Epileptogenesis and drugs with mechaism
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Transcript of Epileptogenesis and drugs with mechaism
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EPILEPTOGENESIS AND DRUGS
Dr AKHIL AGRAWALMD Pharmacology(PG Resident)
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BRIEF OUTLINE-1.DEFINITION2.HISTORY3.INDIVIDUAL EPILEPTOGENIC MECHANISM4.CAUSES OF EPILEPSY5. DRUG INDUCED EPILEPSY6.APPLICATIONS
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An seizure is a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.
A person is considered to have epilepsy if they meet any of the following conditions:(As per ILAE)
1. At least two unprovoked (or reflex) seizures occurring greater than 24 hours apart.
2. One unprovoked (or reflex) seizure and a probability of further seizures similar to the general recurrence risk (at least 60%) after two unprovoked seizures, occurring over the next 10 years.
DEFINITIONS
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Babylonians-presence of demons
Greeks and romans-curse of gods
Hippocrates offered epilepsy as a disease
Electrical hypothesis was discovered by hans berger when he invented the EEG
John Jackson (father of epilepsy)-“occasional sudden,excessive,rapid and local discharge of gray matter”
HISTORY
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The process of the brain acquiring an initial insult and secondarily undergoing a series of epileptic events until the first observable seizure occurs.Sloviter & Bumanglag (2012) have proposed a secondary term “epileptic maturation” to describe the all encompassing processes that happen after epileptogenesis and that influence the secondary changes in the clinical phenotype.
EPILEPTOGENESIS
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GABA GLUTAMATE CHOLINERGIC DOPAMINERGIC SEROTONERGIC NOR-ADRENERGIC
MAJOR PATHWAYS
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It consists of mainly 2 receptors: GABA A
GABA B
GABA PATHWAY
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Location of GABA A receptors-• Synaptic receptors -gamma
subunits(mostly post synaptic)• perisynaptic /extra synaptic -
deltas sub units responsible for phasic and tonic inhibition.
During status epileptics, there is increased neuronal hyper excitability and inhibitory GABAergic synaptic transmission becomes compromised
• Miniature inhibitory post-synaptic currents (mIPSCs) are reduced
• Number of active GABAA receptors per dentate granule cell is also decreased.
GABA A PATHWAY
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Short term(during SE)• In vitro-large
decrease in GABA-gated chloride currents.
• In vivo-rapid reduction in the number of physiologically
active GABA receptors.
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Changes in latency period-1.Minutes to hours – Activation of plasma
membrane receptors result in changes in the intracellular signal transduction pathways involved in the maintenance of vital cellular functions.
2. Hours to days- Long term changes in gene
expression result from the combined effects of repeated seizures, seizure-induced cell death, and subsequent neuronal reorganization
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2 types of receptors: GABA B 1 GABA B2
Types: Slow - downstream
Ca2+/K+ channels upon binding with its endogenous ligand, GABA.
Long term- Ligand activation of GABAB receptors initiates G protein–dependent cell signaling pathways.
GABA B PATHWAY
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Presynaptic receptors prevent neurotransmitter release
• Down-regulating the activity of voltage-sensitive Ca 2+-channels
• Direct inhibition of the release machinery.
Auto receptors inhibit the release of GABA, whereas hetero receptors inhibit the release of glutamate and several other neurotransmitters.
Postsynaptic receptors induce sIPSCs by activating Kir3-type K+-channels, which hyperpolarizes the membrane, favors voltage-sensitive block of NMDA receptors and shunts excitatory currents
Dendritic receptors inhibit back propagating action potentials through activation of K+-channels.
