• Journal of Ginseng Research
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• 제12권2호
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• pp.135-144
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• 1988

갑상선호르몬 분비조절물질(TSH, DB cAMP, NaF, carbachol, isoproterenol, propranolol)과 인삼성분(total saponin, diol saponin, triol saponin)의 복합처리가 갑상선의 cAMP의 양에 미치는 영향을 알아보기 위하여, 흰쥐의 갑상선을 4일 또는 7일간 배양한 후 갑상선호르몬 분비조절물질과 인삼성분을 각각 복합처리, 또는 단독처리하여 cAMP의 양을 조사하였다. 인삼성분만을 처리한 경우, total saponin은 $10^{-5}$%(w/v), diol saponin과 triol saponin은 $10^{-4}$%(w/v)의 농도에서 각각 가장 높은 증가를 나타내었다. 갑상선호르몬 분비조절물질과 복합처리한 인삼성분의 농도는 위의 값으로 하였다. 복합처리한 경우, TSH에 대해서는 증가효과를 나타냈지만 그 양상은 작았다. Total saponin은 DBcAMP와 isoproterennol에 대해서는 증가효과를, carbachol과 propranolol에 대해서는 감소효과를 나타내었고, NaF에 대해서는 영향이 크지 않았다. Diol saponin과 triol saponin은 그 양은 다르지만 isoproterenol을 복합처리한 경우를 제외하고 diol saponin은 감소효과를, triol saponin은 증가효과를 보이는 상반작용을 나타내었다. 억제효과를 가지는 propranolol에 대해서도 diol saponin과 triol saponin은 상반되는 효과를 나타내었다. 인삼성분의 정상화작용은 NaF와 carbachol의 경우에도 두드러지게 나타났다. 이상의 결과들은 인삼성분이 갑상선호르몬의 생성과 분비에 관여하는 cAMP의 생성에 촉진 또는 억제를 가진다는 것을 나타내고 있다.

• 한국미생물·생명공학회지
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• 제13권1호
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• pp.7-11
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• 1985

인삼(人蔘) saponin의 생물학적(生物學的) 활성(活性)을 조사(調査)하기 위하여 세균(細菌) v{\alpha}$-amylase의 작용(作用)에 미치는 인삼(人蔘) saponin의 영향(影響)을 조사(調査)한 결과(結果)를 요약(要約)하면 다음과 같다. Protopanaxadiol계(系), triol계(系) 및 total saponin 모두 ${\alpha}$-amylase의 활성(活性)을 25, 12, 13%정도(程度) 촉진(促進)시켰다. Diol계(系) saponin첨가(添加)경우 $40^{\circ}C$에서 3분간(分間) 전처리(前處理)함으로서 ${\alpha}$-amylase의 활성(活性)을 20%정도(程度) 촉진(促進)시켰으며 酵素(효소)의 열변성(熱變性)에 대(對)한 보호작용(保護作用)은 protopanaxariol계(系) saponin은 $60^{\circ}C$에서 5분(分)까지는 보호작용(保護作用)이 있었으나 protopanaxadiol계(系) saponin은 오히려 열실활(熱失活)을 촉진(促進)하는 경향이었다. Diol 및 triol계(系) saponin의 산가수분해물(酸加水分解物)이 ${\alpha}$-amylase의 활성(活性)을 diol 및 triol계(系) saponin보다 더 촉진(促進)시켰으며 diol, triol계(系) saponin의 첨가(添加)는 고농도(高濃度)의 기질(基質)이 존재(存在)할 때 기질저해(基質沮害)를 막아주었다.

• Journal of Ginseng Research
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• 제9권1호
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• pp.86-94
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• 1985

Attempts were made if diol and triol fractions of ginseng saponin affect on glutamine transport into rat renal cortical mitochondria, swelling, phosphate dependent glutaminase activity, and consumption of oxygen. The following results were obtained. When mitochondrial preparation from rat renal cortex was incubated in medium containing 14C-glutamine and either triol or diol fractions, radioactivity was shown to increase at both 10-6% and 10-5% triol fractions of ginseng saponin, but reduce in case of diol fraction. The remarkable acceleration of the rate of swelling of renal cortical mitochondria was observed in the presence of 10-1% trios and diol fractions but no accerelation at lower concentrations. The activity of phosphate dependent glutaminase from renal cortical mitochondria was slightly activated at 10-2% of triol fraction. However, there was no effect in case of diol fraction. Oxygen consumption by mitochondria from renal cortex was remarkably increased at concentrations of 10-5% and 10-6% triol fractions, but reduced in the case of diol fractions. On the basis of these observations it was concluded that triol fraction of ginseng saponin might increase the transport of glutamine into mitochondria by accelerating the respiratory chain and supplying additional energy to mitochondria, and physiological role of triol fraction was entirely different from that of diol fraction of ginseng saponin.

