PathophysiologyMuscle disorders Flashcards

1
Q

what is tying up disease also known as

A

rhabdomyolysis

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2
Q

name a acquired exertional muscle disease

A

tying up disease - rhabdomyolysis

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3
Q

what is the most common muscular disorder in horses

A

Rhabdomyolysis

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4
Q

List 7 clinical signs of rhabdomyolysis

A

stiff, stilted gait
excessive sweating
increased resp rate after exercise
firm painful muscles
reluctant to move forward
occasional dark urine

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5
Q

why do horses with rhabdomyolysis get dark urine

A

breakdown of myoglobin

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6
Q

List 3 things that can cause rhabdomyolysis

A

overexertion
dietary imbalances
exhaustion

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7
Q

describe how overexertion leads to rhabdomyolysis

A

increase in work intensity without a strong musculoskeletal foundation
Z-disk instability—> overstretching of myofibers—> sarcolemma stretching

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8
Q

Describe how dietary imbalances can lead to rhabdomyolysis

A

Electrolytes (Na and Ca) both important in neural transmission and muscle contraction
Low Vitamin E intake: Poor antioxidant state

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9
Q

Describe how exhaustion can lead to rhabdomyolysis

A

TB and endurance horses training in hot, humid weather : electrolytes loss in sweat and dehydration

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10
Q

why does recurrent exertional rhabdomyolysis occur

A

Intermittent form of rhabdomyolysis in horses likely linked to abnormal calcium regulation in myofibers

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11
Q

List 4 risk factors of recurrent exertional rhabdomyolysis

A

fit horses with nervous temperament
Young mares more at risk, but no associated with oestrus cycle
Lack of turnout
Held back during gallop

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12
Q

what is PSSM-1

A

polysaccharide storage myopathy
genetic mutation means that glycogen synthase enzyme is constantly turned on -unable to adequately breakdown glycogen as it is stored wrong

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13
Q

which horses is PSSM-1 seen

A

most seen in continental European draft brees
very rare in light breeds- unlikely in TB

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14
Q

List the possible risk factors of PSSM-1

A

Breed
exercise of more than 20min in one session

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15
Q

what is the difference between PSSM-1 and PSSM-2

A

PSSM-1 - genetic
PSSM-2- unknown cause- Myofibrillar myopathy: oxidative deficit????

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16
Q

Descrieb how PSSM-1 presents

A

most draft horses aymptomatic
stiffness after a short period of exercise –> reluctance to move forward, poor performance, sweating (most severe sign= myoglobinuria)

17
Q

what is the mean age for diagnosis of PSSM-1

A

4-8 years

18
Q

what is myofibrillar myopathy

A

a type of PSSM-2 that has an abnormal desmin protein and there fore the muscles don’t contract normally

19
Q

List 6 plants that can cause non-exertional muscle damage

A

sycamore
cassia spp
box elder
Malva parviflora
eppatorium spp
Haplopparpus spp

20
Q

What is equine atypical myopathy

A

toxic rhabdomyolysis associated with Hypoglycin A ingestion(sycamore seeds)

21
Q

What are the clinical signs of equine atypical myopathy

A

stiffness
muscle fasciculations
weakness
sweating
myoglobinuria
colic
reduced/ absent GI sounds

22
Q

what is the prognosis of equine atypical myopathy

A

Bad - high mortality rates (68%)

23
Q

what is immune-mediated muscle damage normally associated with

A

previous resp infection

24
Q

Describe how we can confirm sporadic rhabdomyolysis

A

clinical signs and elevated muscle enzymes

25
Q

what type of muscle disease is PSSM

A

exertional - genetic

26
Q

List 2 breeds that get HYPP (hyperkalemic periodic paralysis)

A

quarter horses and QH derived breeds

27
Q

Describe how HYPP occurs

A

sodium channels leak and cause prolonged depolarisation and abnormal action potentials

small increases in potassium cause depolarisations

28
Q

List the clinical signs of HYPP

A

sporadic attacks of stiffness
muscle tremors
weakness and collapse
breathing difficulties
prolapsed third eyelids

29
Q

what contains Hypoglycin A that horses might eat

A

sycamore seeds

30
Q

Describe how does hypoglycin A cause disease

A

hypoglycin A gets metabolised in the liver and in muscles, it then acts in the myofibres to stop fatty acid oxidation

31
Q

what bacteria commonly cause myonecrosis

A

clostridium perfringes

clostridium septicum sometimes

32
Q

what usually is the inciting cause of myonecrosis

A

IM injections (usually biological products) or puncture wounds

33
Q

how soon after injections does myonecrosis occur

A

6-72 hours

34
Q

List the clinical signs of myonecrosis

A

fever
stiffness
severe pain
gangrene
crepitation

35
Q

Describe how do we treat myonecrosis

A

remove all necrotic tissue and allow secondary intention healing

antibiotics - high dose penicillin or metronidazole

analgesia - flunixin or phenylbutazone