GABA B PATHWAY
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Two types of receptors:1.Ionotropic NMDA AMPA Kainate2.Metabotropic(8) Group1 Group2 Group3
GLUTAMATE PATHWAY
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1.NMDA- An increase in glutamate excitatory transmission in the
hippocampus. Increase in the pool of ready-release glutamate at the mossy fiber-
pyramidal cell synapse in the CA3 as well as in DG. Number of NMDA receptors present in neuronal cell membranes
appears to increase.2.AMPA:• Ca2+ influx into neurons causing excitotoxicity and cell death.• Synaptic changes due to alterations in second messenger signaling
Mechanism of action
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3.KAINATE: Causes slow EPSP’s to promote epileptogenesis.4. METABOTROPIC RECEPTORS: Group I- epileptogenic in nature when bound by glutamate. Group II- promote antiepileptogenic effects when bound by
glutamate5.Several morphological changes in the hippocampus occur during epileptogenesis associated with glutamate dysregulation: Hippocampal sclerosis, shrinkage, and reactive gliosis Neuronal loss in hilar mossy cells, interneurons, and pyramidal
neurons of the CA3 and CA1 are also observed in the granule cell layer
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Receptor Mechanism of action
NMDA Glutamate and Glycine mediated
AMPA Influx of Na+,Ca+ and efflux of K+
KAINATE Slow EPSP’s
Group I(1,5) Phospholipase C (PLPC), protein kinase C (PKC)
Group II(2,3) Inhibits c-amp formation, directly activates K+ channels and inhibits voltage sensitiveCa2+ channels
Group III(4,6,7,8) Inhibits neuro-transmitter release
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Promote epileptogenesis such as a decrease in GABAergic interneurons (which could cause an in increase in glutamate neurotransmission)
A decrease in membrane expressed GABAB receptors (which could also cause an increase in glutamate neurotransmission)
NMDA PATHWAY AFFECT BY GABA
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Ach causes increased seizure activity by acting on following brain parts:
Piriform cortex>amydala>hippocampus> thalamus >cortical areas &striatum
Specific areas:Piriform cortex-(substantia nigra & area tempestas)
CHOLINERGIC PATHWAY
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MECHANISM- Cytotoxic activity seen in hippocampus and
cortical neurons Disruption of polymerization of microtubules Altered sensitivity to glutamate
excitotoxicity Decrease in expression of synaptic proteins. Area tempestas-hyperactivity in
hippocampus Direct cholinergic input/indirect to ento-
rhinal cortex.
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DOPAMINERGIC PATHWAYDopamine receptors
Location in brain
D1 CP, nucleus accumbens , substantia nigra
D2 CP, nac, SN pars compacta
D3 Limbic systemD4 Frontal cortex,
amygdala, SN, hippocampus
D5 Entorhinal cortex, SNR, and hippocampus (dentate gyrus)
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DOPAMINERGIC PATHWAYReceptor Action
D1 type(D1,D5)(PRO-CONVULSANT)
increases cAMP levels and protein kinase A (PKA) activity via the stimulation of adenylyl cyclase (AC)
D2 type(ANTI-CONVULSANT)(D2,D3,D4)
inhibit AC activity,antogonises D1 action(c-amp dependent)
Activation of glycogen synthase kinase 3β(c-amp independent)
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Serotonin has a protective mechanism against epilepsy.
Main mechanism: Hyperpolarization of
glutamatergic neurons by 5-HT1A receptors(K+ conductance)
Depolarization of GABAergic neurons by 5-HT2C receptors.
SEROTONERGIC PATHWAY
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5HT1 receptors
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5 HT 2C Receptors
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Considered to have protective role in epilepsy.
Highest affinity for a2
adrenergic receptors. Established role in the
control of limbic seizures by increasing noradrenaline levels in structures that are critically involved in the generation of limbic seizures, such as the hippocampus.
NOR-ADRENERGIC PATHWAY
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VASCULAR METABOLIC INFECTION DRUGS AND COMPOUNDS AUTOIMMUNE SYSTEMIC DISEASES GENETIC
PATHOPHYSIOLOGIC MECHANISMS PRODUCING SEIZURES
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Cerebro-vascular accident(stroke) Congenital vascular
malformation(cavernous)
VASCULAR CAUSES
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METABOLIC CAUSESToxin Mechanism
Increased excitationPyrethrumOrganophosphateAmanita
Na channelCholinergic excitationGlutaminergic stimulation
Decreased inhibitionStrychnineBicuculine
GABA antagonismGlutamate antagonism
Cyanide Interference with energy metabolism
Lead Unknown cause
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Metabolic conditions associated with seizures:
1.Alkalosis 2. Hyponatremia3. Hypoglycemia 4. Hypocalcemia/hypercalcemia5. Hypoxemia 6. Hepatic/Renal failure 7. Hyper osmolality (hypernatremia, nonketotic hyperosmolar diabetes mellictus) Inborn errors of metabolism:• Errors in carbohydrate
metabolism(galactosemia)• Urea cycle enzyme deficiency
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Virus(HSV.measles,rubella) Bacteria(H. influenzae, N. meningitidis) Fungal( C. neoformans, C. immitis, H.
