THROMBOLYTIC DRUGS (Fibrinolytic drugs) By Prof. Hanan Hagar.
DIRECT CHOLINERGIC DRUGS Prof. Hanan Hagar Pharmacology Department.
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Transcript of DIRECT CHOLINERGIC DRUGS Prof. Hanan Hagar Pharmacology Department.
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DIRECT CHOLINERGIC DRUGSDIRECT CHOLINERGIC DRUGSDIRECT CHOLINERGIC DRUGSDIRECT CHOLINERGIC DRUGS
Prof. Hanan HagarPharmacology Department
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By the end of this lecture the student should know
• Classification of nervous system.
• Describe the various steps in cholinergic transmission.
• Mention the different types, locations and actions of cholinergic receptors.
• Describe the effects of acetylcholine on major organs
• Classify cholinomimetic drugs.
• Describe the kinetics, actions and uses of direct and indirect-acting cholinomimetic drugs.
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Nervous system
Peripheral nervous system
Central nervous system
Efferent Division(Motor)
Afferent Division(Sensory)
Autonomic nervous system
Somatic system(skeletal muscles)
Enteric nervous system
Parasympathetic nervous system
Sympathetic nervous system
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What are the differences between the somatic and the autonomic nervous system?
Somatic N.S Autonomic N.S•Control skeletal muscles Control internal viscera
•Voluntary Involuntary
•Somatic nerve is one fiber autonomic nerve is two fibers )Preganglionic &
Postganglionic(
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Pre-ganglionic fiber
Post-ganglionic fiber
ganglia
One fiber
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Divisions of Autonomic Nervous System
• Sympathetic nervous system.
• Parasympathetic nervous system.
• Enteric nervous system.
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ParasympatheticParasympathetic Nervous SystemNervous System)craniosacral outflow()craniosacral outflow(
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Neurotransmitter in parasympathetic or cholinergic system is acetylcholine and nerves are called cholinergic nerves
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Cholinergic transmission
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Cholinergic transmission
• Synthesis
• Storage
• Release
• Binding to receptors
• Metabolism by acetylcholinesterase to give choline and acetate
• Recycling of choline
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Cholinergic transmission
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Cholinergic or parasympathetic receptors
Nicotinic )N, central( receptors. Muscarinic )M, peripheral( receptors.
Central nicotinic receptor
Peripheral muscarinic receptor
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Type I receptors : ion channel linked receptors
Located in:
• Autonomic ganglia )Nn(.• Adrenal medulla )Nn(• CNS )Nn(• Neuromuscular junction )Nm(
Nicotinic receptors
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Type II receptors : G-protein linked receptors
• Located at all target organs that are innervated by parasympathetic fibers )e.g, heart, CVS, eye, bladder, etc(.
• Five subclasses exist )M1 - M5(• M1, M3, M5 are excitatory in function
)stimulation(.• M2, M4 are inhibitory in function )inhibition(.
Muscarinic receptors
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ReceptorLocationsPharmacological actionsM1
ExcitatoryCNS
gastric parietal cells
CNS excitation
Gastric acid secretion
M2 Inhibitory
Heart Cardiac inhibition
)Bradycardia(
M3
Excitatory
Exocrine glands
Smooth muscles
Vascular endothelium
• Secretion of glands
• Smooth muscle contraction
• Vasodilatation )via nitric oxide(
M4 & M5CNSmemory, arousal, attention and
Muscarinic receptors
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Cholinergic or parasympathetic receptors
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Nicotinic receptors
Central cholinoceptor
Muscarinic receptors
Peripheral cholinoceptor
Ion channel linked receptors G protein linked receptors
Autonomic ganglia )sympathetic & parasympathetic( stimulation ) Nn (
On all peripheral organs that receive postganglionic parasympathetic fibers
Adrenal medulla )Nn(
release of catecholamines
(Adrenaline & Noradrenaline)
Heart )M2( inhibition
exocrine glands )M3( contraction
Skeletal muscle
)Neuromuscular junction(
)Nm( Contraction
Smooth muscles )GIT, urinary tract, bronchial muscles(
)M3( contraction
Almost excitatoryExcitatory or inhibitory
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What are the actions of parasympathetic
nervous system?
1. Nicotinic actions
2. Muscarinic actions
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Skeletal muscles: • Low conc. of nicotine muscle contraction• High conc. of nicotine persistent depolarization &
relaxation.
