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AUTACOIDS ,[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HISTAMINES  ,[object Object],[object Object]
Synthesis  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Metabolism : ,[object Object],[object Object],[object Object],[object Object]
Metabolism :
Functions: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Selected Actions of Histamine in Humans H1, H2 H2 H1, H2 H2 (?) H1 H2 H2 H1 H1 H2 H2    TPR Vasodilatation    Blood flow    Blood flow,relaxation Constriction Relaxation Constriction Constriction Vasodilatation    Permeability    SA rate    Force of contraction Atrial & vent automaticity  CARDIOVASCULAR Vascular Facial cutaneous Forearm Gastric mucosa Carotid artery Pulmonary artery Basilar artery Coronary artery Other pre & post cap Arterioles Postcapillary venules Heart Receptor  Action   Organ Tissue
Selected Actions of Histamine in Humans H1 Epinephrine release  ADRENAL MEDULLA  H2 H1 H2 (?) Acid and pepsin secretion, If  Relaxation & Contraction (more prominent) Relaxation (?) GASTROINTESTINAL Oxyntic mucosa GI smooth muscle Gallbladder smooth muscle   H1, H2 (?)  Pain & itching (esp to insect bites & needle stings)   CUTANEOUS NERVE ENDINGS (Sensory)   H1 H2   Contraction (more prominent) Relaxation   RESPIRATORY Bronchiolar smooth muscle   H2 Inhibition of IgE – dependent degranulation BASOPHILS   Receptor  Action   Organ Tissue
Selected Actions of Histamine in Humans ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
H1 RECEPTOR ANTAGONISTS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Adverse Effects: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Therapeutic Uses: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Histamine Antagonists ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Oldest member More prolonged action    Incidence of drowsiness   Chlorcyclizine 4. Piperazine  Most potent Not so prone to develop drowsiness More suitable for older patients Sedation/CNS stimulation   Chlorpheniramine Pheniramine Chlorphenamine   3. Alkylamine  Most specific H1  antagonist    Anticholinergic activity Feeble CNS effects Somnolence GI s/s common   Pyrilamine Mepyramine Pyranesamine 2.Ethylenediamine/  Ethylamine Significant antimuscarinic activity Sedation, somnolence    Incidence of GI symptoms Effective in emesis & motion sickness   Diphenhydramine  First Gen. Agents: 1. Ethanolamine   Characteristics   Prototype   Structural Class
Counters motion sickness & emesis   Meclizine/Meclozine  Counters motion sickness (primarily)   Cyclizine Long acting Widely used for skin allergies CNS depressant More prominent antipruritic action Hydroxyzine Characteristics   Prototype   Structural Class
Rhinitis, urticaria (-) pass BBB  Cetirizine   3. Piperazine   Rapid onset of action (30 mins) (-) anticholinergic effects Reduce both wheal & flare response    Potential to penetrate BBB Skin allergy Allergic  rhinitis   Acrivastine  2. Alkylamine Highly selective for H1 receptor Non-sedating (-) anticholonergic action (-) pass BBB    incidence of S/E Terfenadine  Second Gen.Agents 1. Piperidine   Anticholinergic Prominent sedation Counters motion sickness primarily antiemetic Promethazine  5. Phenothiazine  Characteristics   Prototype   Structural Class
H2 RECEPTOR ANTAGONISTS   ,[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Drug Interactions: ,[object Object],[object Object],[object Object],[object Object]
Vasoactive Peptides ,[object Object],[object Object],[object Object]
BRADYKININ & KALLIDIN  ,[object Object],[object Object],[object Object],[object Object]
Pharmacologic Properties  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Functions ,[object Object],[object Object],[object Object]
Pharmacological Properties  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
5 HYDROXYTRYPTAMINE (5HT)  ,[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],1. Clozapine:   High affinity for dopamine receptors Reduced negative symptoms of schizophrenia 2. Risperidone:   D2 receptor blocker   Reduced negative symptoms of schizophrenia
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],3.  Methysergide:   used for diarrhea & malabsorption in patients    with  carcinoid tumors
[object Object],[object Object],[object Object],[object Object],[object Object]
LIPID-DERIVED AUTOCOIDS  ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object]
Inhibitors of Biosynthesis  ,[object Object],[object Object],[object Object]
Pharmacological Properties
Therapeutic Uses  ,[object Object],[object Object],[object Object],[object Object]
PLATELET ACTIVATING FACTOR (PAF)  ,[object Object]
Pharmacological Properties  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Autacoids....With Slide No

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  • 8. Selected Actions of Histamine in Humans H1, H2 H2 H1, H2 H2 (?) H1 H2 H2 H1 H1 H2 H2  TPR Vasodilatation  Blood flow  Blood flow,relaxation Constriction Relaxation Constriction Constriction Vasodilatation  Permeability  SA rate  Force of contraction Atrial & vent automaticity CARDIOVASCULAR Vascular Facial cutaneous Forearm Gastric mucosa Carotid artery Pulmonary artery Basilar artery Coronary artery Other pre & post cap Arterioles Postcapillary venules Heart Receptor Action Organ Tissue
  • 9. Selected Actions of Histamine in Humans H1 Epinephrine release ADRENAL MEDULLA H2 H1 H2 (?) Acid and pepsin secretion, If Relaxation & Contraction (more prominent) Relaxation (?) GASTROINTESTINAL Oxyntic mucosa GI smooth muscle Gallbladder smooth muscle H1, H2 (?) Pain & itching (esp to insect bites & needle stings) CUTANEOUS NERVE ENDINGS (Sensory) H1 H2 Contraction (more prominent) Relaxation RESPIRATORY Bronchiolar smooth muscle H2 Inhibition of IgE – dependent degranulation BASOPHILS Receptor Action Organ Tissue
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  • 16. Oldest member More prolonged action  Incidence of drowsiness Chlorcyclizine 4. Piperazine Most potent Not so prone to develop drowsiness More suitable for older patients Sedation/CNS stimulation Chlorpheniramine Pheniramine Chlorphenamine 3. Alkylamine Most specific H1 antagonist  Anticholinergic activity Feeble CNS effects Somnolence GI s/s common Pyrilamine Mepyramine Pyranesamine 2.Ethylenediamine/ Ethylamine Significant antimuscarinic activity Sedation, somnolence  Incidence of GI symptoms Effective in emesis & motion sickness Diphenhydramine First Gen. Agents: 1. Ethanolamine Characteristics Prototype Structural Class
  • 17. Counters motion sickness & emesis Meclizine/Meclozine Counters motion sickness (primarily) Cyclizine Long acting Widely used for skin allergies CNS depressant More prominent antipruritic action Hydroxyzine Characteristics Prototype Structural Class
  • 18. Rhinitis, urticaria (-) pass BBB Cetirizine 3. Piperazine Rapid onset of action (30 mins) (-) anticholinergic effects Reduce both wheal & flare response  Potential to penetrate BBB Skin allergy Allergic rhinitis Acrivastine 2. Alkylamine Highly selective for H1 receptor Non-sedating (-) anticholonergic action (-) pass BBB  incidence of S/E Terfenadine Second Gen.Agents 1. Piperidine Anticholinergic Prominent sedation Counters motion sickness primarily antiemetic Promethazine 5. Phenothiazine Characteristics Prototype Structural Class
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