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Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation.
Pluimer, Brock R; Harrison, Devin L; Boonyavairoje, Chanon; Prinssen, Eric P; Rogers-Evans, Mark; Peterson, Randall T; Thyme, Summer B; Nath, Anjali K.
Afiliação
  • Pluimer BR; Cardiovascular Research Center, Massachusetts General Hospital, Charlestown, MA 02129, USA.
  • Harrison DL; Cardiovascular Research Center, Massachusetts General Hospital, Charlestown, MA 02129, USA.
  • Boonyavairoje C; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
  • Prinssen EP; Roche Pharmaceutical Research and Early Development, Roche Innovation Center Basel, Grenzacherstrasse 124, 4070 Basel, Switzerland.
  • Rogers-Evans M; Roche Pharmaceutical Research and Early Development, Roche Innovation Center Basel, Grenzacherstrasse 124, 4070 Basel, Switzerland.
  • Peterson RT; Deparment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, UT 84112, USA.
  • Thyme SB; Department of Neurobiology, University of Alabama, Birmingham, AL 35294, USA.
  • Nath AK; Cardiovascular Research Center, Massachusetts General Hospital, Charlestown, MA 02129, USA.
iScience ; 26(7): 107099, 2023 Jul 21.
Article em En | MEDLINE | ID: mdl-37416451
ABSTRACT
DISC1 is a genetic risk factor for multiple psychiatric disorders. Compared to the dozens of murine Disc1 models, there is a paucity of zebrafish disc1 models-an organism amenable to high-throughput experimentation. We conducted the longitudinal neurobehavioral analysis of disc1 mutant zebrafish across key stages of life. During early developmental stages, disc1 mutants exhibited abrogated behavioral responses to sensory stimuli across multiple testing platforms. Moreover, during exposure to an acoustic sensory stimulus, loss of disc1 resulted in the abnormal activation of neurons in the pallium, cerebellum, and tectum-anatomical sites involved in the integration of sensory perception and motor control. In adulthood, disc1 mutants exhibited sexually dimorphic reduction in anxiogenic behavior in novel paradigms. Together, these findings implicate disc1 in sensorimotor processes and the genesis of anxiogenic behaviors, which could be exploited for the development of novel treatments in addition to investigating the biology of sensorimotor transformation in the context of disc1 deletion.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: IScience Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: IScience Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos