Lemon Balm and Corn Silk Mixture Alleviates Metabolic Disorders Caused by a High-Fat Diet.
Il Je ChoJoung-Hoon ShinBeom-Rak ChoiHye-Rim ParkJeong-Eun ParkSeong-Hwa HongYoung-Sam KwonWon-Seok OhSae Kwang KuPublished in: Antioxidants (Basel, Switzerland) (2022)
We recently reported that varying combination ratios of lemon balm ( Mellissa officinalis L.) and corn silk extracts (Stigma of Zea mays L. fruit) could reduce the obesity caused by a high-fat diet (HFD). The present study investigated the dose-dependent effect of a 1:1 ( w : w ) mixture of lemon balm and corn silk extracts (M-LB/CS) on HFD-mediated metabolic disorders and compared the effect with metformin. Oral administration of 50-200 mg/kg of M-LB/CS for 84 days significantly inhibited HFD-induced body weight gain, adipocyte hypertrophy, and lipogenic gene induction without affecting food consumption in mice. Biochemical analyses showed that M-LB/CS blocked abnormal lipid accumulation in the blood by escalating fecal lipid excretion. In addition, M-LB/CS prevented HFD-mediated pancreatic atrophy, decreased the number of insulin- and glucagon-immunoreactive cells, and inhibited increases in glycated hemoglobin, glucose, and insulin. Moreover, M-LB/CS also reduced hepatic injury, lipid accumulation, gluconeogenesis, and lipid peroxidation in parallel with the induction of AMP-activated protein kinase and antioxidant enzymes. Furthermore, M-LB/CS protected the kidney by inhibiting tubular vacuolation and reducing serum creatinine and blood urea nitrogen levels. The prophylactic effect of 100 mg/kg M-LB/CS-administration was comparable to that of metformin. Therefore, M-LB/CS may be an alternative option for managing obesity and its related metabolic disorders.
Keyphrases
- high fat diet
- insulin resistance
- adipose tissue
- weight gain
- high fat diet induced
- type diabetes
- metabolic syndrome
- skeletal muscle
- protein kinase
- weight loss
- mental health
- body mass index
- fatty acid
- glycemic control
- induced apoptosis
- birth weight
- wound healing
- signaling pathway
- gene expression
- depressive symptoms
- high glucose
- cell death
- endothelial cells
- diabetic rats
- dna methylation
- hepatitis c virus
- cell cycle arrest