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Anti-atherogenic and anti-angiogenic activities of polyphenols from propolis
Authors:Julio Beltrame Daleprane  Vanessa da Silva Freitas  Alejandro Pacheco  Martina Rudnicki  Luciane Aparecida Faine  Felipe Augusto Dörr  Masaharu Ikegaki  Luis Antonio Salazar  Thomas Prates Ong  Dulcinéia Saes Parra Abdalla
Institution:1. Laboratory of Studies on Bioactivity and Animal Morphogenesis, Department of Cell Biology, Embryology and Genetics, CCB, Federal University of Santa Catarina (UFSC), 88.049-900, Trindade, Florianópolis, SC, Brazil;2. Plant Morphogenesis and Biochemistry Laboratory, CCA, Federal University of Santa Catarina (UFSC), 88.040-900, P.O. Box: 476, Florianopolis, SC, Brazil;3. Genomic Engineering Laboratory, CTC, Federal University of Santa Catarina (UFSC), 88.040-900, Florianópolis, SC, Brazil;4. Biosciences National Laboratory, LNBio, Caixa Postal 6192, 13083-100, Campinas, SP, Brazil
Abstract:Propolis is a polyphenol-rich resinous substance extensively used to improve health and prevent diseases. The effects of polyphenols from different sources of propolis on atherosclerotic lesions and inflammatory and angiogenic factors were investigated in LDL receptor gene (LDLr?/?) knockout mice. The animals received a cholesterol-enriched diet to induce the initial atherosclerotic lesions (IALs) or advanced atherosclerotic lesions (AALs). The IAL or AAL animals were divided into three groups, each receiving polyphenols from either the green, red or brown propolis (250 mg/kg per day) by gavage. After 4 weeks of polyphenol treatment, the animals were sacrificed and their blood was collected for lipid profile analysis. The atheromatous lesions at the aortic root were also analyzed for gene expression of inflammatory and angiogenic factors by quantitative real-time polymerase chain reaction and immunohistochemistry. All three polyphenol extracts improved the lipid profile and decreased the atherosclerotic lesion area in IAL animals. However, only polyphenols from the red propolis induced favorable changes in the lipid profiles and reduced the lesion areas in AAL mice. In IAL groups, VCAM, MCP-1, FGF, PDGF, VEGF, PECAM and MMP-9 gene expression was down-regulated, while the metalloproteinase inhibitor TIMP-1 gene was up-regulated by all polyphenol extracts. In contrast, for advanced lesions, only the polyphenols from red propolis induced the down-regulation of CD36 and the up-regulation of HO-1 and TIMP-1 when compared to polyphenols from the other two types of propolis. In conclusion, polyphenols from propolis, particularly red propolis, are able to reduce atherosclerotic lesions through mechanisms including the modulation of inflammatory and angiogenic factors.
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