Altered pupil responses to social and non-social stimuli in Shank3 mutant dogs.
Wei RenKang HuangYumo LiQin YangLi-Ping WangKun GuoPengfei WeiYong Q ZhangPublished in: Molecular psychiatry (2023)
Pupillary response, an important process in visual perception and social and emotional cognition, has been widely studied for understanding the neural mechanisms of neuropsychiatric disorders. However, there have been few studies on pupil response to social and non-social stimuli in animal models of neurodevelopmental disorders including autism spectrum disorder (ASD) and attention deficit hyperactivity disorder. Here, we developed a pupilometer using a robust eye feature-detection algorithm for real-time pupillometry in dogs. In a pilot study, we found that a brief light flash induced a less-pronounced and slower pupil dilation response in gene-edited dogs carrying mutations in Shank3; mutations of its ortholog in humans were repeatedly identified in ASD patients. We further found that obnoxious, loud firecracker sound of 120 dB induced a stronger and longer pupil dilation response in Shank3 mutant dogs, whereas a high reward food induced a weaker pupillary response in Shank3 mutants than in wild-type control dogs. In addition, we found that Shank3 mutants showed compromised pupillary synchrony during dog-human interaction. These findings of altered pupil response in Shank3 mutant dogs recapitulate the altered sensory responses in ASD patients. Thus, this study demonstrates the validity and value of the pupilometer for dogs, and provides an effective paradigm for studying the underlying neural mechanisms of ASD and potentially other psychiatric disorders.
Keyphrases
- autism spectrum disorder
- attention deficit hyperactivity disorder
- wild type
- healthcare
- intellectual disability
- mental health
- end stage renal disease
- high glucose
- newly diagnosed
- ejection fraction
- endothelial cells
- diabetic rats
- chronic kidney disease
- machine learning
- prognostic factors
- mild cognitive impairment
- transcription factor
- dna methylation
- multiple sclerosis
- copy number
- white matter
- genome wide identification