• Journal of Ginseng Research
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• 제14권3호
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• pp.364-372
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• 1990

This experiment was performed to investigate the effects of ginseng saponin fractions (total saponin, triol saponin. diol saponin) and lipopolysacrharide (LPS) on the tllmoricidal activity of macrophage. The ginseng saponin fractions had little effect on the tumoricidal activity of macrophage (less than 10%). When the ginseng saponin fractions were treated with LPS, the effects of tumoricidal activation of macrophage increased a relatively high percent, and the total saponin and triol saponin (20-35%) were ulore effectual than diol saponin (15-25%). The effects of ginseng saponin and LPS on the tumoricidal activity of macrophage were mediated by the induction of macrophage-release factor(5) which has(have) the capacity of tumor cell killing. And the quantity of the (actors) was(were) increased by the contact of macrophage with tumor cell.

• 자연과학논문집
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• 제8권2호
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• pp.27-34
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• 1996

쥐의 복강과 폐포 대식세포를 분리하고 배양하여 효모에 대한 식세포활동 및 화학주성을 관찰하였다. 식세포활동이 일어나는 양상을 wright-Giemsa로 염색하여 사진으로 확인하였다. 복강 대식세포의 경우 diol saponin 처리군에 의해 약 48%까지 식세포활동이 증가되었고 total saponin 처리군에 의해 약 35%까지 식세포활동이 감소되었다. 폐포 대식세포의 경우 모든 인삼분획물 처리군에 의해 최고 50%까지 섭식이 증가되었다. 화학주성은 복강 대식세포의 경우 인삼분획물 처리군 모두 약 17%까지, 폐포 대식세포에서는 diol saponin만 약 16%까지 이동되었다. actin의 증감을 SDS-PAGE로 확인해 보았으나 변화가 없었다.

• Journal of Ginseng Research
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• 제9권1호
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• pp.112-118
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• 1985

It has been known that the ginseng extracts activate the lipid metabolism in animal body. The experiments were undertaken to elucidate the effects of total, diol, and trial saponin of ginseng on the activities of acyl Co-A synthetase and hydroxyacyl Co-A dehydrogenase involved in fatty acid metabolism in normal albino rat liver. The acyl Co-A synthetase activity, in vitro, was increased by 20% with treatment of 2.5${\times}$10-3% total saponin, by 14% with 2.5${\times}$10-3% diol saponin, arid 30% with 2.5${\times}$10-4% triol saponin, respectively. And the enzyme activity was increased by 27% at 2 hours after intraperitoneal injection of total saponin. Hydroxyacyl Co-A dehydrogenase activity, in vitro, was increased by 77% with 10-4% total saponin, by 64% with 10-2% diol saponin, and by 72% with 10-3% triol saponin, respectively. Also, the enzyme activity, in vivo, was increased by 15.3% and 33% at 2 hours and 4 hours.

• Journal of Ginseng Research
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• 제12권1호
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• pp.63-67
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• 1988

인삼사포닌 분획물들(total saponin, diol saponin and triol saponin)이 생쥐의 항체생성에 미치는 영향과 면역억제의 회복에 미치는 영향 그리고 혈청총단백질의 생성에 미치는 영향에 대하여 알아본 결과 아래와 같은 결론을 얻었다. 1. Total saponin은 10mg/kg/day, diol saponin은 10mg/kg/day, triol saponin은 5mg/kg/day로 생쥐에 투여하였을 때 순환성 항체가 가장 많이 생성되는 것으로 나타났다. 2. CY로 면역을 억제시킨 상태에서는 인삼사포닌을 투여하여도 순환성 항체의 생성이 대조군과 차이가 없는 것으로 나타났다. 3. 인삼사포닌은 항체생성과 혈청총단백질의 증가에 서로 다른 농도로 작용을 나타낸다.

