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    • 14. 发明申请
    • METHOD
    • 方法
    • WO2005032567A2
    • 2005-04-14
    • PCT/IB2004/003273
    • 2004-09-24
    • DANISCO A/SRAUTONEN, NinaNURMI, JussiNURMINEN, PäiviPUOLAKKAINEN, Pauli
    • RAUTONEN, NinaNURMI, JussiNURMINEN, PäiviPUOLAKKAINEN, Pauli
    • A61K35/74
    • A61K35/745A23K10/16A23K10/18A23K50/75A61K31/19A61K31/205A61K45/06A61K2300/00
    • The present invention relates to the use of a microorganism and/or a metabolite thereof to at least increase the amount of a COX-1 mRNA in a cell. The present invention further relates to the use of a microorganism and/or a metabolite thereof in the manufacture of a medicament to treat the side effects associated with nonsteroidal anti­inflammatory drugs (NSAIDs). The present invention further relates to a pharmaceutical preparation comprising in combination a nonsteroidal anti­inflammatory drug (NSAIDs) and a microorganism and/or a metabolite thereof which is capable of at least increasing the amount of a COX-1 mRNA in a cell. The present invention yet further relates to a pharmaceutical preparation comprising in combination betaine or a pharmaceutically acceptable salt thereof and a microorganism and/or a metabolite thereof which is capable of at least increasing the amount of a COX-1 mRNA in a cell. The microorganism may suitably be a bacterium, preferably from the genus Bifidobacterium.
    • 本发明涉及使微生物和/或其代谢物至少增加细胞中COX-1mRNA的量的用途。 本发明还涉及微生物和/或其代谢物在制备用于治疗与非甾体抗炎药(NSAID)相关的副作用的药物中的用途。 本发明还涉及一种药物制剂,其包含非甾体抗炎药(NSAID)和能够至少增加细胞中COX-1mRNA量的微生物和/或其代谢物的组合。 本发明还涉及包含组合甜菜碱或其药学上可接受的盐和能够至少增加细胞中COX-1 mRNA的量的微生物和/或其代谢物的药物制剂。 微生物可以适当地是细菌,优选来自双歧杆菌属。