The effects of low and high doses of sugammadex on kidney tissue in streptozotocin-induced diabetic rats. 2015

G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal

BACKGROUND Sugammadex is primarily excreted via renal route. We investigated effects of low and high doses of sugammadex (16 mg/kg versus 96 mg/kg) on renal tissue samples of streptozotocin-induced diabetic rats. METHODS Twenty-four Wistar albino rats were divided into 4 groups. Group C (control - 0.9 % NaCl), Group DC (diabetes control; 55 mg/kg streptozotocin, IP, only), Group DR-16S (diabetes-rocuronium - 16 mg sugammadex, IV.) and Group DR-96S (diabetes- rocuronium - 96 mg sugammadex, IV). Renal tissue histopathological evaluation and antioxidant status (measurements of MDA levels and NO activities) were studied. RESULTS Significantly higher levels of all inflammation parameters (inflammation, degeneration/necrosis, tubular dilatation, tubular cell degeneration, dilatation in Bowman's space, tubular hyaline casts, and lymphocyte infiltration) were found in the 96 mg/kg sugammadex group. Higher MDA tissue levels and lower NO activity were found in the 96 mg/kg sugammadex group. CONCLUSIONS We can conclude that high-dose (96 mg/kg) sugammadex administration resulted in significant renal tissue damage in diabetic rats. As a consequence, low doses of sugammadex have to be preferred in diabetic patients (Tab. 2, Fig. 4, Ref. 26).

UI MeSH Term Description Entries

Related Publications

G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
May 2010, Journal of photochemistry and photobiology. B, Biology,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
November 2017, Canadian journal of physiology and pharmacology,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
January 2009, American journal of nephrology,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
June 2017, Annals of rehabilitation medicine,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
April 2001, Methods and findings in experimental and clinical pharmacology,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
May 2008, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
July 2018, Gene,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
June 2002, Scandinavian journal of medicine & science in sports,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
April 2014, Indian journal of clinical biochemistry : IJCB,
G Kip, and H C Turgut, and M Alkan, and M E Aydin, and M E Erbatur, and H A Kiraz, and S Kartal, and H Boyunaga, and F M Comu, and O Erdem, and M Arslan, and Y Unal
January 2010, Journal of biomedicine & biotechnology,
Copied contents to your clipboard!