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J Biochem Mol Toxicol ; 35(12): e22929, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34676623

RESUMO

Concurrent exposure to antimicrobial and nonsteroidal anti-inflammatory drugs (NSAIDs) is usually inevitable in most infections and postsurgery. Consequently, the present study was designed to assess the intertwining impact of coadministration of cefepime (CP, a wide spectrum antibiotic) and diclofenac sodium (DF, an NSAID) on rat's liver, kidney, and testes. Rats received saline, CP (180 mg/kg/day, IM), DF (10 mg/kg/day, IM), or a combination of CP and DF. After 14 days, CP or DF induced tissue damage expressed by marked biochemical alterations in hepatic and renal function tests. Besides this, disrupted lipid metabolism and testosterone levels along with significant histological changes in hepatic, renal, and testicular tissues were noticed. A significant increase in malondialdehyde and decreases in superoxide dismutase and catalase activities alongside significant upregulated caspase 3 expression in tissues following CP or DF treatment suggested a bearable influence of oxidative stress, lipid peroxidation, and cell death. Accordingly, the simultaneous therapy of CP and DF evoked more obvious tissue damage than their individual treatment. Overall, data concluded that concurrent use of CP and DF in medical practice is a worrisome matter, so it should be done cautiously to avoid synergistic deleterious outcomes.


Assuntos
Antibacterianos/efeitos adversos , Anti-Inflamatórios não Esteroides/efeitos adversos , Cefepima/efeitos adversos , Diclofenaco/efeitos adversos , Metabolismo dos Lipídeos/efeitos dos fármacos , Insuficiência de Múltiplos Órgãos/induzido quimicamente , Estresse Oxidativo/efeitos dos fármacos , Animais , Antibacterianos/administração & dosagem , Anti-Inflamatórios não Esteroides/administração & dosagem , Biomarcadores/metabolismo , Cefepima/administração & dosagem , Diclofenaco/administração & dosagem , Masculino , Ratos , Ratos Wistar
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