Dr. Vishaal Bhat. anti-adrenergic drugs

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Transcription:

Dr. Vishaal Bhat anti-adrenergic drugs

Divisions of human nervous system Human Nervous system Central Nervous System Peripheral Nervous System Autonomic Nervous System

Nervous system Includes neurons and ganglia outside of the brain and spinal cord Peripheral Nervous System *Either fight and flight mode or rest and digest *Autonomic Nervous System (involuntary) Somatic Nervous System (voluntary) With neurotransmitters norepinephrine and acetylcholine Sympathetic Nervous System (adrenergic) Parasympathetic Nervous System (cholinergic)

Sympathomimetic or adrenergic in sympathetic nervous system neurotransmitters are Parasympathomimetic or cholinergic are used to describe parasympathetic system neurotransmitter is

Sympathetic nervous system Fight or flight response results in: 1. Increased BP 2. Increased blood flow to brain, heart and skeletal muscles 3. Increased muscle glycogen for energy 4. Increased rate of coagulation 5. Pupil dilation

Adrenergic receptors Alpha A1 and A2 Beta B1, B2, B3

Review of functions of sympathetic nervous system receptors Alpha 1 smooth muscle contraction Alpha 2-negative feedback causes less norepinephrine to be released so BP is reduced Beta 1 increased heart rate Beta 2 bronchodilation Beta 3 actual site for lipolysis

Sympatholytic Anti-adrenergics Block or decrease the effects of sympathetic nerve stimulation, endogenous catecholamines and adrenergic drugs

Adrenergic Antagonists

ALPHA-BLOCKERS A. Classification Irreversible, Non selective: Phenoxybenzamine Reversible, Non selective: Phentolamine Alpha1-selective: Prazosin, Terazosin, Tamsulosin Alpha2-selective: Yohimbine, rauwolscine

Beta-blockers (antagonists) Selective Non selective Mixed (b 1 ) (b 1 & b 2 ) (b & a ) Atenolol Betaxalol Metoprolol Esmolol Propranolol Sotalol Timolol Carvedilol Labetalol

Beta adrenergic blocking medications Prevent receptors from responding to sympathetic nerve impulses, catecholamines and beta adrenergic drugs.

Effects of Propranolol Decreased heart rate Decreased force of contraction Decreased CO Slow cardiac conduction Decreased automaticity of ectopic pacemakers

Effects of Propranolol Decreased renin secretion from kidneys Decreased BP Bronchoconstriction Less effective metabolism of glucose. May result in more pronounced hypoglycemia and early s/s of hypoglycemia may be blocked (tachycardia)

Effects of Propranolol Decreased production of aqueous humor in eye May increase VLDL and decrease HDL Diminished portal pressure in patients with cirrhosis

Beta Blockers - Indications Mainly for cardiovascular disorders (angina, dysrhythmias, hypertension, MI and glaucoma) In angina, beta blockers decrease myocardial oxygen consumption by decreasing rate, BP and contractility. Slow conduction both in SA node and AV node.

Beta blockers Inhibition of renin, decreasing cardiac output and by decreasing sympathetic stimulation May worsen condition of heart failure as they are negative inotropes May reduce risk of sudden death

Beta blockers Decrease remodeling seen in heart failure In glaucoma, reduce intraocular pressure by binding to beta-adrenergic receptors in ciliary body, thus decrease formation of aqueous humor

Beta blockers Propranolol is prototype Useful in treatment of hypertension, dysrhythmias, angina pectoris, MI Useful in pheochromocytoma in conjunction with alpha blockers (counter catecholamine release) migraines

Beta Blockers In cirrhosis, propranolol may decrease the incidence of bleeding esophageal varices Used to be contraindicated in heart failure, now are standard Known to reduce sudden death Often given with ACEIs Indications include: htn, angina, prevention of MI

Adverse reactions of b-blockers Blockade of b 1 -receptors may cause bradycardia, AV block, heart failure. Blockade of b 2 -receptors may cause bronchospasm, cold extremities,intermittent claudication (reducing peripheral blood flow) and hypoglycemia. CNS effects: sleep disturbance, dreams and hallucinations (more common with lipophilic drugs which cross the BBB).

Fatigue is probably a result of reducing of cardiac output and reduced muscle perfusion in exercise Most beta-blockers raise the plasma concentration of triglycerides and lower the concentration of HDL. Sudden withdrawal syndrome: b-blockers should be stopped gradually.

Drug Interactions Propranolol + lignocaine - reduces the clearance of lignocaine by decreasing hepatic blood flow. This will lead to lignocaine toxicity. Beta Blockers should be used very carefully in diabetic patients who are being treated with Insulin / Sulphonylureas. Propranolol masks the hypoglycemic symptoms such as tachycardia and sweating. It also prevents the synthesis of new glucose molecules and breakdown of glycogen in the liver, preventing recovery from hypoglycaemia.