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              Open Access  
Copyright: The authors. This article is an open access 
article licensed under the terms of the Creative Commons Attribution License 
(http://creativecommons.org/licenses/by/2.0) which permits unrestricted use, 
distribution and reproduction in any medium, provided the work is properly 
cited. 
 
              
              
              Research 
              
              (Published 
online : 01-12-2013) 
2. Preliminary acute toxicity study on imidacloprid in 
Swiss albino mice - Preeti Bagri, Vinod Kumar, Anil Kumar Sikka and 
Joginder Singh PuniaVeterinary World, 6(12): 955-959
 
  
              
              doi: 
              10.14202/vetworld.2013.955-959 
                
              
              
          
 
              Abstract 
 
              Aim: To ascertain the maximum 
              tolerated dose (MTD) and to investigate the acute oral toxic 
              effects of imidacloprid towards Swiss albino male mice.Materials and Methods: The MTD of imidacloprid was 
              determined in pilot dose range finding study following the 
              standard method. Animals were observed for toxic signs and 
              symptoms after oral administration of MTD of imidacloprid in 
              single dose. The body weights of animals were recorded on 
              alternate day. Animals were sacrificed on 14th day and changes in 
              hematological parameters (Hb, TEC, TLC and DLC) and morphometric 
              measurements (length, breadth, thickness and weight) of various 
              body organs (heart, liver, spleen, kidney, testis and epididymis) 
              were examined. The student's t-test was applied to statistically 
              analyze the results.
 Results: The MTD of imidacloprid was determined to be 110 
              mg/kg body weight. The sign and symptoms of acute toxicity were 
              ataxia, rigidity and fasciculation of muscles, protrusion of eye 
              ball and tremors of head. Imidacloprid treatment resulted in 
              decreased body weight gain as compared to the control group. The 
              changes in hematological parameters were not significant between 
              imidacloprid treated and control groups. Also the values of 
              relative organ weights and morphometric measurements of various 
              body organs did not differ significantly between the control and 
              imidacloprid treated animals.
 Conclusions: MTD of imidacloprid in Swiss albino male mice 
              through oral route was determined for the first time. Study 
              revealed a non-toxic effect of imidacloprid on body weight, 
              relative organs weight, hematological parameters and morphometric 
              measurements of various body organs in mice.
 Keywords: hematology, imidacloprid, morphometric 
              measurement, MTD, toxicity
 
 
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