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Few studies have characterize the toxicological effects of exposure to pesticide mixtures. For this reason, the present study aimed to estimate the median lethal doses (LD50) of some new pesticide mixtures; chlorosan, feroban, cygron, engeo and kingbo on albino rats. The in vivo effect of these compounds on some biochemical targets were also investigated. The estimated median lethal doses (LD50) of chlorosan, feroban, engeo and cygron were 140.8, 264.0, 281.5 and 352.0 mg/kg body weight (b.w.), respectively. The estimated median lethal dose was more than 160.0 mg/kg b.w. in the case of kingbo. The symptoms of the affected animals included salivation, bleeding, activity increase and the chlorosan treated rats closed their eyes. Some animals died after doses of chlorosan, feroban and engeo administered at different intervals. The results showed a significant increase in the activities of plasma transaminases [Glutamic Oxaloacetic Transaminase (GOT) and Glutamic Pyruvic Transaminase (GPT)] and glutathione S-transferase (GST). It was found that the tested pesticides significantly inhibited acetylcholinesterase (AChE) activity 1 h after the last dose. Also, there was a significant increase in creatinine and urea levels. The obtained data concluded that chlorosan was the most effective against albino rats followed by feroban and engeo, while kingbo was the least effective. By the end of the experiment, the enzyme activities and kidney functions of animals treated with chlorosan, feroban and engeo did not return to normal.
Filarial nematodes infect more than 150 million people worldwide and are responsible for diseases including elephantiasis, river blindness and tropical pulmonary eosinophilia. Antifílarial agents that can kill all the stages in the life cycle of causative filar- iae have yet to be developed. Very little effort has been made towards rational drug design, employing knowledge gained from studies of the biochemistry and physiology of filarial worms and of their interactions with their specific vertebrate hosts. In this review, we highlight the research and development of rational antifílarial agents and we discuss the pitfalls since the discovery of diethylcarbamazine, the only drug of choice for controlling filariasis, despite its adverse side effects.
Nitric oxide (NO) has become one of the most intensively studied molecules in recent years. Although its beneficial role has been well established, a large body of adverse effects was also attributed to NO and/or its red-ox derivatives in biological systems. Peroxynitrite (ONO-), a product of reaction between NO and superoxide anion (O2•-) was recognized as a potent pro-oxidant endogenous toxicant. The agent was found to induce DNA and protein oxidative damages leading to increased risk(s) of severe human pathologies including cancer. In this review, the discrete chemical aspects of both nitric oxide and peroxynitrite have been discussed in an attempt to elucidate the major biochemical target(s) of NO-and/or peroxynitrite-induced toxicity.
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