Cargando…

Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney

Albuminuria in individuals whose body mass index exceeds 40 kg/m(2) is associated with the presence of large glomeruli, thickened basement membrane and epithelial cellular (podocyte) distortion. Obstructive sleep apnea magnifies glomerular injury as well, probably through a vasoconstrictive mechanis...

Descripción completa

Detalles Bibliográficos
Autores principales: D’Elia, John A, Roshan, Bijan, Maski, Manish, Weinrauch, Larry A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108758/
https://www.ncbi.nlm.nih.gov/pubmed/21694920
_version_ 1782205368657510400
author D’Elia, John A
Roshan, Bijan
Maski, Manish
Weinrauch, Larry A
author_facet D’Elia, John A
Roshan, Bijan
Maski, Manish
Weinrauch, Larry A
author_sort D’Elia, John A
collection PubMed
description Albuminuria in individuals whose body mass index exceeds 40 kg/m(2) is associated with the presence of large glomeruli, thickened basement membrane and epithelial cellular (podocyte) distortion. Obstructive sleep apnea magnifies glomerular injury as well, probably through a vasoconstrictive mechanism. Insulin resistance from excess fatty acids is exacerbated by decreased secretion of high molecular weight adiponectin from adipose cells in the obese state. Adiponectin potentiates insulin in its post-receptor signaling resulting in glucose oxidation in mitochondria. Recent studies of podocyte physiology have concentrated on the structural and functional requirements that prevent glomerular albumin leakage. The architecture of the podocyte involves nephrin and podocin, proteins that cooperate to keep slit pores between foot processes competent to retain albumin. Insulin and adiponectin are necessary for high-energy phosphate generation. When fatty acids bind to albumin, the toxicity to proximal renal tubules is magnified. Albumin and fatty acids are elevated in urine of individuals with obesity related nephrotic syndrome. Fatty acid accumulation and resistin inhibit insulin and adiponectin. Study of cytokines produced by adipose tissue (adiponectin and leptin) and macrophages (resistin) has led to a better understanding of the relationship between weight and hypertension. Leptin, is presumably secreted after food intake to inhibit the midbrain/hypothalamic appetite centers. Resistance to leptin results in excess signaling to hypothalamic sympathetics leading to hypertension. Demonstration of the existence of a cerebral receptor mutation provide evidence for a role in hypertension of a central nervous reflex arc in humans. Further understanding of obesity-related renal dysfunction has been accomplished recently using experimental models. Rapid weight loss following bariatric surgery may reverse renal pathology of obesity with restoration of normal blood pressure.
format Online
Article
Text
id pubmed-3108758
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-31087582011-06-21 Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney D’Elia, John A Roshan, Bijan Maski, Manish Weinrauch, Larry A Int J Nephrol Renovasc Dis Review Albuminuria in individuals whose body mass index exceeds 40 kg/m(2) is associated with the presence of large glomeruli, thickened basement membrane and epithelial cellular (podocyte) distortion. Obstructive sleep apnea magnifies glomerular injury as well, probably through a vasoconstrictive mechanism. Insulin resistance from excess fatty acids is exacerbated by decreased secretion of high molecular weight adiponectin from adipose cells in the obese state. Adiponectin potentiates insulin in its post-receptor signaling resulting in glucose oxidation in mitochondria. Recent studies of podocyte physiology have concentrated on the structural and functional requirements that prevent glomerular albumin leakage. The architecture of the podocyte involves nephrin and podocin, proteins that cooperate to keep slit pores between foot processes competent to retain albumin. Insulin and adiponectin are necessary for high-energy phosphate generation. When fatty acids bind to albumin, the toxicity to proximal renal tubules is magnified. Albumin and fatty acids are elevated in urine of individuals with obesity related nephrotic syndrome. Fatty acid accumulation and resistin inhibit insulin and adiponectin. Study of cytokines produced by adipose tissue (adiponectin and leptin) and macrophages (resistin) has led to a better understanding of the relationship between weight and hypertension. Leptin, is presumably secreted after food intake to inhibit the midbrain/hypothalamic appetite centers. Resistance to leptin results in excess signaling to hypothalamic sympathetics leading to hypertension. Demonstration of the existence of a cerebral receptor mutation provide evidence for a role in hypertension of a central nervous reflex arc in humans. Further understanding of obesity-related renal dysfunction has been accomplished recently using experimental models. Rapid weight loss following bariatric surgery may reverse renal pathology of obesity with restoration of normal blood pressure. Dove Medical Press 2009-11-06 /pmc/articles/PMC3108758/ /pubmed/21694920 Text en © 2009 D’Elia et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
D’Elia, John A
Roshan, Bijan
Maski, Manish
Weinrauch, Larry A
Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
title Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
title_full Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
title_fullStr Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
title_full_unstemmed Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
title_short Manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
title_sort manifestation of renal disease in obesity: pathophysiology of obesity-related dysfunction of the kidney
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108758/
https://www.ncbi.nlm.nih.gov/pubmed/21694920
work_keys_str_mv AT deliajohna manifestationofrenaldiseaseinobesitypathophysiologyofobesityrelateddysfunctionofthekidney
AT roshanbijan manifestationofrenaldiseaseinobesitypathophysiologyofobesityrelateddysfunctionofthekidney
AT maskimanish manifestationofrenaldiseaseinobesitypathophysiologyofobesityrelateddysfunctionofthekidney
AT weinrauchlarrya manifestationofrenaldiseaseinobesitypathophysiologyofobesityrelateddysfunctionofthekidney