a&p exam #3 Flashcards

(39 cards)

1
Q

Describe the anatomical &functional divisions of the nervous system

A

ANATOMICAL: The central nervous system is made up of the brain and spinal cord.
The peripheral nervous system is made up of nerves that branch off from the spinal cord and extend to all parts of the body.

FUNCTIONAL: Sensory and Motor nervous system

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2
Q

Identify the structure of a typical neuron and functions of each component

A

DENDRITES: receive communications from other cells

AXON: conducts electrical impulses away from the neuron’s cell body

CELL BODY: holds all of the general parts of the cell and controls all functions of cell

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3
Q

functions of skeletal muscle tissue

A

PRODUCING MOVEMENT

MAINTAINING POSTURE

SUPPORTING SOFT TISSUES

GUARDING BODY ENTRANCES/EXITS

MAINTAINING BODY TEMP.

STORING NUTRIENTS

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4
Q

identify the molecular components of thick & thin filaments

A

THIN FILAMENT: single thin filaments contain 4 main proteins:
F-ACTIN, NEBULIN, TROPOMYOSIN, TROPONIN

THICK FILAMENT: Each thick filament has a cone of titin and it recoils after stretching.
CONTAINS 300 MYOSIN MOLECULES MADE OF A PAIR OF MYOSIN SUBUNITS TWISTED AROUND EACHOTHER

the long tail in thick filament is bound to other myosin molecules

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5
Q

identify the structural components of a sarcomere

A

A BUNDLE OF MYOSIN THAT CONTAINS THICK FILAMENTS COMBINED WITH BUNDLES OF ACTIN- CONTAINING THIN FILAMENTS

a sarcomere is a basic contractile unit of a myofibril(muscle fiber)

a myofibril consists of approx. 10,000 sarcomeres

A SARCOMERE CONTAINS PROTEINS THAT STABILIZE THE THIN AND THICK FILAMENTS. THE PROTEINS ALSO REGULATE INTERACTIONS BETWEEN THIN AND THICK FILAMENTS

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6
Q

describe the organization of muscle at a tissue level

(CT SHEATHS)

A

EPIMYSIUM: a CT sheath made of collagen fibers that surrounds each each muscle.

PERIMYSIUM: surrounds each bundle of muscle fibers and divided muscle into series of compartments

FASCICLE: each compartment containing muscle fiber bundles

ENDOMYSIUM: surrounds each individual muscle cell.

MYOSATELLITE CELL: stem cells that repair damaged muscle tissue

TENDON: attaches skeletal muscle to bone

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7
Q

describe what happens to the various regions of a sarcomere during muscle contraction

A

SARCOMERES SHORTEN AS THIN/THICK FILAMENTS OVERLAP
this pulls the muscle fiber closer together

interactions between thin/thick filaments are responsible for contraction

WHEN A SARCOMERE CONTRACTS, 2 LINES MOVE CLOSER TOGETHER & THE I BAND GETS SMALLER. THE A BAND STAYS THE SAME WIDTH & AT FULL CONTRACTION THE THIN FILAMENTS OVERLAP

lots of overlap

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8
Q

describe what is involved with excitation contraction coupling

A

the link between the generation of an action potential in the sarcolemma & start of a muscle contraction

the action potential causes the release of ACh into the synaptic cleft which leads to excitation

the action potential travels along the sarcolemma and down the t tubules to the triads. this triggers the release of Ca2+ from the terminal cristernae of the sarcoplasmic reticulum

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9
Q

summarize the events involved in the neural control of skeletal muscle

A

A SKELETAL MUSCLE FIBER CONTRACTS WHEN STIMULATED BY A MOTOR NEURON AT A NEUROMUSCULAR JUNCTION.

