Week 5 Flashcards
What are the determinants of gait
- Pelvic drop - using hip abductors
- Pelvic rotation
- Knee flexion - reduces inertial change
- Ankle joint and foot
- Lateral displacement of body
Gluteus maximus deficit
i. Paralyzed non-functional extensors of the hip
ii. People will walk leaning back
iii. Can accompany paralyzed abductors
1. Lurch-tilt walk
Antalgic gait
i. Occurs with a painful hip or paralysis of abductor mm., primarily gluteus medius m.
ii. Determine competency by Trendelenburg test
iii. We normally walk with a positive Trendelenburg!
Quadriceps deficit
cannot extend knee so they put out a straight leg and “vault” over
Anterior leg deficit (foot drop)
cannot dorsiflex which results in “foot drop” so they walk with a high step to clear foot
-damage to common fibular n.
What anchors actin cytoskeleton to sarcolemma
Dystrophin
Subneural clefts at the NMJ
-Crests vs troughs
Crests - Ach gated channels
Trough - Voltage gated Na+ channels
Dantrolene MoA
blocks RyR1 (ryanodine-1 receptor) -calcium release channel
DHP-ryanodine receptor interaction
-where are each located
DHP -> on T-tubule
Ryanodine -> on terminal cisternae of sarcoplasmic reticulum
2 ways for calcium release in to sarcoplasm
- mechanical couple of DHP-Ryanodine receptors (MAJOR)
- activation of ryanodine receptor by release of Ca++ from DHP receptors (nor required in skeletal muscle)
Components of thin and thick filaments
THIN FILAMENTS
- actin
- tropomyosin
- troponin
THICK
-myosin
Role of calsequestrin
Binds Ca++ in the SR to prevent buildup
Role of ATP in muscle contraction
- causes dissociation of myosin head from actin
- hydrolyzes to place myosin head back into cocked state
What cause the power-stroke
release of phosphate from myosin head
Type 1 vs Type II fibers
Type 1
- slow twitch
- lots of mitochondria
- low glycogen content
Type IIa+b
- fast twitch
- low mitochondria
- high glycogen content
Stains for muscles fibers
- Trichome
- Succinate DH
- ATPase at pH 4.6
- ATPase at pH 10
- Mitochondria and myelin
- Complex 2 of respiratory chain
- Type I is darkest IIa is the lightest
- Type I is light and Type II is dark
Only muscular dystrophy to show inflammation
Fascioscapulohumeral MD
Which muscular dystrophy has high incidence of cardiomyopathy
Becker’s
Duchenne:
Age of onset
Presentation
Labs
- 2-5 y/o
- Pelvic girdle weakness and calf pseudohypertrophy due to fat infiltration and fibrosis
- Highly elevated CPK
Which inflammatory myopathy is associated with perifascicular atrophy?
Dermatomyositis
What are the inclusions seen with Inclusion Body Myositis
Which inflammatory cells?
basophilic inclusions containing beta amyloid and phosphorylated tau protein
T cells and macrophages in endomysium and perimysium
Onset Peaks for inflammatory myopathies
- 5-14 y/o
2. 50s - specially inclusion body myositis
2 skin findings associated w/ dermatomyositis
- Grotten lesions - scaling erythematous eruption or patches over knuckles, elbows and knees
- Heliotrope discoloration of eyelids
Compare inflammations b/w
- Dermatomyositis
- Polymyositis
- Dermatomyositis
- Skin, muscle, GI
- risk of GI ulceration and bleeding - Polymyositis
- no skin lesions
- inflammation in heart, lungs and blood vessels
BOTH STAIN POSITIVE FOR MHC-1
Which muscles are affected w/ inclusions body myositis
distal muscles (extensors of knee and flexors of wrist and fingers)