Muscle Physiology Flashcards

1
Q

Tissue covering of EACH muscle tissue

A

Epimysium

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2
Q

Cover many fascicle of muscle tissue

A

Perimysium

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3
Q

Surround each muscle fiber

A

Endomysium

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4
Q

Smallest anatomic unit capable of contraction

A

Muscle fiber

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5
Q

Thin threadlike substances with light and dark bands of striation

A

Myofibrils

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6
Q

2 types of myofibrils

A

Actin and myosin

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7
Q

Structural functional subunit between 2 adjacent Z lines

A

Sarcomere

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8
Q

Boudaries of sarcomere where actin is inserted

A

Z disk

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9
Q

Proteins bounde to actin and myosin

A

Troponin/tropomyosin

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10
Q

Interconnect sarcolemmal membrane and sarcoplasmic reticulum

A

Transverse tubules

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11
Q

What give the skeletal muscle its striated appearance

A

Overlapping of actin and myosin

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12
Q

Center of sarcomere which contain MYOSIN

A

A band

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13
Q

Contains ACTIN only. Transected by Z disk

A

I band

I- thin “acthin”

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14
Q

Center of sarcomere which contain myosin and DOES NOT OVERLAP

A

H zone

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15
Q

Center of H zone

A

M line

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16
Q

Muscle fiber with Deep red, higher myoglobin content

A

Slow muscle fibers

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17
Q

Muscle fiber with whitish hue

A

Fast muscle fibers

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18
Q

Consist of small specialized muscle fibers encapsulated by connective tissue

A

Muscle spindles

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19
Q

2 types of muscle spindle

A

Nuclear bag

Nuclear chain

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20
Q

2 types of innervation of muscle spindle

A

Primary sensory- annulospiral

Secondary sensory- flower spray

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21
Q

Absence of ATP in muscles will result in

A

Rigor mortis

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22
Q

What is important in the detachment phase of skeletal muscle RELAXATION

A

ATP

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23
Q

What accumulates during rigor mortis?

