Nervous system Flashcards

(60 cards)

1
Q

What are the CNS, PNS and neurotransmitters?

A

Central Nervous System (CNS)- brain and spinal cord.
Peripheral Nervous System (PNS)- composed of nerves that connect the brain or spinal cord with muscles, glands, and sense organs.

The neuron is the basic cell type of both systems (10% of CNS).

Neurotransmitters are chemical messengers released from neurons in response to electrical signals (dopamine, adrenaline, noradrenaline, serotonin, gaba, endorphins, acetylcholine, glutamate).

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2
Q

What makes up neuron?

A

Cell body (soma): contains a nucleus and ribosomes for protein synthesis

Dendrites: branched outgrowths that receive inputs

Dendritic spines: knob-like outgrowths increase the surface area, contain ribosomes

Axon (nerve fibre): a long process extending from the soma that carries output to target cells

Initial segment: ‘trigger zone’

Axon collateral: signal can go sideways

Axon terminal: end of the branch

Varicosities: bulging areas where signal can be released

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3
Q

What are the differences between CNS and PNS?

A

Neurons are wrapped in myelin (20-200 layers of modified plasma membrane) which speed up transduction signalling. They’re made by oligodendrocytes in the CNS and Schwann cells in the PNS.

Axonal transport- organelles must move >1m between the soma and axon terminals.

Anterograde movement- Kinesins: from cell body to axon terminals.

Retrograde movement- Dyneins: axon terminals to cell body.

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4
Q

What are the 3 functional classes of neurons?

A

Afferent neurons- convey information from tissues/organs towards the CNS

Efferent neurons- convey information away from CNS to effector cells

Interneurons- convey information within the CNS (most neurons)

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5
Q

What are nerves and a synapse?

A

Nerves- groups of afferent and efferent neurons together with connective tissue and blood vessels

Synapse- the anatomically specialised junction between neurons

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6
Q

What are glial cells and its components?

A

They surround the soma, axon, dendrites and provide physical and metabolic support.

Astrocyte- regulate extracellular fluid by removing potassium and neurotransmitters. They stimulate epithelial cells to form tight junctions: blood brain barrier.

Microglial cells- specialised macrophage-like cells (remove pathogens, dead/damaged neurons).

Ependymal cells- in fluid filled cavities, regulate flow of cerebrospinal fluid.

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7
Q

What is an axon, a pathway, a commissure, a ganglia, a nuclei and a nerve?

A

Axon- long extension from a single neuron.
A pathway- a group of axons traveling together in the CNS.
A commissure- if the group of axons links the right and left halves of the CNS.
Ganglia- the cell bodies of neurons with similar functions in the PNS.
Nuclei- the cell bodies of neurons with similar functions in the CNS.
Nerve- a group of many axons travelling together to and from the same general location in the peripheral nervous system. (None in the CNS)

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8
Q

What 4 regions make up the brain?

A

The anterior part of the long tube (formed from the CNS) folds to create 4 regions. The brain contains 4 interconnected cavities which are filled with cerebrospinal fluid: cerebral ventricles.

Frontal lobe- good/bad actions, project future

Parietal lobe- sensory, motor, language

Occipital lobe- sight

Temporal lobe- long term memory, process sensory info

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9
Q

What is the part of the forebrain: the cerebrum?

A

It consists of the right and left cerebral hemispheres which consist of the cerebral cortex (an outer shell of grey matter); the inner cerebral cortex is a layer of white matter (mostly myelinated fibre tracts).

Within the grey matter are subcortical nuclei: important for movement. Each cortex area is separated by a deep longitudinal division but connected by a massive bundle of nerve fibres (corpus callosum). Folding gives the brain ridges (gyri) and grooves (sulci).

Cerebral cortex:
Basic afferent information is processed into meaningful perceptual images.
Control over the systems that govern the movement of the skeletal muscles is refined.

Cells of the cerebral cortex:
Pyramidal cells- major output, excitation.
Non-pyramidal cells- major input cells, receive signals.

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10
Q

What is the part of the forebrain: the diencephalon and what does it contain?

A

Thalamus- a collection of several large nuclei, role in general arousal, controlling movement/posture, focusing attention.

Hypothalamus- 1% of brain mass, homeostatic regulation of internal environment.
The master command centre for neural and endocrine coordination controlling: Behaviours to do with preservation of the individual (eating/drinking) and the species (reproduction).
It’s connected by a stalk to pituitary gland (controls several other hormone glands in your body, e.g. thyroid, adrenals, ovaries, testicles) which is regulated by the hypothalamus.

