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Rigor mortis

From Wikipedia, the free encyclopedia
Fourth stage of death
This article is about the sign of death. For other uses, seeRigor mortis (disambiguation).

Look uprigor mortis in Wiktionary, the free dictionary.
Stages ofdeath
  1. Pallor mortis
  2. Livor mortis
  3. Algor mortis
  4. Rigor mortis
  5. Putrefaction
  6. Decomposition
  7. Skeletonization
  8. Fossilization

Rigor mortis[a] (from Latin rigor 'stiffness' and mortis 'of death'), orpostmortem rigidity, is the fourthstage of death. It is one of the recognizablesigns of death, characterized by stiffening of the limbs of thecorpse caused by chemical changes in themuscles postmortem (mainly calcium).[1] In humans, rigor mortis can occur as soon as four hours after death.

Physiology

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Corpses of victims of the1991 Bangladesh cyclone inSandwip displaying signs of rigor mortis

Afterdeath, aerobic respiration in an organism ceases, depleting the source of oxygen used in the making ofadenosine triphosphate (ATP). ATP is required to cause separation of theactin-myosincross-bridges during relaxation of muscle.[2] When oxygen is no longer present, the body may continue to produce ATP via anaerobicglycolysis. When the body'sglycogen is depleted, the ATP concentration diminishes, and the body enters rigor mortis because it is unable to break those bridges.[3][4]

Calcium enters thecytosol after death. Calcium is released into the cytosol due to the deterioration of thesarcoplasmic reticulum. Also, the breakdown of thesarcolemma causes additional calcium to enter the cytosol. The calcium activates the formation of actin-myosin cross-bridging. Once calcium is introduced into the cytosol, it binds to the troponin of thin filaments, which causes the troponin-tropomyosin complex to change shape and allow the myosin heads to bind to the active sites of actin proteins. In rigor mortis,myosin heads continue binding with the active sites of actin proteins viaadenosine diphosphate (ADP), and the muscle is unable to relax until further enzyme activity degrades the complex. Normal relaxation would occur by replacing ADP with ATP, which would destabilize the myosin-actin bond and break the cross-bridge. However, as ATP is absent, there must be a breakdown of muscletissue byenzymes (endogenous or bacterial) duringdecomposition. As part of the process of decomposition, the myosin heads are degraded by the enzymes, allowing the muscle contraction to release and the body to relax.[5]

Decomposition of the myofilaments occurs between 48 and 60 hours after the peak of rigor mortis, which occurs approximately 13 hours after death.[1]

Nysten's rule

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Nysten's rule, first proposed in 1811, describes the sequential onset of rigor mortis in the variousmuscle groups. The basic sequence of the solidifying body begins from the head down the body, in the order:[6]

  • Involuntary muscle first: Heart
  • Upper eyelids
  • Neck
  • Jaw
  • Face
  • Upper extremities
  • Muscles of the trunk
  • Lower extremities

The rule does not occur in all cases.[7] It owes its name to the FrenchpediatricianPierre-Hubert Nysten (1771–1818).

Application in forensic pathology

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Timeline of postmortem changes (stages of death).

The degree of rigor mortis may be used inforensic pathology to determine the approximate time of death. A dead body holds its position as rigor mortis sets in. If the body is moved after death, but before rigor mortis begins, forensic techniques such aslivor mortis can be applied. Rigor mortis is known astransient evidence, as the degree to which it affects a body degrades over time.

Applications in meat industry

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Rigor mortis is very important in themeat industry. The onset of rigor mortis and its resolution partially determines the tenderness ofmeat. If the post-slaughter meat is immediately chilled to 15 °C (59 °F), a phenomenon known as cold shortening occurs, whereby the muscle sarcomeres shrink to a third of their original length.

Cold shortening is caused by the release of storedcalcium ions from thesarcoplasmic reticulum of muscle fibers, in response to the cold stimulus. The calcium ions trigger powerful muscle contraction aided by ATP molecules. To prevent cold shortening, a process known as electrical stimulation is carried out, especially in beef carcasses, immediately afterslaughter andskinning. In this process, thecarcass is stimulated withalternating current, causing it to contract and relax, which depletes the ATP reserve from the carcass and prevents cold shortening.[8]

See also

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Notes

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  1. ^AlthoughBritish English uses the spellingrigour, this is not used inrigor mortis because the phrase is in Latin.

References

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  1. ^abSaladin, K. S. 2010.Anatomy & Physiology: 6th edition. McGraw-Hill.
  2. ^Hall, John E., and Arthur C. Guyton. Guyton and Hall Textbook of Medical Physiology. Philadelphia, PA: Saunders/Elsevier, 2011. MD Consult. Web. 26 January 2015.
  3. ^Fremery, Donald (3 February 1959). "Biochemistry of Chicken Muscle as Related to rigor mortis and Tenderization".Journal of Food Science.25 (1):73–87.doi:10.1111/j.1365-2621.1960.tb17938.x.
  4. ^"Classroom Resources - Argonne National Laboratory". Archived fromthe original on 26 February 2015. Retrieved22 February 2009.
  5. ^"About.com (archived)".[dead link]
  6. ^Hall, Carl W. (28 September 1999).Laws and Models: Science, Engineering, and Technology. CRC Press.ISBN 9781420050547.
  7. ^Madea/ Dettmeyer Basiswissen Rechtsmedizin, Springerverlag 2007, S. 73
  8. ^The Royal Society of New Zealand (1976).New Zealand Journal of Agricultural Research. The Royal Society of New Zealand. p. 13.

Bibliography

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In medicine
Cell death
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Mortality
After death
Body
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Preservation
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