Evidence map›Paper›PMID 36121588›Full record

ArticleInflammopharmacology2022

Geraniol accelerates the gastric healing, minimizes ulcers recurrence, and reduces anxiolytic-like behavior in ulcerated rodents by oral or inhaled route.

Larissa Venzon, Mariane Caroline Meurer, Tauani Caroline Dos Santos França, Bruna Longo, Marihá Mariott, Lincon Bordignon Somensi, Luisa Nathalia Bolda Mariano, Thaise Boeing, Camila André Cazarin, Lucas Natã Pereira and 2 more

Abstract read
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In one paragraph

Article in Inflammopharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% of its field
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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

12 authors at 1 institution in 1 country.

Larissa VenzonPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Mariane Caroline MeurerPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Tauani Caroline Dos Santos FrançaPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Bruna LongoPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Marihá MariottPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Lincon Bordignon SomensiPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Luisa Nathalia Bolda MarianoPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Thaise BoeingPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Camila André CazarinPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Lucas Natã PereiraPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Marcia Maria de SouzaPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil.
Luisa Mota da SilvaPharmaceutical Sciences Graduate Program, University of Itajai Valley, Itajai, SC, Brazil. lu.isamota@hotmail.com.ORCID http://orcid.org/0000-0001-5329-7301
Universidade do Vale do Itajaí · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGeraniol (GE) is dietary acyclic monoterpene alcohol found in essential oils from aromatic plants with therapeutic value against gastric ulcers already described. HYPOTHESIS/PURPOSE: To assess whether oral GE accelerates gastric healing or prevents ulcer recurrence, and to evaluate the hypothesis that GE promotes antiulcer effects by the inhaled route and that promotes changes in the behavior of ulcerated rodents.

methodsGastric healing effects, underlining mechanisms, and behavioral changes were measured in80% acetic acid-induced gastric ulcer model in rats receiving GE by oral (30 mg/kg) or inhaled route (1 mg/L of air/min); whereas the effects of GE to avoid ulcer recurrence was evaluated in mice submitted to 10% acetic acid plus IL-1β ulcer.

resultsGE administered by both routes accelerates gastric healing, increasing mucin and GSH levels, CAT, and GST activities, and reducing MPO activity. Moreover, oral, and inhaled GE minimized ulcer recurrence reducing gastric TNF and IL-6 levels and preserving mucin levels. Interestingly, the inhalation or oral intake of GE promotes anxiolytic-like effects in ulcerated rats.

conclusionData altogether suggest that the GE accelerates gastric healing through the strengthening of protective factors of the gastric mucosa, promoting a quality healing that reduces the recurrence of the lesion. Besides, the anxiolytic-like effect of GE may also contribute to its gastric healing action since anxiety is recognized as one of the etiologic agents of ulcers.

Indexed as

Acyclic MonoterpenesAnti-Anxiety AgentsAnti-Ulcer AgentsStomach UlcerAcetic AcidAnimalsGastric MucosaMiceMucinsRatsRats, WistarAcetic AcidAcyclic MonoterpenesAnti-Anxiety AgentsAnti-Ulcer AgentsgeraniolMucinsGastric ulcersInhalationMonoterpeneUlcer recurrence

Identifiers

PMID36121588
OpenAlexW4296322737

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.