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    • 6. 发明申请
    • SYSTEM FOR SCREENING FATTY ACID TRANSPORT INHIBITORS, METHODS OF USE AND MODULATORS IDENTIFIED THEREBY
    • 用于筛选脂肪酸运输抑制剂的系统,使用方法和鉴定的调节剂
    • WO2002072872A2
    • 2002-09-19
    • PCT/US2002/007884
    • 2002-03-14
    • ALBANY MEDICAL COLLEGEBLACK, PaulDIRUSSO, Concetta
    • BLACK, PaulDIRUSSO, Concetta
    • C12Q
    • C12Q1/25G01N33/92G01N2333/9015G01N2800/044
    • Methods for identifying modulators of fatty acid transport and/or uptake, comprising contacting, under conditions favorable for fatty acid uptake, a putative modulator, e.g., an inhibitor with a system comprising genetic material encoding a fatty acid transport mediator ("TTM"), particularly FAA1, FAA2, FAA3, FAA4. FAT1, fadL, fadD , FATP, CD36 and FABP, or orthologs, homologs, isoforms, variants, analogs, derivatives or fragments thereof, and combinations thereof, or fatty acid transport mediator proteins ("TTMps"), e.g., Faa1p, Faa2p, Faa3p, Faa4p, Fat1p, FadL, fatty acyl CoA synthetase, FATP, CD36 and FABP, or orthologs, homologs, isoforms, variants, analogs, derivatives or fragments thereof, and combinations thereof, and determining the effect of the putative modulator. The test system may be a cell such as Saccharomyces cerevisiae, E. coli, H. sapiens, etc. or an in vitro system.
    • 用于鉴定脂肪酸转运和/或摄取的调节剂的方法包括在有利于脂肪酸摄取的条件下,将推定的调节剂例如抑制剂与包含编码脂肪酸转运介体(“TTM”)的遗传物质的系统接触, 特别是FAA1,FAA2,FAA3,FAA4。 FAT1,fadL,fadD,FATP,CD36和FABP,或直系同源物,同系物,同种型,变体,类似物,衍生物或其片段及其组合,或脂肪酸转运介质蛋白(“TTMps”),例如Faa1p,Faa2p, Faa3p,Faa4p,Fat1p,FadL,脂肪酰辅酶A合成酶,FATP,CD36和FABP,或直系同源物,同系物,同种型,变体,类似物,衍生物或其片段及其组合,并确定推定的调节剂的作用。 测试系统可以是细胞,例如酿酒酵母,大肠杆菌,黑麦草等,或体外系统。
    • 9. 发明申请
    • METHODS AND COMPOSITIONS FOR TREATING ADDICTION DISORDERS
    • 治疗接触性疾病的方法和组合
    • WO2002060425A1
    • 2002-08-08
    • PCT/US2002/002547
    • 2002-01-29
    • ALBANY MEDICAL COLLEGE
    • GLICK, Stanley, D.MAISONNEUVE, Isabelle, M.
    • A61K31/00
    • A61K45/06
    • A method for treating an addiction disorder (such as an addiction to or dependency on stimulants, nicotine, morphine, heroin, other opiates, amphetamines, cocaine, and/or alcohol) in a patient is disclosed. The method includes administering to the patient a first α 3 β 4 nicotinic receptor antagonist and administering to the patient a second α 3 β 4 nicotinic receptor antagonist. The second α 3 β 4 nicotinic receptor antagonist is different than the first α 3 β 4 nicotinic receptor antagonist and the second α 3 β 4 nicotinic receptor antagonist are administered simultaneously or non-simultaneously. Compositions which include a first α 3 β 4 nicotinic receptor antagonist are also described. Examples of suitable α 3 β 4 nicotinic receptor antagonists for use in the present invention's methods and compositions include mecamylamine, 18-methoxycoronaridine, bupropion, dextromethorphan, dextrorphan, and pharmaceutically acceptable salts and solvates thereof. A method of evaluating a compound for its effectiveness in treating addiction disorders is also described.
    • 公开了一种治疗患者的成瘾症状(例如成瘾或依赖兴奋剂,尼古丁,吗啡,海洛因,其他阿片剂,苯丙胺,可卡因和/或酒精)的方法。 该方法包括向患者施用第一α3β4烟碱受体拮抗剂并向患者施用第二α3β4烟碱受体拮抗剂。 第二个α3β4烟碱受体拮抗剂与第一个α3β4烟碱受体拮抗剂不同,第二个α3β4烟碱受体拮抗剂同时或不同时施用。 还描述了包含第一α3β4烟碱受体拮抗剂的组合物。 用于本发明方法和组合物的合适的α3β4烟碱受体拮抗剂的实例包括美加明,18-甲氧基冠醚,安非他酮,右美沙芬,右美沙芬及其药学上可接受的盐和溶剂合物。 还描述了一种评价化合物治疗成瘾症的有效性的方法。