β hydroxybutyrate levels in serum and cerebrospinal fluid under ketone body metabolism in rats
- PMID: 28100888
- PMCID: PMC5411304
- DOI: 10.1538/expanim.16-0090
β hydroxybutyrate levels in serum and cerebrospinal fluid under ketone body metabolism in rats
Abstract
A high-fat, low-carbohydrate diet (KD) or calorie restriction in the form of every-other-day fasting (EODF) results in ketone body metabolism with an increasing β-hydroxybutyrate (βOHB) level. Previous studies have supported that a KD and EODF have a neuroprotective effect. However, the βOHB levels in the cerebrospinal fluid (CSF) resulting from a KD and EODF remain unknown. The aim of this study was to detect βOHB levels in rats fed a KD, EODF diet, and every-other-day ketogenic diet (EODKD) and to compare the serum βOHB level with the CSF βOHB level. Twenty-four male Sprague-Dawley rats were randomly divided into KD, EODF, EODKD, and standard diet (SD) groups. A customized food with a ratio of carbohydrates to fats of 1:4 was used in the KD and EODKD groups. The βOHB level was measured using ELISA kits in 200 µl serum and 100 µl CSF samples for each rat after feeding for 2 weeks. The KD, EODF, and EODKD resulted in a significant increase in βOHB levels in both the serum and CSF. The βOHB levels in the EODKD group were the highest. The CSF βOHB level was, on average, 69% of the serum βOHB level. There was a positive correlation between the overall βOHB levels in serum and that in cerebrospinal fluid. This study demonstrated that the KD, EODF, and EODKD resulted in ketone body metabolism, as the βOHB levels increased significantly compared with those resulting from the standard diet. Our results suggested that the serum βOHB level was an indicator of the CSF βOHB level, and that the EODKD was an effective diet to enhance ketogenic metabolism.
Keywords: CSF; ketone dody metabolism; serum; βOHB concentration.
Figures
Similar articles
-
Ketogenic Metabolism Inhibits Histone Deacetylase (HDAC) and Reduces Oxidative Stress After Spinal Cord Injury in Rats.Neuroscience. 2017 Dec 16;366:36-43. doi: 10.1016/j.neuroscience.2017.09.056. Epub 2017 Oct 9. Neuroscience. 2017. PMID: 29024787
-
Bone microstructure and metabolism changes under the combined intervention of ketogenic diet with intermittent fasting: an in vivo study of rats.Exp Anim. 2019 Aug 14;68(3):371-380. doi: 10.1538/expanim.18-0084. Epub 2019 Apr 3. Exp Anim. 2019. PMID: 30944267 Free PMC article.
-
The Ketone Metabolite β-Hydroxybutyrate Attenuates Oxidative Stress in Spinal Cord Injury by Suppression of Class I Histone Deacetylases.J Neurotrauma. 2017 Sep 15;34(18):2645-2655. doi: 10.1089/neu.2017.5192. Epub 2017 Aug 4. J Neurotrauma. 2017. PMID: 28683591
-
Ketone bodies as signaling metabolites.Trends Endocrinol Metab. 2014 Jan;25(1):42-52. doi: 10.1016/j.tem.2013.09.002. Epub 2013 Oct 18. Trends Endocrinol Metab. 2014. PMID: 24140022 Free PMC article. Review.
-
β-Hydroxybutyrate in the Brain: One Molecule, Multiple Mechanisms.Neurochem Res. 2017 Jan;42(1):35-49. doi: 10.1007/s11064-016-2099-2. Epub 2016 Nov 8. Neurochem Res. 2017. PMID: 27826689 Review.
Cited by
-
β-Hydroxybutyrate Ameliorates Aβ-Induced Downregulation of TrkA Expression by Inhibiting HDAC1/3 in SH-SY5Y Cells.Am J Alzheimers Dis Other Demen. 2020 Jan-Dec;35:1533317519883496. doi: 10.1177/1533317519883496. Epub 2019 Oct 24. Am J Alzheimers Dis Other Demen. 2020. PMID: 31648544 Free PMC article.
-
Metabolism and epilepsy: Ketogenic diets as a homeostatic link.Brain Res. 2019 Jan 15;1703:26-30. doi: 10.1016/j.brainres.2018.05.049. Epub 2018 Jun 6. Brain Res. 2019. PMID: 29883626 Free PMC article. Review.
-
Activation of microglial GPR109A alleviates thermal hyperalgesia in female lupus mice by suppressing IL-18 and glutamatergic synaptic activity.Glia. 2022 Apr;70(4):634-649. doi: 10.1002/glia.24130. Epub 2021 Dec 16. Glia. 2022. PMID: 34919284 Free PMC article.
-
Emerging roles of GPR109A in regulation of neuroinflammation in neurological diseases and pain.Neural Regen Res. 2023 Apr;18(4):763-768. doi: 10.4103/1673-5374.354514. Neural Regen Res. 2023. PMID: 36204834 Free PMC article. Review.
-
Mechanism of Action of Ketogenic Diet Treatment: Impact of Decanoic Acid and Beta-Hydroxybutyrate on Sirtuins and Energy Metabolism in Hippocampal Murine Neurons.Nutrients. 2020 Aug 8;12(8):2379. doi: 10.3390/nu12082379. Nutrients. 2020. PMID: 32784510 Free PMC article.
References
-
- Colombo M., Kruhoeffer M., Gregersen S., Agger A., Jeppesen P., Oerntoft T., Hermansen K.2006. Energy restriction prevents the development of type 2 diabetes in Zucker diabetic fatty rats: coordinated patterns of gene expression for energy metabolism in insulin-sensitive tissues and pancreatic islets determined by oligonucleotide microarray analysis. Metabolism 55: 43–52. - PubMed
-
- de Assis A.M., da Silva J.S., Rech A., Longoni A., Nonose Y., Repond C., de Bittencourt Pasquali M.A., Moreira J.C., Souza D.O., Pellerin L.2016. Cerebral ketone body oxidation is facilitated by a high fat diet enriched with advanced glycation end products in normal and diabetic rats. Front. Neurosci. 10: 509. doi: 10.3389/fnins.2016.00509 - DOI - PMC - PubMed
-
- Holland A.M., Kephart W.C., Mumford P.W., Mobley C.B., Lowery R.P., Shake J.J., Patel R.K., Healy J.C., McCullough D.J., Kluess H.A., Huggins K.W., Kavazis A.N., Wilson J.M., Roberts M.D.2016. Effects of a ketogenic diet on adipose tissue, liver, and serum biomarkers in sedentary rats and rats that exercised via resisted voluntary wheel running. Am. J. Physiol. Regul. Integr. Comp. Physiol. 311: R337–R351. doi: 10.1152/ajpregu.00156.2016 - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources