Pomegranate Extract Augments Energy Expenditure Counteracting the Metabolic Stress Associated with High-Fat-Diet-Induced Obesity.
Marina RegueroMarta Gómez de CedrónAranzazu Sierra-RamírezPablo José Fernández-MarcosGuillermo RegleroJosé Carlos QuintelaAna Ramírez de MolinaPublished in: International journal of molecular sciences (2022)
Obesity is associated to a low grade of chronic inflammation leading to metabolic stress, insulin resistance, metabolic syndrome, dislipidemia, cardiovascular disease, and even cancer. A Mediterranean diet has been shown to reduce systemic inflammatory factors, insulin resistance, and metabolic syndrome. In this scenario, precision nutrition may provide complementary approaches to target the metabolic alterations associated to "unhealthy obesity". In a previous work, we described a pomegranate extract (PomE) rich in punicalagines to augment markers of browning and thermogenesis in human differentiated adipocytes and to augment the oxidative respiratory capacity in human differentiated myocytes. Herein, we have conducted a preclinical study of high-fat-diet (HFD)-induced obesity where PomE augments the systemic energy expenditure (EE) contributing to a reduction in the low grade of chronic inflammation and insulin resistance associated to obesity. At the molecular level, PomE promotes browning and thermogenesis in adipose tissue, reducing inflammatory markers and augmenting the reductive potential to control the oxidative stress associated to the HFD. PomE merits further investigation as a complementary approach to alleviate obesity, reducing the low grade of chronic inflammation and metabolic stress.
Keyphrases
- insulin resistance
- high fat diet induced
- high fat diet
- adipose tissue
- low grade
- metabolic syndrome
- oxidative stress
- high grade
- polycystic ovary syndrome
- skeletal muscle
- type diabetes
- diabetic rats
- cardiovascular disease
- uric acid
- induced apoptosis
- dna damage
- bone marrow
- climate change
- squamous cell carcinoma
- risk assessment
- weight gain
- glycemic control
- young adults
- squamous cell