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Published byRonald Stone Modified over 8 years ago
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Drug action on Sympathetic Nerves: No. 3: Sympatholytic drugs
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Introduction Increased sympathetic nervous system (SNS) activity plays an imp. role in the pathogenesis of various diseases especially, CV diseases. Hence, drugs which reduce SNS activity have a major role in the treatment of CV diseases How can drugs reduce the activity of the SNS?
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Sympatholytic drugs Centrally acting sympatholytics - α2 agonists –
Clonidine, α-methyldopa Ganglion blockers – Trimethaphan Adrenergic neuron blockers - Guanethidine Adrenergic receptor blockers - α blockers – Prazocin β blockers - Propranolol
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1 2 2 1 Adrenoceptors Location Postsynaptic Agonist
Phenylephrine, Oxymetazoline Antagonist Prazocin 1 Receptor block will produce in Blood vessels Vasodilatation ↓PR ↓ BP Kidney Renal artery dilatation Prostatic capsule Relaxation
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2 Adrenoceptors 1 2 Location
Mostly Presynaptic & a few postsynaptic Agonist Clonidine Antagonist Yohimbine Presynaptic 2 block will produce at sympathetic nerve endings ↑ Release of NE ↑ HR (β1) Postsynaptic 2 block in blood vessels will cause Vasodilatation ↓ PR ↓ BP
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Blood vessels – Sympathetic NS
β2 stimulation & block Vasodilatation stimulation & β2 block – Vasoconstriction Blockers cause vasodilatation, decrease peripheral resistance & increase blood flow to organs. Normal
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Effects of alpha receptor blockade
2 block: ↑ NE release from presynaptic S N Tachycardia, ↑ COP, ↑ BP 1 block: Vasodilatation ↓PR ↓ BP
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Sympathetic receptor blocking agents
α blockers – Nonselective α blockers – Phentolamine (reversible) Phenoxybenzamine (irreversible) Selective α blockers – α1 blockers – Prazocin, Terazocin α1A blocker - Tamulosin α2 blockers – Yohimbine β blockers α & β blockers: Carvedilol, Labetolol
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α & β β β Effects of alpha1 block: CVS: Vasodilatation ↓PR ↓ BP
Reflex effects: Tachycardia & ↑ Renin release The more the intrinsic SNS activity, the more will be the effects of α blockade. They block the vasoconstrictor & hypertensive effects of exogenous sympathomimetics. Dale’s reversal α & β β β Adrenaline blocker Adrenaline α, β
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↑ NE release from presynaptic S N Tachycardia, ↑ COP, ↑ BP
Effects of α 2 block: ↑ NE release from presynaptic S N Tachycardia, ↑ COP, ↑ BP Prostate (α1) Relax the Prostatic capsule Decrease tone of the bladder sphincter Facilitate urine flow
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ADR: Reflex tachycardia, Nasal stuffiness, Sodium & water retention, impaired ejaculation & Postural hypotension which occurs when posture is changed from lying down to standing α blockers prevent reflex vasoconstriction required to push blood against gravity ↓Venous return due to peripheral pooling of blood ↓COP Hypotension ↓blood supply to CNS Fainting
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Uses: Hypertension, Hypertensive emergencies Peripheral vascular diseases Local injection following extravasation of sympathomimetic amines after iv injection Rebound hypertension due to clonidine withdrawal Prostatic hypertrophy – Tamsulosin
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Phenoxybenzamine Nonselective alpha (1 & 2) receptor blocker. long duration - 48 h in PR, reflex tachycardia. pressor responses to catecholamines blocked. Uses: Peripheral vascular diseases, Pheochromocytoma- prior to surgery & in medical management Caution: To be given along with betablockers to prevent dangerous tachycardia in pheochromocytoma ADR: postural hypotension
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Prazosin, Terazocin - Selective α1 blockers
PR BP Minimal changes in COP & renal blood flow Minimal tachycardia (since α2 is not inhibited). Duration: prazosin is shorter acting than terazosin Uses : Hypertension, CCF, Benign prostatic hypertrophy (BPH) Precaution: “First dose phenomenon“- marked postural hypotension & fainting minutes after 1st dose. Hence, 1st dose is to be small dose & is given with food at night. ADR: Sedation, postural hypotension, nasal congestion, Sodium and water retention.
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Tamsulosin α1A blocker (bladder & prostate), with little effect on α1B receptors (blood vessels). used in benign prostatic hypertrophy because it decreases the resistance to urinary flow, with minimal hypotensive effect.
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Objectives for self study
Classification of sympatholytic drugs with examples Review of effects of alpha receptor stimulation & inhibition Classification of alpha blockers with examples Actions of alpha blockers on CVS – Dale’s vasomotor reversal Actions on prostate ADR & precautions uses Phenoxybenzamin, Prazocin, Tamsulosin
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What is the Reversal of Dale phenomenon?
What is the Reversal of Dale phenomenon? Ans : Rapid i.v. injection of Adrenaline acts on alfa-1- receptors,produces rise of diastolic BP initially. After some time when concentration of adrenaline is reduced, adrenaline acts on beta-2-receptors, produces vasodilatation, reduces Diastolic BP. This is called as Biphasic response of Adrenaline. If alpha blocker drug (ergotamine) is given then only fall in diastolic BP is seen. This is called as vasomotor reversal phenomenon of Dale.
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