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Status: Bibliographieeintrag

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Verfasst von:Harcourt, Brooke [VerfasserIn]   i
 Sourris, Karly C. [VerfasserIn]   i
 Coughlan, Melinda T. [VerfasserIn]   i
 Walker, Karen Z. [VerfasserIn]   i
 Dougherty, Sonia L. [VerfasserIn]   i
 Andrikopoulos, Sofianos [VerfasserIn]   i
 Morley, Amy L. [VerfasserIn]   i
 Thallas-Bonke, Vicki [VerfasserIn]   i
 Chand, Vibhasha [VerfasserIn]   i
 Penfold, Sally A. [VerfasserIn]   i
 de Courten, Maximilian P. J. [VerfasserIn]   i
 Thomas, Merlin C. [VerfasserIn]   i
 Kingwell, Bronwyn A. [VerfasserIn]   i
 Bierhaus, Angelika [VerfasserIn]   i
 Cooper, Mark E. [VerfasserIn]   i
 Courten, Barbora de [VerfasserIn]   i
 Forbes, Josephine M. [VerfasserIn]   i
Titel:Targeted reduction of advanced glycation improves renal function in obesity
Verf.angabe:Brooke E. Harcourt, Karly C. Sourris, Melinda T. Coughlan, Karen Z. Walker, Sonia L. Dougherty, Sofianos Andrikopoulos, Amy L. Morley, Vicki Thallas-Bonke, Vibhasha Chand, Sally A. Penfold, Maximilian P. J. de Courten, Merlin C. Thomas, Bronwyn A. Kingwell, Angelika Bierhaus, Mark E. Cooper, Barbora de Courten and Josephine M. Forbes
Jahr:2011
Umfang:9 S.
Fussnoten:Gesehen am 02.08.2022
Titel Quelle:Enthalten in: Kidney international
Ort Quelle:New York, NY : Elsevier, 1972
Jahr Quelle:2011
Band/Heft Quelle:80(2011), 2, Seite 190-198
ISSN Quelle:1523-1755
Abstract:Obesity is highly prevalent in Western populations and is considered a risk factor for the development of renal impairment. Interventions that reduce the tissue burden of advanced glycation end-products (AGEs) have shown promise in stemming the progression of chronic disease. Here we tested if treatments that lower tissue AGE burden in patients and mice would improve obesity-related renal dysfunction. Overweight and obese individuals (body mass index (BMI) 26-39kg/m2) were recruited to a randomized, crossover clinical trial involving 2 weeks each on a low- and a high-AGE-containing diet. Renal function and an inflammatory profile (monocyte chemoattractant protein-1 (MCP-1) and macrophage migration inhibitory factor (MIF)) were improved following the low-AGE diet. Mechanisms of advanced glycation-related renal damage were investigated in a mouse model of obesity using the AGE-lowering pharmaceutical, alagebrium, and mice in which the receptor for AGE (RAGE) was deleted. Obesity, resulting from a diet high in both fat and AGE, caused renal impairment; however, treatment of the RAGE knockout mice with alagebrium improved urinary albumin excretion, creatinine clearance, the inflammatory profile, and renal oxidative stress. Alagebrium treatment, however, resulted in decreased weight gain and improved glycemic control compared with wild-type mice on a high-fat Western diet. Thus, targeted reduction of the advanced glycation pathway improved renal function in obesity.
DOI:doi:10.1038/ki.2011.57
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1038/ki.2011.57
 Volltext: https://www.sciencedirect.com/science/article/pii/S0085253815550187
 DOI: https://doi.org/10.1038/ki.2011.57
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:alagebrium chloride
 nephropathy
 obesity
 RAGE
K10plus-PPN:1812841000
Verknüpfungen:→ Zeitschrift

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