Literature DB >> 6422588

Hypoxia induced preferential ketone utilization by rat brain slices.

J R Kirsch, L G D'Alecy.   

Abstract

When exposed to hypoxia, intact mice, with elevated blood ketones, live longer than mice with normal blood ketones. To evaluate a possible mechanism responsible for this phenomenon a rat brain slice preparation was used to determine if brain tissue would utilize glucose or ketones preferentially during exposure to reduced oxygen. Reducing available oxygen in the incubation medium from 95%, in steps, to 5% produced the expected gradual reduction in the carbon dioxide formation from glucose. In contrast, reducing the oxygen level to 40 and 20% resulted in a statistically significant stimulation of the production of carbon dioxide from the ketone beta-hydroxybutyrate. At very low oxygen levels carbon dioxide production from either substrate was reduced. These results are consistent with the hypothesis that ketones can be used in addition to glucose as a substrate for brain energy production even during reduced oxygen availability. If the increase in carbon dioxide production from ketones can be equated with an increase in energy production from this supplemental substrate then ketones may be therapeutically useful in avoiding the collapse of brain function during moderate hypoxia.

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Year:  1984        PMID: 6422588     DOI: 10.1161/01.str.15.2.319

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  10 in total

1.  D-beta-hydroxybutyrate prevents glutamate-mediated lipoperoxidation and neuronal damage elicited during glycolysis inhibition in vivo.

Authors:  Jana Mejía-Toiber; Teresa Montiel; Lourdes Massieu
Journal:  Neurochem Res       Date:  2006-11-18       Impact factor: 3.996

2.  Fasting prior to transient cerebral ischemia reduces delayed neuronal necrosis.

Authors:  C Marie; A M Bralet; S Gueldry; J Bralet
Journal:  Metab Brain Dis       Date:  1990-06       Impact factor: 3.584

3.  Protective effect of fasting upon cerebral hypoxic-ischemic injury.

Authors:  K G Go; G H Prenen; J Korf
Journal:  Metab Brain Dis       Date:  1988-12       Impact factor: 3.584

4.  Effect of D- and L-1,3-butanediol isomers on glycolytic and citric acid cycle intermediates in the rat brain.

Authors:  S Gueldry; J Bralet
Journal:  Metab Brain Dis       Date:  1995-12       Impact factor: 3.584

5.  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

6.  Effect of 1,3-butanediol on cerebral energy metabolism. Comparison with beta-hydroxybutyrate.

Authors:  S Gueldry; J Bralet
Journal:  Metab Brain Dis       Date:  1994-06       Impact factor: 3.584

7.  Ketogenic Ratio Determines Metabolic Effects of Macronutrients and Prevents Interpretive Bias.

Authors:  Tanya Zilberter; Yuri Zilberter
Journal:  Front Nutr       Date:  2018-08-30

8.  Role of glucose and ketone bodies in the metabolic control of experimental brain cancer.

Authors:  T N Seyfried; T M Sanderson; M M El-Abbadi; R McGowan; P Mukherjee
Journal:  Br J Cancer       Date:  2003-10-06       Impact factor: 7.640

9.  How wasting is saving: weight loss at altitude might result from an evolutionary adaptation.

Authors:  Andrew J Murray; Hugh E Montgomery
Journal:  Bioessays       Date:  2014-06-11       Impact factor: 4.345

Review 10.  Investigating Ketone Bodies as Immunometabolic Countermeasures against Respiratory Viral Infections.

Authors:  Brianna J Stubbs; Andrew P Koutnik; Emily L Goldberg; Vaibhav Upadhyay; Peter J Turnbaugh; Eric Verdin; John C Newman
Journal:  Med (N Y)       Date:  2020-07-15
  10 in total

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