6–11 Jul 2014
Palazzo del Bo and Centro Culturale San Gaetano, Padova
Europe/Rome timezone

P66 - Evaluation of the effects of Kolaviron (Garcinia kola) on the elemental metabolism in the rat liver and kidney using PIXE, RBS and SEM.

11 Jul 2014, 13:00
1h
Palazzo del Bo and Centro Culturale San Gaetano, Padova

Palazzo del Bo and Centro Culturale San Gaetano, Padova

Board: 66

Speaker

Dr Johan Mars (Department of Medical Bioscience, University of the Western Cape, Bellville, South Africa)

Description

Poor or no antioxidant activity has been implicated in the aetiology of various pathologies. Since antioxidants are mostly derived from natural resources, the search for medicinal plants, that can either cure or alleviate ailments, has been phenomenal over the past decades. One plant, Garcinia kola, the oil of which is termed kolaviron, has been identified to have possible antioxidant activity [1]. Trace elements such as Fe, Mn, Cu, Zn and Se, form an integral part in antioxidant activity, especially in organ metabolism. In this study organ (liver and kidney) metabolism of major such as C, O, N, S, and trace elements is investigated. The kolaviron was dissolved in corn oil. Two groups (control and experimental) of Wistar rats were selected. The animals were housed in accordance with WHO animal regulations. Both groups had ad libitum access to standard rat chow and potable tap water. The control group was fed, by gavage, with 200 microlitre of the solution of kolaviron in corn oil once per day for a period of 4 weeks. Afterwards the animals were sacrificed by intraperitoneal injection. The organs were excised and homogenised into smaller parts which were freeze-dried -80°C. The freeze-dried organ was then pulverized and press into a palette. Concentrations of trace elements were determined with proton-induced X-ray emission (PIXE). PIXE was selected since with this technique concentrations downto minimum detection limits (MDLs) of parts per million (ppm) can be determined. A beam of 3 MeV protons was used for bombardment and a Be filter of 125 micrometer thickness for absorption. Backscattering spectrometry (BS) and Scanning Electron Microscopy (SEM) were used to determine the matrix composition. PIXE and BS measurements were performed simultaneously. Scanning electron microscopy was used both as complementary and supplementary to PIXE and BS. Statistical tests of p < 0.5 were considered significant. References [1] Ogada & Braide (2009) Nig. J. Physio. Sci., vol. 24(1-2), pp. 53-57

Primary author

Dr Johan Mars (Department of Medical Bioscience, University of the Western Cape, Bellville, South Africa)

Co-authors

Dr Adulkarem Ilfergane (Department of Medical Bioscience, University of the Western Cape, Bellville, South Africa) Ms Carine Kunsevi-Kilola (Department of Molecular Biology and Human Genetics, Stellenbosch University, Tygerberg, South Africa) Prof. Ralph Henkel (Department of Medical Bioscience, University of the Western Cape, Bellville, South Africa)

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