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Serotonin
5-Hydroxytryptamine (5-HT)


        By: Dr. Vahid Nikoui

    Email: nikoui@razi.tums.ac.ir
(Rate limiting)   OH
            COOH                                                     COOH
                                   Tryptophan
            C       NH2            hydroxylase                       C     NH2

      N                                                      N
                In diet. Active
  Tryptophan    CNS transport                        5-Hydroxytryptophan

                                                                 5-OH Tryptophan
                                                                   decarboxylase
            C       COOH
                                                    OH                H
      N

                                                                       C    NH2

5-Hydroxy Indole                                              N
   Acetic Acid                    5-OH Indole
                                  Acetaldehyde           5-Hydroxytryptamine
Distribution (PNS)
   Majority released from gut
       Responsible for smooth muscle contractions
       Release stimulated by food intake
       Inhibits release of gastric acid
       Softens stool

   Cardiovascular system –
    vasoconstrictor/vasodilator of vessels

   Bronchioconstriction

   Uterine contractions
Serotonin roles

   Peripheral
        Peristalsis
        Vomiting
        Platelet aggregation and haemostasis
        Inflammatory mediator
        Sensitisation of nociceptors
        Microvascular control

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Serotonin roles
   Central
        Control of appetite
        Sleep
        Mood
        Hallucinations
        Stereotyped behaviour
        Pain perception
        Vomiting
Hunter Area Toxicology
Service
5-HT Receptors

Receptor 5-HT 1     5-HT 2    5-HT 3    5-HT 4   5-HT 5   5-HT 6   5-HT 7

          5-HT1A    5-HT 2A   5-HT 3A            5–HT5A
          5-HT 1B   5-HT 2B   5-HT 3B            5–HT5B
Subtype   5-HT 1D
                    5-HT 2C
          5-HT 1E

          5-HT 1F



  Major
                                ion
signaling cAMP↓      IP3               cAMP    cAMP ↓ cAMP      cAMP 
                              channel
pathway
Serotonin receptors

   5–HT1
        7 trans–membrane domains
        G protein linked
        cAMP dependant
        Anxiolytic and antidepressant
        Subtypes
              5–HT1A, 5–HT1B, 5–HT1D, 5–HT1E, 5–HT1F


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5-HT1A Receptor




              CNSforum.com
5-HT1A Partial Agonist Mechanism
5-HT1A Antagonist mechanism
5–HT1
   5–HT1A
        Limbic system
              Regulation of emotions
        Neocortex
        Hypothalamus
        Substantia gelatinosa
              Proprioception


   5–HT1B
Hunter Area Toxicology
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5–HT1

   5–HT1D
        Autoreceptors
              Inhibitory feedback
        Heteroreceptors
              Modulate release
                   Acetylcholine
                   Glutamate
        Anti–migraine effect of Sumatriptan

Hunter Area Toxicology
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Serotonin in Migraine

    Neurogenic vs. Vascular theories


1.   Cyproheptadine, Methysergide – prophylaxis

2.   Sumatriptan, Ergotamine – acute attacks

3.   MAO inhibitors and TCAs – both
5–HT1
   5–HT1E
        ? functional role


   5–HT1F
        ? functional role
        Distribution includes CNS, uterus, mesentery
        Inhibit cAMP
        High affinity for
              Sumatriptan, Methysergide

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Serotonin receptors

   5–HT2
        7 trans–membrane domains
        G protein linked
        Phospholipase C dependant
        Subtypes
              5–HT2A, 5–HT2B, 5–HT2C



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5-HT2 Receptor Mechanism
5-HT2 Antagonist Mechanism
5–HT2
   5–HT2A
        Periphery
            Contraction of vascular/non–vascular smooth
             muscle
            Platelet aggregation

            Increased capillary permeability

            Modulation of the release of other
             neurotransmitters and hormones
                   ACh, Adrenaline, Dopamine, Excitatory amino acids,
                    Vasopressin


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5–HT2

   5–HT2A
        CNS
            Motor behaviour
            Head twitch

            Sleep regulation

            Nociception

            Neuroexcitation




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5–HT2
     5–HT2B
           Stomach fundus


     5–HT2C
           CSF production
           Locomotion
           Eating disorders
           Anxiety
           Migraine

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Serotonin receptors
         5–HT3
              Ligand gated cation channels


         5-HT4
              Coupled to adenylyl cyclase


         5-HT5
              Coupled to adenylyl cyclase
              Subtypes
                    5–HT5A, 5–HT5B
Hunter Area Toxicology
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5–HT3
   Peripheral
        Located exclusively on neurons and mediate
         neurotransmitter release - parasympathetic,
         sympathetic, sensory and enteric
                   Cardiac inhibition/activation, pain, initiation of the
                    vomiting reflex

