NLRP3 inflammasome suppression improves longevity and prevents cardiac aging in male mice. Issue 1 (18th October 2019)
- Record Type:
- Journal Article
- Title:
- NLRP3 inflammasome suppression improves longevity and prevents cardiac aging in male mice. Issue 1 (18th October 2019)
- Main Title:
- NLRP3 inflammasome suppression improves longevity and prevents cardiac aging in male mice
- Authors:
- Marín‐Aguilar, Fabiola
Lechuga‐Vieco, Ana V.
Alcocer‐Gómez, Elísabet
Castejón‐Vega, Beatriz
Lucas, Javier
Garrido, Carlos
Peralta‐Garcia, Alejandro
Pérez‐Pulido, Antonio J.
Varela‐López, Alfonso
Quiles, José L.
Ryffel, Bernhard
Flores, Ignacio
Bullón, Pedro
Ruiz‐Cabello, Jesús
Cordero, Mario D. - Abstract:
- Abstract: While NLRP3‐inflammasome has been implicated in cardiovascular diseases, its role in physiological cardiac aging is largely unknown. During aging, many alterations occur in the organism, which are associated with progressive impairment of metabolic pathways related to insulin resistance, autophagy dysfunction, and inflammation. Here, we investigated the molecular mechanisms through which NLRP3 inhibition may attenuate cardiac aging. Ablation of NLRP3‐inflammasome protected mice from age‐related increased insulin sensitivity, reduced IGF‐1 and leptin/adiponectin ratio levels, and reduced cardiac damage with protection of the prolongation of the age‐dependent PR interval, which is associated with atrial fibrillation by cardiovascular aging and reduced telomere shortening. Furthermore, old NLRP3 KO mice showed an inhibition of the PI3K/AKT/mTOR pathway and autophagy improvement, compared with old wild mice and preserved Nampt‐mediated NAD + levels with increased SIRT1 protein expression. These findings suggest that suppression of NLRP3 prevented many age‐associated changes in the heart, preserved cardiac function of aged mice and increased lifespan. Abstract : In this study, we have shown the potential role of the NLRP3 inhibition to modulate several anti‐aging mechanisms during cardiac aging. This work highlights the importance of examining the therapeutic and prophylatic value of small molecule inhibitors of NLRP3 and its effects as potential therapy for preventingAbstract: While NLRP3‐inflammasome has been implicated in cardiovascular diseases, its role in physiological cardiac aging is largely unknown. During aging, many alterations occur in the organism, which are associated with progressive impairment of metabolic pathways related to insulin resistance, autophagy dysfunction, and inflammation. Here, we investigated the molecular mechanisms through which NLRP3 inhibition may attenuate cardiac aging. Ablation of NLRP3‐inflammasome protected mice from age‐related increased insulin sensitivity, reduced IGF‐1 and leptin/adiponectin ratio levels, and reduced cardiac damage with protection of the prolongation of the age‐dependent PR interval, which is associated with atrial fibrillation by cardiovascular aging and reduced telomere shortening. Furthermore, old NLRP3 KO mice showed an inhibition of the PI3K/AKT/mTOR pathway and autophagy improvement, compared with old wild mice and preserved Nampt‐mediated NAD + levels with increased SIRT1 protein expression. These findings suggest that suppression of NLRP3 prevented many age‐associated changes in the heart, preserved cardiac function of aged mice and increased lifespan. Abstract : In this study, we have shown the potential role of the NLRP3 inhibition to modulate several anti‐aging mechanisms during cardiac aging. This work highlights the importance of examining the therapeutic and prophylatic value of small molecule inhibitors of NLRP3 and its effects as potential therapy for preventing cardiac and metabolic aging. … (more)
- Is Part Of:
- Aging cell. Volume 19:Issue 1(2020)
- Journal:
- Aging cell
- Issue:
- Volume 19:Issue 1(2020)
- Issue Display:
- Volume 19, Issue 1 (2020)
- Year:
- 2020
- Volume:
- 19
- Issue:
- 1
- Issue Sort Value:
- 2020-0019-0001-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-10-18
- Subjects:
- autophagy -- cardiac aging -- longevity -- morbidity -- mortality -- NLRP3‐inflammasome
Cells -- Aging -- Periodicals
571.8783605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1474-9726 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/acel.13050 ↗
- Languages:
- English
- ISSNs:
- 1474-9718
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0736.360500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12629.xml