Chemical analysis and potential neuroprotective effects of Newfoundland berries

• Main Author: Hossain, Mohammad Zahid
• Format: Thesis
• Language: English
• Published: Memorial University of Newfoundland 2012
• Subjects: Newfoundland
• Online Access: https://research.library.mun.ca/6128/; https://research.library.mun.ca/6128/1/Hossain_MohammadZahid.pdf; https://research.library.mun.ca/6128/3/Hossain_MohammadZahid.pdf

The research in our laboratory involves the study of nutraceuticals, which are foods claimed to have a medicinal effect on human health. Powdered samples of bilberry, blueberry, black currant and lingonberry were provided from Natural Newfoundland Nutraceuticals (NNN Inc., Markland Newfoundland). Whole berries were also collected. For the analysis, various solvent extractions of the berry samples were conducted. The extract solutions were analyzed using a liquid chromatography-mass spectrometry (LC-MS) method for compound detection. Two distinct elution regions for anthocyanins and flavonols were obtained with near base line separation of different compounds. For proper identification of these compounds, two standards (delphinidin-3-glucoside and cyanidin-3-galactoside) were run to obtain a standard retention peak with MS value. LC-MS analysis revealed that various polyphenolic compounds, such as flavonoids (e.g. anthocyanins and flavonols), are present in these species of berries. In addition, our analysis revealed that bilberry and blueberry extracts appear to contain a greater array of antioxidant compounds when compared to black currant and lingonberry extracts. We have also conducted some quantitative analysis in order to compare compounds from native Newfoundland berries to those detected in these species from other regions. The bilberry extract was examined for neuroprotection by applying them to cultured rat brain cortical cells. Cells were injured using an in vitro model of trauma. High levels of lactate were measured after injury, showing that cells were unhealthy. When extracts were added to the cells 15 minutes before injury lactate levels dropped significantly. Aging experiments showed that up to day 17 cell cultures demonstrated no significant death of neurons, but by day 20 there was a dramatic loss of neurons. For glial cells, proliferation was noticed by day 17, but by day 20 there was no significance further change in glial cells. Extracts were added on days 17, 18 and 19 in vitro . By counting ...