Glechoma hederacea extracts attenuate cholestatic liver injury in a bile duct-ligated rat model. (23rd May 2017)
- Record Type:
- Journal Article
- Title:
- Glechoma hederacea extracts attenuate cholestatic liver injury in a bile duct-ligated rat model. (23rd May 2017)
- Main Title:
- Glechoma hederacea extracts attenuate cholestatic liver injury in a bile duct-ligated rat model
- Authors:
- Wang, Ya-Yu
Lin, Shih-Yi
Chen, Wen-Ying
Liao, Su-Lan
Wu, Chih-Cheng
Pan, Pin-Ho
Chou, Su-Tze
Chen, Chun-Jung - Abstract:
- Abstract: Ethnopharmacological relevance: In traditional Chinese medicine, Glechoma hederacea is frequently prescribed to patients with cholelithiasis, dropsy, abscess, diabetes, inflammation, and jaundice. Polyphenolic compounds are main bioactive components of Glechoma hederacea . Aim of the study: This study was aimed to investigate the hepatoprotective potential of hot water extract of Glechoma hederacea against cholestatic liver injury in rats. Materials and methods: Cholestatic liver injury was produced by ligating common bile ducts in Sprague-Dawley rats. Saline and hot water extract of Glechoma hederacea were orally administrated using gastric gavages. Liver tissues and bloods were collected and subjected to evaluation using histological, molecular, and biochemical approaches. Results: Using a rat model of cholestasis caused by bile duct ligation (BDL), daily oral administration of Glechoma hederacea hot water extracts showed protective effects against cholestatic liver injury, as evidenced by the improvement of serum biochemicals, ductular reaction, oxidative stress, inflammation, and fibrosis. Glechoma hederacea extracts alleviated BDL-induced transforming growth factor beta-1 (TGF-β1), connective tissue growth factor, and collagen expression, and the anti-fibrotic effects were accompanied by reductions in α-smooth muscle actin-positive matrix-producing cells and Smad2/3 activity. Glechoma hederacea extracts attenuated BDL-induced inflammatory cellAbstract: Ethnopharmacological relevance: In traditional Chinese medicine, Glechoma hederacea is frequently prescribed to patients with cholelithiasis, dropsy, abscess, diabetes, inflammation, and jaundice. Polyphenolic compounds are main bioactive components of Glechoma hederacea . Aim of the study: This study was aimed to investigate the hepatoprotective potential of hot water extract of Glechoma hederacea against cholestatic liver injury in rats. Materials and methods: Cholestatic liver injury was produced by ligating common bile ducts in Sprague-Dawley rats. Saline and hot water extract of Glechoma hederacea were orally administrated using gastric gavages. Liver tissues and bloods were collected and subjected to evaluation using histological, molecular, and biochemical approaches. Results: Using a rat model of cholestasis caused by bile duct ligation (BDL), daily oral administration of Glechoma hederacea hot water extracts showed protective effects against cholestatic liver injury, as evidenced by the improvement of serum biochemicals, ductular reaction, oxidative stress, inflammation, and fibrosis. Glechoma hederacea extracts alleviated BDL-induced transforming growth factor beta-1 (TGF-β1), connective tissue growth factor, and collagen expression, and the anti-fibrotic effects were accompanied by reductions in α-smooth muscle actin-positive matrix-producing cells and Smad2/3 activity. Glechoma hederacea extracts attenuated BDL-induced inflammatory cell infiltration/accumulation, NF-κB and AP-1 activation, and inflammatory cytokine production. Further studies demonstrated an inhibitory effect of Glechoma hederacea extracts on the axis of high mobility group box-1 (HMGB1)/toll-like receptor-4 (TLR4) intracellular signaling pathways. Conclusions: The hepatoprotective, anti-oxidative, anti-inflammatory, and anti-fibrotic effects of Glechoma hederacea extracts seem to be multifactorial. The beneficial effects of daily Glechoma hederacea extracts supplementation were associated with anti-oxidative, anti-inflammatory, and anti-fibrotic potential, as well as down-regulation of NF-κB, AP-1, and TGF-β/Smad signaling, probably via interference with the HMGB1/TLR4 axis. Graphical abstract: … (more)
- Is Part Of:
- Journal of ethnopharmacology. Volume 204(2017)
- Journal:
- Journal of ethnopharmacology
- Issue:
- Volume 204(2017)
- Issue Display:
- Volume 204, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 204
- Issue:
- 2017
- Issue Sort Value:
- 2017-0204-2017-0000
- Page Start:
- 58
- Page End:
- 66
- Publication Date:
- 2017-05-23
- Subjects:
- ALT alanine aminotransferase -- ANOVA one-way analysis of variance -- AST aspartate aminotransferase -- BDL bile duct ligation -- CTGF connective tissue growth factor -- ELISA enzyme-linked immunosorbent assay -- EMSA electrophoretic mobility shift assay -- GAPDH glyceraldehyde-3-phosphate dehydrogenase -- γ-GT γ-glutamyl transpeptidase -- H&E hematoxylin/eosin -- HMGB1 high mobility group box-1 -- HPLC high performance liquid chromatography -- IL-1β interleukin-1β -- MDA malondialdehyde -- MMP-2 matrix metalloproteinase-2 -- MMP-9 matrix metalloproteinase-9 -- MPO Myeloperoxidase -- ROS reactive oxygen species -- RT-PCR reverse transcriptase polymerase chain reaction -- α-SMA α-smooth muscle actin -- TAK1 transforming growth factor β-activated kinase-1 -- TBARS thiobarbituric acid reactive substances -- TGF-β1 transforming growth factor beta-1 -- TIMP-1 tissue inhibitor of metalloproteinase-1 -- TIMP-2 tissue inhibitor of metalloproteinase-2 -- TLR4 toll-like receptor-4 -- TNF-α tumor necrosis factor-α
Cholestasis -- Herbal medicine -- Polyphenol -- Rosmarinic acid
Ethnopharmacology -- Periodicals
Pharmacognosy -- Periodicals
Herbs -- Periodicals
Herbs -- Periodicals
Pharmacognosy -- Periodicals
Pharmacognosie -- Périodiques
Herbes -- Périodiques
615.1 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03788741 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jep.2017.04.011 ↗
- Languages:
- English
- ISSNs:
- 0378-8741
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4979.602400
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