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人参(Panax ginseng C. A. Meyer)皂苷的化学药理学研究。II. 药理学部分。

Chemico-pharmacological studies on saponins of Panax ginseng C. A. Meyer. II. Pharmacological part.

作者信息

Kaku T, Miyata T, Uruno T, Sako I, Kinoshita A

出版信息

Arzneimittelforschung. 1975 Apr;25(4):539-47.

PMID:239732
Abstract

The pharmacological properties of seven pure saponins isolated from Panax ginseng C. A. Meyer were studied. 1. The ginseng saponins showed weak toxicities in mice. Especially, Rg1, Rf and Rb 1, which contained glucose as a sugar component, were weaker in their toxicities than the rest, which contained arabinose and/or rhamnose. It was also noted that the saponins containing protopanaxadiol as sapogenin were more toxic than those containing protopanaxatriol. 2. All the saponins diminished ACh-induced contraction of the isolated ileum of the guinea pig. On the other hand high concentrations of Rb 2 caused contraction of the ileum by itself. 3. All of the saponins induced a decrease in heart rate and showed biphasic actions on the blood pressure in rats, while they little affected respiration. They caused blood pressure fall preceded by slight rise. Among them, Rg 1 showed the most prominent action and it produced a blood pressure rise with doses of 30 to 100 mg/kg. The pressor as well as depressor action was not influenced by the pretreatment with any of atropine, diphenhydramine, phentolamine and propranolol. 4. Rg 1 and Re showed vasodilator action in dogs, the potencies of which were 1/20 and 1/50 of that of papaverine, respectively. Rc and Rb 2 showed very weak vasodilator actions but Rb 1 did not. 5. Among the 7 saponins, Rd, Re and Rb 2 showed more potent hemolytic actions than those of the rest and the potencies were proportional to their toxicities. 6. Whereas single administration of Rf, Re and Rd significantly suppressed the conditioned avoidance response, repeated administration of them caused facilitation of the response. On the other hand, Rb 2 always showed very weak suppressant action. 7. Rg 1, Rf, Re and Rd significantly suppressed the fighting of mice induced by foot shock, while Rb 1, Rb 2 and Re little affected the fighting. 8. All the saponins showed antifatigue action. They markedly increased the movement after compulsory gait and the action was consistent and independent of their action on the movement before compulsory gait. 9. The saponins showed moderate depressant actions on the EEG and the behavior in cats. They were qualitatively similar in their actions, although Rg 1, Re and Rb 2 were more potent than the rest. They also suppressed EEG arousal response induced by electrical stimulation of the mid brain in cats.

摘要

对从人参(Panax ginseng C. A. Meyer)中分离出的七种纯皂苷的药理特性进行了研究。1. 人参皂苷对小鼠显示出微弱毒性。特别是,含有葡萄糖作为糖成分的Rg1、Rf和Rb1,其毒性比含有阿拉伯糖和/或鼠李糖的其余皂苷更弱。还注意到,以原人参二醇为皂苷元的皂苷比以原人参三醇为皂苷元的皂苷毒性更大。2. 所有皂苷均能减弱乙酰胆碱诱导的豚鼠离体回肠收缩。另一方面,高浓度的Rb2自身可引起回肠收缩。3. 所有皂苷均导致大鼠心率降低,并对大鼠血压表现出双相作用,而对呼吸影响很小。它们先引起血压轻微升高,随后导致血压下降。其中,Rg1表现出最显著的作用,在剂量为30至100mg/kg时可使血压升高。升压和降压作用均不受阿托品、苯海拉明、酚妥拉明和普萘洛尔任何一种预处理的影响。4. Rg1和Re在犬中显示出血管舒张作用,其效力分别为罂粟碱的1/20和1/50。Rc和Rb2显示出非常微弱的血管舒张作用,但Rb1没有。5. 在这7种皂苷中,Rd、Re和Rb2的溶血作用比其余皂苷更强,且效力与它们的毒性成正比。6. 单次给予Rf、Re和Rd可显著抑制条件回避反应,而重复给予则导致反应增强。另一方面,Rb2始终表现出非常微弱的抑制作用。7. Rg1、Rf、Re和Rd可显著抑制足部电击诱导的小鼠打斗,而Rb1、Rb2和Rc对打斗影响很小。8. 所有皂苷均显示出抗疲劳作用。它们显著增加强迫步态后的活动,且该作用是持续的,与它们对强迫步态前活动的作用无关。9. 皂苷对猫的脑电图和行为表现出适度的抑制作用。它们的作用在性质上相似,尽管Rg1、Re和Rb2比其余皂苷作用更强。它们还抑制了猫中脑电刺激诱导的脑电图觉醒反应。

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