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ADRENERGIC DRUGS
(Sympathomimetics,
Adrenomimetics)
Sponsored
Medical Lecture Notes – All Subjects
USMLE Exam (America) – Practice
The sympathetic preganglionic fibers leave the
CNS through the thoracic and lumbar spinal nerves.
The sympathetic preganglionic neurons (first
neurons) project from the intermediolateral
column of the spinal gray matter to the paired
paravertebral ganglionic chain lying alongside
the vertebral column and to unpaired prevertebral
ganglia. These ganglia represent sites of synaptic
contact between preganglionic axons (1st
neurons)
and nerve cells (2nd
neurons) that emit postgan-
glionic axons terminating on cells in various end
organs. In addition, there are preganglionic neurons
that project either to peripheral ganglia in end organs
or to the adrenal medulla.
(NOR)ADRENERGIC AND DOPAMINERGIC NERVES
NE
Activation of the
Sympathetic Nervous
System can be
considered a means
by which the body
achieves a state of
maximal work capacity
as required in fight
or flight situations.
Whereas ACh serves as the chemical transmitter at
ganglionic synapses between first and second neurons
Norepinephrine (NE, noradrenaline) is the mediator at
synapses of the second neuron. Excitation of the neuron
leads to activation of a larger aggregate of effector cells,
although the action of released NE may be confined to
the region of each junction. Excitation of preganglionic
neurons innervating the adrenal medulla causes
liberation of ACh. This, in turn, elicits a secretion
of epinephrine (adrenaline) into the blood, by
which it is distributed to body tissues as a hormone.
Adrenergic
(catecholamine)
neurotransmitters
Adrenergic
receptors:
α1
α2
β1
β2
β3
Adrenoceptors fall into two major
groups, designated alpha (α1, α2)
and beta (β1, β2, β3) within
each of which further subtypes can be
distinguished pharmacologically. The
different adrenoceptors are differentially
distributed according to region and
tissue. Agonists at adrenoceptors
(direct adrenomimetics) mimic the
actions of the naturally occurring
catecholamines, NA and epinephrine, and
are used for various therapeutic effects.
Within the varicosities, NE is stored in small
membrane-enclosed vesicles (granules,
0.05 to 0.2 µm in diameter). In the axoplasm,
L-tyrosine is converted via two intermediate
steps to dopamine (DA), which is taken up into
the vesicles and there converted to NE by
DA-beta-hydroxylase.
When stimulated electrically, the sympathetic
nerve discharges the contents of part of its
vesicles, including NE, into the extracellular
space. Liberated NE reacts with adrenoceptors
located postjunctionally on the membrane of
effector cells or prejunctionally on the membrane of
varicosities. Activation of presynaptic α2-receptors
inhibits NE (regulative negative feedback).
Presynaptic receptors in adrenergic synapse
and their role in the regulatory negative and
positive feedback
Presynaptic regulation of transmitter release from
noradrenergic and cholinergic nerve terminal
The effect of released NE wanes quickly,
because approximately 90% is actively
transported back into the axoplasm, then
into storage vesicles (neuronal re-uptake).
Small portions of NE are inactivated by the
enzyme catechol-O-methyltransferase
(COMT, present in the cytoplasm of
postjunctional cells, to yield normeta-
nephrine), and monoamine oxidase
(MAO, present in the mitochondria of nerve
cells and postjunctional cells) to yield
3,4-dihydroxymandelic acid).
The liver is richly endowed with
COMT and MAO. It therefore contri-
butes significantly to the degradation
of circulating NE and epinephrine.
The end productThe end product of the combinedof the combined
actions of MAO and COMT isactions of MAO and COMT is
vanillylmandelic acidvanillylmandelic acid..
Antiparkinsonian dopaminergic drugs
moclobemide and selegiline block MAO.
Action on alpha-adrenoceptors
•Arterioles and veins (α1): contraction and rise in BP
•Eye (α1): decreased aqueous secretion and mydriasis
•GIT (α1): contraction of sphincters
•Bladder trigone (α1): contraction
•Uterus (α1): contraction
•Insulin secretion (α2): inhibited
•Male sex organs: ejaculation
•Salivary glands (α1): water secretion
•Nictitating membrane in cats (α1): contraction
Noradrenaline (α1)
PLC
PIP2
IP3
Ca2+
DAG
PKC
ADP
ATP
Ex
In
(+)
Gs
• PLC (phospholipase C) catalyses the
formation of two intracellular messen-
gers − InsP3 and DAG, from memb-
rane phospholipids.
