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Deep fascia

From Wikipedia, the free encyclopedia
Connective tissue around muscle groups
Deep fascia
Details
Identifiers
Latinfascia profunda
Anatomical terminology

Deep fascia (orinvesting fascia) is afascia, a layer ofdense connective tissue that can surround individualmuscles and groups of muscles to separate intofascial compartments.

This fibrous connective tissue interpenetrates and surrounds the muscles, bones, nerves, and blood vessels of the body. It provides connection and communication in the form ofaponeuroses,ligaments,tendons,retinacula,joint capsules, andsepta. The deep fasciae envelop all bone (periosteum andendosteum);cartilage (perichondrium), and blood vessels (tunica externa) and become specialized in muscles (epimysium,perimysium, andendomysium) and nerves (epineurium,perineurium, andendoneurium). The high density ofcollagen fibers gives the deep fascia its strength and integrity. The amount ofelastin fiber determines how muchextensibility and resilience it will have.[1]

Examples

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Examples include:

Fascial dynamics

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Deep fascia is less extensible thansuperficial fascia. It is essentiallyavascular,[2] but is richlyinnervated withsensory receptors that report the presence of pain (nociceptors); change in movement (proprioceptors); change in pressure and vibration (mechanoreceptors); change in the chemical milieu (chemoreceptors); and fluctuation in temperature (thermoreceptors).[3][4] Deep fascia is able to respond to sensory input by contracting; by relaxing; or by adding, reducing, or changing its composition through the process of fascial remodeling.[5]

Fascia may be able to contract due to the activity ofmyofibroblasts which may play a role in wound healing.[6]

The deep fascia can also relax. By monitoring changes in muscular tension, joint position, rate of movement, pressure, and vibration, mechanoreceptors in the deep fascia are capable of initiating relaxation. Deep fascia can relax rapidly in response to sudden muscular overload or rapid movements.Golgi tendon organs operate as a feedback mechanism by causing myofascial relaxation before muscle force becomes so great that tendons might be torn.Pacinian corpuscles sense changes in pressure and vibration to monitor the rate ofacceleration of movement. They will initiate a sudden relaxatory response if movement happens too fast.[7] Deep fascia can also relax slowly as some mechanoreceptors respond to changes over longer timescales. Unlike the Golgi tendon organs, Golgi receptors report joint position independent of muscle contraction. This helps the body to know where the bones are at any given moment.Ruffini endings respond to regular stretching and to slow sustained pressure. In addition to initiating fascial relaxation, they contribute to full-body relaxation by inhibiting sympathetic activity which slows down heart rate and respiration.[3][8]

When contraction persists, fascia will respond with the addition of new material. Fibroblasts secrete collagen and other proteins into theextracellular matrix where they bind to existing proteins, making the composition thicker and less extensible. Although this potentiates thetensile strength of the fascia, it can unfortunately restrict the very structures it aims to protect. The pathologies resulting from fascial restrictions range from a mild decrease in jointrange of motion to severe fascial binding of muscles, nerves and blood vessels, as incompartment syndrome of the leg. However, if fascial contraction can be interrupted long enough, a reverse form of fascial remodeling occurs. The fascia will normalize its composition and tone and the extra material that was generated by prolonged contraction will be ingested by macrophages within the extracellular matrix.[9]

Like mechanoreceptors, chemoreceptors in deep fascia also have the ability to promote fascial relaxation. We tend to think of relaxation as a good thing, however fascia needs to maintain some degree of tension. This is especially true of ligaments. To maintain joint integrity, they need to provide adequate tension between bony surfaces. If a ligament is too lax, injury becomes more likely. Certain chemicals, includinghormones, can influence the composition of the ligaments. An example of this is seen in themenstrual cycle, where hormones are secreted to create changes in theuterine andpelvic floor fascia. The hormones are not site-specific, however, and chemoreceptors in other ligaments of the body can be receptive to them as well. The ligaments of the knee may be one of the areas where this happens, as a significant association between theovulatory phase of the menstrual cycle and an increased likelihood for ananterior cruciate ligament injury has been demonstrated.[10][11]

Art

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The continuity of the deep fasciae within the human body inspired the artistic expression seen in theFascial Net Plastination Project, which is prominently displayed at theBody Worlds exhibition in Berlin.[12]

References

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  1. ^Hedley, Gil (2005).The Integral Anatomy Series Vol. 2: Deep Fascia and Muscle (DVD). Integral Anatomy Productions. Retrieved2006-07-17.
  2. ^Rolf, Ida P. (1989).Rolfing.Rochester, VT:Healing Arts Press. p. 38.ISBN 0892813350.
  3. ^abSchleip, Robert (2003). "Fascial plasticity – a new neurobiological explanation: Part 1".Journal of Bodywork and Movement Therapies.7 (1):11–9.doi:10.1016/S1360-8592(02)00067-0.
  4. ^Gatt, Adrianna; Agarwal, Sanjay; Zito, Patrick M. (2021)."Anatomy, Fascia Layers".StatPearls. StatPearls Publishing.
  5. ^Myers, Thomas W. (2002).Anatomy Trains. London, UK:Churchill Livingstone. p. 15.ISBN 0443063516.
  6. ^Tomasek, James J.; Gabbiani, Giulio; Hinz, Boris; Chaponnier, Christine; Brown, Robert A. (2002). "Myofibroblasts and mechano-regulation of connective tissue remodelling".Nature Reviews Molecular Cell Biology.3 (5):349–63.doi:10.1038/nrm809.PMID 11988769.
  7. ^Chaitow, Leon (1988).Soft Tissue Manipulation. Rochester, VT:Healing Arts Press. pp. 26–7.ISBN 0892812761.
  8. ^Schleip, Robert (2003). "Fascial plasticity – a new neurobiological explanation Part 2".Journal of Bodywork and Movement Therapies.7 (2):104–16.doi:10.1016/S1360-8592(02)00076-1.
  9. ^Paoletti, Serge (2006).The Fasciae: Anatomy, Dysfunction & Treatment. Seattle, WA: Eastland Press. pp. 138,147–9.ISBN 093961653X.
  10. ^Wojtys, E. M.; Huston, L. J.; Lindenfeld, T. N.; Hewett, T. E.; Greenfield, M. L. (1998). "Association between the menstrual cycle and anterior cruciate ligament injuries in female athletes".The American Journal of Sports Medicine.26 (5):614–9.doi:10.1177/03635465980260050301.PMID 9784805.
  11. ^Heitz, N. A.; Eisenman, P. A.; Beck, C. L.; Walker, J. A. (1999)."Hormonal changes throughout the menstrual cycle and increased anterior cruciate ligament laxity in females".Journal of Athletic Training.34 (2):144–9.PMC 1322903.PMID 16558557.
  12. ^"FR:EIA - Fascial Net Plastination Project".Body Worlds. Retrieved2024-08-26.
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