2003
DOI: 10.1097/01.asn.0000077403.06195.d2
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Reactive Oxygen Species and Diabetic Nephropathy

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Cited by 19 publications
(6 citation statements)
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“…Hyperglycaemia leads to the generation of advanced glycation end products (AGEs) [2], which interact with a number of cellular receptors including the receptor for AGE (RAGE) [3]. Recent evidence suggests that AGE-RAGE interaction activates the vascular NAD(P)H oxidase complex resulting in the production of reactive oxygen species (ROS) [4], which is believed to play a pivotal role in the pathogenesis of DN [5]. NAD(P)H oxidase was originally discovered in neutrophils [6].…”
Section: Introductionmentioning
confidence: 99%
“…Hyperglycaemia leads to the generation of advanced glycation end products (AGEs) [2], which interact with a number of cellular receptors including the receptor for AGE (RAGE) [3]. Recent evidence suggests that AGE-RAGE interaction activates the vascular NAD(P)H oxidase complex resulting in the production of reactive oxygen species (ROS) [4], which is believed to play a pivotal role in the pathogenesis of DN [5]. NAD(P)H oxidase was originally discovered in neutrophils [6].…”
Section: Introductionmentioning
confidence: 99%
“…Diabetes is accompanied by neutrophil malfunction caused, to a large extent, by the development of oxidative-nitrative stress [90]. Oxidative stress leads to the activation of immunocompetent blood cells and their aggregation and adhesion.…”
Section: Influence Of Galega Officinalis On Functional State Of Leuko...mentioning
confidence: 99%
“…For instance, ROS can directly damage the DNA and can also alter the expression of ECM glycoproteins. The altered glycoproteins can undergo glycation to form AGEs that can also invariably cause oxidant stress by transducing various intracellular mechanisms via activation of their receptors (RAGE), suggesting that oxidant stress may be the common denominator in the pathogenesis of various complications, as is the case in adult life [12,13,14]. Increased production of ROS related to glucose metabolism could be due to increased oxidative phosphorylation, increased superoxide generation [15] and the relative immaturity of the free radical scavenging system [16], as well as inhibition of free radical scavenging pathways [17].…”
Section: Pathogenetic Mechanisms Relevant To Diabetic Complications Imentioning
confidence: 99%
“…Although ROS are regarded as the common denominator and are pivotal to the development of diabetic complications in adult life [12,13,14], their direct role in diabetic embryopathy is somewhat debatable. An increased production of reactive oxygen species (ROS) is thought to contribute to the development of diabetic vascular complications in adults [18,19,20,21,22,23], since the embryonic tissues are readily susceptible to oxidative damage by ROS, resulting in various congenital abnormalities, including neural tube or genitourinary defects.…”
Section: Pathogenetic Mechanisms Relevant To Diabetic Complications Imentioning
confidence: 99%