Jump to content

Preflexes: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous edit
Content deleted Content added
VisualWikitext
Citation bot (talk | contribs)
Bots
5,436,105 edits
m Alter: isbn, journal. Add: citeseerx. | You can use this bot yourself. Report bugs here. | User-activated.
Open access status updates in citations with OAbot #oabot
 
(9 intermediate revisions by 7 users not shown)
Line 1: Line 1:
{{short description|Latent capacities in the musculoskeletal system}}
'''Preflexes''' are the latent capacities in the [[musculoskeletal system]] that auto-stabilize movements through the use of the [[Nonlinear system|nonlinear]] [[Viscoelasticity|visco-elastic]] properties of [[Skeletal muscle|muscles]] when they [[Muscle contraction|contract]].<ref>{{Cite journal
'''Preflexes''' are the latent capacities in the [[musculoskeletal system]] that auto-stabilize movements through the use of the [[Nonlinear system|nonlinear]] [[Viscoelasticity|visco-elastic]] properties of [[Skeletal muscle|muscles]] when they [[Muscle contraction|contract]].<ref>{{Cite journal
| last1 = Blickhan | first1 = R.
| last1 = Blickhan | first1 = R.
Line 14: Line 15:
| year = 2007
| year = 2007
| pmid = 17148057
| pmid = 17148057
|bibcode = 2007RSPTA.365..199B | s2cid = 1141390
| pmc =
|bibcode = 2007RSPTA.365..199B }}</ref><ref>{{Cite journal
}}</ref><ref>{{Cite journal
| last1 = Valero-Cuevas | first1 = F. J.
| last1 = Valero-Cuevas | first1 = F. J.
| last2 = Yi | first2 = J. W.
| last2 = Yi | first2 = J. W.
Line 30: Line 31:
| year = 2007
| year = 2007
| pmid = 17549909
| pmid = 17549909
| pmc =
| citeseerx = 10.1.1.419.1719
| citeseerx = 10.1.1.419.1719
| s2cid = 1869716
}} [http://ccsl.mae.cornell.edu/papers/TBE07_Valero.pdf PDF]</ref> The term "preflex" for such a zero-delay, intrinsic feedback loop was coined by Loeb. <ref>{{Cite book | last1 = Loeb | first1 = G. E. | doi = 10.1109/IEMBS.1995.579743 | chapter = Control implications of musculoskeletal mechanics | title = Proceedings of 17th International Conference of the Engineering in Medicine and Biology Society | volume = 2 | pages = 1393–1394 | year = 1995 | isbn = 978-0-7803-2475-6 | pmid = | pmc = }}</ref> Unlike stabilization methods using [[neurons]] such as [[reflexes]] and [[Motor coordination|higher brain control]], it happens with minimal time delay. Its chief disadvantage is that it works only to stabilize the main movements of the musculoskeletal system.
}} [http://ccsl.mae.cornell.edu/papers/TBE07_Valero.pdf PDF]</ref> The term "preflex" for such a zero-delay, intrinsic feedback loop was coined by Loeb.<ref>{{Cite book | last1 = Loeb | first1 = G. E. | doi = 10.1109/IEMBS.1995.579743 | chapter = Control implications of musculoskeletal mechanics | title = Proceedings of 17th International Conference of the Engineering in Medicine and Biology Society | volume = 2 | pages = 1393–1394 | year = 1995 | isbn = 978-0-7803-2475-6 | s2cid = 62579032 }}</ref> Unlike stabilization methods using [[neurons]], such as [[reflexes]] and [[Motor coordination|higher brain control]], a preflex happens with minimal time delay; however, it only stabilizes the main movements of the musculoskeletal system.{{Citation needed|date=April 2020}}


