Issues & Opinions: Amyotrophic lateral sclerosis: Lower motor neuron disease spreading to upper motor neurons

Contrary to the recently reemphasized notion that the primary neuron involved in amyotrophic lateral sclerosis (ALS) is the cortical (upper) motor neuron (UMN), we believe that the lower motor neuron (LMN) is primarily involved by the retrograde transport of pathogens from neuromuscular junctions, and the disease process spreads monosynaptically to the UMN. Pathologically and epidemiologically, the LMN hypothesis is more logical than the UMN in light of the recent understanding of neuroaxonal transport systems, particularly in regard to anterograde cytoskeleton transport and the kinetics of the force promoting slow axonal transport. By correlating the early pathologic findings, i.e., the swelling of the initial axons and formation of intracytoplasmic inclusions in the LMN, ALS may be regarded as a disease of axonal transport, especially its slow component (SCa). Therapeutic intervention to facilitate SCa should be attempted in ALS. © 1993 John Wiley & Sons, Inc.

[1]  M. Swash,et al.  Adverse effect of verapamil in myasthenia gravis , 1992, Muscle & nerve.

[2]  B. Pant,et al.  Amyotrophic lateral sclerosis (ALS): A phylogenetic disease of the corticomotoneuron? , 1992, Muscle & nerve.

[3]  S. M. Chou,et al.  Fast axonal transport in amyotrophic lateral sclerosis , 1987, Neurology.

[4]  R. Vallee,et al.  Identification of dynamin, a novel mechanochemical enzyme that mediates interactions between microtubules , 1989, Cell.

[5]  Sanford L. Palay,et al.  THE AXON HILLOCK AND THE INITIAL SEGMENT , 1968, The Journal of cell biology.

[6]  M. Swash,et al.  Ubiquitin deposits in anterior horn cells in motor neurone disease , 1988, Neuroscience Letters.

[7]  M. Swash Amyotrophic lateral sclerosis: A phylogenetic disease of the corticomotoneuron? Comments on the hypothesis , 1992, Muscle & nerve.

[8]  E. G. Jones,et al.  Relationship of intrinsic connections to forelimb movement representations in monkey motor cortex: a correlative anatomic and physiological study. , 1991, Journal of neurophysiology.

[9]  T. Stevens,et al.  A putative GTP binding protein homologous to interferon-inducible Mx proteins performs an essential function in yeast protein sorting , 1990, Cell.

[10]  E. Shooter,et al.  Nerve growth factor-induced neurite outgrowth in PC12 cells involves the coordinate induction of microtubule assembly and assembly-promoting factors , 1985, The Journal of cell biology.

[11]  Polio and ALS , 1990, Neurology.

[12]  D. Price,et al.  Slow axonal transport of neurofilament proteins: impairment of beta,beta'-iminodipropionitrile administration. , 1978, Science.

[13]  Y. Ihara,et al.  Immunocytochemical and ultrastructural studies of lower motor neurons in amyotrophic lateral sclerosis , 1990, Annals of neurology.

[14]  J R Daube,et al.  How frequently does classic amyotrophic lateral sclerosis develop in survivors of poliomyelitis? , 1990, Neurology.

[15]  P. Nunn,et al.  Guam amyotrophic lateral sclerosis-parkinsonism-dementia linked to a plant excitant neurotoxin. , 1987, Science.

[16]  R. Levi‐montalcini,et al.  The nerve growth factor 35 years later. , 1987, Science.

[17]  M. Dalakas,et al.  Post-polio syndrome: concepts in clinical diagnosis, pathogenesis, and etiology. , 1991, Advances in neurology.

[18]  R. Swank,et al.  AMYOTROPHIC LATERAL SCLEROSIS AND RELATED CONDITIONS: A CLINICAL ANALYSIS , 1943 .

[19]  M. Brin,et al.  Primary lateral sclerosis. A clinical diagnosis reemerges. , 1988, Archives of neurology.

[20]  Sanford L. Palay,et al.  The fine structure of the nervous system: The neurons and supporting cells , 1976 .