Epithalamus- controls biological rhythms (via pineal gland which produces melatonin).

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11
Q

What is the cerebellum?

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Doesn’t initiate voluntary movements: an important centre for coordinating movements and for controlling posture and balance. It receives information from the muscles, joints, skin, eyes, ears and parts of the brain involved in control of movement.

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12
Q

What is the brainstem?

A

Contains the reticular formation, essential for life: Midbrain, Pons, Medulla Oblongata. It receives and integrates input from all regions of the CNS and is involved with motor functions, cardiovascular and respiratory control, swallowing, regulates sleep, wakefulness and attention, eye movement.

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13
Q

How are the CNS and PNS supported/protected?

A

Bones support and protect the CNS (cranium) and PNS (vertebrae).

Meninges are membranes that line the structures and add additional support and protections: Dura mater, Arachnoid mater, Pia mater.

Meninges jobs:
Cover and protect CNS.
Protect blood vessels and enclose the venous sinuses.
Contain cerebrospinal fluid.
Form partitions in the skull.

Blood brain barrier- a protective mechanism that helps maintain a stable environment for the brain. Capillaries are the least permeable in the body (very selective barrier). Things that are highly lipid-soluble cross easily.

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14
Q

What is the spinal cord?

A

The Spinal cord is within the bony vertebral column and is a slender cylinder of soft tissue.

Some groups of fibre tracts run longitudinally through the cord: some descend to relay information from the brain; others ascend to transmit information to the brain.

Afferent fibres arrive at the spinal cord from the peripheral nerves enter via the dorsal roots. Efferent fibres exit the spinal cord via the ventral roots. Dorsal and ventral roots from same level form a spinal nerve.

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15
Q

What is the difference between grey and white matter?

A

Grey matter projecting toward the back of the body are dorsal horns. Those orientated toward the front are ventral horns. Grey matter is composed of:

Interneurons.
Cell bodies and dendrites of efferent neurons.
Entering axons of afferent neurons.
Glial cells.

White matter surrounds grey matter and consists of groups of myelinated axons.

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16
Q

How many nerves are in the PNS?

A

43 pairs of nerves, 12 pairs of cranial nerves, 31 pairs of spinal nerves (designated by the vertebral levels from which they exit):

Cervical (8)- control muscles, glands; sensory input- neck, shoulders, arms, hands

Thoracic (12)- associated with the chest and upper abdomen

Lumbar (5)- associated with the lower abdomen, hips, legs

Sacral (5)- associated with the genitals, lower digestive tract

Coccygeal (1)- associated with the tail bone

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17
Q

What is efferent division of the PNS subdivided into?

A

Peripheral nerves can contain nerve fibres that are the axons of efferent neurons, afferent neurons, or both. Efferent neurons carry signals out from the CNS to muscles/glands.

The efferent division of the PNS is subdivided into:
Somatic nervous system- consists of one neuron between CNS and skeletal muscle cells, innervates skeletal muscle, can lead only to muscle excitation.
Autonomic nervous system- has two-neuron chain between CNS and effector organ, innervates smooth and cardiac muscle, glands and GI neurons, can be either excitatory or inhibitory.

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18
Q

What is the autonomic nervous system?

A

The efferent innervation of tissues other than skeletal muscle is by way of the autonomic nervous system. The gastrointestinal tract: enteric nervous system, a subdivision of the autonomic nervous system.

In the sympathetic autonomic nervous system, 80% secretion of Epinephrine, 20% secretion of Norepinephrine. One set of ganglionic neurons form a gland: the adrenal medulla, the nervous system interacting with the endocrine system.

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19
Q

What is the difference between sympathetic and parasympathetic autonomic nervous system?

A

Sympathetic- neurons leave CNS from thoracic and lumbar regions, ganglia are close to spinal cord. Tends to respond as a single unit. Sympathetic system increases activity under physical or psychological stress- fight or flight response.

Parasympathetic- neurons leave CNS from brainstem and sacral region, ganglia within or close to organs they innervate. Tends to activate specific organs in a pattern finely tailored to each physiological situation. Rest or digest: homeostatic processes are predominant.

Some tissues/organs are innervated by both sympathetic and parasympathetic nervous systems: dual innervation. Activating one division usually has the opposite effect to activating the other division. Two divisions activated reciprocally: activity of one increases, activity of the other decreases.

