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[논문] Ginsenoside Rg3, enriched in red ginseng extract, improves lipopolysaccharides‑induced suppression of brown and beige adipose thermogenesis with mitochondrial activation

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논문제목(Title)

[논문] Ginsenoside Rg3, enriched in red ginseng extract, improves lipopolysaccharides‑induced suppression of brown and beige adipose thermogenesis with mitochondrial activation

학술지명(Journal)

Scientific reports

ImpactFactor

3.8

ISSN_ISBN

2045-2322

학술지볼륨권호(Volume)

14

SCI구분

SCIE

초록(Abstract)

Brown adipose tissue (BAT) which is a critical regulator of energy homeostasis, and its activity is inhibited by obesity and low-grade chronic infammation. Ginsenoside Rg3, the primary constituent of Korean red ginseng (steamed Panax ginseng CA Meyer), has shown therapeutic potential in combating infammatory and metabolic diseases. However, it remains unclear whether Rg3 can protect against the suppression of browning or activation of BAT induced by infammation. In this study, we conducted a screening of ginsenoside composition in red ginseng extract (RGE) and explored the anti-adipogenic efects of both RGE and Rg3. We observed that RGE (exist 0.25 mg/mL of Rg3) exhibited signifcant lipid-lowering efects in adipocytes during adipogenesis. Moreover, treatment with Rg3 (60 μM) led to the inhibition of triglyceride accumulation, subsequently promoting enhanced fatty acid oxidation, as evidenced by the conversion of radiolabeled 3 H-fatty acids into 3 H-H2O with mitochondrial activation. Rg3 alleviated the attenuation of browning in lipopolysaccharide (LPS)treated beige adipocytes and primary brown adipocytes by recovered by uncoupling protein 1 (UCP1) and the oxygen consumption rate compared to the LPS-treated group. These protective efects of Rg3 on infammation-induced inhibition of beige and BAT-derived thermogenesis were confrmed in vivo by treating with CL316,243 (a beta-adrenergic receptor agonist) and LPS to induce browning and infammation, respectively. Consistent with the in vitro data, treatment with Rg3 (2.5 mg/kg, 8 weeks) efectively reversed the LPS-induced inhibition of brown adipocyte features in C57BL/6 mice. Our fndings confrm that Rg3-rich foods are potential browning agents that counteract chronic infammation and metabolic complications.

Keywords Ginsenoside Rg3, Beige adipocytes, Brown adipocytes, Adaptive thermogenesis, Infammation, Mitochondrial activation

저자명(Author)

Fang Feng, Hyun‑A Ko , Thi MyTienTruong, Woo‑Jin Song, Eun‑Ju Ko & Inhae Kang

학술지출판일자(PublicationDate)

2024.04.22.

DMP

과제명(영문)

Effects of Jeju-seaweed extract on obesity in diet-induced obesity mouse model

연구책임자 / 소속

강인혜/ 식품영양학과

당해연구기간

2023.03.01-2024.02.29

공개 및 라이선스

공개 일자

2024-09-19

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[강인혜] 만성질환 비만 모델에서 제주 해조류추출물의 항비만 효과 구명 연구(2023)
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2024-09-19
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  • Version 1 2024-09-04
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Fang Feng, Hyun‑A Ko , Thi MyTienTruong, Woo‑Jin Song, Eun‑Ju Ko & Inhae Kang, 2024.04.22., [논문] Ginsenoside Rg3, enriched in red ginseng extract, improves lipopolysaccharides‑induced suppression of brown and beige adipose thermogenesis with mitochondrial activation
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