Week 21 Flashcards

1
Q

What three planes can the brain (and body) be viewed by?

A

sagittal, coronal and transverse (axial)

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2
Q

Brain (and body) key terms for location (/direction): front back, above, below, etc.?

A

Above = superior ​

Below = inferior​

Front = anterior or ventral​

Back = posterior or dorsal​

Medial = close to (midline)​

Lateral = away from/next to (midline)

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3
Q

What are the three main functions of the nervous system?

A

Sensory function​
- detect external & internal changes​

Integrative function​
- analyses & makes decisions based on voluntary and involuntary responses​

Motor function​
- initiates motor movement & glandular secretions​

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4
Q

Three major parts of the brain, what do they do (briefly)?

A

Cerebrum: largest part, containing cerebral cortex and subcortical regions

Cerebellum: located in posterior region, responsible for balance and coordination

Brainstem: contains midbrain, pons and medulla oblongata. Communicated with PNS to control involuntary processes s

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5
Q

What is the cerebral cortex?

A

The outer layer of the cerebrum is composed of the cerebral cortex ​

Four functionally and anatomically distinct lobes: frontal, parietal, temporal and occipital ​

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6
Q

Cerebrum is separated into 2 hemispheres, connected by what?

A

connected by a large fibre bundle called the corpus callosum​

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7
Q

Cortical lobes: function of frontal lobe?

A

higher cognitive functions, e.g. decision-making and problem-solving. It is also responsible for some features of language and voluntary movement​

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8
Q

Cortical lobes: function of parietal lobe?

A

integrates information from the visual pathway, coordinates motor movement and interpretation of sensory information ​

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9
Q

Cortical lobes: function of temporal lobe?

A

interpreting speech and hearing, object recognition and emotion

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10
Q

Cortical lobes: function of occipital lobe?

A

processing primary visual information​

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11
Q

Brain regions that lie underneath the cortex are referred to as?

A

subcortical regions​

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12
Q

What are the main subcortical regions of the brain?

A

hypothalamus, amygdala, hippocampus, thalamus and basal ganglia ​

(The Limbic System)

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13
Q

What are the main subcortical regions of the brain responsible for?

A

many functions including memory, emotions, motor movement & processing sensory information

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14
Q

What is the midbrains role?

A

Serves as a connection between the brainstem and subcortical regions​

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15
Q

Three main structures of the midbrain, briefly what do these do?

A

colliculi – directs eye movement towards objects of interest​

tegmentum – coordination of movement, alertness/sleep ​

cerebral peduncle – control of ocular muscles​

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16
Q

Features of the spinal cord?

A

Critical link between the CNS and PNS

Nerves that branch off from the spinal cord form the PNS and innervate the rest of the body.

Divides into 5 sections

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17
Q

The spinal cord is divided into 5 main sections based on the corresponding body area that is innervated. What are these?

A

cervical (neck), thoracic (chest), lumbar (lower back), sacral (hip) and coccygeal (tail)

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18
Q

Peripheral nervous systems is split into two main parts?

A

Somatic = Voluntary (control skeletal muscles and provides sensory information)

Autonomic = Involuntary and is split further:
- Enteric = Regulates movement of water & solutes between gut and tissues, aiding digestion
- Sympathetic/Parasympathetic = Modulate & balance involuntary functions

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19
Q

Sympathetic and parasympathetic nervous system responsibilities?

A

Sympathetic is responsible for the ‘fight or flight’ reaction that occurs in response to a stressful stimulus​

Parasympathetic nervous system balances the sympathetic response by stimulating ‘rest and digest’ pathways ​

Interaction between the sympathetic and parasympathetic nervous systems is crucial for maintaining homeostasis

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20
Q

What are afferent and efferent pathways?

A
  • Afferent pathways carry sensory information from the periphery up TO the brain via ascending nerve tracts​
  • The brain sends signals down to peripheral nerves along efferent descending nerve tracts to control motor output (OUTPUT)
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21
Q

What are the two main cell groups in the CNS?

