Maintaining the Stability of Neural Function: A Homeostatic Hypothesis
Abstract
The precise regulation of neural excitability is essential for proper nerve cell, neural circuit, and nervous system function. During postembryonic development and throughout life, neurons are challenged with perturbations that can alter excitability, including changes in cell size, innervation, and synaptic input. Numerous experiments demonstrate that neurons are able to compensate for these types of perturbation and maintain appropriate levels of excitation. The mechanisms of compensation are diverse, including regulated changes to synaptic size, synaptic strength, and ion channel function in the plasma membrane. These data are evidence for homeostatic regulatory systems that control neural excitability. A model of neural homeostasis suggests that information about cell activity, cell size, and innervation is fed into a system of cellular monitors. Intracellular- and intercellular-signaling systems transduce this information into regulated changes in synaptic and ion channel function. This review discusses evidence for such a model of homeostatic regulation in the nervous system.
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Perturbations in postsynaptic function can lead to compensatory changes in presynaptic release, and vice versa, at mammalian and invertebrate NMJ.
“More recently work at the mammalian and invertebrate NMJ has shown that perturbations in postsynaptic function can lead to compensatory changes in presynaptic release, and vice versa (Davis and Bezprozvanny 2001).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Davis and Bezprozvanny 2001
Some forms of homeostatic plasticity occur through presynaptic and others through postsynaptic changes in function.
“Similarly, some forms of homeostatic plasticity occur through presynaptic and others through postsynaptic changes in function (Davis and Bezprozvanny 2001).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Davis and Bezprozvanny 2001
Under some circumstances, additional presynaptic changes can be recruited during synaptic scaling.
“It is widely agreed that synaptic scaling involves postsynaptic changes in receptor accumulation (Turrigiano 2008), but under some circumstances additional presynaptic changes can also be recruited (Davis and Bezprozvanny 2001;Rich and Wenner 2007;Thiagarajan et al. 2007).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Davis and Bezprozvanny 2001
The presence of normal EPSPs despite smaller mEPSPs can likely be attributed to a homeostatic increase in quantal content.
“The presence of normal EPSPs despite smaller mEPSPs can likely be attributed to a homeostatic increase in quantal content (Davis and Bezprozvanny, 2001;Heckscher et al, 2007).”
From Ral mediates activity‐dependent growth of postsynaptic membranes via recruitment of the exocyst (2013) · cites this paper as Davis and Bezprozvanny, 2001
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- Authors
- Davis, G. W., & Bezprozvanny, I.
- Affiliations
- University of California, San Francisco (US)
- Department of Biochemistry, University of California, San Francisco, San Francisco, California 94143-0448;
- ORCID
- Davis, Graeme W
- Venue
- Annual Review of Physiology
- Publisher
- Annual Reviews
- Published
- 2001-03
- Volume
- 63
- Issue
- 1
- Pages
- 847-869
- ISSN
- 0066-4278 (ISSN-L)
- 1545-1585
- OpenAlex
- W2168028420
- Cited by
- 302
- References
- 3
- Citations by year
- 2026: 5 · 2025: 6 · 2024: 5 · 2023: 3 · 2022: 7 · 2021: 6 · 2020: 13 · 2019: 8 · 2018: 5 · 2017: 14 · 2016: 7 · 2015: 11 · 2014: 5 · 2013: 17 · 2012: 13
- FWCI
- 1.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS39552, R01NS039313, R01NS039552, NS39313-01)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Keywords
- neuronal homeostasis, neuronal excitability, homeostatic regulation, synaptic plasticity, synaptic efficacy, ion channel modulation, neuron size, innervation, postembryonic development, intracellular signaling, intercellular communication, neural circuit function
- MeSH terms
- Animals, Homeostasis, Neuronal Plasticity, Neurons, Synapses
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