1 / 12

DR. SHABAN ALI

DENSENSITIZATION & TACHYPHYLAXIS. DR. SHABAN ALI. Desensitization & Tachphylaxis. Reduction of effect of a drug after its continuous administration Diminished response of a drug in person after its continuous use b/c body adapts the continuous presence of drug

reed
Download Presentation

DR. SHABAN ALI

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. DENSENSITIZATION & TACHYPHYLAXIS DR. SHABAN ALI

  2. Desensitization & Tachphylaxis Reduction of effect of a drug after its continuous administration Diminished response of a drug in person after its continuous use b/c body adapts the continuous presence of drug • Desensitization & tachyphylaxis= Synonymous

  3. Tachyphylaxis When desensitization occurs rapidly c/d tachyphylaxis (Acute tolerance) Tolerance More gradual d/c in responsiveness to drug (days or weeks) Refractoriness Loss of therapeutic efficacy

  4. Drug resistance • Loss of effectiveness of antimicrobial or antitumour drugs

  5. Mechanisms of Desensitization • Change in receptors • Loss of receptors • Exhaustion of mediators • Increased metabolic degradation • Physiological adaptation • Active extrusion of drug from cells (mainly relevant in chemotherapy)

  6. Change in receptors • Conformational change in receptors • Receptorscoupled to ionic channel=rapid desensitization e.g., NMJ (ion channel)= confirm.change  tight binding of agonist (un opening of channel) β-adrenoceptors (GPCR) =not activate adenylate cyclase although still bound to receptorcont.

  7. Mechanism for change in receptors • Phosphorylation of specific residue (3rd cytoplasmic loop) in receptor protein • Phosphorylated receptor is less efficient at activating G-protein and also exhibits lower affinity for agonists

  8. Receptor desensitization

  9. Loss of receptors • Prolonged exposure to agonists results in a gradual d/c in no of receptors • Receptors taken into cell by endocytosis E.g., β-adrenoceptors studies of cell culture receptor d/c in presence of ISOP • Receptors of various peptides, hormones

  10. Exhaustion of mediators • Depletion of essential intermediate subs. e.g., amphetamine = tachyphylaxis b/c of depletion of stores of NA

  11. Increased metabolic degradation • Tolerance to some drugs b/c of repeated administration of same dose result in low plasma conc. b/c of more metabolic degradation (by metabolic enzyme induction) • Modest tolerance e.g., barbiturates & ethanol

  12. Physiological Adaptation • Diminution of drug effect b/c of nullification by homeostatic response (unknown mech) • E.g., thiazide diuretics = hypotensive effect d/c b/c of stimulation of renin-angiotensin system • Side effect (nausea, sleepiness) subside even drug is continued

More Related