Deterioration in brain and heart functions following a single sub-lethal (0.8 LCt50) inhalation exposure of rats to sarin vapor: A putative mechanism of the long term toxicity

• Published in: Toxicology and applied pharmacology 2011-05, Vol.253 (1), p.31-37
• Main Authors: ALLON, N, CHAPMAN, S, EGOZ, I, RABINOVITZ, I, KAPON, J, WEISSMAN, B. A, YACOV, G, BLOCH-SHILDERMAN, E, GRAUER, E
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Brain - drug effects; Brain - physiopathology; Chemical and industrial products toxicology. Toxic occupational diseases; Gas, fumes; Heart - drug effects; Heart - physiopathology; Inhalation Exposure - adverse effects; Lethal Dose 50; Male; Maze Learning - drug effects; Maze Learning - physiology; Medical sciences; Rats; Rats, Sprague-Dawley; Sarin - administration & dosage; Sarin - toxicity; Time Factors; Toxicology; Volatilization
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2011.03.007

The main injuries among victims of the terrorist act in the Tokyo subway resulted from sub-lethal inhalation and whole body exposure to sarin vapor. In order to study the long term effects of such exposure and to simulate these conditions, freely moving rats were exposed to sarin vapor (27.2±1.7 μg/l) for 10 min. About 50% of the rats showed no overt symptoms and the rest had mild to moderate clinical symptoms that subsided within 4h following exposure. A reduction of weight was noted during the first 3 days with full recovery on the 4th day. Rat's heart was challenged with epinephrine 1 and 6 months post exposure. A significant reduction in the threshold for epinephrine-induced arrhythmia (EPIA) was noted in rats exposed to sarin. A time dependent increase in the kD and Bmax values of muscarinic auto receptors (M2) was recorded in the rat's cortex and striatum. No changes were recorded in the rats' brain trans locator protein (TSPO) levels, concomitant with no observed changes in the animals' performance in A Morris water maze test. A significant increase in open field activity was noted 6 months following exposure to sarin vapor as well as a significant decrease in prostaglandin E₂ (PGE₂) production in the brain. It is speculated that down regulation of the M2 auto receptor function, caused hyper reactivity of the cholinergic system which leads to the changes described above. The continuous reduction in M2 auto-receptor system through an unknown mechanism may be the cause for long lasting decline in sarin-exposed casualties' health.