Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation

Abstract Mitochondrial disorders are among the most prevalent inborn errors of metabolism but largely lack treatments and have poor outcomes. High-fat, low-carbohydrate ketogenic diets (KDs) have shown beneficial effects in mouse models of mitochondrial myopathies, with induction of mitochondrial bi...

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Autores principales: Janne Purhonen, Jayasimman Rajendran, Matthias Mörgelin, Kristiina Uusi-Rauva, Shintaro Katayama, Kaarel Krjutskov, Elisabet Einarsdottir, Vidya Velagapudi, Juha Kere, Matti Jauhiainen, Vineta Fellman, Jukka Kallijärvi
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spelling oai:doaj.org-article:78dd4d8abb004a4485544bb1aa8094972021-12-02T15:05:47ZKetogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation10.1038/s41598-017-01109-42045-2322https://doaj.org/article/78dd4d8abb004a4485544bb1aa8094972017-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-01109-4https://doaj.org/toc/2045-2322Abstract Mitochondrial disorders are among the most prevalent inborn errors of metabolism but largely lack treatments and have poor outcomes. High-fat, low-carbohydrate ketogenic diets (KDs) have shown beneficial effects in mouse models of mitochondrial myopathies, with induction of mitochondrial biogenesis as the suggested main mechanism. We fed KD to mice with respiratory chain complex III (CIII) deficiency and progressive hepatopathy due to mutated BCS1L, a CIII assembly factor. The mutant mice became persistently ketotic and tolerated the KD for up to 11 weeks. Liver disease progression was attenuated by KD as shown by delayed fibrosis, reduced cell death, inhibition of hepatic progenitor cell response and stellate cell activation, and normalization of liver enzyme activities. Despite no clear signs of increased mitochondrial biogenesis in the liver, CIII assembly and activity were improved and mitochondrial morphology in hepatocytes normalized. Induction of hepatic glutathione transferase genes and elevated total glutathione level were normalized by KD. Histological findings and transcriptome changes indicated modulation of liver macrophage populations by the mutation and the diet. These results reveal a striking beneficial hepatic response to KD in mice with mitochondrial hepatopathy and warrant further investigations of dietary modification in the management of these conditions in patients.Janne PurhonenJayasimman RajendranMatthias MörgelinKristiina Uusi-RauvaShintaro KatayamaKaarel KrjutskovElisabet EinarsdottirVidya VelagapudiJuha KereMatti JauhiainenVineta FellmanJukka KallijärviNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-16 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Janne Purhonen
Jayasimman Rajendran
Matthias Mörgelin
Kristiina Uusi-Rauva
Shintaro Katayama
Kaarel Krjutskov
Elisabet Einarsdottir
Vidya Velagapudi
Juha Kere
Matti Jauhiainen
Vineta Fellman
Jukka Kallijärvi
Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
description Abstract Mitochondrial disorders are among the most prevalent inborn errors of metabolism but largely lack treatments and have poor outcomes. High-fat, low-carbohydrate ketogenic diets (KDs) have shown beneficial effects in mouse models of mitochondrial myopathies, with induction of mitochondrial biogenesis as the suggested main mechanism. We fed KD to mice with respiratory chain complex III (CIII) deficiency and progressive hepatopathy due to mutated BCS1L, a CIII assembly factor. The mutant mice became persistently ketotic and tolerated the KD for up to 11 weeks. Liver disease progression was attenuated by KD as shown by delayed fibrosis, reduced cell death, inhibition of hepatic progenitor cell response and stellate cell activation, and normalization of liver enzyme activities. Despite no clear signs of increased mitochondrial biogenesis in the liver, CIII assembly and activity were improved and mitochondrial morphology in hepatocytes normalized. Induction of hepatic glutathione transferase genes and elevated total glutathione level were normalized by KD. Histological findings and transcriptome changes indicated modulation of liver macrophage populations by the mutation and the diet. These results reveal a striking beneficial hepatic response to KD in mice with mitochondrial hepatopathy and warrant further investigations of dietary modification in the management of these conditions in patients.
format article
author Janne Purhonen
Jayasimman Rajendran
Matthias Mörgelin
Kristiina Uusi-Rauva
Shintaro Katayama
Kaarel Krjutskov
Elisabet Einarsdottir
Vidya Velagapudi
Juha Kere
Matti Jauhiainen
Vineta Fellman
Jukka Kallijärvi
author_facet Janne Purhonen
Jayasimman Rajendran
Matthias Mörgelin
Kristiina Uusi-Rauva
Shintaro Katayama
Kaarel Krjutskov
Elisabet Einarsdottir
Vidya Velagapudi
Juha Kere
Matti Jauhiainen
Vineta Fellman
Jukka Kallijärvi
author_sort Janne Purhonen
title Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
title_short Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
title_full Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
title_fullStr Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
title_full_unstemmed Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
title_sort ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex iii deficiency caused by a bcs1l mutation
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/78dd4d8abb004a4485544bb1aa809497
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