2014
DOI: 10.4172/2161-0495.1000232
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Cytotoxic and Anti-inflammatory Activities of Bursera species from Mexico

Abstract: Objective: Organic extracts from nine species (eleven populations) of the Bursera genus native to Mexico, were investigated for cytotoxic and anti-inflammatory activities. The influence of the cytotoxic plant extracts on cell cycle progression and apoptosis were also analyzed. Materials and methods: Cytotoxic activity from B. ariensis (Kunth) McVaugh and Rzed. Kew Bull (two populations), B. bicolor Engl., B. lancifolia Engl., B. glabrifolia Engl. (two populations), B. fagaroides (La Llave) Rez., Calderón and M… Show more

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Cited by 4 publications
(5 citation statements)
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References 35 publications
(32 reference statements)
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“…The antioxidant activity of other Bursera species have been associated with lignans (Nieto-Yañez 2017, Marcotullio et al 2018) and phenols (Martinez-Elizalde et al 2018) Flavonoids such as hesperidin, apigenin, luteolin and quercetin, have anti-inflammatory and analgesic effects (Ferraz et al 2020). In a previous work, anti-inflammatory effects have been reported with an average effective dose (ED 50 ) of B. excelsa (0.26 ± 0.01 mg/ear), B. galeottiana (0.23 ± 0.02 mg/ear) and B. schlechtendalii (0.25 ± 0.02 mg/ear) from bark using chloroform extracts (Acevedo et al 2015). These reports suggested that the highest concentration of anti-inflammatory metabolites was found in the bark, however, our results indicated that the flavonoids were also found in stems and leaves (Table 6).…”
Section: Discussionmentioning
confidence: 98%
“…The antioxidant activity of other Bursera species have been associated with lignans (Nieto-Yañez 2017, Marcotullio et al 2018) and phenols (Martinez-Elizalde et al 2018) Flavonoids such as hesperidin, apigenin, luteolin and quercetin, have anti-inflammatory and analgesic effects (Ferraz et al 2020). In a previous work, anti-inflammatory effects have been reported with an average effective dose (ED 50 ) of B. excelsa (0.26 ± 0.01 mg/ear), B. galeottiana (0.23 ± 0.02 mg/ear) and B. schlechtendalii (0.25 ± 0.02 mg/ear) from bark using chloroform extracts (Acevedo et al 2015). These reports suggested that the highest concentration of anti-inflammatory metabolites was found in the bark, however, our results indicated that the flavonoids were also found in stems and leaves (Table 6).…”
Section: Discussionmentioning
confidence: 98%
“…The chemical study of B. fagaroides over the years shows the characterization of 19 lignans that have been isolated from the bark, using solvents with different polarities and these compounds present cytotoxic activity, and some have been evaluated by their antitumor effect. It has been demonstrated that some of them promote mitotic arrest, delay cell migration, and disrupt microtubules [5][6][7][8][9][10][11]; however, their extraction and purification has been carried out from the bark and requires large amounts of plant biomass. Given the magnitude of tropical deforestation in recent decades, the fact that about 70% of tropical hardwood forests have been drastically lost [12,13], and that it is also one of the most threatened ecosystems in the country, it is necessary to seek alternatives for its extraction.…”
Section: Introductionmentioning
confidence: 99%
“…Its bark is yellowish gray, and it is used in traditional medicine to relieve inflammation, skin tumors and warts [4]. The chemical study of B. fagaroides over the years has included the characterization of 19 lignans structures classified into four groups: eight are aryltetralins: podophyllotoxin (1), β-peltatin-A-methylether (2), 5 ′ -desmethoxy-βpeltatin-A-methylether (3), desoxypodophyllotoxin (4), acetyl podophyllotoxin (5), morelensine (6), burseranin (7) and acetylpicropodophyllotoxin (8); three are dibenzylbutyrolac-tone: desmethoxy-yatein (9), yatein (10) and hinoquinin (11); three are aryldihydronaphtalene: 7 ′ ,8 ′ -dehydropodophyllotoxin (12), 7 ′ ,8 ′ -dehydroacethyl podophyllotoxin (13) and 7 ′ ,8 ′ -dehydro trans-p-cumaroylpodophyllotoxin (14); and five are lignan dibenzylbutanes: 9-acetyl-9 ′ -pentadecanoyldihydroclusin (15), 2,3-desmethoxy-secoisolintetralin monoacetate (16), dihydroclusin diacetate (17), 2,3-demethoxy-secoisolintetralin diacetate (18) and dihydroclusin mono acetate (19) [5][6][7]. These compounds have been isolated from the bark using solvents with different polarities [5,6,[8][9][10], and these compounds present important cytotoxic activity with IC 50 values ranging from 12 µgmL −1 (burseranin, 7) to 4.43 × 10 −6 µgmL −1 (β-peltatin-A-methylether, 2).…”
Section: Introductionmentioning
confidence: 99%
“…Some have been evaluated by their antitumor effect (2 and 3). It has been demonstrated that some of them (1, 2, 5 and 9) promote mitotic arrest, delay cell migration and disrupt microtubules [5][6][7][8][9][10][11]. Their extraction and purification have been carried out from the bark and require large amounts of plant biomass.…”
Section: Introductionmentioning
confidence: 99%
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