• InsP3 (inositol-triphosphate) increases
free cytosolic calcium by releasing
Ca2+
from the endoplasmic reticulum.
• Free calcium initiates contractions, se-
cretion, membrane hyperpolarization
• DAG activates protein kinase C.
Action on beta-adrenoceptors
•Arterioles and veins (β2): dilation and fall in BP
•Heart (β1): increased heart rate,
force, and conduction velocity
•Lung (β2): bronchodilation
•Eye (β2): enhanced aqueous secretion
•GIT (β2): intestinal relaxation
•Bladder detrusor (β2): relaxation
•Uterus (β2): relaxation
•Liver (β2): glycogenolysis
•Insulin and glucagon secretion (β2): augmented
•Fat (β3): lipolysis
•Kidney (β ): renin release
Adr (β1&β2)
Gs AC
ATPcAMP
PKA Effects
Ex
In
(+)
β-ad-
reno-
ceptor
•7 sub-
units
Agents which increase cAMP
(adrenaline, salbutamol,
and other beta-adrenoceptor
agonists) inhibit histamine
secretion and produce
bronchodilation
(antiasthmatic effect).
Autonomic
control
of pupil (A)
and site
of action of
mydriatics (B)
and
miotics (C)
Chemical structure of catecholamines
and affinity for α- and β-receptors
Norepinephrine (noradrenaline):
α1, α2, β1 and β3, but no β2 action
Epinephrine (adrenaline):
α1, α2, β1 and β2, and weak β3 action
Isoproterenol (isoprenaline):
β1 and β2, but no α action
--------------------------------------------------
Clonidine: presynaptic α2 agonist
(with antihypertensive action)
 Direct-acting adrenomimetics
a) α-adrenomimetics (activators of phospholipase C)
- antihypotensive drugs: Etilefrinе, Midodrine, Noradrenaline
- local nasal decongestants: Naphazoline, Oxymetazoline,
Xylometazoline (0.1% nasal drops: 3 x 2 drops daily 5 days)
- eye drops in glaucoma: Phenylephrine
b) Cardioselective β1-adrenomimetics: Dobutamine
c) DA-ergic adrenomimetics: Dopamine
d) Selective β2-adrenomimetics: Clenbuterol, Fenoterol, Hexoprenaline,
Indacaterol, Levosalbutamol, Salbutamol, Salmeterol, Terbutaline
e) Non-selective β-adrenomimetics: Isoprenaline and Orciprenaline
f) α- and β-adrenomimetics: Adrenaline (antiallergic): sol. 0,1% 1 ml s.c.;
Anapen® or EpiPen® (0.3 mg/0.3 ml i.m.) in prefilled syringes
 Indirect-acting adrenomimetics
Antihypotensive drugs
Ephedrine, Mephentermine
http://www.youtube.com/watch?v=ZR5c5VP2rOs
I.M.
Pre-filled syringes: Anapen®
and EpiPen®
: I.M.
Reactive hyperemia due to α-adrenomimetics
(naphazoline, oxymetazoline, xylometazoline)
e.g., following decongestion of nasal mucosa
Some important catecholamines
Isoproterenol (USAN) = Isoprenaline (INN)
BP – blood pressure, HR – heart rate
Dose-response curves of Adr (adrenaline), NA (noradrenaline)
and Iso (isoprenaline) on isolated aortic strip and isolated bron-
chial smooth muscle illustrating two distinct rank orders of po-
tencies respectively for α- and β-adrenergic receptors.
Isolated aortic strip Isolated bronchial
smooth muscle
Effect after 3 to 5 min
and duration 4–6 h:
•Salbutamol
•Fenoterol
Effect after 15–20 min
and duration 12 h:
•Salmeterol
FACTORS THAT EXACERBATE ASTHMA
The primary site of bronchodilation action of inhaled
β2-adrenergic agonists is mainly bronchiolar smooth muscle.
Atropinic drugs cause bronchodilation by blocking cholinergic
constrictor tone, act primarily in large airways.
