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Drug-induced impairment of renal function

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TLDR
This article will review those drugs that are associated with impaired renal function and provide an overview of nephrotoxic drugs that a treating physician is most likely to encounter by focusing on pharmaceutical agents that are currently in clinical practice.
Abstract
Pharmaceutical agents provide diagnostic and therapeutic utility that are central to patient care. However, all agents also carry adverse drug effect profiles. While most of these are clinically insignificant, some drugs may cause unacceptable toxicity that impacts negatively on patient morbidity and mortality. Recognizing adverse effects is important for administering appropriate drug doses, instituting preventive strategies, and withdrawing the offending agent due to toxicity. In the present article, we will review those drugs that are associated with impaired renal function. By focusing on pharmaceutical agents that are currently in clinical practice, we will provide an overview of nephrotoxic drugs that a treating physician is most likely to encounter. In doing so, we will summarize risk factors for nephrotoxicity, describe clinical manifestations, and address preventive and treatment strategies.

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TL;DR: The simplified model summarises the green synthesis, its characterization using physicochemical means and their biomedical applications, and discusses the recent advances in green synthesis of metallic nanoparticles, milestones, therapeutic applications and future perspectives of biosynthesized nanoparticles from some important medicinal plants.
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Ferulic acid protects against methotrexate nephrotoxicity via activation of Nrf2/ARE/HO-1 signaling and PPARγ, and suppression of NF-κB/NLRP3 inflammasome axis.

TL;DR: In this paper, the authors investigated the possible involvement of NLRP3 inflammasome activation in methotrexate (MTX)-induced nephrotoxicity and the protective potential of ferulic acid (FA), pointing out the role of PPARγ and Nrf2/HO-1 signaling.
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Effect of Kidney Function on Drug Kinetics and Dosing in Neonates, Infants, and Children

TL;DR: In this paper, the effects of kidney function on drug exposure and response and fine-tune dosing in pediatric patients, especially in those with impaired kidney function is presented. But the authors do not consider the effect of kidney injury and chronic diseases.
References
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Journal ArticleDOI

The natural history of chronic allograft nephropathy.

TL;DR: Chronic allograft nephropathy represents cumulative and incremental damage to nephrons from time-dependent immunologic and nonimmunologic causes, and was irreversible, resulting in declining renal function and graft failure.
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Prevention of radiographic-contrast-agent-induced reductions in renal function by acetylcysteine.

TL;DR: Prophylactic oral administration of the antioxidant acetylcysteine, along with hydration, prevents the reduction in renal function induced by contrast agents in patients with chronic renal insufficiency.
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VEGF inhibition and renal thrombotic microangiopathy.

TL;DR: To show that local reduction of VEGF within the kidney is sufficient to trigger the pathogenesis of thrombotic microangiopathy, this work used conditional gene targeting to delete V EGF from renal podocytes in adult mice and resulted in a profound thromBotic glomerular injury.
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Mechanisms of Cisplatin nephrotoxicity.

TL;DR: Recent advances in understanding of cisplatin nephrotoxicity are summarized and it is discussed how these advances might lead to more effective prevention.
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