Literature DB >> 30527262

Short-term and long-term ketogenic diet therapy and the addition of exercise have differential impacts on metabolic gene expression in the mouse energy-consuming organs heart and skeletal muscle.

Kozue Shimizu1, Hazuki Saito1, Kanako Sumi1, Yuri Sakamoto2, Yoichi Tachi2, Kaoruko Iida3.   

Abstract

Although a ketogenic diet (KD) is used to treat various metabolic diseases, the organ-specific metabolic changes that occur in response to a KD remain unclear. Therefore, we tested the hypothesis that duration of KD consumption and regular exercise in addition to KD consumption affect metabolic fuel selection at gene levels in heart and skeletal muscle. Six-week-old male C57BL/6J mice were divided into 2 groups, one fed a standard diet and the other fed a KD, and maintained for either 4 weeks (short term) or 12 weeks (long term). The long-term group was further divided into 2 subgroups, and mice in 1 of the 2 groups had an exercise load 5 days a week. Body weight decreased significantly in the KD groups during the first few weeks only. Plasma ketone levels rose and muscle glycogen levels declined significantly in the KD groups, but these changes were less severe in the KD plus exercise group. KD consumption decreased the expression of genes related to glucose utilization in heart and skeletal muscle; however, this decrease did not occur with KD consumption plus exercise. Long-term but not short-term KD consumption increased the expression of genes related to lipid utilization, regardless of exercise. In the KD groups, the expression of genes related to ketolysis was suppressed, and that of genes related to ketogenesis was increased. These results indicate that KD exposure and pairing a KD with exercise have differential impacts on energy substrate selection at gene expression levels in energy-consuming organs, the heart and skeletal muscle.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Exercise; Heart; Ketogenic diet; Metabolic gene; Skeletal muscle

Mesh:

Substances:

Year:  2018        PMID: 30527262     DOI: 10.1016/j.nutres.2018.09.004

Source DB:  PubMed          Journal:  Nutr Res        ISSN: 0271-5317            Impact factor:   3.315


  6 in total

1.  Long-Term Ketogenic Diet Induces Metabolic Acidosis, Anemia, and Oxidative Stress in Healthy Wistar Rats.

Authors:  Aryadi Arsyad; Irfan Idris; Andi A Rasyid; Rezky A Usman; Kiki R Faradillah; Wa Ode U Latif; Zidni I Lubis; Aminuddin Aminuddin; Ika Yustisia; Yulia Y Djabir
Journal:  J Nutr Metab       Date:  2020-06-19

2.  Combined effects of a ketogenic diet and exercise training alter mitochondrial and peroxisomal substrate oxidative capacity in skeletal muscle.

Authors:  Tai-Yu Huang; Melissa A Linden; Scott E Fuller; Felicia R Goldsmith; Jacob Simon; Heidi M Batdorf; Matthew C Scott; Nabil M Essajee; John M Brown; Robert C Noland
Journal:  Am J Physiol Endocrinol Metab       Date:  2021-04-12       Impact factor: 5.900

Review 3.  Changes in Myocardial Metabolism Preceding Sudden Cardiac Death.

Authors:  J Snyder; R Zhai; A I Lackey; P Y Sato
Journal:  Front Physiol       Date:  2020-06-16       Impact factor: 4.566

4.  Effects of the ketogenic diet in mice with hind limb ischemia.

Authors:  Adilan Shalamu; Zhen Dong; Bowen Liu; Lihong Pan; Yun Cai; Liwei Liu; Xiurui Ma; Kai Hu; Aijun Sun; Junbo Ge
Journal:  Nutr Metab (Lond)       Date:  2022-08-29       Impact factor: 4.654

5.  Ketogenic diet feeding improves aerobic metabolism property in extensor digitorum longus muscle of sedentary male rats.

Authors:  Yuji Ogura; Chiaki Kakehashi; Toshinori Yoshihara; Mitsutoshi Kurosaka; Ryo Kakigi; Kazuhiko Higashida; Sei-Etsu Fujiwara; Tatsuo Akema; Toshiya Funabashi
Journal:  PLoS One       Date:  2020-10-30       Impact factor: 3.240

6.  Isonitrogenous low-carbohydrate diet elicits specific changes in metabolic gene expression in the skeletal muscle of exercise-trained mice.

Authors:  Hazuki Saito; Naoko Wada; Kaoruko Iida
Journal:  PLoS One       Date:  2022-01-21       Impact factor: 3.240

  6 in total

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