Forsythia suspensa (Thunb.) Vahl extract ameliorates ulcerative colitis
via inhibiting NLRP3 inflammasome activation through the
TLR4/MyD88/NF-κB pathway
Abstract
Background: Ulcerative colitis (UC) is a chronic inflammatory disease
caused by abnormal immune system reactions resulting in inflammation and
ulcers in the large intestine. Phillygenin (PHI) is a natural compound
found in Forsythia suspensa (Thunb.) Vahl, known for its various
bioactivities, including anti-inflammatory, anti-obesity, and
antipyretic activities. However, the potential anti-inflammatory effects
of PHI on UC and its underlying mechanisms are still poorly understood.
Methods: In this study, we investigated the therapeutic effects of PHI
on acute UC induced by DSS and TNBS. We evaluated the effects of PHI on
disease activity index, body weight, mortality, intestinal mucosal
barrier, cytokine secretion, and macrophage infiltration into colon
tissue using various techniques such as flow cytometry,
immunofluorescence, ELISA, RT-qPCR, and Western blotting. Results: Our
findings revealed that PHI has therapeutic properties in UC treatment.
PHI was able to maintain body weight, reduce disease activity index and
mortality, restore the intestinal mucosal barrier, and inhibit cytokine
secretion. Flow cytometry assay and immunofluorescence indicated that
PHI reduces macrophage infiltration into colon tissue. Additionally,
both in vivo and in vitro results suggested that PHI may exert
anti-inflammatory effects by downregulating the TLR4/MyD88/NF-κB
pathway, inhibiting NLRP3 inflammasome activation. Conclusion: In
conclusion, PHI possesses anti-inflammatory properties and has the
potential as a therapeutic agent for the treatment of UC. Our study
provides insights into the underlying mechanisms of PHI’s therapeutic
effects and highlights the potential for further research in developing
PHI-based treatments for UC.