A

neurons (‘nerve cells’) and glia (‘support cells’)​

(Brain contains ~ 1011 neurons, 1012 glial cells)

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22
Q

Glial cells in the CNS are divided into further groups which are:

A

microglia, astrocytes, oligodendrocytes & ependymal cells ​

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23
Q

Neurons are specialised cells that..

A

receive and send electrical signals within the CNS and between the CNS and PNS​

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24
Q

Features of neurons: Dendrites?

A

Short, bristle-like, highly branched processes​

Receive nerve input (at synapses)​

Not myelinated

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25
Features of neurons: Soma (Cell body)?
Contains the normal cell organelles​ Main site of protein synthesis and degradation​ Has pronounced rough ER = ‘Nissl’ substance​
26
Features of neurons: Axon?
Long, thin process​ Propagates nerve impulse to another neuron, muscle fibre or gland​ Often myelinated​ Terminates at axon terminals or synapses
27
Features of neurons: Synapse?
Release of neurotransmitters to communicate with other cells (post synaptic)​
28
There are different structural classifications of neurons. What are these?
Bipolar neurons – 1 main dendrite and 1 axon ​ - Found: Retina of the eye, inner ear, olfactory area of brain​ Unipolar neurons - Just 1 process from the cell body, part way down the axon​ - Found: Always sensory neurons (pain, temperature, touch, pressure)​ Multipolar neurons - Many dendrites and 1 axon ​ - Found: Most neurons in the CNS​
29
Role of microglia CNS cells? What different states can they be found in?
Immune cells that survey the CNS and respond to signs of infection or damage​​ Exist in a wide-range of morphologies depending on activation state ​: - Surveillant = smaller, with multiple processes​ - Activated = larger, with rounded cell body & shorter processes​
30
What are Astrocytes in the CNS?
Small, star-shaped cells that provide support for the development and homeostatic maintenance of the nervous system and cerebral blood vessels​ Heterogeneity (morphology, protein expression) across different brain regions​ Form a ‘glial scar’ after severe injury
31
What are oligodendrocytes in the CNS?
Cells that form the lipid-rich sheath of myelin that wraps around some neurons to increase the speed at which information is transmitted by the neuron​ In the PNS, these cells are called Schwann cells​
32
What is referred to as white and grey matter?
Areas of brain that contain myelin (bundles of axons) are called white matter, while regions of unmyelinated cell bodies are referred to as the grey matter ​
33
Myelin increases the speed of action potentials. What are the different velocities of nonmyelinated versus myelinated axons?
unmyelinated axon conduction velocities range from about 0.5 to 10 m/s​ myelinated axons can conduct at velocities up to 150 m/s
34
Neuronal health is critically dependent on adequate blood supply. What is the neurovascular unit?
Blood vessels in the brain are made up of endothelial cells, astrocytes, pericytes (capillaries), smooth muscle cells (arteries) and neurons. This is referred to as the neurovascular unit​
35
Neuronal health is critically dependent on adequate blood supply. What is the blood-brain barrier (BBB)?
Endothelial cells of the brain express form tight junction proteins. These junctions allow the brain to create a physical barrier between the blood and the brain, called the blood-brain barrier (BBB) ​ This gives the brain a high degree of selectively, thereby protecting it against entry by potentially harmful substances in the blood (may cause issues when trying to treat brain illness with drugs)
36
What is cerebrospinal fluid (CSF) structure?
- contained within the ventricles and in the subarachnoid spaces of the brain and spinal cord - produced from filtered blood by the choroid plexus in the ventricles ​
37
What is cerebrospinal fluid (CSF) responsible for?
- provides buoyancy for the brain and cushion it against injury, as well as waste removal ​- Because CSF is shared between the brain and spinal cord, samples of CSF collected from the spinal cord are used to provide a ‘snapshot’ of the brain environment
38
Where do neurons receive information?
at dendrites (up to 100,000 synaptic inputs/neuron) and integrate in cell body ​
39
How is information transmitted across neurons?
