Psych 111 - Chapter 3 - Neuroscience and Behaviour - Part II
By the end of this section you should be able to:
- Explain the function of neurons
- Outline the components of the neuron
- Differentiate the three major types of neurons by their function
Neurons: The Origin of Behaviour
- Neurons: cells in the nervous system that communicate w/ each other to perform information-processing tasks
Components of the neuron:
- Cell body (aka soma): coordinates the information-processing tasks; keeps the cell alive; contains a nucleus (houses chromosomes that house DNA); surrounded by a cell membrane that allows molecules to flow in and out of the cell
- Dendrites: receive information from other neurons and relay that information to the cell body
- Axon: carries information to other neurons, muscles, or glands
- Covered by a myelin sheath (insulating layer of fatty material); composed of glial cells
Glial cells (support cells)
- Digest parts of dead neurons
- Provide physical and nutritional support for neurons
- Form myelin to help axon carry information more efficiently
- Demyelination: deterioration of the myelin sheath; e.g.. multiple sclerosis
- Synapse
- Region/gap between the axon of one neuron and the dendrites or cell body of another
- Fundamental to communication between neurons
- Three major types of neurons:
- Sensory: receive information from external world and send this information to the brain via the spinal cord
Motor: carry signals from the spinal cord to the muscles to produce movement
- Interneurons: connect sensory neurons, motor neurons, or other interneurons; carry information and perform information-processing functions
- Specialized by location?
- Purkinje cells: interneuron; information from cerebellum to the rest of the brain and the spinal cord; bush-like dendrites
- Pyramidal cells: cerebral cortex; triangular cell body and single, long dendrite + other smaller dendrites
- Bipolar cells: sensory neuron found in the retinas of the eye; single axon + a single dendrite
The Electrochemical Actions of Neurons:
Information Processing
Learning Outcomes
By the end of this section you should be able to:
- Describe how an electric signal moves across a neuron Outline the steps in synaptic transmission Explain how drugs are able to mimic neurotransmitters
The Electrochemical Actions of Neurons
- Two stages:
- Conduction: movement of an electrical signal within neurons: dendrites -> cell body -> axon
- Transmission: movement of a signal from one neuron to another as a result of chemical signalling across the synapse
- Two stage process = electro/chemical action of neurons
- Conduction
- Cell membrane has small pores (channels) that allow small electrically charged molecules (ions) to flow in and out of the cell
- lons can carry + or - charge
- lons move from high to low [ ]
- K* = potassium; Na* = sodium; CI = chlorine
- But how?
- Resting potential: difference in electric charge between the inside and outside of a neuron's cell membrane; about -70 millivolts
- At rest = high [] of positively charged ions (K*) and negatively charged protein ions (A) inside and high [] of positively charged ions (Na*) and negatively charged ion (CI) outside the neuron's cell membrane
- Builds potential energy that can be released as a electrical impulse
- Action potential
- Electric signal conducted along the length of a neuron's axon to a synapse (+40 millivolts)
- All or none response where electrical stimulation has to be at or above the threshold
- Occurs with same magnitude regardless of whether stimulation is at or above threshold
- Occurs because of a change in the state of the membrane channels
Why does an AP occur?
- When electrical charge reaches threshold level, sodium-specific channels open and Na* ions rush in; this raises the charge of the inside membrane from (-) to (+): up to +40 millivolts
What happens after an AP?
- Sodium channels become inactive (refractory period: the time in which a new AP cannot be initiated)
- Potassium-specific channels open causing K+ ions inside to leave the cell; returns electrical charge back to a negative state (then channels close)
- Pump helps rebalance of ions to -70 millivolts
Saltatory conduction: electric current passing down the length of a myelinated axon
- Myelin facilitates conduction and clumps around the axon with breaks (nodes of Ranvier)
- Charge jumps node to node
- Steps in synaptic transmission
- AP travels down the axon to stimulate release of NTs from vesicles of presynaptic neurons
- NTs are released into the synapse
- Bind w/ receptor sites on a dendrite of postsynaptic neuron; initiates a new AP
- NTs are cleared from the synapse either by reuptake into the presynaptic neuron OR
- Being broken down by enzymes in synapse OR
- Binding to autoreceptors on the presynaptic neuron
- How do NTs know where to go?
