Neurodevelopmental disorders and gut-brain interactions: exploring the therapeutic potential of pycnogenol through

Ling Chen1, Zhiqiang Li1, Yuying Fan1

  • 1Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.

Insights

Neurodevelopmental disorders (NDDs) involve gut-brain axis disruption. Pycnogenol may offer a new treatment strategy by modulating gut microbiota and reducing inflammation in NDDs like ADHD and ASD.

Area of Science:

  • Neuroscience
  • Gastroenterology
  • Pharmacology

Background:

  • Neurodevelopmental disorders (NDDs), including autism spectrum disorder (ASD) and attention-deficit hyperactivity disorder (ADHD), exhibit complex pathogenesis involving genetic, environmental, and neurochemical factors.
  • Disruption of the gut-brain axis and gastrointestinal comorbidities (GIDs) are increasingly recognized as potential contributors to NDD pathophysiology.
  • Key signaling pathways like NF-κB, MAPK, and PI3K/AKT/mTOR are implicated in NDD pathogenesis.

Purpose of the Study:

  • To review the pathological mechanisms of ADHD, ASD, and epilepsy.
  • To analyze the relationship between gut-brain axis dysregulation and GIDs in NDDs.
  • To explore pycnogenol (PYC) as a potential therapeutic agent for NDDs by targeting the gut-brain axis.

Main Methods:

  • Comprehensive literature review of NDD pathogenesis, gut-brain axis, and GIDs.
  • Analysis of signaling pathways (NF-κB, MAPK, PI3K/AKT/mTOR) in NDDs.
  • Evaluation of pycnogenol's (PYC) proposed mechanisms of action on the gut-brain axis.

Main Results:

  • Gut-brain axis disruption and GIDs are linked to NDDs.
  • Abnormal signaling pathways are associated with NDD pathogenesis.
  • Pycnogenol (PYC) demonstrates anti-inflammatory and antioxidant properties, potentially benefiting the gut-brain axis.

Conclusions:

  • Targeting the gut-brain axis presents a novel therapeutic avenue for NDDs.
  • Pycnogenol (PYC) may improve NDDs by regulating gut microbiota (e.g., *Akkermansia muciniphila*) and metabolites.
  • Further research into PYC for NDD treatment is warranted.