Information is transmitted along the axon in the form of electrochemical signals or nerve impulses (= action potentials)​ Action potentials are due to the flow of ions (Na+, K+) through specific protein channels in the membrane​ The lipid bilayer of the membrane is impermeable to these charged ions ​
40
What forces move ions across membranes? What are these?
Chemical force​: - Differences in concentration: diffusion from a region of high concentration to a region of low concentration​ Electrical force​: - Interior of cell is negatively charged so positively charged cations are retained and negative ions will be expelled​ Electrochemical driving force: - A combination of the chemical and electrical forces acting on any particular ion​
41
What 2 categories of io channels facilitate ion movement into and out of cells?
Channels that are gated and require a stimulus to open ​ - ligands, mechanical force or voltage​ - specific to particular ion(s)​ Channels that are always open and allow free movement of ions​
42
Differences between the cell membranes that allow movement of ions?
Ligands gated = open when a ligan binds​ Mechanical gated = Mechanoreceptors – opens when a mechanism occurs such as temp, pressure​ Voltage gated Depends on voltage of neuron, positive or negative, to open – selective, only allow entry of certain ions.​ Open channels AKA leaky channels = selective as they're open all of the time such as only to Na+, electrochemical force only impact on these membranes.
43
Chemical gradient across the neuronal membrane?
Under resting conditions, the concentration of Na+ ions is ~ 10x higher outside the neuron compared to the concentration of Na+ ions inside​ At the same time, levels of K+ ions are ~ 15x higher inside the neuron compared to the extracellular environment ​
44
Movement of potassium in the neuron?
There is a constant flow of K+ ions down their concentration gradient, from the inside of the neuron to the outside​ This movement occurs via open (or leaky) K+ channels that are situated in the membrane of the neuron It will use a Na+/K+ ATPase pump ​to regulate this
45
What is the sodium / potassium ATPase pump?
The ion gradient is maintained by the continuous operation of the Na+/K+ ATPase pump​ It moves 3 Na+ ions from the inside of the neuron to the outside of the cell​ At the same time, 2 K+ ions are moved from outside the neuron to the inside of the cell​
46
Consequence of the Na+/K+ ATPase pump?
At each cycle of the Na+/K+ ATPase pump, the cell loses one positively charged ion from the intracellular environment​
47
Resting membrane potential in a neuron?
The ultimate result between the diffusion of K+ and the action of the Na+/K+ ATPase pump is a more positive charge outside the neuron compared to the inside of the neuron ​ At rest, there is more positive charge outside the neuron compared to the inside of the neuron ​ The difference in charge across the membrane of the neuron is referred to as polarisation​
48
What is polarisation?
The difference in charge across the membrane of the neuron is referred to as polarisation
49
What is the resting membrane potential for most neurons?
~ - 70mv
50
What is The difference in voltage across the plasma membrane when the neuron is at rest is called?
the resting membrane potential ​
51
What forces drive ion movement?
When ion channels open, the chemical gradient drives ion movement from high concentration to low concentration ​ In the absence of polarisation, diffusion would occur until chemical equilibrium was reached ​ However, this does not occur because of electric forces ​
52
Electrochemical gradients of sodium?
When Na+ channels open:​ chemical gradient drives ion movement into the cell electrical force pulls + ions into the cell​ both act in the same direction = Na+ will enter the cell
53
What stops the movement of sodium ions eventually. What causes the equilibrium of sodium movement?
As Na+ moves into the neuron, the charge inside the cell starts to become positive and the electrical gradient decreases, along with the chemical gradient​ Eventually, the chemical and electrical forces will be exactly in balance and there will be no net flow through any open channels ​ ​
54
What is meant by equilibrium potential of sodium?
the membrane potential required to exactly counteract the chemical forces acting to move one particular ion across the membrane.​ Specific to sodium!
55
Electrochemical gradient of potassium?
When K+ channels open:​ chemical gradient drives ion movement out of the cell​ but electrical force pulls + ions into the cell​ two forces act in opposite directions​ chemical force > electrical force, so K+ moves out of the neuron​
