Energy metabolism in feasting and fasting
- PMID: 371355
- DOI: 10.1007/978-1-4757-0734-2_8
Energy metabolism in feasting and fasting
Abstract
During feasting on a balanced carbohydrate, fat, and protein meal resting metabolic rate, body temperature and respiratory quotient all increase. The dietary components are utilized to replenish and augment glycogen and fat stores in the body. Excessive carbohydrate is also converted to lipid in the liver and stored along with the excessive lipids of dietary origin as triglycerides in adipose tissue, the major fuel storage depot. Amino acids in excess of those needed for protein synthesis are preferentially catabolized over glucose and fat for energy production. This occurs because there are no significant storage sites for amino acids or proteins, and the accumulation of nitrogenous compounds is ill tolerated. During fasting, adipose tissue, muscle, liver, and kidneys work in concert to supply, to convert, and to conserve fuels for the body. During the brief postabsorptive period, blood fuel homeostasis is maintained primarily by hepatic glycogenolysis and adipose tissue lipolysis. As fasting progresses, muscle proteolysis supplies glycogenic amino acids for heightened hepatic gluconeogenesis for a short period of time. After about three days of starvation, the metabolic profile is set to conserve protein and to supply greater quantities of alternate fuels. In particular, free fatty acids and ketone bodies are utilized to maintain energy needs. The ability of the kidney to conserve ketone bodies prevents the loss of large quantities of these valuable fuels in the urine. This delicate interplay among liver, muscle, kidney, and adipose tissue maintains blood fuel homeostasis and allows humans to survive caloric deprivation for extended periods.
Similar articles
-
Enzymatic capacities of metabolic fuel use in cuttlefish (Sepia officinalis) and responses to food deprivation: insight into the metabolic organization and starvation survival strategy of cephalopods.J Comp Physiol B. 2016 Aug;186(6):711-25. doi: 10.1007/s00360-016-0991-3. Epub 2016 Apr 30. J Comp Physiol B. 2016. PMID: 27138338
-
Fuel metabolism and energy stores in fasting or suckling newborn guinea pigs.J Dev Physiol. 1983 Dec;5(6):383-93. J Dev Physiol. 1983. PMID: 6655228
-
Protein turnover, ureagenesis and gluconeogenesis.Int J Vitam Nutr Res. 2011 Mar;81(2-3):101-7. doi: 10.1024/0300-9831/a000064. Int J Vitam Nutr Res. 2011. PMID: 22139560 Review.
-
Changes in energy metabolism during the suckling and weaning period in the newborn.Reprod Nutr Dev (1980). 1986;26(2B):619-31. doi: 10.1051/rnd:19860413. Reprod Nutr Dev (1980). 1986. PMID: 3523657 Review.
-
The Banting Memorial Lecture 1971. Physiology of insulin in man.Diabetes. 1971 Dec;20(12):785-99. doi: 10.2337/diab.20.12.785. Diabetes. 1971. PMID: 4941092 Review. No abstract available.
Cited by
-
The ER-Mitochondria Interface as a Dynamic Hub for T Cell Efficacy in Solid Tumors.Front Cell Dev Biol. 2022 Apr 27;10:867341. doi: 10.3389/fcell.2022.867341. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35573704 Free PMC article. Review.
-
KTX 0101: a potential metabolic approach to cytoprotection in major surgery and neurological disorders.CNS Drug Rev. 2005 Summer;11(2):113-40. doi: 10.1111/j.1527-3458.2005.tb00265.x. CNS Drug Rev. 2005. PMID: 16007235 Free PMC article. Review.
-
Burst-like control of lipolysis by the sympathetic nervous system in vivo.J Clin Invest. 2003 Jan;111(2):257-64. doi: 10.1172/JCI14466. J Clin Invest. 2003. PMID: 12531882 Free PMC article.
-
Retinal energy demands control vascular supply of the retina in development and disease: The role of neuronal lipid and glucose metabolism.Prog Retin Eye Res. 2018 May;64:131-156. doi: 10.1016/j.preteyeres.2017.11.002. Epub 2017 Nov 22. Prog Retin Eye Res. 2018. PMID: 29175509 Free PMC article. Review. No abstract available.
-
High-fructose corn syrup causes characteristics of obesity in rats: increased body weight, body fat and triglyceride levels.Pharmacol Biochem Behav. 2010 Nov;97(1):101-6. doi: 10.1016/j.pbb.2010.02.012. Epub 2010 Feb 26. Pharmacol Biochem Behav. 2010. PMID: 20219526 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Research Materials