Usefulness of zebrafish larvae to evaluate drug-induced functional and morphological renal tubular alterations
- 571 Downloads
Prediction and management of drug-induced renal injury (DIRI) rely on the knowledge of the mechanisms of drug insult and on the availability of appropriate animal models to explore it. Zebrafish (Danio rerio) offers unique advantages for assessing DIRI because the larval pronephric kidney has a high homology with its human counterpart and it is fully mature at 3.5 days post-fertilization. Herein, we aimed to evaluate the usefulness of zebrafish larvae as a model of renal tubular toxicity through a comprehensive analysis of the renal alterations induced by the lethal concentrations for 10% of the larvae for gentamicin, paracetamol and tenofovir. We evaluated drug metabolic profile by mass spectrometry, renal function with the inulin clearance assay, the 3D morphology of the proximal convoluted tubule by two-photon microscopy and the ultrastructure of proximal convoluted tubule mitochondria by transmission electron microscopy. Paracetamol was metabolized by conjugation and oxidation with further detoxification with glutathione. Renal clearance was reduced with gentamicin and paracetamol. Proximal tubules were enlarged with paracetamol and tenofovir. All drugs induced mitochondrial alterations including dysmorphic shapes (“donuts”, “pancakes” and “rods”), mitochondrial swelling, cristae disruption and/or loss of matrix granules. These results are in agreement with the tubular effects of gentamicin, paracetamol and tenofovir in man and demonstrate that zebrafish larvae might be a good model to assess functional and structural damage associated with DIRI.
KeywordsNephrotoxicity Proximal tubule Mitochondria Renal clearance Zebrafish
We would like to thank Maysa Franco and Ana Cristina Borges from the Fish Facility of the Gulbenkian Institute of Science.
Compliance with ethical standards
This work was supported by the Calouste Gulbenkian Foundation, Gulbenkian Professorship 121986/2012; the Foundation for Science and Technology through the grant ANR/BEX-BID/0153/2012, contract IF/00951/2012 (to SSL), fellowship PD/BD/52420/2013 (to RJ) and travel ship SFRH/BSAB/114291/2016 (to JM); iNOVA4Health Research Unit, LISBOA-01-0145-FEDER-007344.
All procedures performed in studies involving animals were in accordance with the ethical standards of the institution or practice at which the studies were conducted.
Conflict of interest
The authors declare that they have no conlficts of interest.
- Cook SF, King AD, van den Anker JN, Wilkins DG (2015) Simultaneous quantification of acetaminophen and five acetaminophen metabolites in human plasma and urine by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry: method validation and application to a neonatal pharmacokinetic study. J Chromatogr B Analyt Technol Biomed Life Sci 1007:30–42CrossRefPubMedGoogle Scholar
- Drummond IA, Davidson AJ (2010) Zebrafish kidney development. In: Detrich HW, Westerfiled M, Zon LI (eds) Methods in cell biology. Elsevier Inc., Third Edit, pp 233–260Google Scholar
- Gemer O, Zaltztein E, Gorodischer R (1983) Absorption of orally administered gentamicin in infants with diarrhea. Pediatr Pharmacol (New York) 3:119–123Google Scholar
- Kurmi M, Golla VM, Kumar S et al (2016) Stability behaviour of antiretroviral drugs and their combinations. 4: characterization of degradation products of tenofovir alafenamide fumarate and comparison of its degradation and stability behaviour with tenofovir disoproxil fumarate. J Pharm Biomed Anal 131:146–155CrossRefPubMedGoogle Scholar
- Westhoff JH, Giselbrecht S, Schmidts M et al (2013) Development of an automated imaging pipeline for the analysis of the zebrafish larval kidney. PLoS ONE 8:1–13Google Scholar