Squid giant axon

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The squid giant axon is the very large (up to 1 mm in diameter; typically around 0.5 mm) axon that controls part of the water jet propulsion system in squid. It was first described by L. W. Williams[1] in 1909,[2][page needed] but this discovery was forgotten until English zoologist and neurophysiologist J. Z. Young demonstrated the axon's function in the 1930s while working in the Stazione Zoologica in Naples, the Marine Biological Association in Plymouth and the Marine Biological Laboratory in Woods Hole.[3][4] Squids use this system primarily for making brief but very fast movements through the water.

Between the tentacles of a squid is a siphon through which water can be rapidly expelled by the fast contractions of the body wall muscles of the animal. This contraction is initiated by action potentials in the giant axon. Action potentials travel faster in a larger axon than a smaller one,[5][page needed] and squid have evolved the giant axon to improve the speed of their escape response. The increased diameter of the squid axon decreases the internal resistance of the axon, as resistance is inversely proportional to the cross sectional area of the object. This increases the space constant (), leading to faster local depolarization and a faster action potential ().[6][page needed]

In their Nobel Prize-winning work uncovering ionic mechanism of action potentials, Alan Hodgkin and Andrew Huxley performed experiments on the squid giant axon, using the longfin inshore squid as the model organism. The prize was shared with John Eccles. The large diameter of the axon provided a great experimental advantage for Hodgkin and Huxley as it allowed them to insert voltage clamp electrodes inside the lumen of the axon.

While the squid axon is very large in diameter it is unmyelinated which decreases the conduction velocity substantially. The conduction velocity of a typical 0.5 mm squid axon is about 25 m/s. During a typical action potential in the cuttlefish Sepia giant axon, an influx of 3.7 pmol/cm2 (picomoles per centimeter2) of sodium is offset by a subsequent efflux of 4.3 pmol/cm2 of potassium.[7]

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References[edit]

  1. ^ Kingsley, J. S. (1913). "Obituary. Leonard Worcester Williams". The Anatomical Record. 7: 33–38. doi:10.1002/ar.1090070202. 
  2. ^ Williams, Leonard Worcester (1909). Anatomy of the Common Squid: Loligo pealii, Lesueur. Leiden, Holland: Library and Printing-office late E.J. Brill. OCLC 697639284 – via Internet Archive. 
  3. ^ Young, J.Z. (April 1938). "The Functioning of the Giant Nerve Fibres of the Squid". Journal of Experimental Biology. 15 (2): 170–185 – via The Company of Biologists Ltd. 
  4. ^ Young, J.Z. (June 1985). "Cephalopods and Neuroscience"Paid subscription required. Biological Bulletin. 168 (3S): 153–158. doi:10.2307/1541328 – via University of Chicago Press. 
  5. ^ Gazzaniga, Michael S.; Ivry, Richard B.; Mangun, George R. (1998). Cognitive Neuroscience: The biology of mind. New York: W.W. Norton. ISBN 978-0-393-97219-1. OCLC 301607967. 
  6. ^ Koeppen, Bruce M.; Stanton, Bruce A.; Berne, Robert M. (2010). Berne & Levy Principles of Physiology (Updated ed.). St. Louis, MO: Elsevier Mosby. ISBN 978-0-323-07362-2. OCLC 495598608. 
  7. ^ Plonsey, Robert; Barr, Roger C. (2007). Bioelectricity: A Quantitative Approach (3rd ed.). New York, NY: Springer. p. 109. ISBN 978-0-387-48864-6.