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1.
J Vis Exp ; (203)2024 Jan 12.
Article in English | MEDLINE | ID: mdl-38284527

ABSTRACT

We developed a simple screening system for the evaluation of neuromuscular and general toxicity in zebrafish embryos. The modular system consists of electrodynamic transducers above which tissue culture dishes with embryos can be placed. Multiple such loudspeaker-tissue culture dish pairs can be combined. Vibrational stimuli generated by the electrodynamic transducers induce a characteristic startle and escape response in the embryos. A belt-driven linear drive sequentially positions a camera above each loudspeaker to record the movement of the embryos. In this way, alterations to the startle response due to lethality or neuromuscular toxicity of chemical compounds can be visualized and quantified. We present an example of the workflow for chemical compound screening using this system, including the preparation of embryos and treatment solutions, operation of the recording system, and data analysis to calculate benchmark concentration values of compounds active in the assay. The modular assembly based on commercially available simple components makes this system both economical and flexibly adaptable to the needs of particular laboratory setups and screening purposes.


Subject(s)
Reflex, Startle , Zebrafish , Animals , Zebrafish/physiology , Vibration , Movement , Biological Assay , Embryo, Nonmammalian
2.
Methods Enzymol ; 602: 189-209, 2018.
Article in English | MEDLINE | ID: mdl-29588029

ABSTRACT

General anesthetics are small molecules that interact with and effect the function of many different proteins to promote loss of consciousness, amnesia, and sometimes, analgesia. Owing to the complexity of this state transition and the transient nature of these drug/protein interactions, anesthetics can be difficult to study. The zebrafish is an emerging model for the discovery of both new genes required for the response to and side effects of anesthesia. Here we discuss the tools available to manipulate the zebrafish genome, including both genetic screens and genome engineering approaches. Additionally, there are various robust behavior assays available to study anesthetic and other drug responses. These assays are available for single-gene study or high throughput for genetic or drug discovery. Finally, we present a case study of using propofol as an anesthetic in the zebrafish. These techniques and protocols make the zebrafish a powerful model to study anesthetic mechanisms and drug discovery.


Subject(s)
Anesthesia/methods , Anesthetics/pharmacokinetics , High-Throughput Screening Assays/methods , Pharmacogenetics/methods , Zebrafish/genetics , Anesthesia/adverse effects , Anesthetics/administration & dosage , Anesthetics/adverse effects , Animals , Animals, Genetically Modified/genetics , Behavior, Animal/drug effects , Biotransformation/genetics , Disease Models, Animal , Dose-Response Relationship, Drug , Drug Discovery/methods , Gene Editing/methods , Gene Knockdown Techniques/instrumentation , Gene Knockdown Techniques/methods , High-Throughput Screening Assays/instrumentation , Humans , Mutation , Pharmacogenomic Variants/genetics , Propofol/administration & dosage , Propofol/adverse effects , Propofol/pharmacokinetics , Zebrafish Proteins/genetics
3.
Bioengineered ; 7(4): 261-5, 2016 Jul 03.
Article in English | MEDLINE | ID: mdl-27285638

ABSTRACT

Over the last years, the zebrafish (Danio rerio) has become a key model organism in genetic and chemical screenings. A growing number of experiments and an expanding interest in zebrafish research makes it increasingly essential to automatize the distribution of embryos and larvae into standard microtiter plates or other sample holders for screening, often according to phenotypical features. Until now, such sorting processes have been carried out by manually handling the larvae and manual feature detection. Here, a prototype platform for image acquisition together with a classification software is presented. Zebrafish embryos and larvae and their features such as pigmentation are detected automatically from the image. Zebrafish of 4 different phenotypes can be classified through pattern recognition at 72 h post fertilization (hpf), allowing the software to classify an embryo into 2 distinct phenotypic classes: wild-type versus variant. The zebrafish phenotypes are classified with an accuracy of 79-99% without any user interaction. A description of the prototype platform and of the algorithms for image processing and pattern recognition is presented.


Subject(s)
Pattern Recognition, Automated , Zebrafish/embryology , Zebrafish/genetics , Algorithms , Animals , High-Throughput Screening Assays , Image Processing, Computer-Assisted , Larva/genetics , Larva/metabolism , Models, Genetic , Phenotype , Software
4.
Article in English | MEDLINE | ID: mdl-26738083

ABSTRACT

The zebrafish (Danio rerio) is a well-established vertebrate model organism. Its embryos are used extensively in biology and medicine to perform chemical screens to identify drug candidates or to evaluate teratogenicity and embryotoxicity of substances. Behavioral readouts are increasingly used to assess the effects of compounds on the nervous system. Early stage zebrafish show characteristic behavioral features at stages between 30 and 42 hours post fertilization (hpf) when exposed to a short and bright light flash. This so-called Photomotor Response (PMR) is a reaction of the nervous system of the fish and can be used as a marker in screenings for neuroactive chemicals. To probe a broad and diverse chemical space, many different substances have to be tested and repeated observations are necessary to warrant statistical significance of the results. Although PMR-based chemical screens must use a large number of specimens, there is no sophisticated, automated high-throughput platform available which ensures minimal human intervention. Here we report a PMR platform that was developed by combining an improved automatic sample handling with a remotely controllable microscope setup and an image analysis pipeline. Using infrared illumination during automatic sample preparation, we were able to eliminate excess amounts of visible light that could potentially alter the response results. A remotely controlled microscope setup allows us to screen entire 96-well microtiter plates without human presence that could disturb the embryos. The development of custom video analysis software, including single egg detection, enables us to detect variance among treated specimens and extract easy to interpret numerical values representing the PMR motion. By testing several neuroactive compounds we validated the workflow that can be used to analyze more than one thousand zebrafish eggs on a single 96-well plate.


Subject(s)
Drug Evaluation, Preclinical/methods , Embryo, Nonmammalian/drug effects , Embryo, Nonmammalian/radiation effects , Image Processing, Computer-Assisted/methods , Toxicity Tests/methods , Animals , Humans , Zebrafish
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