Evidence map›Paper›PMID 40987977›Full record

ArticleInflammopharmacology2025

The hydroalcoholic extract of the leaves of red mombin (Spondias purpurea L.) is more effective in accelerating ulcer healing than preventing them in rodents.

Ruan Kaio Silva Nunes, Bruna Longo, Caio Henrique Willrich, Levy Mota da Silva, Luísa Santiago, Thiago Farias de Queiroz Silva, Lucas Matheus Lessa de Olinda, Layla Francielle Pereira, Heloisa Immianovsky Eisendecker, José Roberto Santin and 10 more

Abstract read
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Article in Inflammopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Ruan Kaio Silva NunesGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Bruna LongoLAPHATI - Laboratory of Applied Pharmacology to the Gastrointestinal Tract and Its Interactions, Department of Pharmacology, UFSC, Florianópolis, SC, Brazil.
Caio Henrique WillrichLAPHATI - Laboratory of Applied Pharmacology to the Gastrointestinal Tract and Its Interactions, Department of Pharmacology, UFSC, Florianópolis, SC, Brazil.
Levy Mota da SilvaGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Luísa SantiagoGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Thiago Farias de Queiroz SilvaGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Lucas Matheus Lessa de OlindaGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Layla Francielle PereiraGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Heloisa Immianovsky EisendeckerGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
José Roberto SantinGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Larissa BenvenuttiGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Luiza Felipim CorsiGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Bianca Priscila MirandaGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Hydima Julião CótaGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Larissa VenzonGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Tauani Caroline Santos FrançaGraduate Program in Pharmaceutical Sciences, UNIVALI, Itajaí, SC, Brazil.
Max Vidal-GutiérrezDepartment of Chemical, Biological and Agricultural Sciences, Universidad de Sonora, Campus Navojoa, Sonora, Mexico.
Zuleide Maria IgnacioLaboratory of Physiology Pharmacology and Psychopathology, Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Walter Antônio Roman-JuniorLaboratory of Pharmacognosy, Graduate Program in Health Sciences, Community University of Chapecó Region, Chapecó, SC, Brazil.
Luísa Mota da SilvaLAPHATI - Laboratory of Applied Pharmacology to the Gastrointestinal Tract and Its Interactions, Department of Pharmacology, UFSC, Florianópolis, SC, Brazil. lu.isamota@hotmail.com.ORCID http://orcid.org/0000-0001-5329-7301

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study evaluated the anti-ulcer effects of the hydroalcoholic extract from the leaves of Spondias purpurea L. (SPHE). The gastroprotection was assessed using acidified ethanol-induced gastric ulcer in mice given orally with the vehicle, carbenoxolone (200 mg/kg), or SPHE (10-1.000 mg/kg). The extract's healing activity was evaluated using acetic acid-induced ulcers in rats treated with vehicle, omeprazole (20 mg/kg), or SPHE (3-300 mg/kg). Histological and biochemical analyses were done in ulcerated tissue from both models. SPHE antisecretory action was tested in pylorus-ligated rats. The in vitro antioxidant potential was assessed using the DPPH test; its cytotoxicity and proliferative effects were measured in L929 cells. Mass spectrometry analysis was used to determine the extract's chemical profile and the quantification of phenolic compounds in the extract was performed in LCMS. SPHE induced gastroprotection at a dose of 1.000 mg/kg, and this effect was lost in mice treated with NEM, indomethacin, or yohimbine but not L-NAME. SPHE improves the healing of acetic acid-induced ulcers by 69.5% and 83.7% at 10 and 30 mg/kg, respectively. The microscopic examination confirms the healing effect of SPHE. SPHE enhanced PAS-stained mucins, SOD, and GST activities while decreasing MPO activity, and MDA levels in ulcerated mucosa, and scavenged DPPH radicals but did not change the gastric acid secretion. SPHE showed no cytotoxicity and favored fibroblast proliferation. The presence of hibiscus acid, hydroxy citric acid, hibiscus acid glycoside, ellagic acid, and the flavonoids quercetin and rutin were confirmed and quercetin, caffeic acid, p-coumaric acid, gallic acid, and epigallocatechin were quantified. Therefore, SPHE accumulated chemicals with higher gastric healing potential mediated by gastric protective features, specifically antioxidant resources, mucus barrier, and cell proliferation.

Indexed as

AnacardiaceaeAnti-Ulcer AgentsPlant ExtractsPlant LeavesStomach UlcerAcetic AcidAnimalsAntioxidantsCell LineDisease Models, AnimalEthanolMaleMiceRatsRats, WistarWound HealingAcetic AcidAntioxidantsAnti-Ulcer AgentsEthanolPlant ExtractsGastric healingGastroprotectionHibiscus acidHibiscus acid glycosideHydroxy citric acid

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.