Biology:Escape reflex

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Escape reflex, or escape behavior, is any kind of escape response found in an animal when it is presented with an unwanted stimulus.[1] It is a simple reflectory reaction in response to stimuli indicative of danger, that initiates an escape motion of an animal. The escape response has been found to be processed in the telencephalon.[2]

The above diagram is a simplified version showing that a cockroach will not venture towards a dangerous stimulus. Due to the escape reflex, the cockroach will take an alternative route once it has sensed the stimulus.[3]

Escape reflexes control the seemingly chaotic motion of a cockroach running out from under a foot when one tries to squash it.

As the stimulus on the left side enters the ear, the signal is processed and inhibits the muscles on the same side as the stimulus. Muscles on the opposite side remaining working, which allows the creature to quickly pull away from the stimulus if it is threatening. This depiction is a simplified version and does not contain all accurate structures involved.[4]

In higher animals, examples of escape reflex include the withdrawal reflex (e.g. the withdrawal of a hand) in response to a pain stimulus. Sensory receptors in the stimulated body part send signals to the spinal cord along a sensory neuron. Within the spine, a reflex arc switches the signals straight back to the muscles of the arm (effectors) via an intermediate neuron (interneuron) and then a motor neuron; the muscle contracts. There often is an opposite response of the opposite limb. Because this occurs automatically and independently in the spinal cord, the brain only becomes aware of the response after it has taken place.

Crossed extensor reflex

The crossed extensor reflex is another escape reflex, but it's a type of withdrawal reflex.[5] It is a contralateral reflex that allows for the affected limb to have the flexor muscles contract and the extensor muscles to relax while the unaffected limb has the flexor muscles relax and the extensor muscles to contract.[5] For example, stepping on a piece of glass causes the affected leg to be lifted or withdrawn and the unaffected leg to carry the additional burden of weight and maintain postural support.[6] In this example, the afferent nerve fibers are stimulated on the right foot. The nerve fibers travel up to the spinal cord where they cross the midline, go to the left side, and synapse on an interneuron. When the afferent nerve fibers synapse on the interneuron, they can either inhibit or excite an alpha motor neuron on the muscles on side contralateral to the stimulus.[5]

Escape reflex arcs

Escape reflex arcs have a high survival value enabling organisms to take rapid action to avoid potential danger or physical damage. The effectiveness of escape reflexes can be lowered when an organism is experiencing high levels of fatigue and or stress.[7] These factors cause delays or weakness in the reflex, and they can even develop into learned helplessness, which has been found in animals and Drosophila flies.[8] The reflex can also be habituated as seen in the tail-flip escape reflex of crayfish.[9] More recent studies have also indicated that, once this crayfish escape response is habituated, it can also be recovered.[10] A similar long-term habituation of the C-start escape response has also been studied in the larvae of zebrafish.[11]

Various animals may have specialized escape reflex arcs.

