ANS - Neurotransmitters and receptors Flashcards
ANS
- sympathetic
Sympathetic Preganglion: ACH > Autonomic ganglion:
Nicotinic receptors
> Sympathetic Postganglion: Adrenaline Noradrenaline
> Effector cells:
α1, α2, β1, β2 receptors
sympathetic effector cells
Effector cells:
α1, α2, β1, β2 receptors
- are adrenergic receptors
ANS
parasympathetic
Parasympathetic Preganglion: ACH > Autonomic ganglion:
Nicotinic receptors > Paraympathetic Postganglion: ACH > Effector cells: Muscarinic receptors
cholinergic receptors
Nicotinic and muscarinic receptors are cholinergic receptors
Cholinergic Receptors:
Nicotinic receptor
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
Cholinergic Receptors:
Muscarinic receptors
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
Adrenergic receptors
α1
< Adrenaline & > Noradrenaline - Ca 2+ second- messenger system - Excitatory response, contraction of smooth muscle - Arterioles, most sympathetic target tissues
Adrenergic receptors
α2
< Adrenaline & > Noradrenaline
- Blocks cyclic AMP production
- Inhibitory response, relaxation of smooth muscle
- DIT
Adrenergic receptors
β1
~ Adrenaline & ~ Noradrenaline
Cyclic AMP second- messenger system
- Excitatory response
- Heart (kidney, liver)
Adrenergic receptors
β2
Mostly Adrenaline
- Cyclic AMP second- messenger system
- Inhibitory response, relaxation of smooth muscle
- Bronchioles, arterioles
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….
selectively blocks β1, adrenergic receptors therby reducing the sympathetic effects on the heart such drugs (metoprolol, atenolol) are called β1 antagonists
*** 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….
selectively blocks ACh at the muscuranic receptors, thereby blocking the parasympathetic effects. This drug (Atropine) is called a muscarinic antagonist.
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….
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
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 ….
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/
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
nicotinic antagonist