Class cholinergic drugs
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Transcript of Class cholinergic drugs
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Dr. RAGHU PRASADA M SMBBS,MDASSISTANT PROFESSORDEPT. OF PHARMACOLOGYSSIMS & RC.
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Muscarinic AgonistsNatural Alkaloids:
MuscarinePilocarpineArecholine
Synthetic Alkaloid:Oxotramorine
Mainly Nicotinic AgonistsNatural Alkaloids:
NicotineSynthetic Alkaloids:
Dimethylphenylpiperazinium(DMPP)
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ReversibleTertiary amines
PhysostigmineQuaternary Ammonium compounds
NeostigminePyridostigmineDistigmineAmbenoniumDemecariumTacrine
Miscelloneous DonepezilGalantamineRivastigmine
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Irreversible Anticholinesterases(Organophosphorus Compounds)
Ecothiophate2) War Gases:
SarinTuban,Soman
3) Insecticides:-ParathionMalathionDiisopropyl Flurophosphate (DFP)Tetramethyl Pyrophosphate (TMPP)Octamethyl Pyrophosphotetra amide (OMPA)
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Central Nervous System (CNS) - Brain and spinalcord
Peripheral Nervous System (PNS) - Located outsidethe brain & spinal cord Autonomic NervousSystem (ANS) & the somatic
The PNS receives stimuli from the CNS & initiatesresponses to the stimuli after it’s interpreted by thebrain
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HEMICHOLIUM
VESAMICOL
BOTULINUM
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Sites of Cholinergic Activity-Preganglionic synapses of both sympathetic and parasympathetic ganglia
- Parasympathetic postganglionic neuroeffector junctions
- All somatic motor end plates on skeletal muscles
M2 M4 M5M3M1
Gi Go
Adenylyl cyclasecAMP
Hyperpolarization (heart)Cardiac inhibitionAntagonism of smoothmuscle relaxation
RECEPTOR
INTRACELLULARTRANSDUCER
ELECTRICALMECHANICALPHYSIOLOGICALRESPONSES
Gq
Phospholipase CDiacyl-glycerol IP3
DepolarizationSmooth muscle contractionGlandular secretion
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Eyes: contraction of ciliary muscle and smooth muscle of the irissphincter (miosis) – aqueous humor outflow, drainage of theanterior chamber
Cardiovascular: Bradycardia (possibly preceded by tachycardia),vasodilation (all vascular beds including pulmonary andcoronary – M3) and hypotension, reduction of thecontraction strength (atrial and ventricular cells) diastolicdepolarization ,
Negative chronotropic effect (inhibition of adrenergic activation)Negetive ionotropic effect-activation of SA node M2 receptor
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GI - increases in tone, amplitude of contractions, andperistaltic activity of the stomach and intestines,enhances secretory activity of the gastrointestinal tract.
Urinary bladder - increase ureteral peristalsis, contract thedetrusor muscle of the urinary bladder, increase themaximal voluntary voiding pressure, and decrease thecapacity of the bladder.
Respiratory system-brochoconstriction and increasedbronchial secretions
Other effects – Increased secretion from all glands thatreceive parasympathetic innervation (salivary, lacrimal,tracheobronchial, digestive and exocrine sweat glands)
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CNS-there are complex stimulatory effects-ataxia,behavioral disturbances and restlessness with tremorsand convulsionsBlood vessels-arteries have M3 receptors but noinnervationexagenous cholinomimetic transientbut marked fall in blood pressuredue tovasodilationendothelium release EDRF-EndotheliumDerived Relaxing Factors-NO
Other effects – Increased secretion from all glands thatreceive parasympathetic innervation (salivary, lacrimal,tracheobronchial, digestive and exocrine sweat glands)
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Homotropic receptor interaction Heterotropic receptor interaction
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Is the neurotransmitter of the parasympathetic N.S andcholinergic nerves, it is therapeutically of no importancedue to:1. Multiplicity of actions.2. Rapid inactivation by acetyl-cholinesterase.3. Has both muscarinic and nicotinic activity.
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Structurally related to ACH, has strong muscarinicactivity but no nicotinic actions.It directly stimulates muscarinic receptors of the GITcausing increase intestinal motility and tone,It also stimulates detrusor muscle of the bladdercausing urine expulsion.Clinical uses: Atonic bladder stimulation such as inpostpartum and post operative non obstructiveurine retention.Side effects: Sweating, salivation, flushing,hypotension, nausea, abdominal pain, diarrhea, andbronchospasm.
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Has both muscarinic and nicotinic actions, hasstrong effect on CVS and GIT, it causes release ofepinephrine from adrenal medulla by its nicotinicaction, using it locally on the eye cause Miosis.
Clinical uses: Rarely used because of high potencyand long duration of action except in the eye tocause Miosis and to decrease intraocular pressure.
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Mainly used in ophthalmology, it exhibit muscarinicactivity, it produces rapid miosis and contraction of theciliary muscle.Clinical uses; It is the drug of choice in the emergencylowering of inrtra-ocular pressure in case of glaucoma.Side effects:It can enter the brain and cause CNS disturbances, itstimulate profuse sweating and salivation.painful spasm of accommodation for near vision.
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- sol. 1%, 2%, 4%- in open angle glаucomaApplied to the eye, itpenetrates cornea andpromptly causesmiosis, ciliary muscle contra-ction, and fall in intraocculartension (< 22 mm) lasting 4-8 h.Systemic effects:sweating, salivationCardiovascular effects: in small doses – fall in BP, but in highdoses elicits rise in BP and tachycardia, probably due toganglionic stimulation (through muscarinic receptors
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50
100
150
200A B C D1 min
M- и N-effects of AChBl
ood p
ress
ure[
mm H
g]
ACh2 mcg i.v.
ACh50 mcg
ACh50 mcg
ACh5 mg
M-effect
M-effect
N-effect
Atropine2 mg i.v.
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