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Serotonin.dr.asa

  1. Dr. AMREEN SABA ATTARIYA POST GRADUATE STUDENT DEPT OF PHARMACOLOGY M.R. MEDICAL COLLEGE, GULBARGA INDIA SEROTONIN
  2. Outline Of Presentation Introduction to SEROTONIN Sources, Biosynthesis, Metabolism Receptors in detail Physiological & Pathophysiological roles Drugs Acting On 5HT Receptors Recent Advances Summary & References Mar 6, 2017Dr.ASA:serotonin
  3. HISTORY SEROTONIN -name given to vasoconstrictor substance which appeared in serum when blood clot Named after Latin word serumserum & Greek word tonictonic 1948– first isolation Maurice Rapport & Irvine Page* Earlier called ENTERAMINE by VITTORIO ERSPAMER et al Enteramine found in EC cells In 1950 --both were shown to be 5-hydroxytryptamine Mar 6, 2017Dr.ASA:serotonin * Rapport et al
  4. Physiologic Distribution of 5HT 10% CNS 90% GI tract  90% ECs  10% Neurons 5-Hydroxytryptamine Mar 6, 2017Dr.ASA:serotonin
  5. SOURCE Venom of Wasps, Bees, scorpions Widely distributed in invertebrates Fruits--banana, pear, pineapple, tomato, plums, nuts Mar 6, 2017Dr.ASA:serotonin
  6. SEROTONIN is: Neurotransmitter in CNS Local hormone in the gut Component of the platelet clotting process Potent stimulant of pain and itch nerves Central (CNS) modulator of: Migraine Vomiting Mood, sleep, appetite, temperature, blood pressure Mar 6, 2017Dr.ASA:serotonin
  7. Biosynthesis and metabolism of SEROTONIN Mar 6, 2017Dr.ASA:serotonin
  8. Serotonin Uptake Like NA actively takes up serotonin by Serotonin transporter - amine pump (SERT) – Na+ dependent carrier Inhibited by SSRIs & TCAs Stored in storage vesicles by active uptake – Vesicular monoamine transporter (VMAT 2) – inhibited by Reserpine Mar 6, 2017Dr.ASA:serotonin
  9. SEROTONIN TRANSPORTER[SERT] Member of class of monoamine transporters. Has 12 transmembrane spanning Na+-dependent transporters Mechanism is the transportation of Na+, Cl & substrate intracellularly in exchange for K+ * Location: GIT, pulmonary, peripheral vasculature, platelets Mar 6, 2017Dr.ASA:serotonin* Sneddon, 1973; Torres et al., 2003; Ni & Watts, 2006.
  10. 5HT REC SUBTYPES Earlier[GADDUM &PICARELLI] Mtype= MUSCULOTROPIC Dtype=NEUROTROPIC M type@ cholinergic nerve endingscontrol release of Ach D type @ smooth muscles NEWER [1 to 7] 1– 1A 1B 1D 2-- 2A 2B 2C 3, 4, 5, 6, 7 Mar 6, 2017Dr.ASA:serotonin
  11. 5-HT Rec - Characters All are GPCRs except 5-HT3 Decrease cAMP production – 5-HT1 Increase cAMP production – 5-HT4, 5-HT6, 5-HT7 Generating IP3/DAG – 5-HT2 5-HT3 – Ligand gated Na+ K+ channel – faster depolarization
  12. 5HT REC SUBTYPES Mar 6, 2017Dr.ASA:serotonin
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  14. PHYSIOLOGICAL ROLE OF 5HT Mar 6, 2017Dr.ASA:serotonin
  15. PHYSIOLOGICAL ROLE PLATELETS Lack Tryptophan hydroxylase cant synthesize 5HT Take up from circulation & store VMAT-2 mediated uptake into dense core granules Vascular injury release 5HT 5HT binds on 2A rec on platelets weak Platelet aggregation, augmented by Collagen If injury reaches till smooth muscle direct release of 5HT V/s occlusion & VC Hempostasis 5HT interaction with Endothelium release NO VD [antgonising its own plus other local hormone action] Mar 6, 2017Dr.ASA:serotonin