56
How does equilibrium of potassium movement occur?
As K+ moves out of the neuron, the charge inside the cell starts to become even more negative, so the electrical gradient becomes stronger​ Eventually, the chemical force that drives K+ out of the cell = the electrical force driving K+ back into the cell​ At this point, there will be no net flow of K+ ions​
57
Equilibrium potential (E) can be calculated using what equation?
Nernst Equation E = 61/z log Co / Ci Z = charge (valence) of ion Co = conc of ion outside neuron Ci = Conc of io inside neuron
58
Equilibrium potential for Na+ and K+?
Na+ = +60mV meaning no net movement of sodium at this point. K+ = -94mV meaning no net movement of potassium at this point
59
Overview of How neurons are stimulated?
Incoming signals (from sensory stimulus or other neurons) can depolarise the cell membrane, causing the membrane potential to rise from its resting potential of -70 mV (e.g. open Na+ channels)​ If the membrane potential is depolarised beyond a certain critical level (threshold potential = -55mV) then an action potential is triggered in the neuron​ Other incoming signals can do the reverse and hyperpolarise the membrane (i.e. cause the membrane potential to decrease), so making an action potential less likely
60
What is the threshold potential?
-55mV (triggering an action potential)
61
Does hyperpolarisation trigger or prevent a signal?
Makes an action potential less likely to occur as it is caused by reverse incoming signals causing a decrease to membrane potential
62
Voltage-gated ion channels?
Embedded in the plasma membrane of the neuron are ion channels that are sensitive to the voltage of the cell​ These channels open only when the voltage in the cell reaches a certain value​ These are called voltage-gated ion channels​
63
What are voltage-gated Na+ & K+ channels?
Voltage-gated Na+ channels have both an activation gate and an inactivation gate. At rest, the activation gate is closed and the inactivation gate is open​ Voltage-gated K+ channels have one activation gate, which opens to allow the flow of K+ ions through the channel and closes to stop the flow of K+ ions​
64
Explain the voltage-gated channels when the neuron is at rest (1)?
When the membrane potential is -70mV, voltage-gated Na+ channels are closed and the concentration of Na+ outside the cell is higher than inside the cell​
65
Explain the voltage-gated channels when the neuron experiences initial stimulation (2)?
When the neuron receives an excitatory signal or stimulus, ligand-gated ion Na+ channels open ​ Small amounts of Na+ will move down their concentration gradient into the neuron and the resting potential will start to become more positive​
66
Explain the voltage-gated channels when the neuron experiences depolarisation (3)?
Once the membrane potential reaches a critical threshold of -55 mV, voltage-gated activation gates in the Na+ channel open quickly, allowing Na+ to flood into the neuron​ As a result of the large influx of positively charged Na+, the neuron quickly loses its negative charge and undergoes depolarisation​
67
Explain the voltage-gated channels when the neuron experiences becomes highly positive and Na+ are inactivated (4)?
When the inside of the neuron become highly positive, the pore of the voltage-gated Na+ channels is plugged by the inactivation gate and the flow of Na+ into the neuron stops​
68
Explain the voltage-gated channels when the neuron experiences repolarisation (5)?
Eventually the intracellular environment of the neuron becomes sufficiently positive that voltage-gated K+ channels begin to open slowly​ Opening of these channels allows K+ to flow down its concentration gradient out of the cell ​ This movement of K+ causes the inside of the neuron to quickly regain its negative charge in a process called repolarisation
69
Steps of voltage-gated channel signalling?
1. Neuron at rest 2. Stimulation 3. Depolarisation 4. Inactivation of Na+ channels 5. Repolarisation 6. Hyperpolarisation 7. Refractory period
70
Explain the voltage-gated channels when the neuron experiences hyperpolarisation (6)?
In response to the increasingly negative charge inside the neuron, the voltage-gated K+ channels close. Because this process is slow, some K+ ions continue to move outside the cell while the channel is closing​ This extra efflux of K+ causes the membrane potential to become more negative than the resting potential of -70 mV. This process is called hyperpolarisation
