Updates on Aldose Reductase Inhibitors for Management of Diabetic Complications and Non-diabetic Diseases

被引:166
作者
Grewal, Ajmer Singh [1 ]
Bhardwaj, Shashikant [2 ]
Pandita, Deepti [3 ]
Lather, Viney [1 ]
Sekhon, Bhupinder Singh [4 ]
机构
[1] JCDM Coll Pharm, Dept Pharmaceut Chem, Sirsa 125055, Haryana, India
[2] JCDM Coll Pharm, Dept Pharmacol, Sirsa 125055, Haryana, India
[3] JCDM Coll Pharm, Dept Pharmaceut, Sirsa 125055, Haryana, India
[4] PCTE Inst Pharm, Dept Pharmaceut Chem, Ludhiana 142021, Punjab, India
关键词
Aldose reductase; Aldose reductase inhibitors; Cataract; Diabetes; Nephropathy; Neuropathy; Polyol pathway; Retinopathy; Sepsis complications; NERVE CONDUCTION-VELOCITY; LONG-TERM TREATMENT; NON-CARBOXYLIC ACID; GALACTOSE-FED DOGS; ATTENUATES THERMAL HYPERALGESIA; ALLERGIC AIRWAY INFLAMMATION; OXIDATIVE-NITROSATIVE STRESS; MAGNESIUM LITHOSPERMATE B; POTENT ORAL ACTIVITY; IN-VITRO EVALUATION;
D O I
10.2174/1389557515666150909143737
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diabetes mellitus occurrence has been associated to the modification of the physiological levels of glucose and is often accompanied by several long-term complications, namely neuropathy, nephropathy, retinopathy, cataract, and cardiovascular. Aldose reductase (AR) is an enzyme of aldoketo reductase super-family that catalyzes the conversion of glucose to sorbitol in the polyol pathway of glucose metabolism. In this context, aldose reductase inhibitors (ARIs) have received much attention worldwide. Decreased sorbitol flux through polyol pathway by ARIs could be an emerging target for the management of major complications of diabetes. The present review article describes a brief overview of the role of aldose reductase in the diabetic complications, advances achieved on ARIs and their potential use in the treatment and management of the major diabetic complications such as cataract, retinopathy, neuropathy, nephropathy and cardiovascular. The ARIs developed vary structurally, and representative structural classes of ARIs include i) carboxylic acid derivatives (such as Epalrestat, Alrestatin, Zopalrestat, Zenarestat, Ponalrestat, Lidorestat, and Tolrestat), ii) spirohydantoins and related cyclic amides (such as Sorbinil, Minalrestat, and Fidarestat), and iii) phenolic derivatives (related to Benzopyran-4-one and Chalcone). Among these inhibitors, Epalrestat is the only commercially available inhibitor till date. In addition, some other ARIs such as Sorbinil and Ranirestat had been advanced into late stage of clinical trials and found to be safe for human use. The role of various natural ARIs in management of diabetic complications will be discussed. Adapting ARIs could prevent sepsis complications, prevent angiogenesis, ameliorate mild or asymptomatic diabetic cardiovascular autonomic neuropathy and appear to be a promising strategy for the treatment of endotoxemia and other ROS-induced inflammatory diseases. The role of ARIs in non-diabetic diseases will also be discussed.
引用
收藏
页码:120 / 162
页数:43
相关论文
共 377 条
  • [21] MECHANISM OF HUMAN ALDEHYDE REDUCTASE - CHARACTERIZATION OF THE ACTIVE-SITE POCKET
    BARSKI, OA
    GABBAY, KH
    GRIMSHAW, CE
    BOHREN, KM
    [J]. BIOCHEMISTRY, 1995, 34 (35) : 11264 - 11275
  • [22] Bastaki S., 2005, Int J. Diabetes Metab., V13, P111, DOI DOI 10.1159/000497580
  • [23] Synthesis and aldose reductase inhibitory activity of benzoyl-amino acid derivatives
    Benvenuti, S
    Severi, F
    Costantino, L
    Vampa, G
    Melegari, M
    [J]. FARMACO, 1998, 53 (06): : 439 - 442
  • [24] An aldose reductase inhibitor but not myo-inositol blocks enhanced polyphosphoinositide turnover in peripheral nerve from diabetic rats
    BertiMattera, L
    Day, N
    Peterson, RG
    Eichberg, J
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1996, 45 (03): : 320 - 327
  • [25] ALDOSE REDUCTASE INHIBITION BY 2,4-OXO AND THIOXO DERIVATIVES OF 1,2,3,4-TETRAHYDROQUINAZOLINE
    BILLON, F
    DELCHAMBRE, C
    CLOAREC, A
    SARTORI, E
    TEULON, JM
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1990, 25 (02) : 121 - 126
  • [26] BORHANI DW, 1992, J BIOL CHEM, V267, P24841
  • [27] Synthesis of the human aldose reductase inhibitor rubrolide L
    Boukouvalas, John
    McCann, Lucas C.
    [J]. TETRAHEDRON LETTERS, 2010, 51 (35) : 4636 - 4639
  • [28] SYNTHESIS AND ALDOSE REDUCTASE INHIBITION-ACTIVITY OF SPIRO-[9H-FLUOREN-9,4'-IMIDAZOLIDINE]-2',5'-DIONE DERIVATIVES
    BOVY, P
    LENAERS, A
    CALLAERT, M
    HERICKX, N
    GILLET, C
    ROBA, J
    DETHY, JM
    CALLAERTDEVEEN, B
    JANSSENS, M
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1988, 23 (02) : 165 - 172
  • [29] Synthesis and aldose reductase inhibitory activity of some new chromonyl-2,4-thiazolidinediones
    Bozdak-Dundar, Oya
    Evranos, Begiim
    Das-Evcimen, Net
    Sarikaya, Mutlu
    Ertan, Rahmiye
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2008, 43 (11) : 2412 - 2417
  • [30] Long-term effects of ranirestat (AS-3201) on peripheral nerve function in patients with diabetic sensorimotor polyneuropathy
    Bril, V
    Buchanan, RA
    [J]. DIABETES CARE, 2006, 29 (01) : 68 - 72