==Visco-elastic correction==
==Visco-elastic correction==
Muscles possess nonlinear visco-elastic properties when they contract.<ref name="brown">{{Cite book|author=Brown IE, Loeb GE.|year= 2000|chapter= A reductionist approach to creating and using neuromusculoskeletal models|title= Biomechanical and neurological control of posture and movements|editor=JMC Winters, P.E.|pages=148–63|location= New York|publisher= Springer| isbn= 978-0-471-50908-0}}</ref><ref>{{Cite journal | last1 = Nishikawa | first1 = K. | last2 = Biewener | first2 = A. A. | last3 = Aerts | first3 = P. | last4 = Ahn | first4 = A. N. | last5 = Chiel | first5 = H. J. | last6 = Daley | first6 = M. A. | last7 = Daniel | first7 = T. L. | last8 = Full | first8 = R. J. | last9 = Hale | first9 = M. E. | doi = 10.1093/icb/icm024 | last10 = Hedrick | first10 = T. L. | last11 = Lappin | first11 = A. K. | last12 = Nichols | first12 = T. R. | last13 = Quinn | first13 = R. D. | last14 = Satterlie | first14 = R. A. | last15 = Szymik | first15 = B. | title = Neuromechanics: An integrative approach for understanding motor control | journal = Integrative and Comparative Biology | volume = 47 | issue = 1 | pages = 16–54 | year = 2007 | pmid = 21672819| pmc = }}</ref><ref name="van Soest">{{Cite journal
Muscles possess nonlinear visco-elastic properties when they contract.<ref name="brown">{{Cite book|author=Brown IE, Loeb GE.|year= 2000|chapter= A reductionist approach to creating and using neuromusculoskeletal models|title= Biomechanical and neurological control of posture and movements|editor=JMC Winters, P.E.|pages=148–63|location= New York|publisher= Springer| isbn= 978-0-471-50908-0}}</ref><ref>{{Cite journal | last1 = Nishikawa | first1 = K. | last2 = Biewener | first2 = A. A. | last3 = Aerts | first3 = P. | last4 = Ahn | first4 = A. N. | last5 = Chiel | first5 = H. J. | last6 = Daley | first6 = M. A. | last7 = Daniel | first7 = T. L. | last8 = Full | first8 = R. J. | last9 = Hale | first9 = M. E. | doi = 10.1093/icb/icm024 | last10 = Hedrick | first10 = T. L. | last11 = Lappin | first11 = A. K. | last12 = Nichols | first12 = T. R. | last13 = Quinn | first13 = R. D. | last14 = Satterlie | first14 = R. A. | last15 = Szymik | first15 = B. | title = Neuromechanics: An integrative approach for understanding motor control | journal = Integrative and Comparative Biology | volume = 47 | issue = 1 | pages = 16–54 | year = 2007 | pmid = 21672819| doi-access = free | url = https://biblio.ugent.be/publication/443282/file/6814040 }}</ref><ref name="van Soest">{{Cite journal
| last1 = Van Soest | first1 = A. J.
| last1 = Van Soest | first1 = A. J.
| last2 = Bobbert | first2 = M. F.
| last2 = Bobbert | first2 = M. F.
Line 46: Line 47:
| pmid = 8373890
| pmid = 8373890
| doi=10.1007/bf00198959
| doi=10.1007/bf00198959
| s2cid = 16196068
}}</ref> This property can autocorrect movements when a muscle is forced to change its length, and at a velocity different from that with which it was originally commanded. Such automatic correction is useful when a commanded action is perturbated, for example, if a step goes into a hole as this causes the foot to unexpectedly stretch down. The nonlinear visco-elastic properties of muscles interact with these perturbation induced velocity and length differences such that they counteract directly, as they happen, the effects upon the body of the perturbation.
}}</ref> This property can autocorrect movements when a muscle is forced to change its length, and at a velocity different from that with which it was originally commanded. Such automatic correction is useful when a commanded action is perturbated, for example, if a step goes into a hole as this causes the foot to unexpectedly stretch down. The nonlinear visco-elastic properties of muscles interact with these perturbation induced velocity and length differences such that they counteract directly, as they happen, the effects upon the body of the perturbation.
Part of the resistance to perturbation is passive, by means of the nonlinear increase in passive tension and joint torques produced by muscular and other soft tissues.<ref name="brown">{{Cite book|author=Brown IE, Loeb GE.|year= 2000|chapter= A reductionist approach to creating and using neuromusculoskeletal models|title= Biomechanical and neurological control of posture and movements|editor=JMC Winters, P.E.|pages=148–63|location= New York|publisher= Springer| isbn= 978-0-471-50908-0}}</ref> Tissue prestress is a preflexive property that constitutes a basal level of passive tension which, due to its presence in antagonistic tissues of a joint, increases joint passive stiffness and stability.<ref>{{Cite journal | last1 = Souza | first1 = T.R. | last2 = Fonseca | first2 =S.T. | last3 = Gonçalves | first3 = G.G. | last4 = Ocarino | first4 = J.M. | last5 = Mancini | first5 = M.C. | title = Prestress revealed by passive co-tension at the ankle joint | journal = Journal of Biomechanics | volume = 42 | issue = 14 | pages = 2374–2380 | year = 2009 | doi = 10.1016/j.jbiomech.2009.06.033 | pmid = 19647832 }}</ref>
Part of the resistance to perturbation is passive, by means of the nonlinear increase in passive tension and joint torques produced by muscular and other soft tissues.<ref name="brown">{{Cite book|author=Brown IE, Loeb GE.|year= 2000|chapter= A reductionist approach to creating and using neuromusculoskeletal models|title= Biomechanical and neurological control of posture and movements|editor=JMC Winters, P.E.|pages=148–63|location= New York|publisher= Springer| isbn= 978-0-471-50908-0}}</ref> Tissue prestress is a preflexive property that constitutes a basal level of passive tension which, due to its presence in antagonistic tissues of a joint, increases joint passive stiffness and stability.<ref>{{Cite journal | last1 = Souza | first1 = T.R. | last2 = Fonseca | first2 =S.T. | last3 = Gonçalves | first3 = G.G. | last4 = Ocarino | first4 = J.M. | last5 = Mancini | first5 = M.C. | title = Prestress revealed by passive co-tension at the ankle joint | journal = Journal of Biomechanics | volume = 42 | issue = 14 | pages = 2374–2380 | year = 2009 | doi = 10.1016/j.jbiomech.2009.06.033 | pmid = 19647832 | doi-access = free }}</ref>