- Neurons form pathways in the brain that are characterized by specific neurotransmitters; certain neurotransmitters are found in certain parts of the brain
- Lock-and-key mechanism: certain neurotransmitters bind to specific receptor sites (based on molecular structure)
- Transmission between neurons
- Terminal buttons: knoblike structures at the end of an axon and are filled with vesicles containing neurotransmitters (NTs)
- Neurotransmitters: chemicals that transmit information across the synapse to a receiving neuron's dendrites
- Receptors: parts of the cell membrane that receive neurotransmitters and either initiate or prevent a new electrical signal
- How do NTs leave the synapse?
- Reuptake: NTs are absorbed by the terminal buttons of the presynaptic neuron's axon or neighbouring glial cells
- Enzyme deactivation: NTs are destroyed by enzymes in the synapse; break down NTs
- Diffuslon: NTs drift out of the synapse and can no longer reach receptors
- Autoreceptors: NTs can bind to receptor sites on presynaptic neurons; release signal to stop releasing NTs if there is excess
- Types and Functions of NTs
- Acetylcholine (ACh): voluntary motor control; regulation of attention, learning, sleeping, dreaming, memory; deterioration = Alzheimer's
- Dopamine: regulates motor behaviour, motivation, pleasure, emotional arousal; role in drug addiction; high levels = schizophrenia; low
'levels = Parkinson's
- Serotonin: mood and arousal; regulation of sleep and wakefulness, eating, aggressive behaviour; low levels = mood disorders
- Endorphins: act within pain pathways and emotion centers; dulls experience of pain and elevates mood; e.g., runner's high
o L-dopa: when modified, produces dopamine;
ingestion causes neurons to produce more dopamine; agonist for dopamine (Parkinson's)
o Amphetamines: stimulates release and prevents reuptake of norepinephrine and dopamine; excess NTs flood the synapse which increases the activation of the receptors;
agonist
- Glutamate: excitatory NT; enhances transmission of info btwn neurons; too much = seizures
- GABA: inhibitory NT; stops firing of neurons; too little = seizures
- Norepinephrine: mood and arousal; states of vigilance and awareness of dangers; low levels = mood disorders
How do drugs mimic neurotransmitters?
- Can alter the production or release of NTs
Can bind to a neuron's receptor
- Types:
- Agonists: increase the action of a NT; binds to a receptor and activates the NT
- Antagonists: diminish the function of a NT; prevents the NT from acting or lessens its effect
o Oplolds: agonists for endorphins; feelings of calm and euphoria; highly effective antagonists that decrease the release of NTs involved in the perception of pain; reduces sensitivity to carbon
dioxide levels in the blood = depresses
breathing
o Naloxone: opioid; antagonist as it binds to opioid receptors blocking agonists (heroin) from effecting neurons
o Prozac: blocks reuptake of serotonin - SSRIs; keeps serotonin in synapse longer to activate more receptors to improve mood; agonist for serotonin (depression)
o Propranolol: beta blockers; blocks receptor sites for norepinephrine in the heart; antagonist for NE as it prevents NE from binding to receptors which slows down the heart; antianxiety, antidepressive
Neurons are the building blocks that form nerves
Nerves: bundles of axons and the glial cells that support them
- Nervous system: interacting network of neurons that convey electrochemical information throughout the body
The Organization of the Nervous System
Learning Outcomes
By the end of this section you should be able to:
- Differentiate the functions of the central and peripheral nervous systems
- Understand the nature of the reflex arc
- Demonstrate the hierarchical structure of the central nervous system
_Divisions of the nervous system
- Central nervous system (CNS): brain and spinal cord; receives sensory info from external world, and processes/coordinates info to send commands to the skeletal and muscular systems
- Peripheral nervous system (PNS): connects CNS to the body's organs and muscles; divided into somatic nervous system and autonomic nervous system
- PNS
- Somatic nervous system: set of nerves that convey information between voluntary muscles and the CNS
- Autonomic nervous system: set of nerves that carry involuntary and automatic commands that control blood vessels, body organs, and glands; divided into sympathetic and parasympathetic nervous system
- Subdivisions of ANS
- Sympathetic nervous system: nerves that prepare body for action in challenging or threating situations; fight or flight
- Parasympathetic nervous system: helps body return to resting state; rest and digest
- Components of the CNS
- Brain and spinal cord
