Lecture 7 9/1/23 Flashcards

1
Q

What are the two types of synapses?

A

-electrical synapse
-chemical synapse

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2
Q

What are the characteristics of electrical synapses?

A

-in smooth and cardiac muscle
-gap junctions allow free movement of ions

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3
Q

What are the characteristics of chemical synapses?

A

-majority in CNS and at NMJ
-release neurotransmitters

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4
Q

What are the characteristics of innervation?

A

-one nerve can innervate multiple muscle fibers
-each muscle cell only has one neuron

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5
Q

How does muscle contraction work in terms of action potentials?

A

-each muscle contraction is an all-or-nothing action potential
-the number of motor neurons firing determines the strength of the muscle contraction

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6
Q

What are the synaptic vesicles?

A

packets of acetylcholine neurotransmitters

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7
Q

What are the junctional folds of the post-synaptic membrane?

A

areas of increased surface area allowing for more receptors

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8
Q

What is the synaptic cleft?

A

the space where acetylcholine is released between the presynaptic terminal and the muscle cell

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9
Q

What type of ACh receptors are in skeletal muscle?

A

nicotinic receptors

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10
Q

What is the role of Ca2+ ions in neuro-muscular junctions?

A

-voltage changes associated with APs opens voltage-gated Ca2+ channels
-Ca2+ influxes into pre-synaptic terminal
-Ca2+ triggers vesicles to release ACh

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11
Q

What is the safety factor associated with NMJ?

A

-more than enough ACh and more than enough receptors
-ensures that muscle contraction occurs with every AP

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12
Q

Why is it important that there is a process to stop muscle contraction?

A

we only want one muscle contraction to occur per AP

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13
Q

How is muscle contraction stopped?

A

-acetylcholinesterase exists within synapse and breaks down ACh
-breakdown of ACh stops the muscle contraction
-choline is recycled for use in future APs and contractions

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14
Q

What is myasthenia gravis?

A

-condition in which there are not enough available ACh receptors
-leads to exercise fatigue

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15
Q

What are the two types of myasthenia gravis?

A

-immune-mediated: immune system attacks ACh receptors
-congenital: animal is not born with enough receptors

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16
Q

Why is the lack of NMJ safety factor important in myasthenia gravis?

A

-safety factor typically ensures that, as amount of ACh decreases, there are still enough receptors for the remaining ACh to find
-with fewer receptors, remaining ACh struggles to find receptors and carry out AP/contraction

17
Q

Why is myasthenia gravis a dangerous condition in dogs?

A

-muscles controlling the esophagus and breathing functions are skeletal muscle in dogs
-can lead to difficulty breathing
-also results in animal not being able to properly swallow
-end result can be regurgitation, aspiration, and pneumonia

18
Q

How can immune-mediated myasthenia gravis be treated?

A

suppression of the immune system to prevent it from attacking receptors

19
Q

How can congenital myasthenia gravis be treated?

A

inhibition of acetylcholinesterase to prevent ACh breakdown

20
Q

Why does inhibition of acetylcholinesterase treat myasthenia gravis?

A

it allows for acetylcholine to exist within the synaptic cleft for an extended time, increasing the likelihood it reaches the ACh receptors

21
Q

What are the potential downfalls of acetylcholinesterase inhibition?

A

-can lead to increased weakness due to not having enough time to reset between APs
-can overstimulate parasympathetic nervous system

22
Q

How can neurotransmitters function on a cell?

A

-excitatory/cause APs
-inhibitory/prevent APs

23
Q

How do different neurotransmitters function with different ion channels?

A

-excitatory neurotransmitters will open channels that allow for influx of + ions or efflux of - ions
-inhibitory neurotransmitters will open channels that allow for influx of - ions or efflux of + ions

24
Q

What is glycine?

A

an inhibitory transmitter, especially in the spinal cord/reflexes

25
Q

What is the effect of tetanus?

A

-toxins bind irreversibly to glycine receptors
-animal has no muscle relaxation
-must wait for animal to regenerate new glycine receptors following infection