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Chemical characterization, antioxidant and anti-HIV activities of a Brazilian propolis from Ceará state
Departamento de BotânicaSilva, Caroline Cristina Fernandes da; Departamento de BotânicaSalatino, Antonio; Motta, Lucimar Barbosa da; Departamento de BotânicaNegri, Giuseppina; Departamento de BotânicaSalatino, Maria Luiza Faria.
Affiliation
  • Departamento de BotânicaSilva, Caroline Cristina Fernandes da; Universidade de São Paulo. Instituto de Biociências. Departamento de BotânicaSilva, Caroline Cristina Fernandes da. São Paulo. BR
  • Departamento de BotânicaSalatino, Antonio; Universidade de São Paulo. Instituto de Biociências. Departamento de BotânicaSalatino, Antonio. São Paulo. BR
  • Motta, Lucimar Barbosa da; Universidade Paulista. São Paulo. BR
  • Departamento de BotânicaNegri, Giuseppina; Universidade de São Paulo. Instituto de Biociências. Departamento de BotânicaNegri, Giuseppina. São Paulo. BR
  • Departamento de BotânicaSalatino, Maria Luiza Faria; Universidade de São Paulo. Instituto de Biociências. Departamento de BotânicaSalatino, Maria Luiza Faria. São Paulo. BR
Rev. bras. farmacogn ; 29(3): 309-318, May-June 2019. tab, graf
Article in En | LILACS-Express | LILACS | ID: biblio-1020583
Responsible library: BR1.1
ABSTRACT
ABSTRACT Propolis (bee glue) a product of Apis mellifera L. is a resinous mixture containing chiefly beeswax and resin harvested by bees from plant leaves, buds and exudates. Extracts of a propolis sample from Salitre, a municipality of Ceará state (northeast Brazil) were obtained with solvents of increasing polarity (hexane, chloroform, ethyl acetate and methanol). A chemical profile was carried out by GC-EI-MS and HPLC-DAD-ESI-MS/MS. Lupenone, lupeol, octanoic acid tetracosyl ester and octanoic acid hexacosyl ester were identified by GC-EI-MS. Antioxidant activity was evaluated by the DPPH and β-carotene discoloring methods, and anti-HIV activity by the in vitro inhibition of HIV-1 reverse transcriptase. The ethyl acetate extract exhibited the highest antioxidant and anti-HIV activity and was fractioned by column chromatography using silica gel and seven different eluents. The active fractions were submitted to semi preparative HPLC and the following compounds were isolated caffeic acid, p-coumaric acid, diprenylcinnamic acid, quercetin, naringenin, isorhamnetin, quercetin-3-O-diglucoside,4,2′,4′-trihydroxy-2-methoxychalcone, gossypetin-3,3′,4′,7-tetramethyl ether, myricetin-3,7,3′-trimethyl ether and 5-hydroxy-3,6,7,8,4′-pentamethoxyflavone. The ethyl acetate extract and its fractions F5-F7, as well as quercetin, isorhamnetin, myricetin-3,7,3′-trimethyl ether and p-coumaric acid exhibited high antioxidant activity on both DPPH and β-carotene antioxidant methods. Isorhamnetin exhibited moderate inhibitory effect against HIV-1 reverse transcriptase (56.99 ± 3.91%), followed by naringenin (44.22 ± 1.71%), quercetin (43.41 ± 4.56%) and diprenylcinnamic acid (41.59 ± 2.59%). These results agree with previous authors who reported anti-HIV activity of flavonoids.
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Full text: 1 Index: LILACS Country/Region as subject: America do sul / Brasil Language: En Journal: Rev. bras. farmacogn Journal subject: FARMACIA Year: 2019 Type: Article

Full text: 1 Index: LILACS Country/Region as subject: America do sul / Brasil Language: En Journal: Rev. bras. farmacogn Journal subject: FARMACIA Year: 2019 Type: Article