MOTOR NEURONS CARRY INSTRUCTIONS IN FORM OF ACTION POTENTIALS AT THE AXON TERMINAL

CONTRACTION BEGINS WHEN SARCOPLASMIC RETICULUM RELEASES STORED CALCIUM IONS INTO THE CYTOSOL OF THE MUSCLE FIBER(that release is under control of the nervous system)

AS INTRACELLULAR CALCIUM IONS ARE REABSORBED, CONTRACTION ENDS & MUSCLE RELAXATION OCCURS

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10
Q

identify components of the neuromuscular junction

A

NMJ IS MADE UP OF AN AXON TERMINAL OF A NEURON, A SPECIALIZED REGION OF TGE SARCOLEMMA CALLED THE MOTOR END PLATE, AND IN BETWEEN A NARROW SPACE CALLED THE SYNAPTIC CLEFT

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11
Q

outline the steps that are involved during the contraction cycle

A

calcium ions (CA2+) bind to troponin, resulting in the exposure of the active sites on the thin filaments

this allows cross-bridge formation & will continue as long as ATP is available

CONTRACTION CYCLE IS SERIES OF MOLECULAR EVENTS THAT ENABLE MUSCLE CONTRACTION

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12
Q

explain the mechanisms involved in muscle fiber relaxation

A

ACh is broken down:
ACh broken down by AChE, ends action potential generation

Sarcoplasmic reticulum reabsorbs Ca2+:
As calcium ions are reabsorbed, their concentration in cytosol decreases

Active site covered, cross bridge formation ends:
without calcium ions, the tropomyosin res turns to its normal position & the active sites are covered again

Contraction ends:
* without cross bridge formation, contraction ends*

Muscle relaxation occurs:
* muscled return passively to resting length*

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13
Q

discuss the factors that determine the peak tension developed during a contraction of a muscle fiber

A

FACTORS:
- number of muscle fibers activated
-frequency of neural stimulation to muscle fibers

as tension increases, calcium ions are binding to troponin active sites on thin filaments are being exposed & cross bridging interactions are occurring
^ CONTRACTION PHASE ^

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14
Q

discuss the factors that affect peak tension production during the contraction of an entire skeletal muscle

A

depends on the cross sectional area of the muscle fiber & frequency of neural stimulation

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15
Q

explain the significance of motor units to whole muscle contraction

A

motor units provide electrical input to a muscle in order to generate muscle contraction

a motor unit consists of a neuron & muscle cell that it supplies

the size of a motor unit indicates how precise a movement can be

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16
Q

define muscle tone and it’s relationship to normal everyday activities

A

the resting tension in a skeletal muscle

muscle tone helps to hold body upright when sitting/standing

also contributes to control, speed, and amount of movement we achieve

17
Q

isotonic vs isometric contractions

A

ISOTONIC: tension increases & skeletal muscle length changes

ISOMETRIC: muscle as a whole doesn’t change length and tension produced never exceeds the load

18
Q

concentric vs. essentric in isotonic contractions

A

CONCENTRIC: muscle tension exceeds load and muscle shortens

ESSENTRIC: peak tension developed is less than the load & muscle elongates due to the contraction of another muscle or pull of gravity

19
Q

describe the mechanisms by which muscle fibers obtain the energy to power contractions

A

when muscle fiber is actively contracting, each thick filament breaks down about 2500 ATP molecules per second.

the demand for ATP in a contracting muscle fiber is so high that it would be impossible to have all the necessary energy available as ATP before the contraction begins.

Instead, a resting muscle fiber contains only
enough ATP and other high-energy compounds to sustain acontraction until additional ATP can be generated.

Throughout the rest of the contraction, the muscle fiber will generate ATP at roughly the same rate as it is used.

20
Q

describe the factors that contribute to muscle fatigue

A

muscle fatigue means muscle can’t preform required level of activity

  • DEPLETION OF METABOLIC RESERVES WITHIN MUSCLE FIBER
  • DAMAGE TO SARCOLEMMA AND SARCOPLASMIC RETICULUM

-DECLINE IN pH WITHIN MUSCLE FIBERS

-SENSE OF REDUCTION IN DESIRE TO CONTINUE ACTIVITY

21
Q

discuss the stages of mechanisms involved in muscle recovery

A

after moderate activity, muscles need several hours to recover.

