The Protective Effect of Crataegus aronia Against High-Fat Diet-Induced Vascular Inflammation in Rats Entails Inhibition of the NLRP-3 Inflammasome Pathway.


Journal

Cardiovascular toxicology
ISSN: 1559-0259
Titre abrégé: Cardiovasc Toxicol
Pays: United States
ID NLM: 101135818

Informations de publication

Date de publication:
02 2020
Historique:
pubmed: 12 6 2019
medline: 21 10 2020
entrez: 12 6 2019
Statut: ppublish

Résumé

This study investigated whether the whole-plant aqueous extract of Crataegus aronia (C. aronia) could protect against or alleviate high-fat diet (HFD)-induced aortic vascular inflammation in rats by inhibiting the NLRP-3 inflammasome pathway and examined some mechanisms of action with respect to its antioxidant and hypolipidemic effects. Adult male Wistar rats were divided into five groups (n = 6/each): standard diet (10% fat) fed to control rats, control + C. aronia (200 mg/kg), HFD (40% fat), HFD + C. aronia, and HFD post-treated with C. aronia. The HFD was fed for 8 weeks and C. aronia was administered orally for 4 weeks. In addition, isolated macrophages from control rats were pre-incubated with two doses of C. aronia (25 and 50 μg/mL) with or without lipopolysaccharide (LPS) stimulation. Only in HFD-fed rats, co- and post-C. aronia therapy lowered circulatory levels of LDL-C and ox-LDL-c and aortic protein levels of LOX-1 and CD36. C. aronia also inhibited the nuclear accumulation of NF-κB and lowered protein levels of NLRP-3, caspase-1, and mature IL-1β. In vitro, in the absence of ox-LDL-c, C. aronia led to reduced nuclear levels of NF-κB, ROS generation, and protein NLRP-3 levels, in both LPS-stimulated and unstimulated macrophages, in a dose-dependent manner. However, protein levels of LOX-1 were not affected by C. aronia in unstimulated cells. In conclusion, C. aronia inhibits the NLRP-3 inflammasome pathway, induced by HFD feeding in the aorta of rats, mainly by its hypolipidemic effect and in vitro, in LPS-stimulated macrophages, by its antioxidant effect.

Identifiants

pubmed: 31183600
doi: 10.1007/s12012-019-09534-9
pii: 10.1007/s12012-019-09534-9
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Antioxidants 0
Hypolipidemic Agents 0
Inflammasomes 0
Inflammation Mediators 0
NLR Family, Pyrin Domain-Containing 3 Protein 0
Nlrp3 protein, rat 0
Plant Extracts 0
Reactive Oxygen Species 0
crataegus extract 6OM09RPY36

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

82-99

Auteurs

Abdullah S Shatoor (AS)

Department of Medicine, Cardiology Section, College of Medicine, King Khalid University, Abha, 61421, Saudi Arabia. asshalghamdi@yahoo.com.

Suliman Al Humayed (S)

Department of Medicine, College of Medicine, King Khalid University, Abha, 61421, Saudi Arabia.

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Classifications MeSH