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How do local anesthetics block pain in the body?

Local anesthetics work by blocking the transmission of pain signals in nerves. They do this by interfering with the function of sodium channels in nerve cells, preventing the cells from sending pain signals to the brain. This numbs the area where the anesthetic is applied, temporarily blocking the sensation of pain.


What passive channels are likely found in the pacinian membrane?

The efflux of potassium ions is maintained by passive potassium channels.


What passive channels are likely found in the Pacinian corpuscle?

The efflux of potassium ions is maintained by passive potassium channels.


The channels that transport sodium and potassium within the axon are called?

The channels that transport sodium and potassium within the axon are called voltage-gated sodium channels and voltage-gated potassium channels. These channels play a crucial role in generating and propagating action potentials along the axon.


Why does anesthetic keep you from feeling pain?

There are several different ways that anesthetics work, and they are divide into different classes to reflect that. One of the most commonly used anesthetics, Lidocaine, blocks pain signals from being sent to the brain and also helps them from being created in the first place. This is achieved by blocking sodium channels in the nerve cells, thus leaving the nerve unable depolarize and fire its signal.


What cell gates open immediately after action potential peak?

Voltage-gated potassium channels open immediately after the action potential peak, allowing potassium ions to exit the cell. This repolarizes the cell membrane and helps bring it back to its resting state.


What impact does Lexapro have on potassium ion channels?

Lexapro, also known as Escitalopram is an antidepressant which blocks specific potassium channels in the CNS. While most specific to the HERG channel (Kv11.1) it has also been shown to effect Kv2.1 and Kv2.2 as well as Kv1.5 potassium channels


Name the membrane valves that open and close for potassium efflux and sodium influx?

Potassium efflux is controlled by voltage-gated potassium channels, while sodium influx is controlled by voltage-gated sodium channels. These channels open and close in response to changes in membrane potential, regulating the flow of ions in and out of the cell.


How does the potassium ion channel selectively allow potassium ions k plus to pass through but block sodium ions Na Plus?

Potassium ion channels have a selectivity filter with specific amino acid residues that are the right size and shape to accommodate potassium ions, but not sodium ions. This size exclusion mechanism allows potassium ions to pass through while effectively blocking sodium ions. Additionally, the charge properties of the selectivity filter can also contribute to the selectivity of the potassium ion channel for potassium ions over sodium ions.


Why blocking the sodium channels result in diarrhoea?

Blocking sodium ion channels reduces the uptake of water from the lumen of the intenstine into the epithelial cells of the villus due to osmosis. Water, therefore, remains in the intestine and this causes watery faeces/diarrhoea


How do sodium and potassium travel into and out of cells?

Sodium and potassium travel into and out of cells through specialized proteins called ion channels. These channels allow the ions to move across the cell membrane, maintaining the balance of these ions inside and outside the cell. Sodium ions typically enter the cell through sodium channels, while potassium ions exit the cell through potassium channels. This movement of ions is crucial for various cellular functions, including nerve signaling and muscle contraction.


What allows potassium to diffuse in and out of cells?

Potassium diffuses in and out of cells through potassium channels, which are membrane proteins that selectively allow potassium ions to move down their concentration gradient. These channels help maintain the resting membrane potential and are crucial for many cellular processes, including nerve signaling and muscle contraction.