   Central
        Facilitate dopamine and 5–HT release, inhibit
         ACh and noradrenaline release
                   Anxiety, depression, memory, tolerance and dependence


Hunter Area Toxicology
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Serotonin receptors

   5-HT6
        Coupled to adenylyl cyclase
        Significance unknown


   5-HT7
        Coupled to adenylyl cyclase
        Significance unknown

Hunter Area Toxicology
Service
Serotinergic Drugs
   5-HT1A : Buspirone, Ipsapirone, Tandospirone
    Treat anxiety, depression (partial agonist)

   5-HT 1D/1B : Sumatriptan, Naratriptan, Zolmitriptan
    Treat migraine (partial agonist)

   5-HT 2A/2C : Methysergide, Trazodone,
    Risperidone, Ketanserin, Ritanserin, Mianserin
    Treat migraine, depression, schizophrenia
    (antagonist)
Serotinergic Drugs

   5-HT 3 : Ondansetron, Granisetron,
    Tropisetron, Memantine, Mirtazapine
    Treat chemotherapy-induced emesis
    (antagonist)

   5-HT 4 : Cisapride, Metoclopramide,
    Mosapride, Dazopride, Tegaserod
    Treat GI disorders (agonist)
Serotinergic drugs

   Serotonin precursors
        S–adenyl–L–methionine
        L–tryptophan
        5–hydroxytryptophan
        Dopamine




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Serotinergic drugs

   Serotonin re–uptake inhibitors
        Citalopram, Fluoxetine, Fluvoxamine,
         Paroxetine, Sertraline, Venlafaxine
        Clomipramine, Imipramine
        Nefazodone, Trazodone
        Chlorpheniramine
        Cocaine, Dextromethorphan, Pentazocine,
         Pethidine
Hunter Area Toxicology
Service
Serotinergic drugs

   Serotonin agonists
        Fenfluramine, P–chloramphetamine
        Bromocriptine, Dihydroergotamine, Gepirone
        Eltoprazin, Quipazine




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Serotinergic drugs

   Irreversible Monoamine oxidase inhibitors
    (MAOIs)
        Clorgyline, Isocarboxazid, Nialamide,
         Pargyline, Phenelzine, Tranylcypromine
        Selegiline
        Furazolidone
        Procarbazine

Hunter Area Toxicology
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Serotinergic drugs

   Reversible inhibitors of MAO (RIMAs)
        Brofaramine
        Befloxatone, Toloxatone
        Moclobemide




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Serotinergic drugs

   Miscellaneous/mixed
        Lithium
        Lysergic acid diethylamide (LSD)
        3,4–methylenedioxymethamphetamine
         (MDMA, ecstasy),
         methylenedioxyethamphetamine (eve)
        Propranolol, Pindolol


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Serotonin Syndrome
   Toxic, potentially fatal effects

   Require a combination of serotonergic agents,
    such as an SSRI with an MAOI.

   Other agents is including TCAs,
    Dextromethorphan, Meperidine and MDMA.
Sternbach criteria
                            Mental status changes (confusion, hypomania)
                            Agitation
                            Myoclonus
                            Hyperreflexia
                            Diaphoresis
                            Shivering
                            Tremor
                            Diarrhoea
                            Incoordination
                Diarrhoea
                            Fever
Hunter Area Toxicology Service
Treatment
   Suspected agents should be discontinued.
   OTC drugs containing ingredients known to
    increase serotonin levels, such as
    Dextromethorphan, Pseudoephedrine or
    Phenylpropanolamine, also should be
    discontinued.

   Benzodiazepines for mild to moderate cases

   Cyproheptadine, Methysergide, and Propranolol
    for severe cases
Drugs used to treat serotonin
             syndrome
   Non–specific blocking agents
        Methysergide
        Cyproheptadine


   –blockers
        Propranolol
        Pindolol

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Drugs used to treat serotonin
                 syndrome
         Benzodiazepines
              Lorazepam
              Diazepam
              Clonazepam


         Neuroleptics
              Chlorprothixene
              Chlorpromazine
              Haloperidol
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Drugs used to treat serotonin
               syndrome
    Miscellaneous
          Chlormethiazole
          Nitroglycerine


    Drugs used for neuroleptic malignant
     syndrome
          Dantrolene
          Bromocriptine
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Antagonist potencies
   Ki values (5–HT2)
        Chlorprothixene (0.43 nM) > Chlorpromazine
         > Cyproheptadine > Haloperidol (36 nM)
        limited experience suggests haloperidol
         ineffective


   Ki values (5–HT1)
        Chlorprothixene (230 nM) > Haloperidol >
         Chlorpromazine > Cyproheptadine (3200 nM)

