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Protective effect of Panax ginseng against serum biochemical changes and apoptosis in kidney of rats treated with gentamicin sulphate

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Date

2012

Author

Kalkan, Yıldıray
Kapakin, Kübra Asena Terim
Kara, Adem
Atabay, Tennur
Karadeniz, Ali
Şimşek, Nejdet
Karakuş, Emre
Can, İsmail
Yıldırım, Serap
Özkanlar, Seçkin
Şengül, Emin

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Citation

Kalkan, Y., Kapakin, K. A., Kara, A., Atabay, T., Karadeniz, A., Simsek, N., Karakus, E., Can, I., Yildirim, S., Ozkanlar, S., & Sengul, E. (2012). Protective effect of Panax ginseng against serum biochemical changes and apoptosis in kidney of rats treated with gentamicin sulphate. Journal of molecular histology, 43(5), 603–613. https://doi.org/10.1007/s10735-012-9412-4

Abstract

The protective effects of Panax ginseng (PG) on gentamicin sulphate (GS) induced acute nephrotoxicity were investigated in rats. A total of 32 adult Sprague- Dawley rats were randomly divided into 4 equal groups and treated by intraperitoneous route for 10 days with: 0.5 mL of isotonic saline (group C), GS 100 mg/kg/day (group GS), co treatment PG (100 and 200 mg/kg/day) plus GS (100 mg/kg/day). After the last injection, kidney markers (urea, creatinine and blood urea nitrogen-BUN) and hepatic markers (aspartate aminotransferase-AST, alanine aminotransferase-ALT, gama glutamil transferase- GGT), and biochemical parameters were analyzed using diagnostic kits. Also, kidney changes were evaluated by immunohistochemical and stereological methods. GS treatment induced significant elevation (P<0.05) in kidney and hepatic markers, most of biochemical parameters, and Bax immunoreactivity as well. However, co treatments with both doses of PG (100 and 200 mg/kg/day) significantly alleviated (P<0.05) the GS-induced elevations and have partially protected rats from nephrotoxicity (reduction of kidney damage, and of urea, creatinine and BUN concentrations, and of apoptotic index). Both biochemical results and immunohistochemical evidence showed that administration of PG reduced the gentamicin-induced nephrotoxicity. © Springer Science+Business Media B.V. 2012.

Source

Journal of Molecular Histology

Volume

43

Issue

5

URI

https://doi.org/10.1007/s10735-012-9412-4
https://hdl.handle.net/11436/4195

Collections

  • PubMed İndeksli Yayınlar Koleksiyonu [2443]
  • Scopus İndeksli Yayınlar Koleksiyonu [5931]
  • TF, Temel Tıp Bilimleri Bölümü Koleksiyonu [691]



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