  16. Mar 6, 2017Dr.ASA:serotonin LOCAL INFLUENCES OF PLATELET 5HT
  17. PHYSIOLOGICAL ROLE CVS +VE IONOTROPIC, +VE CHRONOTROPIC Contraction--splanchnic, renal, pulmonary & cerebral vasculatures Also cause release of NO & PGs + block the release of NE from sympatheitic nerves arterial relaxation Other hand, amplifies the local constrictor actions of NE, AngII, and histaminereinforce the hemostatic response to 5-HT Mar 6, 2017Dr.ASA:serotonin
  18. PHYSIOLOGICAL ROLE CVS Effect on BP BEZOLD JARISCH REFLEX Early sharp fall ----chemoreflex. Brief rise---- vasoconstriction and increased CO Prolonged fall ----arterial dilatation & extravasation of fluid. Mar 6, 2017Dr.ASA:serotonin
  19. PHYSIOLOGICAL ROLE GIT 5HT-local hormone in GITinitiation & susutainance of intestinal peristalsis Potent stimulator of GIT Diarrhoea Inhibit gastric acid & pepsin, increases mucus production ULCEROPROTECTIVE PROPERTY Stimulates vomiting (5-HT3rec on vagal afferents & centrally) on 5-HTrec (Physiologically regulates GI motility and peristalsis) Mar 6, 2017Dr.ASA:serotonin
  20. 5HT in GIT Abnormally increased 5-HT is found in a range of gastrointestinal disorders including Chemotherapy- induced Nausea & Vomiting, Carcinoid Syndrome, Coeliac Disease, IBD & IBS-D IBS-D- Impaired SERTincrease in mucosal 5-HT availability. IBS-D -- increased 5-HT postprandially Mar 6, 2017Dr.ASA:serotonin
  21. 5-HT3 rec antagonists inhibit chemotherapy-induced nausea & diarrhoea associated with both carcinoid syndrome & IBS. IBS-C---impaired 5-HT response &responds to 5HT-4 agonists-PRUCALOPRIDE & 5HT-4 partial agonists- TEGASEROD. Mar 6, 2017Dr.ASA:serotonin *Spiller R Recent advances in understanding the role of 5HT in GI motility in functional bowel disorders: alterations in 5-HT signalling & metabolism in human disease.Neurogastroenterol Motil. 2007 Aug;19 Suppl 2:25-31.
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  23. PHYSIOLOGICAL ROLE Mar 6, 2017Dr.ASA:serotonin
  24. PHYSIOLOGICAL ROLE CNS NEUROHUMORAL TRANSMISSION 5HT—released by tryptaminergic neurons Function: Temp Regulation, Endocrine Control, ExtraPyramidal Activity Altered function disturbances in Sleep, Appetite, Mood, Sexual Behaviour, Motor Activity, Perception, Migraine Mar 6, 2017Dr.ASA:serotonin
  25. PHYSIOLOGICAL ROLE CNS SLEEP 5HT—control sleep-wake cycle Depletion INSOMNIA Mar 6, 2017Dr.ASA:serotonin
  26. PHYSIOLOGICAL ROLE CNS BEHAVIOUR 5HT—control mood, emotion, reward, memory Low CSF-5HIAA IMPULSIVE, VIOLENT, SUICIDAL BEHAVIOUR Rx= SSRI[for mental depression] 5HT rec function is altered in EATING disorders – Anorexia Nervosa, Bulimia Nervosa Mar 6, 2017Dr.ASA:serotonin
  27. DRUGS ACTING ON 5-HT Mar 6, 2017Dr.ASA:serotonin
  28. DRUGS ACTING ON 5-HT SYSTEM 5-HT Precursor – Tryptophan in diet↑  5-HT↑ production Inhibit synthesis: p-chlorophenylalanine (PCPA) - irreversible Inhibit neuronal re-uptake: Cocaine, SSRI, TCA Inhibit storage-deplete (VMAT-2): Reserpine Inhibit metabolism: MAO-A inhibitors Promote release: Amphetamines Mar 6, 2017Dr.ASA:serotonin
  29. SSRIs Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Citalopram, Escitalopram MOA: Selectively block reuptake of 5HT Increased extracellular 5HT Increased action on postsynaptic receptors Stimulation Mar 6, 2017Dr.ASA:serotonin
