second messanger pathways Flashcards

1
Q

What is the Second Messenger Pathway, and how does it function?

A

is initiated when the first messenger binds to a G-protein-coupled receptor (GPCR), which activates a G-protein.
The G-protein then interacts with an effector protein, causing the production of intracellular messengers (second messengers). These second messengers activate protein kinases, leading to phosphorylation and a cellular response.

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2
Q

What are G-protein-coupled receptors (GPCRs)?

A

GPCRs are receptors that, when bound by a first messenger, activate G-proteins (composed of α, β, and γ subunits). G-proteins function as intermediates that alter the activity of nearby membrane proteins, which are typically effector proteins involved in the production of second messengers.

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3
Q

What is the role of second messengers in cell signaling?

A

Second messengers are small molecules that relay signals from the activated receptor to target proteins inside the cell. They help transmit and amplify the signal, eventually leading to the desired cellular response, such as changes in metabolism, enzyme activity, or ion channel opening.

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4
Q

What are some examples of second messengers, and what are their roles?

A

Ca2+
IP3
DAG
cAMP
cGMP
1. Ca2+: Binds to calmodulin and other proteins to alter enzyme activity, trigger exocytosis, muscle contraction, cytoskeletal movement, and channel opening.
2. IP3: Releases Ca2+ from intracellular stores, affecting enzyme activity, exocytosis, muscle contraction, and cytoskeletal movement.
3.DAG: Activates protein kinase C (PKC), which phosphorylates target proteins.
4. cAMP: Activates protein kinase A (PKA) and binds to ion channels, leading to protein phosphorylation and altered channel activity.
5. cGMP: Activates protein kinase G (PKG) and binds to ion channels, leading to phosphorylation and changes in channel opening.

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5
Q

What are some examples of effector proteins linked to G-proteins?

A
  1. adenyl cyclase (which produces cAMP),
  2. guanylyl cyclase (which produces cGMP)
    3.phospholipase C (which generates IP3 and DAG).
    These effector proteins produce second messengers that mediate the cellular response.
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6
Q

what does the activatiohn of G-proteins cause

A
  1. open ion channels
  2. alter enzyme activity
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7
Q

Adenulyl cyclase- cAMP by the GPCR describe the steps

A
  1. signal molecule binds to G proteins-linked receptor which activate the G protein
  2. G protein turns on adenyl cyclase (amplifier enzyme)
  3. adenyl cyclase convert ATP to cyclic adenosine monophosphate (cAMP)
  4. protein kinase A phosphorylate other proeins leading to cellular response
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8
Q

what can activating the cAMP pathway lead to

A

1.Modify heart rate
2.Formation of female hormones in ovaries
3.Break down stored glucose in liver
4.Control H2O conservation in kidneys
5.Perception of sweet taste in taste buds

depends on cellular location and cell type

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9
Q

Gyanyl cyclase - cGMP pathway

A
  1. signal molecule binds to G protein linked receptor which activates G protein
  2. G protein turns on guanyl cyclase- amplifier enz
    3, guanyl cyclase converts GTP to cyclic guanosine monophosphate (cGMP)
  3. protein kinase G phosphorylates other proteins leading to celluular response
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10
Q

how is the gyanyl cyclase- cGMP pathway activated and inhibited

A

activated- low calciu,
inhib- high calacum ion

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11
Q

guanyl cyclase cGMP functions

A

1.Drive adaptive/developmental changes
2.Causes relaxation (smooth muscle tissue)
3. increasein cGMP contributes to excessive neuron excitability and locomotor activity
4.Stimulate presynaptic glutamate release

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12
Q

phospholipase C pathway

A
  1. signal molecule activate receptor and associated G protein
  2. G protein activate phospholipase C (PL-C) an amplifier enz
    3.PL-C convert membrane phospholipids into diacylglyferol (DAG) and inositol triphosphate (ip3)
  3. DAG activate protein kinase C (PK-C)
  4. IP3 causes release of Ca drom organelles
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13
Q

What happens to the G-protein after a second messenger response is completed?

A

the alpha (α) subunit of the G-protein cleaves off a phosphate group, converting GTP to GDP. This inactivates the G-protein, helping to terminate the signaling process.

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14
Q

How are second messengers like cAMP and cGMP removed after the response?

A

degraded by phosphodiesterases, enzymes that break them down to stop their activity and help end the signal transduction pathway.

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15
Q

What role do protein phosphatases play in signal termination?

A

remove the phosphate groups added to proteins by protein kinases, thereby shutting off the signal transduction pathway. Unlike protein kinases, which are activated by signals, protein phosphatases are always active.

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16
Q

How do neurotransmitters function through second messenger systems?

A

seratonin, They change the conformation of chemically gated receptor channels, altering membrane permeability and ion fluxes across the synaptic membrane. These are referred to as “slow” synapses, as opposed to “fast” synapses where neurotransmitters act directly on ion channels.

17
Q

What happens to the first messenger after it initiates the response?

A

he first messenger (such as a hormone or neurotransmitter) can be degraded by the liver or excreted in the urine. In some cases, both the first messenger and its receptor are removed from the cell surface through receptor-mediated endocytosis.

18
Q

Why do cells respond differently to the same second messenger signal?

A

The variability in response depends on the specialization of the target cells, not the signaling mechanism itself. Different cell types are equipped with different proteins and pathways that interpret the signal in distinct ways, leading to various outcomes.

19
Q

How important are second messenger systems in drug treatments?

A

Second messenger systems, particularly those involving G-protein-coupled receptors (GPCRs), are vital targets for drugs. About half of all prescribed drugs act on GPCRs, helping to treat conditions like high blood pressure, congestive heart failure, asthma, and allergic reactions by modulating these signaling pathways.

20
Q

hy are second messenger systems particularly important for water-soluble hormones

A

ater-soluble hormones cannot easily cross the lipid bilayer of the cell membrane, so they rely on second messenger systems to relay their signals inside the target cells. This allows them to trigger cellular responses without needing to enter the cell.

21
Q

What is the difference between “fast” and “slow” synapses?

A

“Fast” synapses involve neurotransmitters that directly change the conformation of ion channels, causing immediate effects on membrane permeability and ion flux. In contrast, “slow” synapses, which involve second messenger systems, mediate their effects indirectly and typically result in slower, prolonged responses.

22
Q

ow does receptor-mediated endocytosis help terminate a signal?

A

In receptor-mediated endocytosis, both the first messenger and its receptor are internalized by the cell, effectively removing them from the cell surface and preventing further signaling. This helps to ensure the signal is properly terminated.

23
Q

describe receptor mediated endocytosis via the 2nd messanger oathway

A
  1. substances attach to membrane receptors
  2. membrane pockets inwards
  3. pocket pinches off as endocytotic vesicle containing target molecule