https://pagepressjournals.org/index.php/xeno/issue/feed Journal of Xenobiotics 2018-11-29T17:16:35+01:00 Francesca Baccino francesca.baccino@pagepress.org Open Journal Systems <p>The <strong>Journal of Xenobiotics</strong> publishes original studies concerning the beneficial (pharmacology) and detrimental effects (toxicology) of <em>xenobiotics</em> in all organisms. A xenobiotic (“stranger to life”) is defined as a chemical that is not usually found at significant concentrations or expected to reside for long periods in organisms. In addition to man-made chemicals, natural products could also be of interest if they have potent biological properties, special medicinal properties or that a given organism is at risk of exposure in the environment. Topics dealing with abiotic- and biotic-based transformations in various media (xenobiochemistry) and environmental toxicology are also of interest. Areas of interests include the identification of key physical and chemical properties of molecules that predict biological effects and persistence in the environment; the molecular mode of action of <em>xenobiotics</em>; biochemical and physiological interactions leading to change in organism health; pathophysiological interactions of natural and synthetic chemicals; development of biochemical indicators including new “-omics” approaches to identify biomarkers of exposure or effects for <em>xenobiotics</em>. Studies on the interaction of emerging nano- and biotechnological devices and drug-nanopolymers with living tissues are also of interest to the journal. In addition to research papers, short communications, reviews and mini-reviews, <strong>Journal of Xenobiotics</strong> will publish special issues dealing with the environmental, pharmaceutical and health impacts of new classes of chemicals. In this case, a special issue will be announced and provided at the journal’s web site. Special issues brought by international symposia or other scientific venues are also welcomed.</p> https://pagepressjournals.org/index.php/xeno/article/view/7810 An amplicon-based sequencing approach for the study of aeromycology 2018-11-29T17:16:33+01:00 Hamza Mbareche hamza.mbareche@criucpq.ulaval.ca Marc Veillette hamza.mbareche@criucpq.ulaval.ca Guillaume J. Bilodeau hamza.mbareche@criucpq.ulaval.ca Caroline Duchaine hamza.mbareche@criucpq.ulaval.ca Not available. 2018-10-29T10:52:14+01:00 ##submission.copyrightStatement## https://pagepressjournals.org/index.php/xeno/article/view/7809 Effects of copper on the early development of Xenopus laevis: the case of CuSO4 and Bordeaux mixture solutions 2018-11-29T17:16:34+01:00 P. Titran matthieu.marin@univ-lille.fr S. Slaby matthieu.marin@univ-lille.fr G. Marchand matthieu.marin@univ-lille.fr A. Lescuyer matthieu.marin@univ-lille.fr S. Lemiere matthieu.marin@univ-lille.fr M. Marin matthieu.marin@univ-lille.fr Not available. 2018-10-29T10:52:13+01:00 ##submission.copyrightStatement## https://pagepressjournals.org/index.php/xeno/article/view/7820 Behavioral effects of the neurotoxin ß-N-methylamino-L-alanine on the mangrove rivulus (Kryptolebias marmoratus) larvae 2018-11-29T17:16:33+01:00 Alessandra Carion alessandra.carion@unamur.be Julie Hétru alessandra.carion@unamur.be Angèle Markey alessandra.carion@unamur.be Victoria Suarez-Ulloa alessandra.carion@unamur.be Silvestre Frédéric alessandra.carion@unamur.be Mangrove rivulus, <em>Kryptolebias marmoratus</em>, is a hermaphrodite fish capable of self-fertilization. This particularity allows to naturally produce highly homozygous and isogenic individuals. Despite the low genetic diversity, rivulus can live in extremely variable environments and adjust its phenotype accordingly. This species represents a unique opportunity to clearly distinguish the genetic and non-genetic factors implicated in adaptation and evolution, such as epigenetic mechanisms. It is thus a great model in aquatic ecotoxicology to investigate the effects of xenobiotics on the epigenome, and their potential long-term impacts. In the present study, we used the mangrove rivulus to investigate the effects of the neurotoxin ß-N-methylamino-L-alanine (BMAA) on larvae behaviors after 7 days exposure to two sub-lethal concentrations. Results show that BMAA can affect the maximal speed and prey capture (trials and failures), suggesting potential impacts on the organism’s fitness. 