A pain physician’s tour of mitochondrial diseases.
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Transcript of A pain physician’s tour of mitochondrial diseases.
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A pain physician’s tour of mitochondrial diseases
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OutlineWhy Mitochondria?Who are the Mitochondria?
BiochemistryGenetics
Clinical syndromesManagement StrategiesConclusion
Mitochondria in Pain?
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Why Mitochondria?Mitochondria involved in basic pain mechanisms
NociceptionCentralisation Analgesic tolerance
Mitochondrial dysfunction underlies some clinically unexplained syndromesFibromyalgia, Chronic Fatigue Syndrome
Mitochondrial dysfunction in common disordersNerve and Muscle disease eg Diabetic NeuropathyDepressionNeurodegenerative Disorders
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Who are the Mitochondria ?Mitochondria are the power supply for all
cellsMitochondrial disease can impact on many
systemsBrain, Nerve and Muscle most energy
dependentMitochondrial and Nuclear genetic control
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The humble mitochondrionOriginally a symbiotic bacteriaEach mitochondria has multiple copies of its
own DNACo dependence on nuclear derived genes and
proteinsKey function is oxidative phosphorlyation:
Utilise O2 to produce ATP from ADPRespiratory Chain: 5 complexes working
sequentially
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Mitochondrial BiochemistryComplexes I to IV essentially strip electrons from
hydrogen atoms (NADH/H2O), pumping protons into the INTERMEMBRANE SPACE
This creates a large pH gradient, passage of protons through complex V is coupled to generation of ATP
Process relies on ELECTRON TRANSFER CHAIN including various co-enzymes (Co Q10)
Generates reactive oxygen species which are mopped up by other pathways (ubiquinone, lysosomes)
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Mitochondrial Genetics16,569 base pairs, closed loop of DNAMultiple copies in the matrixDNA encodes for 13 of 90 respiratory chain
proteinsthe rest are coded from nuclear DNA
Almost no noncoding areas, no introns – unstableMitochondrial DNA maternally inheritedNuclear mutations follow Mendelian inheritanceMutations accumulate over time, heteroplasmicTissue mosaicism
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Mitochondrial DNA
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Mitochondrial DNAAlmost no introns, no histones: unstableNo DNA repair enzymesMitochondria dependent upon DNA
replication to continue functioningExposed to free radicals
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Mitochondrial genetic disordersWide range of symptoms and syndromesFatal encephalopathy or acidosis in first weeks of lifeIndolent muscle disorder such as ophthalmoplegiaBRAIN: seizures, myoclonus, infarcts, ataxia, dystoniaNERVE: deafness, blindness, peripheral neuropathyMUSCLE: eye muscles, proximal muscles, weakness,
exercise intolerance, cardiomyopathyOTHER: Diabetes, Deafness, short stature, lactic
acidosis, liver, pancreas, lipodystrophy
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Mitochondrial genetic syndromesMitochondrial MutationsLeber’s Hereditary Optic Neuropathy. Sequential,
severe and irreversible visual loss in young males. LHON gene causes blindness in 50% m, 10% f pts
CPEO: slowly progressive opthalmoplegia. Onset>50 usually a mtDNA deletion, sometimes point mutation
CPEO plus: multiple DNA deletions can result in neuropathy, Parkinsonism, ataxia, retinopathy, cataract, deafness, hypogonadism, depression
Kearns Sayre Syndrome (KSS): single large mt DNA deletion. Retinopathy, CPEO, cardiac conduction block. Limb myopathy, ataxia. Onset < 20. Limited lifespan.
