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106 Cards in this Set
- Front
- Back
- 3rd side (hint)
What is released when Sarcoplasmic Reticulum (SR) is depolarized? |
activated Ca2+ VGC, Ca2+ is released into cytosol |
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Troponin C (of sarcomere) binds to Ca2+ = |
contraction |
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WHere is the location of Ca2+ VGC opening? |
Terminal cisterns of SR |
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Troponin C changes stereochemistry and cause |
grip to loosen on Tropomyosin by Troponin T |
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What causes binding sites to be exposed on actin? |
When Tropomyosin assumes more relaxed lateral position |
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What recognize binding sites? |
Myosin heads |
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What is used to detach from old bond and make new bond at hot spot? |
ATP |
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Once ATP on myosin is cleaved, what happens? |
ATP energy is used to bend myosin head from filament using powerstroke or ratchet movement |
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How many actin filaments are pulled close together? |
12 = 6 actin filaments on each side, sliding on 1 myosin filament` |
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What represents a muscle contraction? |
When H zone narrows (overlap increases), and Z lines come closer together) - |
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Muscle is in a state of contraction when |
500 myosin heads per myosin filament work with 12 actin filaments times thousands of sarcomeres working together |
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What causes skeletal muscle relaxation? |
Ca2+ pumped out of muscle by Ca2+/Mg2+ ATPase pump |
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Troponin C tightens grip on |
Tropomyosin by Troponin T |
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What cause myosin to slide back to resting levels? |
the repositioning of Tropomyosin over binding sites on actin, prevent any further attachment by myosin heads |
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Powerstroke needs ____ to make new and break old attachments between myosin and actin? |
ATP and maintain Ca2+/Mg2+ pump action |
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What is defective in muscular dystrophies disorders? |
protein Dystrophin Example in Becker's Dystrophy |
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Dystrophin protein is absent in what disease? |
Duchenne's Dystrophy |
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What is the cause of dystrophy disorders? |
autoimmune reactions |
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How are muscle cells/fibers classified? |
4 attributes 1. size 2. color 3. twitch speed 4. type of metabolism |
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What is twitch? |
the smallest contraction movement that is detected in a given muscle |
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What are the characteristics of Type 1 muscle |
color = red size = small twitch speed = slow metabolism = oxidative |
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What are the characteristics of Type IIa muscle? |
color = red size = medium twitch speed = fast metabolism = oxidative |
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What are the characteristics of Type IIb muscle? |
color = white (pale) size = large twitch speed = fast metabolism = glycolytic |
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Which muscle is predominant in humans? |
Type I |
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Which muscles are endurance types? |
Type I and IIa |
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Which muscles are capable of generating large amounts of force in a very short period of time? |
Type IIb |
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ATP is produced y what processes? |
glycolysis or oxidative phosphorylation |
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What percent efficiency is ATP used in the body? |
40% |
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Skeletal muscles are controlled in groups called |
motor units |
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what is a motor unit? |
ratio of number of muscle cells stimulated by a single neuron |
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The larger number of muscle cells under control of a single neuron, the LESS control one has over recruiting varying strength of muscle |
coarse control |
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What is Fine control? |
small number of cells being moved by a single neuron = MORE control |
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What are the three types of motor units? |
1, 2, 3, |
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Type 1 |
motor unit = 2-20-:1 Fine control ex: eye muscle |
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Type 2 |
motor unit = 160-220-:1 medium control ex: hands, feet, face muscles |
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Type 3 |
motor unit = 500-2000:1 coarse control ex: torso/extremities |
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What is relaxation? |
When Ca2+ no longer flowing from SR, pumped out of system with Ca2+/Mg2+ pump (1:1) |
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Which muscles are striated? |
skeletal and cardiac |
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Skeletal fiber is known as anatomical syncytium |
made up of numerous embryonic cells so in mature state they have many small nuclei, but essentially just one. |
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Cardiac muscle has a single |
nucleus surrounded by a cloud of glycogen |
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What is the purpose of gap junctions in cardiac cell? |
allow for continuity of sorts between cytoplasm of one cell to next (Na+ and Ca2+ ions enter cytosol can now drift to adjacent cells as though they were part of same cell) |
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ATP is produced by what processes? |
Glycolysis Oxidative Phosphorylation |
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What percent efficiently is ATP used? |
40% |
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What percent efficiently is ATP used? |
40% |
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How is creatinemonophosphate (phosphocreatine) made? |
