Cargando…
Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models
Diseases involving inflammation and oxidative stress can be exacerbated by high blood glucose levels. Due to tight metabolic regulation, safely reducing blood glucose can prove difficult. The ketogenic diet (KD) reduces absolute glucose and insulin, while increasing fatty acid oxidation, ketogenesis...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835632/ https://www.ncbi.nlm.nih.gov/pubmed/31581549 http://dx.doi.org/10.3390/nu11102330 |
_version_ | 1783466718343987200 |
---|---|
author | Ari, Csilla Murdun, Cem Koutnik, Andrew P. Goldhagen, Craig R. Rogers, Christopher Park, Collin Bharwani, Sahil Diamond, David M. Kindy, Mark S. D’Agostino, Dominic P. Kovács, Zsolt |
author_facet | Ari, Csilla Murdun, Cem Koutnik, Andrew P. Goldhagen, Craig R. Rogers, Christopher Park, Collin Bharwani, Sahil Diamond, David M. Kindy, Mark S. D’Agostino, Dominic P. Kovács, Zsolt |
author_sort | Ari, Csilla |
collection | PubMed |
description | Diseases involving inflammation and oxidative stress can be exacerbated by high blood glucose levels. Due to tight metabolic regulation, safely reducing blood glucose can prove difficult. The ketogenic diet (KD) reduces absolute glucose and insulin, while increasing fatty acid oxidation, ketogenesis, and circulating levels of β-hydroxybutyrate (βHB), acetoacetate (AcAc), and acetone. Compliance to KD can be difficult, so alternative therapies that help reduce glucose levels are needed. Exogenous ketones provide an alternative method to elevate blood ketone levels without strict dietary requirements. In this study, we tested the changes in blood glucose and ketone (βHB) levels in response to acute, sub-chronic, and chronic administration of various ketogenic compounds in either a post-exercise or rested state. WAG/Rij (WR) rats, a rodent model of human absence epilepsy, GLUT1 deficiency syndrome mice (GLUT1D), and wild type Sprague Dawley rats (SPD) were assessed. Non-pathological animals were also assessed across different age ranges. Experimental groups included KD, standard diet (SD) supplemented with water (Control, C) or with exogenous ketones: 1, 3-butanediol (BD), βHB mineral salt (KS), KS with medium chain triglyceride/MCT (KSMCT), BD acetoacetate diester (KE), KE with MCT (KEMCT), and KE with KS (KEKS). In rested WR rats, the KE, KS, KSMCT groups had lower blood glucose level after 1 h of treatment, and in KE and KSMCT groups after 24 h. After exercise, the KE, KSMCT, KEKS, and KEMCT groups had lowered glucose levels after 1 h, and in the KEKS and KEMCT groups after 7 days, compared to control. In GLUT1D mice without exercise, only KE resulted in significantly lower glucose levels at week 2 and week 6 during a 10 weeks long chronic feeding study. In 4-month and 1-year-old SPD rats in the post-exercise trials, blood glucose was significantly lower in KD and KE, and in KEMCT groups, respectively. After seven days, the KSMCT group had the most significantly reduced blood glucose levels, compared to control. These results indicate that exogenous ketones were efficacious in reducing blood glucose levels within and outside the context of exercise in various rodent models of different ages, with and without pathology. |
format | Online Article Text |
id | pubmed-6835632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68356322019-11-25 Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models Ari, Csilla Murdun, Cem Koutnik, Andrew P. Goldhagen, Craig R. Rogers, Christopher Park, Collin Bharwani, Sahil Diamond, David M. Kindy, Mark S. D’Agostino, Dominic P. Kovács, Zsolt Nutrients Article Diseases involving inflammation and oxidative stress can be exacerbated by high blood glucose levels. Due to tight metabolic regulation, safely reducing blood glucose can prove difficult. The ketogenic diet (KD) reduces absolute glucose and insulin, while increasing fatty acid oxidation, ketogenesis, and circulating levels of β-hydroxybutyrate (βHB), acetoacetate (AcAc), and acetone. Compliance to KD can be difficult, so alternative therapies that help reduce glucose levels are needed. Exogenous ketones provide an alternative method to elevate blood ketone levels without strict dietary requirements. In this study, we tested the changes in blood glucose and ketone (βHB) levels in response to acute, sub-chronic, and chronic administration of various ketogenic compounds in either a post-exercise or rested state. WAG/Rij (WR) rats, a rodent model of human absence epilepsy, GLUT1 deficiency syndrome mice (GLUT1D), and wild type Sprague Dawley rats (SPD) were assessed. Non-pathological animals were also assessed across different age ranges. Experimental groups included KD, standard diet (SD) supplemented with water (Control, C) or with exogenous ketones: 1, 3-butanediol (BD), βHB mineral salt (KS), KS with medium chain triglyceride/MCT (KSMCT), BD acetoacetate diester (KE), KE with MCT (KEMCT), and KE with KS (KEKS). In rested WR rats, the KE, KS, KSMCT groups had lower blood glucose level after 1 h of treatment, and in KE and KSMCT groups after 24 h. After exercise, the KE, KSMCT, KEKS, and KEMCT groups had lowered glucose levels after 1 h, and in the KEKS and KEMCT groups after 7 days, compared to control. In GLUT1D mice without exercise, only KE resulted in significantly lower glucose levels at week 2 and week 6 during a 10 weeks long chronic feeding study. In 4-month and 1-year-old SPD rats in the post-exercise trials, blood glucose was significantly lower in KD and KE, and in KEMCT groups, respectively. After seven days, the KSMCT group had the most significantly reduced blood glucose levels, compared to control. These results indicate that exogenous ketones were efficacious in reducing blood glucose levels within and outside the context of exercise in various rodent models of different ages, with and without pathology. MDPI 2019-10-01 /pmc/articles/PMC6835632/ /pubmed/31581549 http://dx.doi.org/10.3390/nu11102330 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ari, Csilla Murdun, Cem Koutnik, Andrew P. Goldhagen, Craig R. Rogers, Christopher Park, Collin Bharwani, Sahil Diamond, David M. Kindy, Mark S. D’Agostino, Dominic P. Kovács, Zsolt Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models |
title | Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models |
title_full | Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models |
title_fullStr | Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models |
title_full_unstemmed | Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models |
title_short | Exogenous Ketones Lower Blood Glucose Level in Rested and Exercised Rodent Models |
title_sort | exogenous ketones lower blood glucose level in rested and exercised rodent models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835632/ https://www.ncbi.nlm.nih.gov/pubmed/31581549 http://dx.doi.org/10.3390/nu11102330 |
work_keys_str_mv | AT aricsilla exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT murduncem exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT koutnikandrewp exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT goldhagencraigr exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT rogerschristopher exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT parkcollin exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT bharwanisahil exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT diamonddavidm exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT kindymarks exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT dagostinodominicp exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels AT kovacszsolt exogenousketoneslowerbloodglucoselevelinrestedandexercisedrodentmodels |