Chapter 11 Flashcards

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1
Q

simple motor control

A
  • spinal connections between dorsal (sensory) and ventral (motor) roots provide basis for simple movements
  • REFLEX: basic unit of movement; simple, unvarying, unlearned response to sensory stimuli
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2
Q

complex motor control

A
  • complex set of commands to muscles that is established before behavior starts; present in both humans and animals
  • feedback from movements modifies, fine-tune, and regulates motor sequence
  • involves coordination with different parts of cortex areas (emotions, planning, decision-making)
  • mechanism of closed-loop feedback control system:
    + regulates and controls movement:
    + control signal -> ERROR DETECTOR -> error signal -> CONTROLLER -> command -> CONTROLLED SYSTEM -> output -> TRANSDUER -> feedback signal -> ERROR DETECTOR
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3
Q

hierarchy of motor control systems

A
  • SKELETAL SYSTEM: allow for movement via attached muscles
  • SPINAL CORD: controls skeletal muscles
  • BRAINSTEM: integrates motor commands
  • PRIMARY MOTOR CORTEX: initiates commands for action
  • NONPRIMARY MOTOR CORTEX: provides an additional source of motor commands
    + CEREBELLUM and BASAL GANGLIA modulate activities of these control systems, sometimes via THALAMUS
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4
Q

skeletal system

A

some behavioral properties arise from physical characteristics of the skeleton:

  • limbs shape an animal’s stride
  • type of joint determines direction of movement
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5
Q

muscle

A
  • composed of MUSCLE FIBERS, each containing 2 kinds of regularly arranged, overlapping filaments:
    + THICK filaments made of MYOSIN
    + THIN filaments made of ACTIN
  • filaments overlap -> muscle’s striped appearance (STRIATED MUSCLE)
  • contraction shortens fibers’ length
  • TENDONS connect muscle to bone
  • ANTAGONISTS: muscles that contract when others extend/relax
  • SYNERGISTS: muscles that act together
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6
Q

motoneurons

A

nerve cells in the spinal cord that send their axons to innervate muscles
- FINAL COMMON PATHWAY through which brain and spinal cord control muscles
- firing patterns determine the onset, coordination, and termination of muscle activity
- release only ACh -> muscle contractions BUT respond to a variety of synaptic transmitters (excitatory - glutamate, induces movement, and inhibitory - GABA, prevents firing) released by diverse inputs that motoneurons receive
+ running -> see stop sign -> visual cortex signals stop -> muscles stop
- action potentials travel down motoneuron, which branches into many terminal near its target
- NEUROMUSCULAR JUNCTION (NMJ): where motoneuron terminal and muscle fiber meet -> effective synapse, almost every action potential elicits a contraction

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7
Q

feedback control of muscle movement

A
  • proprioception: collection of information about body movements and positions; perception system in peripheral system) -> inputs feedback and prevents damage + injury
  • receptors:
    + MUSCLE SPINDLES
    + GOLGI TENDON ORGANS
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8
Q

proprioceptive receptors: muscle spindles and Golgi tendon organs

A
  • MUSCLE SPINDLES: responsive to STRETCH, consist of afferent (move toward) and efferent (move away from) elements
    + muscle stretches -> spindle stretches -> afferent nerve impulses to inform brain of stretch
    + e.g. stretching -> sense tension -> sen signal to brain “stop, you’re gonna hurt yourself” -> brain sends signal to stop -> muscles stop
  • GOLGI TENDON ORGANS: responsive to muscle CONTRACTION
    + stimulation inhibits motoneurons acting on muscles -> relax tension and prevent damage
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9
Q

muscle control: spinal cord vs. brain

A
  • STRETCH REFLEX: controlled at SPINAL level
    + example: hold heavy book -> muscle stretches first (can’t hold) -> excitation of muscle spindle afferents (SNa) -> excitatio of motoneurons -> muscles oppose stretch (lift up -> contract + control)
  • BRAIN level: CRANIAL MOTOR NUCLEI in the BRAINSTEM innervate muscles of head and neck -> does not go through spinal cord
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10
Q

major motor pathways

A
  • send signals from brain to spinal cord to control muscles
  • PYRAMIDAL SYSTEM (or CORTICOSPINAL SYSTEM): directly innervate motoneurons of spinal cord or brainstem
    + consists of:
    + neuronal cell bodies in cerebral cortex
    + axons, which pass through brainstem to spinal cord -> form PYRAMIDAL TRACT
    + right cortical regions -> left side of body, vice versa
  • EXTRAPYRAMIDAL SYSTEM: modulate and regulate motor control (indirect)
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11
Q

primary motor cortex (M1)

A
  • many axons in pyramidal tract originate from neurons here
  • initiate and control body movements directly
  • very large regions are devoted to body parts involved in complex movements -> different parts of M1 correspond to different parts of body -> highly organized, allow for specific control of movement
    + disproportionately large regions in M1 map (hand, lips) = devoted to most elaborate and complex movements
  • many neurons rest when certain muscles contracted -> M1 correspond to muscle
    + e.g. move finger -> many groups of neurons fire simultaneously -> flexible system
  • signals from neurons in motor cortex of monkeys and paralyzed humans can be used to control robotic arms in 3D
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12
Q

nonprimary motor cortex

A
  • lies in frontal lobe and anterior to M1, has 2 regions:
    + SUPPLEMENTARY MOTOR AREA (SMA): modulates activity of primary motor cortex -> important for planning movement sequence that is generated internally
    + e.g. planning what to say net -> planning sequence of motor movements (lip contractions)
    + SMA also activated by mental rehearsal of a complex movement
    + e.g. “singing” in your head but not out loud

