| Literature DB >> 35537819 |
Michael Palillo1, Jack Palillo2, Nonyé Williams1, Mary White3, Mael Glon4, Lauren Pintor5, Willie Bidot6, Nguyen K Tram7, Mitchel R Stacy8, Genevieve Kendall9, Dondrae Coble10, Raphael Malbrue11.
Abstract
Crayfish (Decapoda: Astacoidea and Parastacoidea) are among the few animals that have stem cells in hemolymph, with the capacity to continuously produce differentiated neuronal structures throughout life. As the use of crayfish and other invertebrates increases in biomedical research, we must develop laboratory standards and guidelines for performing clinical procedures. This manuscript presents introductory protocols for anesthesia in crayfish during diagnostic imaging. Five anesthetic protocols were evaluated: immersion in buffered tricaine methanesulfonate (MS222; 50 mg/L); immersion in buffered MS222 (150 mg/L); immersion in propofol (65 mg/L); injection of propofol (50 mg/kg); and injection of propofol (100 mg/kg) into the ventral surface of an abdominal somite. MS222 immersion (50 and 150 mg/L) had no observable effect on crayfish. After an extended period of time, immersion in propofol (65 mg/L) created a sedative effect suitable for short-term handling. Propofol injection (50 mg/kg) into the ventral surface of an abdominal somite created an effective plane of anesthesia without adverse effects during or after recovery. Propofol injection at 100 mg/kg had adverse effects and is not recommended for use in crayfish. CT imaging was performed successfully as proof of concept for handling anesthetized crayfish. These findings provide initial data for the anesthetization of crayfish used in research settings.Entities:
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Year: 2022 PMID: 35537819 PMCID: PMC9137292 DOI: 10.30802/AALAS-JAALAS-21-000133
Source DB: PubMed Journal: J Am Assoc Lab Anim Sci ISSN: 1559-6109 Impact factor: 1.706