Literature DB >> 11084206

The cost of an action potential.

G L Aiello1, P Bach-y-Rita.   

Abstract

Neuronal modules, or 'cell-assemblies', comprising millions of mutually interconnected cells have been postulated to form the basis of many functions of the brain, such as mood, sleep, hunger, vigilance, and more. Depending on the extent of the module, neurocommunication in cell-assemblies might exceed metabolic resources. A medium-size (10000 neurons) module would require at least 10 J per l of brain, based on a calculated cost of an isolated action potential (AP) of 10(11)-10(12) molecules of ATP per cm(2) of cell membrane, with an absolute minimum of 10(6) ATP at a node of Ranvier. The figure matches the cost of depolarizing the unmyelinated axon of the large monopolar cell in the blowfly retina. A circuit model of the cell membrane, based on abrupt changes of Na(+) and K(+) conductances, is used to emulate the AP and to assess the resulting ionic unbalance. The cost of an AP is equated to the metabolic energy necessary to fuel ATP-based pumps that restore intracellular K(+). The high metabolic demand of a cell-assembly suggests that less expensive means of neurocommunication may be involved, such as non-synaptic diffusion neurotransmission (NDN), which would comply with a proposed law of conservation of space and energy in the brain.

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Year:  2000        PMID: 11084206     DOI: 10.1016/s0165-0270(00)00308-3

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  16 in total

Review 1.  Nonsynaptic diffusion neurotransmission in the brain: functional considerations.

Authors:  P Bach-y-Rita
Journal:  Neurochem Res       Date:  2001-09       Impact factor: 3.996

2.  A novel hypothesis about mechanisms affecting conduction velocity of central myelinated fibers.

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Journal:  Neurochem Res       Date:  2011-05-08       Impact factor: 3.996

3.  Chronic Dysregulation of Cortical and Subcortical Metabolism After Experimental Traumatic Brain Injury.

Authors:  Jennifer L McGuire; Erica A K DePasquale; Miki Watanabe; Fatima Anwar; Laura B Ngwenya; Gowtham Atluri; Lindsey E Romick-Rosendale; Robert E McCullumsmith; Nathan K Evanson
Journal:  Mol Neurobiol       Date:  2018-08-01       Impact factor: 5.590

Review 4.  Spreading of pathology in neurodegenerative diseases: a focus on human studies.

Authors:  Johannes Brettschneider; Kelly Del Tredici; Virginia M-Y Lee; John Q Trojanowski
Journal:  Nat Rev Neurosci       Date:  2015-01-15       Impact factor: 34.870

Review 5.  Potassium diffusive coupling in neural networks.

Authors:  Dominique M Durand; Eun-Hyoung Park; Alicia L Jensen
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2010-08-12       Impact factor: 6.237

6.  A computational model of motor neuron degeneration.

Authors:  Gwendal Le Masson; Serge Przedborski; L F Abbott
Journal:  Neuron       Date:  2014-07-31       Impact factor: 17.173

7.  Disrupted axo-glial junctions result in accumulation of abnormal mitochondria at nodes of ranvier.

Authors:  Steven Einheber; Manzoor A Bhat; James L Salzer
Journal:  Neuron Glia Biol       Date:  2006-08

Review 8.  Mitochondrial transport and docking in axons.

Authors:  Qian Cai; Zu-Hang Sheng
Journal:  Exp Neurol       Date:  2009-03-31       Impact factor: 5.330

9.  Docking of axonal mitochondria by syntaphilin controls their mobility and affects short-term facilitation.

Authors:  Jian-Sheng Kang; Jin-Hua Tian; Ping-Yue Pan; Philip Zald; Cuiling Li; Chuxia Deng; Zu-Hang Sheng
Journal:  Cell       Date:  2008-01-11       Impact factor: 41.582

10.  KATP channel subunits in rat dorsal root ganglia: alterations by painful axotomy.

Authors:  Vasiliki Zoga; Takashi Kawano; Mei-Ying Liang; Martin Bienengraeber; Dorothee Weihrauch; Bruce McCallum; Geza Gemes; Quinn Hogan; Constantine Sarantopoulos
Journal:  Mol Pain       Date:  2010-01-26       Impact factor: 3.395

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