• 제목/요약/키워드: Ginsenoside Rc

검색결과 250건 처리시간 0.027초

Influence of Ginsenosides on the Kainic Acid-Induced Seizure Activity in Immature Rats

  • Park, Jin-Kyu;Jin, Sung-Ha;Choi, Keum-Hee;Ko, Ji-Hun;Baek, Nam-In;Choi, Soo-Young;Cho, Sung-Woo;Choi, Kang-Ju;Nam, Ki-Yeul
    • BMB Reports
    • /
    • 제32권4호
    • /
    • pp.339-344
    • /
    • 1999
  • We studied the effects of ginsenosides in immature rats based upon the previous results that ginseng has a suppressive or anticonvulsive activity. To examine the suppressive effect of ginsenosides on kainic acid-induced seizures, the severities and frequencies were observed for 4 h after injection of kainic acid (KA; i.p., 2 mg/kg b.w.) using 10-day-old male Sprague-Dawley rats ($22{\pm}2\;g$). Protopanaxadiol saponins such as ginsenoside-Rb1 (Rb1), ginsenoside-Rb2 (Rb2), ginsenoside-Rc (Rc), and ginsenoside-Rd(Rd) generally reduced the seizure activities while protopanaxatriol saponins such as ginsenoside-Rg1 (Rg1) and ginsenoside-Re (Re) rather increased stereotypic "paddling-like" movements. When vinyl-GABA (v-G) was injected together with Rb1 or Rc, KA-induced seizure severities were additionally reduced only by the injection of Rc, but not by Rb1. The level of gamma isozyme of protein kinase C (PKC-${\gamma}$) in the hippocampus increased about three times as much as that of normal rats at 4 h after KA injection. The increased level of PCK-${\gamma}$ by KA was significantly reduced to about 35% by the coinjection with v-G alone, but it was not changed by v-G together with Rb1 or Rc. The increased level of PKC-${\gamma}$ at 4 h after injection of KA was not consistent with the reduction of seizure severities between Rb1 and Rc. These results suggest that Rc and Rb1 may reduce seizure severity independent of PKC-${\gamma}$ levels, and Rc may additionally act with v-G regarding the GABA metabolism during the stage of KA-induced seizures in the immature rats.

  • PDF

Antioxidative effect of active components of red ginseng

  • Kyu Nam;Kim, Jung-Sun;Baek, Bong-Sook;Kim, Yu-Jung;Chung, Hae-Young
    • 한국응용약물학회:학술대회논문집
    • /
    • 한국응용약물학회 1996년도 춘계학술대회
    • /
    • pp.224-224
    • /
    • 1996
  • 홍삼 총 사포닌 투여군은 대조군과 비교시 total free radical 및 malondialdchydc 농도는 유의상 있게 감소되었으며, 단백질의 carbonyl 농도는 다소 감소하는 경향을 나타내었다. 그리고 홍삼 총 사포닌 투여군의 경우 Cu, Zn-SOD, catalasc, GSII reductase 등의 항산화 효소와 nonprotein-SH가 대조군 보다 증가되었다. 홍삼 총 사포닌의 구성성분들인 ginsenoside Rb$_1$, Rb$_2$, Rc, Rd, Re, Rg$_1$, Rh$_1$, Rh$_2$, Rf 중 ginsenoside Rh$_2$는 catalase 활성을 대조군보다 유의성있게 증가시켰으며, ginsenoside Rh$_1$ 및 Rc의 경우 GSII peroxidase 활성이 증가하는 경향을 나타내었다. 그리고 Cu, Zn-SOD의 경우 ginsenoside Rc는 대조군보다 유의성있게 감소시켰으며, GSII reductase의 경우 유의성있는 변화는 관찰되지 않았다.

