Malachite green (MG) had been extensively used worldwide in the past few decades as an effective fungicide, bactericide, ectoparasiticide, and antiprotozoan on fish. It is rapidly and extensively metabolized to leucomalachite green (LMG) in fishes. To study the developmental toxicity of LMG, we evaluated the maternal and embryo/fetal effects of LMG orally administered to Sprague-Dawley rats once daily from day 6-15 of gestation at dose levels of 0, 10, 80, and 160 mg/kg/day. In the current investigation, the unmetabolized compound (LMG) was detected in the plasma of the dams treated with LMG and in the amniotic fluid. At dose levels of 80 and 160 mg/kg/day, LMG induced maternal toxicity, which consisted of severe reduction in maternal weight and food consumption during the treatment period. Doses of 80 and 160 mg/kg/day induced fetal skeletal abnormalities. The major skeletal defects were bipartite ossification of the thoracic centrum. LMG at 160 mg/kg/day also induced marked embryolethality and visceral abnormalities. Based on the results of this study, a dose level of 10mg/kg/day is considered the no-observed-adverse-effect-level (NOAEL) for maternal and fetal developmental toxicity in rats.
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http://dx.doi.org/10.1016/j.fct.2011.10.003 | DOI Listing |
medRxiv
January 2025
Malaria Research Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Background: The WHO malaria treatment guidelines recommend a total dose in the range of 3·5 to 7·0 mg/kg of primaquine to eliminate () hypnozoites and prevent relapses. There are however indications that for tropical isolates, notably from Southeast Asia, the lower dose of 3·5 mg/kg is insufficient. Determining the most effective regimen to eliminate hypnozoites is needed to achieve elimination of this malaria parasite.
View Article and Find Full Text PDFJ Toxicol
December 2024
Department of Physiology, University of Medical Sciences, Ondo, Ondo, Nigeria.
Crude oil, a major key economic driver in developing countries, is also of environmental concern, linked to neurotoxicity and behavioural problems. Despite the known neurotoxic effects of crude oil and the potential benefits of zinc and vitamin E, there is a paucity of research specifically addressing their combined efficacy in mitigating neurochemical changes and behavioural deficits induced by crude oil. Current studies have largely focussed on the individual effects of these supplements in different contexts, but their synergistic potential in a crude oil exposure model remains underexplored.
View Article and Find Full Text PDFToxicol Rep
December 2024
Department of Pre-Clinical Research, Anthem Biosciences Pvt. Ltd., #49, F1 & F2, Canara Bank Road, Bommasandra Industrial Area Phase 1, Bommasandra, Bengaluru, Karnataka-560099, India.
(S)-Equol is a chemically synthesized nutraceutical compound and its consumption provides several health benefits for humans. The new nutraceutical, enantiopure (S)-Equol was studied for acute and sub-chronic toxicity in Sprague Dawley Rats. The oral acute toxicity study showed that (S)-Equol is safe > 2000-5000 mg/kg body weight and it classified into GHS category 5/Unclassified.
View Article and Find Full Text PDFFront Pharmacol
November 2024
Department of Gynaecology, The Second Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Food Chem Toxicol
December 2024
Research Institute for Fragrance Materials, Inc., 1200 MacArthur Blvd, Suite 306, Mahwah, NJ, 07430, USA.
The existing information supports the use of this material as described in this safety assessment. 4-(4-Methyl-3-penten-1-yl)-2(5H)-furanone was evaluated for genotoxicity, repeated dose toxicity, reproductive toxicity, local respiratory toxicity, photoirritation/photoallergenicity, skin sensitization, and environmental safety. Data show that 4-(4-methyl-3-penten-1-yl)-2(5H)-furanone is not mutagenic.
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