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Adrenergic Drugs/Sympathomimetics
• These are the drugs that mimic the response of sympathetic or
adrenergic system.
Neurotramsmitters: Neurotransmitters are the chemical mediators
released by the neurons to transmit the signals through synapse.
Three major endogenous catecholamines are:
 Adrenaline (Adr, Epinephrine)
 Noradrenaline (NA, Norepinephrine)
 Dopamine
Adrenergic Receptors
α β
α1 α2 β1 β2 β3
Tyrosine
Dopa
Dopamine
Noradrenaline
Adrenaline
Synthesis:
Tyrosine hydroxylase
Amino acid decarboxylase
Dopamine β-Hydroxylase
Phenylethanolamine N-methyl transferase
Adrenergic drugs acts through adrenergic receptors.
Adrenergic Receptors/Adenoreceptors are of 2
types: alpha (α) & beta (β).
Receptor Tissue Response
α1 Vascular smooth muscle vasocontraction
Genitourinary tract
smooth muscle
contraction
Smooth muscle
(Sphincter, radial muscle
of iris, gland)
Contraction
(mydriasis, secretion)
Intestinal smooth muscle Relaxation
α2 Prejunctional nerve
ending
NA release
Vascular smooth muscle vasoconstriction
Alpha receptors (α)
Receptor Tissue Response
β1 Heart Rate, FOC,
A-V conduction
Juxtaglomerular cells Rennin release
β2 Smooth muscles
(Bronchial,
gastrointestinal,
genitourinary, uterus)
Relaxation
Skeletal muscle Glycogenolysis
K+ uptake
Liver Glycogenolysis
Gluconeogenesis
β3 Adipose tissue Lipolysis
Beta receptors (β)
Adrenergic drugs/Sympathomimetics
1.Direct
sympathomimetics
Adrenaline,
NorAdrenaline,
Isoprenaline,
Phenylephrine,
Xylometazoline
2.Indirect
sympathomimetics
Amphetamine, Cocaine,
Sellegilline, Entacapone
3.Mixed action
sympathomimetics
Ephedrine,
Mephentermine
Pressor agents Dopamine, NA, Mephentermine, Ephedrine
Cardiac
stimulant
Dobutamine, Adr, Iso
Bronchodilators Salbutamol (albuterol), Salmeterol, Terbutaline, Iso,
Adr
Nasal
decongestant
Xylometazoline, Oxymetazoline, Phenylephrine
Pseudoephedrine
CNS stimulants Amphetamine, Dexamphetamine
Anorectics Fenfluramine, Sibutramine
Uterine relaxant Ritodrine, Isoxsuprine, salbutamol, Terbutaline
Clinical classification of Adrenergic drugs
Adrenaline (Adr) α1+ α2 + β1+ β2+weak β3 action
Noradrenaline (NA) α1+ α2+ β1+ β2 but no β3 action
Isoprenaline (Iso) β1+ β2+ β3 action but no α
action
Pharmacological Actions:
Epinephrine (adrenaline) is a potent stimulant of both α and β
adrenergic receptors. Most of the responses are seen after injection of
epinephrine, although the occurrence of sweating, piloerection, and
mydriasis depends on the physiological state of the patient. Particularly
prominent are the actions on the heart and on vascular and other
smooth muscle.
Norepinephrine (Noradrenaline) and epinephrine both are direct
agonists on effector cells, and their actions differ mainly in the ratio of
their effectiveness in stimulating α and β2 receptors. They are
approximately equipotent in stimulating β1 receptors. Norepinephrine
is a potent αagonist and has relatively little action on β2 receptors.
Heart Positive ionotropic effect (increase in force of contraction)
Positive chronotropic effect (increase in heart rate)
Positive dromotropic effect (increase in heart conduction)
Respiration Bronchodilation , Nasal decongestion
Blood
vessels
Vasoconstriction
Blood
pressure
Increases
GIT Relaxation but sphincter contracts so peristalsis decreases
Eye Mydriasis (Dilation of pupils)
Uterus Non-pregnant-Contraction; Pregnant-Relaxation
Skeletal
muscle
Tremor, glycogenolysis
Metabolic Hyperglycemia, Lipolysis, Hypokalemia
Adverse effects:
• Adr-sc/i.m: restlessness, palpitation, anxiety,
tremor, pallor
• Adr-i.v. high dose: cerebral haemorrhage,
arrhythmias
Contraindications:
• Hypertensive, Hyperthyroidism, Angina Pectoris
• Patient receiving β-blocker.
