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'''Allostasis''' is the process by which the body achieves stability—or [[homeostasis]]—through physiological or behavioral change. This dynamic process enables the organism to maintain internal viability amid external or internal challenges, using anticipatory and adaptive mechanisms.
{{Use Harvard referencing|date=May 2019}}


'''Allostasis''' is the process of achieving stability, or [[homeostasis]], through physiological or behavioral change {{harv|Copstead|Banasik2013}}. This can be carried out by means of alteration in [[Hypothalamic-pituitary-adrenal axis|HPA axis]] hormones, the [[autonomic nervous system]], [[cytokine]]s, or a number of other systems, and is generally adaptive in the short term <!--name="ReferenceA"-->{{harv|McEwen|Wingfield|2003}}.  Allostasis is essential in order to maintain internal viability amid changing conditions ({{harvnb|Sterling|Eyer|1988}}; {{harvnb|McEwen|1998a}}; {{harvnb|McEwen|1998b}}; {{harvnb|Schulkin|2003}}).
Unlike homeostasis, which aims to maintain internal equilibrium through fixed set points, allostasis adjusts physiological systems in a predictive and flexible manner. It involves complex coordination between the [[hypothalamic-pituitary-adrenal axis]] (HPA axis), the [[autonomic nervous system]], [[cytokines]], and other neuroendocrine and immune pathways.


Allostasis provides compensation for various problems, such as in compensated [[heart failure]], compensated [[kidney failure]], and compensated [[liver failure]]. However, such allostatic states are inherently fragile, and [[decompensation]] can occur quickly, as in [[acute decompensated heart failure]].
== Etymology ==
The term "allostasis" comes from the [[Greek language|Greek]] words ''ἄλλος'' (''állos''), meaning "other" or "different," and ''στάσις'' (''stasis''), meaning "standing still". It was introduced by Sterling and Eyer in 1988.


== Etymology ==
== Historical and Conceptual Origins ==
A''llostasis'' {{IPAc-en|ˌ|ɑː|l|oʊ-|ˈ|s|t|eɪ|s|ᵻ|s
The concept of allostasis was proposed by Peter Sterling and Joseph Eyer in 1988 as a more comprehensive and anticipatory model of regulation compared to the classical idea of homeostasis. The authors emphasized that biological systems do not merely react to perturbations but prepare for them through predictive regulation.
}} from the [[Greek language|Greek]] prefix ''ἄλλος'', ''állos'', "other," "different" + the suffix ''[[Stasis|στάσις]]'', ''stasis,'' "standing still".
 
Allostasis emphasizes the role of the brain in initiating and coordinating adaptive responses based on expectations and prior experience. These adjustments allow organisms to effectively cope with both predictable and unpredictable stressors.


==Nature of concept==
In computational models, the analogous term [[heterostasis]] is sometimes used, particularly in systems where state transitions are discrete rather than continuous


The concept of allostasis was proposed by Sterling and Eyer in 1988 as a process of reestablishing stability in response to a challenge. Allostasis was coined from the Greek allo, which means "variable;" thus, "remaining stable by being variable" ({{harvnb|Sterling|Eyer|1988}}; {{harvnb|Klein|2004}}). Allostatic regulation reflects, at least partly, cephalic involvement in primary regulatory events, in that it is anticipatory to systemic physiological regulation ({{harvnb|Sterling|Eyer|1988}}; {{harvnb|Schulkin|2003}}). This is in difference to  [[homeostasis]], which occurs in response to subtle ebb and flow. Both homeostasis and allostasis are endogenous systems responsible for maintaining the internal stability of an organism. Homeostasis, from the Greek homeo, means "similar," while stasis means "stand;" thus, "standing at about the same level." {{harv|Sterling|Eyer|1988}};
== Principles of Allostasis ==
Peter Sterling outlined six principles underlying allostasis:
# Organisms are designed for efficiency.
# Efficiency requires trade-offs.
# Efficiency depends on prediction of future needs.
# Prediction requires sensors to adapt to expected input ranges.
# Effectors must adapt to expected demands.
# Predictive regulation depends on [[behavior]], and [[neural plasticity]] supports such adaptability.