• 약학회지
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• 제29권2호
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• pp.76-89
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• 1985

The effects of ginseng saponin on the activity, phosphorylation, [$^{3}$H] ouabain binding and light scattering (disruption) of purified $Na^{+}$ ,$K^{+}$ -ATPase isolated from the outer medulla of sheep kidney were compared to those of gypsophila saponin, sodium dodecylsulfate (SDS), and Triton X-100 on the same parameters. $Na^{+}$ , $K^{+}$ -ATPase activity, phosphorylation, and [$^{3}H$] ouabain binding were inhibited by ginseng saponin (triol>total>diol), SDS, or Triton X-100, but increased by gypsophila saponin. Low doses of ginseng saponin (3.mu.g saponin/.mu.g protein) decreased phosphorylation sites and ouabain binding site concentration (Bmax) without any change of turnover number and affinity for ouabain binding which were decreased by high dose of ginseng saponin (over 10.mu.g saponin/.mu.g protein), SDS or Triton X-100. On the other hand, gypsophila saponin increased the affinity without any change of Bmax for ouabain binding. Inhibition of $Na^{+}$ ,$K^{+}$ -ATPase activity by ginseng saponin and SDS or Triton X-100 appeared before and after decrease in light scattering, respectively. These data suggest that ginseng saponins (total, diol, triol saponin) inhibit $Na^{+}$ , $K^{+}$ -ATPase activity by specific direct and general detergent action at low and high concentrations, respectively, and this inhibitory action of ginseng sapornin to $Na^{+}$ , $K^{+}$ -ATPase is not general action of all saponins.

• Journal of Ginseng Research
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• 제8권2호
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• pp.153-166
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• 1984

The anticancer activities of petroleum ether extract of Panax ginseng root(crude GX) and its partially purified fraction from silicic acid column chromatography (7:3 GX) were studied with Sarcoma 180(S-180) or Walker carcinosarcoma 256 (Walker 256) in vivo and with L1210 leukemic lympocyte in vitro. Potential cytotoxic activities of the crude GX and against L1210 cells were compared with those of 5-Fluorouracil (5-FU) and saponin derivatives (Panax-diol, Panax-triol, Diol saponin, Triol saponin) in vitro. In order to observe the physiological effects of the crude GX and 7:3 GX on the animals with cancer, hemoglobin(Hb), red blood cell(R.B.C) and white blood cell after treatment with each GX in comparison with corresponding control groups, respectively. The anticancer effects of the crude GX and 7:3 GX were estimated by measuring the survival time of S-180 bearing mice after treatment with them. The experimental results obtained are summarized as follows; 1. The one unit of cytotoxic activity against L1210 cells was equivalent to 2.54$\mu\textrm{g}$ and 0.88$\mu\textrm{g}$of the crude GX and 7:3 GX per ml of culture medium, respectively. 2. The cytotoxic activities of Panax-diol, Panax=triol, Diol saponin and triol saponin against L1210 cells were not detected. 3. The anticancer activities of 5-FU against L1210, S-180 and Walker 256 were very effective in vivo and vitro tests. 4. The significantly increased W.B.C values of mice after inoculation with S-180 cells were reduced to normal range by the crude GX treatment. 5. The significantly decreased Hb values of rats after inoculation with Walker 256 were recovered to normal range by oral administration of the crude GX. 6. The survival times of mice inoculated with S-180 cells were extended about 1.5 to 2 times by the 7:3 GX treatment compared with their control group.

• 한국식품과학회지
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• 제21권3호
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• pp.345-350
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• 1989

부패한 인삼(人蔘) 및 인삼제품(人蔘製品)에서 분리된 3종의 미생물(微生物)을 인삼 crude saponin농도를 달리한 czapek 배지 등에 배양하여 그 배양 미생물에 의한 ginsenoside의 pattern과 함량변화를 조사하였다. Aspergillus sp.는 0.3%에서 최대의 균체량을 9일에서 나타냈으며 Penicillium sp. -A와 B도 같은 경향이었고, 1.0%에서는 대조군보다 균체 증가량이 낮았다. 인삼 saponin pattern의 변화는 Aspergillus sp.를 6일 배양하였을 때 0.3% 첨가한 경우 diol계 saponin이 완전히 분해되었고 1% 첨가 배양에서는 상대적인 함량의 차이가 있었다. Penicillium sp. -A는 saponin pattern 변화에 영향을 주지 않았으며, Penicillium sp. -B는 배양 12일에서 diol계 saponin이 상소하였다. 또한 수삼배지(水蔘培地)및 건삼배지(乾蔘培地)에서 부패미생물은 인삼(人蔘) crude saponin 함량(含量)을 감소시키었다.