- Spinal reflexes: pathways in the nervous system that generate muscle contractions
- Reflex arc: neural pathway that controls reflex actions (e.g., interneurons relay sensory inputs to motor neurons that connect to arm muscles which direct you to retract your hand off a hot stove)
- Location of spinal cord injury = extent of abilities lost; the higher up the injury the worse
Structure of the Brain
Learning Outcomes
By the end of this section you should be able to:
- Differentiate the functions of the major divisions of the brain
- Explain the functions of the cerebral cortex according to organization across hemispheres. within hemispheres, and within specific lobes
Structure of the Brain
Bottom to top approach: higher the level - more complex the function
- Side by side approach: one half of the brain specializes in tasks the other half doesn't
- Identify the causes and consequences of brain plasticity
- Explain the progression of the human brain's evolution
Divisions of the brain
Hindbrain: coordinates information coming into and out of the spinal cord; controls basic functions of life
- Medulla: coordinates heart rate, circulation, respiration
- Reticular formation: cluster of neurons; regulates sleep, wakefulness, levels of arousal
- Cerebellum: "little brain"; controls fine motor skills
- Pons: "bridge"; relays information from cerebellum to the rest of the brain
Across hemispheres
- Divided into left/right hemispheres
- Each hemisphere controls the function of opposite side of the body (contralateral control)
- Corpus callosum: connects two hemispheres and supports communication across hemispheres
- Within hemispheres
- Each hemisphere is divided into four lobes: parietal, temporal, occipital, frontal
- Cerebral cortex: responsible for perception, emotion, movement, and thought
- Gyri: smooth surfaces of cortex
- Sulci: indentations or fissures
Three levels of functioning:
- Across hemispheres
- Within hemispheres
- Within specific lobes
- Occipital lobe: back of the cerebral cortex;
- processes visual information
- Parietal lobe: front of the occipital lobe; processes information about touch; includes somatosensory and motor cortices (strip of brain tissue from top of brain down to the sides)
- Represents skins areas on contralateral surface of the body; more sensitive the area the bigger the portion of the cortex dedicated to it
- Temporal lobe: lower side of each hemisphere; hearing and language; primary auditory cortex (frequencies of sounds); visual association and interpretation areas
- Frontal lobe: behind forehead; specialized areas for movement, abstract thinking, planning, memory, judgment; contains the motor cortex (coordinates muscle movements)
Midbrain: orientation and movement; central location for NTs involved in arousal, mood, and motivation
- Tectum: orients an organism in the environment; receives stimulus input and moves organism in coordinated way toward the stimulus
" Tegmentum: movement and arousal; helps to orient an organism toward sensory stimuli
Subcortical (beneath cortex) structures:
- Thalamus: relays and filters information from the senses and transmits info to the cerebral cortex; controls incoming sensations (especially during sleep!)
- Basal ganglia: set of structures that direct intentional movements; striatum controls posture and movement
Forebrain: controls complex cognitive, emotional, sensory, and motor functions
" Cerebral cortex: outermost layer of the brain;
divided into two hemispheres
- Subcortical structures: areas in forebrain near the center of the brain
Hypothalamus: part of limbic system; regulates body temperature, hunger, thirst, and sexual behaviour
- Hippocampus: part of limbic system; creates new memories and integrates them for long-term storage
- Amygdala: part of limbic system; central role in emotional processes; attaching emotional significance especially fear, punishment, and reward
- Endocrine System
- Network of glands that produce/secrete into the bloodstream chemical messages (hormones); influence metabolism, growth, sexual development
- Includes: thyroid (body temp/HR); adrenals (stress); pancreas (digestion); pineal gland (sleep/wake cycle) and…
- Pituitary: master gland; releases hormones to direct the function of other glands
" Brain plasticity
- Ability for brain to be molded
- Functions assigned to certain areas of the brain can be reassigned to accommodate changing input form the environment
- E.g., phantom limb syndrome
Evolutionary development
- Invertebrates = those w/o a spinal column
- Vertebrates = those w/ a spinal column; hierarchy of CNS: higher levels = more complex functions
- Is it genetics (nature) or environment (nurture)
- that directs a person's behaviour?
