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1. (Article ID: 9647)
Muhaxi M, Liu F, Ng TB
Structural characterization and in vitro hepatoprotective activity of a novel antioxidant polysaccharide from fruiting bodies of the mushroom Pleurotus ferulae
International Journal of Biological Macromolecules 243 (2023)
125124
In the present study, three novel antioxidant polysaccharides (G-1, AG-1, and AG-2) were isolated and purified from Pleurotus ferulae using mouse erythrocyte hemolysis inhibitory activity as an indicator. These components showed antioxidant activity at the chemical and cellular levels. Given that G-1 displayed superior performance in protecting the human hepatocyte L02 cells against oxidative damage caused by H2O2 compared to AG-1 and AG-2 and had a higher yield and purification rate, the detailed structure of G-1 was further characterized. G-1 mainly contains six kinds of linkage type units as A: →4,6)-α-d-Glcp-(1→, B: →3)-β-d-Glcp-(1→, C: →2,6)-β-d-Glcp-(1→, d: β-d-Manp(1→, E: →6)-β-d-Galp-(1→, F: →4)-β-d-Glcp-(1→. Finally, the potential in vitro hepatoprotective mechanism of G-1 was discussed and elucidated. Results suggested that G-1 can protect L02 cells from H2O2-induced damage by reducing the leakage of AST and ALT from the cytoplasm, enhancing the activities of SOD and CAT, and suppressing lipid peroxidation and production of LDH. G-1 could further reduce the production of ROS, stabilize mitochondrial membrane potential and maintain cell morphology. Hence, G-1 could be a valuable functional food with antioxidant and hepatoprotective activities.
Structural characterization, antioxidant and hepatoprotective activity, separation and purification of Pleurotus ferulae polysaccharide (PFLP)
NCBI PubMed ID: 37290546Publication DOI: 10.1016/j.ijbiomac.2023.125124Journal NLM ID: 7909578Publisher: Butterworth-Heinemann
Correspondence: F. Liu
nankai.edu.cn>; T.B. Ng cuhk.edu.hk>
Institutions: School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China, Department of Microbiology, The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Nankai University, Tianjin 300071, China
Methods: 13C NMR, 1H NMR, methylation, NMR-2D, GC-MS, GC, FTIR, composition analysis, HPLC, extraction, statistical analysis, morphological analysis, antioxidant activities, cytotoxicity assay, SEM, Congo Red assay, conformational analysis, UV-vis, hepatoprotective activity assay
The publication contains the following compound(s):
- Compound ID: 17866
Structure type: fragment of a bigger structure
Trivial name: glucan particle, PFLP
Compound class: cell wall polysaccharide, glucan
Reference(s) to other database(s): GTC:G51056AN
- Compound ID: 23308
Structure type: fragment of a bigger structure
Trivial name: polysaccharide LECP, PFLP
- Compound ID: 23531
Structure type: fragment of a bigger structure
Trivial name: PFLP
- Compound ID: 23532
Structure type: fragment of a bigger structure
Trivial name: PFLP
- Compound ID: 23533
Structure type: fragment of a bigger structure
Trivial name: PFLP
- Compound ID: 23534
Structure type: fragment of a bigger structure
Trivial name: PFLP
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2. (Article ID: 12038)
Bhattacharya SK, Bhattacharya A, Kumar A, Ghosal S
Antioxidant activity of Bacopa monniera in rat frontal cortex, striatum and hippocampus
Phytotherapy Research 14(3) (2000)
174-179
The effect of a standardized extract of Bacopa monniera Linn. was assessed on rat brain frontal cortical, striatal and hippocampal superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX) activities, following administration for 7, 14 or 21 days. The effects induced by this extract (bacoside A content 82% +/- 0.5%), administered in doses of 5 and 10 mg/kg, orally, were compared with the effects induced by (-) deprenyl (2 mg/kg, p. o.) administered for the same time periods. Bacopa monniera (BM) induced a dose-related increase in SOD, CAT and GPX activities, in all the brain regions investigated, after 14 and 21 days of drug administration. On the contrary, deprenyl induced an increase in SOD, CAT and GPX activities in the frontal cortex and striatum, but not in the hippocampus, after treatment for 14 or 21 days. The results suggest that BM, like deprenyl, exhibits a significant antioxidant effect after subchronic administration which, unlike the latter, extends to the hippocampus as well. The results suggest that the increase in oxidative free radical scavenging activity by BM may explain, at least in part, the cognition- facilitating action of BM, recorded in Ayurvedic texts, and demonstrated experimentally and clinically.
Bacopa monniera, Ayurvedic medhyarasayana (memory promoting drug), bacoside A, superoxide dismutase, catalase, glutathione peroxidase
NCBI PubMed ID: 10815010Publication DOI: 10.1002/(sici)1099-1573(200005)14:3<174::aid-ptr624>3.0.co;2-oJournal NLM ID: 8904486Publisher: Chichester: Wiley
Correspondence: Bhattacharya SK
baneras.ernet.in>
Institutions: Drug Research and Development Centre, Calcutta, India, Department of Pharmacology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
Methods: biological assays, extraction, HPTLC, CC, enzymatic assay, Lowry method
The publication contains the following compound(s):
- Compound ID: 30757
|
b-D-Glcp-(1-3)-+
|
a-L-Araf-(1-2)-a-L-Arap-(1-3)-Subst
Subst = jujubogenin = SMILES C/C(C)=C/[C@H]1C[C@](C)(O)[C@@H]2[C@H]3CC[C@@H]4[C@@]5(C)CC{3}[C@H](O)C(C)(C)[C@@H]5CC[C@@]4(C)[C@]36C[C@]2(OC6)O1 |
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Structure type: oligomer
Trivial name: jujubogenin isomer of bacopasaponin C
Compound class: saponin glycoside, glycoside
- Compound ID: 31352
|
b-D-Glcp-(1-3)-+
|
a-L-Araf-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = jujubogenin = SMILES C/C(C)=C/[C@H]1C[C@](C)(O)[C@@H]2[C@H]3CC[C@@H]4[C@@]5(C)CC{3}[C@H](O)C(C)(C)[C@@H]5CC[C@@]4(C)[C@]36C[C@]2(OC6)O1 |
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Structure type: oligomer
Trivial name: bacoside A3
Compound class: glycoside
- Compound ID: 31353
|
b-D-Glcp-(1-3)-+
|
a-L-Araf-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = pseudojujubogenin = SMILES C{20}[C@]1(O)[C@H](/C=C(C)/C)CO[C@]2(C3)OC[C@]43[C@]5(C)CC[C@H]6C(C)(C){3}[C@@H](O)CC[C@@](C)6[C@H]5CC[C@@H]4[C@@H]12 |
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Structure type: oligomer
Trivial name: bacopaside II
Compound class: glycoside
- Compound ID: 31354
|
b-D-Glcp-(1-3)-+
|
a-L-Araf-(1-2)-a-L-Arap-(1-3)-Subst
Subst = pseudojujubogenin = SMILES C{20}[C@]1(O)[C@H](/C=C(C)/C)CO[C@]2(C3)OC[C@]43[C@]5(C)CC[C@H]6C(C)(C){3}[C@@H](O)CC[C@@](C)6[C@H]5CC[C@@H]4[C@@H]12 |
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Structure type: oligomer
Trivial name: bacopasaponin C
Compound class: glycoside
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