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Research ArticleOriginal Article
Open Access

The protective effect of NG-nitro-L-arginine methyl ester and insulin on nitric oxide inhibition and pathology in experimental diabetic rat liver

Hilmi Ozden, Neslihan Tekin, Fahrettin Akyuz, Firdevs Gurer, Mehmet C. Ustuner, Fulya Kucuk, Gul Guven and Faik Yaylak
Saudi Medical Journal January 2009, 30 (1) 30-34;
Hilmi Ozden
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Neslihan Tekin
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Fahrettin Akyuz
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Firdevs Gurer
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Mehmet C. Ustuner
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Fulya Kucuk
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Gul Guven
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Faik Yaylak
Department of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
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Abstract

OBJECTIVE: To determine on protective role of NG-nitro-L-arginine methyl ester L-NAME, and insulin on the liver in streptozotocin STZ induced diabetic rats.

METHODS: This study was performed in the Department of Biochemistry, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey in 2007. Forty male Wistar albino rats were divided into 5 groups. These were untreated, diabetic control, STZ+insulin, STZ+L-NAME and STZ+insulin+L-NAME induced groups. The STZ was intraperitonally injected into 3 groups, and includes insulin, L-NAME, and their joint administrations as protective agents. The blood glucose and nitric oxide NO levels were determined. The tissue samples were obtained at the end of the fourth week. The liver tissue distortions were evaluated using hematoxylin and eosin staining.

RESULTS: The serum glucose level was significantly higher in diabetic control p=0.000, than the untreated group. Nitric oxide level was significantly lower in STZ+L-NAME p=0.000 than the untreated group. The focal pseudo lobular structures without vena centralis increased portal fibrillary necrosis, and bile duct stenosis with coagulation necrosis of the peripheral hepatocytes were more observed in diabetic group than the protective agent groups. In addition, insulin, and L-NAME lead to hepatocyte regeneration; and minimal mononuclear cell infiltration was noted.

CONCLUSION: NG-nitro-L-arginine methyl ester inhibits NO level in STZ+L-NAME induced group. NG-nitro-L-arginine methyl ester either alone, or with insulin combination significantly attenuates the liver morphological disarrangements in STZ induced diabetic rats.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 30 (1)
Saudi Medical Journal
Vol. 30, Issue 1
1 Jan 2009
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The protective effect of NG-nitro-L-arginine methyl ester and insulin on nitric oxide inhibition and pathology in experimental diabetic rat liver
Hilmi Ozden, Neslihan Tekin, Fahrettin Akyuz, Firdevs Gurer, Mehmet C. Ustuner, Fulya Kucuk, Gul Guven, Faik Yaylak
Saudi Medical Journal Jan 2009, 30 (1) 30-34;

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The protective effect of NG-nitro-L-arginine methyl ester and insulin on nitric oxide inhibition and pathology in experimental diabetic rat liver
Hilmi Ozden, Neslihan Tekin, Fahrettin Akyuz, Firdevs Gurer, Mehmet C. Ustuner, Fulya Kucuk, Gul Guven, Faik Yaylak
Saudi Medical Journal Jan 2009, 30 (1) 30-34;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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