Gastroprotective xanthones isolated from Garcinia achachairu: Study on mucosal defensive factors and H+, K+-ATPase activity. (25th October 2016)
- Record Type:
- Journal Article
- Title:
- Gastroprotective xanthones isolated from Garcinia achachairu: Study on mucosal defensive factors and H+, K+-ATPase activity. (25th October 2016)
- Main Title:
- Gastroprotective xanthones isolated from Garcinia achachairu: Study on mucosal defensive factors and H+, K+-ATPase activity
- Authors:
- Mariano, Luísa Nathália Bolda
da Silva, Luisa Mota
de Souza, Priscila
Boeing, Thaise
Somensi, Lincon Bordignon
Bonomini, Tiago José
Delle Monache, Franco
Cechinel Filho, Valdir
de Andrade, Sérgio Faloni
Niero, Rivaldo - Abstract:
- Abstract: The present study was designed to investigate the gastroprotective effect of xanthones 7-preniljacareubin (PJB), 1, 3, 5, 6-tetrahydroxy xanthone (THX), 3-demethyl-2-geranyl-4-prenylbellidypholine (DGP) and 1, 5, 8-trihydroxy-4′, 5′-dimethyl-2H-pyrane (2, 3:3, 2)-4-(3-methylbut-2-enyl) xanthone (TDP) isolated of branches from G. achachairu . Their structures were identified through the spectroscopic analysis in comparison with previously reported data. The xanthones were tested at dose of 10 mg/kg against ethanol 60%/HCl 0.3 N-induced gastric ulcer in female swiss mice. The xanthones PJB, THX, DGP and TDP exhibit gastroprotective effect after intraperitoneal treatment, but only the first two displayed anti-ulcer activity after oral administration. Both PJB and THX augmented the antioxidative capacity of tissue by an increase in glutathione levels, as well as were able to prevent an increase in myeloperoxidase activity and tumor necrosis factor level. On the other hand, only THX showed an in vitro free radical scavenger activity, and only PJB avoided mucus depletion on gastric mucosa, which was not associated with an increase in mucin production at glandular level. In addition, PJB and THX inhibited the in vitro H + K + -ATPase activity at similar range as omeprazole. Together, these results demonstrate the anti-ulcer efficacy of xanthones isolated from G. achachairu, which can contribute for future directions in the development of effective strategies to improveAbstract: The present study was designed to investigate the gastroprotective effect of xanthones 7-preniljacareubin (PJB), 1, 3, 5, 6-tetrahydroxy xanthone (THX), 3-demethyl-2-geranyl-4-prenylbellidypholine (DGP) and 1, 5, 8-trihydroxy-4′, 5′-dimethyl-2H-pyrane (2, 3:3, 2)-4-(3-methylbut-2-enyl) xanthone (TDP) isolated of branches from G. achachairu . Their structures were identified through the spectroscopic analysis in comparison with previously reported data. The xanthones were tested at dose of 10 mg/kg against ethanol 60%/HCl 0.3 N-induced gastric ulcer in female swiss mice. The xanthones PJB, THX, DGP and TDP exhibit gastroprotective effect after intraperitoneal treatment, but only the first two displayed anti-ulcer activity after oral administration. Both PJB and THX augmented the antioxidative capacity of tissue by an increase in glutathione levels, as well as were able to prevent an increase in myeloperoxidase activity and tumor necrosis factor level. On the other hand, only THX showed an in vitro free radical scavenger activity, and only PJB avoided mucus depletion on gastric mucosa, which was not associated with an increase in mucin production at glandular level. In addition, PJB and THX inhibited the in vitro H + K + -ATPase activity at similar range as omeprazole. Together, these results demonstrate the anti-ulcer efficacy of xanthones isolated from G. achachairu, which can contribute for future directions in the development of effective strategies to improve gastric diseases. Graphical abstract: Highlights: Xanthones isolated from Garcinia achachairu display gastroprotective activity. Anti-ulcer effect is due the ability of increase protective factors of gastric mucosa. H +, K + -ATPase activity inhibition can explain xanthones anti-secretory effect. Efficacy of xanthones can contribute to improve the management of gastric diseases. … (more)
- Is Part Of:
- Chemico-biological interactions. Volume 258(2016)
- Journal:
- Chemico-biological interactions
- Issue:
- Volume 258(2016)
- Issue Display:
- Volume 258, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 258
- Issue:
- 2016
- Issue Sort Value:
- 2016-0258-2016-0000
- Page Start:
- 30
- Page End:
- 39
- Publication Date:
- 2016-10-25
- Subjects:
- Xanthones -- Gastric ulcer -- Mucin -- Oxidative stress -- Antioxidant -- Spectroscopic analysis
AA ascorbic acid -- CBX Carbenoxolone -- CMEB crude methanolic extract of branches -- DGP 3-demethyl-2-geranyl-4-prenylbellidypholine -- DPPH 2, 2-diphenyl-1- picrylhydrazyl -- GSH reduced glutathione -- H/E hematoxylin and eosin -- MPO myeloperoxidase -- NV naive -- OME omeprazol -- OUA ouabain -- PJB 7-preniljacareubin -- ROS reactive oxygen species -- TDP 1, 5, 8-trihydroxy-4′, 5′-dimethyl-2H-pyrane (2, 3:3, 2)-4-(3-methylbut-2-enyl) xanthone -- THX 1, 3, 5, 6-tetrahydroxy xanthone -- TLC thin-layer chromatography -- TNF tumor necrosis factor -- VEH vehicle
Biochemistry -- Periodicals
Toxicological chemistry -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biochimie -- Périodiques
Toxicologie biochimique -- Périodiques
572 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00092797 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cbi.2016.08.009 ↗
- Languages:
- English
- ISSNs:
- 0009-2797
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3155.500000
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