Analysis of energy restriction and physical activity on brain function: the role of ketone body and brain-derived neurotrophic factor

Article information

J Exerc Rehabil Vol. 13, No. 4, 378-380, August, 2017

Publication date (electronic) : 2017 August 29

doi : https://doi.org/10.12965/jer.1735028.514

Chan Ho Park¹, Yi-Sub Kwak^2,

¹Department of Marine Sports, Pukyong National University, Busan, Korea

²Department of Physical Education, Dong-Eui Uinversity, Busan, Korea

^*Corresponding author: Yi-Sub Kwak, https://orcid.org/0000-0003-4545-7250, Department of Physical Education, College of Arts and Sports Science, Dong-Eui University, 176 Eomgwang-ro, Busanjin-gu, Busan 47340, Korea, Tel: +82-51-890-1546, Fax: +82-505-182-6915, E-mail: ysk2003@deu.ac.kr

Received 2017 June 28; Accepted 2017 August 7.

Abstract

INTRODUCTION

Brain development is a complex process, and stimuli during this development period may modulate the functional maturation of the brain and determine its lifelong integrity. Human and animal studies have shown that environmental stimuli, such as physical activity habits, have a beneficial effect on brain development (Gomes da silva and Arida, 2015). Exercise has many functions not only in the developmental period of the brain but also in adulthood.

Exercise is known to have many beneficial effects on brain function and energy metabolism. Endurance exercise and prolonged fasting state are known to improve brain function including cognition. It is well known that exercise training improves hippocampus-dependent cognition, however optimum exercise intensity is still undetermined. Inoue et al. (2015) showed that continuous mild exercise training leads to enhanced hippocampus-related memory both healthy adults and subjects with low physical capacity.

The hippocampal-dependent memory-enhancing effect of exercise is closely related to exercise-induced increase in hippocampal neurogenesis. Physical exercise most effectively promotes adult hippocampal neurogenesis when exercise is aerobic and lasting (Nokia et al., 2016). Physical exercise is also a strong inducer of reactive oxygen species (ROS), and increased ROS stimulates the regulation of antioxidant enzyme systems in the skeletal and cardiac muscles (Park and Kwak, 2016).

The exact mechanisms of exercise improving brain function are still unknown. However, it can be considered that energy restriction and stressful challenge induced by long-lasting physical exercise might cause direct effect on brain function. The neurotrophin family of signal proteins, including brain-derived neurotrophic factor (BDNF), nerve growth factor, neurotrophin-3 and NT-4/5 determine the survival and differentiation of neuronal cells during development.

BDNF and energy restriction have a great effect on the effects of exercise. In this study, therefore, we discussed two topics: “exercise and BDNF” and “exercise and energy restriction.”

EXERCISE AND BDNF

BDNF is a type of neurotrophic factors involved in memory or cognitive development, and its expression is increased by exercise. Improving memory function of exercise is particularly associated with increased neurotrophic factors such as BDNF and insulin-like growth factor-1 (IGF-1) (Tonoli et al., 2015). BDNF is a major regulator of synaptic transmission and plasticity in adult synapses in many areas of the central nervous system. BDNF activates synaptic consolidation through transcription and rapid dendritic trafficking of mRNA encoded by the immediate early gene, Arc (Bramham and Messaoudi, 2005). There was a difference in BDNF expression by exercise intensity and distance. High intensity intermittent exercise increased BDNF levels in the blood of male subjects at 1.25- or 2.5-km distance, while blood interleukin-6 level was higher in 2.5-km distance (Cabral-Santos et al., 2016).

BDNF is involved in the regulation of adult hippocampal neurogenesis, and tyrosine kinase B (TrkB) is a BDNF receptor. BDNF-TrkB signaling is closely related to progression to neural maturation (Donovan et al., 2008). Regular and prolonged exercise can relieve hippocampal-dependent memory loss caused by chronic stress. Hippocampal adenosine monophosphate-activated protein kinase-dependent BDNF induction is required for exercise-induced protection against chronic stress (Kim and Leem, 2016).

During fasting and intense exercise, brain cell energy substrate utilization moves from glucose to ketone 3-hydroxybutyrate (3OHB). Studies show that 3OHB can protect neurons against excitotoxicity and oxidative stress. 3OHB metabolism increases mitochondrial respiration leading to altered expression of BDNF in cultured cortical neurons (Marosi et al., 2016).

EXERCISE AND ENERGY RESTRICTION

BDNF has been associated with exercise as well as energy restriction. Evolution prefers individuals with excellent cognitive and physical abilities under limited food supply conditions. Mattson (2012) suggested that intermittent energy restriction and prolonged exercise optimize brain function. In the hypothalamus, BDNF inhibits food intake and increases energy consumption. BDNF mediates improvements in cognitive function and neuroprotection caused by exercise and energy restriction through promoting synaptic plasticity and neurogenesis in the hippocampus (Mattson, 2012). Energy restriction also improves cardiovascular stress adaptation by increasing brainstem cholinergic activity (Rothman et al., 2012).

Exercise and energy intake modify the plasticity of neural circuits in a way that affects the health of the brain. By enhancing neurogenesis, synaptic plasticity, and nerve stress robustness, exercise and intermittent energy limitation/fasting can optimize brain function and prevent metabolic and neurodegenerative diseases (van Praag et al., 2014). Caloric restriction improved recognition memory, increased gray matter volume in inferior frontal gyrus and hippocampus, and augmented hippocampal resting-state functional connectivity in the postmenopausal obese women (Prehn et al., 2017).

The ketone body is the most energy efficient fuel and has more ATP per mole of substrate than pyruvic acid and increases the free energy released by ATP hydrolysis. The ketone diet improves rats’ physical function and cognitive function, suggesting that energy conservation characteristics can help cure the condition of people with metabolic disorders (Murray et al., 2016). In the type 2 diabetic mice, increased ketone body improved mitochondrial function in the hippocampus, and this process was considered as the adaptive mechanisms to maintain energy during interrupted glucose metabolism (Andersen et al., 2017).

In recent studies, the effects of exercise on mitochondrial function have also become known. Exercise improves mitochondrial energy in skeletal muscle as well as in other tissues. Gusdon et al. (2017) suggested that exercise training in old mice could improve brain mitochondrial function by affecting electron transport chain function and mitochondrial dynamics without increasing mitochondrial biogenesis. Exercise-trained men consuming a protein-pacing diet along with multicomponent exercise training (PRISE) improved muscular power, strength, and flexibility (Ives et al., 2017). These effects of exercise are not likely related to growth hormone or BDNF but possibly related to IGF-1 response (Ives et al., 2017).

CONCLUSIONS

It is well known that long-term endurance exercise and fasting state improve brain function. Although the precise mechanisms for brain function improvement have not yet been elucidated, ketone body and BDNF have been suggested as the main substances of this action. In future studies, it will be necessary to develop technologies that can clinically use these substances, along with the discovery of other substances that enhance brain function.

Article information Continued