Homeostatic plasticity

Short description: Capacity of neurons to regulate their own excitability relative to network activity

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The relationship between synaptic drive and firing rate for a single neuron. As synaptic drive increases and firing rate rises above the target level, homeostatic mechanisms reduce the strength of the inputs which works to move the neuron back into the target zone. On the other hand, if synaptic drive falls too low and firing rate falls below the target rate, the homeostatic plasticity process will increase the strength of all inputs and bring the neuron back to the target firing zone.

Homeostatic plasticity refers to the capacity of neurons to regulate their own excitability relative to network activity. The term homeostatic plasticity derives from two opposing concepts: 'homeostatic' (a product of the Greek words for 'same' and 'state' or 'condition') and plasticity (or 'change'), thus homeostatic plasticity means "staying the same through change". In the nervous system,the neural circuit has to remain stable in function throughout many plastic challenges through a variety of changes in synapse number and strength . Neurons must be able to evolve with the development of their constantly changing environment while simultaneously staying the same amidst this change whether its on a functional or structural level. While the stability of the neurons is important for neurons to maintain their activity and functionality.On a functional level, the neuronal networks use a complex set of regulatory mechanisms to achieve certain things such as homeostasis over a wide range of temporal and spatial scales. However, neurons need to have flexibility to adapt to changes in the connectivity and synaptic strength during development and learning.

Homeostatic plasticity is also a negative feedback mechanism. This mechanism is used to offset the excessive excitation or inhibition through adjusting the synaptic strength of the neurons. Most of the neurons in the mechanism receive their signals from either a change in the network such as synaptic connectivity or from an external stimulus such as light or sound.

## Contents

* 1 Types
* 1.1 Presynaptic
* 1.2 Postsynaptic
* 1.3 Intrinsic
* 1.4 Synaptic scaling
* 2 Comparison to other types of plasticity
* 2.1 Functional
* 2.2 Structural
* 2.3 Hebbian Plasticity
* 3 Mechanisms
* 4 Role in central pattern generators
* 5 Role in neurological disorders
* 5.1 Epilepsy
* 5.2 Autism
* 5.3 Alzheimer's disease
* 5.4 Neurodegenerative diseases
* 5.5 Schizophrenia
* 6 Prominent Researchers
* 7 References
* 8 External links

## Types

The capacity of neurons to sustain consistent activity levels in response to variations in synaptic input is known as homeostatic synaptic plasticity. Homeostatic synaptic plasticity occurs when neurons modify their synaptic strength in response to variations in activity levels to preserve network stability. This response serves to keep neuronal circuits in the appropriate range of activity for proper functioning. Homeostatic synaptic plasticity can be shown in presynaptic alterations, postsynaptic receptor expression, changes in intrinsic characteristics, and synaptic scaling.

Presynaptic terminal[1][circular reference]

### Presynaptic

Homeostatic presynaptic plasticity refers to the ability of neurons to regulate neurotransmitter release at presynaptic terminals, ensuring a steady range of brain activity. This process involves various mechanisms, such as quantal size adjustment, differential expression of presynaptic proteins, and modification of vesicle recycling. Quantal size adjustment helps maintain steady postsynaptic responses despite changes in synaptic strength. Differential expression of presynaptic proteins, such as calcium channels or synaptic vesicle proteins, can also be altered by neurons to affect neurotransmitter release rate.