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Mitochondrial SyndromesMitochondrial MutationsMELAS: Mitochondrial Encephalomyopathy,
Lactic Acidosis and Stroke like events. Metabolic infarcts cross normal vascular territories. Headache, nausea, vomiting, seizures, hemiparesis, hemianopia or cortical blindness. Defect in mt transfer RNA 3243 A>G
MERRF: Myoclonic Epilepsy with ragged red fibres. Stimulus sensitive Myoclonus, seizures, ataxia, myopathy, cardiomyopathy. Onset in childhood. mtDNA mutation
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MELAS infarction
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Ragged Red Fibre
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Mitochondrial SyndromesNuclear MutationsMNGIE: mitochondrial neurogastrointestinal
encephalomyopathy. CPEO, myopathy, neuropathy, intestinal pseudo obstruction. Laparotomies, malnutrition. May have a leucoencephalopathy. Nuclear DNA mut. thymidine phosphorylase
Leigh Syndrome: childhood onset symmetrical necrosis of brainstem and basal ganglia. Nystagmus, ataxia, dystonia, respiratory disease, pneumonia. Severe, progressive, fatal. Final common pathway of severe defects, many nuc DNA, some mtDNA
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Mitochondrial DysfunctionGenetic syndromes are striking but rareIncreasing recognition of involvement of
mitochondria in more common diseases, especially nerve and muscle disease
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Mitochondrial DysfunctionNeuropathy
HAART neuropathyChemotherapy neuropathy: paclitaxel, Cis-Plat, VincaDiabetic distal symmetric polyneuropathy
MyopathyStatin myopathyFibromyalgia
CNS disordersParkinson’s, Huntington’s, Friedreich’s, Migraine,
DepressionCardiovascular Disorders
Role in Endothelial function. CoQ10 levels predict mortality
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HAART toxicity
Reverse transcriptase inhibitors are nucleoside analogues.
Inhibit mitochondrial as well as viral DNA synthesisAlso inhibit adenylate kinase, ADP/ATP
translocatorR-T side effects include myopathy, neuropathy,
lactic acidosis, fatty liver, pancreatitis, nephrotoxicity. Fatalities reported with Ribavirin (Hep C) plus didanosine
HIV lipodystrophy closely resembles a mitochonrial disorder
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HAART Neuropathy
Occurs in up to two thirds of patients on RTIszalcatibine>didanosine>stavudine>lamivudine>zidovudine
>abacavir
Neuropathic pain, ascending numbnessPoorly responsive to conventional agentsForces a change in therapy, compromising efficacyInhibition of mitochondrial DNA synthesis results
in energy deficiency in peripheral nerve tissuesReduced epidermal nerve fibre density, sweat
gland innervation.
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Chemotherapy NeuropathyPaclitaxel, Doclitaxel, Platinum, Vinca
AlkaloidsInhibit mitochondrial DNA and RNA synthesis
Neuropathy frequent, limits dose and
effectivenessPotential for treatment with metabolic
support
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Diabetic NeuropathyMitochondrial dysfunction a key player in Type 2 DM
Glucose binds to Hexokinase, located on outer mitochondrial membrane
Glucose phosphorylation voltage dependent Glucose -6-P, ADP production stimulate oxidative phosG6P regulates mitochondrial function at several points
NADH donation to complex I FADH to complex II ADP to Complex V
In muscle, ATP turnover stimulates glycolysis, G6P Excess glucose levels PLUS reduced O2 tension lead
to an increase in free radical production0.
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Acetyl L CarnitineMaintains supply of acetyl-Co AContributes to phospholipid synthesisActivates growth factor receptorsPromotes regeneration, neuroprotectiveAnalgesic properties
Acute pain (cholinergic)Chronic pain (glutaminergic)
Increases ACTH and beta endorphin levels
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Acetyl L CarnitineImproves pain scores, NCS in diabetic neuropathy:
333 pts, ACL 2g/d. Pain reduced by 40%, NCV better1364 pts Vibration sense up, Pain down, histological +
Neuroprotective in Laboratory models of antiretroviral and chemotherapy induced neuropathy
Clinically effective in HAART neuropathy21 HIV patients on RTIs: ALC 1.5 grams bd improved neuropathic pain in 76% of ptsskin and sweat gland nerve fibre density inc by 100%
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ALC for Diabetic Neuropathy
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Muscle DiseaseStatin Myopathy
Statins inhibit CoQ10 synthesisMitochondrial dysfunction. Ragged red fibres.