The term [[Heterostasis(Computational)|Heterostasis]] {{harv|Selye|1973}} is also used in place of Allostasis, particularly where state changes are finite in number and therefore discrete (e.g. computational processes).  
== Allostasis vs. Homeostasis ==
Wingfield states:<blockquote>The concept of allostasis, maintaining stability through change, is a fundamental process through which organisms actively adjust to both predictable and unpredictable events... Allostatic load refers to the cumulative cost to the body of allostasis, with allostatic overload... being a state in which serious [[pathophysiology]] can occur... Using the balance between energy input and expenditure as the basis for applying the concept of allostasis, two types of allostatic overload have been proposed {{harv|Wingfield|2003}}.</blockquote>
[[Homeostasis]] is typically defined as the maintenance of a stable internal environment through regulation of variables around a fixed set point (e.g., blood pH, glucose levels). In contrast, '''allostasis''' refers to the active process of achieving stability through change.


{{harvp|Sterling|2004}} proposed six interrelated principles that underlie allostasis:
For example, in response to dehydration, allostasis activates multiple systems:  
# Organisms are designed to be efficient
* Increased [[arginine vasopressin]] (AVP) to conserve water
# Efficiency requires reciprocal trade-offs
* Reduced [[urine]] output by the [[kidneys]]
# Efficiency also requires being able to predict future needs
* Constriction of [[blood vessels]] to maintain blood pressure
# Such prediction requires each sensor to adapt to the expected range of input
* Drying of [[mucous membranes]]
# Prediction also demands that each effector adapt its output to the expected range of demand
# Predictive regulation depends on behavior whilst neural mechanisms also adapt.


==Contrast with homeostasis==
These responses together help preserve function and viability in the face of a stressor.
The difference between allostasis and homeostasis is popularized by [[Robert Sapolsky]]'s book ''[[Why Zebras Don't Get Ulcers]]'':{{cite quote|reason=Can't find this in the book on Google Books|date=May 2019}}


:Homeostasis is the regulation of the body to a balance, by single point tuning such as blood oxygen level, blood glucose or blood pH. For example, if a person walking in the desert is hot, the body will sweat and they will quickly become dehydrated. Allostasis is adaptation but in regard to a more dynamic balance. In dehydration, sweat occurs as only a small part of the process with many other systems also adapting their functioning, both to reduce water use and to support the variety of other systems that are changing to aid this. In this case, kidneys may reduce urine output, mucous membrane in the mouth, nose and eyes may dry out; urine and sweat output will decrease; the release of [[arginine vasopressin]] (AVP) will increase; and veins and arteries will constrict to maintain blood pressure with a smaller blood volume.
== Allostatic Load and Overload ==
While allostasis is adaptive in the short term, prolonged activation of allostatic responses can lead to [[allostatic load]]—the cumulative wear and tear on the body.


==Types==
If allostatic load becomes excessive, it may lead to dysfunction, known as '''allostatic overload'''. This state is associated with various health conditions, including:
McEwen and Wingfield propose two types of allostatic load which result in different responses:-
* [[Hypertension]]
* [[Cardiovascular disease]]
* [[Metabolic syndrome]]
* [[Depression]]


<blockquote>Type 1 allostatic overload occurs when energy demand exceeds supply, resulting in activation of the emergency life history stage. This serves to direct the animal away from normal life history stages into a survival mode that decreases allostatic load and regains positive energy balance. The normal life cycle can be resumed when the perturbation passes.
== Types of Allostatic Overload ==
</blockquote>
According to McEwen and Wingfield (2003), there are two major types of allostatic overload:


<blockquote>
=== Type 1 Allostatic Overload ===
Type 2 allostatic overload begins when there is sufficient or even excess energy consumption accompanied by social conflict and other types of social dysfunction. The latter is the case in human society and certain situations affecting animals in captivity. In all cases, secretion of glucocorticosteroids and activity of other mediators of allostasis such as the autonomic nervous system, CNS [[neurotransmitters]], and inflammatory cytokines wax and wane with allostatic load. If allostatic load is chronically high, then pathologies develop. Type 2 allostatic overload does not trigger an escape response, and can only be counteracted through learning and changes in the social structure ({{harvnb|McEwen|Wingfield|2003}}; {{harvnb|Sterling|Eyer|1988}})</blockquote>
This occurs when the organism faces a deficit in energy availability. The emergency life history stage is activated, prioritizing survival over growth or reproduction. The goal is to reduce allostatic load and reestablish energy balance.


