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Temephos is an organophosphorus pesticide used in control campaigns against vectors that transmit diseases, including dengue, a public health concern. The WHO classifies temephos in category III and its safe concentration (low-observable-adverse-effect level) in male rats is 100 mg/kg/day for up to 44 days. Temephos inhibits acetylcholinesterase (AChE) and is metabolized in different tissues, probably by mixed-function oxidases; one of its metabolites is bisphenol S (BPS), which is considered an endocrine disruptor. The aim of this study was to evaluate the effects of temephos on sperm function and its biotransformation in the testis, epididymis, and other tissues to explore its toxicity in rats treated with 100 mg/kg/day/5 or 7 days (gavage). AChE activity was inhibited 70% starting on day 3 and 13 or 41% mortality was observed at 5 or 7 days, respectively. After 7 days, temephos significantly decreased sperm motility (30%) and viability (10%) and increased (10%) lipoperoxidation, and the sperm DNA exhibited no damage. Temephos was distributed and metabolized in all tissues, with the highest levels observed in the adipose tissue and temephos levels were 16-fold higher in the epididymis than in the testis. Notably, BPS was observed in the testis. At 5 days, decreased sperm motility (12.5%) and viability (5.7%) were observed and sperm fertilization decreased (30%). These results suggest that temephos decreases sperm quality and fertilization capacity at recommended safe concentrations and that it is metabolized in male reproductive tissues. This pesticide places the reproductive health of exposed people at risk, suggesting the need to reevaluate its toxicity.
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http://dx.doi.org/10.1093/toxsci/kfab100 | DOI Listing |
Am J Trop Med Hyg
August 2025
ICMR-National Institute of Malaria Research Field Unit, Chennai, India.
This study aimed to evaluate the susceptibility of immature Anopheles stephensi to temephos formulation, a primary antilarval intervention currently in operational use. The assessment was conducted against both the WHO-recommended discriminatory dosage with temephos (0.25 parts per million [ppm]) and the operational field dosage with temephos 50% emulsifiable concentrate (EC; 1 ppm).
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
August 2025
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques of Fez, Sidi Mohamed Ben Abdellah University, Fez, Morocco.
The growing need for sustainable mosquito control solutions led us to develop an optimized larvicidal formulation against Culex pipiens Linnaeus, 1758 (Diptera: Culicidae), a key disease vector. Based on preliminary LC evaluations, we developed a synergistic essential oil (EO) blend composed of Artemisia absinthium Linnaeus (58%), A. arborescens L.
View Article and Find Full Text PDFInsects
July 2025
Office of Administrative Interdisciplinary Program on Agricultural Technology, School of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang, Ladkrabang, Bangkok 10520, Thailand.
The present study evaluated the larvicidal and pupicidal activities of pure and mixed monoterpene formulations-eucalyptol, geranial, -anethole, and -cinnamaldehyde-against and compared them with 1% (/) temephos. Safety bioassays of all formulations on non-target species confirmed their safety. The combined mixture of eucalyptol + -anethole at 400 µg/mL exhibited stronger larvicidal activity, with an LC of 176 µg/mL, while the combination of -anethole + geranial at 400 µg/mL exhibited stronger pupicidal activity with an LC of 167 µg/mL.
View Article and Find Full Text PDFJ Med Entomol
July 2025
Insect Biochemistry and Molecular Biology Laboratory, Department of Zoology, University of North Bengal, Darjeeling, West Bengal, India.
Dengue cases are increasing every year in the sub-Himalayan part of West Bengal, where Aedes albopictus (Skuse 1894) has emerged as a predominant dengue vector. Dengue management heavily relies on the recurrent application of chemical insecticides such as temephos (larvicide) and deltamethrin (adulticide). However Ae.
View Article and Find Full Text PDFJ Biomol Struct Dyn
July 2025
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research Raebareli (NIPER-R), Lucknow, UP, India.
A series of novel dichloroindolizine carboxylate analogues () have been prepared by using 3,5-dichloropyridine, and substituted phenacyl bromide with electron-deficient acetylene a [3 + 2] cycloaddition reaction. This methodology features a reaction that is free from transition metal or catalyst, providing an eco-friendly synthesis for developing dichloroindolizines. All the synthesized products () were characterized by H NMR,C NMR, and HRMS spectroscopic techniques.
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