1,2,4-Triethylbenzene (1,2,4-TEB) and 1,3,5-triethylbenzene (1,3,5-TEB) were administered orally to male Sprague-Dawley rats. Experimental and appropriate control rats were examined electrophysiologically for motor and sensory conduction velocities (MCV and SCV), and the amplitudes of the sensory (A
Diethylbenzene-induced sensorimotor neuropathy in rats
✍ Scribed by F. Gagnaire; B. Marignac; J. de Ceaurriz
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 530 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0260-437X
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✦ Synopsis
Abstract
The commercial isomer mixture of diethylbenzene (DEB mixture), 1,2‐diethylbenzene (1,2‐DEB), 1,3‐diethylbenzene (1,3‐DEB) and 1,4‐diethylbenzene (1,4‐DEB) were administered orally to male Sprague‐Dawley rats. The experimental rats and the appropriate controls were examined electrophysiologically for motor and sensory conduction velocities (MCV and SCV), and for the amplitude of the sensory action potential (ASAP) of the tail nerve, at weekly or bi‐weekly intervals. Oral administration of DEB mixture (750 or 500 mg kg^−1^, once daily, 5 days per week for 10 weeks) and 1,2‐DEB (100 mg kg^−1^, once daily, 4 days per week for 8 weeks) produced a time‐dependent decrease in MCV, SCV and ASAP. Rats treated with DEB mixture and 1,2‐DEB exhibited a blue discoloration of tissues and urine.
No changes in MCV, SCV and ASAP developed in rats administered orally with 1,3‐DEP and 1,4‐DEB (500 mg kg^−1^, once daily, 5 days per week for 8 weeks).
The results indicate that 1,2‐DEB is the isomer responsible for neurotoxicity and suggest that a metabolic pathway giving rise to coloured compounds is involved in the neurotoxicity of DEB.
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The role of 1,2-diacetyIbenzene (1,2-DAB) in the peripheral nerve toxicity of 1,2-diethyIbenzene (1,2-DEB) was investigated in rats. Gas chromatography-mass spectrometry identified 1,2-DAB in the urine samples of rats given 165 mg kg-' 1,2-DEB orally on four consecutive days. I,2-DAB shared not only
## Abstract Motor and sensory conduction velocities (MCV and SCV), amplitude of the sensory action potential (ASAP) of the tail nerve and parameters of brainstem auditory evoked potentials (BAEP) were studied in male Sprague‐Dawley rats after prolonged inhalation exposure to a commercial isomer mix