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Abstract 1.1. Pyrethroids 1.1.1 Types and structure The widespread use of pesticides in public health protection and agricultural programs has caused severe environmental pollution and health hazard, particularly in developing countries including cases of severe acute and chronic human and animal poisoning as well as damage to other non-target organisms (Assayed, et al., 2010). Humans are potentially exposed to pesticides either directly, as workers in greenhouse and in agriculture, or indirectly, via food consumption. In addition, it is likely that a significant amount of these pesticides and their metabolites reach rivers and estuaries via run-off from farmland that are potentially toxic to wildlife (EL-Shenawy, 2010). The pesticides featured belong to two major different classes of insecticides, namely organophosphate and pyrethroids.Synthetic pyrethroids a unique group of insecticides having pyrethrin-like structure with better performance characteristics and globally account for over 30% of insecticides use (Shulka, et al., 2002). Pyrethroids are modified derivates of pyrethrin, natural substance from the flowers of pyrethrum species (Luty, et al., 2000). Various classes of insecticides include organophosphate, organochlorine, carbamate and pyrethroid. Pyrethroids use has increased much for the last 10 years (Wolansky, et al., 2006). The incidence of major outcomes and fatalities attributable to pyrethroids are considerably less than organophosphates (Sudakin, 2006). However, their pathological effects have been encountered in experimental studies in different animals (Manna, et al., 2004 and Khan, et al., 2009). Initially, pyrethroids were extracted from the dried and powdered flower heads of Chrysanthemum cinerariaefolium. The extract contains chrysanthemic (pyrethrin I) and pyrethric acid esters (pyrethrin II) in about equal quantities. Natural pyrethrin is a mixture (1:1) of pyrethrin I and pyrethrin II (Davies, 1985). The toxicity of pyrethroids insecticides to mammals has received much attention in recent years because animals exposed to these insecticides showed change in their physiological activities besides other pathological features (Glass, 2008). Good solubility of pyrethroids in fats facilitates their absorption, spread in an organism and penetration to the nervous tissue. Pyrethroid insecticides show neurotoxic effect which is manifested by an increased excitatory effect of central and peripheral nervous systems (Crafton, et al., 1995). Pyrethroids, the synthetic analogues of pyrethrin, fall into two distinct categories (Type I and Type II) based on the symptoms in experimental animals receiving acute toxic doses (Verschoyle and Aldridge 1980). Type I pyrethroids, e.g. pyrethrin and permethrin, do not have an alpha cyano group while Type II pyrethroids such as cypermethrin and fenvalerate, contain an alpha cyano group. It is generally agreed that Type II pyrethroids are more potent insecticides Introduction 2 due to the alpha cyano group in their structure (Vijverberg. |