The effects of Ginsenosides on PI3K/AKT signaling pathway

被引:12
作者
Ghafouri-Fard, Soudeh [1 ]
Balaei, Neda [2 ]
Shoorei, Hamed [3 ]
Hasan, Syed Muhammad Farid [4 ]
Hussen, Bashdar Mahmud [5 ]
Talebi, Seyedeh Fahimeh [6 ]
Taheri, Mohammad [7 ]
Ayatollahi, Seyed Abdulmajid [8 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
[2] Tabriz Univ Med Sci, Dept Pharmacol, Tabriz, Iran
[3] Birjand Univ Med Sci, Fac Med, Dept Anat Sci, Birjand, Iran
[4] Univ Karachi, Fac Pharm & Pharmaceut Sci, Dept Pharmaceut, Karachi, Pakistan
[5] Hawler Med Univ, Coll Pharm, Dept Pharmacognosy, Kurdistan Region, Iraq
[6] Birjand Univ Med Sci, Coll Pharm, Dept Pharmacol, Birjand, Iran
[7] Jena Univ Hosp, Inst Human Genet, Jena, Germany
[8] Shahid Beheshti Univ Med Sci, Phytochem Res Ctr, Tehran, Iran
关键词
Ginsenoside; Gene expression; Signaling pathway; CELL-CYCLE ARREST; ANTICANCER ACTIVITY; INDUCED APOPTOSIS; HEPATOCELLULAR-CARCINOMA; 20(S)-GINSENOSIDE RG3; MOLECULAR-MECHANISMS; PANCREATIC-CANCER; OXIDATIVE STRESS; DOWN-REGULATION; MODULATING AKT;
D O I
10.1007/s11033-022-07270-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ginsenosides belong to a group of steroid glycosides that are extracted from the plant genus Panax (ginseng). This plant has been used for a long time for the treatment of a variety of disorders in traditional medicine. Recent studies have assessed the biological impact of Ginsenosides in cell culture or animal models. Animal studies have shown their beneficial impacts in the remedy of pathological conditions in different tissues. The ameliorating effects of Ginsenosides in diverse pathogenic conditions can be attributed to their effects on the production of reactive oxygen species. These substances mainly affect the activity of AMPK/AKT and PI3K/AKT pathways. The beneficial effects of Ginsenosides have been appraised in diabetes-related complications, spinal cord injury, cerebral ischemia, myocardial ischemia, and other disorders which are associated with oxidative stress. Moreover, these substances have been shown to interfere with the pathologic conditions during carcinogenesis. In the current study, we explain these impacts in two distinct sections including non-neoplastic conditions and neoplastic conditions.
引用
收藏
页码:6701 / 6716
页数:16
相关论文
共 70 条
[31]  
LI Y, 2018, BIOMED RES INT, V2018, DOI DOI 10.1155/2018/4306579
[32]   Ginsenoside Rg1 Inhibits Glucagon-Induced Hepatic Gluconeogenesis through Akt-FoxO1 Interaction [J].
Liu, Qun ;
Zhang, Fei-Ge ;
Zhang, Wen-Song ;
Pan, An ;
Yang, Yi-Lin ;
Liu, Jin-Feng ;
Li, Ping ;
Liu, Bao-Lin ;
Qi, Lian-Wen .
THERANOSTICS, 2017, 7 (16) :4001-4012
[33]   Ginsenoside Rd promotes neurogenesis in rat brain after transient focal cerebral ischemia via activation of PI3K/Akt pathway [J].
Liu, Xin-yu ;
Zhou, Xin-yu ;
Hou, Jin-cai ;
Zhu, Hua ;
Wang, Zhong ;
Liu, Jian-xun ;
Zheng, Yong-qiu .
ACTA PHARMACOLOGICA SINICA, 2015, 36 (04) :421-428
[34]   Ginsenoside Rg5 induces apoptosis and autophagy via the inhibition of the PI3K/Akt pathway against breast cancer in a mouse model [J].
Liu, Yannan ;
Fan, Daidi .
FOOD & FUNCTION, 2018, 9 (11) :5513-5527
[35]  
Liu Y, 2019, FOOD FUNCT, V10, P2538, DOI [10.1039/c9fo00095j, 10.1039/C9FO00095J]
[36]   Ginsenoside Rg1 protects human umbilical cord blood-derived stromal cells against tert-Butyl hydroperoxide-induced apoptosis through Akt-FoxO3a-Bim signaling pathway [J].
Liu, Ying ;
Yi, Long ;
Wang, Lu ;
Chen, Linbo ;
Chen, Xiongbin ;
Wang, Yaping .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2016, 421 (1-2) :75-87
[37]   Synergistic anticancer activity of 20(S)-Ginsenoside Rg3 and Sorafenib in hepatocellular carcinoma by modulating PTEN/Akt signaling pathway [J].
Lu, Mingxia ;
Fei, Zhenghua ;
Zhang, Ganlu .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 97 :1282-1288
[38]   Ginseng Compounds: An Update on their Molecular Mechanisms and Medical Applications [J].
Lue, Jian-Ming ;
Yao, Qizhi ;
Chen, Changyi .
CURRENT VASCULAR PHARMACOLOGY, 2009, 7 (03) :293-302
[39]   Inhibition of Autophagy via Activation of PI3K/Akt Pathway Contributes to the Protection of Ginsenoside Rb1 against Neuronal Death Caused by Ischemic Insults [J].
Luo, Tianfei ;
Liu, Guiying ;
Ma, Hongxi ;
Lu, Bin ;
Xu, Haiyang ;
Wang, Yujing ;
Wu, Jiang ;
Ge, Pengfei ;
Liang, Jianmin .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (09) :15426-15442
[40]  
Luo Y., 2020, J AGR FOOD CHEM, V68, P51