Examples

See also

References

  1. "Escape behaviour". APA Dictionary of Psychology. Washington, DC: American Psychological Association. n.d.. https://dictionary.apa.org/escape-behavior. Retrieved 2020-01-31. 
  2. "Avoidance conditioning in bamboo sharks (Chiloscyllium griseum and C. punctatum): behavioral and neuroanatomical aspects". Journal of Comparative Physiology A: Neuroethology, Sensory, Neural & Behavioral Physiology 199 (10): 843–56. October 2013. doi:10.1007/s00359-013-0847-1. PMID 23958858. 
  3. Booth, D.; Marie, B.; Domenici, P.; Blagburn, J. M.; Bacon, J. P. (2009-06-03). "Transcriptional Control of Behavior: Engrailed Knock-Out Changes Cockroach Escape Trajectories" (in en). Journal of Neuroscience 29 (22): 7181–7190. doi:10.1523/JNEUROSCI.1374-09.2009. ISSN 0270-6474. PMID 19494140. 
  4. Catania, Kenneth C. (April 2011). "The brain and behavior of the tentacled snake". Annals of the New York Academy of Sciences 1225 (1): 83–89. doi:10.1111/j.1749-6632.2011.05959.x. ISSN 0077-8923. PMID 21534995. 
  5. 5.0 5.1 5.2 "Reflexes". Boundless Anatomy and Physiology. courses.lumenlearning.com. https://courses.lumenlearning.com/boundless-ap/chapter/reflexes/. 
  6. "Flexion Reflex Pathways". Neuroscience (2nd ed.). Sunderland (MA): Sinauer Associates. 2001. https://www.ncbi.nlm.nih.gov/books/NBK11091/. 
  7. "Differential effects of stress on escape and reflex responses to nociceptive thermal stimuli in the rat". Brain Research 987 (2): 214–22. October 2003. doi:10.1016/S0006-8993(03)03339-0. PMID 14499966. 
  8. "Inescapable Stress Changes Walking Behavior in Flies - Learned Helplessness Revisited". PLOS ONE 11 (11): e0167066. 2016-11-22. doi:10.1371/journal.pone.0167066. PMID 27875580. 
  9. "Habituation of an invertebrate escape reflex due to modulation by higher centers rather than local events". Proceedings of the National Academy of Sciences of the United States of America 92 (8): 3362–6. April 1995. doi:10.1073/pnas.92.8.3362. PMID 7724567. 
  10. "Auditory stimulation dishabituates anti-predator escape behavior in hermit crabs (Coenobita clypeatus)". Behavioural Processes 88 (1): 7–11. September 2011. doi:10.1016/j.beproc.2011.06.009. PMID 21756986. 
  11. Roberts, Adam C.; Pearce, Kaycey C.; Choe, Ronny C.; Alzagatiti, Joseph B.; Yeung, Anthony K.; Bill, Brent R.; Glanzman, David L. (October 2016). "Long-term habituation of the C-start escape response in zebrafish larvae" (in en). Neurobiology of Learning and Memory 134 (Pt B): 360–368. doi:10.1016/j.nlm.2016.08.014. PMID 27555232. 
  12. "Excitation and habituation of the crayfish escape reflex: the depolarizing response in lateral giant fibres of the isolated abdomen". The Journal of Experimental Biology 50 (1): 29–46. February 1969. doi:10.1242/jeb.50.1.29. PMID 4304852. https://jeb.biologists.org/content/50/1/29. 
  13. "Altered excitability of the crayfish lateral giant escape reflex during agonistic encounters". The Journal of Neuroscience 17 (2): 709–16. January 1997. doi:10.1523/JNEUROSCI.17-02-00709.1997. PMID 8987792. 
  14. Otis, T. S.; Gilly, W. F. (1990-04-01). "Jet-propelled escape in the squid Loligo opalescens: concerted control by giant and non-giant motor axon pathways." (in en). Proceedings of the National Academy of Sciences 87 (8): 2911–2915. doi:10.1073/pnas.87.8.2911. ISSN 0027-8424. PMID 2326255. 
  15. Frost, W. N.; Hoppe, T. A.; Wang, J.; Tian, L.-M. (August 2001). "Swim Initiation Neurons in Tritonia diomedea" (in en). American Zoologist 41 (4): 952–961. doi:10.1093/icb/41.4.952. ISSN 0003-1569. 
  16. Frost, W. N.; Katz, P. S. (1996-01-09). "Single neuron control over a complex motor program." (in en). Proceedings of the National Academy of Sciences 93 (1): 422–426. doi:10.1073/pnas.93.1.422. ISSN 0027-8424. PMID 8552652. 
  17. "The Mauthner cell and other identified neurons of the brainstem escape network of fish". Progress in Neurobiology 63 (4): 467–85. March 2001. doi:10.1016/s0301-0082(00)00047-2. PMID 11163687. 
  18. "Regeneration of Rapid Escape Reflex Pathways in Earthworms" (in en). Integrative and Comparative Biology 28 (4): 1077–1089. 1988-11-01. doi:10.1093/icb/28.4.1077. https://academic.oup.com/icb/article/28/4/1077/166348.