• During anesthesia by Halothane
• Dopamine is the immediate metabolic precursor of
norepinephrine and epinephrine. It is a central neurotransmitter
particularly important in the regulation of movement and
possesses important intrinsic pharmacological properties.
• In the periphery, it is synthesized in epithelial cells of the
proximal tubule and is thought to exert local diuretic and
natriuretic effects.
• Dopamine is a substrate for both MAO and COMT and thus is
ineffective when administered orally.
• It doesn’t cross BBB.
• In moderate dose (0.2-1mg) it increases BP & urine flow.
Mechanism of action:
• Dopamine can activate α- and β-adrenergic receptors. It acts on
dopaminergic receptors (D1-D5) present on peripheral
mesenteric and renal vascular beds. Binding of dopamine
produces vasodilation. D2 receptors are also found on
presynaptic adrenergic neurons, where their activation interferes
with norepinephrine release.
Indication:
• Given as i.v. infusion to patients with cardiogenic & septic
shock.
• Severe Congestive Heart Failure
• Dose regulated by monitoring BP & urine formation.
• At high concentrations, dopamine activates vascular a1
receptors, leading to more general vasoconstriction.
Adverse Effects:
Nausea, vomiting, tachycardia, anginal pain, arrhythmias,
headache, hypertension, and peripheral vasoconstriction
may be encountered during dopamine infusion.
Contraindication:
Hypovolemic shock, depression (patients receiving MAO
inhibitors or tricyclic antidepressants)
Dobutamine
Mechanism of Action:
• Dobutamine is a derivative of dopamine that directly acts
on adrenergic receptors(β1).
Indications:
• Dobutamine is used to increase cardiac output in acute
congestive heart failure as well as for inotropic support
after cardiac surgery.
• It increases cardiac output and does not significantly
elevate oxygen demands of the myocardium, a major
advantage over other sympathomimetic drugs.
• It is used in pump failure (Myocardial Infarction, Cardiac
surgery, CHF)
Contraindication:
• Atrial fibrillation
• May cause tolerance
Ephedrine
• Mixed action adrenergic drugs
• Orally effective & long acting than Adr
• Crosses BBB so stimulation
• Used in mild chronic bronchial asthma & hypotension during
spinal anaesthesia
Amphetamine
• Synthetic compound similar to ephedrine but have more CNS
action
• Improves alertness, attention, concentration & performance
• Included in dope test (drug for abuse)
• Used in attention deficit hyperactive disorder (ADHD)
Phenylephrine
• alpha1 agonist
• used as mydriatics, decreases ocular tension
• Oral or nasal decongestant
Nasal Decongestants
• Topical: Oxymetazoline, Xylometazoline,
Naphazoline
• alpha2 agonist, long duration of action
• Use cautiously in hypertensive patients
• Oral: Phenylephrine, Pseudoephedrine,
Phenylpropanolamine (PPA)
• Produce vasoconstriction in mucosa & skin
• Used orally as decongestant of upper respiratory
tract, nose & eustachian tubes
• Avoided in hypertensive patients
• PPA banned in Nepal (risk of haemorrhagic stroke)
Indications:
1.Vascular Uses:
• Hypotensive states (shock, spinal anaesthesia, hypotensive drugs)
• Along with local anaesthetics
• Control of local bleeding
• Nasal Decongestants
2. Cardiac Use
• Cardiac arrest (drowning, electrocution, etc.) – In combination
with external cardiac massage
• Partial or complete A-V block – Isoprenaline as temporary
measure
• Congestive Heart Failure
3. Bronchial asthma
4. Allergic disorders (histamine mediated)
5. Mydriatic
• Fundus examination
• Wide angle glaucoma
6. Insulin Hypoglycaemia
7. Nocturnal enuresis in children and urinary
incontinence – Amphetamine
8. Uterine relaxant – Ritoridine: to postpone labour –
Isosuxprine: threatened abortion and dysmenorrhoea
9. Central Uses
• Attention Deficit Hyperkinetic Disorders –
Amphetamine
• Narcolepsy – Amphetamine, Modafinil – Imipramine
like drugs
• Epilepsy – Amphetamines
• Parkinsonism – Amphetamine
• Obesity – Considered in severe obesity

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adrenergic-180630054152.pdf

  • 1. Adrenergic Drugs/Sympathomimetics • These are the drugs that mimic the response of sympathetic or adrenergic system. Neurotramsmitters: Neurotransmitters are the chemical mediators released by the neurons to transmit the signals through synapse. Three major endogenous catecholamines are:  Adrenaline (Adr, Epinephrine)  Noradrenaline (NA, Norepinephrine)  Dopamine Adrenergic Receptors α β α1 α2 β1 β2 β3
  • 2. Tyrosine Dopa Dopamine Noradrenaline Adrenaline Synthesis: Tyrosine hydroxylase Amino acid decarboxylase Dopamine β-Hydroxylase Phenylethanolamine N-methyl transferase
  • 3.
