Vet World   Vol.11   September-2018  Article-15

Research Article

Veterinary World, 11(9): 1291-1297

https://doi.org/10.14202/vetworld.2018.1291-1297

Acute oral toxicity of pesticide combination (acephate 50% and imidacloprid 1.8% as active ingredients) in Sprague-Dawley rats

Rajendra Palkhade1, Suresh Yadav2, SukhDev Mishra3, and Jaseer Muhamed4
1. Laboratory Animal Facility, ICMR-National Institute of Occupational Health, Ahmedabad, Gujarat, India.
2. Toxicology Division, ICMR-National Institute of Occupational Health, Ahmedabad, Gujarat, India.
3. Biostatistics and Data Management Division, ICMR-National Institute of Occupational Health, Ahmedabad, Gujarat, India.
4. Poison Information Center, ICMR-National Institute of Occupational, Ahmedabad, Gujarat, India.

Background and Aim: The aim of this study was to assess the acute toxic interaction and lethal dose (LD50) of pesticide combination product (acephate 50% and imidacloprid 1.8% as active ingredients) available in the market in Sprague-Dawley female rats by oral route.

Materials and Methods: A total of 10 Sprague-Dawley female rats were divided into two groups, comprising five rats in each dose group. Both groups were identified as control and test groups, respectively. Control group received sterile water as vehicle and test group received pesticide combination (acephate 50% and imidacloprid 1.8% as active ingredients) at a dose of 0 and 2000 mg/kg body weight. As per the Organization for Economic Cooperation and Development Guideline 420, initially one animal each from both the control and test groups were dosed with 0 and 2000 mg/kg, respectively, as sighting study. Based on the results of sighting study, additionally, four animals each from both groups were dosed with the same dose to make a total of five animals in each group. Dose volume was constant as 10 mL/kg. All animals were observed daily twice for clinical signs and mortality. Body weight was recorded on day 0 and weekly thereafter during 14 days' observation period; last body weight (fasted) was recorded on day 15. All the rats of both the groups were humanely sacrificed on day 15 for gross pathology, collection of organs for histopathology, organ weighing, and morphometry. Organ weights were taken as absolute values, and relative organ weights to last fasted body weights were calculated.

Results: Pesticide combination (acephate 50% and imidacloprid 1.8% as active ingredients) treated rats showed cholinergic signs with one mortality in the test group. No significant difference was observed in body weight, relative organ weights, and organ morphometry between pesticide combination exposed and non-exposed groups. Gross pathology of the treated rats was also comparable with respect to control group. Histopathological changes in the liver, kidneys, heart, lung, adrenaline, spleen, and ovaries of test group rats were found to be comparable with control group rats.

Conclusion: The present study demonstrated the LD50 of one of the combination products available in the market having acephate 50% and imidacloprid 1.8% as active ingredients in Sprague-Dawley female rats which is >2000 mg/kg body weight. Furthermore, gross, histopathology and histoarchitectural alterations of all the vital organs of the test group were comparable to the control. Keywords: acephate 50%, acute oral toxicity, histopathology, imidacloprid 1.8%.

Keywords: acephate 50%, acute oral toxicity, histopathology, imidacloprid 1.8%.

How to cite this article: Palkhade R, Yadav S, Mishra S, Muhamed J (2018) Acute oral toxicity of pesticide combination (acephate 50% and imidacloprid 1.8% as active ingredients) in Sprague-Dawley rats, Veterinary World, 11(9): 1291-1297.

Received: 16-05-2018  Accepted: 01-08-2018     Published online: 18-09-2018

Corresponding author: Rajendra Palkhade   E-mail: drpalkhade@rediffmail.com

DOI: 10.14202/vetworld.2018.1291-1297

Copyright: Palkhade, et al. This article is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http:// creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.