Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractPotato tuber herbivory increases resistance to aboveground lepidopteran herbivores    Next AbstractPollutant Levels at Cooking Place and Their Association with Respiratory Symptoms in Women in a Rural Area of Delhi-NCR »

Toxicol Ind Health


Title:Prenatal developmental toxicity study of n-heneicosane in Wistar rats
Author(s):Kumar P; Lomash V; Jatav PC; Kumar A; Pant SC;
Address:"Pharmacology and Toxicology Division, Defence Research and Development Establishment, Gwalior, India pravinkumar43@hotmail.com. Pharmacology and Toxicology Division, Defence Research and Development Establishment, Gwalior, India"
Journal Title:Toxicol Ind Health
Year:2016
Volume:20130923
Issue:1
Page Number:118 - 125
DOI: 10.1177/0748233713498438
ISSN/ISBN:1477-0393 (Electronic) 0748-2337 (Linking)
Abstract:"n-Heneicosane (C21) is one of the vital pheromone for attracting mosquitoes of Aedes spp to lay their eggs in areas of stagnant fresh water, for their subsequent destruction, thus controlling spread of dangerous disease transmission by the vectors. As part of a safety evaluation, we have investigated embryo toxic and teratogenic potential, if any, of C21 following OECD Test Guideline 414. C21 was offered at a dose of 1 g/kg body weight mixed in the standard rat pellet diet to treated rats, whereas the control group received only standard rat pellet diet. There were no mortalities and animals did not show any clinical signs of toxicity. A similar pattern of body weight gain, feed and water intake was observed in treated and control groups. Analysis of maternal toxic response, maternal end points of development of the foetus and developmental end points for litters did not show any gross structural abnormality in dams or foetus of treated group compared to that of the control group. Thus, it was concluded that C21 at a dose of 1 g/kg was neither embryo toxic nor teratogenic in Wister rats. Furthermore, the no observed adverse effect level for teratogenicity for C21 in rats may be considered as 1 g/kg body weight under the present experimental conditions"
Keywords:"Alkanes/*toxicity Animals Dose-Response Relationship, Drug Female Fetal Development/*drug effects Fetus/*drug effects Male No-Observed-Adverse-Effect Level Organ Size/drug effects Rats Rats, Wistar Teratogens/toxicity Weight Gain developmental toxicity em;"
Notes:"MedlineKumar, Pravin Lomash, Vinay Jatav, P C Kumar, A Pant, S C eng England 2013/09/26 Toxicol Ind Health. 2016 Jan; 32(1):118-25. doi: 10.1177/0748233713498438. Epub 2013 Sep 23"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024