==Evolutionary opportunity==
==Evolutionary opportunity==
Line 63: Line 65:
| year = 2007
| year = 2007
| pmid = 16458022
| pmid = 16458022
⚫
}}</ref> Within each muscle segment, there exists a complex internal structure that goes down to one in which each muscle unit consists of a tendon, [[aponeurosis]], and a [[Muscle fascicle|fascicle]] of active contractile and passive elements.<ref name="brown" /> Another source of variation is in the internal architecture of the fiber orientation relative to a muscle's line of action, for example, as found in [[Pennate_muscle|pennate muscles]].<ref>{{Cite journal
| pmc =
⚫
}}</ref> Within each muscle segment, there exists a complex internal structure that goes down to one in which each muscle unit consists of a tendon, [[aponeurosis]], and a [[Muscle fascicle|fascicle]] of active contractile and passive elements.<ref name="brown" /> Another source of variation is in the internal architecture of the fiber orientation relative to a muscle’s line of action, for example, as found in [[Pennate_muscle|pennate muscles]].<ref>{{Cite journal
| last1 = Azizi | first1 = E.
| last1 = Azizi | first1 = E.
| last2 = Brainerd | first2 = E. L.
| last2 = Brainerd | first2 = E. L.
Line 78: Line 79:
| pmc =2234215
| pmc =2234215
| bibcode = 2008PNAS..105.1745A
| bibcode = 2008PNAS..105.1745A
| doi-access = free
}}</ref> The complexities of the different visco-elastic length- and velocity-force relationships of these subparts provides the opportunity for the adaptive selection of structurally complex muscle biocomposites with highly task-tuned nonlinear visco-elastic length- velocity- force relationships. This nature of muscles to be composite structures thus provides the adaptive opportunity for evolution to modify the visco-elastic reactions of the musculoskeletal system so they counteract perturbations without the need for spinal or higher levels of control.
}}</ref> The complexities of the different visco-elastic length- and velocity-force relationships of these subparts provides the opportunity for the adaptive selection of structurally complex muscle biocomposites with highly task-tuned nonlinear visco-elastic length- velocity- force relationships. This nature of muscles to be composite structures thus provides the adaptive opportunity for evolution to modify the visco-elastic reactions of the musculoskeletal system so they counteract perturbations without the need for spinal or higher levels of control.


Line 83: Line 85:
=== Leg step recovery ===
=== Leg step recovery ===


[[Helmeted guineafowl]] like many other [[bipedal]] birds [[walk]] upon rough ground. When a guineafowl's leg steps into a hole (a common disruption against which evolution has tuned the nonlinear visco-elastic properties of its musculoskeletal system), a momentarily uncommanded velocity and length change in the muscles that span its leg joints occurs. This length/velocity discrepancy interacts with the nonlinear length and velocity-force relationships that have evolved in response to such a disruption with the result that the leg extends further into the hole, and thus keeps the bird’s body stable and upright.<ref>{{Cite journal
[[Helmeted guineafowl]] like many other [[bipedal]] birds [[walk]] upon rough ground. When a guineafowl's leg steps into a hole (a common disruption against which evolution has tuned the nonlinear visco-elastic properties of its musculoskeletal system), a momentarily uncommanded velocity and length change in the muscles that span its leg joints occurs. This length/velocity discrepancy interacts with the nonlinear length and velocity-force relationships that have evolved in response to such a disruption with the result that the leg extends further into the hole, and thus keeps the bird's body stable and upright.<ref>{{Cite journal
| last1 = Daley | first1 = M. A.
| last1 = Daley | first1 = M. A.
| last2 = Biewener | first2 = A. A.
| last2 = Biewener | first2 = A. A.
Line 96: Line 98:
| pmc =1622881
| pmc =1622881
| bibcode = 2006PNAS..10315681D
| bibcode = 2006PNAS..10315681D
| doi-access = free
}}</ref>
}}</ref>


