The proposal seeks to continue studies to define the molecular pathogenesis of the neuropathy caused by n-hexane, a hazard of occupational exposure and inhalant abuse. The working hypothesis guiding this work has been that n-hexane is metabolized to the gamma-diketone, 2,5-hexanedione, which reacts with lysyl amino groups of proteins to form pyrrolyl derivatives; the pyrrole rings then undergo autoxidation, resulting in covalent crosslinking of proteins; the extreme stability of the neurofilament predisposes this axonal filament to progressive derivatization and crosslinking; periodic constrictions of the axon at nodes of Ranvier present obstructions to the proximo-distal transport of the growing mass of neurofilaments; continued transport up to the point of occlusion results in large paranodal swellings filled with neurofilaments; subsequent impairment of axonal transport results in degeneration of the distal axon. To test this hypothesis the following.
Specific Aims shall be pursued: (1) to determine the specificity and generality of the gamma-diketone structure in the genesis of the neurotoxicity of alkanes; (2) to define the mechanism of pyrrole synthesis and the relationship between the rate of pyrrole formation and neurotoxicity; (3) to determine whether pyrrole autoxidation and crosslinking are necessary steps in the pathogenetic sequence: (4) to determine the structure of the crosslinking adducts; (5) to determine whether neurofilamentous crosslinking is progressive during chronic intoxication; (6) to determine the role of axonal constrictions at nodes of Ranvier in the development of axonal swellings; (7) to determine the mechanism of degeneration of the distal axon; and (8) to determine what steps in the proposed pathogenetic scheme for n-hexane neuropathy have parallels in the pathogenesis of the neuropathies caused by beta,beta'-iminodipropionitrile, carbon disulfide and acrylamide. The major approach taken in this project is to synthesize novel analogues of 2,5-hexanedione and the putative crosslinking metabolites of other toxicants in order to test specific steps in the pathogenetic schemes and to define the identities of the crosslinking adducts. This includes the synthesis of a series of gamma-diketones which, through the presence of electron-withdrawing or electron-donating groups, enhance or impair the rate of pyrrole formation and retard or facilitate oxidation of the resulting pyrrole ring. Further, the role of oxidation of intermediates in the crosslinking of neurofilaments by beta,beta'- iminodipropionitrile and carbon disulfide will be explored. The participation of different neurofilament subunits in the crosslinking reactions will be sought as will the role of fast axonal transport in the genesis of distal axonal degeneration.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37ES002611-13
Application #
3483784
Study Section
Toxicology Subcommittee 2 (TOX)
Project Start
1981-07-01
Project End
1994-06-30
Budget Start
1993-07-01
Budget End
1994-06-30
Support Year
13
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
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Zhang, J; Graham, D G; Montine, T J et al. (2000) Enhanced N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine toxicity in mice deficient in CuZn-superoxide dismutase or glutathione peroxidase. J Neuropathol Exp Neurol 59:53-61
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Zhang, J; Price, J O; Graham, D G et al. (1998) Secondary excitotoxicity contributes to dopamine-induced apoptosis of dopaminergic neuronal cultures. Biochem Biophys Res Commun 248:812-6
Amarnath, V; Valentine, W M; Montine, T J et al. (1998) Reactions of 4-hydroxy-2(E)-nonenal and related aldehydes with proteins studied by carbon-13 nuclear magnetic resonance spectroscopy. Chem Res Toxicol 11:317-28
Montine, K S; Olson, S J; Amarnath, V et al. (1997) Immunohistochemical detection of 4-hydroxy-2-nonenal adducts in Alzheimer's disease is associated with inheritance of APOE4. Am J Pathol 150:437-43

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