### Postsynaptic

Homeostatic postsynaptic plasticity is crucial for maintaining consistent levels of synaptic activity in neurons, which are formed at specific synapses in the brain. Homeostatic processes involve changes in the expression of receptors, changes in receptor sub-unit composition, and changes to intracellular signaling pathways. For example, the NMDA receptor can change its sub-unit composition to improve sensitivity to neurotransmitters. Additionally, changes in the expression and location of neurotransmitter receptors can impact synaptic transmission when specific signaling pathways are activated. Synaptic adhesion molecules can also be influenced by homeostatic processes. Overall, homeostatic postsynaptic plasticity contributes to the stability and proper functioning of neural circuits, allowing the brain to adapt to changing conditions without compromising the overall stability of neuronal activity.[2]

### Intrinsic

Homeostatic intrinsic plasticity refers to the ability of neurons to change their intrinsic electrical characteristics in response to changes in synaptic or network activity. This process involves alterations in the excitability or firing characteristics of individual neurons, rather than primarily adjusting synaptic strength. Intrinsic plasticity processes associated with homeostasis include ion channel expression alterations, membrane conductance modifications, action potential threshold alterations, and regulation of intrinsic excitability. Neurons can up-regulate the expression of sodium channels to maintain firing rates and increase excitability in case of a drop in synaptic activity. These changes impact the input-output link between neurons and the homeostatic control of neuronal activity.

### Synaptic scaling

Synaptic scaling is a homeostatic mechanism that allows neurons to modulate the strength of all synapses to maintain stable activity levels within a specific range. This process is characterized by changes in the quantity or sensitivity of neurotransmitter receptors on the postsynaptic membrane. Neurons can reduce the number of neurotransmitter receptors in response to network activity spikes, reducing synaptic strength, or increase the density in response to network activity drops, increasing sensitivity and boosting synaptic strength. This homeostatic regulation of brain circuits supports other types of synaptic plasticity, such as long-term depression and long-term potentiation.

## Comparison to other types of plasticity

### Functional

Functional plasticity is a type of plasticity that allows the brain the ability to adapt to changes in its functions with changes in their environment. At every point in the child's life, their brain is able to balance malleable processes that represent neural plasticity and promote the change with homeostatic process in order to promote stability.[3] This means that regardless of a child's brain development as a fetus, typical brain development or atypical brain development, can depend on their environment.

The functions and abilities of a certain part of the brain can be moved to another part of the brain when damaged. When a fetus is developing, this type of plasticity occurs rapidly establishing the brain systems.[4]

### Structural

Structural plasticity refers to morphological changes in the structure of the brain through the growth of new synaptic connections.[5] This process is done through synaptogenesis, neuronal migration, and neurogenesis. These processes are a foundational part of fetal neuron development, but has recently also been found in adult brains. Neurogenesis occurs in the ventricular or subventricular zone of the brain. Neural migration is the process of neurons traveling from these zones towards their final destination in development.[6] Synaptic remodeling in response to learning and memory lead to function consequences in the brain throughout life.[7]

### Hebbian Plasticity

Homeostatic synaptic plasticity is a means of maintaining the synaptic basis for learning, respiration, and locomotion, in contrast to the Hebbian plasticity associated with learning and memory. Although Hebbian forms of plasticity, such as long-term potentiation (LTP) and long-term depression (LTD) occur rapidly, homeostatic plasticity (which relies on protein synthesis) can take hours or days. Homeostatic plasticity is thought to balance Hebbian plasticity by modulating the activity of the synapse or the properties of ion channels.

## Mechanisms

Synaptic scaling has been labeled as a potential mechanism of homeostatic plasticity.[8] Homeostatic plasticity is often used to describe a process that maintains stability of neuronal functions through a coordinated plasticity among subcellular compartments, such as the synapses versus the neurons and the cell bodies versus the axons.[9] Synaptic scaling aids in that regulation of neurons as the role of synaptic scaling is to adjust the strength of neuron's excitatory synapses, helping to keep the neurons in check so homeostatic plasticity can achieve its function properly.[10] Recently, it was proposed that homeostatic synaptic scaling may play a role in establishing the specificity of an associative memory.[11]

Homeostatic plasticity also uses a separate mechanism to help maintain neuronal excitability in a real-time manner through the coordinated plasticity of threshold and refractory period at voltage-gated sodium channels, keeping them balanced so the barrier remains constant for stable firing actions.[12]