  • PDF

고속액체(高速液體) chromatography에 의(依)한 Ginsenoside $-Rb_1,\;-Rb_2,\;-Rc,\;-Rd,\;-Re$$-Rg_1$의 대량분리(大量分離) (Larqe guantity isolation of Ginsenoside $-Rb_1,\;-Rb_2,\;-Rc,\;-Rd,\;-Re\;and\;-Rg_1$ in Panax ginseng C.A. Meyer by High Performance Liquid Chromatography)

  • 최진호;김우정;배효원;오성기;대포언길
    • Applied Biological Chemistry
    • /
    • 제23권4호
    • /
    • pp.199-205
    • /
    • 1980
  • 인삼의 유효약리성분으로 밝혀진 saponin중의 각 ginsenosides를 효과적이고 능률적으로 분리하기 위하여 대량분취전용 고속액체 chromatograph인 preparative HPLC의 응용을 검토하였다. 조(粗) saponin획분을 preparative HPLC인 Prep LC/system-500를 사용하여 부분분획을 하고 각 획분에 함유되어 있는 ginsenosides의 조성을 Analytical HPLC로 동정한 후 Semi-preparative HPLC를 사용하여 인삼주성분 saponin을 단리했다. 그 결과 인삼 주성분 saponin인 $ginsenoside-Rb_1,\;-Rb_2,\;-Rc,\;-Rd,\;-Re$$-Rg_1$은 약 20 mg / 2.0 ml / injection으로 chromatography를 행하여 $300{\sim}400mg/day$로 대량분취가 가능하였다. 따라서 ginsenosides의 약리 및 임상효능 연구에 크게 기여하게 될 것이다.

  • PDF

백삼 및 홍삼의 이화학적 특성 및 말로닐 진세노사이드 함량 비교 (Comparison of Physicochemical Properties and Malonyl Ginsenoside Contents between White and Red Ginseng)

  • 오명환;박영식;이환;김나영;장영부;박지훈;곽준영;박영순;박종대;표미경
    • 생약학회지
    • /
    • 제47권1호
    • /
    • pp.84-91
    • /
    • 2016
  • Korean ginseng (Panax ginseng C. A. Meyer) has been used as a traditional herbal medicine in East Asia and is very popular in the world, because of its health benefits. To comparison of pharmacological components and physiochemical properties between white and red ginseng from same body, we analyzed ginsenoside and malonyl ginsenoside, ash, crude lipid/protein, fatty acid, mineral contents, total/reducing sugar, and total phenolic and acidic polysaccharide contents. The general components did not show any significant difference between white and red ginseng. Whereas, the content of neutral ginsenoside $Rb_1$, $Rb_2$, Rc and Rd were higher in red ginseng than those of white ginseng. However, malonyl ginsenoside such as $m-Rb_1$, $m-Rb_2$, m-Rc and m-Rd in white ginseng were similar to neutral ginsenoside $Rb_1$, $Rb_2$, Rc and Rd in white ginseng and far higher than those of red ginseng. These results exhibit that malonyl ginsenosides were converted to neutral ginsenosides in steaming process for red ginseng. So, we suggest that malonyl ginsenoside are necessary to applies in ginsenoside analysis of Korean ginseng.

Study on biosynthesis of ginsenosides in the leaf of Panax ginseng by seasonal flux analysis

  • Kim, Dongmin;Han, Jaehong
    • Journal of Applied Biological Chemistry
    • /
    • 제62권4호
    • /
    • pp.315-322
    • /
    • 2019
  • Seasonal ginsenoside flux in the leaves of 5-year-old Panax ginseng was analyzed from the field-grown ginseng, for the first time, to study possible biosynthesis and translocation of ginsenosides. The concentrations of nine major ginsenosides, Rg1, Re, Rh1, Rg2, R-Rh1, Rb1, Rc, Rb2, and Rd, were determined by UHPLC during the growth in between April and November. It was confirmed total ginsenoside content in the dried ginseng leaves was much higher than the roots by several folds whereas the composition of ginsenosides was different from the roots. The ginsenoside flux was affected by ginseng growth. It quickly increased to 10.99±0.15 (dry wt%) in April and dropped to 6.41±0.14% in May. Then, it slowly increased to 9.71±0.14% in August and maintained until October. Ginsenoside Re was most abundant in the leaf of P. ginseng, followed by Rd and Rg1. Ginsenosides Rf and Ro were not detected from the leaf. When compared to the previously reported root data, ginsenosides in the leaf appeared to be translocated to the root, especially in the early vegetative stage even though the metabolite translocated cannot be specified. The flux of ginsenoside R-Rh1 was similar to the other (20S)-PPT ginsenosides. When the compositional changes of each ginsenoside in the leaf was analyzed, complementary relationship was observed from ginsenoside Rg1 and Re, as well as from ginsenoside Rd and Rb1+Rc. Accordingly, ginsenoside Re in the leaf was proposed to be synthesized from ginsenoside Rg1. Similarly, ginsenosides Rb1 and Rc were proposed to be synthesized from Rd.

