Resistant hypertension (RH) is a clinical condition in which the hypertensive patient has become resistant to drug therapy and is often associated with increased cardiovascular morbidity and mortality. Several signalling pathways have been studied and related to the development and progression of RH: modulation of sympathetic activity by leptin and aldosterone, primary aldosteronism, arterial stiffness, endothelial dysfunction and variations in the renin–angiotensin–aldosterone system (RAAS). miRNAs comprise a family of small non-coding RNAs that participate in the regulation of gene expression at post-transcriptional level. miRNAs are involved in the development of both cardiovascular damage and hypertension. Little is known of the molecular mechanisms that lead to development and progression of this condition. This review aims to cover the potential roles of miRNAs in the mechanisms associated with the development and consequences of RH, and explore the current state of the art of diagnostic and therapeutic tools based on miRNA approaches.
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December 2017
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Wheat germ agglutinin staining of the adult mouse heart transverse section. In their study, Diniz et al., shows microRNA-22 regulates dyslipidemia and energy expenditure. For more information please see pages 2885-2900. Image kindly provided by Da-Zhi WangClose Modal
Review Article|
November 28 2017
Decoding resistant hypertension signalling pathways
Ricardo Cambraia Parreira;
Ricardo Cambraia Parreira
1Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antôniol Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil
2Instituto Nanocell, Research Department, Rua Santo Antônio, 420, Divinópolis 35500-041, MG, Brazil
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Leandro Heleno Guimarães Lacerda;
Leandro Heleno Guimarães Lacerda
3College of Sete Lagoas - FACSETE, Department of Pharmacology, Rua Itália Pontelo, 50/86, Chácara do Paiva 35700-170 -Sete Lagoas, MG, Brazil
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Rebecca Vasconcellos;
Rebecca Vasconcellos
1Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antôniol Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil
2Instituto Nanocell, Research Department, Rua Santo Antônio, 420, Divinópolis 35500-041, MG, Brazil
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Swiany Silveira Lima;
Swiany Silveira Lima
1Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antôniol Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil
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Anderson Kenedy Santos;
Anderson Kenedy Santos
1Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antôniol Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil
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Vanessa Fontana;
Vanessa Fontana
4Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, Wolfson Centre for Personalised Medicine, University of Liverpool, Liverpool, United Kingdom
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Valéria Cristina Sandrim;
Valéria Cristina Sandrim
5Department of Pharmacology, Institute of Biosciences of Botucatu, Universidade Estadual Paulista (UNESP), Distrito Rubiao Junior, Botucatu, São Paulo 18680-000, Brazil
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Rodrigo Ribeiro Resende
1Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Av. Antôniol Carlos, 6627, Belo Horizonte 31270-901, MG, Brazil
2Instituto Nanocell, Research Department, Rua Santo Antônio, 420, Divinópolis 35500-041, MG, Brazil
Correspondence: Rodrigo Ribeiro Resende (rrresende@institutonanocell.org.br) or (rrresende@hotmail.com)
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Clin Sci (Lond) (2017) 131 (23): 2813–2834.
Article history
Received:
September 28 2017
Revision Received:
October 16 2017
Accepted:
October 23 2017
Citation
Ricardo Cambraia Parreira, Leandro Heleno Guimarães Lacerda, Rebecca Vasconcellos, Swiany Silveira Lima, Anderson Kenedy Santos, Vanessa Fontana, Valéria Cristina Sandrim, Rodrigo Ribeiro Resende; Decoding resistant hypertension signalling pathways. Clin Sci (Lond) 1 December 2017; 131 (23): 2813–2834. doi: https://doi.org/10.1042/CS20171398
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