- Neuronal synapses questions
- Mini MCAT passage: Neurotransmitter removal from the synapse
- Mini MCAT passage: Manipulating synaptic transmission between neurons
- Signal propagation: The movement of signals between neurons
- Synapse structure
- Neurotransmitter release
- Types of neurotransmitters
- Types of neurotransmitter receptors
- Neurotransmitter removal
Explore the intricate world of neurotransmitter receptors in neurons. Learn how they can be excitatory or inhibitory, and how neurotransmitters can bind to multiple types of receptors. Discover the role of ionotropic and metabotropic receptors, and how they influence neuron behavior, from rapid effects to long-lasting changes. Created by Matthew Barry Jensen.
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- Are there other types of metabotropic receptors in the nervous system than the g-protein-coupled type?(11 votes)
- Yep, but very few that we understand very well. Metabotropic is just a receptor that acts through a second messenger system (not through an ion channel). An example of a non-G-protein metabotropic receptor would be a tyrosine kinase receptor, where the receptor either phosphorylates itself to become activated, or phosphorylates proteins other than g proteins to activate them and transmit the signal.(17 votes)
- Does the target cells have to be only neurons? Can it be other types of cells ?(5 votes)
- Target cells include neurons, muscle cells, and gland cells.
The target may even be a blood vessel, so that the neuron can secret NT into the bloodstream!
Matthew mentioned this in the first video of this section, Synapse Structure.(6 votes)
- I don't understand the general 5 steps of the neurotransmitters relating to neurons synapse. Can you please explain it in simple steps. I have reviewed this over & over & I just don't understand it.(4 votes)
- I reviewed this video and did not see 5 steps. This video is giving a wide overview of how a neuron can be affected. I think it is more detailed than it needs to be and he concentrated more on vocabulary then on concepts. What I would say is first understand how an action potential, AP, is carried down an axon and the neuron releases neurotransmitter. Here in this video, there more details that complicate the story. A neuron can have 1000 other neurons telling it what to do. Some encourage or excite by allowing sodium into the cell. Some are inhibitory by allowing potassium out or Cl ions in. Whether or not the neuron sends an action potential depends on the sum of these occurrences. It has to be overall excited to trigger an action potential. In addition, further fine tuning can occur at the axon terminal. If you get that, you are doing well. For more background read Wikipedia or a college level textbook from open stax at Rice University web site.(8 votes)
- What exactly does he mean by "graded potentials" when talking about ionotopic receptors? I understand action potential and resting potential, but what does graded mean?(3 votes)
- Let's say you need a total of +5 stimulatory messages to trigger an action potential. If you receive 5 stimulatory signals, you'll reach that action potential threshold. But what if you get 5 stimulatory signals AND 2 inhibitory signals at the same time? The graded potential is essentially the sum of all of the inputs. So +5 stimulatory -2 inhibitory = a graded potential of +3, which in this case is not enough to trigger an action potential.(1 vote)
- So lack of nutrients such as minerals and vitamins could affect the effectiveness of neurotransmitter which could cause muscle-spasms?(4 votes)
- Are metabotropic receptors responsible for epigenetic changes?(2 votes)
- It's possible that a signal cascade initiated by a metabotropic receptor:ligand binding could produce certain epigenetic effects to include DNA methylation, histone modification, and non coding RNA.(3 votes)
- in what way does an increase in neurotransmitters (quantity) affect the amount of information passed from one cell to the next, specifically in relation to metabotropic transmitter receptors?(2 votes)
- No, there are not always an excess of neurotransmitters. Take Parkinson's disease for an enormously simplified example; the brain cells that are responsible for the production of the neurotransmitter dopamine slowly die. Dopamine is the messenger with which the brain instructs the muscles about movement. The using of muscles becomes increasingly harder when there is not enough dopamine to carry orders from the brain to the muscles.(2 votes)
- So, if the inside of the cell becomes more positive due to an action potential, it is excitatory. If it becomes more negative, it is inhibitory. Correct?(2 votes)
- yes. this is because neurons have a resting potential of -70mV but in order to fire an action potential they need to reach a threshold potential around -55mV. Thus, if an action potential is excitatory, it will cause the membrane potential in the postsynaptic neuron to become more positive (depolarized) and closer to that threshold potential. In contrast, an inhibitor signal would cause it to become even more negative (hyperpolarized).(1 vote)
- If acetylcholine causes muscle contraction, so when at night, what happen to our skeletal muscle? should the muscles contract at night?(2 votes)
- what is depolarization?(1 vote)
- Depolarization occurs when a cell moves away from its resting potential in the positive direction. This is commonly accomplished with Na+ entry into a cell, causing the cell to become more positive. if the cell becomes depolarized past a set threshold, an action potential is fired. This is how all the nervous system works, and the main function of neurotransmitters is to cause or inhibit action potential firing in the post-synaptic cell.(3 votes)