  • 4. Adrenergic drugs acts through adrenergic receptors. Adrenergic Receptors/Adenoreceptors are of 2 types: alpha (α) & beta (β). Receptor Tissue Response α1 Vascular smooth muscle vasocontraction Genitourinary tract smooth muscle contraction Smooth muscle (Sphincter, radial muscle of iris, gland) Contraction (mydriasis, secretion) Intestinal smooth muscle Relaxation α2 Prejunctional nerve ending NA release Vascular smooth muscle vasoconstriction Alpha receptors (α)
  • 5. Receptor Tissue Response β1 Heart Rate, FOC, A-V conduction Juxtaglomerular cells Rennin release β2 Smooth muscles (Bronchial, gastrointestinal, genitourinary, uterus) Relaxation Skeletal muscle Glycogenolysis K+ uptake Liver Glycogenolysis Gluconeogenesis β3 Adipose tissue Lipolysis Beta receptors (β)
  • 6.
  • 8.
  • 9. Pressor agents Dopamine, NA, Mephentermine, Ephedrine Cardiac stimulant Dobutamine, Adr, Iso Bronchodilators Salbutamol (albuterol), Salmeterol, Terbutaline, Iso, Adr Nasal decongestant Xylometazoline, Oxymetazoline, Phenylephrine Pseudoephedrine CNS stimulants Amphetamine, Dexamphetamine Anorectics Fenfluramine, Sibutramine Uterine relaxant Ritodrine, Isoxsuprine, salbutamol, Terbutaline Clinical classification of Adrenergic drugs
  • 10. Adrenaline (Adr) α1+ α2 + β1+ β2+weak β3 action Noradrenaline (NA) α1+ α2+ β1+ β2 but no β3 action Isoprenaline (Iso) β1+ β2+ β3 action but no α action Pharmacological Actions: Epinephrine (adrenaline) is a potent stimulant of both α and β adrenergic receptors. Most of the responses are seen after injection of epinephrine, although the occurrence of sweating, piloerection, and mydriasis depends on the physiological state of the patient. Particularly prominent are the actions on the heart and on vascular and other smooth muscle. Norepinephrine (Noradrenaline) and epinephrine both are direct agonists on effector cells, and their actions differ mainly in the ratio of their effectiveness in stimulating α and β2 receptors. They are approximately equipotent in stimulating β1 receptors. Norepinephrine is a potent αagonist and has relatively little action on β2 receptors.
