Temperature in freshwater ecosystems fluctuates daily, seasonally and yearly. Climate change further induces temperature variations. In this study, we hypothesise that water temperatures, in particular thermal extremes, can significantly influence chemical toxicity to ectothermic organisms. Although temperature-dependent chemical toxicity (TDCT) is a classic research area in ecotoxicology, a unified model for predicting TDCT for freshwater species is yet to be developed. This study aimed to address this challenging issue through a meta-analysis by comparing acute toxicity endpoints (i.e. median lethal or effective concentration data; LC or EC) of 13 chemicals for various freshwater species generated from different temperatures. Our results suggest that in most cases, freshwater species exhibit the highest tolerance towards chemicals at their physical optimal temperature (T), and chemical toxicity exacerbates when temperature is higher or lower than T (i.e. inverted V-shaped model between temperature and LC or EC). Such observations are further supported by temperature-dependent hazardous concentration 10% (HC) values derived from species sensitivity distributions constructed using toxicity data generated at different temperatures. A unified mathematical model was also developed to describe the inverted V-shape relationship between temperature and HC derivations. Overall, considering the natural variations of freshwater temperatures, the inverted V-shaped TDCT model can be readily applied to derive water quality guidelines and assess ecological risks of chemical contaminants.
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http://dx.doi.org/10.1016/j.chemosphere.2019.02.103 | DOI Listing |
Sci Prog
January 2025
UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
The recent severe acute respiratory syndrome coronavirus 2 pandemic has clearly exemplified the need for broad-spectrum antiviral (BSA) medications. However, previous outbreaks show that about one year after an outbreak, interest in antiviral research diminishes and the work toward an effective medication is left unfinished. Martin et al.
View Article and Find Full Text PDFFront Pharmacol
January 2025
State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Atherosclerotic cardiovascular disease (ASCVD) causes significant morbidity and mortality globally. Most of the chemicals specifically target certain pathways and minimally impact other diseases associated with ASCVD. Moreover, interactions of these drugs can cause toxic reactions.
View Article and Find Full Text PDFCutaneous absorption of methylene chloride is rarely toxic. This case shows that it can lead to carboxyhemoglobinemia. Exposure to methylene chloride should warrant a carboxyhemoglobin check and oxygen support.
View Article and Find Full Text PDFJ Toxicol Pathol
January 2025
Department of Molecular Pathology, Graduate School of Medicine, Osaka Metropolitan University, 1-4-3 Asahi-machi, Abeno-ku, Osaka, Japan.
Occupational exposure to aromatic amines is a major risk factor for urinary bladder cancer. Our previous studies showed that acetoaceto--toluidine, which is produced using -toluidine as a raw material, promotes urinary bladder carcinogenesis in rats. We also found high concentrations of -toluidine, a human bladder carcinogen, in the urine of acetoaceto--toluidine-treated rats, indicating that urinary -toluidine derived from acetoaceto--toluidine may play an important role in bladder carcinogenesis.
View Article and Find Full Text PDFJ Toxicol Pathol
January 2025
Laboratory of Veterinary Pathology, Osaka Metropolitan University, 1-58 Rinku-Ourai-Kita, Izumisano City, Osaka 598-8531, Japan.
The liver, a major organ involved in substance metabolism, is highly susceptible to toxicity induced by chemicals and their metabolites. Although damage-associated molecular patterns (DAMPs) have been implicated in the development of sterile inflammation following cell injury, their involvement in chemically induced hepatocellular injury remains underexplored. This study aimed to determine the role of high-mobility group box 1 (HMGB1), a DAMP, in a rat model of liver injury treated with thioacetamide, a hepatotoxicant.
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