Physiological Psychology Module 7 Notes
Module 7.1 The Control of Movement
Introduction
Ultimately, the brain is linked to the concept of doing something, that is, movement
Internal processing would be useless without the ability to react to the environments (e.g. move)
Muscles and Movements
All animal movement depends on muscle contractions
Smooth muscles: control the digestive system and other organs
Skeletal muscles/striated muscles: control movement of the body in relation to the environment
Cardiac muscles: heart muscles that have properties of skeletal and smooth muscles
Muscles are composed of many individual fibers
Each muscle fiber receives information from only one axon but a single axon may innervate many muscle fibers
A neuromuscular junction is a synapse between a motor neuron axon and a muscle fiber
Release of acetylcholine causes the muscle to contract
Movement requires the alternation contraction of opposing sets of muscles called antagonistic muscles
Acetylcholine always excited skeletal muscles to contract
A flexor muscle is one that flexes or raises an appendage
An extensor muscle is one that extends an appendage or straightens it
Fast and Slow Muscles
Skeletal muscle types range from:
-Fast-twitch: fibers produce fast contractions but fatigue rapidly
-Slow-twitch: fibers produce less vigorous contraction without fatigue
People have varying percentages of fast-twitch and slow-twitch muscles
Slow-twitch fibers are aerobic and require oxygen during movement and therefore do not fatigue
-Nonstrenuous activities utilize slow-twitch and intermediate fibers
Fast-twitch fibers are anaerobic and use reactions that do not require oxygen, resulting in fatigue
-Behaviors requiring quick movements utilize fast-twitch fibers
Muscle Control by Proprioceptors
Proprioceptors: receptors that detect the position or movement of a part of the body
Muscle spindles are proprioceptors parallel to the muscle that respond to a stretch: cause a contraction of the muscle
A stretch reflex occurs when muscle proprioceptors detect the stretch and tension of a muscle and send messages to the spinal cord to contract it
The Golgi tendon organ is another type of proprioceptor that responds to increases in muscle tension
Located in the tendons at the opposite ends of the muscle
Acts as a “brake” against excessively vigorous contraction by sending an impulse to the spinal cord where motor neurons are inhibited
Units of Movement
Movements include speaking, walking, threading a needle, and throwing a basketball while of balance and evading two defenders
Different kinds of movement needs different kinds of control by the nervous system
Voluntary and Involuntary Movements
Reflexes are involuntary, consistent, and automatic responses to stimuli
Most movements are a combination of voluntary and involuntary; reflexive and nonreflexive
Movements vary with respect to feedback
Some are ballistic and cannot be changed once initiated
Others are guided by feedback
Sequences of Behaviors
Many behaviors consist of rapid sequences of individual movements
Central pattern generators are neural mechanisms in the spinal cord or elsewhere that generate rhythmic patterns of motor output
-Example: wing flapping in birds or “wet dog shake”
A motor program refers to a foxed sequence of movements that is either learned or built into the nervous system
Once begun, the sequence is fixed from beginning to end
Automatic in the sense that thinking or talking about it interferes with the action
Examples: mouse grooming itself; yawning
Module 7.2 Brain Mechanisms of Movement
Introduction
Understanding how the brain controls movement offers hope for spinal cord damage or limb amputations
However, the technology has limitation
-Electrodes implanted into the brain can drift out of position and damage neurons
The Cerebral Cortex
The primary motor cortex is located in the precentral gyrus located in the frontal lobe
Axons from the precentral gyrus connect to the brainstem and the spinal cord, which generate impulses that control the muscles
Cerebral cortex is additionally involved in complex movements
Planning a Movement
Specific areas of the primary motor cortex are responsible for control of specific areas of the opposite side of the body
-Some overlap does exist
The primary motor cortex is active when people intend a movement
The primary motor cortex “orders” an outcome
Other areas near the primary motor cortex also contribute to movement
Posterior parietal cortex: keeps track of the position of the body relative to the world
Damage to this area causes difficulty in coordinating visual stimuli with movement
Important for planning
Other Areas for Planning a Movement
Supplementary motor cortex
-Organizes rapid sequence of movements in a specific order; inhibitory if necessary
-Active seconds before the movement
-Active following an error in movement so you can inhibit the incorrect movement the next time
Premotor cortex
-Active during preparation for movement
-Receive information about a target
-Integrates information about position and posture of the body; organizes the direction of the movement in space
Prefrontal cortex
-Active during a delay before movement
-Stores sensory information relative to a movement
-Necessary for you to consider the probable outcomes of a movement
Inhibiting of Movements
Antisaccade task: inhibits a saccade, a voluntary eye movement from one target to another
Performing this task well requires sustained activity in parts of the prefrontal cortex and basal ganglia before seeing the moving stimulus
Ability to perform this task matures through adolescence
Performance declines in old age and as a result of schizophrenia, attention-deficit disorder, or alcohol intoxication
Mirror Neurons
Neurons that are active during both preparation of a movement and while watching someone else perform the same or similar movement
-May be important for understanding, identifying, and imitating other people
-May be involved in social behaviors
-Unknown whether they cause or result from social behavior
From the Brain to the Spinal Cord
Messages from the brain must reach the medulla and the spinal cord to control the muscles
Corticospinal tracts are paths from the cerebral cortex to the spinal cord
Two such tracts:
Lateral corticospinal tract
-Extends from the primary motor cortex, nearby areas of the cortex, and the red nucleus
Medial corticospinal tract
-Extends from many areas of the cerebral cortex, as well as from several areas of the midbrain and medulla
