Tanshinone IIA improves impaired nerve functions in experimental diabetic rats

被引:64
作者
Liu, Yanwu [1 ]
Wang, Lingjuan [1 ]
Li, Xinkui [1 ]
Lv, Changwei [1 ]
Feng, Dapeng [2 ]
Luo, Zhuojing [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Inst Orthopaed, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Xijing Hosp, Dept Anesthesiol, Xian 710032, Peoples R China
关键词
Tanshinone ILA; Diabetic neuropathy; Motor nerve conducting velocity; Hyperalgesia; Antioxidant; NA+-K+ PUMP; OXIDATIVE STRESS; PATHOGENESIS; DAMAGE;
D O I
10.1016/j.bbrc.2010.07.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Diabetic neuropathy is one of the most common complications in diabetes mellitus. Thus far, effective therapeutic agents for restoring the impaired motor and sensory nerve functions in diabetic neuropathy are still lacking. The antioxidant and neuroprotective properties of tanshinone IIA make it a promising candidate for the treatment of diabetic neuropathy. Therefore, the present study investigated the possible beneficial effect of tanshinone IIA on the impaired nerve functions displayed by a rat diabetic model. Insulin-dependent diabetes in rats was developed by a single dose of streptozotocin (STZ) at 50 mg/kg. The diabetic rats were randomly divided into four groups (n = 10 in each group), and were intraperitoneally administrated daily for 4 weeks with tanshinone IIA (20 mg/kg, 50 mg/kg and 100 mg/kg), or normal saline from the fourth day after STZ injection, respectively. At the end of tanshinone IIA administration, thermal and mechanical nociceptive threshold were determined by a hot plate test and Von Frey hairs; motor nerve conducting velocity (MNCV) was determined by an electrophysiological method; nerve blood flow (NBF) was detected using a laser Doppler flow meter; Na+,K(+)ATPase activity, the level of superoxide dismutase (SOD), catalase and malondialdehyde (MDA) in sciatic nerves, and the serum total antioxidant capability were also determined. We found that tanshinone IIA was capable of restoring diabetes-induced deficit in nerve functions (MNCV and NBF), and impairment in thermal and mechanical nociceptive capability. In addition, tanshinone IIA significantly increased the serum total antioxidant capability, improved the activities of Na+,K(+)ATPase, increased the levels of SOD and catalase, and reduced the MDA level in sciatic nerves in diabetic rats. All the findings indicate the beneficial effect of tanshinone IIA on impaired nerve functions and raise the possibility of developing tanshinone IIA as a therapeutic agent for diabetic neuropathy. Crown Copyright (C) 2010 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:49 / 54
页数:6
相关论文
共 26 条
[1]
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]
ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[3]
Calcutt NA, 2002, INT REV NEUROBIOL, V50, P205
[4]
Effect of natural antioxidant tanshinone II-A on DNA damage by lipid peroxidation in liver cells [J].
Cao, EH ;
Liu, XQ ;
Wang, JJ ;
Xu, NF .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (06) :801-806
[5]
Effect of M40403 treatment of diabetic rats on endoneurial blood flow, motor nerve conduction velocity and vascular function of epineurial arterioles of the sciatic nerve [J].
Coppey, LJ ;
Gellett, JS ;
Davidson, EP ;
Dunlap, JA ;
Lund, DD ;
Salvemini, D ;
Yorek, MA .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (01) :21-29
[6]
Lipoic Acid Alters δ-Aminolevulinic Dehydratase, Glutathione Peroxidase and Na plus ,K plus -ATPase Activities and Glutathione-Reduced Levels in Rat Hippocampus After Pilocarpine-Induced Seizures [J].
de Freitas, Rivelilson Mendes .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2010, 30 (03) :381-387
[7]
Neuroprotective Effects of Tanshinone IIA on Permanent Focal Cerebral Ischemia in Mice [J].
Dong, Kenan ;
Xu, Wei ;
Yang, Jun ;
Qiao, Hongxiang ;
Wu, Limao .
PHYTOTHERAPY RESEARCH, 2009, 23 (05) :608-613
[8]
DRAPER HH, 1990, METHOD ENZYMOL, V186, P421
[9]
New insights into the pathogenesis of diabetic neuropathy [J].
Feldman, EL ;
Russell, JW ;
Sullivan, KA ;
Golovoy, D .
CURRENT OPINION IN NEUROLOGY, 1999, 12 (05) :553-563
[10]
Reversible Oxidative Modification A Key Mechanism of Na+-K+ Pump Regulation [J].
Figtree, Gemma A. ;
Liu, Chia-Chi ;
Bibert, Stephanie ;
Hamilton, Elisha J. ;
Garcia, Alvaro ;
White, Caroline N. ;
Chia, Karin K. M. ;
Cornelius, Flemming ;
Geering, Kaethi ;
Rasmussen, Helge H. .
CIRCULATION RESEARCH, 2009, 105 (02) :185-U187