Whereas both types of allostasis are associated with increased release of [[cortisol]] and [[catecholamines]], they differentially affect [[thyroid homeostasis]]: Concentrations of the [[thyroid hormone]] [[triiodothyronine]] are decreased in type 1 allostasis, but elevated in type 2 allostasis {{harv|Chatzitomaris et al.|2017}}.
=== Type 2 Allostatic Overload ===
This occurs despite adequate or even excessive energy intake. It is typically driven by psychosocial stress, conflict, or other chronic environmental stressors. Unlike Type 1, it does not activate an escape response and can lead to long-term pathophysiological conditions.


==Allostatic load==
Both types involve increased secretion of [[glucocorticoids]] such as [[cortisol]] and activation of [[neurotransmitters]], [[cytokines]], and the [[autonomic nervous system]]. However, their effects on [[thyroid hormone]] regulation differ:
{{main|Allostatic load}}
* In Type 1, levels of [[triiodothyronine]] (T3) are reduced
In the long run, the maintenance of allostatic changes over a long period may result in wear and tear, the so-called [[allostatic load]]. If a dehydrated individual is helped but continues to be stressed and hence does not reinstate normal body function, the individual's body systems will wear out.{{cn|date=May 2019}}
* In Type 2, T3 levels may be elevated


==Controversy==
== Allostasis in Chronic Conditions ==
In 2005, Trevor A. Day has argued that the concept of allostasis is no more than a renaming of the original concept of homeostasis {{harv|Day|2005}}.
Allostasis underlies many compensated states in chronic diseases, such as:
* [[Heart failure]] (compensated and decompensated)
* [[Kidney failure]]
* [[Liver failure]]


==See also==
These states are fragile and can lead to rapid decompensation when compensatory mechanisms fail.
* [[Homeostasis]]


==Notes==
== Criticisms and Controversies ==
{{Reflist}}
Some scholars, such as Trevor A. Day (2005), have argued that allostasis may be redundant with homeostasis, suggesting it is merely a rebranding of older ideas. However, proponents argue that allostasis provides a more integrative and predictive framework, accounting for the brain’s central role and the dynamic interplay between systems.


