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...
Guardado en:
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 |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/78dd4d8abb004a4485544bb1aa809497 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
A spontaneous mitonuclear epistasis converging on Rieske Fe-S protein exacerbates complex III deficiency in mice
por: Janne Purhonen, et al.
Publicado: (2020) -
Myxedema Coma and Acute Hepatopathy in a Dog with Severe Atherosclerosis
por: Leah C. Giralico, et al.
Publicado: (2021) -
Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease
por: Omar Hikmat, et al.
Publicado: (2021) -
Human pluripotent reprogramming with CRISPR activators
por: Jere Weltner, et al.
Publicado: (2018) -
Congestive Hepatopathy Secondary to Right Ventricular Hypertrophy Related to Monocrotaline-Induced Pulmonary Arterial Hypertension
por: Douglas Mesadri Gewehr, et al.
Publicado: (2021)