ATP stored in muscle by transfer of high energy bond with a phosphate to protein creatine |
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What enzyme is used for reaction in making phosphocreatine? |
CreatinePhosphoKinase (CPK) |
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What happens when phosphorylcreatine decays into creatine as waste? |
Creatine is removed from muscle and into blood then into urine by Kidneys |
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What happens when phosphorylcreatine decays into creatine as waste? |
Creatine is removed from muscle and into blood then into urine by Kidneys |
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What is the normal blood level range of creatinine in the body? |
0.6-1.5 mg/dl Suggest normal kidney or muscle |
Higher levels in kidney/muscle damage, pregnancy, growing children, post IM injections and large adults |
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Motor Units? |
The groups that skeletal muscles are controlled in |
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Which muscle types have striations? |
Cardiac and Skeletal |
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Which muscle types have striations? |
Cardiac and Skeletal |
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Does cardiac muscle go into Tetany? |
No |
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Which muscle types have striations? |
Cardiac and Skeletal |
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Does cardiac muscle go into Tetany? |
No |
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What is the benefit of gap junctions in smooth and cardiac muscles? |
Able to stimulate action potentials: migrate easily and set off another action potential - depolarization wave |
Sodium and calcium ions can drift to adjacent cells - laws of diffusion Promote depolarization Cardiac muscle - intercalated discs
Smooth muscles - branchings |
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What is the difference between propagating action potential down cardiac muscles and skeletal muscles? |
Cardiac muscles membrane is wider, different in morphology, action potential takes a long time - relative refractory could be reached and by that time muscle cells already in relaxation phrase |
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Why do Cardiac muscles show evidence of spontaneous depolarization? |
Because cardiac muscle have slow sodium gated channels that open upon hyper polarization - why heart (pacemaker) cells AKA funny channels |
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Why are skeletal muscles not automatic? |
Because their action potential more or less mimic neuronal AP except for excitation contraction coupling that follows in muscle |
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Why is the action potential wide in cardiac muscle ? |
Because Ca2+ stays longer in cytosol than in skeletal muscle |
This increase refractory period which prevents a significant summation of contractions
Cardiac muscle stimulation do not tetanize like skeletal muscle (but known to shred) |
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Troponin T interact with |
Tropomyosin |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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What is A band? |
Middle area in sarcomere where thick and thin filaments are found |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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What is A band? |
Middle area in sarcomere where thick and thin filaments are found |
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What is I band? |
Contains thin filaments because it's lighter in color |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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What is A band? |
Middle area in sarcomere where thick and thin filaments are found |
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What is I band? |
Contains thin filaments because it's lighter in color |
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What are Z discs? |
Separate one sarcomere from the next |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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What is A band? |
Middle area in sarcomere where thick and thin filaments are found |
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What is I band? |
Contains thin filaments because it's lighter in color |
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What are Z discs? |
Separate one sarcomere from the next |
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What is H zone? |
Area of only thick filaments |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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What is A band? |
Middle area in sarcomere where thick and thin filaments are found |
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What is I band? |
Contains thin filaments because it's lighter in color |
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What are Z discs? |
Separate one sarcomere from the next |
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What is H zone? |
Area of only thick filaments |
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What is M line? |
Supporting proteins that hold thick filaments together in H zone |
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Troponin T interact with |
Tropomyosin |
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Troponin C interact with |
Ca2+ |
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What cause mechanical movement of myosin head? (Ratchet style or power stroke ) |
Catalized ATP |
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What is A band? |
Middle area in sarcomere where thick and thin filaments are found |
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What is I band? |
Contains thin filaments because it's lighter in color |
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What are Z discs? |
Separate one sarcomere from the next |
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What is H zone? |
Area of only thick filaments |
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What is M line? |
Supporting proteins that hold thick filaments together in H zone |
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What is the function of sarcoplasmic reticulum? |
Stores and release Ca2+ into sarcoplasmic after nervous stimulation |
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Gross contracture of sarcomeres are a cause of |
Lack of ATP |
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