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20
Q

What is membrane potential and what does the magnitude of resting membrane potential depend on?

A

All cells under resting conditions have a potential difference across their membranes. The inside is negatively charged with respect to the outside; extracellular fluid is assigned a voltage of zero. The excess charge inside is what is called the membrane potential.

Magnitude of resting membrane potential depends on:
Differences in specific ion concentrations.
Differences in membrane permeability for the different ions.

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21
Q

What happens if a membrane contains K+ channels but no Na+ or Cl- channels?

A

No ion movement as channels are closed. No potential difference due to equal numbers of + and – ions.
Ions are different (Na+ vs K+) but charges are equal

K+ channels open so K+ diffuses down the concentration gradient. As Na+ can’t diffuse, compartment 1 has a net + charge. Compartment 2 gains a net – charge

Compartment 2 become more -.

As compartment 2 is more – then K+ is attracted back into compartment 2.

Eventually the membrane potential generates an equal flux of K+. This equilibrium potential for K+ results in a difference in electrical charge which can be measured in mV.

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22
Q

What is depolarisation, repolarisation and hyperpolarisation?

A

Neurons process and transmit information from transient changes in the membrane potential from its resting level produce electrical signals.

Depolarisation is the potential moving resting membrane potential to less negative values.

Repolarisation is the potential moving back to resting membrane potential.

Hyperpolarisation is the potential moving away from resting membrane potential in a more negative direction.

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23
Q

What are graded potentials?

A

Changes in membrane potential that are confined to a relatively small region of the plasma membrane, they signal over short distances. They’re given names related to the location of the potential or function they perform (receptor potential, synaptic potential, pacemaker potential).

A small region of the membrane has been depolarised by the transient application of a chemical signal. Membrane cation channels open and produce a membrane potential that’s less negative than adjacent areas. Different stimulus intensities result in different degrees of depolarisation.

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24
Q

How do graded potentials work?

A

The magnitude of the potential change can vary (is graded), therefore graded potentials.

Depending on the initiating event, graded potentials can depolarise or hyperpolarise.
The magnitude of the change in membrane potential is related to the magnitude of the stimulus.
Charge is lost across the membrane because the membrane is permeable to ions through open membrane channels.