- Within specific lobes
- Assoclation areas: composed of neurons that help provide sense and meaning to information registered in the cortex
- Mirror neurons: active when an animal performs or observes a behaviour being performed; found in frontal lobe and parietal lobe
The Adaptive Brain: Evolution Discussion
- Prenatal development
- How the nervous system develops/changes within each member of a species
- Evolutionary development How the nervous system in humans evolved and adapted from other species
Genes, Epigenetics, and the Environment Learning Outcomes
By the end of this section you should be able to:
Outline the structure of a gene
- Differentiate between monozygotic and dizygotic twins
- Explain how epigenetic influences work
- Give examples of the influence of genetics and the environment to human behaviour
- Monozygotic twins: identical twins; splitting of a single fertilized egg; share 100% of genes
- Dizygotic twins: fraternal twins; two separate fertilized eggs; share 50% of genes
- Twin studies can help researchers understand the role of genetics and environment on behaviour
- DNA methylation: adding a methyl group to
DNA; special enzymes (epigenetic writers) add a methyl group which switches off methylated gene to prevent expression
- Histone modification: adding chemical modifications to proteins (aka histones) involved in packaging DNA; influence gene expression w/o altering DNA
- Genes: unit of heredity transmission; sections on a strand of DNA that code for the protein molecules that affect traits; organized into large threads (chromosomes) Chromosomes: strands of DNA wound around each other in a double-helix configuration; 23 pairs; e.g., XX (female), XY (male) Degree of relatedness: probability of sharing genes
- Epigenetics: study of environmental influences that determine whether or not genes are expressed or the degree to which they are expressed, w/o altering the basic DNA sequences that constitute the genes themselves
- Epigenetic marks: chemical modifications to DNA that turn genes on or off; two main types
Heritability: measure of the variability of behavioural traits among individuals that can be accounted for by genetics; range of 0 to
1.00 (1.00 = genes are 100% responsible for
individual differences)
" BUT, remember heritability is a(n):
- Abstract concept - tells us nothing about specific genes that contribute to a trait
- Population concept - tells us nothing about an individual specifically
- Dependent on the environment
- Not fate - behaviours can be modified
Investigating the Brain
Learning Outcomes
By the end of this section you should be able to:
- Identify the three main ways that researchers study the human brain
- Compare and contrast advantages and disadvantages of techniques used to study the brain in action
Studying damaged brains
- E.g., Phineas Gage
- Split-brain procedures (consequences?)
- Relating specific psychological and behavioural disruptions to damage helps better understand how the brain area normally functions
" Studying brain's electrical activity
- Electroencephalograph (EEG); records electrical activity in the brain
- Electrodes placed on the head amplify electrical signals of synapses/APs to produce a visual record of electric activity
- Used to record brain activity during different states of consciousness
- Types of brain imaging
- Neuroimaging: advanced technology used to create images of the brain
- Structural imaging: basic structure of the brain; used to find abnormalities (CT scan, MRI, DTI)
- Functional imaging: activity of the brain when performing tasks (PET, fMRI, resting state functional connectivity)
- Brain injuries: transcranial magnetic stimulation
- Brain imaging to study brain structure
- CT scan: scanner rotates a device around a person's head that takes x-ray photos at different angles; shows densities of tissue in the brain; tumours are less dense than cortex (appear darker)
- MRI: uses a strong magnetic field to line up the nuclei of specific molecules in the brain tissue; pulses of radio waves cause nuclei to rotate out of alignment; mesures energy given off by nuclei when they snap back into alignment; reveals localization of damage but not extent of damage
- DTI: special type of MRI; used to visualize white matter pathways (connections btwn brain regions); mesures the rate and direction of diffusion of water molecules; assesses the integrity of a white matter pathway
- Brain imaging to study brain function
- PET: radioactive substance injected into the bloodstream; brain is scanned by radiation detectors to determine energy/ blood flow (level of activity) while performing tasks; more radiation = more activity
- fMRI: detects difference between oxygenated and deoxygenated hemoglobin when exposed to magnetic pulses; active neurons require more blood/oxygen; tells us about levels of activation
- Resting state functional connectivity: same fMRI task but at rest; measures the extent to which spontaneous brain activity is correlated over time; higher the correlation, the greater the functional connection
- Mimicking brain damage
- TMS: magnetic pulse passes through the skull and temporarily deactivates neurons in the cerebral cortex
- Can direct TMS pulses to certain brain regions (i.e., turning them off) and measure temporary changes in perception, thought, memory, speech, emotion etc.