===Leg wiping ===
===Leg wiping ===


It is the intrinsic musculoskeletal properties of a [[Frog|frog’s]] leg, not neurally mediated spinal reflexes, that stabilize its wiping movements at irritants when the leg movement is instigated.<ref>{{Cite journal
It is the intrinsic musculoskeletal properties of a [[frog]]'s leg, not neurally mediated spinal reflexes, that stabilize its wiping movements at irritants when the leg movement is instigated.<ref>{{Cite journal
| last1 = Richardson | first1 = A. G.
| last1 = Richardson | first1 = A. G.
| last2 = Slotine | first2 = J. J.
| last2 = Slotine | first2 = J. J.
Line 113: Line 116:
| year = 2005
| year = 2005
| pmid = 15788775
| pmid = 15788775
| pmc =
| pmc = 6725085
| doi-access = free
}}</ref>
}}</ref>


Latest revision as of 10:11, 6 August 2024

Preflexes are the latent capacities in the musculoskeletal system that auto-stabilize movements through the use of the nonlinear visco-elastic properties of muscles when they contract.[1][2] The term "preflex" for such a zero-delay, intrinsic feedback loop was coined by Loeb.[3] Unlike stabilization methods using neurons, such as reflexes and higher brain control, a preflex happens with minimal time delay; however, it only stabilizes the main movements of the musculoskeletal system.[citation needed]

Visco-elastic correction

[edit]

Muscles possess nonlinear visco-elastic properties when they contract.[4][5][6] This property can autocorrect movements when a muscle is forced to change its length, and at a velocity different from that with which it was originally commanded. Such automatic correction is useful when a commanded action is perturbated, for example, if a step goes into a hole as this causes the foot to unexpectedly stretch down. The nonlinear visco-elastic properties of muscles interact with these perturbation induced velocity and length differences such that they counteract directly, as they happen, the effects upon the body of the perturbation. Part of the resistance to perturbation is passive, by means of the nonlinear increase in passive tension and joint torques produced by muscular and other soft tissues.[4] Tissue prestress is a preflexive property that constitutes a basal level of passive tension which, due to its presence in antagonistic tissues of a joint, increases joint passive stiffness and stability.[7]

Evolutionary opportunity

[edit]

Muscles contain many different systems on which the evolutionary selection of preflex stabilization can operate. The deltoid muscle, for example, consists of at least seven segments with different bone attachments and neural control.[8] Within each muscle segment, there exists a complex internal structure that goes down to one in which each muscle unit consists of a tendon, aponeurosis, and a fascicle of active contractile and passive elements.[4] Another source of variation is in the internal architecture of the fiber orientation relative to a muscle's line of action, for example, as found in pennate muscles.[9] The complexities of the different visco-elastic length- and velocity-force relationships of these subparts provides the opportunity for the adaptive selection of structurally complex muscle biocomposites with highly task-tuned nonlinear visco-elastic length- velocity- force relationships. This nature of muscles to be composite structures thus provides the adaptive opportunity for evolution to modify the visco-elastic reactions of the musculoskeletal system so they counteract perturbations without the need for spinal or higher levels of control.

