Carnitine palmitoyltransferase inhibitors in the management of type 2 diabetes: an old promise to be maintained

被引:7
作者
Giannessi, F [1 ]
机构
[1] Sigma Tau Pharmaceut Ind SpA, Dept Endocrinol & Metab, I-00040 Pomezia, Rome, Italy
关键词
D O I
10.1358/dof.2003.028.04.725499
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Type 2 diabetes is a complex metabolic disease of epidemic proportions, and is more prevalent in People with a Western life-style. Present treatments consist mainly of insulin secretagogues, metformin and insulin sensitizers. This review will focus on the therapeutic potential of carnitine palmitoyltransferase (CPT) inhibitors, which act on long-chain fatty acids transport into the mitochondria. Particular attention will be devoted to the group of structurally related carnitine inhibitors, where a new selective molecule has now entered clinical development. In the past, a number of compounds have shown interesting characteristics without producing, for several reasons, a clinically available drug.
引用
收藏
页码:371 / 381
页数:11
相关论文
共 101 条
[1]   Hypoglycemic prodrugs of 4-(2,2-dimethyl-1-oxopropyl)benzoic acid [J].
Aicher, TD ;
Bebernitz, GR ;
Bell, PA ;
Brand, LJ ;
Dain, JG ;
Deems, R ;
Fillers, WS ;
Foley, JE ;
Knorr, DC ;
Nadelson, J ;
Otero, DA ;
Simpson, R ;
Strohschein, RJ ;
Young, DA .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (01) :153-163
[2]  
Amos AF, 1997, DIABETIC MED, V14, pS7, DOI 10.1002/(SICI)1096-9136(199712)14:5+<S7::AID-DIA522>3.3.CO
[3]  
2-I
[4]  
Anderson RC, 1998, CURR PHARM DESIGN, V4, P1
[5]   ANTIDIABETIC AGENTS - A NEW CLASS OF REVERSIBLE CARNITINE PALMITOYLTRANSFERASE-I INHIBITORS [J].
ANDERSON, RC ;
BALESTRA, M ;
BELL, PA ;
DEEMS, RO ;
FILLERS, WS ;
FOLEY, JE ;
FRASER, JD ;
MANN, WR ;
RUDIN, M ;
VILLHAUER, EB .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (18) :3448-3450
[6]  
ATKINSON L, 1979, BRIT J PHARMACOL, V66, pP444
[7]  
ATTWOOD PV, 1984, CURR TOP CELL REGUL, V23, P1
[8]   Drug therapy - Metformin [J].
Bailey, CJ ;
Turner, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (09) :574-579
[9]   Elucidation of the mechanism by which (+)-acylcarnitines inhibit mitochondrial fatty acid transport [J].
Baillet, L ;
Mullur, RS ;
Esser, V ;
McGarry, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :36766-36768
[10]   The impact of fatty acid oxidation on energy utilization: Targets and therapy [J].
Bebernitz, GR ;
Schuster, HF .
CURRENT PHARMACEUTICAL DESIGN, 2002, 8 (14) :1199-1227