1. Academic Validation
  2. Ceftriaxone improves hepatorenal damages in mice subjected to D-galactose-induced aging

Ceftriaxone improves hepatorenal damages in mice subjected to D-galactose-induced aging

  • Life Sci. 2020 Oct 1;258:118119. doi: 10.1016/j.lfs.2020.118119.
Elham Hakimizadeh 1 Jalal Hassanshahi 2 Ayat Kaeidi 2 Mohammad Hadi Nematollahi 3 Zahra Taghipour 4 Mohammadreza Rahmani 5 Iman Fatemi 6
Affiliations

Affiliations

  • 1 Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
  • 2 Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran; Department of Physiology and Pharmacology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
  • 3 Department of Clinical Biochemistry, Kerman University of Medical Sciences, Kerman, Iran.
  • 4 Department of Anatomy, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
  • 5 Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran; Department of Clinical Biochemistry, Kerman University of Medical Sciences, Kerman, Iran.
  • 6 Research Center of Tropical and Infectious Diseases, Kerman University of Medical Sciences, Kerman, Iran. Electronic address: i.fatemi@kmu.ac.ir.
Abstract

Ceftriaxone (CTX) is a third-generation cephalosporin Antibiotic that has broad-spectrum antimicrobial activity. This agent also has anti-inflammatory and antioxidant characteristics. In the current study, the effects of CTX against hepatorenal damages in a D-galactose (DGL) induced aging model were investigated. We used twenty-eight male mice which equally and randomly were separated into four groups as follows: Control, DGL group (treated with 500 mg/kg/day DGL orally for six weeks), DGL + CTX group (treated with 500 mg/kg/day DGL orally plus 200 mg/kg/day CTX intraperitoneally for six weeks), and CTX group (treated with 200 mg/kg/day CTX intraperitoneally for six weeks). The liver and kidney function indices such as serum creatinine, blood urine nitrogen, alanine aminotransferase, and aspartate aminotransferase were measured. Also, levels of malondialdehyde, catalase, and Glutathione Peroxidase in hepatic and renal tissues were evaluated. Moreover, the expression profiles of interleukin 1 beta and tumor necrosis factor alpha were assessed. The liver and kidney tissues were assessed for histopathological lesions. The results showed that aging induced by DGL leads to abnormalities in functional indices of the liver and kidneys. DGL also induced significant oxidative stress and inflammation, as well as histopathological lesions, in these organs. CTX improved functional indices, as well as the parameters of oxidative stress and inflammation, compared with the DGL-treated Animals. These results were also confirmed by histological evaluations of the liver and kidneys. These data provide evidence for the therapeutic value of CTX in clinical practice for mitigating the hepatorenal damages of aging.

Keywords

Aging; Ceftriaxone; D-galactose; Inflammation; Kidney; Liver; Oxidative stress.

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