• 생약학회지
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• 제37권4호
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• pp.217-220
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• 2006

This study compared the contents of ginsenoside according to the extract conditions of red ginseng to provide basic information for developing functional food using red ginseng. According to the result, the content of crude saponin was highest in 72 hours of extraction at $82^{\circ}C$ (RG-823). The content of prosapogenin (ginsenoside $Rh_1,\;Rh_2,\;Rg_2,\;Rg_3$) was highest in 48 hours of extraction, and followed by 72 and 24 hours at $82^{\circ}C$. And at $93^{\circ}C$ the prosapogenin contents were highest in the order of 48 hours, and next in 24 and 72 hours. In addition, ginsenoside $Rb_1,\;Rb_2$ Rc and Re were not detected in 72 hours of extraction at $93^{\circ}C$ (RG-933) presumedly due to hydrolysis, but ginsenoside Rd, Rf and $Rg_1$ were detected as long as 72 hours of extraction. These results show that protopanaxatriol group is relatively more resistant to heat than protopanaxadiol group.

• Journal of Ginseng Research
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• 제41권4호
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• pp.435-443
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• 2017

Panax ginseng is one of the most universally used herbal medicines in Asian and Western countries. Most of the biological activities of ginseng are derived from its main constituents, ginsenosides. Interestingly, a number of studies have reported that ginsenosides and their metabolites/derivatives-including ginsenoside (G)-Rb1, compound K, G-Rb2, G-Rd, G-Re, G-Rg1, G-Rg3, G-Rg5, G-Rh1, G-Rh2, and G-Rp1-exert anti-inflammatory activities in inflammatory responses by suppressing the production of proinflammatory cytokines and regulating the activities of inflammatory signaling pathways, such as nuclear factor-${\kappa}B$ and activator protein-1. This review discusses recent studies regarding molecular mechanisms by which ginsenosides play critical roles in inflammatory responses and diseases, and provides evidence showing their potential to prevent and treat inflammatory diseases.

• Journal of Ginseng Research
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• 제30권2호
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• pp.70-77
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• 2006

Ginseng has an anti-cancer effect in several cancer models. As a mechanism study of ginsenoside-induced growth inhibition in cancer cells, we measured change of membrane potential in prostate cancer and glioma cells by ginsenosides, active constituents of ginseng. Membrane potential was estimated by measuring fluorescence change of DiBAC-Ioaded cells. Among 11 ginsenosides tested, ginsenosides $Rb_2$, $Rg_3$, and $Rh_2$ increased significantly and robustly the membrane potential in a concentration-dependent manner in prostate cancer and glioma cells. Ginsenosides Rc, Ro, and $Rb_1$ slightly increased membrane potential. The ginsenoside-induced membrane potential increase was not affected by treatment with pertussis toxin or U73122. The ginsenoside-induced membrane potential increase was not diminished in $Na^+$-free or $HCO_3^-$-free media. Furthermore, the ginsenoside-induced increase of membrane potential was not changed by EIPA (5-(N-ethyl-N-isopropyl)-amiloride), SITS (4-acetoamido-4'-isothiocyanostilbene-2,2'-disulfonic acid), and omeprazole. In summary, ginsenosides $Rb_2$, $Rg_3$, and $Rh_2$ increased membrane potential in prostate cancer and glioma cells in a GPCR-independent and $Na^+$ independent manner.

• 한국식품과학회지
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• 제38권4호
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• pp.521-525
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• 2006

인삼을 처리온도 및 처리시간을 변수로 하여 열처리한 다음 80% 메탄올로 추출하여 성분 및 생리활성 변화를 분석하였다. 총 폴리페놀 함량은 고온고압처리에 따라 증가하다가 $140^{\circ}C$, 4시간 이후에 감소하였으며, $150^{\circ}C$, 1시간 처리구에서 29.46mg/g으로 가장 높은 함량을 나타내었다. 총 플라보노이드 함량은 고온고압처리에 따라 증가하다가 $150^{\circ}C$에서는 2시간 처리구에서 4.75mg/g으로 가장 높은 함량을 나타내었다. $IC_{50}$은 처리온도와 시간이 증가할수록 감소하여 항산화활성이 무처리구(17.68mg/g)보다 증가한 것을 알 수 있었으며, 가장 활성이 높은 처리구는 $140^{\circ}C$, 3시간 처리구로 0.22mg/g으로 나타났다. 4년근 인삼의 조사포닌 함량은 1.18%이었으며, 고온고압처리에 따라 ginsenoside는 대부분 처리온도가 높아질수록, 처리시간이 길어질수록 감소하는 경향을 보였다. $Rg_1$, Re, $Rb_2,\;Rb_3$은 비교적 낮은 온도에서는 안정하였으나 $130^{\circ}C$ 이상의 온도에서는 불안정하여 감소하였다. Rf는 열처리에 비교적 안정하였으며, $Rg_3,\;Rh_2$는 고온고압처리에 의해 새로이 생성되거나 함량이 증가하여 최대 생성 조건은 $130^{\circ}C$에서는 4-5시간, $140^{\circ}C$에서는 2-4시간, $150^{\circ}C$에서는 2시간으로 나타났다.

