The essential oil from Baccharis trimera (Less.) DC improves gastric ulcer healing in rats through modulation of VEGF and MMP-2 activity.
Acetic Acid
/ toxicity
Animals
Anti-Ulcer Agents
/ pharmacology
Baccharis
/ chemistry
Brazil
Caspases
/ metabolism
Cyclooxygenase 1
/ metabolism
Cyclooxygenase 2
/ metabolism
Disease Models, Animal
Ethanol
/ toxicity
Gastric Mucosa
/ drug effects
Lansoprazole
/ pharmacology
Male
Matrix Metalloproteinase 2
/ metabolism
Matrix Metalloproteinase 9
/ metabolism
Medicine, Traditional
Membrane Proteins
/ metabolism
Oils, Volatile
/ pharmacology
Organ Size
/ drug effects
Rats, Wistar
Stomach Ulcer
/ chemically induced
Vascular Endothelial Growth Factor A
/ metabolism
Baccharis trimera (Less.) DC
Essential oil
Gastric ulcer healing
MMP-2
VEGF
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
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
113832Informations de copyright
Copyright © 2021 Elsevier B.V. All rights reserved.