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Acute toxicity studies of α-Ketoglutarate: a promising antidote for cyanide poisoning

✍ Scribed by R. Bhattacharya; Deo Kumar; K. Sugendran; S. C. Pant; R. K. Tulsawani; R. Vijayaraghavan


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
97 KB
Volume
21
Category
Article
ISSN
0260-437X

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✦ Synopsis


Abstract

Recently we have shown that cyanide poisoning by the oral (p.o.) route could be antagonized significantly by pretreatment or simultaneous treatment of α‐ketoglutarate (α‐KG), administered p.o. in rodents. The protective effect of α‐KG was dose dependent (0.125–2.0 g kg^−1^) and the effect was significant at a dose above 1.0 g kg^−1^. In order to establish the safety of α‐KG, various haematological, biochemical and histological parameters were studied following p.o. administration of 2.0 g kg^−1^α‐KG in female rats, and various physiological parameters were studied following p.o. administration of 2.0 or 4.0 g kg^−1^α‐KG in anaesthetized male rats. The p.o. LD~50~ of α‐KG in male and female rats was >5.0 g kg^−1^ and no toxic signs were observed in the surviving animals. Except for an increase in plasma alkaline phosphatase and urea levels after 1 h and a decrease in inorganic phosphorus levels after 7 days of treatment, no significant change in haematology, biochemistry or histology of the vital organs were observed. Mean arterial pressure and neuromuscular transmission were decreased at 4.0 g kg^−1^α‐KG but other physiological variables such as heart rate, respiratory rate, rectal temperature, left ventricular pressure (systolic), arterial pressure (systolic) and arterial pressure (diastolic) were not altered. The changes observed at 4.0 g kg^−1^α‐KG are unlikely to be of toxicological concern. The results indicate that α‐KG at 2.0 g kg^−1^ (p.o.)—a dose offering maximum antidotal efficacy—is non‐toxic and therefore can be considered suitable for cyanide poisoning. Copyright © 2001 John Wiley & Sons, Ltd.