L10: Adrenergic Transmission Flashcards
What is noradrenaline?
The chemical transmitter of the sympathetic nervous system.
What are catecholamines?
- Noradrenaline.
- Adrenaline.
- Dopamine.
What are the sites of the release of catecholamines?
1- All postganglionic sympathetic fibers except those supplying skin, skeletal ms blood vessels, and sweat glands.
2- Some synapses in CNS.
3- Suprarenal medulla: adrenaline (80%) and noradrenaline (20%).
How is catecholamine synthesized?
- Noradrenaline is derived from tyrosine amino acids.
- Synthesis begins in the cytoplasm of terminal nerve endings and is completed in vesicles present in adrenergic nerve fibers.
- Synthesis occurs in the chromaffin cells of SRM and in the CNS neurons.
In liver:
• Phenylalanine - hydroxylation ——> tyrosine.
In axoplasm of adrenergic nerve fiber:
• Tyrosine - hydroxylation ——> DOPA - decarboxylation ——> dopamine
In adrenergic vesicles at nerve ending: Transport of dopamine. • Dopamine - +OH ——> Noradrenaline.
In SRM and CNS neurons: this reaction goes one step to form adrenaline. Noradrenaline - +CH3 ——> Adrenaline
Where is dopamine present in higher conc. Than noradrenaline?
In basal ganglia of the brain
Where are catecholamines stored?
- NA is stored inside the nerve terminals in tiny vesicles (1000 molecules or more).
- But some molecules are found free in the cytoplasm.
- In the adrenal medulla, adrenaline and NA are stored in the form of granules in the
chromaffin cells.
How is catecholamine released?
- when the action potential reaches the axon terminal it opens the voltage-gated Ca+2 channels → Ca2+ influx →increase Ca2+ level → move the vesicles toward the membrane and fuse with it → vesicles rupture and empty their content outside nerve fiber NA cross the cleft (10-30 nm) & bind to its receptors on effector organ.
- Stimulation of Symp. preganglionic nerve fibers relaying on chromaffin cells in SRM causes adrenaline and NA release.
What is the mechanism of action of Noradrenaline?
When NA binds with its receptors on the postsynaptic membrane, it leads to :
- change of cell membrane permeability to various ions. It either:
➢ ↑es membrane permeability to Na and Ca → ↑ed Na and Ca influx → depolarization (stimulation).
➢ ↑es membrane permeability to K and Cl → ↑ed K and Cl influx → hyperpolarization (inhibition) - Activation of adenyl cyclase → conversion of ATP into cAMP→ initiates many intracellular activities.
How is noradrenaline removed?
Once, NA produces its action, it is rapidly removed in three different ways:
- Neuronal uptake (85 %)
• NA is actively reuptaken into the adrenergic nerve end where it is stored in the vesicles or oxidized by monoamine oxidase (MAO).
- Extra neuronal uptake (15 %)
• NA is inactivated by catechol-o-methyl transferase (COMT). - Excretion in urine
• Small amount of NA escapes enzymatic destruction and is excreted in urine (conjugated with glucuronic acid)
Compare between MOA and COMT in terms of:
Name: Site of uptake: Type of process: Amount removed: Sites:
Mono-amino-oxidase
Catecholamine o- methyltransferase
Neuronal.
Extra –neuronal.
Produce oxidation Produce methylation (then Excretion by glucuration)
Removal of 85% of adrenaline.
Removal of 15% of adrenaline.
-Present in mitochondria of
adrenergic fibers, liver, and kidney (ALK)
-Present in all tissues especially the kidney
and brain (KB)
What is the definition of adrenergic receptors?
adrenergic receptors are receptors that respond to NA and adrenaline.
What is the classification of adrenergic receptors?
- α adrenergic receptors: subclassified into (α 1: excitatory and α 2: inhibitory)
• They are equally sensitive to adrenaline and NA. - β adrenergic receptors: subclassified into (β 1 , β 2 , β 3 , β 4 , β 5 )
• β1:
o Are sensitive to both norepinephrine and epinephrine
o Are more sensitive than the α1 receptors
• β2:
o Are more sensitive to epinephrine than to norepinephrine.
o Are more sensitive to epinephrine than the α1 receptors.
N.B
➢ β3 receptors: located in the adipose tissues → increase lipolysis.
➢ β4 and β5 receptors: under research.
What are the sites of alpha 1 receptors?
-Are postsynaptic receptors located on smooth ms of blood vessels in the skin and splanchnic regions, the GIT and bladder sphincters, and dilator pupillae ms of the iris and piloerector ms
What is the mechanism of action of alpha 1 receptors?
Are G-protein coupled receptors that activate phospholipase C, and increase in inositol 1,4,5-triphosphate (IP3) and intracellular [Ca2+] to make contraction or excitation
What are the physiological actions of alpha 1 receptors?
Mainly excitatory:-
➢ Vasoconstriction
➢ Contraction of piloerector muscle.
➢ Contraction of splenic capsule.
➢ Contraction of the seminal vesicle, ejaculatory duct.
➢ Contraction of bladder & intestinal sphincters.
➢ Adrenergic sweating in the palm.
-Inhibitory effects as
➢ Intestinal relaxation.
➢ Inhibition of insulin secretion.