Supplementation with a carob (Ceratonia siliqua l.) fruit extract attenuates the cardiometabolic alterations associated with metabolic syndrome in mice
Author
De La Fuente-Fernández, María; González-Hedström, Daniel; Amor, Sara; Tejera-Muñoz, Antonio; Fernández Monsalve, Nuria





Entity
UAM. Departamento de Anatomía, Histología y Neurociencia; UAM. Departamento de Fisiología; UAM. Departamento de Química Física AplicadaPublisher
MDPI, Basel, SMwitzerlandDate
2020-04-21Citation
10.3390/antiox9040339
Antioxidants 9.4 (2020): 339
ISSN
2076-3921DOI
10.3390/antiox9040339Funded by
This work has been funded by Pharmactive Biotech Products S.L. and by Grants from Community of Madrid awarded to Daniel González-Hedström (IND2017/BIO7701,) and María de la Fuente-Fernández (PEJ-2018-AI/SAL-11315)Editor's Version
http://doi.org/10.3390/antiox9040339Subjects
Anti-inflammatory; Antioxidant; Cardiovascular; Carob; Coronary ischemia; Endothelial dysfunction; Insulin resistance; Metabolic syndrome; MedicinaRights
© 2020 The AuthorsAbstract
The incidence of metabolic syndrome (MetS) is increasing worldwide which makes necessary the finding of new strategies to treat and/or prevent it. The aim of this study was to analyze the possible beneficial effects of a carob fruit extract (CSAT+®) on the cardiometabolic alterations associated with MetS in mice. 16-week-old C57BL/6J male mice were fed for 26 weeks either with a standard diet (chow) or with a diet rich in fats and sugars (HFHS), supplemented or not with 4.8% of CSAT+®. CSAT+® supplementation reduced blood glucose, Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) and circulating levels of total cholesterol, low-density lipoprotein (LDL) cholesterol (LDL-c), insulin, and interleukin-6 (IL-6). In adipose tissue and skeletal muscle, CSAT+® prevented MetS-induced insulin resistance, reduced macrophage infiltration and the expression of pro-inflammatory markers, and up-regulated the mRNA levels of antioxidant markers. Supplementation with CSAT+® prevented MetS-induced hypertension and decreased the vascular response of aortic rings to angiotensin II (AngII). Moreover, treatment with CSAT+® attenuated endothelial dysfunction and increased vascular sensitivity to insulin. In the heart, CSAT+® supplementation reduced cardiomyocyte apoptosis and prevented ischemia-reperfusion-induced decrease in cardiac contractility. The beneficial effects at the cardiovascular level were associated with a lower expression of pro-inflammatory and pro-oxidant markers in aortic and cardiac tissues.
Files in this item
Google Scholar:De La Fuente-Fernández, María
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González-Hedström, Daniel
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Amor, Sara
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Tejera-Muñoz, Antonio
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Fernández Monsalve, Nuria
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Monge Sánchez, Luis
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Almodóvar, Paula
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Andrés Delgado, Laura
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Santamaría Solís, Luis
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Prodanov Prodanov, Marin
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Inarejos-García, Antonio Manuel
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García-Villalón, Angel Luis
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Granado García, Miriam
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