Int J Med Sci 2020; 17(8):1048-1055. doi:10.7150/ijms.43979 This issue Cite

Research Paper

Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis

Si-Jia Zhong1,3*, Lin Wang1*, Run-Ze Gu1*, Wen-Hao Zhang1, Rongfeng Lan2✉, Xiao-Yan Qin1✉

1. Center on Translational Neuroscience, College of Life and Environmental Sciences, Minzu University of China, Beijing 100081, China.
2. Department of Cell Biology & Medical Genetics, School of Basic Medical Sciences, Shenzhen University Health Science Center, Shenzhen 518060, China.
3. College of Economics and management, North China Electric Power University, Beijing 102206, China.
* These authors contributed equally as first authors.

Citation:
Zhong SJ, Wang L, Gu RZ, Zhang WH, Lan R, Qin XY. Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis. Int J Med Sci 2020; 17(8):1048-1055. doi:10.7150/ijms.43979. https://www.medsci.org/v17p1048.htm
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Abstract

Ginsenoside Rg1 is the main active ingredient of Panax ginseng with the activity of neuroprotective, antioxidant and strengthening the immune system. Therefore, we hypothesized that Rg1 may afford anti-aging effects although the mechanism remains to be elucidated. In this study, chemically induced aging mice were established by consecutive administration of D-galactose and AlCl3. We found that Rg1 effectively ameliorates spatial learning and memory deficits in aging mice demonstrated by their improved performance in step down avoidance tests and Morris water maze experiments. Rg1 restored aging-induced decline of FGF2 and BDNF, reactivated TrkB/Akt signaling pathways in the hippocampus and prefrontal cortex to inhibit apoptosis, for the expression of anti-apoptotic protein Bcl-2 and apoptosis promoting enzyme cleaved-Caspase3 were antagonistically restored. Therefore, these results established the anti-aging effects of Rg1, and FGF2, BDNF and associated signaling pathways might be promising targets. Our data may provide a new avenue to the pharmacological research and diet therapeutic role of ethnic products such as Rg1 in anti-aging and aging associated diseases.

Keywords: estradiol, ginsenoside Rg1, learning and memory, Morris water maze, step down avoidance test


Citation styles

APA
Zhong, S.J., Wang, L., Gu, R.Z., Zhang, W.H., Lan, R., Qin, X.Y. (2020). Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis. International Journal of Medical Sciences, 17(8), 1048-1055. https://doi.org/10.7150/ijms.43979.

ACS
Zhong, S.J.; Wang, L.; Gu, R.Z.; Zhang, W.H.; Lan, R.; Qin, X.Y. Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis. Int. J. Med. Sci. 2020, 17 (8), 1048-1055. DOI: 10.7150/ijms.43979.

NLM
Zhong SJ, Wang L, Gu RZ, Zhang WH, Lan R, Qin XY. Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis. Int J Med Sci 2020; 17(8):1048-1055. doi:10.7150/ijms.43979. https://www.medsci.org/v17p1048.htm

CSE
Zhong SJ, Wang L, Gu RZ, Zhang WH, Lan R, Qin XY. 2020. Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl3-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis. Int J Med Sci. 17(8):1048-1055.

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