• Journal of Ginseng Research
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• 제34권1호
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• pp.1-7
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• 2010

본 논문은 백삼 추출물의 코팅 처리에 의한 인삼 커피의 품질 특성에 대한 것으로 주요 내용은 다음과 같다. 백삼 추출물 (WGC-2)의 농도에 따라 커피의 품질 속성을 실험하였다. 대조군과 $5^{\circ}$ Brix (WGC-1)와 $20^{\circ}$ Brix의 사포닌 농도는 8.29%, 8.74%와 8.93% 였고, WGC-1과 WGC-2의 총 진세노사이드 농도는 0.3 mg/g과 0.6 mg/g 였다. 특히 주요 진세노사이드 $Rg_1,\;Rg_2,\;Rb_1,\;Rb_2,\;Rg_2,\;Rh_1$와 $Rg_3$ 함량은 백삼 추출물의 농도에 따라 증가하였다. 커피 맛은 WGC-2가 상업적 커피콩보다 유의하게 낮았고, 소비자 관능 평가에서는 별 차이가 없다는 내용이다.

• 한국약용작물학회지
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• 제19권4호
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• pp.271-275
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• 2011

In this study, ginseng flower water extracts were analyzed to set up the ginsenoside content and quality optimization condition. The highest total ginsenoside content among the ginseng flower water extracts was 67.44mg/g which was extracted at $85^{\circ}C$ for 3 hours. In addition, the ginsenoside content decreased according to the increased extraction temperature and time. The highest total content of $Rb_2$ and Re was 37.42mg/g at $75^{\circ}C$ for 6 hours. Total content of $Rb_2$ and Re decreased according to the increased extraction temperature and time. The highest prosapogenin ($Rg_2$ + $Rg_3$ + $Rh_1$) content among the total of ginseng flower water extracts was 18.58mg/g which was extracted at $95^{\circ}C$ for 12 hours. The sweetness, absorbance were increased according to the increased extraction temperature and time. But pH was decreased according to the increased extraction time.

• 한국약용작물학회지
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• 제21권5호
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• pp.401-414
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• 2013

Ginsenoside Rg3 (G-Rg3) contained only in red ginseng has been found to show various pharmacological effects such as an anticancer, antiangiogenetic, antimetastastic, liver protective, neuroprotective immunomodulating, vasorelaxative, antidiabetic, insulin secretion promoting and antioxidant activities. It is well known that G-Rg3 could be divided into 20(R)-Rg3 and 20(S)-Rg3 according to the hydroxyl group attached to C-20 of aglycone, whose structural characteristics show different pharmacological activities. It has been reported that G-Rg3 is metabolized to G-Rh2 and protopanaxadiol by the conditions of the gastric acid or intestinal bacteria, thereby these metabolites could be absorbed, suggesting its absolute bioavailability (2.63%) to be very low. Therefore, we reviewed the chemical, physical and biological transformation methods for the production on a large scale of G-Rg3 with various pharmacological effects. We also examined the influence of acid and heat treatment-induced potentials on for the preparation method of higher G-Rg3 content in ginseng and ginseng products. Futhermore, the microbial and enzymatic bio-conversion technologies could be more efficient in terms of high selectivity, efficiency and productivity. The present review discusses the available technologies for G-Rg3 production on a large scale using chemical and biological transformation.

• 한국식품영양과학회지
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• 제45권12호
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• pp.1740-1746
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• 2016

