Open Access
Issue |
Med Sci (Paris)
Volume 35, Number 6-7, Juin-Juillet 2019
Modèles alternatifs
|
|
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Page(s) | 544 - 548 | |
Section | M/S Revues | |
DOI | https://doi.org/10.1051/medsci/2019110 | |
Published online | 05 July 2019 |
- Wu JP, Li MH. The use of freshwater planarians in environmental toxicology studies: advantages and potential. Ecotoxicol Environ Saf 2018 ; 161 : 45–56. [CrossRef] [PubMed] [Google Scholar]
- Rink JC. Stem cell systems and regeneration in planaria. Dev Genes Evol 2013 ; 223 : 67–84. [CrossRef] [PubMed] [Google Scholar]
- Torre C, Ghigo E. La planaire : un ver immortel pour élucider la réponse immunitaire de l’homme. Med Sci (Paris) 2015 ; 31 : 20–22. [Google Scholar]
- Morgan TH. Experimental studies of the regeneration of Planaria maculata. Rouxs Arch Dev Biol 1898 ; 7 : 364–397. [Google Scholar]
- Saló E.. The power of regeneration and the stem-cell kingdom: freshwater planarians (Platyhelminthes). BioEssays 2006 ; 28 : 546–559. [CrossRef] [PubMed] [Google Scholar]
- Reddien PW, Alvarado AS. Fundamentals of planarian regeneration. Annu Rev Cell Dev Biol 2004 ; 20 : 725–757. [CrossRef] [PubMed] [Google Scholar]
- Newmark PA, Alvarado AS. Not your father’s planarian: a classic model enters the era of functional genomics. Nat Rev Genet 2002 ; 3 : 210–219. [CrossRef] [PubMed] [Google Scholar]
- Byrne JH. The Oxford handbook of invertebrate neurobiology 2019 ; Oxford Oxford University Press 778 p [CrossRef] [Google Scholar]
- Brown DDR, Molinaro AM, Pearson BJ. The planarian TCF/LEF factor Smed-tcf1 is required for the regeneration of dorsal-lateral neuronal subtypes. Dev Biol 2018 ; 433 : 374–383. [CrossRef] [PubMed] [Google Scholar]
- Sarnat HB, Netsky MG. The brain of the planarian as the ancestor of the human brain. Can J Neurol Sci J Can Sci Neurol 1985 ; 12 : 296–302. [CrossRef] [Google Scholar]
- Kitamura Y, Kakimura J, Taniguchi T. Protective effect of talipexole on MPTP-treated planarian, a unique parkinsonian worm model. Jpn J Pharmacol 1998 ; 78 : 23–29. [CrossRef] [PubMed] [Google Scholar]
- Inden M, Kitamura Y, Taniguchi T, et al. Parkinsonian model of planarian, an invertebrate flatworm. Int Congr Ser 2004 ; 1260 : 291–295. [Google Scholar]
- Zhang S, Hagstrom D, Hayes P, et al. Multi-behavioral endpoint testing of an 87-chemical compound library in freshwater planarians. Toxicol Sci 2019 ; 167 : 26–44. [CrossRef] [PubMed] [Google Scholar]
- Ofoegbu PU, Lourenço J, Mendo S, et al. Effects of low concentrations of psychiatric drugs (carbamazepine and fluoxetine) on the freshwater planarian. Schmidtea mediterranea. Chemosphere 2019 ; 217 : 542–549. [Google Scholar]
- Mazzitelli J-Y, Budzinski H, Cachot J, et al. Evaluation of psychiatric hospital wastewater toxicity: what is its impact on aquatic organisms?. Environ Sci Pollut Res 2018 ; 25 : 26090–26102. [CrossRef] [Google Scholar]
- Ofoegbu PU, Campos D, Soares AMVM, et al. Combined effects of NaCl and fluoxetine on the freshwater planarian, Schmidtea mediterranea (Platyhelminthes: Dugesiidae). Environ Sci Pollut Res 2019; Feb 23. doi: 10.1007/s11356-019-04532-4. [Google Scholar]
- Bezerra da Silva C, Pott A, Elifio-Esposito S, et al. Effect of Donepezil, Tacrine, Galantamine and Rivastigmine on acetylcholinesterase inhibition in Dugesia tigrina. Molecules 2016 ; 21 : 53. [CrossRef] [PubMed] [Google Scholar]
