Protective effect of sucrose esters from cape gooseberry (Physalis peruviana L.) in TNBS-induced colitis

PLoS One. 2024 Mar 21;19(3):e0299687. doi: 10.1371/journal.pone.0299687. eCollection 2024.

Abstract

Phytotherapy is an attractive strategy to treat inflammatory bowel disease (IBD) that could be especially useful in developing countries. We previously demonstrated the intestinal anti-inflammatory effect of the total ethereal extract from the Physalis peruviana (Cape gooseberry) calyces in TNBS-induced colitis. This work investigates the therapeutic potential of Peruviose A and B, two sucrose esters that constitute the major metabolites of its calyces. The effect of the Peruvioses A and B mixture on TNBS-induced colitis was studied after 3 (preventive) and 15-days (therapy set-up) of colitis induction in rats. Colonic inflammation was assessed by measuring macroscopic/histologic damage, MPO activity, and biochemical changes. Additionally, LPS-stimulated RAW 264.7 macrophages were treated with test compounds to determine the effect on cytokine imbalance in these cells. Peruvioses mixture ameliorated TNBS-induced colitis in acute (preventive) or established (therapeutic) settings. Although 3-day treatment with compounds did not produce a potent effect, it was sufficient to significantly reduce the extent/severity of tissue damage and the microscopic disturbances. Beneficial effects in the therapy set-up were substantially higher and involved the inhibition of pro-inflammatory enzymes (iNOS, COX-2), cytokines (TNF-α, IL-1β, and IL-6), as well as epithelial regeneration with restoration of goblet cells numbers and expression of MUC-2 and TFF-3. Consistently, LPS-induced RAW 264.7 cells produced less NO, PGE2, TNF-α, IL-6, and MCP-1. These effects might be related to the inhibition of the NF-κB signaling pathway. Our results suggest that sucrose esters from P. peruviana calyces, non-edible waste from fruit production, might be useful as an alternative IBD treatment.

MeSH terms

  • Animals
  • Colitis* / chemically induced
  • Colitis* / drug therapy
  • Colitis* / metabolism
  • Colon / pathology
  • Cytokines / metabolism
  • Esters / metabolism
  • Inflammatory Bowel Diseases* / pathology
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / pharmacology
  • Physalis*
  • Rats
  • Ribes*
  • Sucrose / metabolism
  • Trinitrobenzenesulfonic Acid / toxicity
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Tumor Necrosis Factor-alpha
  • Esters
  • Sucrose
  • Interleukin-6
  • Lipopolysaccharides
  • Cytokines
  • Trinitrobenzenesulfonic Acid

Grants and funding

This work was supported by Colciencias, actually Minciencias [Grant 110751929179–2010 and 597-2012], and the Universidad de Cartagena (Grant 055-2013). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.