11.2 - movement Flashcards

1
Q

what is an exoskeleton?

A
  • the external skeleton surrounds and protecting most of the body surface of animals including insects and crustaceans
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are bones?

A
  • the internal skeletons found in animals with an endoskeleton such as mammals and fish
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are muscles?

A
  • connected to the outside of bones by tendons, and attached to the
    insides of exoskeletons
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what are levers?

A
  • Bones and exoskeletons facilitate movement by providing an anchor for muscles, thus acting as levers.
  • This allows for changing size and direction of forces generated.
  • The relative position of the effort force (E), the fulcrum (F, aka pivot point), and the resultant force (R); in which these determine the class of lever
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are Synovial joints?

A
  • The structure of a joint (joint capsule and ligaments) determines the movements that are possible
  • Synovial joints are the most movable joints in the body and therefore provide the greatest range of motion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is synovial fluid?

A
  • In synovial joints, the surfaces of the bones are covered in a thin layer of strong cartilage and a very thin layer of slippery joint fluid
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what are skeletal muscles?

A
  • Skeletal muscles occur in pairs and are called antagonistic because when one muscle contracts, the other relaxes
  • antagonistic muscles produce opposite movements at a joint
  • the elbow joint, the triceps extends the forearm and the biceps flex the forearm
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

drawing a diagram of an elbow?

A
  • include cartilage, synovial fluid, joint capsule, named bones and named antagonistic muscles
  • elbow joint works on both a hinge
    joint and pivot joint –together it allows for a vast range of movements
  • joint is where the bones meet
  • cartilage is tough, smooth tissue that prevents bones rubbing together (friction) and absorbs shocks to decrease fractures of bones
  • Synovial fluid fills the cavity between the joint and cartilage
  • The joint capsule is a tough ligamentous covering to the joint
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the Antagonistic pairs in an insect leg?

A
  • The hindlimb of a grasshopper is specialised for jumping, and it is a jointed limb with three parts
  • When the grasshopper prepares to jump, the flexor muscles will contract and the extensor muscles relax (antagonistic pair), bringing the femur and tibia closer together. This is known as flexing
  • When the extensor muscles contract and the flexor muscles relaxes, the tibia is extended and it produces a powerful propelling force
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is the structure of a skeletal muscle?

A
  • Skeletal muscles are attached to bones (outside) and used to move the body
  • Skeletal muscles consist of bundles of large multinucleate striated cells called muscle fibres
  • The term fibres is used as it provides structural support, and it is striated as the muscles viewed using a microscope will have visible stripes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the structure of muscle cells?

A
  • Each muscle cell is surrounded by a plasma membrane called the sarcolemma
  • The muscle cell has special cytoplasm called sarcoplasm
  • An internal membrane called the sacroplasmic reticulum (SR) conveys the signal for muscle contraction
  • Large numbers of mitochondria are present to provide sufficient ATP for muscle contraction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are Myofibrils?

A
  • sacroplasmic reticulum surrounds structures called myofibrils found inside each muscle cell
  • myofibrils are thin parallel and elongated fibres
  • has alternating light and dark bands, which gives the striped pattern on skeletal muscles
  • the centre of each light band is a discshaped structure called the Z-line
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

how are Myofibrils made up of sacromeres?

A
  • The sacromere is the functional unit of the muscle.
  • The myofibrils are divided into compartments by Z-lines.
  • The distance between two Z-lines is called the sacromere.
  • Therefore, myofibrils consist of repeating units called sacromeres.
  • Myofibrils have two types of myofilaments: myosin and actin.
  • Both myosin and actin are proteins.
  • The myosin filaments are thick and seen as dark bands.
  • The actin filaments are thin and seen as light bands.
  • Actin filaments are attached to one end of the Z-line.
  • Six actin filaments surround one myosin filament to form cross-bridges during contraction.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

drawing the sacromere.

A
  • Diagrams of the sacromere structure should include Z-lines, actin filaments, myosin filament heads, and the region of light and dark bands.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

how is a muscle contracted?