The Cerebellum
A structure in the brain often associated with balance and coordination
-More neurons in the cerebellum than in all other brain areas combined
Damage to the cerebellum causes trouble with rapid movements requiring aim/timing
-Examples: clapping hands, speaking, writing, and so on
Important for the establishment of new motor program that allow the execution of a sequence of actions as a whole, for example tasks that require timing
Also critical for certain aspects aspects of attention, such as the ability to shift attention and attend to visual stimuli
The symptoms of cerebellar damage resemble those of alcohol intoxication: clumsiness, slurred speech, and inaccurate eye movements
-Finger to nose test
Cellular Organization of the Cerebellum
The cerebellum receives input from the spinal cord, from each of the sensory systems and the cerebral cortex, and sends it to the cerebellar cortex
The cerebellar cortex is the surface of the cerebellum
Cerebellar cortex neurons are arranged in precise geometrical patterns that provide outputs of well-controlled duration
-Purkinje cells: flat parallel cells in sequential planes
-Parallel fibers: axons parallel to one another; perpendicular to planes of Purkinje cells
The greater the number of excited Purkinje cells, the greater their collective duration of response
Parallel fibers excite Purkinje cells
Purkinje cells transmits inhibitory messages to the cells in the nuclei of the cerebellum (clusters of cell bodies in the interior of the cerebellum) and the vestibular nuclei in the brain stem
Messages then sent to the midbrain and the thalamus
Functions Other than Movements
Responds to sensory information even in absence of movement
Responds strongly to violations of sensory information
-Example: reaching to touch something and not feeling it or feeling something when you don’t expect to feel it
Important for certain aspects of attention
The cerebellum contributes to many tasks that have little to do with one another
The Basal Ganglia
When axons initially reach their targets, they form synapses with several cells
Postsynaptic cells strengthen connection with some cells and eliminate connections with others
The formation or elimination of these connections depends on the pattern of input from incoming axons
Caudate nucleus and putamen receive input from the cerebral cortex and send output to the globus pallidus
Globus pallidus connects to the thalamus, which relays information to the motor areas and the prefrontal cortex
Basal ganglia select a movement to make by ceasing to inhibit it
That basal ganglia are particularly important for spontaneous, self-initiated behaviors
The basal ganglia are also critical for learning new habits
Conscious Decisions and Movement
The conscious decision to move, and the movement itself, occurs at two different times
A readiness potential is a particular type of activity on the motor cortex that occurs before any type of voluntary movement
-Begins at least 500 ms before the movement
-Implies that we become conscious of the decision to move after the process has already begun
Module 7.3 Movement Disorders
Introduction
Brain disorders, such as Parkinson’s disease and Huntington’s disease, not only affect movement but also impair mood, memory, and cognition
Parkinson’s Disease
A movement disorder characterized by muscle tremors, rigidity, slow movements, and difficult initiating physical and mental activity
-Associated with an impairment in initiating spontaneous movement in the absence of stimuli to guide the action
Many, but not all, Parkinson’s patients may experience depression, and many may have problems with attention, language, or memory
Causes of Parkinson’s
Caused by gradual and progressive deaths of neurons, especially in the substania nigra
-Substania nigra usually sends dopamine-releasing axons to the caudate nucleus and putamen
Loss of dopamine leads to less stimulation of the motor cortex and slower onset of movements
Studies suggest early-onset Parkinson’s has a genetic link
Genetic factors are only a small factor of late onset Parkinson’s disease (after 50)
Environmental influences such as exposure to toxins
-Insecticides, herbicides, certain drugs, and fungicides
Traumatic head injury
Cigarette smoking and coffee drinking are related to a decreased chance of developing Parkinson’s disease
Damaged mitochondria of cells seems to be common to most factors that increase the risk of Parkinson’s disease
L-Dopa Treatment
The drug L-dopa is the primary treatment for Parkinson’s and is a precursor to dopamine that easily crosses the blood-barrier
-They are more effective in some people than in others, probably because of variation in the intestinal bacteria that metabolize L-dopa before it can enter the blood
Does not prevent the continued loss of neurons
Enters other brain cells, producing unpleasant side effects
Non-pharmaceutical Therapies
Drugs that directly stimulate dopamine receptors, implanting electrodes to stimulate areas deep in the brain
Experimental strategies such as:
-transplanting brain tissue of aborted fetuses
-Implantation of stem cells that are programmed to produce large quantities of L-dopa
Huntington’s Disease
A neurological disorder characterized by various motor symptoms
-Affects 17 in 100,00 in the US
-Usually onset occurs between the ages of 30 and 50
Associated with gradual and extensive brain damage especially in the basal ganglia but also in the cerebral cortex
Initial motor symptoms include arm jerks and facial twitches
Motor symptoms progress to tremors and writhing that affect the persons walking, speech, and other voluntary movements
Also associated with other psychological disorders
-Depression, memory impairment, anxiety, hallucinations/delusions, poor judgment, alcoholism, drug abuse, sexual disorders
Heredity and Presymptomatic Testing
Huntington’s disease can be traced to a single gene
-The gene is an autosomal dominant gene
-As a rule, a mutant gene that causes the loss of a function is recessive
The fact that the huntington’s gene is dominant implies that it produces the gain of an undesirable function
A variety of neurological diseases are related to C-A-G repeats in genes
-For a variety of disorders, the earlier the onset, the greater the probability of a strong genetic influence
Identification of the gene for Huntington’s disease led to the discovery of the protein that codes it (huntingtin)
-Mutant form impairs neurons in the brain; future drug therapy may address huntingtin