Functional food for ameliorating engogenous melatonin secretion rhythm and functional food for ameliorating circadian rhythm
a melatonin secretion and circadian rhythm technology, applied in the field of functional food for improving the secretion rhythm of engogenous melatonin, can solve the problems of completely different quality of sleep, unfulfilled assurance of safety of melatonin products, and the side effects of exogenous melatonin products per se, so as to prevent or ameliorate sleep disorder or prolonged sleep latency, improve the amplitude of endogenous melatonin secr
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[0049] The present invention will now be explained in more detail with reference to Examples, which do not intend to limit the present invention.
examples 1 and 2
[0050] Commercially available skim milk was dissolved in distilled water at a solid content of 9 mass %, subjected to high temperature pasteurization in an autoclave at 105° C. for 10 minutes, allowed to cool to the room temperature, inoculated with 3 mass % of a pre-cultured CM4 starter, and cultured at 37° C. for 24 hours, to thereby obtain fermented milk. This fermented milk was centrifuged at 12000 G for 20 minutes for removing the solids, to prepare fermented milk whey.
[0051] On the other hand, commercially available skim milk was dissolved in distilled water at a solid content of 9 mass %, subjected to high temperature pasteurization in an autoclave at 105° C. for 10 minutes, and allowed to cool to the room temperature. Lactic acid was added to increase the acidity to 2.2%. Then the product was centrifuged at 12000 G for 20 minutes for removing the solids, to prepare casein whey.
[0052] Each of the obtained fermented milk whey (Example 1) and casein whey (Example 2) was dilut...
examples 3 and 4
[0057] Thirty three male Wistar rats at 3 weeks of age were pre-bred for 1 week. During the pre-breeding, the rats were allowed free access to solid feed (trade name MF, manufactured by ORIENTAL YEAST CO., LTD.) and distilled water. The daily light-dark cycle during the pre-breeding was set such that the light cycle was from 8:00 to 20:00 and the dark cycle was for 12 hours after that. After the pre-breeding, the rats were divided into three groups (1) to (3) of 11 animals each in the same way as in Examples 1 and 2, and bred with free access to the respective drinks and solid feed for 1 month. After 1 month of breeding, 5 animals in each group was slaughtered at 12:00, and the remaining 6 animals in each group at 0:00, and the corpus pineale of each animal was taken out of the brain. The NAT activity in the corpus pineale was measured by the method of Thomas et al.
[0058] Specifically, 100 ml of 0.25 M calcium phosphate buffer (pH 1.5) containing 1.5 mM of acetyl CoA was added to t...
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