Functional and morphological effects of repeated sodium arsenite exposure on rat peripheral sensory nerves
Article
-
- Overview
-
- Research
-
- Identity
-
- Additional Document Info
-
- View All
-
Overview
abstract
-
Exposure to inorganic arsenic (iAs) is known to result in peripheral neuropathy. To better understand the functional and morphological consequences of iAs exposure, we examined the electrophysiological and histological characteristics of the sensory sural nerves in adult Male Wistar rats following 30 days of sodium arsenite administration by gavage (10 mg/kg body weight/day). Arsenic (As) levels in the peripheral nerves of exposed animals were about 150 times greater than those in controls. Lipid peroxidation was also increased in iAs-exposed animals. Compound action potentials (CAPs) evoked in iAs-exposed nerves were characterized by a slower conduction velocity (∼ 26%25). iAs-exposed nerves also showed a trend towards a decreased CAP area (∼ 35%25). These electrophysiological changes were consistent with histological alterations such as a ∼ 56%25 decrease in myelin thickness. In addition, the perimeter and transverse area of axons were reduced to 29%25 and 45%25 of control, respectively. Our results suggest that accumulation of As produced by iAs exposure induces oxidative damage, severe demyelination, and other morphological alterations in axons of peripheral nerves. These changes may, in turn, induce changes in the generation and propagation of action potentials in peripheral nerves, leading to decreased transmission of information from peripheral sensory organs to the central nervous system. © 2007 Elsevier B.V. All rights reserved.
publication date
funding provided via
published in
Research
keywords
-
Arsenic; Demyelination; Oxidative damage; Peripheral nervous system; Sural nerve arsenite sodium; myelin; action potential; animal experiment; animal model; animal tissue; article; body weight; controlled study; demyelinating disease; disease severity; electrophysiology; histopathology; lipid peroxidation; male; morphology; myelin sheath; nerve conduction; nerve fiber; nerve function; nonhuman; oxidative stress; peripheral nerve; priority journal; rat; sensory nerve; sural nerve; Action Potentials; Animals; Arsenites; Electric Stimulation; Enzyme Inhibitors; Lipid Peroxidation; Male; Neural Conduction; Rats; Rats, Wistar; Sodium Compounds; Sural Nerve
Identity
Digital Object Identifier (DOI)
PubMed ID
Additional Document Info
start page
end page
volume
issue