Crataegus Aronia protects and reverses vascular inflammation in a high fat diet rat model by an antioxidant mechanism and modulating serum levels of oxidized low-density lipoprotein.


Journal

Pharmaceutical biology
ISSN: 1744-5116
Titre abrégé: Pharm Biol
Pays: England
ID NLM: 9812552

Informations de publication

Date de publication:
Dec 2019
Historique:
entrez: 1 2 2019
pubmed: 1 2 2019
medline: 8 2 2019
Statut: ppublish

Résumé

Crataegus aronia (Willd.) Bosc (Rosaceae) (syn. Azarolus L) is traditionally used to treat cardiovascular disorders. To investigate C. aronia protection against a high-fat diet (HFD)-induced vascular inflammation in rats. Wistar Male rats (180-220 g) were divided (n = 10/group) as control fed a standard diet (STD), STD + C. aronia (200 mg/kg, orally), HFD, HFD + C. aronia and HFD post-treated with C. aronia. Simvastatin (20 mg/kg) was co- or post-administered as a positive control drug. HFD was given for 8 weeks, and all other treatments were administered for 4 weeks. Most significantly, co-administration of C. aronia to HFD-fed rats reduced the thickness of aorta tunica media (90 ± 5 vs. 160 ± 11.3 µm) and adventitia (54.3 ± 3.8 vs. 93.6 ± 9.4 µm). It also lowered protein levels of TNF-α (0.51 ± 0.15 and 0.15 ± 0.16 vs. 0.1 ± 0.09%) and IL-6 (0.52 ± 0.19 vs. 1.0 ± 0.2%) in their aorta or serum (5.9 ± 0.91 vs. 12.98 ± 1.3 ng/mL and 78.1 ± 6.7 vs. 439 ± 78 pg/mL, respectively). It also lowered all serum lipids and increased aorta levels of GSH levels (70.4 ± 4.0 vs. 40.7 µM) and activity of SOD (5.7 ± 0.7 vs. 2.9 ± 0.6 U/mg) and decreased serum levels of ox-LDL-c (566.7 ± 46 vs. 1817 ± 147 ng/mL). Such effects were more profound than all other treatments. C. aronia inhibits the HFD-induced vascular inflammation and its use in clinical trials is recommended.

Identifiants

pubmed: 30702358
doi: 10.1080/13880209.2018.1564930
pmc: PMC6366417
doi:

Substances chimiques

Antioxidants 0
Lipids 0
Lipoproteins, LDL 0
Plant Extracts 0
oxidized low density lipoprotein 0
crataegus extract 6OM09RPY36
Simvastatin AGG2FN16EV
Superoxide Dismutase EC 1.15.1.1
Glutathione GAN16C9B8O

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

38-48

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Auteurs

Abdullah S Shatoor (AS)

a Department of Medicine, Cardiology Section, College of Medicine, King Khalid University (KKU), Abha, Saudi Arabia.

Suliman Al Humayed (S)

a Department of Medicine, Cardiology Section, College of Medicine, King Khalid University (KKU), Abha, Saudi Arabia.

Mahmoud A Alkhateeb (MA)

b Department of Basic Medical Sciences, College of Medicine, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi Arabia.

Khalid A Shatoor (KA)

c An intern, College of Medicine, King Khalid University (KKU), Abha, Saudi Arabia.

Hussain Aldera (H)

b Department of Basic Medical Sciences, College of Medicine, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi Arabia.
d King Abdullah International Medical Research center (KAIMRC), Riyadh, Saudi Arabia.

Mohammed Alassiri (M)

b Department of Basic Medical Sciences, College of Medicine, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi Arabia.
d King Abdullah International Medical Research center (KAIMRC), Riyadh, Saudi Arabia.

Ali A Shati (AA)

e Department of Biology College of Science, College of Medicine, King Khalid University (KKU), Abha, Saudi Arabia.

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Classifications MeSH