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  31.  PK of SSRI: Orally absorbed Metabolism=liver 2D6 & 2C19 t1/2=18hrs-7d SSRI(t1/2) DOSES (mg/d) Fluoxetine(2d) 10-60 Fluvoxamine(18hrs) 50-300 Paroxetine(20hrs) 10-40 Sertraline(26hrs) 50-200 Citalopram(33hrs) 10-40 Mar 6, 2017Dr.ASA:serotonin
  32. AE-SSRIs Pharmacological Action Adverse Effect GIT Nausea, Vomiting, Diarrhea Neuropsychiatry Agitation, Tremor, Insomnia And Daytime Somnolence, Seizures, Mania Sexual Dysfunctions Ejaculatory Delay, Anorgasmia Mar 6, 2017Dr.ASA:serotonin
  33. SEROTONERGIC DRUGS Mar 6, 2017Dr.ASA:serotonin
  34. SEROTONERGIC DRUGS PARTIAL AGONIST- AZAPIRONES AGONISTS TRIPTANS ERGOT & ERGOT ALKALOIDS D-LYSERGIC ACID DIETHYLAMIDE(LSD) ANTAGONISTS-- CYPROHEPTADINE METHYSERGIDE KETANSERIN ATYPICAL ANTIPSYCHOTICS Mar 6, 2017Dr.ASA:serotonin
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  36. PARTIAL AGONIST- AZAPIRONES BUSPIRONE, GEPIRONE, IPSAPERONE Selective partial agonists of 5HT-1A Effective in the treatment of anxiety Mimics antianxiety properties of BDZs but donot interact with GABAA rec Do not display sedative & anticonvulsant properties of BDZs. Mar 6, 2017Dr.ASA:serotonin
  37. AGONISTS TRIPTANS ERGOT & ERGOT ALKALOIDS D-LYSERGIC ACID DIETHYLAMIDE(LSD) PROKINETICS- CISAPRIDE, MOSAPRIDE Mar 6, 2017Dr.ASA:serotonin
  38. TRIPTANS Almotriptan, Eletriptan, Frovatriptan, Naratriptan, Rizatriptan, Sumatriptan, Zolmitriptan Agonist of 5-HT1D 5-HT1B Low / no affinity for other subtypes of 5-HTrec or for adrenergic, dopaminergic, muscarinic cholinergic, GABAA receptors
  39. TRIPTANS-MOA MOA: 2 hypothesis of migraine pathophysiology I: unknown events lead to abnormal dilation of carotid AV anastomoses in headdiverting blood from capillary bedscerebral ischemia & hypoxia. Rx: Triptans constrict IC blood vessels, including AV anastomoses & restores blood flow to brain II: 5-HT1D & 5-HT1Bserve as presynaptic autoreceptorsmodulate neurotransmitter release from neuronal terminals 5-HT1 agonists block the release of proinflammatory neuropeptides Mar 6, 2017Dr.ASA:serotonin
  40. TRIPTANS-PK SUMATRIPTAN(SC, ORAL, NASAL SPRAY) SCpeak conc 12min,BA=97% ORAL 1-2hrs,BA14-17% t1/2 = 1-2hrs, Metabolised by MAO-A, Excretion in urine  ZOLMITRIPTAN(ORAL) ORAL peak conc 1.5-2hrs, BA=40% t1/2 =2-3hrs  NARATRIPTAN(ORAL) ORAL peak conc 2-3hrs, BA =70% t1/2 =6hrs  RIZATRIPTAN(ORAL) ORAL peak conc 1-1.5hrs, BA=45% Metabolised by MAO-A Mar 6, 2017Dr.ASA:serotonin
  41. TRIPTANS-AE Cardiac events--coronary artery vasospasm, transient MI,atrial & ventricular arrhythmias, MI SC Sumatriptanirritation at the site of injection (transient mild pain, stinging, or burning sensations). Nasal spray Sumatriptan bitter taste. Oralparesthesias, asthenia,fatigue,flushing, feelings of pressure, tightness, or pain in chest,neck, & jaw; drowsiness, dizziness, nausea, sweating. Mar 6, 2017Dr.ASA:serotonin
  42. TRIPTANS-C/I H/o ischemic or vasospastic CAD (strokeTIA), cerebrovascular, PVD hemiplegic or basilar migraines, other significant cardiovascular diseases, or IBD Uncontrolled HTN. Naratriptan C/I-severe renal/hepatic impairment. Rizatriptan--with caution in renal/hepatic disease but not C/I Eletriptan C/I--hepatic disease. Almotriptan,rizatriptan, sumatriptan, zolmitriptan are C/I in patients who have taken MAO-I within the preceding 2 weeks All triptans C/I--near-term prior exposure to ergot alkaloids or other 5-HT agonists Mar 6, 2017Dr.ASA:serotonin