Hunter Area Toxicology
Service
Receptor Overview
5-HT2 Subtypes
Thanks for Your Attention

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Serotonin

  • 1. Serotonin 5-Hydroxytryptamine (5-HT) By: Dr. Vahid Nikoui Email: nikoui@razi.tums.ac.ir
  • 2. (Rate limiting) OH COOH COOH Tryptophan C NH2 hydroxylase C NH2 N N In diet. Active Tryptophan CNS transport 5-Hydroxytryptophan 5-OH Tryptophan decarboxylase C COOH OH H N C NH2 5-Hydroxy Indole N Acetic Acid 5-OH Indole Acetaldehyde 5-Hydroxytryptamine
  • 3. Distribution (PNS)  Majority released from gut  Responsible for smooth muscle contractions  Release stimulated by food intake  Inhibits release of gastric acid  Softens stool  Cardiovascular system – vasoconstrictor/vasodilator of vessels  Bronchioconstriction  Uterine contractions
  • 4. Serotonin roles  Peripheral  Peristalsis  Vomiting  Platelet aggregation and haemostasis  Inflammatory mediator  Sensitisation of nociceptors  Microvascular control Hunter Area Toxicology Service
  • 5. Serotonin roles  Central  Control of appetite  Sleep  Mood  Hallucinations  Stereotyped behaviour  Pain perception  Vomiting Hunter Area Toxicology Service
  • 6. 5-HT Receptors Receptor 5-HT 1 5-HT 2 5-HT 3 5-HT 4 5-HT 5 5-HT 6 5-HT 7 5-HT1A 5-HT 2A 5-HT 3A 5–HT5A 5-HT 1B 5-HT 2B 5-HT 3B 5–HT5B Subtype 5-HT 1D 5-HT 2C 5-HT 1E 5-HT 1F Major ion signaling cAMP↓ IP3 cAMP cAMP ↓ cAMP cAMP  channel pathway
  • 7. Serotonin receptors  5–HT1  7 trans–membrane domains  G protein linked  cAMP dependant  Anxiolytic and antidepressant  Subtypes  5–HT1A, 5–HT1B, 5–HT1D, 5–HT1E, 5–HT1F Hunter Area Toxicology Service
  • 8. 5-HT1A Receptor CNSforum.com
  • 11. 5–HT1  5–HT1A  Limbic system  Regulation of emotions  Neocortex  Hypothalamus  Substantia gelatinosa  Proprioception  5–HT1B Hunter Area Toxicology Service
  • 12. 5–HT1  5–HT1D  Autoreceptors  Inhibitory feedback  Heteroreceptors  Modulate release  Acetylcholine  Glutamate  Anti–migraine effect of Sumatriptan Hunter Area Toxicology Service
  • 13. Serotonin in Migraine  Neurogenic vs. Vascular theories 1. Cyproheptadine, Methysergide – prophylaxis 2. Sumatriptan, Ergotamine – acute attacks 3. MAO inhibitors and TCAs – both
  • 14. 5–HT1  5–HT1E  ? functional role  5–HT1F  ? functional role  Distribution includes CNS, uterus, mesentery  Inhibit cAMP  High affinity for  Sumatriptan, Methysergide Hunter Area Toxicology Service
  • 15. Serotonin receptors  5–HT2  7 trans–membrane domains  G protein linked  Phospholipase C dependant  Subtypes  5–HT2A, 5–HT2B, 5–HT2C Hunter Area Toxicology Service
  • 18. 5–HT2  5–HT2A  Periphery  Contraction of vascular/non–vascular smooth muscle  Platelet aggregation  Increased capillary permeability  Modulation of the release of other neurotransmitters and hormones  ACh, Adrenaline, Dopamine, Excitatory amino acids, Vasopressin Hunter Area Toxicology Service
  • 19. 5–HT2  5–HT2A  CNS  Motor behaviour  Head twitch  Sleep regulation  Nociception  Neuroexcitation Hunter Area Toxicology Service
  • 20. 5–HT2  5–HT2B  Stomach fundus  5–HT2C  CSF production  Locomotion  Eating disorders  Anxiety  Migraine Hunter Area Toxicology Service
  • 21. Serotonin receptors  5–HT3  Ligand gated cation channels  5-HT4  Coupled to adenylyl cyclase  5-HT5  Coupled to adenylyl cyclase  Subtypes  5–HT5A, 5–HT5B Hunter Area Toxicology Service
  • 22. 5–HT3  Peripheral  Located exclusively on neurons and mediate neurotransmitter release - parasympathetic, sympathetic, sensory and enteric  Cardiac inhibition/activation, pain, initiation of the vomiting reflex  Central  Facilitate dopamine and 5–HT release, inhibit ACh and noradrenaline release  Anxiety, depression, memory, tolerance and dependence Hunter Area Toxicology Service
