Literature DB >> 22944656

Effect of tenofovir, an antiretroviral drug, on hepatic and renal functional indices of Wistar rats: protective role of vitamin E.

Oluwatosin Adekunle Adaramoye1, Olubusuyi Moses Adewumi, Omolola Abidemi Adesanoye, Opeyemi Olubunmi Faokunla, Ebenezer Olatunde Farombi.   

Abstract

BACKGROUND: Tenofovir (TFR) is a nucleotide reverse transcriptase inhibitor with activity against human immunodeficiency virus. We studied the effect of TFR administered to Wistar rats on hepatic and renal function markers and the possible modulatory role of vitamin E (Vit E).
METHODS: The study consists of four groups of six rats each. The first group served as control, the second group received TFR at 50 mg/kg/day for 4 weeks, third group received TFR and Vit E, and the last group received Vit E alone.
RESULTS: TFR administration caused a significant (p<0.05) increase in the levels of serum urea, creatinine, urinary glucose, and protein by 65%, 51%, 88%, and 79%, respectively, relative to controls. This was followed by a significant (p<0.05) reduction in creatinine clearance of TFR-treated rats. There were no significant differences (p>0.05) in the activities of serum aminotransferases, γ-glutamyltransferase, and alkaline phosphatase in TRF-treated rats relative to controls. TFR administration caused a marked elevation of malondialdehyde (MDA; index of lipid peroxidation) in the animals. Specifically, serum, hepatic, and renal MDA levels increased by 75%, 90%, and 102%, respectively. TRF-treated rats had significantly (p<0.05) reduced activities of renal catalase, glutathione-S-transferase, and superoxide dismutase. Supplementation of Vit E ameliorated TFR-induced effects by decreasing the levels of MDA and enhancing the activities of renal antioxidative enzymes. The biochemical data were supported by histopathological findings from the slides.
CONCLUSIONS: TFR increased oxidative stress and altered kidney function markers in the rats, whereas supplementation of Vit E attenuated these effects.

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Year:  2012        PMID: 22944656     DOI: 10.1515/jbcpp.2011.0042

Source DB:  PubMed          Journal:  J Basic Clin Physiol Pharmacol        ISSN: 0792-6855


  8 in total

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2.  Tenofovir disoproxil fumarate: toxicity, toxicokinetics, and toxicogenomics analysis after 13 weeks of oral administration in mice.

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Review 4.  Mitochondria-targeted senotherapeutic interventions.

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5.  Depletion of the cellular antioxidant system contributes to tenofovir disoproxil fumarate - induced mitochondrial damage and increased oxido-nitrosative stress in the kidney.

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Authors:  Helen Kovari; Caroline A Sabin; Bruno Ledergerber; Lene Ryom; Peter Reiss; Matthew Law; Christian Pradier; Francois Dabis; Antonella d'Arminio Monforte; Colette Smith; Stephane de Wit; Ole Kirk; Jens D Lundgren; Rainer Weber
Journal:  Open Forum Infect Dis       Date:  2016-01-21       Impact factor: 3.835

7.  The Effect of Switching from Tenofovir Disoproxil Fumarate (TDF) to Tenofovir Alafenamide (TAF) on Liver Enzymes, Glucose, and Lipid Profile.

Authors:  Nicola Squillace; Elena Ricci; Barbara Menzaghi; Giuseppe Vittorio De Socio; Simone Passerini; Canio Martinelli; Maria Sabrina Mameli; Paolo Maggi; Katia Falasca; Laura Cordier; Benedetto Maurizio Celesia; Elena Salomoni; Antonio Di Biagio; Giovanni Francesco Pellicanò; Paolo Bonfanti
Journal:  Drug Des Devel Ther       Date:  2020-12-15       Impact factor: 4.162

8.  Renal Dysfunction and Tubulopathy Induced by High-Dose Tenofovir Disoproxil Fumarate in C57BL/6 Mice.

Authors:  Eungyeong Jang; Jong Kil Lee; Kyung-Soo Inn; Eun Kyoung Chung; Kyung-Tae Lee; Jang-Hoon Lee
Journal:  Healthcare (Basel)       Date:  2020-10-21
  8 in total

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