Ma; Jun Xia; Chaoqun Lian
Journal:  Front Med       Date:  2021-06-04       Impact factor: 4.592

2.  NADPH accumulation is responsible for apoptosis in breast cancer cells induced by fatty acid synthase inhibition.

Authors:  Yanfen Cui; Pan Xing; Yuanyuan Wang; Miao Liu; Li Qiu; Guoguang Ying; Binghui Li
Journal:  Oncotarget       Date:  2017-05-16
  2 in total

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