Examples

[edit]

Leg step recovery

[edit]

Helmeted guineafowl like many other bipedal birds walk upon rough ground. When a guineafowl's leg steps into a hole (a common disruption against which evolution has tuned the nonlinear visco-elastic properties of its musculoskeletal system), a momentarily uncommanded velocity and length change in the muscles that span its leg joints occurs. This length/velocity discrepancy interacts with the nonlinear length and velocity-force relationships that have evolved in response to such a disruption with the result that the leg extends further into the hole, and thus keeps the bird's body stable and upright.[10]

Leg wiping

[edit]

It is the intrinsic musculoskeletal properties of a frog's leg, not neurally mediated spinal reflexes, that stabilize its wiping movements at irritants when the leg movement is instigated.[11]

Squat jumps

[edit]

A human example of a preflex stabilization occurs when a person explosively jumps up from a squat position, and the leg muscles act to provide a minimal time delay against perturbations from the vertical.[6]

References

[edit]
  1. ^ Blickhan, R.; Seyfarth, A.; Geyer, H.; Grimmer, S.; Wagner, H.; Gunther, M. (2007). "Intelligence by mechanics". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences. 365 (1850): 199–220. Bibcode:2007RSPTA.365..199B. doi:10.1098/rsta.2006.1911. PMID 17148057. S2CID 1141390.
  2. ^ Valero-Cuevas, F. J.; Yi, J. W.; Brown, D.; McNamara, R. V.; Paul, C.; Lipson, H. (2007). "The Tendon Network of the Fingers Performs Anatomical Computation at a Macroscopic Scale". IEEE Transactions on Biomedical Engineering. 54 (6): 1161–1166. CiteSeerX 10.1.1.419.1719. doi:10.1109/TBME.2006.889200. PMID 17549909. S2CID 1869716. PDF
  3. ^ Loeb, G. E. (1995). "Control implications of musculoskeletal mechanics". Proceedings of 17th International Conference of the Engineering in Medicine and Biology Society. Vol. 2. pp. 1393–1394. doi:10.1109/IEMBS.1995.579743. ISBN 978-0-7803-2475-6. S2CID 62579032.
  4. ^ a b c Brown IE, Loeb GE. (2000). "A reductionist approach to creating and using neuromusculoskeletal models". In JMC Winters, P.E. (ed.). Biomechanical and neurological control of posture and movements. New York: Springer. pp. 148–63. ISBN 978-0-471-50908-0.
  5. ^ Nishikawa, K.; Biewener, A. A.; Aerts, P.; Ahn, A. N.; Chiel, H. J.; Daley, M. A.; Daniel, T. L.; Full, R. J.; Hale, M. E.; Hedrick, T. L.; Lappin, A. K.; Nichols, T. R.; Quinn, R. D.; Satterlie, R. A.; Szymik, B. (2007). "Neuromechanics: An integrative approach for understanding motor control". Integrative and Comparative Biology. 47 (1): 16–54. doi:10.1093/icb/icm024. PMID 21672819.
  6. ^ a b Van Soest, A. J.; Bobbert, M. F. (1993). "The contribution of muscle properties in the control of explosive movements". Biological Cybernetics. 69 (3): 195–204. doi:10.1007/bf00198959. PMID 8373890. S2CID 16196068.
  7. ^ Souza, T.R.; Fonseca, S.T.; Gonçalves, G.G.; Ocarino, J.M.; Mancini, M.C. (2009). "Prestress revealed by passive co-tension at the ankle joint". Journal of Biomechanics. 42 (14): 2374–2380. doi:10.1016/j.jbiomech.2009.06.033. PMID 19647832.
  8. ^ Brown, J. M. M.; Wickham, J. B.; McAndrew, D. J.; Huang, X. -F. (2007). "Muscles within muscles: Coordination of 19 muscle segments within three shoulder muscles during isometric motor tasks". Journal of Electromyography and Kinesiology. 17 (1): 57–73. doi:10.1016/j.jelekin.2005.10.007. PMID 16458022.
  9. ^ Azizi, E.; Brainerd, E. L.; Roberts, T. J. (2008). "Variable gearing in pennate muscles". Proceedings of the National Academy of Sciences. 105 (5): 1745–1750. Bibcode:2008PNAS..105.1745A. doi:10.1073/pnas.0709212105. PMC 2234215. PMID 18230734.
  10. ^ Daley, M. A.; Biewener, A. A. (2006). "Running over rough terrain reveals limb control for intrinsic stability". Proceedings of the National Academy of Sciences. 103 (42): 15681–15686. Bibcode:2006PNAS..10315681D. doi:10.1073/pnas.0601473103. PMC 1622881. PMID 17032779.
  11. ^ Richardson, A. G.; Slotine, J. J.; Bizzi, E.; Tresch, M. C. (2005). "Intrinsic Musculoskeletal Properties Stabilize Wiping Movements in the Spinalized Frog". Journal of Neuroscience. 25 (12): 3181–3191. doi:10.1523/JNEUROSCI.4945-04.2005. PMC 6725085. PMID 15788775.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Preflexes&oldid=1238910876"