capsulatum, C. albicans) Protozoal (Plasmodium ,Toxoplasma ) Helminthic (taenia solium, Echinoccocus
granulosis)
INFECTIVE CAUSES
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Various Diseases:1. SLE2. Sjögren’s
Syndrome3. Wegener’s
Granulomatosis4. Sarcoidosis5. Celiac Disease
Mechanism: Vascular disease • Platelet-fibrin thrombi
(e.g., TTP)• Prothrombotic state• Anticardiolipin antibody• Emboli Vasculitis Antineuronal antibodies Immune complexes Cytokines
AUTO-IMMUNE CAUSE
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Various mechanism seen are: A particular body system has been
sufficiently impaired to produce a lowering of the seizure threshold and the induction of “reactive seizures.
A state of cortical neuronal instability, such as a (stroke with infarction, hemorrhage, embolus)
Encephalopathy
SYSTEMIC CAUSE
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GENETIC CAUSE
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Study of inheritance of heritable changes in gene expression that occur with no modifications to the DNA sequence.
Different types: DNA methylation histone modification action of non-coding RNA
EPIGENETICS AND EPILEPSY
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DNA methylation
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Histone modification
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Action of non-coding RNA
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Various mechanism of action are: Cerebral receptors Electrolytic disturbance Brain edema(vasogenic& cytotoxic) Metabolic effects Posterior reversible leukoencephalopathy
syndrome
DRUG INDUCED EPILEPSY
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Drug MechanismAnti-infective Peniciilin and related drugs Inhibits GABA binding to GABAA receptor(allosteric
modulation)Blocks GABAA chloride channel
Fluoroquinolones Inhibit GABA binding to GABAA receptorIsoniazid Inhibits pyridoxine kinase, resulting in decreased
GABA synthesis(formation of IPH)
Bromocriptine,pergolide Blocks dopaminergic transmissionMetronidazole Leads to accumulation of hydroxy- and 1-acetic
acid metaboliteTCA Inhibition of serotonin uptake in the cleftPhenothiazine Dopamine blocking propertyMOA –A inhibitor Produces serotergic activation(alpha-motor
neuron excitability)Selective serotonin reuptakeInhibitor
Decreases GABA transmission in the hippocampus
Phenothiazines Antagonizes postsynaptic, mesolimbic dopamine receptors in the brain
CEREBRAL RECEPTORS
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Local anesthetics Antagonizes Na1 channelsMeperidine Leads to accumulation of normeperidine
metaboliteTramadol Inhibits monoamine uptakeTheophylline Antagonizes anticonvulsant effects of brain
adenosineCalcineurin Down regulates GABAA receptor activationBrain-stem stimulantsPentetrazolPicro-toxin
GABA excitation and inhibits GABA inhibition respectively
Spinal stimulantsstrychnine
Blocks inhibitory action of glycine at post synaptic receptor
General anesthesiaEnfluraneetomidate
Increased excitability in limbic systemDisinhibit ion of sub-cortical activity
Local anaesthesia+epinephrine Ischemia in spinal cord(transient epilepsy)Radio contrast dye(gadolinium) Direct action on cerebral cortex
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Electrolyte disturbance Drugs
Hypo-natremia Vincristine,vinblastine,cyclophosphamide
hypokalemia Theophylline
ELECTROLYTE DISTURBANCES
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Drugs Mechanism
Metronidazole Vasogenic edema
IVIg
An intramyelinic edema in the myelin sheathCytotoxic edema
VASOGENIC AND CYTOTOXIC EDEMA
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Drug Mechanism
Salicyclate High anion gap metabolic acidosis
Malnutrition Inhibits glucoronidation(valproate)
METABOLIC EFFECTS
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The PRES has been described after the intake of immunosuppressants such as tacrolimus, Cyclosporine.
