CLARIFICATION OF THE BIOLOGICAL MEANING OF MENAQUINONE-4 SYNTHESIS IN ANIMAL ORGANS
| Project/Area Number |
16580095
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Food science
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| Research Institution | TOHOKU UNIVERSITY |
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Principal Investigator |
SHIRAKAWA Hitoshi GRADUATE SCHOOL OF AGRICULTURAL SCIENCE, TOHOKU UNIVERSITY, ASSOCIATE PROFESSOR, 大学院農学研究科, 助教授 (40206280)
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| Co-Investigator(Kenkyū-buntansha) |
KOMAI Michio GRADUATE SCHOOL OF AGRICULTURAL SCIENCE, PROFESSOR, 大学院農学研究科, 教授 (80143022)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,800,000 (Direct Cost: ¥3,800,000)
Fiscal Year 2005: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2004: ¥2,500,000 (Direct Cost: ¥2,500,000)
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| Keywords | vitamin K / menaquinone-4 / anti-inflammation / gene regulation / steroidogenesis / 食品 / 生体内変換 / 抗炎症 / DNAマイクロアレイ |
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| Research Abstract |
Vitamin K (K) is well known for its role in post-translational activation of a family of nascent proteins to Gla-proteins, such as blood clotting factors and bone Gla-proteins. There are two forms of naturally occurring K: Ki, plant-synthesized phylloquinone; and K2, a family of homologues designated as menaquinone-n (MK-n), which are synthesized by microorganisms including intestinal microflora. However, reports indicate that K analogues are converted into MK-4 in various organs outside the gastrointestinal tract without involvement of bacterial enzymes. Although studies indicate that MK-4 has unique functions related to cell differentiation, induction of apoptosis, and stimulation of transcription of a ligand for the nuclear receptor, these cannot totally explain the physiological significance of MK-4 synthesis in diverse tissues. To help elucidate the biological role of MK-4 production, we used germfree rats to eliminate MK-n synthesized by intestinal flora, and identified patterns of gene expression as a function of K status.
Wistar germfree rats were fed either K-deficient, Control (normal level of 1(1), Ki-supplemented, or MK-4-supplemented diets. We obtained testicular gene expression profiles using DNA microarray techniques. Expression of genes involved in cholesterol synthesis and isoprenoid metabolism was down-regulated in the K-deficient group compared with Ki-supplemented animals. Quantitative RT-PCR analysis revealed that testicular MK-4 concentrations were positively correlated with expression of CYP11a, a rate-limiting enzyme involved in testicular testosterone synthesis. Moreover, plasma testosterone concentrations were reduced in K-deficient relative to Control and MK-4-supplemented animals. Together, these results suggest that testicular MK-4 could be a key factor involved in steroid hormone synthesis via regulation of gene expression related to steroidogenesis.
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Report
(3 results)
Research Products
(14 results)