Homeostatic plasticity can also be mediated by extracellular signals such as BDNF or TNF-α. These factors are released in an activity-dependent manner and can regulate both excitatory and inhibitory synapses across neurons, contributing to circuit-wide homeostatic adjustments.[13]

## Role in central pattern generators

Homeostatic plasticity is also very important in the context of central pattern generators. Central pattern generators control rhythmic and repeating pattern. Moreover, central pattern regulators are crucial for vital functions (i.e. respiration and digestion) and any disruptions can cause immense consequences. Therefore, homeostatic plasticity works to stabilize a given activity pattern. Central pattern generators maintain their rhythmic activity through homeostatic regulation using various intrinsic and network properties. One example of an intrinsic neuronal property is ion channel expression. For instance, neuron activity is influenced by the expression of ion channel levels. Moreover, changes in membrane voltage are used as feedback signals and those signals can modify the effects of the ion channels.[14] Furthermore, the changes allow neurons to adjust and maintain stable activity patterns with various inputs. An example of a network property is synaptic reorganization. Synaptic reorganization refers to the formation and elimination of neuron connections that change synapse function and is key in brain plasticity.[15] Overall homeostatic plasticity is important for central pattern generators, as neuronal properties are modulated in response to environmental changes in order to maintain an appropriate and balanced neural output.[16]

## Role in neurological disorders

Homeostatic plasticity plays a crucial role in neurological disorders such as epilepsy, autism, Alzheimer's disease, and other neurodegenerative diseases. In these disorders, neurons ability to maintain stability in response to changes in activity levels or external stimuli is often altered.[17]

### Epilepsy

In a healthy brain, neuronal excitability and synaptic strength are homeostatically regulated to maintain balance between excitation and inhibition. Homeostatic plasticity aids the brain by maintaining balance by adjusting neural activity in response to changes in stimulation. In epilepsy, this process can become semi-uncontrolled, leading to excessive neural excitability. This can cause an event where after prolonged network inactivity and/or brain injuries, neurons may become more active to compensate for the irregularity, which can cause the person to be more prone to seizures. Homeostatic plasticity is essential for normal brain function, the overcompensation due to brain dysregulation can contribute to the epileptic activity, highlighting its complex role in both stability and dysfunction.[18] There are ways to attempt to regulate the over-excitability, such as cortical stimulation which increases controlled activity and might decrease excessive excitability, achieving the balance homeostatic plasticity seeks. Some studies also show that electrical stimulation helps those who suffer from drug-resistant epilepsy.[19] Traditional pharmacological approaches may be ineffective in restoring physiological balance in the neuronal network. However, therapeutic strategies targeting homeostatic plasticity mechanisms may offer a potential solution.[17]

### Autism

Autism spectrum disorder is a neurodevelopment disorder that is characterized by repetitive patterns of behavior, along with difficulties in social interaction and communication. Dysregulation of homeostatic plasticity and neural imbalance can contribute to the cognitive and behavioral symptoms associated with autism. Sensory inputs and intrinsic brain activity can cause long-term changes in synaptic efficiency and eventually lead to an increase or decrease in the ratio between excitatory and inhibitory neurotransmissions is found in Autism.[20] Alterations in the expression of synaptic proteins that regulate excitatory or inhibitory leads to dysfunction as the ratio changes. An example linked to autism is Neuroligins 1-4. Neuroligin 1 is mainly present in excitatory synapses, neuroligin 2 is more present in inhibitory synapses, and neuroligin 3 is present in both. Neuroligin 4 is present in glycinergic synapses which are major contributors to the regulation of neuronal excitability as they control fluxes of sensory information. Mutations in neuroligins 3 & 4 have been shakily linked to autism, but neuroligins 1-3 have been found to cause primary inhibitory dysfunction in autism.[21] Pruning of developing synapses in the central nervous system regulates brain size and shape into the third decade of life. It is a necessary process to keep the brain from being too small or large. Underpruning has been associated autism and results in enlarged brain size due to overgrowth of dendrites from the lack of pruning and modification of neuron number. Motor impairment in autism has been linked specifically to an abundance of white matter in the primary motor cortex. Due to 22q11.2 gene deletion syndrome, found to be connected to autism spectrum disorder, both thicker and thinner cortical regions along with regions of increased cerebral cortex folding can be found in the brain.[22] Environmental factors that effect normal homeostasis are heightened in autism, stopping neurons from maintaining optimum levels of activity.[23]

