Deugchan Lee

Prof. Deugchan Lee

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2016 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
EKEunhee Kim
Eunhee Kim
SASejin Ahn
Sejin Ahn
HRHae-Ik Rhee
Hae-Ik Rhee
DLDeugchan Lee
Deugchan Lee

1 September 2016 in International Immunopharmacology
Verified
Journal Article
Closed access
SASejin Ahn
Sejin Ahn
EKEunhee Kim
Eunhee Kim
KLKooyeon Lee
Kooyeon Lee
DLDeugchan Lee
Deugchan Lee

24 August 2022 in Molecules
Verified
Journal Article
Open access
PDF file
SKSeo-Young Kim
Seo-Young Kim
SKSung-Pil Kwon
Sung-Pil Kwon
SPSeonJu Park
SeonJu Park
SCSu-Hyeon Cho
Su-Hyeon Cho
YOYoungse OH
Youngse OH
Kil-Nam KimKil-Nam Kim
Kil-Nam Kim
Growth and maintenance of skeletal muscle is essential for athletic performance and a healthy life. Stimulating the proliferation and differentiation of muscle cells may help prevent loss of muscle mass. To discover effective natural substances enabling to mitigate muscle loss without side effects, we evaluated muscle growth with several compounds extracted from Catalpa bignonioides Walt. Among these compounds, pinoresinol and vanillic acid increased C2C12, a mouse myoblast cell line, proliferation being the most without cytotoxicity. These substances activated the Akt/mammalian target of the rapamycin (mTOR) pathway, which positively regulates the proliferation of muscle cells. In addition, the results of in silico molecular docking study showed that they may bind to the active site of insulin-like growth factor 1 receptor (IGF-1R), which is an upstream of the Akt/mTOR pathway, indicating that both pinoresinol and vanillic acid stimulate myoblast proliferation through direct interaction with IGF-1R. These results suggest that pinoresinol and vanillic acid may be a natural supplement to improve the proliferation of skeletal muscle via IGF-1R/Akt/mTOR signaling and thus strengthen muscles.

1 January 2021 in Yonsei Medical Journal
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Journal Article
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JKJi Tae Kim
Ji Tae Kim
HKHyunho Kim
Hyunho Kim
SKSung Hyun Kim
Sung Hyun Kim
DKDong Jun Kim
Dong Jun Kim
YSYeji Shin
Yeji Shin
JPJung-Won Park
Jung-Won Park
Kim JT, et al. Yonsei Med J. 2021 Jan;62(1):86-90. https://doi.org/10.3349/ymj.2021.62.1.86

27 June 2017 in American Journal of Reproductive Immunology
Verified
Journal Article
Closed access
PDF file
SASejin Ahn
Sejin Ahn
EJEunbee Jeong
Eunbee Jeong
JMJae Woong Min
Jae Woong Min
EKEunhee Kim
Eunhee Kim
SCSun Shim Choi
Sun Shim Choi
DLDeugchan Lee
Deugchan Lee

31 May 2023 in Microorganisms
Verified
Journal Article
Open access
PDF file
HKHee-woong Kim
Hee-woong Kim
SCSooyoung Choi
Sooyoung Choi
DLDeugchan Lee
Deugchan Lee
HRHae-Ik Rhee
Hae-Ik Rhee
This study examines the possibility of directly producing and utilizing useful substances in the intestines of animals using anaerobic bacteria that can grow in the intestines of animals. A facultative anaerobe producing a large amount of α-glucosidase inhibitor was isolated from hay and identified and named Bacillus coagulans CC. The main compound of α-glucosidase inhibitor produced by Bacillus coagulans CC was identified as 1-deoxynojirimycin. α-glucosidase inhibitor activity was confirmed in the intestinal contents and feces of mice orally administered with spores of this strain, and it was confirmed that this strain could efficiently reach the intestines, proliferate, and produce α-glucosidase inhibitors. As a result of administering Bacillus coagulans CC to mice at 109 cells per 1 kg body weight of spores for 8 weeks, the high-carbohydrate diet and the high-fat diet showed a 5% lower weight gain compared to the non-administrated group. At this point, in the spore-administered group, a decrease was observed in both the visceral and subcutaneous fat layers of the abdomen and thorax in both high-carbohydrate and high-fat diet groups compared to the non-administered group on computed tomography. The results of this study show that α-glucosidase inhibitors produced in the intestine by specific strains can work efficiently.