Xu_2024_BMC.Gastroenterol_24_151

Reference

Title : Vitamin B6 ameliorates acute pancreatitis by suppressing the caspase3 signaling pathway - Xu_2024_BMC.Gastroenterol_24_151
Author(s) : Xu H , Yue H , Ge H , Wang F
Ref : BMC Gastroenterol , 24 :151 , 2024
Abstract :

BACKGROUND: Acute pancreatitis (AP) is a prevalent exocrine inflammatory disorder of the pancreas characterized by pancreatic inflammation and injury to acinar cells. Vitamin B6 (VB6) is a vital nutrient that plays a significant role in preserving human health and has anti-inflammatory and anti-apoptotic effects. METHODS: This study aimed to explore the potential pancreatic protective effects of VB6 in mitigating pancreatic inflammation and apoptosis induced by taurocholate sodium (TLCS) in an AP model and to assess the underlying mechanism of action. AP was induced in SpragueDawley (SD) rats through TLCS administration and lipopolysaccharide (LPS)-treated AR42J cells, followed by treatment with VB6. RESULTS: Various parameters associated with AP were assessed in both plasma and pancreatic tissues. VB6 has been shown to ameliorate the severity of AP through various mechanisms. It effectively reduces the levels of serum amylase, lipase, and inflammatory factors, thereby mitigating histological injury to the pancreas. Moreover, VB6 inhibited pancreatic apoptosis by downregulating bax expression and up-regulating Bcl2 expression in TLCS-treated rats. Additionally, VB6 suppressed the expression of caspase3. The anti-inflammatory and anti-apoptotic effects of VB6 observed in LPS-treated AR42J cells are consistent with those observed in a rat model of AP. CONCLUSIONS: These results suggest that VB6 exerts anti-inflammatory and anti-apoptotic effects through inhibition of the caspase3 signaling pathway and has a protective effect against AP.

PubMedSearch : Xu_2024_BMC.Gastroenterol_24_151
PubMedID: 38698325

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Citations formats

Xu H, Yue H, Ge H, Wang F (2024)
Vitamin B6 ameliorates acute pancreatitis by suppressing the caspase3 signaling pathway
BMC Gastroenterol 24 :151

Xu H, Yue H, Ge H, Wang F (2024)
BMC Gastroenterol 24 :151