본 연구는 산양삼의 이용가치를 높이고, 기능성 식품소재 개발을 위하여 산양삼의 이화학적 특성과 추출용매를 달리하여 추출한 각각의 추출물의 항산화 활성을 비교하였다. 산양삼의 일반성분은 수분 7.56%, 탄수화물 73.01%, 단백질 12.58%, 지질 1.99%, 회분 5.54%를 나타내었고, 총아미노산 함량은 16.17 mg/100 g이었으며, 그중 필수아미노산은 1.42 mg/100 g을 나타내었다. 총 ginsenoside 함량은 15.98 mg/g을 나타내었고, 그중 major ginsenoside($Rb_1$, $Rb_2$, $Rb_3$, Rc, Rd, Re, Rf, $Rg_1$)의 함량은 15.94 mg/g, minor ginsenoside($Rg_3$, $Rh_1$, $Rh_2$) 함량은 0.04 mg/g을 나타내었다. 1 mg/mL 농도로 조정한 증류수를 이용한 산양삼 추출물(KGW), 70% 에탄올을 이용한 산양삼 추출물(KGE)의 항산화 활성을 측정한 결과 KGE가 모든 항목에서 가장 높게 활성을 나타냈으며, 각각 8.93 mg/g(총폴리페놀 함량), 3.96 mg/g(총플라보노이드 함량), 57.57%(DPPH 라디칼 소거능), 70.73%(ABTS 라디칼 소거능), 44.12%(아질산염 소거능), 78.05%(SOD 유사활성), $1.08O.D_{700nm}$(환원력), 55.33%(ferrous ion chelating activity)를 나타내었다. 또한, 각각의 산양삼 추출물의 elastase, collagenase 및 tyrosinase 저해활성을 측정한 결과 역시 KGE가 모든 항목에서 가장 높은 활성을 나타내었으며, 각각 81.96%, 78.96%, 30.96%를 나타내었다.

• 고려인삼학회:학술대회논문집
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• 고려인삼학회 2002년도 학술대회지
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• pp.376-384
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• 2002

Object To find out which of the 27 ginsenosides isolated from Panax ginseng C.A. Mey that may inhibit the proliferation of human osteosaocoma cell line $U_2OS$. Methods Effects of each individual ginsenoside on the proliferation of $U_2OS$ cell were studied by determining the viability of cancer cells during culture with or without the presence of the test compound. DNA assay was determined by flow cytometry. Results Ginsonosides -Ro, $-Rh_l,\;-Rh_2,\;-F_1\;and\;-L_8$ at concentrations of 5 ,umol/L could obviously suppress the proliferation of $U_2OS$ cells while ginsenosides $-Rg_1,\;-F_3,$ -Rf, PPT and PT significantly inhibited the cancer cells. Flow cytometry revealed that ginsenosides $-Ro,-Rg_1-Rf,-F_1-Rh_2,PPT$ and PT induced cell cycle arrest at $G_0/G_1$ phase with obvious decrease of cell count at Sand $G_2+M$ phase, Moreover, ginsenosides $-Rf_1,-Rg_1,\;-F_1$ and PPT induced significantly high rates of cell death as compared with the control. Conclusion These data suggested that ginsenosides inhibited $U_2OS$ proliferation Via cell cycle arrest or induction of cell death.

• Molecules and Cells
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• 제21권1호
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• pp.52-62
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• 2006

In previous reports we demonstrated that ginsenosides, active ingredients of Panax ginseng, affect some subsets of voltage-dependent $Ca^{2+}$ channels in neuronal cells expressed in Xenopus laevis oocytes. However, the major component(s) of ginseng that affect cloned $Ca^{2+}$ channel subtypes such as ${\alpha}_{1C}$(L)-, ${\alpha}_{1B}$(N)-, ${\alpha}_{1A}$(P/Q)-, ${\alpha}_{1E}$(R)- and ${\alpha}_{1G}$(T) have not been identified. Here, we used the two-microelectrode voltage clamp technique to characterize the effects of ginsenosides and ginsenoside metabolites on $Ba^{2+}$ currents ($I_{Ba}$) in Xenopus oocytes expressing five different $Ca^{2+}$ channel subtypes. Exposure to ginseng total saponins (GTS) induced voltage-dependent, dose-dependent and reversible inhibition of the five channel subtypes, with particularly strong inhibition of the ${\alpha}_{1G}$-type. Of the various ginsenosides, $Rb_1$, Rc, Re, Rf, $Rg_1$, $Rg_3$, and $Rh_2$, ginsenoside $Rg_3$ also inhibited all five channel subtypes and ginsenoside $Rh_2$ had most effect on the ${\alpha}_{1C}$- and ${\alpha}_{1E}$-type $Ca^{2+}$ channels. Compound K (CK), a protopanaxadiol ginsenoside metabolite, strongly inhibited only the ${\alpha}_{1G}$-type of $Ca^{2+}$ channel, whereas M4, a protopanaxatriol ginsenoside metabolite, had almost no effect on any of the channels. $Rg_3$, $Rh_2$, and CK shifted the steady-state activation curves but not the inactivation curves in the depolarizing direction in the ${\alpha}_{1B}$- and ${\alpha}_{1A}$-types. These results reveal that $Rg_3$, $Rh_2$ and CK are the major inhibitors of $Ca^{2+}$ channels in Panax ginseng, and that they show some $Ca^{2+}$ channel selectivity.