Metabolic Profiling in Plasma and Brain Induced by 17β-Estradiol Supplementation in Ovariectomized Mice.
So Hwi YangYe Jin KimHye Rim YangSang Un ParkJae Geun KimJae Kwang KimPublished in: ACS omega (2024)
17β-Estradiol is an ovarian hormone that regulates energy circulation and storage by acting on the central nervous system. However, the metabolic differences between the blood and brain when stimulated by 17β-estradiol are poorly understood. Moreover, research using menopause-induced models to investigate primary metabolites in the blood and brain is limited. Thus, this study aimed to identify metabolic changes in the plasma and brain resulting from 17β-estradiol supplementation in an estrogen-deficient mouse model. Three groups of mice were utilized: sham-operated mice (Sham), ovariectomized mice (OVX), and ovariectomized mice that received a weekly supplementation of 17β-estradiol (E2). Plasma and brain samples from these mice were subjected to metabolic analysis using gas chromatography-time-of-flight-mass spectrometry. Compared with the plasma samples from the Sham and OVX groups, the plasma samples from the E2 group contained higher contents of branched-chain amino acids (BCAAs), such as valine, isoleucine, and leucine. Meanwhile, the brain samples from the E2 group contained higher contents of most metabolites, including BCAAs, neurotransmitters, tricarboxylic acid cycle intermediates, and fatty acids, than those from the two other groups. This study is the first to reveal differences in energy metabolism induced by 17β-estradiol supplementation through brain metabolic profiling of ovariectomized mice, emphasizing the importance of brain metabolic profiling in menopausal hormone research.
Keyphrases
- resting state
- white matter
- high fat diet induced
- functional connectivity
- estrogen receptor
- cerebral ischemia
- mouse model
- wild type
- clinical trial
- ms ms
- fatty acid
- multiple sclerosis
- type diabetes
- insulin resistance
- amino acid
- metabolic syndrome
- high resolution
- adipose tissue
- oxidative stress
- brain injury
- diabetic rats
- gene expression
- blood brain barrier
- postmenopausal women
- double blind
- drug induced
- high resolution mass spectrometry