Effect of the consumption of hesperidin in orange juice on the transcriptomic profile of subjects with elevated blood pressure and stage 1 hypertension: A randomized controlled trial (CITRUS study).
3-Hydroxysteroid Dehydrogenases
/ metabolism
Adult
Blood Pressure
/ genetics
Citrus sinensis
Double-Blind Method
Down-Regulation
Female
Fruit and Vegetable Juices
Gene Expression
/ drug effects
Hesperidin
/ administration & dosage
Humans
Hypertension
/ genetics
Leukocytes, Mononuclear
/ metabolism
Male
Middle Aged
Selenium-Binding Proteins
/ metabolism
Transcriptome
/ drug effects
Hesperidin
Hypertensive subjects
Orange juice
PBMCs
Plasma
Transcriptomic analysis
Journal
Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603
Informations de publication
Date de publication:
12 2021
12 2021
Historique:
received:
25
03
2021
revised:
21
09
2021
accepted:
14
10
2021
pubmed:
21
11
2021
medline:
24
2
2022
entrez:
20
11
2021
Statut:
ppublish
Résumé
Hesperidin exerts cardiovascular beneficial effects, but its mechanisms of action remain undefined. In a previous study we demonstrated that a single dose and a 12-week treatment of hesperidin decreased systolic blood pressure. The aim of this study was to ascertain the action mechanisms of hesperidin consumption in subjects with elevated blood pressure or with stage 1 hypertension, by determining their transcriptomic profile after a single dose or a 12-week treatment. For transcriptomic analysis, peripheral blood mononuclear cells were obtained from 37 subjects with elevated blood pressure and stage 1 hypertension from CITRUS study who were randomized to receive for 12 weeks: control drink (CD; n = 11), OJ (containing 345 mg of hesperidin; n = 15) or EOJ (containing 600 mg of hesperidin; n = 11). Before starting the 12-weeks treatment, a single dose study with a 6 h of follow-up in each group was performed. After the single dose consumption, EOJ versus OJ, downregulated DHRS9 gene which is related with insulin resistance. Compared to CD, 12-week treatment of EOJ downregulated 6 proinflammatory genes while after OJ consumption only 1 proinflammatory gene was downregulated. Moreover, 12-week treatment of EOJ versus OJ, downregulated acute coronary syndrome gene related (SELENBP1). A single dose consumption of EOJ could protect from insulin resistance. Moreover, EOJ decrease the expression of proinflammatory genes after 12-week treatment providing a possible mechanism of action on inflammation pathway.
Identifiants
pubmed: 34800819
pii: S0261-5614(21)00478-7
doi: 10.1016/j.clnu.2021.10.009
pii:
doi:
Substances chimiques
SELENBP1 protein, human
0
Selenium-Binding Proteins
0
Hesperidin
E750O06Y6O
3-Hydroxysteroid Dehydrogenases
EC 1.1.-
DHRS9 protein, human
EC 1.1.-
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
5812-5822Informations de copyright
Copyright © 2021. Published by Elsevier Ltd.
Déclaration de conflit d'intérêts
Conflict of interest The authors declare that they have not conflicts of interest with the content of this article.