Cholesterol absorption inhibitors in development as potential therapeutics

被引:8
作者
Kajinami, K [1 ]
Takekoshi, N [1 ]
机构
[1] Kanazawa Med Univ, Dept Cardiol, Uchinada, Ishikawa 9200293, Japan
关键词
ATP-binding cassette transporter; bile acid sequestrant; bile acid transporter inhibitor; cholesterol absorption inhibitor;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drugs that lower low-density lipoprotein cholesterol through their actions in the gastrointestinal tract have been used for > 30 years. Bile acid sequestrants have very excellent safety profiles but their poor tolerability means they have limited clinical use. Recently developed new compounds are better tolerated in clinical trials and show greater benefit in reducing low-density lipoprotein cholesterol level, as compared to 'older' sequestrants. Cholesterol absorption inhibitors and bile acid transporter inhibitors have recently been reported to show clinical efficacy and safety as novel gut-acting drugs for lowering cholesterol. Further advances in, our understanding of the cholesterol absorption mechanism will provide novel therapeutic targets, such as the ATP-binding cassette transporter. This approach in the treatment of lowering cholesterol appears to play a more significant role in the clinical field of atherosclerotic vascular disease.
引用
收藏
页码:831 / 835
页数:5
相关论文
共 21 条
[1]   Effective lipid modification by partial ileal bypass reduced long-term coronary heart disease mortality and morbidity: Five-year posttrial follow-up report from the POSCH [J].
Buchwald, H ;
Varco, RL ;
Boen, JR ;
Wiliams, SE ;
Hansen, BJ ;
Campos, CT ;
Campbell, GS ;
Pearce, MB ;
Yellin, AE ;
Edmiston, WA ;
Smink, RD ;
Sawin, HS .
ARCHIVES OF INTERNAL MEDICINE, 1998, 158 (11) :1253-1261
[2]   Ezetimibe: a selective inhibitor of cholesterol absorption [J].
Catapano, AL .
EUROPEAN HEART JOURNAL SUPPLEMENTS, 2001, 3 (0E) :E6-E10
[3]   Molecular mechanisms of sterol absorption [J].
Chen, HC .
JOURNAL OF NUTRITION, 2001, 131 (10) :2603-2605
[4]   Colesevelam hydrochloride: a non-absorbed, polymeric cholesterol-lowering agent [J].
Davidson, MH ;
Dicklin, MR ;
Maki, KC ;
Kleinpell, RM .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2000, 9 (11) :2663-2671
[5]   Colesevelam hydrochloride (Cholestagel) - A new, potent bile acid sequestrant associated with a low incidence of gastrointestinal side effects [J].
Davidson, MH ;
Dillon, MA ;
Gordon, B ;
Jones, P ;
Samuels, J ;
Weiss, S ;
Isaacsohn, J ;
Toth, P ;
Burke, SK .
ARCHIVES OF INTERNAL MEDICINE, 1999, 159 (16) :1893-1900
[6]   Drug interactions with colesevelam hydrochloride, a novel, potent lipid-lowering agent [J].
Donovan, JM ;
Stypinski, D ;
Stiles, MR ;
Olson, TA ;
Burke, SK .
CARDIOVASCULAR DRUGS AND THERAPY, 2000, 14 (06) :681-690
[7]  
ENDO A, 1992, J LIPID RES, V33, P1569
[8]   Specific reduction of plasma large, light low-density lipoprotein by a bile acid sequestering resin, cholebine (MCI-196) in type II hyperlipoproteinemia [J].
Homma, Y ;
Kobayashi, T ;
Yamaguchi, H ;
Ozawa, H ;
Sakane, H ;
Nakamura, H .
ATHEROSCLEROSIS, 1997, 129 (02) :241-248
[9]   Coadministration of colesevelam hydrochloride with atorvastatin lowers LDL cholesterol additively [J].
Hunninghake, D ;
Insull, W ;
Toth, P ;
Davidson, D ;
Donovan, JM ;
Burke, SK .
ATHEROSCLEROSIS, 2001, 158 (02) :407-416
[10]  
Ichihashi T, 1998, J PHARMACOL EXP THER, V284, P43