2009
DOI: 10.1016/j.etp.2008.11.002
|View full text |Cite
|
Sign up to set email alerts
|

ROS scavenging capacity and neuroprotective effect of α-mangostin against 3-nitropropionic acid in cerebellar granule neurons

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

3
92
3

Year Published

2012
2012
2018
2018

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 110 publications
(98 citation statements)
references
References 40 publications
3
92
3
Order By: Relevance
“…Consistently, Mahabusarakam et al [45] reported that α-MG and its synthetic derivatives inhibited the decrease of α-tocopherol consumption in copper-induced LDL oxidation, and the structural modifications of α-MG differently affected the antioxidant activity: (i) substitution of C-3 and C-6 hydroxyl groups with aminoethyl increased the activity, and (ii) substitution of C-3 and C-6 hydroxyl groups with methyl, acetate, propanediol, or nitrile reduced the activity. There is substantial evidence supporting the capacity of α-MG to scavenge superoxide anion (O 2 -• ), hydroxyl radicals (OH·), and H 2 O 2 [46][47][48][49]. On the other hand, α-MG was shown to possess peroxynitrite (ONOO − ) scavenging activity using authentic and 3-morpholinosydnonimine-derived peroxynitrite methods [32,46].…”
Section: Antioxidant Activitymentioning
confidence: 99%
See 1 more Smart Citation
“…Consistently, Mahabusarakam et al [45] reported that α-MG and its synthetic derivatives inhibited the decrease of α-tocopherol consumption in copper-induced LDL oxidation, and the structural modifications of α-MG differently affected the antioxidant activity: (i) substitution of C-3 and C-6 hydroxyl groups with aminoethyl increased the activity, and (ii) substitution of C-3 and C-6 hydroxyl groups with methyl, acetate, propanediol, or nitrile reduced the activity. There is substantial evidence supporting the capacity of α-MG to scavenge superoxide anion (O 2 -• ), hydroxyl radicals (OH·), and H 2 O 2 [46][47][48][49]. On the other hand, α-MG was shown to possess peroxynitrite (ONOO − ) scavenging activity using authentic and 3-morpholinosydnonimine-derived peroxynitrite methods [32,46].…”
Section: Antioxidant Activitymentioning
confidence: 99%
“…There is substantial evidence supporting the capacity of α-MG to scavenge superoxide anion (O 2 -• ), hydroxyl radicals (OH·), and H 2 O 2 [46][47][48][49]. On the other hand, α-MG was shown to possess peroxynitrite (ONOO − ) scavenging activity using authentic and 3-morpholinosydnonimine-derived peroxynitrite methods [32,46]. Moreover, studies carried out in several cell/tissue models have confirmed the effectiveness of α-MG in counteracting lipoperoxidation and oxidative stress-mediated damage by its ability of quenching free radicals.…”
Section: Antioxidant Activitymentioning
confidence: 99%
“…Its chemical structure of 1,3,6-trihydroxy-7-methoxy-2,8-bis(3-methyl-2-butenyl)-9H-xanthen-9-one ( Figure 1) was elucidated by Yates et al [3]. Alphamangostin represented the major active constituent among the detected xanthones and therefore, it has been considered as analytical marker for the quality control of GM products [4,5]. Recently, alpha-mangostin has been commonly employed as ingredient in nutritional supplements, herbal cosmetics [4] and some topical pharmaceutical preparations [6] owing to its previously investigated multi-pharmacological activities that were previously reviewed by Pedraza-Chaverri et al [7].…”
Section: Introductionmentioning
confidence: 99%
“…Previously described method [4] for the assay of pure alpha-mangostin using methanol as solvent could not be applied to quantify alpha-mangostin from the PLGA microspheres. This was due to poor solubilising property of the methanol to completely dissolve the polymeric PLGA.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation