Dr. AMREEN SABA ATTARIYA
POST GRADUATE STUDENT
DEPT OF PHARMACOLOGY
M.R. MEDICAL COLLEGE, GULBARGA
INDIA
SEROTONIN
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
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
Physiologic Distribution of 5HT
10% CNS
90% GI tract
90% ECs
10% Neurons 5-Hydroxytryptamine
Mar 6, 2017Dr.ASA:serotonin
SOURCE
Venom of Wasps, Bees, scorpions
Widely distributed in invertebrates
Fruits--banana, pear, pineapple, tomato, plums, nuts
Mar 6, 2017Dr.ASA:serotonin
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
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
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.
5HT REC SUBTYPES
Earlier[GADDUM &PICARELLI]
Mtype= MUSCULOTROPIC
Dtype=NEUROTROPIC
M type@ cholinergic nerve
endingscontrol 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
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
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
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 histaminereinforce the hemostatic response to 5-HT
Mar 6, 2017Dr.ASA:serotonin
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
PHYSIOLOGICAL ROLE
GIT
5HT-local hormone in GITinitiation & 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
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 SERTincrease in mucosal 5-HT
availability.
IBS-D -- increased 5-HT postprandially
Mar 6, 2017Dr.ASA:serotonin
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.
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
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
TRIPTANS-MOA
MOA: 2 hypothesis of migraine pathophysiology
I: unknown events lead to abnormal dilation of carotid AV
anastomoses in headdiverting blood from capillary bedscerebral
ischemia & hypoxia.
Rx: Triptans constrict IC blood vessels, including AV anastomoses
& restores blood flow to brain
II: 5-HT1D & 5-HT1Bserve as presynaptic autoreceptorsmodulate
neurotransmitter release from neuronal terminals
5-HT1 agonists block the release
of proinflammatory neuropeptides
Mar 6, 2017Dr.ASA:serotonin
TRIPTANS-AE
Cardiac events--coronary artery vasospasm, transient
MI,atrial & ventricular arrhythmias, MI
SC Sumatriptanirritation at the site of injection
(transient mild pain, stinging, or burning sensations).
Nasal spray Sumatriptan bitter taste.
Oralparesthesias, asthenia,fatigue,flushing, feelings of
pressure, tightness, or pain in chest,neck, & jaw;
drowsiness, dizziness, nausea, sweating.
Mar 6, 2017Dr.ASA:serotonin
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
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
ERGOT & ERGOT ALKALOIDS
Partial agonists/antagonists at adrenergic, dopaminergic & 5HT rec
Effects depends onagent, 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
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
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
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
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
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 chronicallyRx should be interrupted for 3 weeks or
more every 6 months.
Mar 6, 2017Dr.ASA:serotonin
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
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
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
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
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.
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.
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.
Sternbach’s criteria for serotonin
syndrome*
Mar 6, 2017Dr.ASA:serotonin
* Sternbach, 1991;Brown et al., 1996
Agents that have potential to induce serotonin
toxicity &
their MOA for increasing serotonin levels
Mar 6, 2017Dr.ASA:serotonin
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
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
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
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
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.
4 FAMILIES WITH 14 RECEPTOR SUBTYPES
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-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.
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
IN ADDITION TO UPTAKE BLOCKADE THEY HAVE SHOW MUSCURANIC, ADRENERGIC, HISTAMINIC EFFECTS
EITHER BY REPLACING THEM FOR PPB SITE OR REDUCING THEIR METABOLISM
HPERTENSION CRISIS WIT EXCITATION AND HALLUCINATION
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
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.
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.
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
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