Exp Clin Endocrinol Diabetes 2015; 123(08): 479-484
DOI: 10.1055/s-0035-1550019
Article
© Georg Thieme Verlag KG Stuttgart · New York

The Protective Effect of Losartan on Diabetic Neuropathy in a Diabetic Rat Model

T. Cavusoglu
1   Department of Histology & Embryology, Ege University Faculty of Medicine, Izmir, Turkey
2   Cord Blood, Cell and Tissue Research and Application Center, Ege University, Izmir, Turkey
,
T. Karadeniz
3   Departmen of Pathology, Izmir Tepecik Training and Research Hospital, Izmir, Turkey
,
E. Cagiltay
4   Department of Endocrinology & Metabolism, GATA Haydarpasa Teaching Hospital, Istanbul,Turkey
,
M. Karadeniz
5   Department of Endocrinology, Sifa University Faculty of Medicine, Izmir, Turkey
,
G. Yigitturk
1   Department of Histology & Embryology, Ege University Faculty of Medicine, Izmir, Turkey
,
E. Acikgoz
1   Department of Histology & Embryology, Ege University Faculty of Medicine, Izmir, Turkey
,
Y. Uyanikgil
1   Department of Histology & Embryology, Ege University Faculty of Medicine, Izmir, Turkey
2   Cord Blood, Cell and Tissue Research and Application Center, Ege University, Izmir, Turkey
,
U. Ates
6   Department of Histology & Embryology, Bilim University Faculty of Medicine, Istanbul, Turkey
,
M. İ. Tuglu
7   Department of Histology & Embryology, Celal Bayar University Faculty of Medicine, Manisa, Turkey
,
O. Erbas
8   Department of Physiology, Bilim University Faculty of Medicine, Istanbul, Turkey
› Author Affiliations
Further Information

Publication History

received 28 December 2014
first decision 20 April 2015

accepted 05 May 2015

Publication Date:
26 May 2015 (online)

Abstract

Aim: Involvement of the peripheral and autonomic nervous systems is possibly the most frequent complication of diabetes. Important risk factors included hyperglycemia, dyslipidemia, hypertension, and smoking. Angiotensin-converting-enzyme inhibitor (ACE) inhibitors should be beneficial in all vascular beds, including neuropathy and retinopathy. In this study we aimed to evaluate the effect of the angiotensin receptor blocker losartan on diabetic neuropathy in a diabetic rat model.

Material and Methods: 24 male, Sprague Dawley albino mature rats were divided into 3 groups; (1) control group: No drug was administered to the remainder of rats which blood glucose levels were under 120 mg/dl, (2) diabetic control: rats were given no medication, but 4 ml per day of tap water was given by oral gavage, (3) losartan groups: rats were given 10 mg/kg/day oral of losartan for 4 weeks. Electromyography (EMG) was applied to anesthetized rats at the end of 4th weekend. Then, the animals were euthanized and sciatic nerve was performed for histopathological examination.

Results: Compound Muscle Action Potential (CMAP) amplitude of diabetic rats receiving the Saline in the EMG was significantly reduced when compared to the control group. Distal latency value and CMAP duration of diabetic rats receiving the saline were meaningfully increased when compared to the control group. CMAP amplitude and CMAP duration of diabetic rats receiving the Losartan treatment in the EMG were meaningfully reduced when compared to diabetic rats receiving the Saline.

Perineural thickness in the rats receiving the Losartan treatment was found to be significantly reduced when compared to the group receiving the Saline.

Conclusions: As a result, it has been shown in this study that perineural thickness of the Losartan treatment was significantly reduced when compared to saline receiving group, significantly increased the immunoexpression of NGF, and also provided a significantly recovery in EMG when compared to Saline receiving group.

 
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