2018-10-29T10:52:13+01:00 ##submission.copyrightStatement## https://pagepressjournals.org/index.php/xeno/article/view/7674 Effects of chronic exposure to benzophenone and diclofenac on DNA methylation levels and reproductive success in a marine copepod 2018-11-29T17:16:35+01:00 Anais Guyon guyon.anais@hotmail.fr Kirsty F. Smith Kirsty.Smith@cawthron.org.nz Maria P. Charry Maria.Charry@cawthron.org.nz Olivier Champeau Olivier.Champeau@cawthron.org.nz Louis A. Tremblay louis.tremblay@cawthron.org.nz The UV-filter benzophenone and the anti-inflammatory diclofenac are commonly detected in the environment. The aim of this study was to assess the multigenerational effects of chronic exposure to low concentrations of these chemicals on toxicity and DNA methylation levels in the copepod <em>Gladioferens</em> <em>pectinatus</em>. Acute toxicity tests were conducted to determine the sensitivity of <em>G. pectinatus</em> to the chemicals. All chemicals impacted breeding, hatching and egg viability. Diclofenac (1 mg.L<sup>-1</sup>) reduced the number of eggs per gravid female. Benzophenone (0.5 mg.L<sup>-1</sup>) decreased egg hatching success. Exposure to the reference toxicant copper (0.02 mg.L<sup>-1</sup>) led to unsuccessful hatching. Effects on DNA methylation was estimated by the percentage of 5- methylcytosine. The treatments resulted in strong differences in DNA methylation with increased methylation in the exposed animals. The two chemicals impacted both egg viability and the induction of differential DNA methylation, suggesting potential intra- and trans-generational evolutionary effects. 2018-10-29T10:52:12+01:00 ##submission.copyrightStatement## https://pagepressjournals.org/index.php/xeno/article/view/7149 Thiamethoxam Actara® induced alterations in kidney liver cerebellum and hippocampus of male rats 2018-10-29T11:14:45+01:00 Hassina Khaldoun-Oularbi khaldounhassina@hotmail.fr Noura Bouzid hkhaldoun2005@yahoo.fr Soumia Boukreta hkhaldoun2005@yahoo.fr Chahrazed Makhlouf hkhaldoun2005@yahoo.fr Fariza Derriche hkhaldoun2005@yahoo.fr Nadia Djennas hkhaldoun2005@yahoo.fr Thiamethoxam (TMX), a second-generation neonicotinoid insecticide, is one of the most widely used insecticides in Algeria. The present study assessed the effects of repeated subchronic exposure to the commercial formulation of thiamethoxam (Actara®, 25% WG) in albino male rats. The toxic effects of thiamethoxam (TMX) were studied biochemically and histopathologically. Twenty-eight male albino rats weighing between 226 and 243 g were randomly assigned to four groups. One group served as control, and the other three were served as experimental groups administered a neonicotinoid thiamethoxam (TMX; 26, 39 and 78 mg/kg/day) for 6 weeks. The effects of the insecticide on various biochemical parameters were evaluated at 2, 4 and 6 weeks. Histopathological studies were carried out in the liver, kidney, cerebellum and hippocampus at the end of the experiment. Changes in biochemical parameters glucose, ALT (alanine aminotransferase), AST (aspartate aminotransferase), γGT (gamma-glutamyltransferase) ALP (alkaline phosphatase) urea and creatinine were observed in treated-groups in a dose dependent manner when compared to the control. Histopathological alterations were more intense in male rats from the TMX high dose group than those from group 2 and 3. Based on these results, subchronic oral administration of thiamethoxam altered the biochemical parameters, which correlated with histopathological changes in the liver kidney and brain. 2017-12-21T12:42:08+01:00 ##submission.copyrightStatement## https://pagepressjournals.org/index.php/xeno/article/view/7173 Metal contamination of the St. Lawrence River following a major release of untreated wastewater 2018-10-29T11:14:45+01:00 C. Gagnon Christian.gagnon@canada.ca M. Pilote Christian.gagnon@canada.ca P. Turcotte Christian.gagnon@canada.ca C. André Christian.gagnon@canada.ca Not available 2017-11-28T17:09:33+01:00 ##submission.copyrightStatement##