  43. TRIPTANS-Use in Migraine In acute Rx of migraine (with/without aura), but not for prophylaxis. Begin as soon as possible after onset of a migraine attack Oral – most convenient, but Nausea & Vomiting occurs. SUMATRIPTAN SC=6mg(max 12mg/d), Nasal spray=5-20mg Oral=25-100mg(max 200mg/d) ZOLMITRIPTAN oral =1.25-2.5 mg(max10mg/d) NARATRIPTAN oral=1-2.5 mg,should not be repeated until 4 hours after previous dose. Donot exceed 5mg/day RIZATRIPTAN oral= 5-10 mg, max 30mg/d Donot use concurrently with other tripans / ergot derivativesMar 6, 2017
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  45. ERGOT & ERGOT ALKALOIDS Partial agonists/antagonists at adrenergic, dopaminergic & 5HT rec Effects depends onagent, dosage,species, tissue, physiological & endocrinological state, & experimental conditions. Ergot derivative-METHYSERGIDE-2A>2C blocker—Rx of acute migraine Ergot for migraine should be restricted to patients having frequent, moderate migraine / infrequent, severe migraine attacks Ergotamine, Ergonovine, Methyl-ergonovine, Dihydroergotamine(DHE) Mar 6, 2017Dr.ASA:serotonin
  46. ERGOTAMINE Most effective ergot alkaloid in Migraine MOA: Partial agonist of 5-HT1B/1D – 1. Constriction of dilated cranial vessels Or, 2. by specific Constriction of carotid AV shunt channels 3. Reduction of neurogenic inflammation Doses: oral/SL (1mg every half an hourly) till relief – 6 mg/d DIHYDROERGOTAMINE(DHE) Preferred for parenteral administration Mar 6, 2017Dr.ASA:serotonin
  47. Current Status of Ergots in Migraine Not popular anymore Regular use is hazardous No prophylactic value – precipitate on discontinuation Dull headache Available prep=Combination with caffeine, paracetamol etc Mar 6, 2017Dr.ASA:serotonin
  48. 5HT AGONIST- LSD D-Lysergic acid diethyl amide Chemical precursor=lysergic acid, occurs naturally in a fungus-that grows on wheat & rye-but is devoid of hallucinogenic actions. LSD has indolealkylamine moiety which interacts with 5- HT rec Agonist 5-HT1A marked slowing of firing in Raphe cellbodies Studies of 5-HT2Arec knockout mice confirm the role for this rec in LSD hallucinogenic effects* Mar 6, 2017Dr.ASA:serotonin * Gonzalez-Maeso et al., 2007
  49. ANTAGONISTS CYPROHEPTADINE METHYSERGIDE KETANSERIN OTHERS:ATYPICAL ANTIPSYCHOTICS ONDANSETRON, GRANISETRON METACHLOPRAMIDE Mar 6, 2017Dr.ASA:serotonin
  50. CYPROHEPTADINE 5-HT2Ablocking property Weak H1 antihistaminic, anticholinergic & sedative Famous for increasing appetite Uses: good antipruritic – used in allergies (no 5-HT Role) Carcinoid syndrome Gastrectomy dumping syndrome Priapism (caused by fluoxetine) Appetite stimulation in children Migraine Prophylaxis AE: weight gain, drowsiness, dry mouth, ataxia Mar 6, 2017Dr.ASA:serotonin
  51. METHYSERGIDE Congener of methyl-ergonovine Related to ergot alkaloids – but without ergot like effects Weak vasoconstrictor, oxytocic 5-HT2A/2C antagonist - also tissue specific agonistic action – also acts on 5-HT1 receptor Uses: Prophylaxis of Migraine & other headaches, carcinoid syndrome, post gastrectomy dumping syndrome ADR: Abdominal, pulmonary and endocardial FIRBOSIS If used chronicallyRx should be interrupted for 3 weeks or more every 6 months. Mar 6, 2017Dr.ASA:serotonin
