The light/dark preference test is commonly used to assess anxiety-like phenotypes and validate the pharmacological effects of neuroactive compounds. This test has been recently adapted for adult zebrafish but has not yet been characterized and pharmacologically validated for young juvenile zebrafish. In the present study, we provide a detailed description of the pattern of exploratory behaviours encountered in juvenile zebrafish when exposed to the light/dark preference test. We report that juveniles display strong dark-avoidance behaviours in this test. Specifically, juveniles spent significantly less time, displayed high latency to enter and moved significantly less in the dark compartment relative to the white compartment of the testing apparatus. The expression of these dark-avoidance behaviours was significantly attenuated and increased by commonly used anxiolytic (diazepam, buspirone, ethanol) and anxiogenic (caffeine but not FG-7142) drugs, respectively. We also show that the expression of dark-avoidance behaviours can be significantly reduced in a manner similar to what is achieved with anxiolytic drugs, simply by decreasing the contrast between the white and dark zones, which made the dark zone less dark. Taken together, these findings provide the first pharmacological validation of the light/dark preference test for juvenile zebrafish and ascertain the nature of dark-avoidance behaviours as anxiety-like behaviours in young juvenile zebrafish. This behavioural-based assay is also versatile and can accommodate drug screening of both anxiolytic and anxiogenic compounds while eventually amenable to automation and high-throughput capacity in a near future.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.bbr.2011.03.025 | DOI Listing |
PLoS Genet
January 2025
Department of Developmental Biology and Cancer Research, The Hebrew University of Jerusalem Faculty of Medicine, Ein- Kerem Campus, Jerusalem, Israel.
Germ cells are essential for fertility, embryogenesis, and reproduction. Germline development requires distinct types of germ granules, which contains RNA-protein (RNP) complexes, including germ plasm in embryos, piRNA granules in gonadal germ cells, and the Balbiani body (Bb) in oocytes. However, the regulation of RNP assemblies in zebrafish germline development are still poorly understood.
View Article and Find Full Text PDFComp Biochem Physiol C Toxicol Pharmacol
January 2025
Center for Clinical Medicine Research, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, Jiangxi Province, China. Electronic address:
The compound m-Cresol, also referred to as 3-methylphenol,acts as a precursor in the creation of pesticides and plasticizers. This research has conducted a thorough evaluation of the toxic effects of m-cresol on the cardiac development of juvenile zebrafish, from 6 to 72 hpf. The study's results reveal that higher concentrations of m-Cresol, compared to lower ones, result in more severe heart abnormalities in zebrafish larvae.
View Article and Find Full Text PDFWhile pancreatic beta-cell proliferation has been extensively studied, the role of cell death during islet development remains incompletely understood. Using a genetic model of caspase inhibition in beta cells coupled with mathematical modeling, we here discover an onset of beta-cell death in juvenile zebrafish, which regulates beta-cell mass. Histologically, this beta-cell death is underestimated due to phagocytosis by resident macrophages.
View Article and Find Full Text PDFAquat Toxicol
December 2024
School of Emergency Management, School of the Environment and Safety, Jiangsu University, 301 Xuefu Rd., Zhenjiang, Jiangsu 212013, China. Electronic address:
Monoethylhexyl phthalate (MEHP) is the primary metabolite of di(2-ethylhexyl) phthalate (DEHP), the most prevalent phthalate plasticiser globally. It has been demonstrated that MEHP exerts more potent toxic effects than DEHP. Nevertheless, the full extent of the toxicity of MEHP to neurodevelopmental organisms remains unclear.
View Article and Find Full Text PDFBio Protoc
December 2024
Division of Life Science, Graduate School of Science and Engineering, Saitama University, Shimo-Okubo 255, Sakura-ku, Saitama, Japan.
Zebrafish and medaka are valuable model vertebrates for genetic studies. The advent of CRISPR-Cas9 technology has greatly enhanced our capability to produce specific gene mutants in zebrafish and medaka. Analyzing the phenotypes of these mutants is essential for elucidating gene function, though such analyses often yield unexpected results.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!