  • 11. Heart Positive ionotropic effect (increase in force of contraction) Positive chronotropic effect (increase in heart rate) Positive dromotropic effect (increase in heart conduction) Respiration Bronchodilation , Nasal decongestion Blood vessels Vasoconstriction Blood pressure Increases GIT Relaxation but sphincter contracts so peristalsis decreases Eye Mydriasis (Dilation of pupils) Uterus Non-pregnant-Contraction; Pregnant-Relaxation Skeletal muscle Tremor, glycogenolysis Metabolic Hyperglycemia, Lipolysis, Hypokalemia
  • 12. Adverse effects: • Adr-sc/i.m: restlessness, palpitation, anxiety, tremor, pallor • Adr-i.v. high dose: cerebral haemorrhage, arrhythmias Contraindications: • Hypertensive, Hyperthyroidism, Angina Pectoris • Patient receiving β-blocker. • During anesthesia by Halothane
  • 13. • Dopamine is the immediate metabolic precursor of norepinephrine and epinephrine. It is a central neurotransmitter particularly important in the regulation of movement and possesses important intrinsic pharmacological properties. • In the periphery, it is synthesized in epithelial cells of the proximal tubule and is thought to exert local diuretic and natriuretic effects. • Dopamine is a substrate for both MAO and COMT and thus is ineffective when administered orally. • It doesn’t cross BBB. • In moderate dose (0.2-1mg) it increases BP & urine flow. Mechanism of action: • Dopamine can activate α- and β-adrenergic receptors. It acts on dopaminergic receptors (D1-D5) present on peripheral mesenteric and renal vascular beds. Binding of dopamine produces vasodilation. D2 receptors are also found on presynaptic adrenergic neurons, where their activation interferes with norepinephrine release.
  • 14. Indication: • Given as i.v. infusion to patients with cardiogenic & septic shock. • Severe Congestive Heart Failure • Dose regulated by monitoring BP & urine formation. • At high concentrations, dopamine activates vascular a1 receptors, leading to more general vasoconstriction. Adverse Effects: Nausea, vomiting, tachycardia, anginal pain, arrhythmias, headache, hypertension, and peripheral vasoconstriction may be encountered during dopamine infusion. Contraindication: Hypovolemic shock, depression (patients receiving MAO inhibitors or tricyclic antidepressants)
  • 15. Dobutamine Mechanism of Action: • Dobutamine is a derivative of dopamine that directly acts on adrenergic receptors(β1). Indications: • Dobutamine is used to increase cardiac output in acute congestive heart failure as well as for inotropic support after cardiac surgery. • It increases cardiac output and does not significantly elevate oxygen demands of the myocardium, a major advantage over other sympathomimetic drugs. • It is used in pump failure (Myocardial Infarction, Cardiac surgery, CHF) Contraindication: • Atrial fibrillation • May cause tolerance
  • 16. Ephedrine • Mixed action adrenergic drugs • Orally effective & long acting than Adr • Crosses BBB so stimulation • Used in mild chronic bronchial asthma & hypotension during spinal anaesthesia Amphetamine • Synthetic compound similar to ephedrine but have more CNS action • Improves alertness, attention, concentration & performance • Included in dope test (drug for abuse) • Used in attention deficit hyperactive disorder (ADHD) Phenylephrine • alpha1 agonist • used as mydriatics, decreases ocular tension • Oral or nasal decongestant
  • 17. Nasal Decongestants • Topical: Oxymetazoline, Xylometazoline, Naphazoline • alpha2 agonist, long duration of action • Use cautiously in hypertensive patients • Oral: Phenylephrine, Pseudoephedrine, Phenylpropanolamine (PPA) • Produce vasoconstriction in mucosa & skin • Used orally as decongestant of upper respiratory tract, nose & eustachian tubes • Avoided in hypertensive patients • PPA banned in Nepal (risk of haemorrhagic stroke)
  • 18. Indications: 1.Vascular Uses: • Hypotensive states (shock, spinal anaesthesia, hypotensive drugs) • Along with local anaesthetics • Control of local bleeding • Nasal Decongestants 2. Cardiac Use • Cardiac arrest (drowning, electrocution, etc.) – In combination with external cardiac massage • Partial or complete A-V block – Isoprenaline as temporary measure • Congestive Heart Failure 3. Bronchial asthma 4. Allergic disorders (histamine mediated) 5. Mydriatic • Fundus examination • Wide angle glaucoma
  • 19. 6. Insulin Hypoglycaemia 7. Nocturnal enuresis in children and urinary incontinence – Amphetamine 8. Uterine relaxant – Ritoridine: to postpone labour – Isosuxprine: threatened abortion and dysmenorrhoea 9. Central Uses • Attention Deficit Hyperkinetic Disorders – Amphetamine • Narcolepsy – Amphetamine, Modafinil – Imipramine like drugs • Epilepsy – Amphetamines • Parkinsonism – Amphetamine • Obesity – Considered in severe obesity