  52. KETANSERINE Selective 5-HT2 receptor blocker[5-HT2A > 5-HT2C] No effects on 5-HT1, 5-HT3, or 5-HT4 Additional H1, α1 and DAergic blocking action Antagonizes VC, platelet aggregation & airway constriction actions of 5-HT – antihypertensive Also in vasospastic conditions – Raynauds disease RITANSERIN= more 2A selective Mar 6, 2017Dr.ASA:serotonin
  53. OTHER ANTAGONISTS Clozapine: Atypical antipsychotic--5HT2A/2C blocker – weaker dopaminergic antagonist than typical ones – used for resistant cases of Schizophrenia Risperidone: 5-HT2A + D2 antagonist - similar to clozapine – used in Schizophrenia Ondansetron: 5-HT3 antagonist – Chemo & radiotherapy induced vomiting Mar 6, 2017Dr.ASA:serotonin
  54. DRUG REC TYPE USE CYPROHEPTADINE 2A ANTAGONIS T SEROTONIN SYNDROME METHYSERGIDE 2A/2C ANTAGONIS T CARCINOID & POST- GASTRECTOMY DUMPING SYNDROMES. CLOZAPINE 2A/2C ANTAGONIS T ANTIPSYCHOTIC RESPERIDONE 2A ANTAGONIS T ANTIPSYCHOTIC KETANSERIN 2A ANTAGONIS T ANTIHYPERTENSIVE Mar 6, 2017Dr.ASA:serotonin
  55. DRUG REC TYPE USE DOSE METACLOPRAMIDE 4 AGONIST GERD IBS 10mg TDS orally CISAPRIDE 4 AGONIST GERD IBS 10-20mg TDS MOSAPRIDE 4 AGONIST GERD, IBS 5mg TDS ONDANSETRON 3 ANTAGONIST CINV 8mg OD orally GRANISTERON 3 ANTAGONIST CINV 2mg orally PALANOSETRON 3 ANTAGONIST CINV Mar 6, 2017Dr.ASA:serotonin
  56. USES Major Depression– SSRIs like Fluoxetine, Sertraline Obsessive compulsive disorder – SSRIs Phobic disorders - SSRIs PMS - SSRIs Somatoform disorders (Hypochondriasis) - SSRIs Post traumatic stress disorder - SSRIs Neuropathic pain & Fibromyalgia pain Anxiety neurosis – Azapirones(5- HT1A partial agonist)Mar 6, 2017
  57. USES Migraine – Triptans 5-HT 1B/1D agonist Appetite stimulant – Cyproheptadine (5-HT2A antagonist) Schizophrenia – Clozapine (2A/2C antagonist) CINV –Ondansetron (Emeset 4,8mg tabs ,2mg/ml inj in 2ml & 4ml amps), Granisetron (Granicip 1,2mg tabs ,1mg/ml inj in 1ml & 3ml amps) Tropisetron (5-HT 3 antagonist). GERD – Mosaprid[Moza 2.5mg ,5mg tabs] (5-HT4 agonist ) IBS – Mosapride, Prucalopride (5-HT4 agonist) Mar 6, 2017Dr.ASA:serotonin
  58. Mar 6, 2017Dr.ASA:serotonin Carcinoid Syndrome Over 90% of the serotonin in the body is found in enterochromaffin cells in GI tract. Carcinoid tumor secrets serotonin and is a neoplasm of enterochromaffin cells. Carcinoid syndrome causes subendocardial fibroplasia and valvular or electrical malfunction. In patients whose tumor is not operable, a serotonin antagonist is a useful treatment.
  59. Mar 6, 2017Dr.ASA:serotonin CARCINOID SYNDROME Cyproheptadine is a H1 and 5-HT2blocker. It also has antimuscarinic effects and causes sedation. It is used in the treatment of the smooth muscle manifestations of carcinoid tumor and in cold-induced urticaria.
  60. Mar 6, 2017Dr.ASA:serotonin Carcinoid Syndrome 5-hydroxyindoleacetic acid (5-HIAA) is a metabolite of serotonin. The excretion of 5-HIAA is a measure of serotonin synthesis. The 24-hour excretion of 5-HIAA can be used as a diagnostic test for carcinoid tumor. Banana contains large amounts of serotonin and must be prohibited during such tests.
