4.4 Article

Rubus chingii var. suavissimus alleviates high-fat diet-induced lipid metabolism disorder via modulation of the PPARs/SREBP pathway in Syrian golden hamsters

Journal

JOURNAL OF NATURAL MEDICINES
Volume 75, Issue 4, Pages 884-892

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s11418-021-01536-8

Keywords

Rubus chingii var; suavissimus; Lipid metabolism disorder; PPAR alpha; PPAR gamma; C/EBP alpha; SREBP1

Funding

  1. National Natural Science Foundation of China [31660095, 81903918]
  2. Guangxi Natural Science Foundation [2019JJA140644]
  3. First-class discipline of Chinese materia medica in Guangxi [2019XK117]
  4. Graduate Education Innovation Program Project from Guangxi University of Chinese Medicine [YCSZ2020011, YCSZ20190028]
  5. Guangxi Key Laboratory of Zhuang and Yao Ethnic Medicine [32]

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Rubus chingii var. suavissimus or Rubus suavissimus, a sweet plant in southwest China, has potential in improving obesity and hyperlipidemia. Studies showed that it can alleviate lipid metabolism disorder by modulating the PPARs/SREBP pathway in Syrian golden hamsters.
While the underlying mechanism remains unknown, Rubus chingii var. suavissimus (S. K. Lee) L. T. Lu or Rubus suavissimus S. Lee (RS), a sweet plant distributed in southwest of China, has been used as beverage and folk medicine. Pharmacological studies indicated the potential of RS improving the obesity phenotype and hyperlipidemia. The mechanism is still not yet to be put forward. To verify the substantial effects of RS on lipid metabolism, a Syrian golden hamster model was adopted. The physiological and pathological evaluation of experimental animals demonstrated that RS can relieve the lipid metabolism disorder induced by high-fat diet and alleviated liver injury. RS upregulation the expressions of peroxisome proliferator-activated receptor alpha (PPAR alpha), PPAR gamma and CCAAT/enhancer binding protein alpha (C/EBP alpha), as well as adipocyte-specific genes, glucose transporter 4 (Glut4), lipoprotein lipase (LPL) and fatty acid binding protein 4 (aP2). On the other side, RS suppressed the sterol regulatory element binding protein 1 (SREBP1) and downstream acetyl-CoA carboxylase 1 (ACC1), stearoyl-CoA desaturase-1 (SCD1) and fatty acid synthase (FAS). In conclusion, RS alleviated lipid metabolism disorder symptoms caused by high-fat diet accompanied with 8 weeks of treatment, involving enhanced beta-oxidation, increased adipogenesis and decreased the metabolism of fatty acids, via modulation of the PPARs/SREBP pathway in Syrian golden hamsters.

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