Citrus Pomace-Derived Plant Complexes Enhance Caco-2 Wound Closure In Vitro and Modulate Selected Probiotic Strains

Citrus processing by-products represent a sustainable source of bioactive plant complexes with potential applications in intestinal health. This study investigated the effects of standardized food-grade orange (OE) and lemon (LE) pomace extracts and their simulated gastrointestinal digestates (DIGs) on intestinal epithelial responses and selected probiotic strains. Caco-2 cells were used to assess cytotoxicity, epithelial wound closure, and, in differentiated monolayers challenged with lipopolysaccharide (LPS), extracellular levels of SOD2, catalase, Nrf2, IL-6, IL-8, TNF-α, and IL-1β. In parallel, the effects of OE, LE, and their corresponding DIGs on the growth and cell-surface hydrophobicity of four probiotic lactic acid bacteria were evaluated. OE and LE DIGs were non-cytotoxic and promoted epithelial wound closure in a concentration- and time-dependent manner. In LPS-challenged monolayers, both DIGs counteracted alterations in extracellular oxidative stress-related proteins and reduced pro-inflammatory cytokine levels without affecting cell viability. OE and LE also produced strain-dependent effects on probiotic growth and cell-surface hydrophobicity, which were modified by gastrointestinal digestion. Overall, these findings extend previous evidence on the intestinal bioactivity of Citrus pomace-derived plant complexes and support their further investigation as sustainable food-grade ingredients for gut health applications.

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Publication Details

Journal
Antioxidants
Published
2026-09-11
DOI
https://doi.org/10.3390/antiox15091161
Primary Topic
Wound Healing and Treatments
Type
article
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article

Citrus Pomace-Derived Plant Complexes Enhance Caco-2 Wound Closure In Vitro and Modulate Selected Probiotic Strains

Filomena Nazzaro, Maria Neve Ombra, Domenico Trombetta, Mariarosaria Ingegneri et al.
Antioxidants
Wound Healing and Treatments
article

Citrus Pomace-Derived Plant Complexes Enhance Caco-2 Wound Closure In Vitro and Modulate Selected Probiotic Strains

Filomena Nazzaro, Maria Neve Ombra, Domenico Trombetta, Mariarosaria Ingegneri, Souda Belaïd, Antonella Smeriglio, Martina Imbesi, Marta Mangano
article en

Abstract

Citrus processing by-products represent a sustainable source of bioactive plant complexes with potential applications in intestinal health. This study investigated the effects of standardized food-grade orange (OE) and lemon (LE) pomace extracts and their simulated gastrointestinal digestates (DIGs) on intestinal epithelial responses and selected probiotic strains. Caco-2 cells were used to assess cytotoxicity, epithelial wound closure, and, in differentiated monolayers challenged with lipopolysaccharide (LPS), extracellular levels of SOD2, catalase, Nrf2, IL-6, IL-8, TNF-α, and IL-1β. In parallel, the effects of OE, LE, and their corresponding DIGs on the growth and cell-surface hydrophobicity of four probiotic lactic acid bacteria were evaluated. OE and LE DIGs were non-cytotoxic and promoted epithelial wound closure in a concentration- and time-dependent manner. In LPS-challenged monolayers, both DIGs counteracted alterations in extracellular oxidative stress-related proteins and reduced pro-inflammatory cytokine levels without affecting cell viability. OE and LE also produced strain-dependent effects on probiotic growth and cell-surface hydrophobicity, which were modified by gastrointestinal digestion. Overall, these findings extend previous evidence on the intestinal bioactivity of Citrus pomace-derived plant complexes and support their further investigation as sustainable food-grade ingredients for gut health applications.

AntioxidantsVol. 15(9)
University of Messina (IT), Institute of Food Science (IT)
Responsible consumption and production
Openalex Percentile: Top 14%
Wound Healing and Treatments
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Citrus Pomace-Derived Plant Complexes Enhance Caco-2 Wound Closure In Vitro and Modulate Selected Probiotic Strains — Filomena Nazzaro, Maria Neve Ombra, et al. · Antioxidants (2026) | TGRS Research Map | TGRS