A
  • The contraction of muscle is due to the sacromeres in the myofibrils becoming shorter.
  • This is achieved by the sliding of actin and myosin filaments over each other with the use of energy (ATP).
  • Contraction shortens the sacromeres by about 35% and therefore shortens the overall length of the muscle fibres.
  • However, it does not change the length of the thick (myosin) and thin (actin) filaments.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

how are muscle contraction controlled with ATP and Ca2+ ions?

A
  • depolarisation and calcium (Ca2+) ion release,
  • actin and myosin cross-bridge formation,
  • sliding mechanism of actin and myosin filaments, and
  • sacromere shortening for muscle contraction.
17
Q

how does Depolarisation and calcium (Ca2+) ion release work?

A
  • action potential from a motor neuron triggers the release of acetylcholine into the motor end plate
  • causes the sacrolemma to depolarise and this is transmitted down the T-tubules to all muscle fibres.
  • This triggers the release of calcium (Ca2+) ions from the sacroplasmic reticulum
18
Q

how does the Actin and myosin cross bridge formation work?

A
  • Actin filaments have a binding site for the myosin heads and also have two proteins, tropomyosin and troponin
  • In a relaxed muscle, tropomyosin blocks the myosin binding sites on actin by forming two strands that wind around the actin filament
  • Ca2+ ions bind to troponin, troponin
    causes the myosin to move and so it reconfigures the complex to expose the myosin binding sites
  • myosin filament heads can attach to the binding side of actin filaments in order to pull them together for cross-bridge formation.
19
Q

how does the Sliding mechanism of actin and myosin filaments work?

A
  • ATP binds to the myosin head and causes it to break the cross-bridges between actin and myosin
  • The myosin head gains energy from the hydrolysis of ATP to ADP and Pi, and changes shape ready to bind to the next binding site on actin
  • The myosin head binds to the new exposed actin binding site and returns to the original conformation.
  • This reorientation drags the actin further from the centre along the myosin in a sliding mechanism.
  • The ADP and Pi are released, and the myosin head push the actin filament towards the centre of the sacromere.
  • This is called the power-stroke
20
Q

how does the Sacromere shortening for muscle contraction.

A
  • The repeated reorientation of the myosin heads drags the actin filaments along the length of the myosin.
  • As the actin filaments are anchored to the Z-lines, the Z-lines are pulled closer together; thus shortening the sacromere.
  • As individual sacromeres become shorter, the muscle fibres as a whole contracts.
  • When no more nerve impulse arrives, Ca2+ ions move back into vesicles of the sacroplasmic reticulum by active transport.
  • The binding sites on actin are covered again and the muscle relaxes.
21
Q

how to look at a muscle contraction.

A
  • Next to the Z-line is the light band of actin, this is called the I band (i for light).
  • The I band is longer in a relaxed muscle.
  • In the centre of the sacromere is the darkest band consisting of myosin and actin, this is called the A band (a for dark).
  • There is no change in length of the A band in both relaxed and contracted muscle.
  • In the centre of the A band is a grey zone of only myosin. This is called the M-line.
  • In a relaxed muscle, there is more visible light on either side of the M-line.
  • The Z-lines are farther apart when the sacromere is relaxed, and so the light bands are wider for a longer sacromere.
  • The Z-lines are closer together when the sacromere is contracted, and so the sacromere is shorter as the myosin and actin have slid over one another.
  • The I band becomes smaller and there is less light on either side of the M-line.
22
Q

what are the results of Muscle contractions and fluorescence studies?

A
  • Fluorescence is the emission of electromagnetic radiation, often visible light, by a substance after it has been illuminated by electromagnetic radiation of a different wavelength
  • Muscle research relies on fluorescence, in particular calcium-sensitive bioluminescent protein, aequorin found in Aequorea victoria (jellyfish)
  • injected into giant single muscle fibres of Balanus nubilus and the when muscles were stimulated, there was a strong bioluminescence coinciding with the release of Ca2+
    from the sacroplasmic reticulum. The bioluminescence decreased as the stimulus was removed.
  • Separately, scientists cut open Nitella axillaris cells that have a network of actin filaments below the membranes.
  • Researchers added a fluorescent dye to myosin molecules to show that myosin “walks along” actin filaments. Researchers also showed the ATP-dependence of myosin too