Ganglia:
stimulation of sympathetic& parasympathetic ganglia.
Adrenal medulla
release of catecholamines )A & NA(.
Nicotinic actions
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Muscarinic actionsOrgansCholinergic actionsEyeContraction of circular muscle of iris
(miosis)(M3)Contraction of ciliary muscles for near
vision (M3)Decrease in intraocular pressure
Heartendothelium
bradycardia ( heart rate ) (M2)Release of NO (EDRF)
LungConstriction of bronchial smooth musclesIncrease bronchial secretion M3
GITIncrease motility (peristalsis)Increase secretionRelaxation of sphincter M3
Urinary bladder
Contraction of muscles Relaxation of sphincter M3 - Urination
Exocrine glands
Increase of all secretionssweat, saliva, lacrimal, bronchial, intestinal secretions M3
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Drugs that produce actions similar to stimulation of parasympathetic system )or similar to natural neurotransmitter, Ach(.
CholinomimeticsCholinomimeticsParasympathomimeticsParasympathomimetics
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Types of cholinomimetics
Direct cholinomimetics
cause direct stimulation of cholinergic receptors.
Indirect cholinomimetics )anticholinesterases(
increase action of Ach indirectly by inhibiting acetylcholinesterase thus prevent the degradation of Ach.
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Direct cholinomimetics• Acetylcholine )M,N(
• Carbachol )M,N(
• Bethanechol )M(
• Pilocarpine )M(
Direct CholinomimeticsDirect Cholinomimetics
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Acetylcholine )Ach(
Muscarinic and nicotinic agonist
Not used clinically because Ach
– Is not selective )N, M(
– Has short duration of action. Why?
– Due to rapid metabolism by acetycholinesterase
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Synthetic choline esters
include drugs as bethanechol, carbacholQuaternary ammonium compounds )polar( Poor distribution can not cross BBB (No CNS effects) Not metabolized by cholinesterase. Have longer duration of action than Ach.Never given I.V. or I.M BUT S.C.
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Carbachol1. Orally-S.C.2. Not metabolized by cholinesterases.3. Longer duration of action than Ach4. Muscarinic actions on Eye, GIT, UT. )Table5. Has nicotinic actions )what are these
actions?(.6. Used for
Mainly in glaucoma Urinary retention & paralytic ileus (rarely
used due to its nicotinic actions)
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Bethanechol Orally-SC Prominent muscarinic actions on GIT, UT. No nicotinic action Not metabolized by cholinesterases. Longer duration of action than Ach Used for
In paralytic ileus In urinary retention )in cases of post-operative
atony, neurogenic bladder(
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Pilocarpine
Natural alkaloids
Tertiary amine lipophilic
Pharmacokinetics
• It is well absorbed
• Good distribution
• Cross BBB (has central effects).
• Long duration of action
• Direct muscarinic agonist
)mainly on eye & secretion).
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Pilocarpine
Uses:
• Xerostomia )dry mouth(.
• Drug of choice in emergency glaucoma applied as eye drops.
Adverse effects:
• Profuse sweating
• Salivation
• Bronchoconstriction
• Diarrhea
• CNS effects
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ACh CarbacholBethanechol Pilocarpine
Chemistry Quaternary Polar
Quaternary Polar
Quaternary Polar
Tertiarynon polar
AbsorptionNOT better absorbed than
Ach
better absorbed than
Ach
Complete
Metabolismby
cholinesterase
metabolized by
cholinesterase
NOT NOT NOT
DurationVery shortLonger )++(Longer )++(Longer )++(
Administ.I.V.eye drops
Oral, eye drops
S.C.
Oral S.C.
oral, eye drops
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ACh Carbachol Bethanechol Pilocarpine
ReceptorsMuscarinicNicotinic
MuscarinicNicotinic
MuscarinicMuscarinic
Muscarinic+++ +++ ++++++
SelectivityNOTEye, GITUrinary bladder
GIT, Urinary
bladder
More on eye, secretion
Nicotinic+++ +++ NONO
UsesNOGlaucoma
Paralytic ileus
Urinary retention
Paralytic ileus
Urinary retention
GlaucomaXerostomia
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Cevimeline –Direct acting muscarinic agonist
–Used for treatment of dry mouth symptom
associated with Sjogren's syndrome.
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Contraindications of cholinomimetics
1. Bronchial asthma.2. Peptic ulcer.3. Angina pectoris4. Incontinence5. Intestinal obstruction
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Thank you