The Effect of Drugs, Toxins, and Other Molecules on Synapse and Synapse Transmission.

If the frequency of action potentials in the excitatory presynaptic cell increases than the number of action potentials in the postsynaptic cell will increase as well. This is due to temporal summation of EPSP at very frequent times. This causes the postsynaptic cell to produce many action potential in succession.

Once a presynaptic neuron is passive, an electrical current is spread along the length of the axon (Schiff, 2012). This is known as action potential (Pinel, 2011). Action potential happens once an abundant amount of depolarisation reaches the limit through the entry of sodium, by means of voltage gated sodium channels

As an action potential travels down the axon of the presynaptic neuron, the action potential reaches the axon terminal synaptic vesicles which migrate toward the synapse. They then release neurotransmitters into the synaptic cleft. The neurotransmitters travel through the synaptic cleft and bind to ligand-gated ion channels on the postsynaptic neuron membrane. The channels open and allow chemicals to enter the cell (i.e. sodium). Then positively charged sodium enters the cell and causes the cell to depolarize. The depolarization spreads down the axon and an action potential is generated. The process then starts over at the axon terminals.

When substances like Acetylcholine (Ach) and norepinephrine which are small- molecular neurotransmitters are released into the body they bind to receptors on tissue or neurons through our ANS and PNS system. Ach is released by many PNS neurons and some CNS neurons. In the PNS Ach is an excitatory neurotransmitter at some synapses, such as the neuromuscular junction where it binds to ionotropic receptors which open cation channels. Ach can also be an inhibitory neurotransmitter at other synapses, where it binds to metabotropic receptors while opening potassium channels. The enzyme acetylcholinesterase (AchE) inactivates Ach by splitting into acetate and choline fragments. Norepinephrine (NE) is a biogenic amine; most biogenic amines may cause

The main components of the synapses are as follows: The Axon terminal, found at the end of the Axon, passes neurotransmitters to other neurons via synaptic transmission. Synaptic Vesicles contain neurotransmitters within the Axon. Neurotransmitters themselves are chemical messengers that travel through the neurons and activate receptors on the receiving cell. The neurotransmitters are diffused through the synaptic cleft—a region between the two neurons and gap the neurotransmitter needs to cross to make it to the receiving cell. Said receiving cell is what receives the neurotransmitters and starts the process over again. The receptors on the cell are structures that receive the neurotransmitters and

A synapse is a link where neurons communicate with other cells across narrow gaps using neurotransmitters or pulses (I learned this in my biology course last semester).

The structure of neuromuscular junction consists of a neuron and skeletal muscle cell. The motor neurons, which arise from the spinal cord, supply the skeletal muscle fibers. The neuromuscular junction is un-myelin nerve with a bulb shape at the endings that contract the muscle fiber. The schwann cells form a covering over the postsynaptic membrane and nerve membrane of the fiber that is located under the terminal and is categorized as a post-junction folds. The area between the folds and the bulbs create the synaptic cleft. This consists of proteins and proteoglycans. The enzyme acetylcholinesterase; exist only at high levels in the synaptic basal lamina (UMN,

The end of the axon spread into some shorter fibers that have swellings on the ends called synaptic knobs. The synaptic knob has a number of little saclike structures in it called synaptic vesicles. Inside the synaptic vesicles are chemicals hung in fluid, which are molecules of substances called neurotransmitters which are inside a neuron and are going to transmit a message. Neurotransmitter are released into the synapse from synaptic vesicles. The neurotransmitter molecules bind to receptor sites on the releasing neuron and the second neuron or glands or even muscles causing a reaction.

In a normal and healthy nervous system, many electrical signals are received and sent through neurons. The arrival of those signals at the end of the neuron triggers the release of many chemicals, in specific, neurotransmitters (Brooker, 2011). These chemicals travel into a gap between the presynaptic (end of one neuron) and the beginning of he postsynaptic (next neuron). This gap is named a synapse (Brooker, 2011). Neurotransmitters are then released into the synapse and then bind to the ibid (post -synaptic neuron). When this

Glutamate-receptor-interacting protein (GRIP) is the interacting protein which is associated with AMPAR protein receptor in the postsynaptic cell. Amount of GRIP is associated with AMPAR receptors can lead to the prediction of activity in the presynaptic cell. AMPAR receptor change shape to be ready to receive neurotransmitter when GRIP bind. The presynaptic cell contains vesicle which neurotransmitters are accommodated. When calcium enters the presynaptic cell by calcium channel, vesicles dock to the presynaptic cell to become ready to release neurotransmitters to the synaptic gap. Neurotransmitters are released in a packet called quanta. AMPAR receptor has to change its shape by GRIP to receive the release of quanta in the synaptic

Neurons have a part called the dendrites and this is where the neuron fires a correct impulse to another neuron through the axon. Axon is a long projection that connects nerve cells.

Dr. Harlow’s central focus is to find out what are the molecules contained within, and released from cholinergic synaptic vesicles. He explained that in 1974, studies found that ATP was being loaded into the cholinergic synapse vesicle, and that it is important for signaling molecules. In the central nervous system, the cholinergic neurons can posses many types of neurotransmission. One question about these concepts is how neurotransmitters unload in the

Synaptic signaling is a the main form of signaling utilized in the central and peripheral nervous systems which utilizes neurons to transfer the signal throughout the body (Williams College). When a neuron receives an electrical signal at the dendrites (branch-like receptors) it is transferred to the cell body called the soma, then down the axon (tail-like area) and finally to the terminals (branch-like endings of the neuron) (Williams College). In most cases, the electrical signal at the terminals causes a release of neurotransmitters into the space between this neuron, and the neighboring neuron called the synaptic cleft which would either excite or inhibit the next neuron (Campbell). So, synaptic signaling involves a specific neuron transmitting its signal into only its neighboring cell not into the environment. Therefore it is not synaptic signaling which releases a signal molecule into the environment and a number of cells in the immediate vicinity

As soon as the electrical signal reaches the end of the axon, mechanism of chemical alteration initiates. First, calcium ion spurt into the axon terminal, leading to the release of neurotransmitters “molecules released neurons which carries information to the adjacent cell”. Next, inside the axon terminal, neurotransmitter molecules are stored inside a membrane sac called vesicle. Finally, the neurotransmitter molecule is then discharged in synapse space to be delivered to post synaptic neuron.

Most neurons do not make direct connections with surrounding neurons, signals (molecules) must make the transition from the presynaptic (upstream) neuron to the postsynaptic (downstream) neuron. This transition space is called the synaptic cleft. The exchange of information from the pre- to postsynaptic neuron is called a synapse.