LACTATE REMOVAL & RECYCLING

OXYGEN DEBT:
* happens when the body can no longer distribute oxygen to muscle cells to aid the processes that make them function, resulting in muscular fatigue*

HEAT PRODUCTION & LOSS:

22
Q

relate the type of muscle fibers to muscle muscle performance

A

FAST FIBERS: reach peak twitch tension in 0.01 seconds and is prevalent in quick and powerful movement such as sprinting/ weight lifting

SLOW FIBERS: takes 3 times as long to reach peak tension after stimulation but is prevalent in long distance running

INTERMEDIATE FIBERS: BETWEEN FAST AND SLOW FIBERS

23
Q

distinguish between aerobic vs anaerobic endurance and implications for muscle performance

A

AEROBIC: length of time & muscle can continue to contract with while supported by mitochondrial activities. -does not promote hypertrophy

ANAEROBIC: length of time & muscular contraction can continue to be supported by existing energy reserves of ATP & CP & by glycolysis

24
Q

classify neurons based on structure

A

MULTIPOLAR: more than 2 processes, single axon, and multiple dendrites

UNIPOLAR: single elongated process, cell body off to the side

BIPOLAR: 2 processes separated by cell body

25
describe how peripheral neurons can respond to injury
*more repair is possible for PNS than CNS* 1) fragment of axon& myelin occurs in distal stump 2) schwann cells form cord, grow into cut & unite stumps. macrophages engulf degenerating axon & myelin 3) axon sends buds into network of schwann cells that starts growing along cord of schwann cells 4) axon continues to grow distal stump and is enclosed by shwann cells
26
explain how resting potential is created and maintained
potassium that leaks from inside of the cell to the outside via leak potassium channels & generates a negative charge in the inside of membrane vs. outside. MAINTAINED: sodium potassium pumps move 2 potassium ions inside the cell as 3 sodium ions are pumped out to maintain negatively charged membrane inside the cell
27
identify various types of gated channels found in neuron plasma membranes & where they can be found
CHEMICALLY GATED ION CHANNEL: found on densities and cell body of neuron. open/close when they bind specific chemicals VOLTAGE GATED ION CHANNEL: found in axons. open/close in response to changes in membrane potential MECHANICALLY GATED ION CHANNEL: found in sensory receptors. open/close in response to physical distortion of membranes/surfaces
28
describe how graded potential is generated & describe factors which can keep it from beginning an action potential
GRADED POTENTIAL: changes in the membrane potential that can not spread far from the site of stimulation any stimulus that opens a gated channel produces a graded potential if a graded potential causes hyperpolarization an action potential becomes less likely
29
differentiate between the absolute refractory period and the relative refractory period
ABSOLUTE: 1st part of refractory period. period of time during which no amount of external stimulus will generate an action potential RELATIVE: begins when sodium ion channels regain their normal resting conditions. only a large stimulus will generate an action potential
30
duchess the events that occur at a chemical synapse
action potential triggers the pre synaptic neuron to release neurotransmitters where 1 neuron finds chemical signals to another cell, often a second neuron. every chemical synapse involves 2 cells
31
discuss the factors involved in synaptic delays and synaptic fatigue
DELAY: occurs between arrival of action potential at the axon terminal and the effect on the postsynaptic membrane. due to time necessary for transmitter to be released. diffuse across the cleft and bind with receptors on postsynaptic membrane FATIGUE: occurs often, response of the synaptic weakens until ACh has been replenished. temp. depletion of synaptic vesicles that house neurotransmitters in the synapse
32
structural vs. functional differences between skeletal muscle fibers & smooth muscle cells
*SMOOTH MUSCLE CELLS* structure: relatively long, slender, spindle shaped cell, centrally located nucleus, no t tubules function: contracts 4x greater than skeletal muscle fibers. triggers 4 contractions appearance free calcium ions in cystoplasm SKELETAL MUSCLE FIBERS: structure: thousands of muscle fibers wrapped in sheath, fascicle function:allows muscles to move bones to preform lots of movements
33
classify neurons based on function
motor neurons sensory neurons interneurons
34
discuss the role that smooth muscle tissue plays in systems throughout the body
