AI Article Synopsis

  • Clinical trials on L-carnosine supplementation in children with autism spectrum disorder (ASD) have shown mixed results, and animal studies had not yet been conducted until this research.
  • In CD157KO mice, a model for ASD, oral L-carnosine supplementation improved social behavior deficits and increased c-Fos-positive neurons in brain regions related to social behavior.
  • The findings suggest that L-carnosine may enhance social recognition impairments by boosting oxytocin levels, indicating a potential safe nutritional intervention for some individuals with ASD.

Article Abstract

The outcomes of supplementation with L-carnosine have been investigated in clinical trials in children with autism spectrum disorder (ASD). However, reports on the effects of L-carnosine in humans have been inconsistent, and the efficacy of L-carnosine supplementation for improving ASD symptoms has yet to be investigated in animal studies. Here, we examined the effects of oral supplementation with L-carnosine on social deficits in CD157KO mice, a murine model of ASD. Social deficits in CD157KO mice were assessed using a three-chamber social approach test. Oral supplementation with L-carnosine attenuated social behavioral deficits. The number of c-Fos-positive oxytocin neurons in the supraoptic nucleus and paraventricular nucleus was increased with L-carnosine supplementation in CD157KO mice after the three-chamber social approach test. We observed an increase in the number of c-Fos-positive neurons in the basolateral amygdala, a brain region involved in social behavior. Although the expression of oxytocin and oxytocin receptors in the hypothalamus was not altered by L-carnosine supplementation, the concentration of oxytocin in cerebrospinal fluid was increased in CD157KO mice by L-carnosine supplementation. These results suggest that L-carnosine supplementation restores social recognition impairments by augmenting the level of released oxytocin. Thus, we could imply the possibility of a safe nutritional intervention for at least some types of ASD in the human population.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879915PMC
http://dx.doi.org/10.3390/nu14040803DOI Listing

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