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Differential sympathetic response to lesion-induced chronic kidney disease in rabbits.
Sata, Yusuke; Burke, Sandra L; Watson, Anna M D; Jha, Jay C; Gueguen, Cindy; Eikelis, Nina; Lim, Kyungjoon; Jackson, Kristy L; Lambert, Gavin W; Jandeleit-Dahm, Karin A M; Denton, Kate M; Esler, Murray D; Schlaich, Markus P; Head, Geoffrey A.
Afiliação
  • Sata Y; Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Human Neurotransmitters Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Faculty of Medicine, Nursing and Health Sciences, Central Clinical School, Monash University, Melb
  • Burke SL; Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
  • Watson AMD; Department of Diabetes, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Jha JC; Department of Diabetes, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Gueguen C; Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
  • Eikelis N; Human Neurotransmitters Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Iverson Health Innovation Research Institute and School of Health Science, Swinburne University of Technology, Hawthorn, Victoria, Australia.
  • Lim K; Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Department of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, Victoria, Australia.
  • Jackson KL; Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
  • Lambert GW; Human Neurotransmitters Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Iverson Health Innovation Research Institute and School of Health Science, Swinburne University of Technology, Hawthorn, Victoria, Australia.
  • Jandeleit-Dahm KAM; Department of Diabetes, Central Clinical School, Monash University, Melbourne, Victoria, Australia; German Diabetes Centre, Leibnitz Institute for Diabetes Research at the Heinrich Heine University, Dusseldorf, Germany.
  • Denton KM; Monash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
  • Esler MD; Human Neurotransmitters Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Faculty of Medicine, Nursing and Health Sciences, Central Clinical School, Monash University, Melbourne, Victoria, Australia; Department of Cardiology, Alfred Hospital, Melbourne, Victoria, Austra
  • Schlaich MP; Human Neurotransmitters Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Dobney Hypertension Centre, School of Medicine, Royal Perth Hospital Unit, University of Western Australia and Departments of Cardiology and Nephrology, Royal Perth Hospital, Perth, Western Austra
  • Head GA; Neuropharmacology Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Department of Pharmacology, Monash University, Melbourne, Victoria, Australia. Electronic address: geoff.head@baker.edu.au.
Kidney Int ; 98(4): 906-917, 2020 10.
Article em En | MEDLINE | ID: mdl-32763117
ABSTRACT
Chronic kidney disease (CKD) is associated with greater sympathetic nerve activity but it is unclear if this is a kidney-specific response or due to generalized stimulation of sympathetic nervous system activity. To determine this, we used a rabbit model of CKD in which quantitative comparisons with control rabbits could be made of kidney sympathetic nerve activity and whole-body norepinephrine spillover. Rabbits either had surgery to lesion 5/6th of the cortex of one kidney by electro-lesioning and two weeks later removal of the contralateral kidney, or sham lesioning and sham nephrectomy. After three weeks, the blood pressure was statistically significantly 20% higher in conscious rabbits with CKD compared to rabbits with a sham operation, but their heart rate was similar. Strikingly, kidney nerve activity was 37% greater than in controls, with greater burst height and frequency. Total norepinephrine spillover was statistically significantly lower by 34%, and kidney baroreflex curves were shifted to the right in rabbits with CKD. Plasma creatinine and urine output were elevated by 38% and 131%, respectively, and the glomerular filtration rate was 37% lower than in sham-operated animals (all statistically significant). Kidney gene expression of fibronectin, transforming growth factor-ß, monocyte chemotactic protein1, Nox4 and Nox5 was two- to eight-fold greater in rabbits with CKD than in control rabbits. Overall, the glomerular layer lesioning model in conscious rabbits produced a moderate, stable degree of CKD characterized by elevated blood pressure and increased kidney sympathetic nerve activity. Thus, our findings, together with that of a reduction in total norepinephrine spillover, suggest that kidney denervation, rather than generalized sympatholytic treatments, may represent a preferable management for CKD associated hypertension.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Kidney Int Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Kidney Int Ano de publicação: 2020 Tipo de documento: Article