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  62. Sternbach’s criteria for serotonin syndrome* Mar 6, 2017Dr.ASA:serotonin * Sternbach, 1991;Brown et al., 1996
  63. Agents that have potential to induce serotonin toxicity & their MOA for increasing serotonin levels Mar 6, 2017Dr.ASA:serotonin
  64. RECENT ADVANCES TANDOSPIRONE – A/k/a Metanopirone--5HT1A partial agonist—Use--anxiolytic & antidepressant. Dose =30mg/d. AGOMELATINE – 5HT2C antagonist & agonist at melatonin rec. Used in depression. NELOTANSERIN (APD-125) – selective 5HT2A inverse agonist developed by Arena pharmaceuticals for insomnia. PALONOSETRON (Aloxi) – approved by FDA in 2003 for IV use in preventing delayed CINV Mar 6, 2017Dr.ASA:serotonin
  65. RECENT ADVANCES RAMOSETRON – 5HT 3 antagonist available in Japan & South east Asian countries—used in CINV. CILANSETRON – 5HT 3 antagonist used in IBS where diarrhoea is the dominant symptom. LASMIDITAN-5HT1F agonist without vasoconstriction—1F is expresses in trigeminal nerve pathway– Rx of Migraine --mainly for individuals with CV risk factors, CVS diseases or dissatisfied with current therapies Newer drugs for chronic migraine OLCEGEPANT TELCAGEPANT Mar 6, 2017Dr.ASA:serotonin
  66. SUMMARY Mar 6, 2017Dr.ASA:serotonin
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  69. References… Sander E: 5Hydroxytryptamine and dopamine Goodman & Gilman’s The pharmacological Basis of Therapeutics 12th ed(335-363) 5Hydroxytryptamine :Pharmacology & Pharmacotherapeutics by R.S Satoskar, 24th ed (333-343) 5Hydroxytryptamine,its antagonist and drug therapy: Essentials of medical pharmacology by KD Tripathi, 7th ed(170-181) HL Sharma, KK Sharma. Histamine, serotonin,ergot alkoloid and bradykinin In: HL Sharma editor. Principles of pharmacology, 2nd edn. New Delhi: Para Publishers; 2011. Zadeh M, et al: Serotonin: J. vet. Pharmacol. Therap. 31, 187–199, doi: 10.1111/j.1365-2885.2008.00944.x. REVIEW ARTICLE *Spiller R Recent advances in understanding the role of 5HT in GI motility in functional bowel disorders: alterations in 5-HT signalling & metabolism in human disease.Neurogastroenterol Motil. 2007 Aug;19 Suppl 2:25-31. Mar 6, 2017Dr.ASA:serotonin
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Editor's Notes

  1. As you all know, serotonin is a biogenic amine that is predominantly located in the gastrointestinal tracts. In fact, it has been estimated that 95% of all the serotonin in the body is in the digestive tract. 90% of this is in the enterochromaffin cells in the mucosa, 10% is in the neurons in different plexuses, which we will discuss later. About 5% of the body serotonin is in the central nervous system. Next slide, please
  2. SERT is a member of a more general class of monoamine transporters All monoamine transporters, including SERT, are 12 transmembrane spanning sodium-dependent transporters. The basic mechanism is the transportation of Na+, Cl) and the substrate intracellularly in exchange for K+ (Sneddon, 1973; Torres et al., 2003; Ni & Watts, 2006). SERT has been identified in the CNS, gastrointestinal tract, pulmonary and peripheral vasculature, and platelets. This is the mechanism by which serotonin is taken up by platelets and enterochromaffin cells.
  3. 4 FAMILIES WITH 14 RECEPTOR SUBTYPES
  4. Abnormally increased 5-HT is found in a range of gastrointestinal disorders including chemotherapy-induced nausea and vomiting, carcinoid syndrome, coeliac disease, inflammatory bowel disease and irritable bowel syndrome (IBS) with diarrhoea (IBS-D), especially that developing following enteric infection Impaired SERT has been described in IBS-D and might account for some of the increase in mucosal 5-HT availability.
  5. 5-HT(3) receptor antagonists inhibit chemotherapy-induced nausea and diarrhoea associated with both carcinoid syndrome and IBS. While IBS-D is associated with increased 5-HT postprandially, IBS with constipation (IBS-C) is associated with impaired 5-HT response and responds to 5-HT(4) agonists such as Prucalopride and 5-HT(4) partial agonists such as Tegaserod.
