Download - CHOLINERGIC AGONISTS. DIRECT ACTING Acetyl choline Bethanecol Carbachol cevimeline pilocarpine
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CHOLINERGIC AGONISTS
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DIRECT ACTING
Acetyl choline
Bethanecol
Carbachol
cevimeline
pilocarpine
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INDIRECT ACTING ( reversible)AmbenomiumDonepezilEdrophoniumGalantamineNeostigminePhysostigminePyridostigmineRivastigminetacrine
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INDIRECT ACTING (irreversible)
Ecothiophate
isoflurophate
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REACTIVATION OF ACETYLCHOLINEESTERASE
pralidoxime ( PAM )
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CHOLINERGIC AGONISTS
Neurotransmission at cholinergic neuronsSynthesis, storage, release, and binding of acetyl choline.Synthesis—choline cotransport system involving sodium.Storage in vesicles.—contains ach & ATP.Release—opening of ca channels. Binding—ach binds to either of two receptors muscarinic or nicotinic.
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Degradation-acetylcholine esterace cleaves acetyl choline to choline and acetate in synaptic cleft.
Recycling- choline recaptured by sodium and gets transported back to the neuron.
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Muscarinic receptors – decreased HR, increased glandular secretory activity, stimulation of smooth muscle contractions.M1,M2,M3,M4 & M5
Nicotinic receptors – increased B.P (peripheral vasoconstriction), contraction of skeletal muscle. NM, NN.
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Location of muscarinic receptors
Ganglia of pns
Autonomic effector organs—heart, smooth muscle, brain and exocrine glands.
Location of nicotinic receptors
Cns, adrenal medulla, neuro muscular junction.
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Cholinergic agonists
Direct acting
Indirect acting
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Direct acting
Choline esters
Acetylcholine
Bethanechol
Carbachol
Methacholine
Alkaloids
Muscarine
Pilocarpine
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Acetyl choline —both muscarinic and nicotinic activities.
Actions---decrease in heart rate & cardiac output. Mimics effects of vagal stimulation.
Decrease in blood pressure—due to vasodilatation.---rise in intracellular calcium.
Increases salivary, intestinal, bronchial secretion.
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ACH – both muscarinic (M) and nicotinic (N) receptors
Bethanechol – strong M and low or no N
Carbachol – both (Strong N)
Pilocarpine – more M
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Gastrointestinal & Genitourinary
Bethanechol
GI smooth muscle stimulant >> postoperative abdominal distention >> paralytic ileus >>esophageal reflux; (promotes increased
esophageal motility)
Urinary bladder stimulant post-operative; post-partum urinary retention
Carbachol not used due to more prominent nicotinic receptor activation
Methacholine used for diagnostic purposes. testing for bronchial hyper reactivity and asthma
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Opthalmological Uses Acetylcholine and Carbachol may be used for intraocular use as a miotic in surgery Carbachol may be used also in treatment of glaucoma.
Pilocarpine is used in management of glaucoma and has become the standard initial drug for treating the closed-angle form. effective even in open angle type.Opens the trab mesh work around schlemm canal. Sequential administration of atropine (mydriatic) and Pilocarpine (miotic) is used to break iris-lens adhesions
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Major contraindication to the use of muscarinic agonists
Asthma Choline esters (muscarinic agonists) can produce bronchoconstriction. In the
predisposed patient, an asthmatic attack may be induced.
Hyperthyroidism Choline esters (muscarinic agonists) can induce atrial fibrillation in
hyperthyroid patients.
Peptic ulcer Choline esters (muscarinic agonists), by increasing gastric acid secretion,
may exacerbate ulcer symptoms.
Coronary vascular disease Choline esters (muscarinic agonists), as a result of their hypotensive effects,
can further compromise coronary blood flow.
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Adverse Effects:
Muscarinic Agonists
salivation diaphoresis
colic GI hyperactivity
headache loss of accommodation
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Indirect actingthru enzyme
Reversible inhibitors
Irreversible inhibitors
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Reversible" Anticholinesterases Used Clinically
Edrophonium
Pyridostigmine - Used in treatment of myasthenia gravis
Neostigmine
Physostigmine
Demecarium
Ambenonium - Used in treatment of myasthenia gravis
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Physostigmine
Actions – muscarinic and nicotinic actions.
Miosis and spasm of accomodation.
Decreases iop.
High doses can cause convulsions
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Neostigmine
Has a quarternary nitrogen. there fore it does not enter the cns.
Use – antidote for tubocurarine & treatment of myasthenia gravis.
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Acetylcholinesterase Inhibitors ("Irreversible")
Soman Parathion Malathion
Isoflurophate Echothiophate
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Organo phosphate poisoning
Reactivation of acetylcholine esterase
Pralidoxime (PAM)
(Pyridine – 2 aldoxime chloride)
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Drugs affecting the release:
· Drugs which increase Ach release (mainly venom toxins)
· b bungarotoxin
· Banded krait venom
· Black widow spider venom
· These toxins cause a massive release of Ach which results in fasciculations of muscle
followed by paralysis as all of the Ach is drained from the nerve terminal
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Drugs which decrease Ach release
· Botulinum toxin· Produced by the Clostridium botulinum· This bacterium lives in unsterilised canned foods.
Drug that interfere with the synthesisCholine uptake inhibition· Hemicholinium
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Glaucoma a disease of the eye marked by increased
pressure within the eyeball that can result in damage to the optic disk and gradual loss of vision.
Myasthenia gravis a disease characterized by progressive weakness
and exhaustibility of voluntary muscles without atrophy or sensory disturbance and caused by an autoimmune attack on acetylcholine receptors at neuromuscular junctions.
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