ANS - Neurotransmitters and receptors Flashcards

1
Q

ANS

- sympathetic

A

Sympathetic Preganglion: ACH > Autonomic ganglion:
Nicotinic receptors
> Sympathetic Postganglion: Adrenaline Noradrenaline
> Effector cells:
α1, α2, β1, β2 receptors

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2
Q

sympathetic effector cells

A

Effector cells:
α1, α2, β1, β2 receptors

  • are adrenergic receptors
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3
Q

ANS

parasympathetic

A

Parasympathetic Preganglion: ACH > Autonomic ganglion:

Nicotinic receptors > Paraympathetic Postganglion: ACH > Effector cells: Muscarinic receptors

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4
Q

cholinergic receptors

A

Nicotinic and muscarinic receptors are cholinergic receptors

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5
Q

Cholinergic Receptors:

Nicotinic receptor

A

site of receptor:
All autonomic ganglia
Motor end plate of skeletal muscle fibres
Some CNS cell bodies and dendrites

Respond to ACH release from Sympathetic and parasympathetic preganglionic fibres
Motor neurons
Some CNS presynaptic terminals

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6
Q

Cholinergic Receptors:

Muscarinic receptors

A

Site of receptor:
Effector cells (cardiac muscle, smooth muscle, glands)
Some CNS cell bodies and dendrites

Respond to ACH release from
Parasympathetic postganglionic fibres
Some CNS presynaptic terminals

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7
Q

Adrenergic receptors

α1

A
< Adrenaline &amp; > Noradrenaline
- Ca 2+ second- messenger system
- Excitatory response, contraction of smooth muscle
- Arterioles,
most sympathetic target tissues
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8
Q

Adrenergic receptors

α2

A

< Adrenaline & > Noradrenaline

  • Blocks cyclic AMP production
  • Inhibitory response, relaxation of smooth muscle
  • DIT
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9
Q

Adrenergic receptors

β1

A

~ Adrenaline & ~ Noradrenaline
Cyclic AMP second- messenger system
- Excitatory response
- Heart (kidney, liver)

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10
Q

Adrenergic receptors

β2

A

Mostly Adrenaline

  • Cyclic AMP second- messenger system
  • Inhibitory response, relaxation of smooth muscle
  • Bronchioles, arterioles
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11
Q

You are a drug designer and being asked to develop a drug that reduces heart rate in the treatment of hypertension. Based on todays’ information you would develop a drug that….

A
selectively blocks β1, adrenergic receptors therby reducing the sympathetic effects on the heart 
such drugs (metoprolol, atenolol) are called β1 antagonists
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12
Q

*** You are a drug designer and being asked to develop a drug that suppresses salivary and bronchial secretion before surgery. Based on todays’ information you would develop a drug that….

A

selectively blocks ACh at the muscuranic receptors, thereby blocking the parasympathetic effects. This drug (Atropine) is called a muscarinic antagonist.

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13
Q

You are a drug designer and being asked to develop a drug that dilates bronchioles in the treatment of asthma without undesirably stimulating the heart. Based on todays’ information you would develop a drug that….

A

selectively activates β2 adrenergic receptors at low doeses thereby relaxing bronchioal smooth muscles (the heart has mostly β1 adrenergic receptors). This drug (salbutamol) is called β2 agonist

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14
Q

You are a drug designer and being asked to develop a drug that increases heart rate and that leads to general vasoconstriction in the treatment of acute cardiac failure. Based on todays’ information you would develop ….

A

Human adrenaline. Adrenaline activates a and b adrenergic receptors thereby increasing HE, and promoting smooth muscle contraction of peripheral arterioles, which results in increases arterial BP/

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15
Q

You are a drug designer and being asked to develop a drug that reduces the effects of both, sympathetic and parasympathetic NS. Based on todays’ information you would develop a/an

A

nicotinic antagonist

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16
Q

Autonomic agonists and antagonists

A

drugs are available that selectively enhance or mimic (agonists) or block (antagonists) autonomic responses