The essential oil from Baccharis trimera (Less.) DC improves gastric ulcer healing in rats through modulation of VEGF and MMP-2 activity.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
10 May 2021
Historique:
received: 29 09 2020
revised: 12 12 2020
accepted: 11 01 2021
pubmed: 19 1 2021
medline: 17 8 2021
entrez: 18 1 2021
Statut: ppublish

Résumé

Baccharis trimera (Less.) DC known as "carqueja" in Brazil has been acknowledged as a medicinal plant in folk medicine for the treatment of stomach aches and gastrointestinal disorders. The present study aimed to evaluate the gastroprotective and healing effects of essential oil from B. trimera (EOBT) against gastric ulcer lesions caused by absolute ethanol and acetic acid, respectively, and to identify the mechanism of action of this essential oil in male Wistar rats. The plant material used to obtain EOBT was collected in the southern region of Brazil and was analyzed by chromatography-mass spectrometry (GCMS) demonstrate its characteristic chemical composition, with carquejyl acetate as its main component. Different doses of EOBT (50, 100, and 200 mg/kg) were administered orally in male Wistar rats as an acute treatment against absolute ethanol-induced gastric lesions. The gastric healing effect of EOBT (100 mg/kg) was evaluated once a day after 7, 10, and 14 days of treatment. After treatment, the stomachs of rats from all groups were collected to measure the lesion area (mm Pretreatment with EOBT (100 and 200 mg/kg) significantly decreased the severity of gastric damage induced by absolute ethanol and decreased MPO activity in gastric tissue. After 10 and 14 days of treatment with EOBT (100 mg/kg) once a day, the lesion area was significantly reduced by 61% and 65.5%, respectively, compared to the negative control group. The gastric healing effect of EOBT was followed by a decrease in the expression of COX-1 compared to that in the negative control group. Notably, treatment with EOBT for 14 days increased the expression of VEGF compared to that using an anti-ulcer drug (lansoprazole). Additionally, analyses of MMP-2 and MMP-9 activities in the gastric mucosa confirmed the accelerated gastric healing effect of EOBT, with a significant decrease in the activity of pro-MMP-2. No sign of toxicity was observed after treatment with EOBT for 14 consecutive days. These findings indicated that EOBT was effective in preventing and accelerating ulcer healing by decreasing MPO activity, increasing VEGF expression, and decreasing MMP-2 activity. These actions collectively contribute to the rapid recovery of gastric mucosa following treatment with EOBT, without any observed toxicity.

Identifiants

pubmed: 33460758
pii: S0378-8741(21)00058-1
doi: 10.1016/j.jep.2021.113832
pii:
doi:

Substances chimiques

Anti-Ulcer Agents 0
Membrane Proteins 0
Oils, Volatile 0
Vascular Endothelial Growth Factor A 0
vascular endothelial growth factor A, rat 0
Lansoprazole 0K5C5T2QPG
Ethanol 3K9958V90M
Cyclooxygenase 1 EC 1.14.99.1
Cyclooxygenase 2 EC 1.14.99.1
Ptgs1 protein, rat EC 1.14.99.1
Ptgs2 protein, rat EC 1.14.99.1
Caspases EC 3.4.22.-
Matrix Metalloproteinase 2 EC 3.4.24.24
Mmp2 protein, rat EC 3.4.24.24
Matrix Metalloproteinase 9 EC 3.4.24.35
Mmp9 protein, rat EC 3.4.24.35
Acetic Acid Q40Q9N063P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113832

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Gabriela Bueno (G)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Stefanni Liliane Chavez Rico (SL)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Larissa Lucena Périco (LL)

Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Alberta, Canada.

Rie Ohara (R)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Vinicius Peixoto Rodrigues (VP)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Maycon Tavares Emílio-Silva (MT)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Renata Assunção (R)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Lucia Regina Machado da Rocha (LR)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Domingos Sávio Nunes (DS)

Department of Chemistry, UEPG-Ponta Grossa State University, CEP, 84030-900, Ponta Grossa, Paraná, Brazil.

Michele Aparecida Besten (MA)

Federal Institute of Paraná, CEP, 85860-000, Foz Do Iguaçu, Paraná, Brazil.

Gustavo Heiden (G)

Herbário ECT - Embrapa Clima Temperado, Rodovia BR 392, Km 78, CEP, 96010-971, Pelotas, RS, Brazil.

Ana Carolina Lima Camargo (AC)

Department of Structural and Functional Biology (Morphology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Luis Antonio Justulin (LA)

Department of Structural and Functional Biology (Morphology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil.

Clélia Akiko Hiruma-Lima (CA)

Department of Structural and Functional Biology (Physiology), Biosciences Institute, UNESP-São Paulo State University, CEP, 18618-689, Botucatu, São Paulo, Brazil. Electronic address: clelia.hiruma@unesp.br.

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Classifications MeSH