Professor DON SHARKEY don.sharkey@nottingham.ac.uk
PROFESSOR OF NEONATAL MEDICINE AND TECHNOLOGIES
Professor DON SHARKEY don.sharkey@nottingham.ac.uk
PROFESSOR OF NEONATAL MEDICINE AND TECHNOLOGIES
Hernan P. Fainberg
Vicky Wilson
Emma Harvey
Professor DAVID GARDNER DAVID.GARDNER@NOTTINGHAM.AC.UK
PROFESSOR OF PHYSIOLOGY
Michael E. Symonds
Professor Helen Budge HELEN.BUDGE@NOTTINGHAM.AC.UK
PROFESSOR OF NEONATAL MEDICINE
Childhood obesity has reached epidemic proportions. Obesity is an independent risk factor for the development of end-stage renal disease. Endoplasmic reticulum stress and subsequent activation of the unfolded protein response (UPR) are implicated in the development of adipose tissue dysregulation and type 2 diabetes mellitus in obesity. The present study explored the impact of adolescent-onset obesity on the UPR after obesity-related hypertension and nephropathy, using an ovine model in which obesity was induced by increased food intake and reduced activity. Obese young adults had a higher mean arterial pressure (lean, 89.6±1.7 mm Hg versus obese, 101±3.0 mm Hg; P<0.01) and greater sensitivity to low physiological doses of angiotensin II. Obesity increased the glomerular area and was associated with activation of the UPR in renal cells with a greater abundance of glucose-regulated protein 78, C/EBP homologous protein, Bax, phosphorylated c-Jun amino-terminal kinase, and activating transcription factor 6 (all P<0.05). In addition, there was a marked upregulation of proinflammatory genes, most notably those involved in macrophage signaling. Reactive oxygen species production and handling were also perturbed in obese adults. Renal endoplasmic reticulum stress was positively correlated with macrophage content (r=0.83; P<0.001), phosphorylated c-Jun amino-terminal kinase (r=0.73; P<0.01), and adiposity (r=0.71; P<0.01). In conclusion, adolescent-onset, obesity-related renal endoplasmic reticulum stress was associated with activation of the UPR, apoptosis, and inflammation, potentially increasing the associated renal damage observed in young adults. The UPR may prove to be a useful therapeutic target for the treatment and prevention of obesity-related nephropathy and associated hypertension, thereby reducing the burden of end-stage renal disease.
Sharkey, D., Fainberg, H. P., Wilson, V., Harvey, E., Gardner, D. S., Symonds, M. E., & Budge, H. (2009). Impact of early onset obesity and hypertension on the unfolded protein response in renal tissues of juvenile sheep. Hypertension, 53(6), 925-931. https://doi.org/10.1161/HYPERTENSIONAHA.108.122812
Journal Article Type | Article |
---|---|
Acceptance Date | Apr 2, 2009 |
Online Publication Date | May 4, 2009 |
Publication Date | Jun 1, 2009 |
Deposit Date | Mar 3, 2025 |
Journal | Hypertension |
Print ISSN | 2224-1485 |
Electronic ISSN | 2307-1095 |
Publisher | Publishing House Zaslavsky |
Peer Reviewed | Peer Reviewed |
Volume | 53 |
Issue | 6 |
Pages | 925-931 |
DOI | https://doi.org/10.1161/HYPERTENSIONAHA.108.122812 |
Keywords | obesity, hypertension, unfolded protein response, nephropathy, adolescence, kidney |
Public URL | https://nottingham-repository.worktribe.com/output/3084934 |
Publisher URL | https://www.ahajournals.org/doi/10.1161/HYPERTENSIONAHA.108.122812 |
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