Membranes are so ‘leaky’ to ions that electrical currents die out- decremental

Additional stimuli can be added- summation

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25
What are action potentials?
Large alterations in membrane potential, e.g. a change of 100mV. This change is an ‘all or nothing’ response. Action potentials are very rapid and may repeat at frequencies of several hundred per second. The ability to generate action potential is excitability, possessed by neurons, muscles cells and some others. Action potential signal over long distances.
26
How do different channels interact with an action potential?
Ligand-gated channels and mechanically gated channels often serve as the initial stimulus for an action potential. Voltage-gated channels give a membrane the ability to undergo action potentials by allowing the rapid depolarisation and repolarisation. Many voltage-gated ion channels vary by the ion and how they behave as the membrane voltage changes. Similarity- Na+ and K+ have charged amino acid residues allowing a change in shape in response to membrane potential. Difference- Na+ are much faster to respond and have an ‘inactivation gate’.
27
What is the action potential mechanism?
Resting membrane potential close to K+ equilibrium as normal K+ channels are leaky. Action potential begins when a stimulus binds to a specific ion channel, allowing Na+ to enter. Other Na+ channels stimulated to open by the depolarisation- positive feedback. Na+ channels become inactivated and K+ channels now open with a delayed effect halting depolarisation. K+ fluxes out of the cell rapidly repolarising the membrane. The return of resting membrane potential closes Na+ channels, but the sluggish K+ results in hyperpolarisation. As K+ channels close, resting membrane potential returns.
28
What are threshold and subthreshold potentials/stimuli?
Not all membrane depolarisations in excitable cells trigger the positive feedback relationship leading to an action potential. The initial stimulus and the current through the Na+ channels must be sufficient to elevate the membrane potential beyond the threshold potential. Stimuli that are just strong enough to depolarise the membrane to this level are threshold stimuli. The threshold of most excitable membranes is 15mV less negative than the resting membrane potential. Weak polarisations- subthreshold potentials, caused by subthreshold stimuli.
29
What is an absolute refractory period?
Refractory periods limit the number of action potentials an excitable membrane can produce in each period. They also contribute to the separation of these action potentials so that electrical signals pass down the axon. Two types of refractory periods that cells undergo following an action potential: Absolute and Relative. A second stimulus will never produce a second action potential if one is already happening, that region of the membrane is in its absolute refractory period, occurring when the voltage-gated Na+ channels are already open or have proceeded to the inactivated state during the first action potential.
30
What is a relative refractory period?
After the absolute refractory period, an interval allows a second action potential to be produced, if the strength is much greater than usual- this is the relative refractory period. Some voltage-gated Na+ channels will have returned to a resting state; the magnitude of the action potential is temporarily reduced and some K+ channels that repolarised the membrane are still open. During the relative refractory period, a new stimulus can depolarise the membrane above the threshold potential, if the stimulus is large in magnitude or outlasts the relative refractory period.
31
What is action potential propagation?
New action potentials produce local currents of its own that depolarise the region adjacent to it, producing another action potential at the next site, causing action potential propagation along the length of the membrane. There is a sequential opening and closing of Na+ and K+ channels. The action potential doesn’t move but ‘sets off’ a new action potential in the region of the axon just ahead of it. The end of the membrane is virtually identical in form to the initial one, so they don’t decrease in magnitude with distance.
32
Why can action potentials only travel in one direction?
Action potentials in neurons are unidirectional (can only go forward down the axon, as the space behind is in its refractory period). If the membrane through which the action potential travels is not refractory, excitable membranes can conduct action potentials in either direction. In most neurons, action potentials are initiated at one end of the cell and propagate toward the other end. The larger the fibre diameter, the faster the action potential propagates, larger fibres offer less internal resistance to local current.
33
What is myelin and the nodes of Ranvier?
Myelin is an insulator that makes it harder for charge to flow between intracellular and extracellular fluid compartments. As there’s less leakage of charge across the myelin, a local current can spread farther along an axon. Action potentials occur only at the nodes of Ranvier, where the myelin coating is interrupted and the concentration of voltage-gated Na+ channels is high.
34
What is saltatory conduction?
Action potentials jump from one node to the next as they propagate along a myelinated fibre; an action potential is regenerated at each node. Saltatory conduction is faster than propagation in non-myelinated fibres of the same axon diameter: less charge leakage, membrane pumps need to restore fewer ions.
35
What are the key points of a graded potential?
Amplitude varies with size of the initiating event. Can be summed. Has no threshold. Has no refractory period. Is conducted decrementally- amplitude decreases with distance. Duration varies with initiating conditions. Can be a depolarisation or a hyperpolarisation. Initiated by receptor, synapse, or randomly. Mechanism depends on ligand-gated channels or other changes.
36
What are the key points of an action potential
