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System-level investigation of anti-obesity effects and the potential pathways of Cordyceps militaris in ovariectomized ratsopen access

Authors
Jang, DongyeopLee, EunjooLee, SullimKwon, YongsamKang, Ki SungKim, Chang-EopKim, Daeyoung
Issue Date
May-2022
Publisher
BMC
Keywords
Cordyceps militaris; Menopause; Obesity; Estrogen receptor; Mitogen-activated protein kinase; Network pharmacology
Citation
BMC COMPLEMENTARY MEDICINE AND THERAPIES, v.22, no.1
Journal Title
BMC COMPLEMENTARY MEDICINE AND THERAPIES
Volume
22
Number
1
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/84413
DOI
10.1186/s12906-022-03608-y
ISSN
2662-7671
Abstract
Background Cordyceps species have been used as tonics to enhance energy, stamina, and libido in traditional Asian medicine for more than 1600 years, indicating their potential for improving reproductive hormone disorders and energy metabolic diseases. Among Cordyceps, Cordyceps militaris has been reported to prevent metabolic syndromes including obesity and benefit the reproductive hormone system, suggesting that Cordyceps militaris can also regulate obesity induced by the menopause. We investigated the effectiveness of Cordyceps militaris extraction (CME) on menopausal obesity and its mechanisms. Methods We applied an approach combining in vivo, in vitro, and in silico methods. Ovariectomized rats were administrated CME, and their body weight, area of adipocytes, liver and uterus weight, and lipid levels were measured. Next, after the exposure of MCF-7 human breast cancer cells to CME, cell proliferation and the phosphorylation of estrogen receptor and mitogen-activated protein kinases (MAPK) were measured. Finally, network pharmacological methods were applied to predict the anti-obesity mechanisms of CME. Results CME prevented overweight, fat accumulation, liver hypertrophy, and lowered triglyceride levels, some of which were improved in a dose-dependent manner. In MCF-7 cell lines, CME showed not only estrogen receptor agonistic activity through an increase in cell proliferation and the phosphorylation of estrogen receptors, but also phosphorylation of extracellular-signal-regulated kinase and p38. In the network pharmacological analysis, bioactive compounds of CME such as cordycepin, adenine, and guanosine were predicted to interact with non-overlapping genes. The targeted genes were related to the insulin signaling pathway, insulin resistance, the MARK signaling pathway, the PI3K-Akt signaling pathway, and the estrogen signaling pathway. Conclusions These results suggest that CME has anti-obesity effects in menopause and estrogenic agonistic activity. Compounds in CME have the potential to regulate obesity-related and menopause-related pathways. This study will contribute to developing the understanding of anti-obesity effects and mechanisms of Cordyceps militaris.
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