Transcript
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ANGIOTENSIN RECEPTOR BLOCKERS [ARBS]

DR PADMAVATHI SASSOCIATE PROFESSOR - DEPT OF PHARMACOLOGY

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ANGIOTENSIN ANTAGONISTS

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ANGIOTENSIN RECEPTORSAT1

VASCULAR S. M, MYOCARDIUM GPCR

VASOCONSTRICTIONCELL GROWTH IN HEART & ARTERIESSECRETION OF ALDOSTERONEPERIPHERAL SYM. ACTIVITY INCREASED

AT2 FOETUS, ADRENAL MEDULLA –

ADULTS GPCR

VASODILATATIONANTI-PROLIFERATIVEAPOPTOSIS

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COMPETITIVE blockers

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ARBS SARTANS

LO SARTAN CANDESARTAN IRBESARTAN VALSARTAN OLMESARTAN TELMISARTAN

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MAJOR ADVERSE EFFECT DUE TO TREATMENT WITH ACE INHIBITORS

NOT SEEN WITH ARBS ?

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ARBS VS ACE INHIBITORS

DO NOT INTERFERE WITH DEGRADATION OF BRADYKININ – COUGH IS RARE

COMPLETE INHIBITION OF AT1 RECEPTOR ACTIVATION

INDIRECT AT2 ACTIVATION

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INDIVIDUAL DRUGS LOSARTAN – HIGH FIRST PASS METABOLISM,

NO DOSE ADJUSTMENT – RENAL / LIVER DISEASE

CANDESARTAN – NON COMPETITIVE ANTAGONISM

VALSARTAN – ABSORPTION AFFECTED BY FOOD

OLMESARTAN – NO DOSE ADJUSTMENTPRODRUG

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ADVERSE EFFECTS

HYPOTENSION

HYPERKALEMIA

TERATOGENECITY

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USES

HYPERTENSIONCONGESTIVE HEART FAILUREMYOCARDIAL INFARCTIONDIABETIC NEPHROPATHY

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PREVENTS REMODELING

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CONTRAINDICATI

ONBilateral

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CAN WE COMBINE

ARBS WITH ACE INHIBITORS?

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THEORETICAL REASONS

MORE COMPLETE SUPPRESSION OF RAS

ANGIOTENSIN II GENERATED BY ALTERNATE PATHWAYS BLOCKED BY ARBS

ACE INHIBITORS – BRADYKININ RELATED VASODILATATION

ARBS – COMPENSATORY RISE IN ANG II checked by ACEI

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DIRECT RENIN INHIBITOR

ALISKIREN


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