All-or-none. Cannot be summed. Has a threshold (15mV) depolarised relative to the resting potential. Has a refractory period. Depolarisation is amplified to a constant value at each point along the membrane. Duration is constant under constant conditions. Only depolarisation. Initiated by graded potential. Mechanism depends on voltage-gated channels.
37
What are chemical messengers: neurotransmitters and neuromodulators?
Certain chemical messengers elicit complex responses that can’t be described as ESPSs or IPSPs. Modulation is used for these complex responses and the messengers that cause them are neuromodulators. Certain neuromodulators are co-released with the neurotransmitter. Many messengers used by the immune system serve as neuromodulators. Receptors for neurotransmitters influence ion channels that directly affect excitation or inhibition of the post-synaptic cell. Receptors for neuromodulators more often bring about changes in metabolic processes in neurons via G-proteins coupled to second-messenger systems. Neurotransmitters are involved in rapid communication. Neuromodulators are associated with slower events (learning, development states).
38
What are the neurotransmitters: Acetylcholine and Biogenic Amines?
Acetylcholine (ACh)- neurons that release it are cholinergic neurons. It’s synthesised from chlorine and acetyl coenzyme A. It’s concentration at the postsynaptic membrane decreases due to the action of enzyme acetylcholinesterase, which destroys ACh, releasing choline and acetate. The two types of ACh receptors are Nicotinic Acetylcholine Receptors and Muscarinic Acetylcholine Receptors. Biogenic Amines- small, charged molecules that are synthesised from amino acids and contain an amino group. These include: Catecholamines (dopamine, norepinephrine, epinephrine), Serotonin and Histamine.
39
What are the neurotransmitters: Amino acid neurotransmitters and Neuropeptides?
Amino Acid Neurotransmitters- the most prevalent neurotransmitter in the CNS. The most common excitatory amino acid is glutamate. GABA is the major inhibitory neurotransmitter in the brain, it’s a modified form of glutamate. Neuropeptides- composed of two or more amino acids linked together by peptide bonds. Many function as hormones or paracrine substances. They’re derived from larger precursor proteins. Neurons that release one or more of the peptide neurotransmitters are called peptidergic. Often, neuropeptides are co-secreted with another neurotransmitter and act as neuromodulators.
40
What are the neurotransmitters: Gases and Purines?
Gases- nitric oxide, carbon monoxide and hydrogen sulphide are emitted by neurons as signals. They’re produced by enzymes in axon terminals and diffuse from their sites of origin in one cell into the intracellular fluid of other neurons, where they bind to activate proteins. Purines- ATP and adenosine act as neuromodulators. ATP is co-released with one or more neurotransmitters in response to Ca2+ influx into the terminal. Adenosine is derived from ATP via enzyme activity in the extracellular compartment.
41
What are the types of synapses?
A synapse is an anatomically specialised junction between two neurons, either chemical or electrical. Activity at synapses can increase or decrease the likelihood that the post-synaptic neuron will fire action potentials by producing a brief graded potential. Excitatory synapse- membrane potential of post-synaptic neuron is brought closer to threshold (depolarised) Inhibitory synapse- membrane potential of post-synaptic is either driven farther from threshold (hyperpolarised) or stabilised at resting potential
42
What are the differences between electrical and chemical synapses?
In an electrical synapse, the electrical activity of the presynaptic neuron affects the electrical activity of the postsynaptic neuron. Pre and post synaptic cells are connected by gap junctions. In chemical synapses, neurotransmitters transmit the signal. Pre-synaptic neurons release neurotransmitters from their axon terminals.
43
What are the mechanisms of synaptic release?
Neurotransmitters are stored in vesicles within lipid bilayer membranes; vesicles are docked on the presynaptic membrane in release regions called ‘active zones’. Receptors can be ionotropic (ion channels) or metabotropic (G protein/second messenger signalling). To terminate the signal in a chemical synapse the neurotransmitter must be removed. Diffusion of the transmitter from the cleft. Degradation of the transmitter by enzymes. Reuptake into the pre-synaptic cells for reuse.
44
What are the differences between excitatory and inhibitory chemical synapses?
Excitatory chemical synapses generate an excitatory postsynaptic potential (EPSP)- a graded potential. EPSPs serve to bring the membrane potential closer to threshold for generating an action potential. Inhibitory chemical synapses generate an inhibitory postsynaptic potential (IPSP) which make the cell membrane potential more negative, making it harder to generate an action potential.
45
What is temporal and spatial summation?
If synapses become active simultaneously the stimulus can be summed. Temporal summation- one axon is stimulated again before the first EPSP has died down, so second synaptic potential adds to the first, resulting in greater depolarisation. Spatial summation- two axons are stimulated resulting in input from two different neurons, which results in summation and greater depolarisation.
46
How does motor control move down the hierarchy?
The neurons involved in controlling skeletal muscle can be thought of as being organised in a hierarchical fashion, with each level having a certain function. General intention at the highest level of the hierarchy is generated for a consciously planned movement. Information is then relayed to middle level structures that specify posture and movements needed to carry out the action. As neurons in the middle level receive input from the command neurons, they also receive afferent information from receptors in the muscles, tendons, joints, skin, etc (local level).
47
What are voluntary and involuntary movements?
Voluntary movements- movement accompanied by a conscious awareness of what we are doing and why we’re doing it; our attention is directed toward the action or its purpose. Involuntary movements describe actions that are unconscious and automatic, described by ‘reflex’.
48
