Positive symptoms in multiple sclerosis: their treatment with sodium channel blockers, lidocaine and mexiletine

Patients with multiple sclerosis (MS) often show positive symptoms of painful tonic seizure and dysesthesia as well as negative symptoms of paralysis and hypesthesia. Positive manifestation is paroxysmal and/or persistent. These are considered to be mediated by ectopic impulses generated at the site of demyelination, whereas negative symptoms are caused by conduction block. Conduction block at a demyelinated segment should reduce positive symptoms, but worsen negative ones. As reported previously, lidocaine, an Na channel blocker unmasks silent negative symptoms presumably by further reducing the action current in demyelinated portions and blocking conduction. Furthermore, because it blocks Na channels in a voltage- and frequency dependent manner, fibers that mediate positive symptoms are preferentially blocked. We administered lidocaine to 30 MS patients with positive symptoms. Lidocaine (mean plasma level, 2.4 pg/ml) almost completely abolished the paroxysmal manifestation of painful tonic seizures, neuralgic attacks, paroxysmal itching, and Lhermitte's sign. It also markedly alleviated persistent symptoms, but less so than paroxysmal symptoms. Similar effects were obtained with orally-administered mexiletine (300-400 mg/day), a derivative of lidocaine, but to a lesser extent. Na channel blockers have a dual effect on symptoms in MS, depending on whether symptoms are positive or negative. The mechanism that produces positive symptoms and the effects of the drugs on these symptoms are discussed.

[1]  L. Weiner,et al.  Remyelination following viral‐induced demyelination: Ferric ion—ferrocyanide staining of nodes of ranvier within the CNS , 1980, Annals of neurology.

[2]  C. Schauf,et al.  Impulse conduction in multiple sclerosis: a theoretical basis for modification by temperature and pharmacological agents , 1974, Journal of neurology, neurosurgery, and psychiatry.

[3]  W. Matthews TONIC SEIZURES IN DISSAMINATED SCLEROSIS , 1958 .

[4]  D. Bergen Antiepileptic Drugs, 4th Ed , 1996, Neurology.

[5]  M. Rasminsky Hyperexcitability of pathologically myelinated axons and positive symptoms in multiple sclerosis. , 1981, Advances in neurology.

[6]  T. Guthrie,et al.  Influence of temperature changes on multiple sclerosis: critical review of mechanisms and research potential , 1995, Journal of the Neurological Sciences.

[7]  D. Clifford,et al.  Pain in multiple sclerosis. , 1984, Archives of neurology.

[8]  Y.-G. Li,et al.  Slow sodium-dependent potential oscillations contribute to ectopic firing in mammalian demyelinated axons. , 1997, Brain : a journal of neurology.

[9]  W. Matthews,et al.  Paroxysmal symptoms in multiple sclerosis , 1975, Journal of the Neurological Sciences.

[10]  M. Espir,et al.  Treatment of paroxysmal disorders in multiple sclerosis with carbamazepine (Tegretol) , 1970, Journal of neurology, neurosurgery, and psychiatry.

[11]  H. Shibasaki,et al.  Painful tonic seizure in multiple sclerosis. , 1974, Archives of neurology.

[12]  S. Waxman The Axon : structure, function, and pathophysiology , 1995 .

[13]  W. Catterall,et al.  Molecular determinants of state-dependent block of Na+ channels by local anesthetics. , 1994, Science.

[14]  P. Schwindt,et al.  Properties of persistent sodium conductance and calcium conductance of layer V neurons from cat sensorimotor cortex in vitro. , 1985, Journal of neurophysiology.

[15]  K. Foley,et al.  Pain syndromes in multiple sclerosis , 1988, Neurology.

[16]  P. Gage,et al.  Effects of lignocaine and quinidine on the persistent sodium current in rat ventricular myocytes , 1992, British journal of pharmacology.

[17]  M. Rasminsky Ephaptic transmission between single nerve fibres in the spinal nerve roots of dystrophic mice. , 1980 .

[18]  Stephen G. Waxman,et al.  Pathophysiology of demyelinated axons , 1995 .

[19]  W. I. McDonald,et al.  Spontaneous and evoked electrical discharges from a central demyelinating lesion , 1982, Journal of the Neurological Sciences.

[20]  S G Waxman,et al.  Noninactivating, tetrodotoxin-sensitive Na+ conductance in rat optic nerve axons. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[21]  D. Silberberg,et al.  New diagnostic criteria for multiple sclerosis: Guidelines for research protocols , 1983, Annals of neurology.

[22]  Stephen G. Waxman,et al.  Impulse conduction in inhomogeneous axons: Effects of variation in voltage-sensitive ionic conductances on invasion of demyelinated axon segments and preterminal fibers , 1984, Brain Research.

[23]  C. Westerberg,et al.  Paroxysmal attacks in multiple sclerosis. , 1975, Brain : a journal of neurology.

[24]  W. Matthews,et al.  McAlpine's multiple sclerosis , 1985 .

[25]  W. Catterall Common modes of drug action on Na+ channels: local anesthetics, antiarrhythmics and anticonvulsants , 1987 .

[26]  K. Burchiel Abnormal impulse generation in focally demyelinated trigeminal roots , 1980 .

[27]  M. Sakurai,et al.  Lidocaine unmasks silent demyelinative lesions in multiple sclerosis , 1992, Neurology.