BACKGROUND: Gentamicin (GM) is an antibiotic whose clinical use is limited by its nephrotoxicity. Thus the present study was undertaken to investigate if carnosine, an antioxidant, could protect the kidney in this experimental model. MATERIAL/ METHODS: The animals were divided into seven groups each of 10 animals: one control group, two healthy carnosine groups (10 mg/kg/day), two GM groups (80 mg/kg/day), and two carnosine-GM groups. Kidney function tests, histopathological, ultrastructural, and enzymatic histochemical studies clarified GM nephrotoxicity. RESULTS: GM rat showed early kidney function failure as blood creatinine and blood urea were significantly increased after one and two weeks. Experimental evidence suggested a role of reactive oxygen species in GM-induced nephrotoxicity. Histopathological examination revealed degenerative changes in glomeruli and tubules. Ultrastructural study showed glomerular changes, some degeneration of both distal and collecting tubules. The proximal tubules showed marked degrees of changes and necrosis. Enzymatic histochemical studies of GM rats revealed marked elevation of lactate dehydrogenase (LDH) and inhibition of succinic dehydrogenase (SDH), alkaline phosphatases (ALP), acid phosphatases (ACP), and adenosine triphosphatase (ATPase). Blood creatinine and urea were normalized in the carnosine-GM group after one and two weeks. Structural and enzymatic histochemical pictures were greatly ameliorated. CONCLUSIONS: The mechanism by which carnosine has a protective effect on GM-induced nephrotoxicity was attributed to its many actions: double antioxidant action, protein molecule protection, removal of harmfully modified ones, activation of immune system, preservation of membrane fluidity, and cytosolic buffering. Carnosine thus offers a promise of ameliorating GM nephrotoxicity.
BACKGROUND:Gentamicin (GM) is an antibiotic whose clinical use is limited by its nephrotoxicity. Thus the present study was undertaken to investigate if carnosine, an antioxidant, could protect the kidney in this experimental model. MATERIAL/ METHODS: The animals were divided into seven groups each of 10 animals: one control group, two healthy carnosine groups (10 mg/kg/day), two GM groups (80 mg/kg/day), and two carnosine-GM groups. Kidney function tests, histopathological, ultrastructural, and enzymatic histochemical studies clarified GMnephrotoxicity. RESULTS:GMrat showed early kidney function failure as blood creatinine and blood urea were significantly increased after one and two weeks. Experimental evidence suggested a role of reactive oxygen species in GM-induced nephrotoxicity. Histopathological examination revealed degenerative changes in glomeruli and tubules. Ultrastructural study showed glomerular changes, some degeneration of both distal and collecting tubules. The proximal tubules showed marked degrees of changes and necrosis. Enzymatic histochemical studies of GMrats revealed marked elevation of lactate dehydrogenase (LDH) and inhibition of succinic dehydrogenase (SDH), alkaline phosphatases (ALP), acid phosphatases (ACP), and adenosine triphosphatase (ATPase). Blood creatinine and urea were normalized in the carnosine-GM group after one and two weeks. Structural and enzymatic histochemical pictures were greatly ameliorated. CONCLUSIONS: The mechanism by which carnosine has a protective effect on GM-induced nephrotoxicity was attributed to its many actions: double antioxidant action, protein molecule protection, removal of harmfully modified ones, activation of immune system, preservation of membrane fluidity, and cytosolic buffering. Carnosine thus offers a promise of ameliorating GMnephrotoxicity.
Authors: Saud Alarifi; Amin Al-Doaiss; Saad Alkahtani; S A Al-Farraj; Mohammed Saad Al-Eissa; B Al-Dahmash; Hamad Al-Yahya; Mohammed Mubarak Journal: Saudi J Biol Sci Date: 2011-12-03 Impact factor: 4.219
Authors: Barbora de Courten; Timea Kurdiova; Maximilian P J de Courten; Vitazoslav Belan; Inge Everaert; Marek Vician; Helena Teede; Daniela Gasperikova; Giancarlo Aldini; Wim Derave; Jozef Ukropec; Barbara Ukropcova Journal: PLoS One Date: 2015-10-06 Impact factor: 3.240