Diabetic neuropathy: therapies on the horizon

被引:0
|
作者
Mahmood, Danish [1 ]
Singh, Bhulan Kumar [1 ]
Akhtar, Mohammad [1 ]
机构
[1] Hamdard Univ, Dept Pharmacol, Fac Pharm, New Delhi 110062, India
关键词
diabetic neuropathy; poly(ADP-ribose) polymerase inhibitors; non-immunosuppressive immunophilin ligand; ALPHA-LIPOIC ACID; GLYCATION END-PRODUCTS; ACETYL-L-CARNITINE; ALDOSE REDUCTASE INHIBITOR; MOTOR-NERVE CONDUCTION; KINASE-C ACTIVATION; PROTEIN-KINASE; PERIPHERAL NEUROPATHY; INTRAVENOUS IMMUNOGLOBULIN; GROWTH-FACTOR;
D O I
10.1211/jpp/61.09.0002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives This is a review of emerging interventions from the recent preclinical and clinical literature that demonstrate the potential for effectiveness in the therapy of diabetic neuropathy (DN). DN is the most common complication of diabetes mellitus and up to 50% of patients with type 1 and type 2 forms have some or other form of neuropathy. The pathology of DN is characterized by progressive nerve fibre loss that gives rise to positive and negative clinical signs and symptoms such as pain, paraesthesiae and loss of sensation. Key findings There are very few drugs available to directly treat DN. Those that are clinically indicated provide symptomatic relief but do not repair or reverse underlying nerve damage. However, some agents are in clinical development that may support adult neurons and direct reparative processes after injury stages. Several disease modifying drugs such as aldose reductase inhibitors and protein kinase C inhibitors are in phase Ill development. Agents on the horizon include neurotrophic factors, growth factors, gene therapy, immunotherapy, poly(ADP-ribose) polymerase inhibitors and non-immunosuppressive immunophilin ligands. Summary Progress has been made toward understanding the biochemical mechanisms leading to diabetic neuropathy, and as a result, new treatment modalities are being explored. The pathogenesis, types and approaches for treating DN together with the newer therapeutic interventions on the horizon are discussed.
引用
收藏
页码:1137 / 1145
页数:9
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