{{Short description|Animal behavioural test}} {{more citations needed|date=November 2019}} [[File:201407 tail suspension test.png|thumb|tail suspension test (TST)]] [[File:Nigral-proteasome-inhibition-in-mice-leads-to-motor-and-non-motor-deficits-and-increased-expression-Video1.ogv|thumb|The video is shown at 4x its normal speed : after a period of initial struggle, control mice demonstrate intervals of immobile behavior, reflecting reluctance to maintain active escape-oriented behavior.]] {{Animal testing}}

The '''tail suspension test''' ('''TST''') is an experimental method used in [[Scientific method|scientific research]] to measure [[Stress (psychological)|stress]] in rodents. It is based on the observation that if a mouse is subjected to short term inescapable stress then the mouse will become [[Paralysis|immobile]]. It is used to measure the effectiveness of [[antidepressant]]-like agents but there is significant controversy over its interpretation and usefulness.

== History == The TST was introduced in 1985 due to the popularity of a similar test called the [[Behavioural despair test|forced swim test (FST)]]. However this test only recently became popular in the 2000s where data has shown that animals do show a change in behavior when injected with antidepressants. TST is more reliable when done in conjunction with other depression models such as FST, [[Animal models of depression#Adult stress models|learned helplessness]], [[Animal models of depression#Endophenotypes in animal model of depression|anhedonia models]], and [[Animal models of depression#Other models|olfactory bulbectomy]].<ref name=":0">{{cite journal |last1=Cryan |first1=John F. |last2=Mombereau |first2=Cedric |last3=Vassout |first3=Annick |title=The tail suspension test as a model for assessing antidepressant activity: Review of pharmacological and genetic studies in mice |journal=Neuroscience and Biobehavioral Reviews |date=2005 |volume=29 |issue=4–5 |pages=571–625 |doi=10.1016/j.neubiorev.2005.03.009 |pmid=15890404 |s2cid=2758433}}</ref>

== Modeling depression== [[Depression (mood)|Depression]] is a complex multi-faceted disorder with symptoms that can have multiple causes such as [[Psychology|psychological]], behavioral, and [[genetics]]. Since there are so many variables it is hard to model in a lab setting. Patients with depression do not always show the same set of symptoms and often present with co-occurring psychiatric conditions.

A major difficulty in modeling depression is that psychiatrists who clinically diagnose depression follow the [[Diagnostic and Statistical Manual of Mental Disorders|Diagnostic and Statistical Manual (DSM IV) of the American Psychiatric Association]], which involves self-reporting from patients on how they feel. Since animals cannot explain to us how they feel, animals cannot be diagnosed as clinically depressed.<ref>{{cite book|title=Diagnostic and Statistical Manual of Mental Disorders: DSM-5|last=American Psychiatric Association|date=2013|publisher=American Psychiatric Association|edition=fifth|location=Washington D.C.}}</ref> While there are theories that animals can experience a condition similar to depression, it is important to keep in mind that depression is, by definition, a human disease. Human and animal brains are considerably different, and care must be taken when interpreting animal behavior and [[Anthropomorphism|assigning emotional states to various behaviors]].

However, there are discrete elements of depression that can be modeled in a lab setting.<ref>{{cite book|last1=Koob|first1=George|last2=Zimmer|first2=Andreas|title=Neurobiology of Psychiatric Disorders |chapter=Animal models of psychiatric disorders|series=Handbook of Clinical Neurology|year=2012|volume=106|issue=2012|pages=136–166|doi=10.1016/B978-0-444-52002-9.00009-7|pmid=22608620|isbn=9780444520029}}</ref><ref>{{cite journal|last1=Cryan|first1=J F|last2=Mombereau|first2=C|title=In search of a depressed mouse: utility of models for studying depression-related behavior in genetically modified mice|journal=Molecular Psychiatry|date=13 January 2004|volume=9|issue=4|pages=326–357|doi=10.1038/sj.mp.4001457|pmid=14743184|doi-access=|s2cid=14937344 }}</ref> [[Stress (psychological)|Stress]] induced immobilization is a behavior that can be useful in modelling aspects of depression. If a rodent is subjected to the short term inescapable stress of being suspended in the air it will develop an immobile posture. [[Paralysis|Immobility]] in the TST can be interpreted as the animal ceasing to put in the effort to try to escape. This is often interpreted as behavioral despair, and could be considered a model of the hopelessness and despair experienced by those with depression.<ref name=":0" />

