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Published on: December 16, 2022
Genistein and daidzein decrease food intake and body weight gain in mice, and alter LXR signaling in vivo and in
Ting Luo1, Omar Miranda-Garcia, Geoff Sasaki
1Food Science and Technology, Oregon State University, Corvallis, OR 97330, USA. Neil.Shay@oregonstate.edu.
Abstract:
The study is designed to determine whether consumption of the soy isoflavones, genistein and daidzein, differentially influence metabolic syndrome, and to further investigate the involvement of Liver X Receptor (LXR) regulation. C57BL/6J mice were fed diets as follows: low fat diet (LF), western-style diet (WD), and WD containing 0.16% (w/w) of genistein (WD + G) or daidzein (WD + D) for 10 weeks. Intake of WD + G and WD + D produced a robust decrease in body weight gain by 40% and 19%, respectively (p < 0.05). Genistein reduced energy intake by 26%, and daidzein decreased energy intake by 8% (p < 0.05). A glucose tolerance test indicated that genistein consumption significantly decreased the incremental areas under the curve (AUC) from 60-120 min, compared to WD-fed mice. Gene array profiling of hepatic mRNA, and cell studies utilizing transiently-transfected HepG2 cells and mouse embryonic fibroblast cells devoid of or expressing LXRα, indicate that genistein and daidzein induce LXR-mediated pathways. In summary, addition of genistein, compared to daidzein, to a western-style diet, more profoundly decreased food intake, body weight gain, while both appear to regulate LXR-mediated pathways.
Insights
Soy isoflavones genistein and daidzein consumption reduced body weight gain and food intake in mice. Both compounds appear to regulate Liver X Receptor (LXR)-mediated pathways, with genistein showing more profound effects.
Area of Science:
- Nutritional Science
- Metabolic Health
- Molecular Biology
Background:
- Metabolic syndrome is a growing health concern.
- Soy isoflavones, like genistein and daidzein, are plant compounds with potential health benefits.
- The role of soy isoflavones in metabolic regulation and their interaction with Liver X Receptor (LXR) pathways require further investigation.
Purpose of the Study:
- To determine if soy isoflavones, genistein and daidzein, differentially affect metabolic syndrome.
- To investigate the involvement of Liver X Receptor (LXR) regulation in the effects of these isoflavones.
Main Methods:
- C57BL/6J mice were fed a low-fat diet, a western-style diet (WD), or WD supplemented with genistein or daidzein for 10 weeks.
- Body weight gain, energy intake, and glucose tolerance were assessed.
- Hepatic mRNA gene array profiling and cell-based studies (HepG2, mouse embryonic fibroblasts) were used to examine LXR pathway involvement.
Main Results:
- Both genistein and daidzein significantly reduced body weight gain and energy intake compared to the western-style diet alone.
- Genistein demonstrated a more pronounced reduction in body weight gain and food intake than daidzein.
- Genistein consumption significantly improved glucose tolerance.
- Gene expression analysis and cell studies indicated that both genistein and daidzein activate LXR-mediated pathways.
Conclusions:
- Soy isoflavones, particularly genistein, can mitigate adverse effects of a western-style diet in mice.
- Genistein and daidzein exert their effects, at least partly, through the regulation of LXR-mediated pathways.
- Dietary interventions with soy isoflavones may offer a strategy for managing metabolic syndrome.
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