Skeletal muscle Flashcards

1
Q

Cause of denervation atrophy

A

caused by lost connection to peripheral nerves

- unaffected motor neuron has compensatory hypertrophy

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2
Q

Type 1 muscle fiber v. type 2

A

type 1- slow (marathon runner)

Type 2- fast twitch (sprinter)

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3
Q

Cause of disuse atrophy

A

decreased contractile activity of innervated muscles causing a uniform atrophy (ex. painful lameness, fx, bone disease)

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4
Q

Cause atrophy from malnutrition/cachexia

A

caused by inability to support dietary nutrition to maintain muscle mass~ causes generalized atrophy
- cachexia is associated with neoplasia & chronic illness

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5
Q

Cause atrophy of endocrine disease

A

associated with hypothyroidism & hyperglucocorticoidism

i. Primarily selective type 2 atrophy with no compensatory type 1 hypertrophy

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6
Q

myopathic atrophy

A

muscle atrophy after primary muscle disease (ex. inflammatory muscle disease)

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7
Q

4 different patterns of myofiber necrosis

A

Focal monophasic rxn- infarct
Multifocal monophasic rxn- toxin
Focal polyphasic rxn- repeat injury/same site
Multifocal polyphasic rxn- nutritional myopathies

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8
Q

What gene is responsible for “double muscling”

A

defective myostatin gene affecting cattle, dogs & sheep

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9
Q

What is muscular dystrophy?

A

X-linked recessive disorder caused by defects in the gene encoding dystrophin.

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10
Q

hyperkalemic periodic paralysis (HYPP) disease mechanism

A

ion channel defect affecting sodium channel (muscle) that alters muscle membrane potential.

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11
Q

HYPP clinical signs

A

muscle fasciculations (spams), 3rd eyelid flashing, collapse

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12
Q

Best way to confirm HYPP

A

DNA testing

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13
Q

What breeds are predisposed to polysaccharide storage myopathy

A

draft horses, warmbloods & quarter horses

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14
Q

CS of PSM

A

recurrent exertional rhabdomyolysis–> progressive weakness

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15
Q

What gene is associated with the PSM?

A

mutated GYS1

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16
Q

Mechanism of congenital myasthenia gravis

A

inherited defect in acetylcholine end plate receptor (autosomal recessive in dogs)

17
Q

Mechanism of acquired myasthenia gravis

A

circulating antibodies to motor end plate acetylcholine receptors bind & form immune complexes at NM junction

18
Q

What is the diagnostic method for myasthenia gravis?

A

Electrodiagnostic testing, positive response to anti-cholinesterase therapy & detection of circulating anti-acetylcholine receptor antibodies.

19
Q

Malignant hyperthermia mechanism

A

defective ryanodine receptor causes a calcium release from sarcoplasmic reticulum.

20
Q

MH pathogenesis

A

prolonged myofiber contraction & muscle rigidity –> tachycardia, metabolic acidosis & hyperthermia (life threatening)

21
Q

domestic animal species affected by malignant hyperthermia

A

humans, pigs, horses & dogs

22
Q

Splayleg (condition with corresponding lesion)

A

congenital muscle condition of piglets and corresponding histopathologic lesion is myofibrillar hypoplasia.

23
Q

Compartment pathogenesis

A

increase muscle contraction causes increased muscle diameter & pressure

  • -> venous outflow collapse, continuous arterial blood supply that causes muscle metabolite accumulation and increases interstitial water
  • -> exacerbates intramuscular pressure & blood flow stops causing ischemic necrosis of muscle (worsens in 1-4 hr.)
24
Q

Compartment disease example

A

pectoral muscles in turkeys and chickens

25
Q

Nutritional myopathy- gross changes

A

muscle pallor, pale streaking affecting weight bearing muscles (though, shoulder, intercostal muscles, diaphragm & tongue)

26
Q

What type of histologic change occurs with nutritional myopathy?

A

polyphasic myofiber necrosis

27
Q

What is an underlying cause of equine exertional rhabdomyolysis?

A

equine polysaccharide storage myopathy

28
Q

What are potential effects of widespread rhabdomyolysis on the kidney?

A

myoglobininuric nephrosis & renal failure

29
Q

Ionophore effect on muscle

A

acute monophasic myofiber necrosis (affect skeletal & cardiac m.), once cardiac muscle is damaged it is replaced with fibrosis

30
Q

Senna spp. effect on muscle

A

acute monophasic myofiber necrosis (skeletal muscle)

31
Q

Gossypol effect on muscle

A

acute segmental myofiber necrosis ( skeletal & myocardium) + hepatotoxic

32
Q

What are different types of immune-meditated myositis in dogs?

A

Masticatory myositis
Polymyositis
Bilateral extra-ocular muscle myositis

33
Q

How do you diagnose immune mediated myositis in dogs?

A

distribution of affected muscles
histopathology
detection of serum type 2M antibodies (masticatory myositis)

34
Q

What are different bacterial agents of clostridial myositis?

A

a. Blackleg: C. chauvoei
b. Malignant edema: C. speticum
c. Gas gangrene: C. perfringes
d. Swelled head (sheep): C. novyi

35
Q

Gross changes observed with black leg?

A

i. Muscle is dark red/black, emphysematous & smell like rancid butter
ii. Fibrinous/ fibrohemorrhagic pleuritis & pericarditis

36
Q

What is the best diagnostic method for detecting black leg?

A

fluorescent antibody testing (hard to culture)

37
Q

What is a benign tumor of striated myofiber?

A

rhabdomyoma

38
Q

What is malignant neoplasm of myofiber?

A

Rhabdomyosarcoma

39
Q

List 5 primary muscle tumors of non- muscle origin

A

soft tissue sarcomas, HAS, LSA, granular cell tumor & infiltrative lipoma