What are the local control systems of motor control?
Local control systems are the relay points for instructions to the motor neurons from centres higher in the motor control hierarchy. They play a major role in adjusting motor unit activity to unexpected obstacles to movement and to painful stimuli in the surrounding environment. To do this: Carry out adjustments based on information from sensory receptors. Also, by transmitting information via afferent fibres to higher levels of the hierarchy.
49
What are length monitoring systems?
Stretch receptors embedded within muscles monitor muscle length and the rate of change in muscle length. Receptors consist of peripheral endings of afferent nerve fibres wrapped around modified muscle fibres enclosed within a connective tissue capsule, collectively called a muscle spindle. Intrafusal fibres- modified muscle fibres. Extrafusal- fibres that form the bulk of the muscle.
50
What are tension monitoring systems?
Tension depends on muscle length, load on the muscle and fatigue. Golgi tendon organs are the endings of afferent nerve fibres that wrap around collagen bundles in the tendons near their junction with the muscle. These sensors discharge action potentials upon stretching or contraction.
51
What is the process of a stretch reflex?
Afferent fibres from the muscle spindle enter the CNS and divide: Excitatory synapse directly onto motor neurons in extensor muscle. Inhibitory synapse with interneuron that inhibit motor neurons in flexor muscle. Reciprocal innervation. Excitatory synapse directly onto motor neurons of other synergistic extensor muscles. Information to higher centres.
52
What is the process of the withdrawal reflex?
Stand on a pin. Pain detected by nociceptor and signal sent to CNS. Ipsilateral extensor muscle in thigh relaxes due to inhibitory synapse. Ipsilateral flexor muscle contracts due to excitatory synapse. Contralateral effects: Contraction of extensor muscle. Relaxation of flexor muscle. Result: stand up on other leg. Signal sent to brain.
53
What is an electroencephalogram (EEG)?
A recording of brain electrical activity. EEG patterns are due to graded potential, summed postsynaptic potentials in the many brain neurons that underlie the recording electrodes. The alpha rhythm is associated with decreased levels of attention. When alpha rhythms are generated, subjects are often relaxed and happy. When people are attentive to external stimulus or are thinking hard about something, the alpha rhythm is replaced by the beta rhythm.
54
What does the sensory system consist of?
Sensory receptors that receive stimuli from the external or internal environment. Neural pathways that conduct information from receptors to the brain/spinal cord. The parts of the brain that deal with this information (sensory information). Sensation- aware of the information. Perception- aware and understand the meaning.
55
When do sensation and perception often occur?
After the CNS has modified/processed the sensory information: Transduction of stimulus to graded potentials (receptor potentials). Action potentials in afferent neurons. Pattern of action potentials is the code providing info about stimulus. Primary sensory areas of CNS receive this input. Further communication with other brain regions/spinal cord.
56
What are the types of sensory receptors?
Sensory receptors are specialised cells that generate graded potentials called receptor potentials in response to a stimulus. 5 major divisions of these sensory receptors based on stimuli that they respond to: Mechanoreceptors- pressure/stretch. Thermoreceptors- cold/warmth. Photoreceptors- different ranges of light. Chemoreceptors- binding of chemical to the receptor (smell, taste, pH, O2). Nociceptors- painful stimuli (heat, tissue damage). Sensory receptors are the ends of afferent neurons and can convert stimuli into graded potentials. Stimuli open ion channels directly or indirectly.
57
How is a receptor potential formed?
Transduction in sensory neurons involve opening or closing ion channels, directly by the stimulus, or through a second messenger system. Ion channels present at the distal tip of a single axon or are on a specialised receptor cell. An ion flux results in a change in membrane potential which results in a local graded potential (receptor potential). Current flows to a region where there are membrane voltage gated channels, usually at the first node of Ranvier. A larger stimulus results in a larger graded potential which results in more frequent action potentials.
58
What is coding and modality?
Coding is the conversion of a stimulus into a signal that conveys the relevant information. The area of the body that when stimulated, leads to activity in a particular afferent neuron: receptive field. Modality- a term for a type of stimulus (heat, cold, sound, pressure). Modalities can be sub-divided (salty, sweet, bitter, sour of Taste). A given receptor is particularly sensitive to one stimulus modality the ‘adequate stimulus’. This is optimal for the signal transduction mechanism and ion channels.
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How do intensity and location affect sensory coding?
As the strength of a stimulus increases, receptors on adjacent branches of an afferent neuron are activated, resulting in a summation of their currents. Stimulus location is coded by the site of a stimulated receptor and potentials travelling along unique pathways to a specific part of the CNS. In vision, hearing and smell, the stimulus location is interpreted as outside the body, rather than at the site of receptor stimulation. A neuron responds vigorously when stimulus is in the middle of the receptive filed (more receptors activated=more action potentials). The precision (acuity) for locating the stimulus depends on convergence. Greater convergence=less acuity.
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What is lateral inhibition?
It enables the localisation of a stimulus site for some sensory systems. Information form afferent neurons whose receptors are at the edge of a stimulus is strongly inhibited compared to information from the stimulus’ centre. It enhances the contrast between the centre and periphery of a stimulated region.