It is characterized by capillary-leak syndrome in the brain caused by changes affecting the vascular endothelium.
Clinical symptoms are headache, vomiting, confusion, seizures, cortical blindness and other visual symptoms.
Posterior reversible leukoencephalopathy syndrome
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Drug EffectVariant methionine synthetase, modified effect of methotrexateOn homocysteine metabolism
Methotrexate encephalopathy
Human thymidylate synthetase gene
5- fluorouracil-associated hyperammonemic encephalopathy
DRUGS PROMOTING GENETIC SUSCEPTIBILITY
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Benzodiazepine- in association with LENNOX GASTAUT Syndrome or WEST Syndrome
Valproate/carbamazepine induced encephalopathy(accumulation of CBZ epoxide) esp. in children
Vigabatrin-increased GABA in brain
Anti-epileptic drug induced seizure
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NOVEL TARGETS FOR EPILEPTOGENESIS
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Use in animal experimental model PENICILLIN MODEL PENTYLENTETRAZOL MODEL BICUCULLINE MODEL KAINIC ACID MODEL
Application of epileptogenic drug
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1.Marco I. Gonzáleza, Amy Brooks-Kayala; Altered GABAA receptor expression during epileptogenesis; Neuroscience Letters 497 (2011) 218–2222. Amy R. Brooks-Kayal, M.D.; Regulation of GABAA Receptor Gene Expression and Epilepsy; Jasper's Basic Mechanisms of the Epilepsies3. Mauro DiNuzzoa, Silvia Mangiab; REVIEW Physiological bases of the K+and the glutamate/GABA hypotheses of epilepsy; Epilepsy Research ;1st April(2014)4. Seth R. Batten; GLUTAMATE DYSREGULATION AND HIPPOCAMPAL DYSFUNCTION IN EPILEPTOGENESIS; University of Kentucky, Theses and Dissertations--Medical Sciences Medical Sciences,2013.5. YuriBozzi, EmilianaBorrelli; The role of dopamine signaling in epileptogenesis; Frontiers in Cellular Neuroscience; September 2013 | Volume7 | Article 1576. Carl J. Vaughan, MD, MRCPI and Norman Delanty, MB, FRCPI; Pathophysiology of Acute Symptomatic Seizures; Seizures: Medical Causes and Management; 7. Niels Hansen; Drug-Induced Encephalopathy; Miscellanea on Encephalopathies – A Second Look; 25, April, 20128. L. Pulido Fontesa, P. Quesada Jimeneza, M. Mendioroz Iriarte ; Epigenetics and epilepsy; NEUROLOGÍA; 2015;30(2):111—1189. Rocio Sanchez-Carpintero;Genetic causes of epilepsy; THE NEUROLOGIST; DECEMBER 200710. PRATIBHA SINGHI; Infectious causes of seizures and epilepsy in the developing world; Developmental Medicine & Child Neurology 2011, 53: 600–60911.Dennis o brien; Toxic and Metabolic Causes of Seizures; Clinical Techniques m Small Animal Practice, Vol 13, No 3 (August), 1998: pp 159-16612. Todd H Ahern, Martin A Javors, Douglas A Eagles, Jared Martillotti, Heather A Mitchell, Larry Cameron Liles and David Weinshenker; The Effects of Chronic Norepinephrine Transporter Inactivation on Seizure Susceptibility in Mice; Neuropsychopharmacology (2006) 31, 730–73813. Gyorgy Bagdy, Valeria Kecskemeti; Serotonin and epilepsy; Journal of Neurochemistry, 2007, 100, 857–87314. LEONARDO COCITO, M.D., EMILIO FAVALE, M.D.; Epileptic Seizures in Cerebral Arterial Occlusive Disease; Stroke, Vol 13, No 2, 198215. ROBRECHT RAEDT;VNS, noradrenaline and seizure suppression |; Journal of Neurochemistry, 2011; International Society for Neurochemistry, J. Neurochem. (2011) 117, 461–469
References
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HOPE THIS HAS NOT HAPPENED!!!!
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