### Alzheimer's disease

In Alzheimer's disease, synaptic function and neuronal integrity are impaired. In a healthy brain, these mechanisms are tightly maintained by homeostatic plasticity. In the brain, there are constant changes in synaptic input. Therefore, neurons use homeostatic plasticity to keep their activity stable and prevents neurons from becoming too excited or too quiet. According to researchers, if a neuron does not receive enough activity, the synapses become stronger by adding receptors that help transmit signals.[8] On the other hand, researchers argue that if the neuron receives too much activity the neuron will remove the receptors and weaken the synaptic connection.[8] Researchers describe the regulation of receptors as synaptic scaling. In addition, neurons are able to adjust their intrinsic excitability and the changes help maintain the stability of neuron firing rates.[8] Therefore, homeostatic plasticity potentially plays a significant role in neural stability. Deficits in homeostatic plasticity contribute to cognitive decline and memory impairment which are characteristic symptoms of Alzheimer's disease.

### Neurodegenerative diseases

Purjunkie cells in neurons[24][circular reference]

Several neurological disorders are affected by homeostatic plasticity. Dysregulation of homeostatic plasticity can cause an excitatory or inhibitory network activity. Parkinson's disease, Huntington's disease, and ALS are all examples of disorders where dysregulation of neuronal networks contributes to the pathophysiology of the disorders.[25] For instance, synaptic impairments occur early in ALS, so the early chances may serve as a method to counteract neuron dysfunction. Although the nervous system does attempt to adapt using synaptic plasticity, the attempts to maintain neural function are most times temporary and may eventually become harmful. For example, researchers believe that the spinal cord attempts to adapt by increasing the size of synaptic contacts, such as glutamatergic synapses to preserve motor function before the disease becomes detrimental.[26] However, the increased excitatory synaptic activity becomes too excessive and leads to excitotoxicity. Thus, the neurodegenerative disease progresses further.

### Schizophrenia

Schizophrenia is characterized by disruptions in thought processes, perceptions, and emotions. Alterations in synaptic strength and connectivity potentially due to dysregulation in homeostatic mechanisms may lead to the symptoms observed in schizophrenic patients. These dysregulation contribute to the cognitive deficits and delusions observed in schizophrenia.[27] In fact, a study was conducted to prove that disturbance in the homeostasis of Purkinje cells is an example of how developmental plasticity homeostasis is crucial in preventing mental illnesses like Schizophrenia. Purkinje cells are neurons located in the cerebellum and are involved in cognitive functions.[28] Moreover, research has shown that Purkinje cells keep the brain's activity stable after traumatic experiences, and unregulated responses to trauma disrupt normal brain activity, which leads to mental illnesses.[29]

## Prominent Researchers

Gina G. Turrigiano is an American neuroscientist known for her work on homeostatic plasticity mechanisms in the brain. Her research focused on synaptic strength and intrinsic excitability of neurons. Turrigiano discovered and characterized several types of homeostatic plasticity, most notably Synaptic scaling and intrinsic homeostatic plasticity. She considers homeostatic plasticity as how brains "tune themselves up" to remain dynamic and stable. More recently, she and her colleagues have been working to uncover the role of homeostatic plasticity in the development of the neocortex, in tandem with LTP/LTD, through experience-dependent refinement and learning.[2]