==References==
== See Also ==
*{{cite journal|last1=Chatzitomaris|first1=Apostolos|last2=Hoermann|first2=Rudolf|last3=Midgley|first3=John E.|last4=Hering|first4=Steffen|last5=Urban|first5=Aline|last6=Dietrich|first6=Barbara|last7=Abood|first7=Assjana|last8=Klein|first8=Harald H.|last9=Dietrich|first9=Johannes W.|title=Thyroid Allostasis–Adaptive Responses of Thyrotropic Feedback Control to Conditions of Strain, Stress, and Developmental Programming|journal=Frontiers in Endocrinology|date=20 July 2017|volume=8|pages=163|pmid=28775711|pmc=5517413|doi=10.3389/fendo.2017.00163|ref={{SfnRef|Chatzitomaris et al.|2017}}}}
* [[Homeostasis]]
*{{cite book|last1=Copstead|first1=Lee-Ellen|last2=Banasik|first2=Jacquelyn|title=Pathophysiology|date=2013|publisher=Elsevier Saunders|location=St Louis, Missouri|isbn=978-1-4557-2650-9|edition=5th|ref=harv}}
* [[Allostatic load]]
* {{Cite journal|title = Defining stress as a prelude to mapping its neurocircuitry: No help from allostasis|year = 2005|last = Day|first = Trevor A.|ref = harv|journal = Prog. Neuropsychopharmacol. Biol. Psychiatry|issn = 0278-5846|volume = 29|issue = 8|pages = 1195–1200|doi=10.1016/j.pnpbp.2005.08.005|pmid = 16213079}}{{Closed access}}
* [[Stress (biology)]]
* {{Cite thesis|ref = harv|last = Klein|first = Robyn|title = Phylogenetic and phytochemical characteristics of plant species with adaptogenic properties|chapter = Chapter 3|chapter-url = http://www.rrreading.com/files/Thesis%203.pdf|archiveurl = https://web.archive.org/web/20061017061323/http://www.rrreading.com/files/Thesis%203.pdf|archivedate = October 17, 2006|type = MS|publisher = Montana State University|year = 2004}}{{open access}}
* [[Neuroendocrinology]]
* {{Cite journal|title = Protective and Damaging Effects of Stress Mediators|ref = harv|last = McEwen|first = Bruce S.|journal = [[N. Engl. J. Med.]]|doi = 10.1056/NEJM199801153380307|volume = 338|issue = 3|pages = 171–9|department = Seminars in Medicine of the Beth Israel Deaconess Medical Center|year = 1998a|pmid=9428819|citeseerx = 10.1.1.357.2785}}{{Closed access}}
* [[Autonomic nervous system]]
* {{Cite journal|title = Stress, Adaptation, and Disease: Allostasis and Allostatic Load|last = McEwen|first = Bruce S.|journal = [[Ann. N. Y. Acad. Sci.]]|doi = 10.1111/j.1749-6632.1998.tb09546.x|pmid = 9629234|volume = 840|issue = 1|pages = 33–44|year = 1998b|ref=harv|bibcode = 1998NYASA.840...33M}}{{Closed access}}
* {{Cite journal|title = The concept of allostasis in biology and biomedicine|year = 2003|ref = harv|last = McEwen|first = Bruce S.|last2 = Wingfield|first2 = John C.|journal = Horm. Behav.|volume = 43|issue = 1|pages = 2–15|issn = 0018-506X|doi=10.1016/S0018-506X(02)00024-7|pmid = 12614627}}{{Closed access}}
* {{Cite book|title = Rethinking homeostasis : allostatic regulation in physiology and pathophysiology|last = Schulkin|first = Jay|publisher = [[MIT Press]]|year = 2003|isbn = 9780262194808|location = Cambridge, MA|pages = |oclc = 49936130 |ref=harv}}
* {{Cite book|title = Handbook of life stress, cognition, and health|last = Sterling|first = P.|publisher = Wiley|year = 1988|isbn = 9780471912699|location = Chicester, NY|pages = |oclc = 17234042|chapter = Allostasis: A new paradigm to explain arousal pathology|last2 = Eyer|first2 = J.|editor-last = Fisher|editor-first = S.|editor2-last = Reason|editor2-first = J. T. |ref=harv}}
* {{Cite book|title = Allostasis, homeostasis, and the costs of physiological adaptation|last = Sterling|first = Peter|publisher = [[Cambridge University Press]]|year = 2004|isbn = 9780521811415|location = New York, NY|pages = |oclc = 53331074|chapter = Chapter 1. Principles of Allostasis|ref = harv|editor-last = Schulkin|editor-first = Jay}}
* {{cite journal|last=Selye|first=H.|year=1973|title=Homeostasis and Heterostasis|journal=Perspectives in Biology and Medicine|volume=16|issue=3|pages=441–445|ref=harv|doi=10.1353/pbm.1973.0056}}
* {{Cite journal|title = Control of behavioural strategies for capricious environments|journal = [[Anim. Behav.]]|department = Anniversary Essays|year = 2003|ref = harv|first = John C.|last = Wingfield|volume = 66|issue = 5|pages = 807–16|doi = 10.1006/anbe.2003.2298}}{{Closed access}}


==Further reading==
== External Links ==
* {{cite journal |doi=10.3389/fnevo.2010.00111|pmid=21369352|title=Social Allostasis: Anticipatory Regulation of the Internal Milieu|journal=Frontiers in Evolutionary Neuroscience|volume=2|year=2011|last1=Schulkin|first1=Jay|pmc=3037529}} Contains an entire paragraph dedicated to defining allostasis.
* [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974761/ Allostasis and Allostatic Load — NIH]
* [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1993982/ The concept of allostasis — Sterling and Eyer]


[[Category:Anxiety]]
[[Category:Stress]]
[[Category:Neuroendocrinology]]
[[Category:Immune system]]
[[Category:Physiology]]
[[Category:Homeostasis]]
[[Category:Homeostasis]]
[[Category:Immune system]]
[[Category:Neuroendocrinology]]
[[Category:Stress]]

Latest revision as of 10:46, 26 March 2025

Allostasis is the process by which the body achieves stability—or homeostasis—through physiological or behavioral change. This dynamic process enables the organism to maintain internal viability amid external or internal challenges, using anticipatory and adaptive mechanisms.

