Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
Evid Based Complement Alternat Med
2013 Jan 01;2013:619361. doi: 10.1155/2013/619361.
Show Gene links
Show Anatomy links
Cytotoxic Activity of Six Samples of Brazilian Propolis on Sea Urchin (Lytechinus variegatus) Eggs.
Fernandes-Silva CC
,
Freitas JC
,
Salatino A
,
Salatino ML
.
???displayArticle.abstract???
The cytotoxic activities of extracts of four samples of propolis from the state of Minas Gerais (Southeast Brazil) and two from the state of Paraná (South Brazil) were evaluated using sea urchin (Lytechinus variegatus) eggs. Cytotoxic activity was observed, characterized mainly by the inhibition of the first cleavage of newly fertilized eggs. Methanol extracts at 32 µg mL(-1) of all samples were highly active (97-100%). Extracts were also prepared by successive treatments of the samples with hexane, chloroform, ethyl acetate, and methanol. High activity was observed using the ethyl acetate fractions of all samples, but hexane and chloroform fractions of some samples also had high activity. Based on the chemical composition of the extracts and fractions (published previously), it is hypothesized that the cytotoxic activities observed are due mainly to artepillin C, p-coumaric acid, and kaempferide. The results suggest that caffeoylquinic acids have no cytotoxic activity in sea urchin eggs.
Figure 1. Micrographs evidencing the effect of methanol extract and fractions of samples of Brazilian propolis at 32 μg mL−1 on the initial development of sea urchin (Lytechinus variegatus) embryos. (a) control (ethanol): normal development; (b) effect of methanol extract of sample D: inhibition of egg cleavage; (c) effect of chloroform fraction of sample D: eggs with abnormal division; (d) effect of ethyl acetate fraction of sample A: eggs with abnormal division or inhibition of cleavage. A and D: samples from Minas Gerais state. For detailed information regarding the activity of extracts of all samples and extracts, see Table 1. Scale bars = 100 μm.
Ahn,
Suppression of tumor-induced angiogenesis by Brazilian propolis: major component artepillin C inhibits in vitro tube formation and endothelial cell proliferation.
2007, Pubmed
Ahn,
Suppression of tumor-induced angiogenesis by Brazilian propolis: major component artepillin C inhibits in vitro tube formation and endothelial cell proliferation.
2007,
Pubmed
Banskota,
Chemical constituents of Brazilian propolis and their cytotoxic activities.
1998,
Pubmed
Chernysheva,
Synthesis and comparative evaluation of 4-oxa- and 4-aza-podophyllotoxins as antiproliferative microtubule destabilizing agents.
2012,
Pubmed
,
Echinobase
Hattori,
Isolation, identification, and biological evaluation of HIF-1-modulating compounds from Brazilian green propolis.
2011,
Pubmed
Inoue,
Anti-tumor effects of water-soluble propolis on a mouse sarcoma cell line in vivo and in vitro.
2008,
Pubmed
Ishihara,
Growth inhibitory activity of ethanol extracts of Chinese and Brazilian propolis in four human colon carcinoma cell lines.
2009,
Pubmed
Janicke,
Differential effects of ferulic acid and p-coumaric acid on S phase distribution and length of S phase in the human colonic cell line Caco-2.
2005,
Pubmed
Janicke,
The antiproliferative effect of dietary fiber phenolic compounds ferulic acid and p-coumaric acid on the cell cycle of Caco-2 cells.
2011,
Pubmed
Messerli,
Artepillin C (ARC) in Brazilian green propolis selectively blocks oncogenic PAK1 signaling and suppresses the growth of NF tumors in mice.
2009,
Pubmed
Mishima,
Identification of caffeoylquinic acid derivatives from Brazilian propolis as constituents involved in induction of granulocytic differentiation of HL-60 cells.
2005,
Pubmed
Naves,
Cytotoxicity in the marine dinoflagellate Prorocentrum mexicanum from Brazil.
2006,
Pubmed
,
Echinobase
Orsolić,
Immunomodulation by water-soluble derivative of propolis: a factor of antitumor reactivity.
2003,
Pubmed
Pellicanò,
The sea urchin embryo: a model to study Alzheimer's beta amyloid induced toxicity.
2009,
Pubmed
,
Echinobase
Salatino,
Propolis research and the chemistry of plant products.
2011,
Pubmed
Szliszka,
Ethanolic extract of Brazilian green propolis sensitizes prostate cancer cells to TRAIL-induced apoptosis.
2011,
Pubmed
Yoshimoto,
Antimutagenicity of mono-, di-, and tricaffeoylquinic acid derivatives isolated from sweetpotato (Ipomoea batatas L.) leaf.
2002,
Pubmed