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Ciliotherapy: a novel intervention in polycystic kidney disease
BACKGROUND: Ciliopathies are a group of diseases associated with abnormal structure or function of primary cilia. Ciliopathies include polycystic kidney disease (PKD), a pathology associated with vascular hypertension. We previously showed that cilia length regulates cilia function, and cilia functi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Science Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981986/ https://www.ncbi.nlm.nih.gov/pubmed/24748884 http://dx.doi.org/10.3969/j.issn.1671-5411.2014.01.001 |
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author | Kathem, Sarmed H. Mohieldin, Ashraf M. Abdul-Majeed, Shakila Ismail, Sajida H. Altaei, Qaiss H. Alshimmari, Ibrahim K. Alsaidi, Mohanned M. Khammas, Hussein Nauli, Andromeda M. Joe, Bina Nauli, Surya M. |
author_facet | Kathem, Sarmed H. Mohieldin, Ashraf M. Abdul-Majeed, Shakila Ismail, Sajida H. Altaei, Qaiss H. Alshimmari, Ibrahim K. Alsaidi, Mohanned M. Khammas, Hussein Nauli, Andromeda M. Joe, Bina Nauli, Surya M. |
author_sort | Kathem, Sarmed H. |
collection | PubMed |
description | BACKGROUND: Ciliopathies are a group of diseases associated with abnormal structure or function of primary cilia. Ciliopathies include polycystic kidney disease (PKD), a pathology associated with vascular hypertension. We previously showed that cilia length regulates cilia function, and cilia function is required for nitric oxide (NO) biosynthesis in endothelial cells. Because patients with PKD show abnormal sensory cilia function, the aim of our current study was to search for a targeted therapy focused on primary cilia, which we refer to as ‘ciliotherapy’. METHODS AND RESULTS: In the present studies, our in vitro analyses refined fenoldopam as an equipotent and more specific dopaminergic agonist to regulate cilia length and function. Our in vivo studies indicated that fenoldopam increased cilia length and serum NO thereby reducing blood pressure in a PKD mouse model. Our crossover, multicenter, double-blind and placebo-controlled clinical study further indicated that cilia-targeting therapy showed an overall reduction in mean arterial pressure in PKD patients. CONCLUSIONS: Overall, our studies provide the first evidence of ciliotherapy as an innovative intervention in patients with abnormal primary cilia. |
format | Online Article Text |
id | pubmed-3981986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39819862014-04-18 Ciliotherapy: a novel intervention in polycystic kidney disease Kathem, Sarmed H. Mohieldin, Ashraf M. Abdul-Majeed, Shakila Ismail, Sajida H. Altaei, Qaiss H. Alshimmari, Ibrahim K. Alsaidi, Mohanned M. Khammas, Hussein Nauli, Andromeda M. Joe, Bina Nauli, Surya M. J Geriatr Cardiol Research Article BACKGROUND: Ciliopathies are a group of diseases associated with abnormal structure or function of primary cilia. Ciliopathies include polycystic kidney disease (PKD), a pathology associated with vascular hypertension. We previously showed that cilia length regulates cilia function, and cilia function is required for nitric oxide (NO) biosynthesis in endothelial cells. Because patients with PKD show abnormal sensory cilia function, the aim of our current study was to search for a targeted therapy focused on primary cilia, which we refer to as ‘ciliotherapy’. METHODS AND RESULTS: In the present studies, our in vitro analyses refined fenoldopam as an equipotent and more specific dopaminergic agonist to regulate cilia length and function. Our in vivo studies indicated that fenoldopam increased cilia length and serum NO thereby reducing blood pressure in a PKD mouse model. Our crossover, multicenter, double-blind and placebo-controlled clinical study further indicated that cilia-targeting therapy showed an overall reduction in mean arterial pressure in PKD patients. CONCLUSIONS: Overall, our studies provide the first evidence of ciliotherapy as an innovative intervention in patients with abnormal primary cilia. Science Press 2014-03 /pmc/articles/PMC3981986/ /pubmed/24748884 http://dx.doi.org/10.3969/j.issn.1671-5411.2014.01.001 Text en Institute of Geriatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission. |
spellingShingle | Research Article Kathem, Sarmed H. Mohieldin, Ashraf M. Abdul-Majeed, Shakila Ismail, Sajida H. Altaei, Qaiss H. Alshimmari, Ibrahim K. Alsaidi, Mohanned M. Khammas, Hussein Nauli, Andromeda M. Joe, Bina Nauli, Surya M. Ciliotherapy: a novel intervention in polycystic kidney disease |
title | Ciliotherapy: a novel intervention in polycystic kidney disease |
title_full | Ciliotherapy: a novel intervention in polycystic kidney disease |
title_fullStr | Ciliotherapy: a novel intervention in polycystic kidney disease |
title_full_unstemmed | Ciliotherapy: a novel intervention in polycystic kidney disease |
title_short | Ciliotherapy: a novel intervention in polycystic kidney disease |
title_sort | ciliotherapy: a novel intervention in polycystic kidney disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981986/ https://www.ncbi.nlm.nih.gov/pubmed/24748884 http://dx.doi.org/10.3969/j.issn.1671-5411.2014.01.001 |
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