Journal
NEUROBIOLOGY OF DISEASE
Volume 176, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2022.105944
Keywords
Autism spectrum disorder; Amygdala; cFos; Circadian; Cntnap2 knock out; Light pollution; Melanopsin; Mice
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Many patients with autism spectrum disorders (ASD) have disrupted sleep/wake cycles and may be more vulnerable to the effects of circadian disruptors. Previous research has shown that exposure to dim light at night (DLaN) for 2 weeks disrupts diurnal rhythms, increases repetitive behaviors, and reduces social interactions. This study found that shifting the DLaN stimulus to longer wavelengths mitigated the negative impact on activity rhythms and 'autistic' behaviors in both neurotypical and vulnerable populations. These findings highlight the importance of considering the spectral properties of light at night for optimizing health.
Many patients with autism spectrum disorders (ASD) show disturbances in their sleep/wake cycles, and they may be particularly vulnerable to the impact of circadian disruptors. We have previously shown that a 2-weeks exposure to dim light at night (DLaN) disrupts diurnal rhythms, increases repetitive behaviors and reduces so-cial interactions in contactin-associated protein-like 2 knock out (Cntnap2 KO) mice. The deleterious effects of DLaN may be mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopig-ment melanopsin, which is maximally sensitive to blue light (480 nm). In this study, the usage of a light-emitting diode array enabled us to shift the spectral properties of the DLaN while keeping the intensity of the illumination at 10 lx. First, we confirmed that the short-wavelength enriched lighting produced strong acute suppression of locomotor activity (masking), robust light-induced phase shifts, and cFos expression in the suprachiasmatic nucleus in wild-type (WT) mice, while the long-wavelength enriched lighting evoked much weaker responses. Opn4DTA mice, lacking the melanopsin expressing ipRGCs, were resistant to DLaN effects. Importantly, shifting the DLaN stimulus to longer wavelengths mitigated the negative impact on the activity rhythms and 'autistic' behaviors (i.e. reciprocal social interactions, repetitive grooming) in the Cntnap2 KO as well as in WT mice. The short-, but not the long-wavelength enriched, DLaN triggered cFos expression in in the basolateral amygdala (BLA) as well as in the peri-habenula region raising that possibility that these cell populations may mediate the effects. Broadly, our findings are consistent with the recommendation that spectral properties of light at night should be considered to optimize health in neurotypical as well as vulnerable populations.
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