71
Explain the voltage-gated channels when the neuron experiences refractory period (7)?
During the period of hyperpolarization, the neuron will not be able to fire another action potential. This is termed the refractory period​ Eventually, the action of the Na+/K+ ATPase pump will restore the resting membrane potential to -70mV and the neuron will be ready to fire another action potential
72
Give an overview of an action potential?
The process of depolarisation and repolarisation is referred to as an action potential​ A single action potential takes only milliseconds to complete, enabling the neuron to fire quickly in response to the hundreds of signals it receives every second​
73
What is referred to as an action potential?
The process of depolarisation and repolarisation of a neurone cell due to a threshold being reached (-55mV)
74
Where are action potentials initiated?
At the base of the neuron in the region called the axon hillock
75
Movement of action potentials after initiation has occurred at the axon hillock?
The action potential will be transmitted down the axon​ Small gaps in the myelin, called nodes of Ranvier, allow ion movement across the axon membrane at these sites ​ This effectively permits the action potential to ‘jump’ from one node to another, thereby allowing the signal to be transmitted very quickly. This is type of transmission is called saltatory conduction​
76
Myelinated versus unmyelinated axons propagation of action potentials?
Unmyelinated = Each segment has to undergo the process of action potentials​ Myelinated = Only nodes of Ranvier have to undergo the process of action potentials, therefore the ions are propagated along the neuron quicker.
77
Properties of action potentials: All-or-nothing principle? How is information coded?
An action potential will not be triggered if the excitatory stimulus is not strong enough to raise the membrane potential to reach the threshold potential​ Action potentials are “all or none” – they either fire or they do not​ Information is coded by the frequency of the firing of action potentials (i.e. the number of spikes over a given period of time), rather than the size of the action potential, which is always the same ​
78
Chemical versus electrical synapses: communication of a single neuron with the next?
Neurons communicate with other cells via synapses​ Electrical synapses use gap junctions that directly connect the cytoplasm between 2 cells​ Chemical synapses involve the release of neurotransmitters from a pre-synaptic neuron that diffuse across the synaptic cleft & bind to post-synaptic neurons ​ Chemical synapses are the most common type​
79
Physiology of a chemical synapse?
- NT & Synaptic Vesicles = Neurotransmitters are stored in synaptic vesicles. Amount in one vesicle is called a quantum​ - Voltage-gated Ca2+ channel: Arrival of action potential causes influx of Cz2+ and fusion of vesicles with pre-synaptic membrane and release of transmitter into synaptic cleft - Receptor = Transmitter (crosses synaptic cleft and) Binds to receptor on post-synaptic membrane - Reuptake molecule/ enzyme = End of transmitter activity via i) End i) Catabolism (degradation) or ii) Uptake of transmitter into axon terminal or glial cells​
80
Summary of how signalling in a chemical synapse can end?
Eventually, synaptic communication is terminated when the neurotransmitter is either taken back up into the presynaptic neuron (reuptake) or broken down in the synapse by enzymes.
80
Summary of signalling at a chemical synapse?
When the depolarisation of the action potential reaches the presynaptic terminal, the voltage-gated Ca2+ ion channels open. ​ In response to the increase in intracellular Ca2+, vesicles containing neurotransmitter fuse with the plasma membrane of the neuron. This causes the neurotransmitter to be released into the synapse. ​ Neurotransmitter diffuses across the synapse and binds to receptors on the postsynaptic neuron. For excitatory neurotransmitters, this causes Na+ ion channels to open and entry of Na+ triggers an action potential in the postsynaptic neuron. ​ ​
81
Integration of multiple synaptic inputs: when are neurotransmitters classified as excitatory or inhibitory?
excitatory = if they raise the membrane potential towards the critical threshold (membrane potential less negative) inhibitory = if they lower the membrane potential away the critical threshold (membrane potential more negative) A single neuron communicates with hundreds of other neurons and therefore constantly receives both excitatory (EPSP = excitatory postsynaptic potential) and inhibitory (IPSP = inhibitory postsynaptic potential) signals
