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Open AccessJournal ArticleDOI

Cilastatin Attenuates Cisplatin-Induced Proximal Tubular Cell Damage

TLDR
It is suggested that the affinity of cilastatin for renal dipeptidase makes this effect specific for proximal tubular cells and may be related to a reduction in intracellular drug accumulation.
Abstract
A major area in cancer therapy is the search for protective strategies against cisplatin-induced nephrotoxicity. We investigated the protective effect of cilastatin on cisplatin-induced injury to renal proximal tubular cells. Cilastatin is a specific inhibitor of renal dehydrodipeptidase I (DHP-I), which prevents hydrolysis of imipenem and its accumulation in the proximal tubule. Primary cultures of proximal cells were treated with cisplatin (1-30 microM) in the presence or absence of cilastatin (200 microg/ml). Apoptosis and mitochondrial injury were assessed by different techniques. Cisplatin uptake and DNA binding were measured by inductively coupled plasma spectrometry. HeLa cells were used to control the effect of cilastatin on the tumoricidal activity of cisplatin. Cisplatin increased cell death, apoptotic-like morphology, caspase activation, and mitochondrial injury in proximal tubular cells in a dose- and time-dependent way. Concomitant treatment with cilastatin reduced cisplatin-induced changes. Cilastatin also reduced the DNA-bound platinum but did not modify cisplatin-dependent up-regulation of death receptors (Fas) or ligands (tumor necrosis factor alpha, Fas ligand). In contrast, cilastatin did not show any effects on cisplatin-treated HeLa cells. Renal DHP-I was virtually absent in HeLa cells. Cilastatin attenuates cisplatin-induced cell death in proximal tubular cells without reducing the cytotoxic activity of cisplatin in tumor cells. Our findings suggest that the affinity of cilastatin for renal dipeptidase makes this effect specific for proximal tubular cells and may be related to a reduction in intracellular drug accumulation. Therefore, cilastatin administration might represent a novel strategy in the prevention of cisplatin-induced acute renal injury.

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Citations
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Journal ArticleDOI

Rutin attenuates cisplatin induced renal inflammation and apoptosis by reducing NFκB, TNF-α and caspase-3 expression in wistar rats

TL;DR: It is found that the beneficial effect of rutin pretreatment is mediated partially by its inhibitory effect on NFκB and TNF-α pathway mediated inflammation, caspase-3 mediated-tubular cell apoptosis, as well as by restoration of histopathological changes against cisplatin administration.
Journal ArticleDOI

Quercetin reduces cisplatin nephrotoxicity in rats without compromising its anti-tumour activity

TL;DR: In a model of tumour-bearing rats, quercetin prevents the nephrotoxic effect of cisplatin without affecting its anti-tumour activity.
Journal ArticleDOI

Elemental Bioimaging in Kidney by LA–ICP–MS As a Tool to Study Nephrotoxicity and Renal Protective Strategies in Cisplatin Therapies

TL;DR: Pt turned out to accumulate in the kidney cortex and corticomedullary junction, corresponding to areas where the proximal tubule S3 segments (the most sensitive cells to cisplatin nephrotoxicity) are located, demonstrating the connection between platinum accumulation and renal damage proved by histological examination of HE-stained sections.
Journal ArticleDOI

ELABELA and an ELABELA Fragment Protect against AKI

TL;DR: Treatment of mice with ELA32 or ELA11 but not an ELA 11 mutant with a cysteine to alanine substitution at the N terminus inhibited I/R injury-induced renal fibrosis, inflammation, apoptosis, and the DNA damage response and markedly reduced the renal tubular lesions and renal dysfunction.
References
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Journal ArticleDOI

Cisplatin nephrotoxicity: Mechanisms and renoprotective strategies

TL;DR: Examination of tumor-bearing animals and identification of novel renoprotective strategies that do not diminish the anticancer efficacy of cisplatin are essential to the development of clinically applicable interventions.
Journal ArticleDOI

Cisplatin Nephrotoxicity: A Review

TL;DR: Understanding the mechanisms of injury has led to multiple approaches to prevention and potential approaches to treatment and the experimental approaches in these studies with cisplatin are potentially applicable to other drugs causing renal dysfunction.
Journal ArticleDOI

Cisplatin and platinum drugs at the molecular level. (Review).

Teni Boulikas, +1 more
- 01 Nov 2003 - 
TL;DR: This review summarizes the molecular mechanisms of platinum compounds for DNA damage, DNA repair and induction of apoptosis via activation or modulation of signaling pathways and explores the basis of platinum resistance.
Journal ArticleDOI

Review of the Comparative Pharmacology and Clinical Activity of Cisplatin and Carboplatin

TL;DR: Carboplatin does not possess equivalent activity to cisplatin in all platinum-sensitive tumors, and its role in limited-stage small-cell lung cancer needs to be investigated further.
Book

Drug Prescribing in Renal Failure: Dosing Guidelines for Adults

TL;DR: The data base for rational guidelines to safe, efficacious drug prescribing in adults with renal insufficiency is presented in tabular form in this paper, where recommendations are based on pharmacokinetic variables in normal subjects.
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