## References

1. ↑ "File:Synapse figure.png - Wikipedia" (in en). 2022-04-26. https://en.wikipedia.org/wiki/File:Synapse_figure.png.
2. ↑ 2.0 2.1 "The dialectic of Hebb and homeostasis". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 372 (1715). March 2017. doi:10.1098/rstb.2016.0258. PMID 28093556.
3. ↑ "Functional plasticity in childhood brain disorders: when, what, how, and whom to assess". Neuropsychology Review 24 (4): 389–408. December 2014. doi:10.1007/s11065-014-9261-x. PMID 24821533.
4. ↑ "Functional plasticity before the cradle: a review of neural functional imaging in the human fetus". Neuroscience and Biobehavioral Reviews. CNTRICS: Modeling psychosis related cognition in animal systems to enhance translational research + Life-Span Plasticity of Brain and Behavior: A Cognitive Neuroscience Perspective 37 (9 Pt B): 2220–2232. November 2013. doi:10.1016/j.neubiorev.2013.03.013. PMID 23542738.
5. ↑ "The dark side of neuroplasticity". Experimental Neurology 235 (1): 133–141. May 2012. doi:10.1016/j.expneurol.2011.11.004. PMID 22116043.
6. ↑ "Mechanisms of neuronal migration in the adult brain". Journal of Neurochemistry 141 (6): 835–847. June 2017. doi:10.1111/jnc.14002. PMID 28251650.
7. ↑ "Structural plasticity upon learning: regulation and functions". Nature Reviews. Neuroscience 13 (7): 478–490. June 2012. doi:10.1038/nrn3258. PMID 22714019. https://archive-ouverte.unige.ch/unige:26265.
8. ↑ 8.0 8.1 8.2 8.3 "Unraveling mechanisms of homeostatic synaptic plasticity". Neuron 66 (3): 337–351. May 2010. doi:10.1016/j.neuron.2010.04.028. PMID 20471348.
9. ↑ "Homeostasis established by coordination of subcellular compartment plasticity improves spike encoding". Journal of Cell Science 121 (Pt 17): 2961–2971. September 2008. doi:10.1242/jcs.022368. PMID 18697837.
10. ↑ "Unraveling mechanisms of homeostatic synaptic plasticity". Neuron 66 (3): 337–351. May 2010. doi:10.1016/j.neuron.2010.04.028. PMID 20471348.
11. ↑ "Homeostatic synaptic scaling establishes the specificity of an associative memory". Current Biology 31 (11): 2274–2285.e5. June 2021. doi:10.1016/j.cub.2021.03.024. PMID 33798429. Bibcode: 2021CBio...31E2274W.
12. ↑ "Real-time neuronal homeostasis by coordinating VGSC intrinsic properties". Biochemical and Biophysical Research Communications 387 (3): 585–589. September 2009. doi:10.1016/j.bbrc.2009.07.066. PMID 19616515. Bibcode: 2009BBRC..387..585G.
13. ↑ Turrigiano, G. (2012-01-01). "Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function" (in en). Cold Spring Harbor Perspectives in Biology 4 (1). doi:10.1101/cshperspect.a005736. ISSN 1943-0264. PMID 22086977.
14. ↑ Temporal, Simone; Lett, Kawasi M.; Schulz, David J. (2014-08-18). "Activity-Dependent Feedback Regulates Correlated Ion Channel mRNA Levels in Single Identified Motor Neurons". Current Biology 24 (16): 1899–1904. doi:10.1016/j.cub.2014.06.067. ISSN 0960-9822. PMID 25088555. Bibcode: 2014CBio...24.1899T.
15. ↑ Wolff, J. R.; Missler, M. (1992). "Synaptic reorganization in developing and adult nervous systems". Annals of Anatomy 174 (5): 393–403. doi:10.1016/s0940-9602(11)80257-8. ISSN 0940-9602. PMID 1449216.
16. ↑ "Molecular mechanisms of homeostatic plasticity in central pattern generator networks". Developmental Neurobiology 80 (1–2): 58–69. January 2020. doi:10.1002/dneu.22727. PMID 31778295.
