2019
DOI: 10.3390/molecules24224112
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Anti-Amyloidogenic and Cyclooxygenase Inhibitory Activity of Guettarda speciosa

Abstract: Guettarda speciosa is known in traditional folk medicine for treating cough, cold, sore throat, fever, wounds, epilepsy, and headaches. To discover the scientific pharmacological potential of G. speciosa, we explore its anti-inflammatory, cytotoxicity, and inhibition of amyloid-beta (Aβ) aggregation effects. Cyclooxygenase assay of the G. speciosa CHCl3 (GSC) extract and G. speciosa MeOH (GSM) extract are more selective to COX-1 inhibition with a 50% inhibitory concentration (IC50) of 3.56 μg/mL for the GSC ex… Show more

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Cited by 15 publications
(15 citation statements)
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“…Of all documented Philippine medicinal plants, the top list of medicinal plants used for TCAM has been enumerated by [12]. Most of these Philippine medicinal plants have been evaluated to scientifically validate folkloric claims like the recent studies of [13][14][15][16][17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…Of all documented Philippine medicinal plants, the top list of medicinal plants used for TCAM has been enumerated by [12]. Most of these Philippine medicinal plants have been evaluated to scientifically validate folkloric claims like the recent studies of [13][14][15][16][17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…As part of our continuing search for potential anti-AD agents exhibiting anti-amyloidogenic activity (Tan et al 2019(Tan et al , 2020, the crude extracts of Pandanus clementis Merr. (Pandanaceae) were observed to inhibit the Aβ aggregation using the ThT assay.…”
Section: Introductionmentioning
confidence: 99%
“…The procedure for the ThT assay was previously reported [ 2 , 19 , 20 ]. Briefly, Aβ 1-42 (Aggresure™ (AnaSpec) Fremont, CA, USA) was dissolved in phosphate buffered saline (PBS) and incubated with or without the compounds or phenol red (positive control) at 37 °C for 24 h. ThT solution was added and incubated for 15 min.…”
Section: Methodsmentioning
confidence: 99%
“…Cell viability measurement was performed using the ATP luminescence assay as previously described [ 19 , 20 ]. SH-SY5Y cells were counted by Eve cell counter (NanoEntek, Inc., Seoul, Korea), and 2 × 10 4 cells/well density were sub-cultured in 96-well plate and incubated for 24 h. After incubation, cells were treated with the compounds for 24 h. The media were removed, cells were washed with PBS, fresh media were added, and incubated for another 30 min.…”
Section: Methodsmentioning
confidence: 99%