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note
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6): δ 167.40, 166.94, 155.69, 139.77, 134.34, 130.63, 130.54, 130.31, 128.20, 125.87, 124.61, 124.45, 121.89, 115.61, 113.02, 68.77.
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0141680857
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Mouse experiment: Twenty-four mice (4-wk old, 17-19 g, Japan SLC, Haruno Breeding branch, Hamamatsu, Japan) were individually housed and maintained in a 12 h dark-light cycle at 22 ± 2 °C. They were fed ad libitum. After acclimatization for 1 wk by feeding a LFD, the mice were divided into two groups; LFD (8 mice) and HFD (16 mice) groups. The LFD-fed lean control group was maintained on a LFD throughout the study. The HFD group of mice was provided with a HFD for the first 8 wk of the study for development of obesity/diabetes. Then, they were separated into two groups with the same mean body weight. Each group was then given a HFD or HFD plus 3e for 4 wk. Compound 3e was administered as a mixture with the food (2.0 g of 3e per kg of diet). For this, 3e (400 mg) was dissolved in 0.5 mL DMSO and homogenized with 1% aqueous solution of polyglycerol fatty acid ester (19.5 mL, Mitsubishi-kagaku foods, Tokyo, Japan). The homogeneous suspension was mixed thoroughly in a powder form of HFD (200 g) and kneaded into a dough. Body weight and food intake were recorded every third day during the drug feeding period. At the end of the drug feeding period, glucose tolerance tests were performed. After a 5 d recovery period on their own diet (the test group on HFD plus 3e), mice were fasted overnight and blood collected by cardiac puncture under secobarbital anesthesia. Liver, lung, kidney, and white adipose tissue were excised and weighed.
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