82
What is summation?
the process by which the neuron ‘sums up’ all the excitatory and inhibitory signals it receives over a period of time​
83
What is the criteria for transmitter substance?
1. Synthesised in the neuron​ 2. Present at presynaptic terminals, packaged within synaptic vesicles​ 3. Exogenous substance (drug) at reasonable concentration mimics exactly the action of endogenously released transmitter​ 4. Specific mechanism exists for removing transmitter from synaptic cleft​
84
What does EPSP and IPSP stand for?
Excitatory postsynaptic potential Inhibitory postsynaptic potential
85
Give a few examples of neurotransmitters?
Acetylcholine - Excitatory at skeletal muscle, and both at other sites. Secretion = PNS & CNS, Neuromuscular junction Norepinephrine & Epinephrine - Both. Secretion = CNS & PNS Dopamine (Secretion = CNS + PNS) and serotonin (CNS) - Generally excitatory. Gamma aminobutyric acid - Inhibitory (CNS + Neuromuscular junction) ETC
86
What are the two types of neurotransmitter receptors?
1. Ionotropic receptors – transmitter binding = direct opening of ion channel​ - also termed ligand-gated ion channels​ - always stimulatory​ - fast – effect lasts a few milliseconds​​ 2. Metabotropic receptors – transmitter binding = indirect activation of G-protein ​ - also termed G-protein coupled receptors ​ - can trigger opening or closing of a separate ion channel and downstream signalling cascade​ - slow – effect takes up to several hours ​ ​
87
What is the structure of ionotropic receptors (neurotransmitter receptors)?
omposed of 4 or 5 subunits arranged around a central pore in the membrane​ Receptors can be made up of different combinations of subunits = increase diversity between different tissues ​
88
Give examples of ionotropic receptors?
nicotinic acetylcholine (ACh)​ GABAA​ glycine​ 5-HT3 receptors​
89
What is the structure of metabotropic receptors?
Composed of a single protein with 7 membrane-spanning regions (α-helices) ​ seven transmembrane (7TM) receptor​
90
Examples of a metabotropic receptors?
muscarinic acetylcholine​ alpha and beta adrenergic receptor​ all 5-HT receptors except 5-HT3​ rhodopsin​ olfactory receptors​ many others​
91
Ionotropic receptors before and after a neurotransmitter has bound
At rest, the channel pore is closed and there is no movement of ions ​ Binding of neurotransmitter to its receptor, causes the channel to open​ Ions will flow down their concentration gradient ​ Channels will be permeable to anions (e.g. Na+, K+) or cations (Cl-)​
92
Metabotropic receptors before and after a neurotransmitter has bound?
Binding of neurotransmitter to its receptor causes activation of a G-protein​ The G-protein can act directly on an ion channel, causing the ion pore to open and/or​ the G-protein can activate a second messenger​ If a second messenger activated then Second messenger can bind to and open an ion channel or initiate a signalling cascade (enzymes, gene transcription, etc.) ​
93
Give a summary of the sequence of event of G protein activation?
Transmitter binds to receptor ​ GTP exchanges for GDP on the G protein a subunit​​ G protein dissociates from receptor – then ligand as well​ The 3 subunits (a, b, and g) of the G protein also dissociate​ The a subunit activates the ion channel​ The a subunit is inactivated by the hydrolysis of GTP to form GDP (GTPase activity is intrinsic to this subunit)​ The a subunit recombines with b and g subunits and attaches to the receptor, which can then bind another agonist​
94
Second messengers as neurotransmitter receptors?
G proteins can stimulate (Gs) or inhibit (Gi) enzymes​ Most common enzyme targets:​ ​Cyclic AMP, cyclic GMP, inositol triphosphate & diacylglycerol. = All of which slow intracellular response, eg decrease heart rate
95
Agonists versus antagonists drugs on neurotransmission?
Agonists are drugs that mimic the actions of the neurotransmitter​ - Binding to the receptor = activation ​ Antagonists are drugs that block the action of the neurotransmitter​ - Binding to the receptor = no activation​
97
Explain the effects of Multiple Sclerosis in terms of neuronal communication?
A neurodegenerative disease where neurones become demyelinated. This can be seen as lesions on in the brain and spinal cord. Therefore, this slows down action potential conduction causing problems with cognitive development and mobility