[21]  D. Barker,et al.  MOTONEURON DISEASE AND PAST POLIOMYELITIS IN ENGLAND AND WALES , 1988, The Lancet.

[22]  P N Leigh,et al.  Cytoskeletal pathology in motor neuron diseases. , 1991, Advances in neurology.

[23]  M. Swash,et al.  Selective and asymmetric vulnerability of corticospinal and spinocerebellar tracts in motor neuron disease. , 1988, Journal of neurology, neurosurgery, and psychiatry.

[24]  James R. Miller,et al.  Prolonged intracerebral infection with poliovirus in asymptomatic mice , 1981, Annals of neurology.

[25]  V. Meininger,et al.  Modifications of microtubule proteins in ALS nerve precede detectable histologic and ultrastructural changes , 1988, Neurology.

[26]  C. Davison AMYOTROPHIC LATERAL SCLEROSIS: ORIGIN AND EXTENT OF THE UPPER MOTOR NEURON LESION , 1941 .

[27]  Mulder Dw,et al.  Late progression of poliomyelitis or forme fruste amyotrophic lateral sclerosis , 1972 .

[28]  J Tanji,et al.  Digit-muscle responses evoked from multiple intracortical foci in monkey precentral motor cortex. , 1989, Journal of neurophysiology.

[29]  S. Carpenter Proximal axonal enlargement in motor neuron disease , 1968, Neurology.

[30]  R Porter,et al.  Morphology of pyramidal neurones in monkey motor cortex and the synaptic actions of their intracortical axon collaterals. , 1988, The Journal of physiology.

[31]  P. Averback,et al.  Regular involvement of Clarke's nucleus in sporadic amyotrophic lateral sclerosis. , 1982, Archives of neurology.

[32]  R. Vallee,et al.  MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties , 1987, The Journal of cell biology.

[33]  H. Kuypers,et al.  Viruses as transneuronal tracers , 1990, Trends in Neurosciences.

[34]  S. Maruyama,et al.  Swelling of neuronal processes in motor neuron disease , 1988, Neurology.

[35]  R. P. Mackay,et al.  Course and Prognosis in Amyotrophic Lateral Sclerosis , 1963 .

[36]  G. Bloom,et al.  Mechanisms of fast and slow axonal transport. , 1991, Annual review of neuroscience.

[37]  D. Price,et al.  Cytoskeletal disorganization induced by local application of β,β′‐iminodipropionitrile and 2,5‐hexanedione , 1983, Annals of neurology.

[38]  J. Kimura,et al.  Amyotrophic lateral sclerosis: A critique of a hypothesis , 1992, Muscle & nerve.

[39]  W. Hammond ART. I.—THE BRAIN NOT THE SOLE ORGAN OF THE MIND , 1876 .

[40]  L. Autilio‐Gambetti,et al.  Reorganization of axoplasmic organelles following beta, beta'- iminodipropionitrile administration , 1981, The Journal of cell biology.

[41]  R. Lasek,et al.  Cytotypic differences in the protein composition of the axonally transported cytoskeleton in mammalian neurons , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  T. Lentz,et al.  Is the acetylcholine receptor a rabies virus receptor? , 1982, Science.

[43]  S. Maruyama,et al.  Swellings of proximal axons in a case of motor neuron disease , 1989, Annals of neurology.

[44]  L. Thal,et al.  Dementia and motor neuron disease: Morphometric, biochemical, and Golgi studies , 1984, Annals of neurology.

[45]  S. Carpenter,et al.  Neurofibrillary axonal swellings and amyotrophic lateral sclerosis , 1984, Journal of the Neurological Sciences.

[46]  R. Lasek,et al.  The slow component of axonal transport. Identification of major structural polypeptides of the axon and their generality among mammalian neurons , 1975, The Journal of cell biology.

[47]  B. Brownell,et al.  The central nervous system in motor neurone disease , 1970, Journal of neurology, neurosurgery, and psychiatry.

[48]  S H Appel,et al.  A unifying hypothesis for the cause of amyotrophic lateral sclerosis, parkinsonism, and alzheimer disease , 1981, Annals of neurology.