  6. UPTAKE BLOCKADE OCCURS QUICKLY BT ANTIDEPRESSANT EFFECTS TAKES WEEKS TO APPEAR
  7. ORALLY ABSORBED THOUGH SLOW LARGE VOLUME OF DISTRIBUTION METABOLISED BY CYP2D6, CYP3A4,CYP1A2 ACTIVE METABOLITIES DESIPREMINE AND NORTRIPTYLINE ARE FORMED AFTER DEMYTHYLATION Inactivation is by glucunoride conjugation n oxidation
  8. IN ADDITION TO UPTAKE BLOCKADE THEY HAVE SHOW MUSCURANIC, ADRENERGIC, HISTAMINIC EFFECTS
  9. EITHER BY REPLACING THEM FOR PPB SITE OR REDUCING THEIR METABOLISM HPERTENSION CRISIS WIT EXCITATION AND HALLUCINATION
  10. ORALLY ABSORBED THOUGH SLOW LARGE VOLUME OF DISTRIBUTION METABOLISED BY CYP2D6, CYP3A4,CYP1A2 ACTIVE METABOLITIES DESIPREMINE AND NORTRIPTYLINE ARE FORMED AFTER DEMYTHYLATION Inactivation is by glucunoride conjugation n oxidation
  11. DISCONTINUATION REACTION : PARAESTHESIA, AGITATION, BOWEL UPSET,BODTACH, SLEEP DISTURBANCES
  12. I: unknown events lead to theabnormal dilation of carotid arteriovenous anastomoses in the head, diverting blood from the capillary beds and thereby producing cerebral ischemia and hypoxia.
  13. Two classes of 5-HT autoreceptors with differential localizations. Somatodendritic 5-HT1A autoreceptors decrease raphe cell firing when activated by 5-HT released from axon collaterals of the same or adjacent neurons. The receptor subtype of the presynaptic autoreceptor on axon terminals in the forebrain has different pharmacological properties and has been classified as 5-HT1D (in humans) or 5-HT1B (in rodents). This receptor modulates the release of 5-HT. Postsynaptic 5-HT1 receptors are also indicated.
  14. Naratriptan is contraindicated in patients with severe renal or hepatic impairment. Rizatriptan should be used with caution in patients with renal or hepatic disease but is not contraindicated in such patients. Eletriptan is contraindicated in hepatic disease. Almotriptan, rizatriptan, sumatriptan, and zolmitriptan are contraindicated in patients who have taken a monoamine oxidase inhibitor within the preceding 2 weeks, and all triptans are contraindicated in patients with near-term prior exposure to ergot alkaloids or other 5-HT agonists
  15. CYPROHEPTADINE=HAS ADDITIONAL HISTAMINIC,ANTICHOINERGIC,SEDATIVE PROPERTIES, USED TO INCREASE APPETITE,CARCINOID SYNDROME, POSTGASTRECTOMY DUMPING SYNDROME, TOXICITY OF SSRI ,TO TEAT SEXUAL DYSFUNCTION CAUSED BY SSRI & TRAZODONE. SIDE EFFECTS=DROWZINESS , DRY MOUTH METHYSERGIDE=RELATED TO ERGOT ALKOLOID, ANTAGONISES 5HT ON SMOOTH MUSCLES, USED IN MIGRAINE PROPHYLAXIS.S/E=ABDOMINAL,PILMONAR FIBROSIS CLOZAPINE=WEAK D2 BLOCKING THUS LESS EXTRAPYRADIMAL SIDE EFFECTS,NO RISE IN PRLACTIN LEVEL, METABOLISED IN LIVER BY CYP3A4.T1/2=12HRS. S/E=AGRANULOCYTOSIS, SEDATION,WGHT GAIN, URINARY INCONTINENCE,SEIZURES.USED IN SCHIZO RESPERIDONE=PROLACTIN LEVEL INCREASE, EXTRAPYRAMIDAL EFFECTS PRESENT OTHER DRUGS=OLANZAPINE t1/2=24hrs,QUITIAPINE t1/2=6hrs,ARIPIPRAZOLE t1/2=3days
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