Novel molecular targets for prevention of obesity and osteoporosis |
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Authors: | Rayalam Srujana Yang Jeong-Yeh Della-Fera Mary Anne Baile Clifton A |
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Affiliation: | a Department of Animal and Dairy Science, University of Georgia, Athens, GA 30602, USAb Department of Foods and Nutrition, University of Georgia, Athens, GA 30602, USA |
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Abstract: | Evidence from both epidemiological studies and basic research suggests that obesity and osteoporosis are interrelated. Though there is an increase in the prevalence of these disorders, a limited number of treatments are available, one of the reasons being the complexity of the pathways involved and difficulty in identifying a single molecular target. Due to adverse effects of pharmaceuticals, intake of herbal drugs by patients without a physician's recommendation is increasing globally. Lack of success with targeted monotherapy has encouraged scientists to determine whether combinations of phytochemicals that interfere with numerous cell-signaling pathways can be a more effective approach to treat complex diseases. For example, evidence is emerging that specific combinations of phytochemicals are far more effective than single compounds in decreasing adipogenesis and promoting bone formation. Since multiple pathways are dysfunctional in obesity and osteoporosis, an ideal approach for preventing and treating these diseases may be to use a combination of phytochemicals to address several targets simultaneously. |
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Keywords: | AHR, aryl hydrocarbon receptor ARNT, AHR nuclear translocator BAs, bile acids cAMP, cyclic adenosine monophosphate CRE, cAMP response element CYP24, cytochrome P450 enzyme 24-hydroxylase CYP27B1, 1 α-hydroxylase D2, type 2 iodothyronine deiodinase FXR, farnesoid X receptor FXRE, FXR responsive element VDR, vitamin D receptor VDRE, vitamin D responsive element TCDD, 2,3,7,8-tetrachlorodibenzo-p-dioxin T3, triiodothyronine T4, thyroxine |
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