MyalgiaCo Q10 supplements reduce pain AND improve
function by 40% (no improvement with Vit E) Am J Cardiol 2007;99(10):1409
FibromyalgiaSeveral lines of evidence indicating CoQ10
deficiency in fibromyalgia, chronic fatigue/ME
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More DisordersDepression
CoQ10 levels lower in depressed pts p<0.0002Lower again in patients with CFS or treatment
resistant depressionLink to cardiovascular mortality
Cardiovascular DiseaseEfficacy of statins predicted by CoQ10 levelsCoQ10 levels an independent predictor of
survival CoQ10 improves CHF: increased LVEF, Cardiac
OP
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Coenzyme Q10
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Coenzyme Q10Q is for Quinone, 10 is the number of isoprene units Complex synthesis, Quinone group from tyrosine,
isoprene side chains from acetyl CoA (Cholesterol)Statins reduce CoQ10 levels by 40%Oil soluble, poor oral absorptionFound in heart, liver, nuts, soy or grapeseed oil.Average intake 3-6mg/d, supplement at 150-300mg/dCan lower BP by 17mmHg. Reduces insulin resistanceStudies in aging, dementia, PAIN….
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Mitochondrial Mechanisms in PainCapsaicin induced hyperalgesia
Reactive Oxygen species (ROS) from mitochondriaSuperoxide Dismutase SOD2
Mechanical HyperalgesiaROS scavengers powerful antinociceptivesMitochondrial Complex I or complex III inhibitors
induce long lasting hyperalgesiaMorphine Antinociceptive tolerance
Inactivation of mitoSOD leads to excess peroxynitriteNitrative and Oxidative stress results in sensitisationEffect reversed by peroxynitrite scavengers
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Making the DiagnosisWell developed syndromes present no difficultyPointers to possible mitochondrial disorder:
Myopathy, Neuropathy, Deafness, Diabetes, Cardiomyopathy or conduction defect.Stroke, migraine, seizure, dementia
Serum Lactate, lactate/ pyruvate ratio. CK rise. Changes on ncs/EMG. CNS imaging.
Muscle BiopsyGomori trichrome stain demonstrates
accumulation of abnormal mitochondria – Ragged Red Fibre
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Ragged Red Fibre
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DiagnosisMuscle Biopsy: other techniques
Cytochrome C (COX) and Succinate DH staining
Specific enzymatic analysis. Tricky: sample handling, differing lab evaluations. Age related changes. Looking for reduced biochemical activity of various complexes.
Genetic AnalysisSpecific tests for specific syndromes: MELAS,
MERRF, LHON, adult Leigh syndrome. Deletion analysis for CPEO, KSS, myopathies
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ManagementSupportiveDiabetes – due to energy failure not insulin
resistance. OHAs, minimal insulin. NO metformin!!
Seizures – AVOID valproate as it inhibits function. Levetiracetam, Lamotrigene, Clonazepam
Respiratory and Bulbar weakness. Noninvasive ventilation, PEG tubes etc.
Cardiac – KSS and others may require Pacemaker. Be alert for WPW and SVT.
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ManagementPharmacologyCoenzyme Q10Acetyl CarnitineLimited efficacy: Riboflavin, alpha lipoic acid,
Vitamin A,D,E,KTrials: benzafibrate, reservatrol, PCC1 alpha.
L-arginine for MELASMetabolic agents: bicarbonate,
dichloroacetateMNGIE- stem cell transplantation
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ManagementResistance TrainingMitochondrial genetic material is heteroplasmic,
and dynamic. Mitochondria have a social life!Proportions of mutant and wild type DNA are
not stable.Resistance training can apply selection pressure
in favour of more functional DNA. Population of “satellite cells” in muscle with
high proportions of wild type DNA.Exercise physiologist supervised protocols
available.
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Resistance Training
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ConclusionComplex group of diseasesGenetic disorders have CPEO, Myopathy,
Neuropathy, Retinopathy, Cardiomyopathy, myoclonus, seizures, funny stroke syndromes, migraine, ataxia, dystonia, acidosis, diabetes, deafness, short stature
Metabolic and Neurological Disease: Diabetes, Heart Disease, Neurodegenerative disease.
Pain and related disorders: Depression, Fibromyalgia, CFS
Important role in basic pain mechanisms
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ConclusionTreatment is largely supportiveCoenzyme Q10 supplements generally
worthwhile Resistance training useful for muscle diseaseIncreasingly wide spectrum of disorders
affecting or affected by mitochondrial function.