- Margotta V, Caronti B, Meco G, et al. Effects of cocaine treatment on the nervous system of planaria (Dugesia gonocephala s. l.). Histochemical and ultrastructural observations. Eur J Histochem 1997 ; 41 : 223–230. [PubMed] [Google Scholar]
- Duruibe J., Ogwuegbu M.O., Egwurugwu J.. Heavy metal pollution and human biotoxic effects. Int J Phys Sci 2007 ; 2 : 112–118. [Google Scholar]
- Medvedev IV. Regeneration in two freshwater planarian species exposed to methylmercury compounds. Russ J Dev Biol 2008 ; 39 : 232–235. [CrossRef] [Google Scholar]
- Knakievicz T, Ferreira HB. Evaluation of copper effects upon Girardia tigrina freshwater planarians based on a set of biomarkers. Chemosphere 2008 ; 71 : 419–428. [CrossRef] [PubMed] [Google Scholar]
- García-Medin S, García-Medina L, Galar-Martinez M, et al. Genotoxicity and oxidative stress induced by cadmium and zinc in the planarian. Dugesia dorotocephala. Afr J Biotechnol 2013 ; 12 : 4028–4038. [Google Scholar]
- Wu JP, Lee HL, Li MH. Cadmium neurotoxicity to a freshwater planarian. Arch Environ Contam Toxicol 2014 ; 67 : 639–650. [CrossRef] [PubMed] [Google Scholar]
- Leynen N, Bellegem FGAJV, Wouters A, et al. In vivo toxicity assessment of silver nanoparticles in homeostatic versus regenerating planarians. Nanotoxicology 2019 ; 0 : 1–16. [Google Scholar]
- Villar D, Gonzalez M, Gualda MJ, et al. Effects of organophosphorus insecticides on Dugesia tigrina: cholinesterase activity and head regeneration. Bull Environ Contam Toxicol 1994 ; 52 : 319–324. [CrossRef] [PubMed] [Google Scholar]
- Poirier L, Brun L, Jacquet P, et al. Enzymatic degradation of organophosphorus insecticides decreases toxicity in planarians and enhances survival. Sci Rep 2017 ; 7 : 15194. [CrossRef] [PubMed] [Google Scholar]
- Rodrigues ACM, Henriques JF, Domingues I, et al. Behavioural responses of freshwater planarians after short-term exposure to the insecticide chlorantraniliprole. Aquat Toxicol 2016 ; 170 : 371–376. [CrossRef] [PubMed] [Google Scholar]
- Hagstrom D, Cochet-Escartin O, Zhang S, et al. Freshwater planarians as an alternative animal model for neurotoxicology. Toxicol Sci 2015 ; 147 : 270–285. [CrossRef] [PubMed] [Google Scholar]
- Hagstrom D, Hirokawa H, Zhang L, et al. Planarian cholinesterase: in vitro characterization of an evolutionarily ancient enzyme to study organophosphorus pesticide toxicity and reactivation. Arch Toxicol 2017 ; 91 : 2837–2847. [CrossRef] [PubMed] [Google Scholar]
- Feldhaus JM, Feldhaus AJ, Ace LN, et al. Interactive effects of pesticide mixtures on the neurobehavioral responses and ache levels of Planaria. Environ Toxicol Risk Assess 1998 ; 1333 : 140–150. [Google Scholar]
- Yuan Z, Shao X, Miao Z, et al. Perfluorooctane sulfonate induced neurotoxicity responses associated with neural genes expression, neurotransmitter levels and acetylcholinesterase activity in planarians Dugesia japonica. Chemosphere 2018 ; 206 : 150–156. [CrossRef] [PubMed] [Google Scholar]
- Zhang S, Ireland D, Sipes NS, et al. Screening for neurotoxic potential of 15 flame retardants using freshwater planarians. bioRxiv 2019; doi: https://doi.org/10.1101/538280. [Google Scholar]
- Hagstrom D, Truong L, Zhang S, et al. Comparative analysis of zebrafish and planarian model systems for developmental neurotoxicity screens using an 87-compound library. Toxicol Sci 2019 ; 167 : 15–25. [CrossRef] [PubMed] [Google Scholar]
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