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1.
J Ethnopharmacol ; 155(2): 1243-55, 2014 Sep 11.
Article in English | MEDLINE | ID: mdl-25046825

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Ginseng, the root of Panax ginseng C.A. Meyer, is a traditional medicinal herb that has been widely used in Asia for the treatment of many diseases through its effects of reinforcing vitality, strengthening the bodily resistance to pathogenic factors, engendering body liquids and allaying thirst, relieving uneasiness of the body and mind and benefiting intelligence, reducing body weight and prolonging life. Ginsenosides are the most important biologically active substances in ginseng. Many reports have suggested that ginsenosides could exert prominent neuroprotective and neurotrophic effects, promote neural stem/progenitor cell (NSC) proliferation and promote neurite outgrowth and neuronal network formation. The present study aimed to investigate whether treatment with ginsenosides could facilitate NSC proliferation in the hippocampal formation after traumatic brain injury (TBI) and contribute to the recovery of neurological functions including learning and memory. MATERIALS AND METHODS: The modified Feeney׳s method was used to induce a TBI in rats. Ginseng total saponins (GTS) were treated intraperitoneally twice a day for 1 week after the TBI. The neurological functions, morphology of the hippocampus, expression of nerve growth-related factors and number of NSCs in the hippocampal formation ipsilateral to the trauma were determined. RESULTS: We determined 1) GTS (5-80 mg/kg) treatment after a TBI improved the recovery of neurological functions, including learning and memory, and reduced cell loss in the hippocampal area. The effects of GTS at 20, 40, 60, and 80 mg/kg were better than the effects of GTS at 5 and 10 mg/kg. 2) GTS treatment (20 mg/kg) after a TBI increased the expression of NGF, GDNF and NCAM, inhibited the expression of Nogo-A, Nogo-B, TN-C, and increased the number of BrdU/nestin positive NSCs in the hippocampal formation. CONCLUSIONS: GTS treatment in rats after a TBI alleviated the secondary brain injury and ameliorated the neurological functions with an effective dose limit of 5-80 mg/kg. GTS regulated the expression of nerve growth-related factors and improved the proliferation of neural stem/progenitor cells, which might facilitate neural regeneration and tissue repair, and might contribute to the recovery of neurological functions, including learning and memory. These effects of GTS might provide a foundation for the use of ginseng as a medicinal herb to enhance intelligence, reduce the aging process and prolong life in the traditional medicine.


Subject(s)
Brain Injuries/drug therapy , Hippocampus/drug effects , Nerve Regeneration/drug effects , Neural Stem Cells/drug effects , Neuroprotective Agents/pharmacology , Panax , Plant Extracts/pharmacology , Saponins/pharmacology , Animals , Behavior, Animal/drug effects , Brain Injuries/metabolism , Brain Injuries/pathology , Brain Injuries/physiopathology , Brain Injuries/psychology , Cell Proliferation/drug effects , Disease Models, Animal , Dose-Response Relationship, Drug , Glial Cell Line-Derived Neurotrophic Factor/metabolism , Hippocampus/metabolism , Hippocampus/pathology , Hippocampus/physiopathology , Male , Memory/drug effects , Nerve Growth Factor/metabolism , Neural Cell Adhesion Molecules/metabolism , Neural Stem Cells/metabolism , Neural Stem Cells/pathology , Neuroprotective Agents/isolation & purification , Panax/chemistry , Phytotherapy , Plant Extracts/isolation & purification , Plant Roots , Plants, Medicinal , Rats, Sprague-Dawley , Recovery of Function , Saponins/isolation & purification , Time Factors
2.
Zhongguo Ying Yong Sheng Li Xue Za Zhi ; 28(2): 179-83, 2012 Mar.
Article in Chinese | MEDLINE | ID: mdl-22737925

ABSTRACT

OBJECTIVE: To investigate the neuroprotective effect, effective dose and time window of ginseng total saponins (GTS) treatment in rat after traumatic brain injury (TBI). METHODS: The modified Feeney's method was used to establish TBI model in rat. GTS was treated intraperitoneally. The neurological function and histological morphology of brain tissue were observed. RESULTS: Different doses of GTS were used 6 h after TBI. The neurological and histological results showed that: compared with the TBI group, significant efficacy was observed 2 - 14 days after injury with GTS treatment at 10, 20, 40, 60 and 80 mg/kg (P < 0.05); The effects of GTS at 20, 40, and 60 mg/kg were better than those of GTS at 10 and 80 mg/kg. During the research on the time window of GTS intervention, GTS (20 mg/kg) showed significant effect when used at 3 h and 6 h after TBI; however 12 h, 24 h after TBI, application of GTS did not exert any significant effect. CONCLUSION: GTS intervention after TBI could reduce brain damage and promote recovery of the neurological function. Among doses of GTS 5 - 80 mg/kg, 20 - 60 mg/kg is the best dose limit. The effective time window of GTS is 6 h after TBI.


Subject(s)
Brain Injuries/drug therapy , Phytotherapy , Saponins/administration & dosage , Saponins/therapeutic use , Animals , Male , Neuroprotective Agents , Panax/chemistry , Rats , Rats, Sprague-Dawley , Time Factors , Treatment Outcome
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