Rate of neurotoxicant exposure determines morphologic manifestations of distal axonopathy

被引:35
作者
LoPachin, RM
Lehning, EJ
Opanashuk, LA
Jortner, BS
机构
[1] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Anesthesiol, Bronx, NY 10467 USA
[2] Virginia Polytech Inst & State Univ, Virginia Maryland Reg Coll Vet Med, Blacksburg, VA 24061 USA
关键词
D O I
10.1006/taap.2000.8984
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exposure to a variety of agricultural, industrial, and pharmaceutical chemicals produces nerve damage classified as a central-peripheral distal axonopathy. Morphologically, this axonopathy is characterized by distal axon swellings and secondary degeneration. Over the past 25 years substantial research efforts have been devoted toward deciphering the molecular mechanisms of these presumed hallmark neuropathic features. However, recent studies suggest that axon swelling and degeneration are related to sub-chronic low-dose neurotoxicant exposure rates (i.e., mg toxicant/ kg/day) and not to the development of neurophysiological deficits or behavioral toxicity. This suggests these phenomena are nonspecific and of uncertain pathophysiologic relevance. This possibility has significant implications for research investigating mechanisms of neurotoxicity, development of exposure biomarkers, design of risk assessment models, neurotoxicant classification schemes, and clinical diagnosis and treatment of toxic neuropathies. In this commentary we will review the evidence for the dose-related dependency of distal axonopathies and discuss how this concept might influence our current understanding of chemical-induced neurotoxicities. (C) 2000 Academic Press.
引用
收藏
页码:75 / 86
页数:12
相关论文
共 83 条
[71]  
SPENCER PS, 1974, CAN J NEUROL SCI, V1, P170
[72]  
Spencer PS., 1976, PROGR NEUROPATHOLOGY, VIII, P253
[73]   2,5-HEXANEDIONE AND ACRYLAMIDE PRODUCE REORGANIZATION OF MOTONEURON PERIKARYA [J].
STERMAN, AB ;
SPOSITO, N .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1985, 11 (03) :201-212
[75]   ACRYLAMIDE INDUCES EARLY MORPHOLOGIC REORGANIZATION OF THE NEURONAL CELL BODY [J].
STERMAN, AB .
NEUROLOGY, 1982, 32 (09) :1023-1026
[76]   Anoxic and ischemic injury of myelinated axons in CNS white matter: From mechanistic concepts to therapeutics [J].
Stys, PK .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (01) :2-25
[77]   SLOWING OF FAST AXOPLASMIC-TRANSPORT IN ACRYLAMIDE NEUROPATHY [J].
SUMNER, A ;
PLEASURE, D ;
CIESIELKA, K .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1976, 35 (03) :319-319
[78]   ACRYLAMIDE NEUROPATHY IN RATS - ELECTRON-MICROSCOPIC STUDY OF DEGENERATION AND REGENERATION [J].
SUZUKI, K ;
PFAFF, LD .
ACTA NEUROPATHOLOGICA, 1973, 24 (03) :197-213
[79]   NEUROTOXICITY OF ACRYLAMIDE AND RELATED-COMPOUNDS IN RATS - EFFECTS ON ROTAROD PERFORMANCE, MORPHOLOGY OF NERVES AND NEUROTUBULIN [J].
TANII, H ;
HASHIMOTO, K .
ARCHIVES OF TOXICOLOGY, 1983, 54 (03) :203-213
[80]  
Trump BF, 1979, SCANNING ELECTRON MI, V3, P1