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The influence of HINT1 protein in nucleus accumbens on aggressive behavior and anxiety-like behavior

  • Yongkang Ma,
  • Dianying Liu,
  • Ruichao Wen,
  • Shaofu Li,
  • Leile Zhang,
  • Huiling Hu,
  • Jingmiao Xu,
  • Zhengqi Li,
  • Tong Su,
  • Sareen Akhtar,
  • Hang Jing,
  • Xiaogang Li,
  • Hui Zhang,
  • Yonghui Dang

摘要

Objective

Histidine triad nucleotide-binding protein 1 (HINT1), implicated in psychiatric disorders, is highly expressed in the nucleus accumbens (NAc). Although previous work has linked HINT1 to aggression and anxiety, its specific role and mechanism remain unclear. This study aimed to delineate HINT1 distribution in the NAc and its regulatory function in aggressive and anxiety-like behaviors.

Materials and methods

Using immunofluorescence, we mapped HINT1 expression in wild-type (WT) mouse NAc. Behavioral and molecular analyses were performed on Hint1-knockout (KO) and WT littermates. Adeno-associated virus (AAV) vectors were then used to knock down (KD) or overexpress (OE) Hint1 in the NAc of WT mice for further validation.

Results

HINT1 was expressed in medium spiny neurons (MSN), microglia, oligodendrocytes and cholinergic interneurons (ChINs) in the NAc. The Hint1-KO mice exhibited increased aggression, accompanied by elevated levels of dopamine D1 receptor (D1R), CREB, ΔFOSB, and heightened p-PKA and p-CREB in the NAc. AAV-mediated KD of Hint1enhanced both aggressive and anxiety-like behaviors, whereas OE produced no significant behavioral changes. Molecular upregulation in KD mice mirrored KO alterations but was absent in OE mice. These findings indicate that NAc HINT1 inhibits aggression, likely via suppression of the D1R-PKA-CREB-ΔFOSB pathway, although its role in anxiety-like behavior requires further investigation.

Conclusion

Our findings indicate that HINT1 in the NAc inhibits aggressive behavior. Loss of Hint1 likely leads to enhanced aggression through aberrant activation of the D1R-PKA-CREB-ΔFOSB pathway. The role of HINT1 in anxiety-like behavior and its underlying mechanisms warrants further investigation.