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The effects of baicalein on gastric mucosal ulcerations in mice: Protective pathways and anti-secretory mechanisms.
- Source :
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Chemico-biological interactions [Chem Biol Interact] 2016 Dec 25; Vol. 260, pp. 33-41. Date of Electronic Publication: 2016 Oct 22. - Publication Year :
- 2016
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Abstract
- Many flavonoids have been shown to present good results for the treatment of gastric ulcers. Baicalein, a bioactive flavonoid derived from the Scutellaria baicalensis Georgi root, possesses several biological effects, such as anti-inflammatory and antioxidant. This study was conducted to assess the gastroprotective properties of baicalein. Anti-ulcerogenic assay was performed using the protocol of ulcer induced by ethanol/HCl in mice; then, the role of presynaptic α <subscript>2</subscript> -receptors, sulfhydryl (SH) compounds, nitric oxide (NO), prostaglandin (PG) and ATP-sensitive K <superscript>+</superscript> (K <subscript>ATP</subscript> ) channels in gastroprotection of baicalein was investigated. The levels of reduced glutathione (GSH) and the myeloperoxidase (MPO) activity were measured in the gastric mucosa. Parameters of gastric secretion (volume, [H <superscript>+</superscript> ] and pH) were determined with or without the presence of the secretagogue agent histamine, as well as mucus in gastric contents, by the pylorus ligation model. In vitro H <superscript>+</superscript> ,K <superscript>+</superscript> -ATPase activity was also determined. Baicalein (10, 30 and 100 mg/kg) exhibited a dose related gastroprotective effect (P < 0.001) against acidified ethanol-induced lesions. The intraperitoneal treatment of mice with a α <subscript>2</subscript> -adrenoreceptor antagonist (yohimbine; 2 mg/kg), a SH compounds blocker (N-ethylmaleimide, NEM; 10 mg/kg), a non-selective inhibitor of NO synthase (N <subscript>w</subscript> -nitro-L-arginine methyl ester hydrochloride, L-NAME; 10 mg/kg), a non-selective inhibitor of cyclo-oxygenase (indomethacin; 10 mg/kg) or a K <subscript>ATP</subscript> channel blocker (glibenclamide; 10 mg/kg) was able to reverse (P < 0.001) the gastroprotective response caused by baicalein (30 mg/kg). Baicalein (30 mg/kg; P < 0.05) was able to increase GSH levels and decreasing MPO activity. The intraduodenal treatment with baicalein (30 and 100 mg/kg) significantly increased (P < 0.05) the gastric mucus secretion. Additionally, the treatment with baicalein reduced (30 and 100 mg/kg; P < 0.05) the secretion volume and total acid secretion, and also increased (10, 30 and 100 mg/kg; P < 0.001) the pH value, after pylorus ligature. Baicalein (30 mg/kg) was also effective in inhibiting the effects of histamine on gastric secretion (volume, [H <superscript>+</superscript> ] and pH; P < 0.001). Baicalein at 10 and 30 μg/mL showed anti-H <superscript>+</superscript> ,K <superscript>+</superscript> -ATPase activity. In conclusion, the present results provide convincing evidence that baicalein could be used as a cytoprotective (preventive effect) and anti-ulcerogenic (anti-secretory effect) agent in the gastric ulcers.<br /> (Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.)
- Subjects :
- Animals
Ethanol
Female
Flavanones administration & dosage
Flavanones pharmacology
Gastric Juice metabolism
Gastric Mucosa drug effects
Glutathione metabolism
H(+)-K(+)-Exchanging ATPase metabolism
Hydrochloric Acid
KATP Channels metabolism
Male
Mice
Peroxidase metabolism
Prostaglandins metabolism
Protective Agents administration & dosage
Protective Agents pharmacology
Stomach drug effects
Stomach Ulcer chemically induced
Stomach Ulcer drug therapy
Stomach Ulcer pathology
Flavanones therapeutic use
Gastric Mucosa metabolism
Gastric Mucosa pathology
Protective Agents therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7786
- Volume :
- 260
- Database :
- MEDLINE
- Journal :
- Chemico-biological interactions
- Publication Type :
- Academic Journal
- Accession number :
- 27780710
- Full Text :
- https://doi.org/10.1016/j.cbi.2016.10.016