Long-chain polyunsaturated fatty acids may mutually benefit both obesity and osteoporosis |
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Authors: | Owen J. Kelly Jennifer C. Gilman Youjin Kim Jasminka Z. Ilich |
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Affiliation: | 1. Abbott Nutrition Research and Development, Columbus, OH 43219-3034, USA;2. Department of Nutrition and Food Sciences, Texas Woman''s University, Denton, TX, 76204, USA;3. Bayer CropScience Ltd., Gangnam-gu, Seoul 135-979, Korea;4. Department of Nutrition, Food and Exercise Sciences, 418 SAN, Florida State University, Tallahassee, FL, 32306-1491 |
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Abstract: | The overconsumption of n-6 polyunsaturated fatty acids (PUFA), resulting in a high ratio of n-6 to n-3 PUFA, may contribute to the increased pathogenesis of obesity and osteoporosis by promoting low-grade chronic inflammation (LGCI). As evidence suggests, both obesity and osteoporosis are linked on a cellular and systemic basis. This review will analyze if a relationship exists between LGCI, fat, bone, and n-3 PUFA. During the life cycle, inflammation increases, fat mass accumulates, and bone mass declines, thus suggesting that a connection exists. This review will begin by examining how the current American diet and dietary guidelines may fall short of providing an anti-inflammatory dose of the n-3 PUFA eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). It will then define LGCI and outline the evidence for a relationship between fat and bone. Inflammation as it pertains to obesity and osteoporosis and how EPA and DHA can alleviate the associated inflammation will be discussed, followed by some preliminary evidence to show how mesenchymal stem cell (MSC) lineage commitment may be altered by inflammation to favor adipogenesis. Our hypothesis is that n-3 PUFA positively influence obesity and osteoporosis by reducing LGCI, ultimately leading to a beneficial shift in MSC lineage commitment. This hypothesis essentially relates the need for more focused research in several areas such as determining age and lifestyle factors that promote the shift in MSC commitment and if current intakes of EPA and DHA are optimal for fat and bone. |
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Keywords: | 2010 DG, 2010 Dietary Guidelines for Americans 5-Lox, 5-lipoxygenase AA, arachidonic acid AHA, American Heart Association ALA, α-linolenic acid AMDR, acceptable macronutrient distribution ranges BMD, bone mineral density CB2, cannabinoid receptor type 2 CRP, C-reactive protein Cox-2, cyclooxygenase-2 DHA, docosahexaenoic acid DPA, docosapentaenoic acid EPA, eicosapentaenoic acid IL-6, interleukin-6 IFNγ, interferon-γ LA, linoleic acid LGCI, low-grade chronic inflammation LTB4, leukotriene B4 LTB5, leukotriene B5 MCP-1, monocyte chemoattractant protein&ndash 1 MSC, mesenchymal stem cell NHANES, National Health and Nutrition Examination Survey NO, nitric oxide PGE2, prostaglandin E2 PUFA, polyunsaturated fatty acids SDA, stearidonic acid TNF-α, tumor necrosis factor&ndash α |
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