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Saponins from Panax japonicus improve neuronal mitochondrial injury of aging rats.
Fan, Cheng; Wang, Jin-Xin; Xiong, Zhang-E; Hu, Shan-Shan; Zhou, Ao-Jia; Yuan, Ding; Zhang, Chang-Cheng; Zhou, Zhi-Yong; Wang, Ting.
Affiliation
  • Fan C; Institute of Pharmaceutical Process, Academy of Nutrition and Health Hubei Province Key Laboratory of Occupational Hazard Identification and Control School of Medicine, Wuhan University of Science and Technology Wuhan, China.
  • Wang JX; College of Medical Science, Three Gorges University, Yichang, Hubei, China.
  • Xiong ZE; Department of Gastroenterology, Wuhan Third Hospital, Wuhan, China.
  • Hu SS; College of Medical Science, Three Gorges University, Yichang, Hubei, China.
  • Zhou AJ; Institute of Pharmaceutical Process, Academy of Nutrition and Health Hubei Province Key Laboratory of Occupational Hazard Identification and Control School of Medicine, Wuhan University of Science and Technology Wuhan, China.
  • Yuan D; College of Medical Science, Three Gorges University, Yichang, Hubei, China.
  • Zhang CC; College of Medical Science, Three Gorges University, Yichang, Hubei, China.
  • Zhou ZY; College of Medical Science, Three Gorges University, Yichang, Hubei, China.
  • Wang T; Institute of Pharmaceutical Process, Academy of Nutrition and Health Hubei Province Key Laboratory of Occupational Hazard Identification and Control School of Medicine, Wuhan University of Science and Technology Wuhan, China.
Pharm Biol ; 61(1): 1401-1412, 2023 Dec.
Article in En | MEDLINE | ID: mdl-37667488
ABSTRACT
CONTEXT Panax japonicus is the dried rhizome of Panax japonicus C.A. Mey. (Araliaceae). Saponins from Panax japonicus (SPJ) exhibit anti-oxidative and anti-aging effects.

OBJECTIVE:

We evaluated the neuroprotective effects of SPJ on aging rats. MATERIALS AND

METHODS:

Sprague-Dawley rats (18-months-old) were randomly divided into aging and SPJ groups (n = 8). Five-month-old rats were taken as the adult control (n = 8). The rats were fed a normal chow diet or the SPJ-containing diet (10 or 30 mg/kg) for 4 months. An in vitro model was established by d-galactose (d-Gal) in the SH-SY5Y cell line and pretreated with SPJ (25 and 50 µg/mL). The neuroprotection of SPJ was evaluated via Nissl staining, flow cytometry, transmission electron microscopy and Western blotting in vivo and in vitro.

RESULTS:

SPJ improved the neuronal degeneration and mitochondrial morphology that are associated with aging. Meanwhile, SPJ up-regulated the protein levels of mitofusin 2 (Mfn2) and optic atrophy 1 (Opa1) and down-regulated the protein level of dynamin-like protein 1 (Drp1) in the hippocampus of aging rats (p < 0.05 or p < 0.01 vs. 22 M). The in vitro studies also demonstrated that SPJ attenuated d-Gal-induced cell senescence concomitant with the improvement in mitochondrial function; SPJ, also up-regulated the Mfn2 and Opa1 protein levels, whereas the Drp1 protein level (p < 0.05 or p < 0.01 vs. d-Gal group) was down-regulated. DISCUSSION AND

CONCLUSIONS:

Further research on the elderly population will contribute to the development and utilization of SPJ for the treatment of neurodegenerative disorders.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Panax / Neuroblastoma Limits: Aged / Animals / Humans Language: En Journal: Pharm Biol Year: 2023 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Panax / Neuroblastoma Limits: Aged / Animals / Humans Language: En Journal: Pharm Biol Year: 2023 Type: Article Affiliation country: China