Back to Search
Start Over
Ghrelin mediates exercise endurance and the feeding response post-exercise
- Source :
- Molecular Metabolism, Molecular Metabolism, Vol 9, Iss, Pp 114-130 (2018)
- Publication Year :
- 2017
-
Abstract
- Objective Exercise training has several well-established health benefits, including many related to body weight, appetite control, and blood glucose homeostasis. However, the molecular mechanisms and, in particular, the hormonal systems that mediate and integrate these beneficial effects are poorly understood. In the current study, we aimed to investigate the role of the hormone ghrelin and its receptor, the growth hormone secretagogue receptor (GHSR; ghrelin receptor), in mediating the effects of exercise on food intake and blood glucose following exercise as well as in regulating exercise endurance capacity. Methods We used two mouse models of treadmill running to characterize the changes in plasma ghrelin with exercise. We also assessed the role of the ghrelin system to influence food intake and blood glucose after exercise, exercise endurance, and parameters potentially linked to responses to exercise. Mice lacking GHSRs (GHSR-null mice) and wild-type littermates were studied. Results An acute bout of exercise transiently elevated plasma acyl-ghrelin. Without the action of this increased ghrelin on GHSRs (as in GHSR-null mice), high intensity interval exercise markedly reduced food intake compared to control mice. The effect of exercise to acutely raise blood glucose remained unmodified in GHSR-null mice. Exercise-induced increases in plasma ghrelin positively correlated with endurance capacity, and time to exhaustion was reduced in GHSR-null mice as compared to wild-type littermates. In an effort to mechanistically explain their reduced exercise endurance, exercised GHSR-null mice exhibited an abrogated sympathoadrenal response, lower overall insulin-like growth factor-1 levels, and altered glycogen utilization. Conclusions Exercise transiently increases plasma ghrelin. GHSR-null mice exhibit decreased food intake following high intensity interval exercise and decreased endurance when submitted to an exercise endurance protocol. These data suggest that an intact ghrelin system limits the capacity of exercise to restrict food intake following exercise, although it enhances exercise endurance.<br />Highlights • High intensity exercise transiently increases plasma ghrelin. • Without ghrelin action on its receptors (growth hormone secretagogue receptors), exercise markedly reduces food intake. • An intact ghrelin system enhances exercise endurance.
- Subjects :
- 0301 basic medicine
Male
Food intake
Growth hormone secretagogue receptor
RT-PCR, reverse transcriptase-polymerase chain reaction
Endurance
PC, pyruvate carboxylase
chemistry.chemical_compound
Eating
Mice
Medicine
Glucose homeostasis
AMP 5′, adenosine monophosphate
Treadmill
Receptor
Receptors, Ghrelin
2. Zero hunger
Glycogen
digestive, oral, and skin physiology
Ghrelin
PYGL, glycogen phosphorylase, liver
HIIE, high intensity interval exercise
GHSR, growth hormone secretagogue receptor
G6P, glucose-6-phosphatase
Original Article
PCG1α, peroxisome proliferator-activated receptor gamma coactivator 1α
lcsh:Internal medicine
medicine.medical_specialty
IGFBP-1, insulin-like growth factor binding protein-1
IGF-1, insulin-like growth factor-1
CNS, central nervous system
HNF4α, hepatocyte nuclear factor 4α
03 medical and health sciences
Internal medicine
Physical Conditioning, Animal
Animals
lcsh:RC31-1245
Molecular Biology
Exercise
ACC, acetyl coA carboxylase
business.industry
VMH, ventromedial hypothalamus
Cell Biology
COX IV, cytochrome c oxidase subunit 4
GH, growth hormone
Mice, Inbred C57BL
AMPK, AMP-activated protein kinase
030104 developmental biology
Endocrinology
chemistry
Physical Endurance
PEPCK, phosphoenolpyruvate carboxykinase
GHSR
business
Hormone
Subjects
Details
- ISSN :
- 22128778
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Molecular metabolism
- Accession number :
- edsair.doi.dedup.....a38cb4afba235476a0547e55762f6cd8