Pathways for oxidative fuel provision to working muscles: ecological consequences of maximal supply limitations
- PMID: 1612135
- DOI: 10.1007/BF01920239
Pathways for oxidative fuel provision to working muscles: ecological consequences of maximal supply limitations
Abstract
The study of metabolic fuel provision and its regulation has reached an exciting stage where specific molecular events can be correlated with parameters of the organism's ecology. This paper examines substrate supply pathways from storage sites to locomotory muscle mitochondria and discusses ecological implications of the limits for maximal flux through these pathways. The relative importance of the different oxidative fuels is shown to depend on aerobic capacity. Very aerobic, endurance-adapted animals such as long distance migrants favor the use of lipids and intramuscular fuels over carbohydrates and circulatory fuels. The hypothesis of functional co-adaptation between oxygen and metabolic fuel supply systems allows us to predict that the capacity of several biochemical processes should be scaled with maximal oxygen consumption. Key enzymes, transmembrane transporter proteins, glucose precursor supply and soluble fatty acid transport proteins must all be geared to support higher maximal glucose and fatty acid fluxes in aerobic than in sedentary species.
Similar articles
-
Design of the oxygen and substrate pathways. IV. Partitioning energy provision from fatty acids.J Exp Biol. 1996 Aug;199(Pt 8):1667-74. doi: 10.1242/jeb.199.8.1667. J Exp Biol. 1996. PMID: 8708574
-
Metabolic fuels: regulating fluxes to select mix.J Exp Biol. 2011 Jan 15;214(Pt 2):286-94. doi: 10.1242/jeb.047050. J Exp Biol. 2011. PMID: 21177948
-
Fuel selection in rufous hummingbirds: ecological implications of metabolic biochemistry.Proc Natl Acad Sci U S A. 1990 Dec;87(23):9207-10. doi: 10.1073/pnas.87.23.9207. Proc Natl Acad Sci U S A. 1990. PMID: 2251266 Free PMC article.
-
Design of the oxygen and substrate pathways. VII. Different structural limits for oxygen and substrate supply to muscle mitochondria.J Exp Biol. 1996 Aug;199(Pt 8):1699-709. doi: 10.1242/jeb.199.8.1699. J Exp Biol. 1996. PMID: 8708577 Review.
-
Metabolic fuel kinetics in fish: swimming, hypoxia and muscle membranes.J Exp Biol. 2016 Jan;219(Pt 2):250-8. doi: 10.1242/jeb.125294. J Exp Biol. 2016. PMID: 26792337 Review.
Cited by
-
Recycling and utilization of metabolic wastes for energy production is an index of biochemical adaptation of fish under environmental pollution stress.Environ Monit Assess. 2003 Aug;86(3):255-64. doi: 10.1023/a:1024009505008. Environ Monit Assess. 2003. PMID: 12858966
-
Energy substrate utilization during nightly vocal activity in three species of Scinax (Anura/Hylidae).J Comp Physiol B. 2008 May;178(4):447-56. doi: 10.1007/s00360-007-0236-6. Epub 2008 Jan 8. J Comp Physiol B. 2008. PMID: 18185935
-
Energy metabolism during endurance flight and the post-flight recovery phase.J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2017 Jul;203(6-7):431-438. doi: 10.1007/s00359-017-1150-3. Epub 2017 Feb 21. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2017. PMID: 28224277 Review.
-
Effects of Repeated Sublethal External Exposure to Deep Water Horizon Oil on the Avian Metabolome.Sci Rep. 2019 Jan 23;9(1):371. doi: 10.1038/s41598-018-36688-3. Sci Rep. 2019. PMID: 30674908 Free PMC article.
-
Carnitine palmitoyl transferase activity and whole muscle oxidation rates vary with fatty acid substrate in avian flight muscles.J Comp Physiol B. 2011 May;181(4):565-73. doi: 10.1007/s00360-010-0542-2. Epub 2010 Dec 14. J Comp Physiol B. 2011. PMID: 21153644