2011
DOI: 10.1016/j.foodchem.2010.09.043
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In vivo and in vitro studies to identify the hypoglycaemic constituents of Momordica charantia wild variant WB24

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Cited by 42 publications
(49 citation statements)
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“…abbreviata Seringe) is a wild variety of Momordica charantia and is consumed as both a vegetable and as folk medicine in Taiwan. Bitter melon is known to contain numerous components such as alkaloids, steroidal glucosides, phenolics (Krawinkel & Keding, 2006), lysophosphatidylcholines (Kobori et al, 2008), conjugated linolenic acid isomers (Chuang et al, 2006), and cucurbitane-type triterpenoids (Chang et al, 2011;Hsu, Hsieh, Kuo, & Huang, 2011). 1-R-linolenoyl-LPC and 1-linoleoyl-LPC has been shown to negatively regulate TNF-a production in endotoxin lipopolysaccharide (LPS)-activated RAW264.7 macrophages (Kobori et al, 2008).…”
Section: Introductionmentioning
confidence: 99%
“…abbreviata Seringe) is a wild variety of Momordica charantia and is consumed as both a vegetable and as folk medicine in Taiwan. Bitter melon is known to contain numerous components such as alkaloids, steroidal glucosides, phenolics (Krawinkel & Keding, 2006), lysophosphatidylcholines (Kobori et al, 2008), conjugated linolenic acid isomers (Chuang et al, 2006), and cucurbitane-type triterpenoids (Chang et al, 2011;Hsu, Hsieh, Kuo, & Huang, 2011). 1-R-linolenoyl-LPC and 1-linoleoyl-LPC has been shown to negatively regulate TNF-a production in endotoxin lipopolysaccharide (LPS)-activated RAW264.7 macrophages (Kobori et al, 2008).…”
Section: Introductionmentioning
confidence: 99%
“…The obtained powder was extracted with methanol (3 × 120 L) at room temperature (7 d each) (Chang et al, 2006(Chang et al, , 2011. The combined methanol extract was evaporated under reduced pressure to afford a black residue, which was suspended in H2O (6 L), and then partitioned sequentially, using ethyl acetate (EA) and n-butanol (3 × 4 L) as the solvents.…”
Section: Source Extraction Fractionation and Purification Of C Momentioning
confidence: 99%
“…Glucose uptake assays in insulinresistant FL83B cells were performed by treating cells with 20 ng/ mL TNF-α for 5 h, followed by treating the cells with the investigated chemical and 100 nM insulin for 5 h. At 0, 1, 2, 3, 4, and 5 h after the addition of the chemical, glucose concentration of the culture medium was assayed, as previously described (Chang et al, 2011). For assays using normal FL83B cells, experiments were performed similarly except that cells were not pretreated with TNF-α.…”
Section: 4mentioning
confidence: 99%
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“…17) BHK-21 cells, purchased from the Bioresource Collection and Research Centre, were grown and counted to 10000 cells in a 96-well microplate. The cells were then treated with various concentrations (0 to 20 mm) of butyrate, 2-PB, 3-PB and 4-PB for 24 h in quadruplicate.…”
Section: )mentioning
confidence: 99%