Selective β2-adrenomimetics with tocolytic effect
•Fenoterol (Partusisten®
: tab. 5 mg)
•Hexoprenaline
•Salbutamol (Salbupart®
)
•Terbutaline
Ephedra
equisetina
-Ephedrine
(indirect adreno-
mimetic with
antihypotensive
and
antiasthmatic
effects
ADR: tachy-
phyllaxis
Indirect
sympathomimetics
with central
stimulant
activity and
abuse potential
•Amphetamine
•Cocaine
Erythroxylum
coca L.

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Adrenergic drugs

  • 2. Sponsored Medical Lecture Notes – All Subjects USMLE Exam (America) – Practice
  • 3. The sympathetic preganglionic fibers leave the CNS through the thoracic and lumbar spinal nerves. The sympathetic preganglionic neurons (first neurons) project from the intermediolateral column of the spinal gray matter to the paired paravertebral ganglionic chain lying alongside the vertebral column and to unpaired prevertebral ganglia. These ganglia represent sites of synaptic contact between preganglionic axons (1st neurons) and nerve cells (2nd neurons) that emit postgan- glionic axons terminating on cells in various end organs. In addition, there are preganglionic neurons that project either to peripheral ganglia in end organs or to the adrenal medulla.
  • 5. Activation of the Sympathetic Nervous System can be considered a means by which the body achieves a state of maximal work capacity as required in fight or flight situations.
  • 6. Whereas ACh serves as the chemical transmitter at ganglionic synapses between first and second neurons Norepinephrine (NE, noradrenaline) is the mediator at synapses of the second neuron. Excitation of the neuron leads to activation of a larger aggregate of effector cells, although the action of released NE may be confined to the region of each junction. Excitation of preganglionic neurons innervating the adrenal medulla causes liberation of ACh. This, in turn, elicits a secretion of epinephrine (adrenaline) into the blood, by which it is distributed to body tissues as a hormone.
  • 7.
  • 9. Adrenoceptors fall into two major groups, designated alpha (α1, α2) and beta (β1, β2, β3) within each of which further subtypes can be distinguished pharmacologically. The different adrenoceptors are differentially distributed according to region and tissue. Agonists at adrenoceptors (direct adrenomimetics) mimic the actions of the naturally occurring catecholamines, NA and epinephrine, and are used for various therapeutic effects.
  • 10. Within the varicosities, NE is stored in small membrane-enclosed vesicles (granules, 0.05 to 0.2 µm in diameter). In the axoplasm, L-tyrosine is converted via two intermediate steps to dopamine (DA), which is taken up into the vesicles and there converted to NE by DA-beta-hydroxylase. When stimulated electrically, the sympathetic nerve discharges the contents of part of its vesicles, including NE, into the extracellular space. Liberated NE reacts with adrenoceptors located postjunctionally on the membrane of effector cells or prejunctionally on the membrane of varicosities. Activation of presynaptic α2-receptors inhibits NE (regulative negative feedback).
  • 11. Presynaptic receptors in adrenergic synapse and their role in the regulatory negative and positive feedback
  • 12. Presynaptic regulation of transmitter release from noradrenergic and cholinergic nerve terminal
  • 13. The effect of released NE wanes quickly, because approximately 90% is actively transported back into the axoplasm, then into storage vesicles (neuronal re-uptake). Small portions of NE are inactivated by the enzyme catechol-O-methyltransferase (COMT, present in the cytoplasm of postjunctional cells, to yield normeta- nephrine), and monoamine oxidase (MAO, present in the mitochondria of nerve cells and postjunctional cells) to yield 3,4-dihydroxymandelic acid).
  • 14. The liver is richly endowed with COMT and MAO. It therefore contri- butes significantly to the degradation of circulating NE and epinephrine. The end productThe end product of the combinedof the combined actions of MAO and COMT isactions of MAO and COMT is vanillylmandelic acidvanillylmandelic acid..
  • 15.
  • 17. Action on alpha-adrenoceptors •Arterioles and veins (α1): contraction and rise in BP •Eye (α1): decreased aqueous secretion and mydriasis •GIT (α1): contraction of sphincters •Bladder trigone (α1): contraction •Uterus (α1): contraction •Insulin secretion (α2): inhibited •Male sex organs: ejaculation •Salivary glands (α1): water secretion •Nictitating membrane in cats (α1): contraction
  • 19.
  • 20. • PLC (phospholipase C) catalyses the formation of two intracellular messen- gers − InsP3 and DAG, from memb- rane phospholipids. • InsP3 (inositol-triphosphate) increases free cytosolic calcium by releasing Ca2+ from the endoplasmic reticulum. • Free calcium initiates contractions, se- cretion, membrane hyperpolarization • DAG activates protein kinase C.
  • 21. Action on beta-adrenoceptors •Arterioles and veins (β2): dilation and fall in BP •Heart (β1): increased heart rate, force, and conduction velocity •Lung (β2): bronchodilation •Eye (β2): enhanced aqueous secretion •GIT (β2): intestinal relaxation •Bladder detrusor (β2): relaxation •Uterus (β2): relaxation •Liver (β2): glycogenolysis •Insulin and glucagon secretion (β2): augmented •Fat (β3): lipolysis •Kidney (β ): renin release
  • 22. Adr (β1&β2) Gs AC ATPcAMP PKA Effects Ex In (+)
  • 24. Agents which increase cAMP (adrenaline, salbutamol, and other beta-adrenoceptor agonists) inhibit histamine secretion and produce bronchodilation (antiasthmatic effect).
  • 25. Autonomic control of pupil (A) and site of action of mydriatics (B) and miotics (C)
  • 26.
  • 27.
  • 28. Chemical structure of catecholamines and affinity for α- and β-receptors
  • 29. Norepinephrine (noradrenaline): α1, α2, β1 and β3, but no β2 action Epinephrine (adrenaline): α1, α2, β1 and β2, and weak β3 action Isoproterenol (isoprenaline): β1 and β2, but no α action -------------------------------------------------- Clonidine: presynaptic α2 agonist (with antihypertensive action)
  • 30.  Direct-acting adrenomimetics a) α-adrenomimetics (activators of phospholipase C) - antihypotensive drugs: Etilefrinе, Midodrine, Noradrenaline - local nasal decongestants: Naphazoline, Oxymetazoline, Xylometazoline (0.1% nasal drops: 3 x 2 drops daily 5 days) - eye drops in glaucoma: Phenylephrine b) Cardioselective β1-adrenomimetics: Dobutamine c) DA-ergic adrenomimetics: Dopamine d) Selective β2-adrenomimetics: Clenbuterol, Fenoterol, Hexoprenaline, Indacaterol, Levosalbutamol, Salbutamol, Salmeterol, Terbutaline e) Non-selective β-adrenomimetics: Isoprenaline and Orciprenaline f) α- and β-adrenomimetics: Adrenaline (antiallergic): sol. 0,1% 1 ml s.c.; Anapen® or EpiPen® (0.3 mg/0.3 ml i.m.) in prefilled syringes  Indirect-acting adrenomimetics Antihypotensive drugs Ephedrine, Mephentermine
  • 32.
  • 33. Reactive hyperemia due to α-adrenomimetics (naphazoline, oxymetazoline, xylometazoline) e.g., following decongestion of nasal mucosa
  • 34. Some important catecholamines Isoproterenol (USAN) = Isoprenaline (INN)
  • 35. BP – blood pressure, HR – heart rate
  • 36. Dose-response curves of Adr (adrenaline), NA (noradrenaline) and Iso (isoprenaline) on isolated aortic strip and isolated bron- chial smooth muscle illustrating two distinct rank orders of po- tencies respectively for α- and β-adrenergic receptors. Isolated aortic strip Isolated bronchial smooth muscle
  • 37. Effect after 3 to 5 min and duration 4–6 h: •Salbutamol •Fenoterol Effect after 15–20 min and duration 12 h: •Salmeterol
  • 38.
  • 40. The primary site of bronchodilation action of inhaled β2-adrenergic agonists is mainly bronchiolar smooth muscle. Atropinic drugs cause bronchodilation by blocking cholinergic constrictor tone, act primarily in large airways.
  • 41. Selective β2-adrenomimetics with tocolytic effect •Fenoterol (Partusisten® : tab. 5 mg) •Hexoprenaline •Salbutamol (Salbupart® ) •Terbutaline