Background Hypertension is a multifactorial and chronic cardiovascular condition whose complications are responsible for worldwide morbidity and mortality. An increasing body of experimental data, recognize low-grade inflammation as a basic process in hypertension onset and development since there is a strong contribution of both the innate and the adaptive immune system according to the so-called Danger-Model. In this contest, NLRP3 inflammasome represents a key signaling platform as demonstrated by its implication in several hypertension-associated conditions, such as vascular smooth muscle remodeling and proliferation. This intracellular receptor is activated by Pathogen-associated molecular pattern molecules/damage-associated molecular pattern molecules signals and its mechanism of action converges on the final production of caspase-1 and, consequently, of the pro-inflammatory cytokines IL-1β and IL-18. Objective The aim of the present work was to point the role of the NLRP3 inflammasome complex in the hypertensive pathology and to describe it as a new potential therapeutic target. Method A systematic review of the literature data related to NLRP3 and hypertension correlation has been performed. Results Numerous and well-designed experiments demonstrate that the inflammasome plays a crucial role in essential and high-salt dependent hypertension, as well as in preeclampsia, in pulmonary hypertension, and in its related secondary disorders; its mechanism includes both a central nervous and a peripheral modulation of the inflammatory pathways. To date, research is trying to design inflammasome antagonists or equivalent inhibition strategies. Conclusion The inflammasome represents a leading promoter of hypertensive inflammation opening new perspective in the field of the clinical approach in this pathology.

Role of NLRP-3 inflammasome in hypertension: A potential therapeutic target

Pagliaro, Pasquale;Penna, Claudia
Last
2018-01-01

Abstract

Background Hypertension is a multifactorial and chronic cardiovascular condition whose complications are responsible for worldwide morbidity and mortality. An increasing body of experimental data, recognize low-grade inflammation as a basic process in hypertension onset and development since there is a strong contribution of both the innate and the adaptive immune system according to the so-called Danger-Model. In this contest, NLRP3 inflammasome represents a key signaling platform as demonstrated by its implication in several hypertension-associated conditions, such as vascular smooth muscle remodeling and proliferation. This intracellular receptor is activated by Pathogen-associated molecular pattern molecules/damage-associated molecular pattern molecules signals and its mechanism of action converges on the final production of caspase-1 and, consequently, of the pro-inflammatory cytokines IL-1β and IL-18. Objective The aim of the present work was to point the role of the NLRP3 inflammasome complex in the hypertensive pathology and to describe it as a new potential therapeutic target. Method A systematic review of the literature data related to NLRP3 and hypertension correlation has been performed. Results Numerous and well-designed experiments demonstrate that the inflammasome plays a crucial role in essential and high-salt dependent hypertension, as well as in preeclampsia, in pulmonary hypertension, and in its related secondary disorders; its mechanism includes both a central nervous and a peripheral modulation of the inflammatory pathways. To date, research is trying to design inflammasome antagonists or equivalent inhibition strategies. Conclusion The inflammasome represents a leading promoter of hypertensive inflammation opening new perspective in the field of the clinical approach in this pathology.
2018
19
9
708-714
714
http://www.eurekaselect.com/607/journal/current-pharmaceutical-biotechnology
Cytokines; Hypertension; Inflammasome; Inflammation; Preeclampsia; Vascular remodeling; Adaptive Immunity; Animals; Humans; Hypertension; Immunity, Innate; Inflammasomes; Inflammation; Molecular Targeted Therapy; NLR Family, Pyrin Domain-Containing 3 Protein; Signal Transduction; Vascular Remodeling; Biotechnology; 3003
Pasqua, Teresa; Pagliaro, Pasquale; Rocca, Carmine; Angelone, Tommaso; Penna, Claudia
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1674580
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