coordinates movement of substances through internal passageways Integumentary System: helps regulate the flow of blood to the superficial dermis - Cardiovascular System: control blood flow through vital organs and help regulate blood pressure. -Respiratory System: contract or relax to alter the diameters of the respiratory passageways and change their resistance to airflow.
35
structural vs functional differences of skeletal muscle fibers and cardiac muscle cells
CARDIAC MUSCLE CELLS: Structure: found only in heart, relatively small, single nucleus, typically branched Function: contractions last 10 times longer than skeletal, longer refractory periods and do not readily fatigue SKELETAL MUSCLE FIBERS: structure: unbranched function: action potential triggers release of calcium from SR& contraction of sarcomeres
36
discuss the factors involved in synaptic delay & synaptic fatigue
SYNAPTIC DELAY: occurred between arrival of action potential at the axon terminal & the effect on the postsynaptic membrane. Delay is due to time necessary for transmitter to be released, diffuse across the cleft & bind w/ receptors in post synaptic membrane SYNAPTIC FATIGUE: occurs after, response of the synapse weakens until ACh has been replenished temp. depletion of synaptic vesicles that house neurotransmitters in the synapse
37
factors that affect the speed w/ which action potentials propagated
* Because myelin limits the movement of ions across the axon membrane, the action potential must "jump" from node to node during propagation. This results in much faster propagation along the axon.* A local current produces a graded depolarization that brings the axon membrane (axolemma) at the next node to threshold. An action potential develops at node (2). A local current produces a graded depolarization that brings the axolemma at node (3 to threshold.
38
discuss the factors that affect the speed w which action potentials are propagated
* In an unmyelinated axon, an action potential moves along by continuous propagation. The action potential spreads by depolarizing the adjacent region of the axon membrane. This process continues to spread as a chain reaction down the axon.* As an action potential develops at the initial segment 1, the membrane polential at this site depolarizes to +30 mV. A local current then develops as the sodium lons entering at 1 spread away from the open voltage-gated channels. A graded depolarization quickly brings the axon membrane (axolemma) in segment (2) to threshold. An action potential now occurs in segment I while segment 2 begins repolarization. as the sodium ions entering at segment (2) spread laterally, a graded depolarization quickly brings the membrane in segment (3 to threshold, and the cycle is repeated.
39
describe the events involved in the generation and propagation of an action potential
*if graded potential causes depolarization, action potential becomes more likely to occur* Depolarization to Threshold The stimulus that initiates an action potential is a graded depolarization large enough to open voltage-gated sodium channels. The opening of the channels occurs at a membrane potential known as the threshold. Activation of Sodium lon channels and Rapid Depolarization When the sodium channel activation gates open, the plasma membrane becomes much more permeable to Na*. Driven by the large electrochemical gradient, sodium ions rush into the cytosol, and rapid depolarization occurs. The inner membrane surface now has more positive ions than negative ones, and the membrane potential has changed from -60 mV to a positive value. inactivation of Sodium lon channels and Activation of potassium Ion Channels starts repolarization as the membrane potential approaches +30 mV, the inactivation gates of the voltage-gated sodium channels close. This step is known as sodium channel inactivation, and it coincides with the opening of voltage-gated potassium channels. Positively charged potassium lons move out of the cytosol, shifting the membrane potential back toward the resting level. Repolarization now begins. Time Lag in Closing All Potassium Ion Channels Leads to Temporary Hyperpolarization The voltage-gated sodium channels remain inactivated until the membrane has repolarized to near threshold level. At this time, they regain their normal status: closed but capable at opening. The voltage-gated potassium channels begin closing as the membrane reaches the normal resting membrane potential (about -70 mV). Until all of these potassium channels nave closed, potassium ions continue to leave the cell. This produces a briet hyperpolarization.