The main strength of the tail suspension test is its predictive validity– performance on the test can be altered by drugs that improve depressive symptoms in people. Specifically, if [[antidepressant]] agents are administered before the test, the animal will struggle for a longer period of time than if not and exhibit more escape behaviors.<ref name=":0" /> Thus, it is widely used for assessing the antidepressant effects of new pharmacological compounds.

== Procedure == The animal is hung from a tube by its tail for five minutes approximately 10&nbsp;cm away from the ground. During this time the animal will try to escape and reach for the ground. The time it takes until it remains immobile is measured. Each animal is tested only once and out of view from the other animals. Within the study there should be two sets of rats, one group which is the control which has been injected with [[Saline (medicine)|saline]] and the group being tested which has been injected with the antidepressant-like agents.<ref>{{cite web|title=Tail Suspension Test|url=http://www.research.psu.edu/arp/experimental-guidelines/rodent-behavioral-tests-1/rodent-behavioral-tests|website=Penn State Animal Resource Program|access-date=30 March 2016}}</ref>

==Controversy== There are mixed opinions about the TST. A common criticism is that it can be weeks before a noticeable effect is observed in patients who take antidepressants regularly, however the TST only measures one acute antidepressant dose for 5–6 minutes.{{Citation needed|date=April 2019}}

The TST has predictive reliability for known antidepressant agents. However, when testing drugs of unknown mechanisms, the prediction rate is unclear. While the TST detects [[NK1 receptor antagonist]]s, which have known antidepressant action, it doesn't detect [[CRF1|CRF1 receptor antagonists]] which also have antidepressant functions.

Some consider the TST to be a test of antidepressant function, rather than a model of depression itself.<ref name=Hoffman>{{cite book |last1=Hoffman |first1=Kurt Leroy |title=Modeling Neuropsychiatric Disorders in Laboratory Animals, 2 - What can animal models tell us about depressive disorders? |date=2016 |publisher=Woodhead Publishing |pages=35–36 |doi=10.1016/B978-0-08-100099-1.00002-9 |url=https://doi.org/10.1016/B978-0-08-100099-1.00002-9 |access-date=26 February 2022}}</ref> This is largely because the test measures behavioral response to a short-term stressor, whereas human depression is a long-term condition.<ref name=Hoffman/>

==Difference from the forced swim test== TST is more sensitive to antidepressant agents than the FST because the animal will remain immobile longer in the TST than the FST.<ref name=":0" /> The FST is not as reliable as the TST because the immobility in the animal could be due to the shock of being dropped in water. This also risks hypothermia.<ref>{{cite journal|last1=Liu|first1=X|last2=Peprah|first2=D|last3=Gershenfield|first3=H.K|title=Tail-suspension induced hyperthermia: a new measure of stress reactivity.|journal=J Psychiatr Res|date=2003|volume=37|issue=3|pages=249–259|doi=10.1016/s0022-3956(03)00004-9|pmid=12650744}}</ref> While the mechanisms through which the TST and FST produce stress are unknown it is clear that while overlapping the tests produce immobility through stress differently.

==See also== * [[Animal models of depression]] * [[Behavioural despair test]] * [[Learned helplessness]] * [[Open field (animal test)]]

== References== {{Reflist}}

[[Category:Animal testing techniques]] [[Category:Psychology experiments]]