Muscles 1 Flashcards

(59 cards)

1
Q

composed of actin and mysoin filaments

A

myofibrils

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2
Q

calcium ion storage

A

sarcoplasmic reticulum

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3
Q

thin undifferentiated cells that have the ability to undergo mitosis – muscle regeneration

A

satellite cells

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4
Q

skeletal muscle response to injury

A

degeneration

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5
Q

pale due to sublethal muscle fiber damage and edema or dark due to extensive myofiber damage

A

degenerative muscle reponse

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6
Q

skeletal muscle necrosis

A

rhabdomyolysis

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7
Q

more pale than normal and mildly to moderately swollen

A

early necrotic muscle

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8
Q

result of replacement of necrotic muscle

A

smaller and firmer muscle

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9
Q

muscle fiber hyper-contraction
muscle fiber swelling
hypereosinophilia

A

microscopic early necrotic muscle lesions

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10
Q

responsible for driving muscle fiber regeneration

A

satellite cells

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11
Q

if basal lamina of a damaged myofiber is left intact…

A

satellite cells with activate forming myoblasts along the endomysium to regenerate

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12
Q

if endomysioum does not survive…

A

muscle regeneration will be inhibited and muscle will be replaced by fibrous tissue leading to scarring and reduced muscle function

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13
Q

ischemic myopathy

A

compartment syndrome
deep pectoral myopathy of poultry

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14
Q

muscle degeneration and necrosis secondary to insufficient blood flow caused by muscle swelling in non-expandable space

A

compartment syndrome

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15
Q

cause of compartment syndrome

A

tissue swelling within the compartment leads to increased compartmental pressure and increased resistance to flow of blood into space

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16
Q

green muscle disease of turkeys and chickens caused by vigorous flapping of wings leading to compartment syndrome in the supracoracoid muscles

A

deep pectory myopathy in poultry

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17
Q

nutritional myopathy in calves

A

white muscle disease

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18
Q

nutritional myopathy in sheep

A

stiff lamb disease

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19
Q

nutritional myopathy in pigs

A

mulberry heart disease

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20
Q

muscle damage secondary to a deficiency of free radical scavengers (vitamin E and selenium)

A

nutritional myopathy

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21
Q

reason for muscle susceptibility to nutritional myopathy

A

high oxygen requirements and contractile activity of striated cardiac muscle

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22
Q

species most susceptible to ionophore toxicity

A

horses

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23
Q

most toxic ionophore

A

monensin

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24
Q

location of ionophore toxicity in horses

25
location of ionophore toxicity in sheep and pigs
skeletal muscle
26
location of ionophore toxicity in cattle
skeletal cardiac
27
classic clinical sign of ionophore muscle toxicity
myoglobinuria
28
caused by anthraqinones and their derivatives or various plant glycosides and alkaloids
cassia toxicosis
29
CS of cassia toxicosis
diarrhea muscle weakness reluctance to walk myoglobinuria recumbency
30
massive muscle necrosis in wild and zoo animals can be observed secondary to extreme muscle exertion
capture myopathy
31
pathophys of captive myopathy
stress = muscle exertion to exhaustion and elevated catecholamines hyperthermia and metabolic acidosis
32
types of exertional rhabdomyolysis
sporadic exertional rhabdomyolysis chronic exertional rhabdomyolysis
33
CS of sporadic exertional rhabdomyolysis
azoturia paralytic myoglobinuria monday-morning sickness black water and tying up
34
triggering of sporadic exertional rhabdomyolysis
week of hard work followed by weekend stall rest with high grain feed
35
physical CS signs of sporadic exertional rhabdomyolysis
swollen, edematous affected muscles dark red-brown uring **renal failure, profuse sweating, acidosis, muscle weakness
36
categories of chronic exertional rhabdomyolysis
recurrent exertional rhabdomyolysis polysaccharide storage myopathy (PSSM)
37
breeds affected by RER
thoroughbreds standardbreds
38
trigger of RER
acutely by exercise resulting in sharp spikes in serum myoglobin and creatine kinase excitement
39
cause of PSSM
mutation in glycogen synthase 1 gene
40
process of glycogen synthase 1 gene mutation
enhances synthesis and storage of amylase-resistant glycogen disrupt normal metabolism of the glycogen
41
sequelae of Type 1 PSSM
abnormal accumulation of intracytoplasmic glycogen within Type 2 myofibers
42
abnormal appearing amylase-sensitive or amylase-resistant polysaccharide in muscle biopsies of horses lacking the GYS1 mutation
PSSM type 2
43
CS of chronic exertional rhabdomyolysis
exhibit stiff gait, bilaterally symmetrical muscle atrophy, muscle cramping and pain, shivers and generalized weakness
44
affected animals found dead observed sick are lame, run a fever, have swollen muscle and gas in muscle and subQ tissue
C. chauvoei blackleg
45
cause of death in blackleg
cardiovascular collapse and shock due to exotoxemia
46
seen at necropsy of black leg
hemorrhagic and gas-filled muscles hemorrhagic rhabdomyolysis
47
suppurative myositis in cattle
trueperella
48
suppurative mysositis in horses
streptococcus
49
suppurative myositis in small animals
staph and strep
50
young dog fever/anorexia general body pain gait abnormalities respiratory signs xray shows irregular periosteal proliferations *marked leukocytosis and increased CK
Hepatozoon americanum
51
an inherited progressive myopathies characterized histologically by ongoing muscle fiber necrosis and regeneration
muscular dystrophy
52
pathophys of muscular dystrophy
defects in sarcolemmal-associated proteins such as dystrophin
53
sequelae of defects and/or deficiencies in dystrophin
progressive muscle damage and myofiber necrosis leads to muscle atrophy and fibrosis
54
inherited myotonia
HYPP
55
pathophys of HYPP
defective sodium channel activity increasing myofiber excitability increasing potassium outflow from cells (hyperkalemia)
56
initial signs of HYPP
sweating muscle fasciculations flashing of third eye lid muscle spasm inspiratory difficulty
57
pathophys of myasthenia gravis
autoantibodies bind to acetylcholine receptors causing receptor cross-linking and internalization leading to damage to neuromuscular junctions and severe decreases in number of acetylcholine receptors
58
what has a strong association with myasthenia gravis
thymoma
59