Voiceover: In this video I want to talk about the types of neurotransmitter receptors. Neurons are often referred to as excitatory or inhibitory, but more accurately it's the synapse that's excitatory or inhibitory, and even more specifically, it's the combination of the neurotransmitter that's released at the synapse and the receptor that it binds to on the post synaptic membrane. Because many neurotransmitters can bind to multiple types of receptors so that the neurotransmitter can sometimes be excitatory and it can sometimes be inhibitory to the target cell so that this axon terminal might be releasing this neurotransmitter here at the synapse and perhaps when it binds to this purple receptor, that causes an excitatory potenetial in the target cell, but if it binds to this orange receptor on the post synaptic membrane, that would cause inhibition of the target cell, would cause inhibitory potential. When the target cell is another neuron, excitatory or inhibitory synapses can be scattered around all over the surface of the neuron. Or there are many neurons where the dendrites are receiving predominately excitatory synapses so that there can be a large number of neurons synapsing on the dendrites and releasing neurotransmitters that will cause depolarizations in the dendrites. So let me just draw little purple pluses in here to represent that these are excitatory synapses. And then many neurons like this will have more inhibitory synapses on the soma. So I'll just draw some little orange minus signs here to represent that these could be inhibitory synapses on the soma. And then often neurons have synapses on their axon terminals so that other axon terminals are synapsing on the axon terminal of the target neuron and these will often be a mix of excitatory and inhibitory synapses. And there's a big variety in how the synapses are set up on neurons. And there would be a mix of some excitatory and inhibitory synapses at all these locations. But for neurons that are set up like this, kind of a general way of thinking about how information would flow to the neuron is that they can receive lots of excitatory input through the dendrites, causing depolarizations to spread down the dendrites into the soma. But then if these neurons are inhibiting the soma, that can block those depolarizations from reaching the trigger zone to trigger an action potential. And then when action potentials are conducted from the trigger zone down the axon to the axon terminal, the excitatory and inhibitory synapses on the axon terminal can increase or decrease the amount of neurotransmitter that is released when an action potential reaches the axon terminal. So that there can be fine tuning of the output of the neuron at multiple levels all the way from the dendrites through the soma and to the actual individual axon terminals, can have their output turned up or turned down in response to the information flowing in from all these synapses. So that one way you can categorize synapses is if they're predominately excitatory or predominately inhibitory. But there are some other big differences in neurotransmitter receptors and how they pass information from neurotransmitters in the chemical synapse to the target cell. So let me just draw a big axon terminal here that's releasing neurotransmitter into the synaptic cleft. And this will be the post synaptic membrane of the target cell. And I'm gonna draw the two big types of neurotransmitter receptors here. Let me draw this one in grey with its little receptor to bind to the neurotransmitter. And I'll draw this other one in yellow over here with its little pocket to bind to its neurotransmitter. So this first type of neurotransmitter receptor is called ionotropic. And ionotropic neurotransmitter receptors are ligand gated ion channels. So they have ion right in the name. And when their ligand binds to their receptor, which in this case is their neurotransmitter, they open and allow certain ions to pass. And when the neurotransmitter leaves the receptor, then they close and they don't let ions pass through anymore. The ionotropic neurotransmitter receptors cause graded potentials when they're activated, which have a rapid effect on the potential of the near by membrane that is brief and local. The target cell will usually be excited if the activated ionotropic neurotransmitter receptor allows sodium or calcium ions to pass because they will usually flow into the neuron, bringing their positive charges in and causing depolarization. Or the ionotropic neurotransmitter receptor will usually cause inhibition of the target cell if it allows chloride or potassium ions to pass. Chloride ions will usually flow into the neuron, bringing negative charges in, making it more negative inside and potassium ions will usually flow out of the neuron, carrying their positive charges outside and also making it more negative inside. Now the other big class of neurotransmitter receptors are called metabotropic. And these are not ion channels. Instead, when their neurotransmitter binds to the receptor, they activate second messengers inside the neuron. And there are a number of different types of second messenger systems that can be activated by metabotopic neurotransmitter receptors. And these second messengers can do a lot of different things. They can go and effect the behavior of ion channels, causing them to be more or less active. Or they can change the activity of proteins inside the neuron. And some can even effect the activity of genes and change the pattern of gene expression inside of neurons. When these metabotropic neurotransmtter receptors are activated, the response of the target cell occurs more slowly than it does with activation of ionotropic neurotransmitter receptors, but the effects may be larger and they may be more widespread because there can be amplification through these second messenger systems. The effects of activation of these second messenger systems by metabotropic receptors may involve just brief excitation or inhibition of the target cell, or it may cause longer lasting changes to how the target cell behaves, either when it's at rest or when it's responding to input.