# Carbohydrate-Rich Extract from Pereskia aculeata Leaves: In Vitro Prebiotic-Related Properties and Metabolic Effects in an Experimental Model of Obesity

**Authors:** Martha Eunice de Bessa, Vivian Tomasco Andrade, Gabriele Moreira Guimarães, Ana Flávia Lawall Werneck Cerqueira, Carolina Carvalho Ramos Viana, Marianna Miranda Furtado, Renata de Freitas Mendes, Mirian Pereira Rodarte, Anderson S. Sant’Ana, Maria José Valenzuela Bell, Maria Christina Marques Nogueira Castañon, Maria Silvana Alves, Elisabeth Neumann, Elita Scio

PMC · DOI: 10.1007/s11130-026-01486-0 · Plant Foods for Human Nutrition (Dordrecht, Netherlands) · 2026-03-21

## TL;DR

This study shows that a carbohydrate-rich extract from Pereskia aculeata leaves has prebiotic and metabolic benefits in an obesity model, reducing fat and improving blood markers.

## Contribution

The study demonstrates the prebiotic and metabolic benefits of a carbohydrate-rich extract from Pereskia aculeata in an experimental obesity model.

## Key findings

- The extract reduced visceral adiposity and serum triglycerides in obese rats by 20% and 31%, respectively.
- Supplementation lowered fasting blood glucose by 10% in the obesity model.
- The extract showed antioxidant activity and supported lactic acid bacteria growth in vitro.

## Abstract

Pereskia aculeata Mill. is a leafy cactus native to Brazil, whose leaves are traditionally used as food and are characterized by high nutritional value and significant mucilage content. This study aimed to evaluate the functional potential of the carbohydrate-rich extract obtained from leaves and to investigate its metabolic effects in obese male rats subjected to a litter-size reduction model. The extract was chemically characterized by physicochemical analysis and FTIR-MIR spectroscopy, which revealed spectral features consistent with arabinogalactan-type carbohydrates (absorption bands between 1,000 and 1,050 cm⁻¹). In vitro assays demonstrated antioxidant activity, with DPPH radical inhibition exceeding 60% and nitric oxide reduction exceeding 30%. In addition to promoting the growth of lactic acid bacteria in culture medium supplemented with the extract, it also showed antagonistic activity against selected Gram-negative pathogens. FTIR-MIR analysis during an in vitro gastrointestinal simulation indicated relative spectral stability. In vivo, obese rats were supplemented with the extract for 75 days (0.3%, w/v, in drinking water; 300 mg/kg body weight/day). Supplemented animals showed a reduction in visceral adiposity (-20%) and serum triglycerides (-31%) compared to obese controls (p < 0.05). The obesity model increased fasting blood glucose by approximately 19%, and supplementation reduced blood glucose by approximately 10%. Data were analyzed using appropriate parametric tests (p < 0.05). Liver parameters and histological analyses indicated protection against non-alcoholic fatty liver disease. Overall, these results corroborate the functional potential of carbohydrate fractions and provide a basis for future studies addressing microbiota-mediated mechanisms and metabolic effects.

The online version contains supplementary material available at 10.1007/s11130-026-01486-0.

## Linked entities

- **Chemicals:** nitric oxide (PubChem CID 145068)
- **Diseases:** obesity (MONDO:0011122), non-alcoholic fatty liver disease (MONDO:0013209)
- **Species:** Pereskia aculeata (taxon 3597), Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}
- **Diseases:** dyslipidemia (MESH:D050171), excess (MESH:D006970), Gram (MESH:D016908), non-alcoholic steatohepatitis (MESH:D005235), non-alcoholic fatty liver disease (MESH:D065626), Obese (MESH:D009765), impaired glucose tolerance (MESH:D018149), Hypercholesterolemia (MESH:D006937), fat (MESH:D004620), hyperlipidemia (MESH:D006949), metabolic disorders (MESH:D008659), hepatic alterations (MESH:D056486), fibrosis (MESH:D005355), endotoxemia (MESH:D019446), hepatic lipid (MESH:D011017), liver injury (MESH:D017093), visceral adiposity (MESH:D007418), adiposity (MESH:D018205), inflammation (MESH:D007249), Hepatic steatosis (MESH:D005234)
- **Chemicals:** cholesterol (MESH:D002784), EDe (-), NO (MESH:D009569), gallic acid (MESH:D005707), lactic acid (MESH:D019344), eosin (MESH:D004801), Inulin (MESH:D007444), AG (MESH:D012834), triglyceride (MESH:D014280), hemicelluloses (MESH:C007916), amide (MESH:D000577), Lipid (MESH:D008055), polysaccharides (MESH:D011134), formalin (MESH:D005557), xylazine (MESH:D014991), paraffin (MESH:D010232), arabinogalactan (MESH:C005653), creatinine (MESH:D003404), AA (MESH:D000596), Blood glucose (MESH:D001786), oligosaccharide (MESH:D009844), sodium nitroprusside (MESH:D009599), DPPH (MESH:C004931), Carbohydrate (MESH:D002241), ascorbic acid (MESH:D001205), Hematoxylin (MESH:D006416), water (MESH:D014867), sugars (MESH:D000073893), dextrose (MESH:D005947)
- **Species:** Leptospira sp. AB (species) [taxon 103236], Lactiplantibacillus plantarum (species) [taxon 1590], Lactobacillus acidophilus NCFM (strain) [taxon 272621], Pisonia aculeata (species) [taxon 363212], Limosilactobacillus fermentum (species) [taxon 1613], Pereskia aculeata (species) [taxon 3597], Enterovirus F (no rank) [taxon 1330520], Rattus norvegicus (brown rat, species) [taxon 10116], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13005867/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC13005867/full.md

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Source: https://tomesphere.com/paper/PMC13005867