AI Article Synopsis

  • The study aimed to investigate the effects of diammonium glycyrrhizinate (DG) on AQP-5 expression in a mouse model of acute lung injury induced by lipopolysaccharides (LPS).
  • Thirty male BALB/c mice were divided into control, LPS+DG, and LPS groups to assess lung damage and AQP-5 levels through various tests, including staining and genetic analysis.
  • The results indicated that DG treatment improved lung pathology and increased AQP-5 expression, likely by inhibiting NF-kappaB activation.

Article Abstract

Objective: To determine the therapeutic value and associated mechanism of diammonium glycyrrhizinate (DG) on the expression of AQP-5 in lipapolysacchairides (LPS)-induced acute lung injury in mice.

Methods: Thirty male BALB/c mice were randomly divided into three groups equally: Control, LPS+DG and LPS. HE staining and lung injury score system were used to evaluate the pathological changes in the lung tissues. Wet to dry ratio (W/D) was used to measure the degree of lung edema. RT-PCR and Western blot were obtained to measure AQP-5 expression. Total NF-kappaB p65 and phospho-NF-kappaB p65 (p-NF-kappaB p65) were evaluated by Western blot.

Results: After 3 days of LPS intratracheal injection, severe pathological changes, increased W/D, down-regulated AQP-5 expression and increased p-NF-kappaB p65/total NF-kappaB p65 were observed. Compared with mice in the LPS group, mice in the LPS+DG group had more significantly ameliorated pathological changes and increased W/ D, up-regulated AQP-5 expression, and reduced p-NF-kappaB p65/total NF-kappaB p65.

Conclusion: DG up-regulates AQP-5 in vivo, possibly resulting from inactivation of NF-kappaB.

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