CHEN Yan-zhi, LIN Fei, LI Ping-ping. Acute Toxicity and Anti-stress Effect of Ginseng Tonic Decoction in Mice[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(8): 225-229.
CHEN Yan-zhi, LIN Fei, LI Ping-ping. Acute Toxicity and Anti-stress Effect of Ginseng Tonic Decoction in Mice[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(8): 225-229.DOI:
21.0 g ·kg-1)和十一味参芪片组(1 g ·kg-1)可延长小鼠不间断走动疲劳过度从转棒上跌落的时间;人参养荣汤的高剂量组可延长小鼠断头后喘息时间和小鼠常压下的窒息时间;人参养荣汤的高、中剂量组和十一味参芪片组具有延长小鼠45 ℃高温下死亡的时间和小鼠-5 ℃低温下死亡时间
具有统计学意义(P<0.05或P<0.01)。 结论: 人参养荣汤的最大耐受量按生药量计>160 g ·kg-1
相当于人临床每天口服用量的76.2倍。人参养荣汤可以提高小鼠的抗疲劳、耐缺氧和耐高低温能力
具有抗疲劳和抗应激作用。
Abstract
Objective: To oberseve the acute toxicity
anti-fatigue effect and anti-stress effect of Ginseng Tonic Decoction in mice. Method: Mice of KM species were used to test the maximum tolerance dose (MTD)of Ginseng Tonic Decoction. The mouse anti-fatigue test
the mouse acute cerebral ischemia anti-hypoxia test
the mouse anti-hypoxia test and the mouse resistant test to high and low-temperature were used to evaluate anti-stress effect of Ginseng Tonic Decoction at doses of 42.0
21.0 and 10.5 g ·kg-1 ·d-1. Result: the oral MTD of Ginseng Tonic Decoction in mice was>160 g ·kg-1 ·d-1
equal to 76.2 times of human adult’s clinical dose per day. Compared with the control group
mice in Ginseng Tonic Decoction in high dosage group
moderate dosage group and positive control group could prolong the falling time that mice drop from rotating bar because of fatigue;Ginseng Tonic Decoction in high dosage group could prolong the asthmatic time after decapitation and the death time under ambient pressure in mice; Decoction in high dosage group
moderate dosage group and positive control group could prolong the death time under high temperature of 45 ℃ and under low temperature of -5 ℃
there were significant differences(P<0.05 or P<0.01). Conclusion: Tonic Decoction can improve the ability of anti-fatigue
anti-hypoxia and resistance to high and low-temperature. So
the decoction shows anti-stress effects without detectable acute toxicity.