Lesson 5 - Receptor Potentials, Adaptation; PNS/CNS Flashcards
how does the stimulus for the change in potential differ between membrane potentials and receptor potentials
- we have learned that the membrane potential of the post synaptic neuron changes due to the binding of neurotransmitters from the presynaptic neuron
- however when it comes to the sensory system and receptor potentials, the change in membrane potential comes from the exterior sensory environment instead
- The energy from the environment will react with membrane proteins and in general this will cause depolarization
- in general this will cause depolarization of sensory receptors upon receipt of specific energy (like pressure) – much like an EPSP
- Exception: photoreceptors hyperpolarize
where are receptor proteins found and what will happen if a signal is sent to the receptor proteins?
- instead of post synaptic proteins (either ionotropic or metabotropic receptors) we have receptor proteins (similar pathway)
- these receptor proteins are found in the sensory cell membrane
- if a signal is sent to these receptor proteins of the sensory cells (like a touch stimulus), the cells will change shape and generally depolarize the membrane
what are two things that could happen when a receptor protein changes shape?
- Directly open ion channels (ex. cation channels –> leads to depolarization of the membrane) - similar to ionotropic
- Enzyme is activated via G protein coupling –> leading to production of 2nd messenger (cAMP, cGMP, lnP3) –> lots of 2nd messenger –> amplifying the signal – similar to metabotropic
What happens when a chemical stimulus binds to a specific metabotropic receptor?
- Chemical stimulus (signal) binds to specific metabotropic receptor (G-protein coupled) > changes shape? > activation of G-protein > activate adjacent enzyme (adenyl cyclase) > produces 2nd messengers (cAMP) > cAMP activate kinases > directly interact with ion channels or phosphorylate other proteins
how does the metabotropic effect for receptor proteins lead to the two stages of amplification?
- receptor proteins that are metabotropic exhibit an extra advantage: the metabotropic effect
- the advantage effect is the process of amplification
the two stages of amplification:
- G-protein can activate a number of different enzyme molecules
- each of these enzyme molecules will produce lots of 2nd messenger (cAMP)
* Thus, one stimulus molecule can produce lots of 2nd messenger (cAMP) leading to amplification
how can the depolarizing current in your olfactory pathways lead to an AP
- much like PSPs, the receptors in nose produce graded potentials
- thus the depolarizing current that is produced needs to travel from the dendrites along the membrane passively to the trigger zone for the olfactory neurons
- if the current is strong enough and brings the trigger zone to threshold, an AP will fire and signal to your brain that you smell smth (ex. roses)
use the olfactory receptor to explain how the metabotropic and amplification effect takes place when a stimulus is triggered
- there are olfactory neurons in the nasal epithelium and there is a coating of mucus on top of it
- the olfactory receptor cells line the mucus layer
- chemical stimuli or odorant (ex. smell of roses) dissolved in the mucus bind to the receptors in the olfactory cell membrane
- activates a G-protein –> activates adynyl cyclase –> produces cAMP –> cAMP directly binds to ion channels –> allows (Na+ and Ca++) to go through —> depolarizes the membrane
what happens if we bind odour molecules to the olfactory receptor ionotropically instead
- because we are generating a current indirectly through the metabotropic system, this will result in the amplification system
- this makes the olfactory cells very very sensitive to one or two molecules in the air
- instead if the odor molecules were to bind directly to an ion channel (ionotropic pathway), then you will get one or two ion channels open and you will never be able to detect that odorant (doesnt amplify and send an AP to brain)
(smell bypasses the thalamus – goes straight to the brain – this may be why smell is important)
what are the two categories of sensory cell transmission?
- sensory cell generates an action potential at the trigger zone aka spike generating zone
- sensory cell releases vesicles when depolarized; impulses generated in post synaptic neuron
explain how sensory cells like the mechanoreceptors in our skin generate an AP at the trigger zone / branch point
1st category of sensory cell transmission
- depolarizing current has to reach the trigger zone and bring it to threshold for an AP
- mechanoreceptors are found in your skin and respond to pressure
- the first patch of excitable membrane is located at the branch point (like the trigger zone)
- when pressure is applied, ion channels will open at the membrane and produce a depolarizing current (receptor graded potential)
- the graded potential will have to summate and travel to the branch point (like the trigger zone) so that it can reach threshold for an AP
- depolarizing current spreads to the first patch of excitable membrane, and through summation reaches an AP
- receptor potential has to summate enough at the branch point to generate an AP (like EPSPs summating at trigger zone for AP)
what is the second category of sensory cell transmission?
- sensory cell here doesn’t have to generate its own AP as long as it can release neurotransmitters
–Sensory cell releases vesicles when depolarized; impulses generated in post-synaptic
neuron
how is there a transmission of a signal in sensory cells through vesicles
2nd category of sensory cell transmission
- if the sensory cell can release transmitters then the next cell in line will pick this up and act as the postsynaptic neuron and fire an AP
- the release of transmitters is due to the depolarizing current which does not generate an AP but instead opens up an influx of Ca++ ions that triggers the exocytosis of vesicles
- thus sensory cell is releasing vesicles with neurotransmitters but no AP
explain the 2nd category of sensory cell transmission using the example of the taste receptor
- there are specialized cells that have taste receptor proteins in the taste buds inside your mouth
- taste receptors will bind chemicals stimulus through the receptor surface of the tongue and mucus layer and produce a depolarizing current (receptor potential not AP - no axon) that will result in the release of transmitters
- this depolarizing current travels passively and reaches the other end of the current
- the depolarizing current opens the voltage gated calcium channels and leads to a calcium influx which subsequently releases transmitters (exocytosis of vesicles)
- after the release of the transmitters the next cell generates the AP so your brain knows what you tasted (no AP in the sensory cell itself)
what is the concept of adaptation in relation to stimulus and receptor/membrane potential
what are the two types
- Adaptation in sensory receptors refers to how they respond to a continuous stimulus over time.
- The MP can decay over time leading to ‘Adaptation’
- The original voltage is not sustained and it’s dropped over time, even though the stimulus may be constant
- ex. when you enter a hot bath its very hot at first, but you adapt and you may not feel it to be hot over time even though the temperature is the same
- Types of adaptations
- slowly adapting
- rapidly adapting
what is slow adaptation
- receptor potential is sustained for duration (slowly decayed) of a stimulus as long as the stimulus intensity remains
- it is interested in the overall magnitude of the stimulus
- Example: Merkel cells in the skin, which are slowly adapting receptors, detect sustained pressure or touch. For example, when you hold a pencil, Merkel cells keep firing while you’re holding it, providing information about the pressure and shape of the object.