17. ↑ 17.0 17.1 "Derailment of Sleep Homeostatic Plasticity Affects the Most Plastic Brain Systems and Carries the Risk of Epilepsy". Journal of Integrative Neuroscience 22 (5). August 2023. doi:10.31083/j.jin2205111. PMID 37735129.
18. ↑ "Derailment of Sleep Homeostatic Plasticity Affects the Most Plastic Brain Systems and Carries the Risk of Epilepsy". Journal of Integrative Neuroscience 22 (5). August 2023. doi:10.31083/j.jin2205111. PMID 37735129.
19. ↑ "Cortical stimulation for treatment of neurological disorders of hyperexcitability: a role of homeostatic plasticity". Neural Regeneration Research 14 (1): 34–38. January 2019. doi:10.4103/1673-5374.243696. PMID 30531066.
20. ↑ "Cerebral plasticity: Windows of opportunity in the developing brain" (in English). European Journal of Paediatric Neurology 21 (1): 23–48. January 2017. doi:10.1016/j.ejpn.2016.07.007. PMID 27567276.
21. ↑ Nelson, Sacha B.; Valakh, Vera (2015-08-19). "Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders" (in English). Neuron 87 (4): 684–698. doi:10.1016/j.neuron.2015.07.033. ISSN 0896-6273. PMID 26291155.
22. ↑ Dennis, Maureen; Spiegler, Brenda J.; Juranek, Jenifer J.; Bigler, Erin D.; Snead, O. Carter; Fletcher, Jack M. (2013-12-01). "Age, plasticity, and homeostasis in childhood brain disorders". Neuroscience & Biobehavioral Reviews 37 (10, Part 2): 2760–2773. doi:10.1016/j.neubiorev.2013.09.010. ISSN 0149-7634. PMID 24096190.
23. ↑ "Key role for gene dosage and synaptic homeostasis in autism spectrum disorders" (in English). Trends in Genetics 26 (8): 363–372. August 2010. doi:10.1016/j.tig.2010.05.007. PMID 20609491. https://hal-pasteur.archives-ouvertes.fr/pasteur-01967134/file/TIGS-D-09-00224NEW-1.pdf.
24. ↑ "File:Neurons (Purkinje cells).jpg - Wikipedia" (in en). 2021-09-14. https://en.wikipedia.org/wiki/File:Neurons_(Purkinje_cells).jpg.
25. ↑ "Apolipoprotein E and Alzheimer disease: pathobiology and targeting strategies". Nature Reviews. Neurology 15 (9): 501–518. September 2019. doi:10.1038/s41582-019-0228-7. PMID 31367008.
26. ↑ Gulino, Rosario (2023-02-27). "Synaptic Dysfunction and Plasticity in Amyotrophic Lateral Sclerosis" (in en). International Journal of Molecular Sciences 24 (5): 4613. doi:10.3390/ijms24054613. ISSN 1422-0067. PMID 36902042.
27. ↑ "Emerging links between homeostatic synaptic plasticity and neurological disease". Frontiers in Cellular Neuroscience 7: 223. November 2013. doi:10.3389/fncel.2013.00223. PMID 24312013.
28. ↑ "Histology, Purkinje Cells". StatPearls. Treasure Island (FL): StatPearls Publishing. 2025. https://www.ncbi.nlm.nih.gov/books/NBK545154/#:~:text=Purkinje cells are a unique type of neuron-specific to the cerebellar cortex.&text=[6] In the 3-layered cerebellar cortex, the,cells, make up the outer molecular layer.. Retrieved 2025-02-22.
29. ↑ "Intrinsic plasticity of Purkinje cell serves homeostatic regulation of fear memory". Molecular Psychiatry 29 (2): 247–256. February 2024. doi:10.1038/s41380-023-02320-8. PMID 38017229.

## External links

* "Homeostatic Regulation of Neuronal Excitability". http://www.scholarpedia.org/article/Homeostatic_Regulation_of_Neuronal_Excitability.

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