A

Phosphoric acid

Lactic acid

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24
Q

MC form of progressive motor neuron disease

A

ALS

aka Lou Gehrig disease

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25
Rapidly progressive fatal neurologic disease that attack the nerve cells responsible for controlling voluntary muscle
ALS
26
Gene mutation in ALS
Superoxide dismutase gene Result to ROS damage
27
What neurotransmitter in increased in ALS?
Glutamate--- lead to increased excitation--- death of neuron
28
Gene that regulates glutamate release
SOD-1
29
Part of spinal cord affected in ALS
Anterior horn cells-- both UMN and LMN symptoms
30
Telltale sign of ALS
Atrophy of tongue
31
Small intracytoplasmic eosinophilic inclusions seen in LMN of pt with ALS
Bunina bodies
32
Drug that increase survival of pt with ALS
Riluzole
33
Median survival of ALS
3-5 years
34
Type of contraction where there is change in muscle length
Isotonic muscle contraction | Ex: biceps curls
35
Type of contraction where there is NO change in muscle length,and only EXERT TENSION
Isometric muscle contraction
36
Electrical stimulation of myocytes above the threshold potential results in a limited efflux of calcium from SER stimulating a SINGLE CONTRACTION
Twitch
37
Occurs if muscle is stimulated high enough, and individual muscles twitches combine to produce SUSTAINED contraction
Summation and tetany
38
Type of muscle contraction/training where there js an increase in NUMBER OF MYOFILAMENT leading to INCREASED MUSCLE MASS
Strength training
39
Type of muscle contraction/training where there js an increase in NUMBER OF BLOOD VESSELS and MITOCHONDRIA, NO increase in muscle mass
Endurance training
40
A single alpha neuron plus all the corresponding muscle fibers it innervates
Motor unit
41
Most common disease that affect the motor unit
ALS
42
Characteristics of smooth muscle
Non striated No t tubule Spindle shaped (+) dense bodies--- analogous to z disk
43
Predominant type of smooth muscle
Single unit/ unitary/visceral smooth muscle
44
Type of smooth muscle in which each fiber function separately
Multiunit
45
Single unit or multiunit | Found in GIT,bladder,ureter
Single unit
46
Single unit or multiunit: | Function as syncytium
Single unit
47
Single unit or multiunit: | (+) gap junctions
Single unit
48
Single unit or multiunit: | (+) pacemaker activity
Single unit
49
Single unit or multiunit: | Primary regulator is slow waves
Single unit
50
Single unit or multiunit: | Found in iris,ciliary muscle, arrector pili, vas deferens
Multiunit
51
Single unit or multiunit: | Each fiber function separately
Multiunit
52
Single unit or multiunit: No gap junction No pacemaker
Multiunit
53
Single unit or multiunit: | Regulated by ANS
Multiunit
54
Slow twitch/fast twich: | Red muscle due to high myoglobin content
Slow | Slow red ox
55
Slow twitch/fast twich: | Primarily aerobic
Slow
56
Slow twitch/fast twich: | More mitochondria
Slow
57
Slow twitch/fast twich: | Function is to provide endurance
Slow
58
Slow twitch/fast twich: More capillary supply Highly sensitive to hypoxia High resistance to fatigue
Slow twitch
59
Slow twitch/fast twich: | Soleus muscle
Slow
60
Slow twitch/fast twich: | Source of energy is oxidative system
Slow | Slow red ox
61
Slow twitch/fast twich: | White muscle
Fast
62
Slow twitch/fast twich: | Example is stapedius m
Fast
63
Slow twitch/fast twich: | Primarily anaerobic
Fast
64
Slow twitch/fast twich: | Deliver power surge for few seconds or minutes
Fast
65
Slow twitch/fast twich: | Source of energy is phosphagen/glycolytic system
Fast twitch
66
Skeletal/cardiac/smooth muscle: | Striated
cardiac and skeletal muscle
67
Skeletal/cardiac/smooth muscle: | Gap junctions
Cardiac and skeletal m
68
Skeletal/cardiac/smooth muscle: | Presence of sarcomere
Cardiac and skeletal muscle
69
Normal EMG in normal muscle
SNAP-sensory nerve action potential
70
Abnormal EMG seen in myopathy
Abnormal spontaneous activity- Fibrillation
71
Dive bomber sound in EMG
Myotonic dystrophy
72
Characterized by calf pseudohypertrophy and progressive weakness of girdle muscles
DMD
73
Due to gene deletion of dystrophin
DMD
74
Pathognomonic of DMD
(+)gower sign
75
Aka steinert's disease
Myotonic dystrophy
76
CTG trinucleotide repeat in DMPK gene
Myotonic dystrophy
77
Characterized by weakness, myotonia(sustained contraction) christmas tree cataract, frontal balding/bossing Carp mouth
Myotonic dystrophy
78
Aka thomsen disease
Myotonia congenita
79
Gene mutation in chloride channel
Myotonia congenita
80
Characterized by myotonia, muscle hypertrophy and HERCULEAN appearance
Myotonia congenita | Maskulado
81
Glucose 6 phosphatase def
Von gierke's disease | Type 1: 1st bf is always a jerk
82
Severe hypoglycemia Lactic acidosis Hepatomegaly Hyperlipidemia,xanthoma
Von gierke
83
Acid maltase/alpha glucosidase deficiency
Type 2Pompe disease
84
Death due to cardiomyopathy and heart failure
Pompe disease
85
Debranching enzyme deficiency
Type 3 Cori disease
86
Accumulation in cori disease
Limit dextrin
87
Branching enzyme deficiency
Type 4 andersen disease
88
Accumulation of amylopectin
Andersen disease
89
Muscle phosphorylase def
Type 5 mc ardle disease
90
Poor exercise intolerance
Mc ardle
91
Liver phosphorylase def
Type 6: her's disease | Hep hep herry
92
Phosphofructokinase def
Type 7: Tarui disease
93
Only GSD with hemolytic anemia
Tarui