  • 23. Serotonin receptors  5-HT6  Coupled to adenylyl cyclase  Significance unknown  5-HT7  Coupled to adenylyl cyclase  Significance unknown Hunter Area Toxicology Service
  • 24. Serotinergic Drugs  5-HT1A : Buspirone, Ipsapirone, Tandospirone Treat anxiety, depression (partial agonist)  5-HT 1D/1B : Sumatriptan, Naratriptan, Zolmitriptan Treat migraine (partial agonist)  5-HT 2A/2C : Methysergide, Trazodone, Risperidone, Ketanserin, Ritanserin, Mianserin Treat migraine, depression, schizophrenia (antagonist)
  • 25. Serotinergic Drugs  5-HT 3 : Ondansetron, Granisetron, Tropisetron, Memantine, Mirtazapine Treat chemotherapy-induced emesis (antagonist)  5-HT 4 : Cisapride, Metoclopramide, Mosapride, Dazopride, Tegaserod Treat GI disorders (agonist)
  • 26. Serotinergic drugs  Serotonin precursors  S–adenyl–L–methionine  L–tryptophan  5–hydroxytryptophan  Dopamine Hunter Area Toxicology Service
  • 27. Serotinergic drugs  Serotonin re–uptake inhibitors  Citalopram, Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Venlafaxine  Clomipramine, Imipramine  Nefazodone, Trazodone  Chlorpheniramine  Cocaine, Dextromethorphan, Pentazocine, Pethidine Hunter Area Toxicology Service
  • 28. Serotinergic drugs  Serotonin agonists  Fenfluramine, P–chloramphetamine  Bromocriptine, Dihydroergotamine, Gepirone  Eltoprazin, Quipazine Hunter Area Toxicology Service
  • 29. Serotinergic drugs  Irreversible Monoamine oxidase inhibitors (MAOIs)  Clorgyline, Isocarboxazid, Nialamide, Pargyline, Phenelzine, Tranylcypromine  Selegiline  Furazolidone  Procarbazine Hunter Area Toxicology Service
  • 30. Serotinergic drugs  Reversible inhibitors of MAO (RIMAs)  Brofaramine  Befloxatone, Toloxatone  Moclobemide Hunter Area Toxicology Service
  • 31. Serotinergic drugs  Miscellaneous/mixed  Lithium  Lysergic acid diethylamide (LSD)  3,4–methylenedioxymethamphetamine (MDMA, ecstasy), methylenedioxyethamphetamine (eve)  Propranolol, Pindolol Hunter Area Toxicology Service
  • 32. Serotonin Syndrome  Toxic, potentially fatal effects  Require a combination of serotonergic agents, such as an SSRI with an MAOI.  Other agents is including TCAs, Dextromethorphan, Meperidine and MDMA.
  • 33. Sternbach criteria Mental status changes (confusion, hypomania) Agitation Myoclonus Hyperreflexia Diaphoresis Shivering Tremor Diarrhoea Incoordination Diarrhoea Fever Hunter Area Toxicology Service
  • 34. Treatment  Suspected agents should be discontinued.  OTC drugs containing ingredients known to increase serotonin levels, such as Dextromethorphan, Pseudoephedrine or Phenylpropanolamine, also should be discontinued.  Benzodiazepines for mild to moderate cases  Cyproheptadine, Methysergide, and Propranolol for severe cases
  • 35. Drugs used to treat serotonin syndrome  Non–specific blocking agents  Methysergide  Cyproheptadine  –blockers  Propranolol  Pindolol Hunter Area Toxicology Service
  • 36. Drugs used to treat serotonin syndrome  Benzodiazepines  Lorazepam  Diazepam  Clonazepam  Neuroleptics  Chlorprothixene  Chlorpromazine  Haloperidol Hunter Area Toxicology Service
  • 37. Drugs used to treat serotonin syndrome  Miscellaneous  Chlormethiazole  Nitroglycerine  Drugs used for neuroleptic malignant syndrome  Dantrolene  Bromocriptine Hunter Area Toxicology Service
  • 38. Antagonist potencies  Ki values (5–HT2)  Chlorprothixene (0.43 nM) > Chlorpromazine > Cyproheptadine > Haloperidol (36 nM)  limited experience suggests haloperidol ineffective  Ki values (5–HT1)  Chlorprothixene (230 nM) > Haloperidol > Chlorpromazine > Cyproheptadine (3200 nM) Hunter Area Toxicology Service
  • 41. Thanks for Your Attention