Line 31: |
Line 31: |
| | | |
| | | |
− | ===Regeneration===
| |
− | [[Image:Muscle regeneration.jpg|right|thumb|100px|<small><center>Muscle regeneration (Image sourced from Bristol Biomed Image Archive with permission)</center></small>]]
| |
− |
| |
− | *Skeletal muscle myofibres have substantial regenerative ability
| |
− | *Success depends on:
| |
− | **An intact '''sarcolemmal tube''' - to act as a support and guide
| |
− | **Availability of '''satellite cells''' - to act as progenitor cells for new sarcoplasm production
| |
− | **Macrophages to clear up cell debris
| |
− | **If these conditions are not met (e.g. severe thermal damage) '''fibrosis''' will occur
| |
− | *Stages:
| |
− | #Nuclei in [[Muscles - degenerative#Necrosis|necrotic segement]] disappear, hyalinased sarcoplasm due to loss of normal myofibrillar structure, may separate from adjacent normal myofibrils and/or [[Muscles - degenerative#Calcification|mineralise]]
| |
− | #Monocytes from capillaries -> macrophages in necrotic portion, satellite cells swell -> vesicular with prominent nucleoli -> mitosis (within 1-4 days after initial injury)
| |
− | #Satellite cells move to centre
| |
− | #Macrophages clear the sacrolemmal tube, plasmalemma disappears, shape maintained by basal lamina
| |
− | #Satellite cells -> myoblasts (contain myosin) -> fuse forming myotubes with row of central nuclei; cytoplasmic processes fusing
| |
− | #Growing and differentiating fibre, striations appear - formation of sarcomeres
| |
− | #Nuclei move to peripheral position (2-3 weeks after initial injury)
| |
− | *Regeneration by '''budding'''
| |
− | **When conditions are not optimal, disrupted sacrolemma
| |
− | **E.g. injection of irritating substance, trauma, [[Muscles - degenerative#Ischaemia|infarction]]
| |
− | **Myoblasts proliferate -> sacrolamma bulges from cut part -> club-shaped with numerous central nuclei = muscle giant cells
| |
− | *Monophasic lesions - all at same phase above
| |
− | **Damage occured at one time, e.g. trauma or one toxin exposure
| |
− | *Multiphasic lesions - different stages as described above
| |
− | **Ongoing damage, e.g. vitamin E - selenium deficiency, continuous exposure to toxin
| |
| | | |
| | | |