Literature DB >> 19201746

Ketogenic diet reduces cytochrome c release and cellular apoptosis following traumatic brain injury in juvenile rats.

Zhi Gang Hu1, Han Dong Wang, Wei Jin, Hong Xia Yin.   

Abstract

Ketone bodies have been shown to be favorable alternative metabolic substrates and are protective under neuropathologies. At the same time, cytochrome c release has been reported following traumatic brain injury (TBI) and precipitates apoptosis via the mitochondrial pathway. The present study investigated the effects of a ketogenic diet (KD) on TBI. TBI was produced using the Feeney weight-drop model and the animals were fed either normal diet (ND) or KD. Brain edema was estimated by wet/dry weight ratio; cytochrome c was detected by Western blotting; cellular apoptosis in the penumbra area was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and active caspase-3 immunohistochemical staining. The results show that brain edema, cytochrome c release, and cellular apoptosis were induced after TBI and that KD reduced these changes dramatically. These findings suggest that KD has potential therapeutic benefit in TBI.

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Year:  2009        PMID: 19201746

Source DB:  PubMed          Journal:  Ann Clin Lab Sci        ISSN: 0091-7370            Impact factor:   1.256


  24 in total

1.  Ketogenic diet prevents alterations in brain metabolism in young but not adult rats after traumatic brain injury.

Authors:  Ying Deng-Bryant; Mayumi L Prins; David A Hovda; Neil G Harris
Journal:  J Neurotrauma       Date:  2011-08-04       Impact factor: 5.269

2.  Protection of hypoglycemia-induced neuronal death by β-hydroxybutyrate involves the preservation of energy levels and decreased production of reactive oxygen species.

Authors:  Alberto Julio-Amilpas; Teresa Montiel; Eva Soto-Tinoco; Cristian Gerónimo-Olvera; Lourdes Massieu
Journal:  J Cereb Blood Flow Metab       Date:  2015-02-04       Impact factor: 6.200

Review 3.  Purines and neuronal excitability: links to the ketogenic diet.

Authors:  S A Masino; M Kawamura; D N Ruskin; J D Geiger; D Boison
Journal:  Epilepsy Res       Date:  2011-08-30       Impact factor: 3.045

4.  The mitochondrial permeability transition pore provides a key to the diagnosis and treatment of traumatic brain injury.

Authors:  Richard L Veech; C Robert Valeri; Theodore B VanItallie
Journal:  IUBMB Life       Date:  2012-02       Impact factor: 3.885

Review 5.  Glucose metabolism in pediatric traumatic brain injury.

Authors:  Mayumi L Prins
Journal:  Childs Nerv Syst       Date:  2017-09-06       Impact factor: 1.475

Review 6.  Cerebral ketone metabolism during development and injury.

Authors:  Mayumi L Prins
Journal:  Epilepsy Res       Date:  2011-11-21       Impact factor: 3.045

7.  A ketogenic diet delays weight loss and does not impair working memory or motor function in the R6/2 1J mouse model of Huntington's disease.

Authors:  David N Ruskin; Jessica L Ross; Masahito Kawamura; Tiffany L Ruiz; Jonathan D Geiger; Susan A Masino
Journal:  Physiol Behav       Date:  2011-04-09

8.  D-beta-hydroxybutyrate prevents MPP+-induced neurotoxicity in PC12 cells.

Authors:  Baohua Cheng; Xinxin Yang; Chengchun Chen; Danfu Cheng; Xudong Xu; Xuewen Zhang
Journal:  Neurochem Res       Date:  2009-10-23       Impact factor: 3.996

Review 9.  Ketogenic diet, neuroprotection, and antiepileptogenesis.

Authors:  Madhuvika Murugan; Detlev Boison
Journal:  Epilepsy Res       Date:  2020-08-19       Impact factor: 3.045

Review 10.  Ketone bodies as signaling metabolites.

Authors:  John C Newman; Eric Verdin
Journal:  Trends Endocrinol Metab       Date:  2013-10-18       Impact factor: 12.015

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