+ PREMOTOR CORTEX: contains neurons that fire when motor sequences are guided externally by stimuli (e.g. auditory/visual cues)
+ e.g. want to lift table -> as for help

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13
Q

mirror neurons

A
  • become active when an individual makes a particular movement (monkey picks up a ball) OR when an individual sees another individual make that same movement (monkey sees someone pick up a ball)
  • important in the understanding of other individuals’ actions and in attempts to imitate those actions (empathy, understanding intention, self-awareness, imitation - language, autism - difficulty talking to people and maintaining eye contact comes from not being able to copy others?)
  • many vertebrates have mirror neurons but only those with high cognitive functions have a lot
  • females have more mirror neurons than males -> show more empathy
  • e.g. yawning -> if you yawn or see others do -> trigger yawn
  • e.g. musicians vs. non-musicians (NM)
    + when musicians just listen w/o playing: motoneurons still fire
    + NM don’t show same action, because they haven’t been exposed to the same experience before
    + experiment: use electrodes to observe neural activity when engage in a physical one (pick up ball) -> see if same circuit light up
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14
Q

extrapyramidal system

A
  • includes motor tracts that do not run through medulla
    + system = “extrapyramidal” -> distinguish from tracts of motor cortex that reach targets by traveling through pyramids of medulla
  • most important components:
    + BASAL GANGLIA: forebrain nuclei that modulates movement -> determine attitude/direction of movement, initiation of movement
    + important for memory-based motor movement/learning -> reinforcement learning/conditioning
    + has complex feedback loop connecting to cortex, mediated by dopamine produced by substantia nigra
    + CEREBELLUM: receives information from sensory systems, spiral cord, other parts of brain -> regulates and coordinates voluntary motor movements (posture, balance, coordination, speech)
    + in vertebrates, size varies according to range and complexity of movements
    + CEREBELLAR CORTEX: contains PURKINJE cells, only end inhibitory messages -> guide movement through inhibition
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15
Q

muscular dystrophy (MD)

A
  • disorders that lead to degeneration and changes in muscle structure
    + caused by gene mutation in X chromosome -> more likely in males
    + DYSTROPHIN: protein needed for normal muscle function, produced by gene on X chromosome
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16
Q

amyotrophic lateral sclerosis (ALS)

Lou Gehrig’s disease

A

progressive degeneration of motoneurons and subsequent loss of target muscles - 100% fatal
- motoneurons die -> brain loses ability to initiate + control motor movement -> voluntary muscle actions are affected -> can’t speak, eat, move, and breathe
- heritable (rare form) but there are also other causes
+ single gene mutation in SOD1 accounts for 20% of ALS heritable cases

17
Q

strategies to reconnect a severed spinal cord

A
  • provide STEM cells -> differentiates into new neurons
  • transplant GLIAL cells -> promotes regeneration
  • using NEUROTROPHIC FACTORS or ADHESION MOLECULES -> assist new growth
18
Q

Parkinson’s disease

A
  • causes tremors, loss of muscle tone, difficulty in motor movement
  • patients show degeneration of dopamine-containing cells in basal ganglia neurons in the SUBSTANTIA NIGRA, which projects to the striatum
  • inherited cause: defective gene that encodes for α-synuclein, a basal ganglia protein
    + the proteins normally interact -> defects in either protein lead to abnormal aggregates of protein, LEWY BODIES, in the cell
  • NOT curable BUT can be treated to reduce symptoms
    + treatment is in early stage of development
    + L-DOPA: precursor to dopamine -> injected to increase dopamine level and relieve tremors
    + electrical stimulation within basal ganglia can reduce symptoms but DEEP-BRAIN STIMULATION (DBS) requires an implanted eletrode
    + experimental: neurotrophic factors, stem cells
19
Q

Huntington’s disease: general

A

cause by basal ganglia damage (neuronal death) -> excessive, involuntary movement + tremor, dementia, speech + language dysfunction

  • not curable, hard to treat fatal progressive neuron degeneration in basal ganglia
  • cerebral cortex may also show impairment -> motor turns mental disorder
  • impairments in retrieval of lexical information and application of combinatorial rules -> repetition of sounds (stuttering)
20
Q

Huntington’s disease: mechanism and treatment exploration (transgenic bird)

A
  • cause of disease: mutation of single gene HTT, which encores protein HUNTINGTIN
    + gene has TRINUCLEOTIDE REPEAT (e.g. CAG) variable in length -> if repeats 36+ time, it will form abnormal protein of mutant huntingtin -> cells die -> develop disease
    + the more repeats, the more severe the disorder
  • dominant orthosomial disorder: mutant gene is dominant over normal gene -> 50/50 chance of having it -> if 1 of 2 parents, you do
    + Parkinson’s and Alzheimer’s are partially genetics, but environment factors are also involved
  • express mutant HTT in canary:
    + no good animal models yet but birds are chosen because they have vocal learning in basal ganglia
    + inject human gene to canary embryo -> transgenic birds who express same behavior as humans with disease (tremors, behavior deteriorate over time