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NADPH Oxidases, Reactive Oxygen Species, and the Kidney: Friend and Foe

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TLDR
The role of NADPH oxidases and ROS in renal physiology and pathology is provided and Nox4 has been implicated in the basal production of ROS in the kidney and in pathologic conditions such as diabetic nephropathy and CKD.
Abstract
Reactive oxygen species (ROS) play an important role in normal cellular physiology. They regulate different biologic processes such as cell defense, hormone synthesis and signaling, activation of G protein-coupled receptors, and ion channels and kinases/phosphatases. ROS are also important regulators of transcription factors and gene expression. On the other hand, in pathologic conditions, a surplus of ROS in tissue results in oxidative stress with various injurious consequences such as inflammation and fibrosis. NADPH oxidases are one of the many sources of ROS in biologic systems, and there are seven isoforms (Nox1–5, Duox1, Duox2). Nox4 is the predominant form in the kidney, although Nox2 is also expressed. Nox4 has been implicated in the basal production of ROS in the kidney and in pathologic conditions such as diabetic nephropathy and CKD; upregulation of Nox4 may be important in renal oxidative stress and kidney injury. Although there is growing evidence indicating the involvement of NADPH oxidase in renal pathology, there is a paucity of information on the role of NADPH oxidase in the regulation of normal renal function. Here we provide an update on the role of NADPH oxidases and ROS in renal physiology and pathology.

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Current Mechanistic Concepts in Ischemia and Reperfusion Injury.

TL;DR: This review article presents recent advances focusing on the basic pathophysiology of ischemia-reperfusion injury, especially the involvement of reactive oxygen species and cell death pathways and highlights the latest mechanistic insights into reperfusion-injury-induced cell death via these different processes.
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Mitochondrial energetics in the kidney

TL;DR: Implementing compounds that stimulate mitochondrial biogenesis can restore mitochondrial and renal function in mouse models of AKI and diabetes mellitus and inhibiting the fission protein dynamin 1-like protein (DRP1) might ameliorate ischaemic renal injury by blocking mitochondrial fission.
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Renal tubule injury: a driving force toward chronic kidney disease.

TL;DR: A better understanding of the mechanisms by which tubular injury drives inflammation and fibrosis is necessary for the development of therapeutics to halt the progression of chronic kidney disease.
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Oxidative stress and autophagy: Crucial modulators of kidney injury

TL;DR: The potential relationships between oxidative stress and autophagy that may enable the development of better therapeutic intervention to halt the progression of kidney disease and promote its repair and resolution are discussed.
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The Hippo Pathway Effector TAZ Regulates Ferroptosis in Renal Cell Carcinoma.

TL;DR: It is found that cell density-regulated ferroptosis is mediated by TAZ through the regulation of EMP1-NOX4, suggesting its therapeutic potential for RCC and other TAZ-activated tumors.
References
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Journal ArticleDOI

The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology

TL;DR: This review summarizes the current state of knowledge of the functions of NOX enzymes in physiology and pathology.
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Cell transformation by the superoxide-generating oxidase Mox1

TL;DR: The cloning of mox1 is described, which encodes a homologue of the catalytic subunit of the superoxide-generating NADPH oxidase of phagocytes, gp91phox, which is expressed in colon, prostate, uterus and vascular smooth muscle, but not in peripheral blood leukocytes.
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Homologs of gp91phox: cloning and tissue expression of Nox3, Nox4, and Nox5.

TL;DR: The cloning and tissue expression of three additional homologs of gp91phox, termed Nox3, Nox4 and Nox5, members of a growing family of gp 91phox homologicals are reported, which are predicted to encode proteins of around 65 kDa.
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Role of the kidney in normal glucose homeostasis and in the hyperglycaemia of diabetes mellitus: therapeutic implications

TL;DR: In this paper, a review of the development of glucose-lowering drugs involving inhibition of renal glucose reabsorption is presented, in light of the fact that the human kidney is involved in the regulation of glucose via gluconeogenesis, taking up glucose from the circulation, and by reabsorbing glucose from glomerular filtrate.
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Contributions of gluconeogenesis to glucose production in the fasted state.

TL;DR: Healthy subjects ingested 2H2O and after 14, 22, and 42 h of fasting the enrichments of deuterium in the hydrogens bound to carbons 2, 5, and 6 of blood glucose and in body water determined and rates of gluconeogenesis can be determined without corrections required in other tracer methodologies.
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