Aromatase activating agent
a technology of activating agent and aromatase, which is applied in the direction of algae medical ingredients, drug compositions, metabolic disorders, etc., can solve the problems that direct administration is not appropriate for prevention or amelioration, and achieve the effect of prevention, amelioration or treatmen
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production example 1
Production of Mulberry Bark Extract
[0030] Mulberry bark (10 g) was subjected to extraction with an aqueous ethanol solution (50 v / v %, 25 mL) for about seven days at room temperature, followed by filtration, to thereby yield a mulberry bark extract (yield: 11 mL, evaporation residue: 11.6 w / v %).
production example 2
[0031] Extracts of the plants and chlorella listed in Table 1 below were prepared in accordance with the process of Production Example 1.
TABLE 1Portion subjectedSolvent employedPlantto extractionfor extractionGinsengRoot90% EthanolCucumberImmature fruit40% 1,3-ButanediolPhellodendron barkBark50% EthanolChlorellaWhole algaeWater
referential example 1
Construction of Reporter Gene Assay System
[0032] Genomic DNA was extracted from a human normal keratinocyte sample. A DNA fragment in the genomic DNA, the fragment containing a transcriptional control region of human aromatase gene exon 1c and a portion of the exon 1c, was amplified through PCR by use of the following primers.
upper primer5′-GACTAGTAAACAACCACAAAACTGCTC-3′(SEQ ID NO: 1)lower primer5′-AACTGCAGACAAGTCAAAACAAGGAAGC-3′(SEQ ID NO: 2)
[0033] The PCR product was treated with restriction enzymes SpeI and PstI, and the product was transferred into a SeaPansy null control vector (TOYO INK MFG. CO., LTD.) at SpeI and PstI sites thereof. The product was used as an Ex1c-luc plasmid in the luciferase assay described below.
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