Unlike homeostasis, which aims to maintain internal equilibrium through fixed set points, allostasis adjusts physiological systems in a predictive and flexible manner. It involves complex coordination between the hypothalamic-pituitary-adrenal axis (HPA axis), the autonomic nervous system, cytokines, and other neuroendocrine and immune pathways.

Etymology[edit]

The term "allostasis" comes from the Greek words ἄλλος (állos), meaning "other" or "different," and στάσις (stasis), meaning "standing still". It was introduced by Sterling and Eyer in 1988.

Historical and Conceptual Origins[edit]

The concept of allostasis was proposed by Peter Sterling and Joseph Eyer in 1988 as a more comprehensive and anticipatory model of regulation compared to the classical idea of homeostasis. The authors emphasized that biological systems do not merely react to perturbations but prepare for them through predictive regulation.

Allostasis emphasizes the role of the brain in initiating and coordinating adaptive responses based on expectations and prior experience. These adjustments allow organisms to effectively cope with both predictable and unpredictable stressors.

In computational models, the analogous term heterostasis is sometimes used, particularly in systems where state transitions are discrete rather than continuous

Principles of Allostasis[edit]

Peter Sterling outlined six principles underlying allostasis:

  1. Organisms are designed for efficiency.
  2. Efficiency requires trade-offs.
  3. Efficiency depends on prediction of future needs.
  4. Prediction requires sensors to adapt to expected input ranges.
  5. Effectors must adapt to expected demands.
  6. Predictive regulation depends on behavior, and neural plasticity supports such adaptability.

Allostasis vs. Homeostasis[edit]

Homeostasis is typically defined as the maintenance of a stable internal environment through regulation of variables around a fixed set point (e.g., blood pH, glucose levels). In contrast, allostasis refers to the active process of achieving stability through change.

For example, in response to dehydration, allostasis activates multiple systems:

These responses together help preserve function and viability in the face of a stressor.

Allostatic Load and Overload[edit]

While allostasis is adaptive in the short term, prolonged activation of allostatic responses can lead to allostatic load—the cumulative wear and tear on the body.

If allostatic load becomes excessive, it may lead to dysfunction, known as allostatic overload. This state is associated with various health conditions, including:

Types of Allostatic Overload[edit]

According to McEwen and Wingfield (2003), there are two major types of allostatic overload:

Type 1 Allostatic Overload[edit]

This occurs when the organism faces a deficit in energy availability. The emergency life history stage is activated, prioritizing survival over growth or reproduction. The goal is to reduce allostatic load and reestablish energy balance.

Type 2 Allostatic Overload[edit]

This occurs despite adequate or even excessive energy intake. It is typically driven by psychosocial stress, conflict, or other chronic environmental stressors. Unlike Type 1, it does not activate an escape response and can lead to long-term pathophysiological conditions.

Both types involve increased secretion of glucocorticoids such as cortisol and activation of neurotransmitters, cytokines, and the autonomic nervous system. However, their effects on thyroid hormone regulation differ:

  • In Type 1, levels of triiodothyronine (T3) are reduced
  • In Type 2, T3 levels may be elevated

Allostasis in Chronic Conditions[edit]

Allostasis underlies many compensated states in chronic diseases, such as:

These states are fragile and can lead to rapid decompensation when compensatory mechanisms fail.

Criticisms and Controversies[edit]

Some scholars, such as Trevor A. Day (2005), have argued that allostasis may be redundant with homeostasis, suggesting it is merely a rebranding of older ideas. However, proponents argue that allostasis provides a more integrative and predictive framework, accounting for the brain’s central role and the dynamic interplay between systems.

See Also[edit]

External Links[edit]