18 research outputs found

    Estimation of Caffeine, Niacin and Calorie Content in Tea Commonly Consumed by Dhaka City Residents

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    Tea is largest consuming drink in the world. Many health claims is attributed towards the tea due to its distinguished phytochemical array. Role of tea is well established as a neutraceutical and many studies elucidate its pharmacological worth. The objective of this study was to calculate the calorie content by determining total lipid, crude fiber, total protein and available carbohydrate contents and estimation of caffeine and niacin content in Bangladeshi teas. The lipid, crude fiber, protein and available carbohydrate contents of the tea samples were found to be in the range of 3.25-5.53, 10.15-15.41, 12.97-17.08 and 4.78-6.21 g/100g fresh weight respectively while calorie contents were found in the range of 83.54- 101.46 Kcal/100g fresh weight of tea. The total caffeine and niacin content in teas ranged from 1.31 - 3.58 and 0.038 – 0.056 g/100g fresh weight respectively. Tea leaf contained the highest amount of caffeine (3.58 g/100g) and niacin (0.056 g/100g). As tea has different health effects it is essential to estimate the update nutrient contents of tea

    Acute Multiple Organ Failure in Adult Mice Deleted for the Developmental Regulator Wt1

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    There is much interest in the mechanisms that regulate adult tissue homeostasis and their relationship to processes governing foetal development. Mice deleted for the Wilms' tumour gene, Wt1, lack kidneys, gonads, and spleen and die at mid-gestation due to defective coronary vasculature. Wt1 is vital for maintaining the mesenchymal–epithelial balance in these tissues and is required for the epithelial-to-mesenchyme transition (EMT) that generates coronary vascular progenitors. Although Wt1 is only expressed in rare cell populations in adults including glomerular podocytes, 1% of bone marrow cells, and mesothelium, we hypothesised that this might be important for homeostasis of adult tissues; hence, we deleted the gene ubiquitously in young and adult mice. Within just a few days, the mice suffered glomerulosclerosis, atrophy of the exocrine pancreas and spleen, severe reduction in bone and fat, and failure of erythropoiesis. FACS and culture experiments showed that Wt1 has an intrinsic role in both haematopoietic and mesenchymal stem cell lineages and suggest that defects within these contribute to the phenotypes we observe. We propose that glomerulosclerosis arises in part through down regulation of nephrin, a known Wt1 target gene. Protein profiling in mutant serum showed that there was no systemic inflammatory or nutritional response in the mutant mice. However, there was a dramatic reduction in circulating IGF-1 levels, which is likely to contribute to the bone and fat phenotypes. The reduction of IGF-1 did not result from a decrease in circulating GH, and there is no apparent pathology of the pituitary and adrenal glands. These findings 1) suggest that Wt1 is a major regulator of the homeostasis of some adult tissues, through both local and systemic actions; 2) highlight the differences between foetal and adult tissue regulation; 3) point to the importance of adult mesenchyme in tissue turnover
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