Effect of sodium tungstate on visual evoked potentials in diabetic rats

被引:4
作者
Bulut, Mehmet [1 ]
Donmez, Baris Ozgur [2 ]
Ozturk, Nihal [3 ]
Basaranlar, Goksun [3 ]
Manas, Ceren Kencebay [3 ]
Derin, Narin [3 ]
Ozdemir, Semir [3 ]
机构
[1] Antalya Educ & Res Hosp, Dept Ophthalmol, TR-07070 Antalya, Turkey
[2] Akdeniz Univ, Sch Hlth, Dept Nutr & Dietet, TR-07070 Antalya, Turkey
[3] Akdeniz Univ, Fac Med, Dept Biophys, TR-07070 Antalya, Turkey
关键词
diabetes; retinopathy; sodium tungstate; visual evoked potentials; lipid peroxidation; OXIDATIVE STRESS; GLUCOSE; BRAIN; PATHOPHYSIOLOGY; COMPLICATIONS; RETINOPATHY; RESISTANCE; EXERCISE;
D O I
10.18240/ijo.2016.05.06
中图分类号
R77 [眼科学];
学科分类号
100212 [眼科学];
摘要
AIM: To evaluate the effect of sodium tungstate on visual evoked potentials (VEPs) in diabetic rats. METHODS: Wistar rats were randomly divided into three groups as normal control, diabetic control and diabetic rats treated with sodium tungstate. Diabetes was induced by single intraperitoneal injection of streptozotocin (50 mg/kg). Sodium tungstate [40 mg/(kg.d)] was administered for 12wk and then VEPs were recorded. Additionally, thiobarbituric acid reactive substance (TBARS) levels were measured in brain tissues. RESULTS: The latencies of P1, N1, P2, N2 and P3 waves were significantly prolonged in diabetic rats compared with control group. Diabetes mellitus caused an increase in the lipid peroxidation process that was accompanied by changes in VEPs. However, prolonged latencies of VEPs for all components returned to control levels in sodium tungstate-treated group. The treatment of sodium tungstate significantly decreased brain TBARS levels and depleted the prolonged latencies of VEP components compared with diabetic control group. CONCLUSION: Sodium tungstate shows protective effects on visual pathway in diabetic rats, and it can be worthy of further study for potential use.
引用
收藏
页码:677 / 681
页数:5
相关论文
共 41 条
[1]
Methods for monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins [J].
Abuja, PM ;
Albertini, R .
CLINICA CHIMICA ACTA, 2001, 306 (1-2) :1-17
[2]
Neuromodulatory Effects of Hesperidin in Mitigating Oxidative Stress in Streptozotocin Induced Diabetes [J].
Ashafaq, Mohammad ;
Varshney, Laxmi ;
Khan, Mohammad Haaris Ajmal ;
Salman, Mohd. ;
Naseem, Mehar ;
Wajid, Saima ;
Parvez, Suhel .
BIOMED RESEARCH INTERNATIONAL, 2014, 2014
[3]
A new view of diabetic retinopathy: a neurodegenerative disease of the eye [J].
Barber, AJ .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2003, 27 (02) :283-290
[4]
Tungstate is an effective antidiabetic agent in streptozotocin-induced diabetic rats:: a long-term study [J].
Barberà, A ;
Gomis, RR ;
Prats, N ;
Rodríguez-Gil, JE ;
Domingo, M ;
Gomis, R ;
Guinovart, JJ .
DIABETOLOGIA, 2001, 44 (04) :507-513
[5]
ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[6]
Bertinat R, 2015, J CLIN CELL IMMUNOL, V6
[7]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]
The role of oxidative stress in corneal diseases and injuries [J].
Cejkova, Jitka ;
Cejka, Cestmir .
HISTOLOGY AND HISTOPATHOLOGY, 2015, 30 (08) :893-900
[9]
Caffeic acid phenethyl ester (CAPE) protects brain against oxidative stress and inflammation induced by diabetes in rats [J].
Celik, Sefa ;
Erdogan, Suat .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2008, 312 (1-2) :39-46
[10]
Effects of streptozotocin-induced type 1 diabetes mellitus on total protein concentrations and cation contents in the isolated pancreas, parotid, submandibular, and lacrimal glands of rats [J].
Changrani, Navin R. ;
Chonkar, Apurva ;
Adeghate, Ernest ;
Singh, Jaipaul .
DIABETES MELLITUS AND ITS COMPLICATIONS: MOLECULAR MECHANISMS, EPIDEMIOLOGY, AND CLINICAL MEDICINE, 2006, 1084 :503-519