인삼 뿌리 부위별 및 모상근 세포주간 ginsenoside 양상 및 함량 (Patterns and Contents of Ginsenoside in Normal Root Parts and Hairy Root Lines of Panax ginseng C. A. Meyer)

  • 양덕춘;양계진
    • 식물조직배양학회지
    • /
    • 제27권6호
    • /
    • pp.485-489
    • /
    • 2000
  • 생장이 우수한 인삼모상근 세포주 (KGHR-1, KGHR-5, KGHR-8) 및 6년생 인삼근의 부위별로 ginsenoside 양상 및 생성특성을 조사하였다. 인삼모상근 및 6년생 인상근에서 ginsenoslde-Rb$_1$, Rb$_2$, Rc, Rd, Re, Rf, Rg$_1$, Rg$_2$을 확인하였으며, 인삼모상근 세포주간 및 인삼근 부위별로 ginsenoside의 함량은 큰 차이를 나타내었다. 8종류의 ginsenoside함량이 가장 높은 인삼모상근은 KGHR-1 세포주로 17.42 mg/g dry wt와 함량을 나타내었다. 모상근세포주 KGHR-1은 ginsenoside-Rd, Rg$_1$을, KGHR-5는 ginsenoside-Rb$_1$, Rg$_1$을, 그리고 KGHR-8은 ginsenoside-Rd, Re을 상대적으로 많이 생성하는 특징을 지니고 있으며, ginsenoside-Rf의 생성은 매우 낮았다. 6년생 인삼근의 부위별 ginsenoside의 함량은 주근, 지근, 세근순으로 많았으며, 주근에서 ginsenoside-Rc의 생성은 ginsenoside의 50.99%로써 모상근 세포주의 4.90~6.89%보다 매우 높았다. 6년생 인삼근의 총 ginsenoside에 대한 ginsenoside-Rg$_1$의 비율은 3.43~14.18% 수준으로 주근, 지근, 세근순으로 급격히 감소하였으며, 모상관의 17.14~24.43%와 비교할 때 매우 낮은 수준을 나타내었다. 따라서 인삼모상근 배양을 통하여 특정 ginsenosides생산이 가능하리라 생각된다.

  • PDF

Agrobacterium rhisogense에 의해 형질 전환된 인삼의 모상근 배양에서 Ginsenoside의 생산 (Ginsenoside Production by Hairy Root Cultures of Panax ginseng Transformed With Agrobacterium rhizogenes)

  • 고경수;허인옥고정삼이윤진
    • KSBB Journal
    • /
    • 제5권3호
    • /
    • pp.263-268
    • /
    • 1990
  • 인삼의 조직에 Agrobacterium rhizogenes strain 15834와 A4을 감염하여 형질전화체를 얻었다. 이는 인삼에서처럼 무균식물을 얻기어려운 경우 leaf disk 방법으로 모상근을 유도할 수 있었다. 모상근의 ginsenoside(Rg2,Rg1,Rf,Rd,Rc,Rbl, and Rb2)는 HPLC에 의해 定量하였으며, 진탕배양한 모상근의 ginsenoside의 함량은 0.34-1.19% 건량이었다. 이러한 결과는 재배 인삼과 배양 인삼의 ginsenoside의 함량에 비해 좋은 성과라고 사료된다.

  • PDF

Preparation of minor ginsenosides C-Mc, C-Y, F2, and C-K from American ginseng PPD-ginsenoside using special ginsenosidase type-I from Aspergillus niger g.848

  • Liu, Chun-Ying;Zhou, Rui-Xin;Sun, Chang-Kai;Jin, Ying-Hua;Yu, Hong-Shan;Zhang, Tian-Yang;Xu, Long-Quan;Jin, Feng-Xie
    • Journal of Ginseng Research
    • /
    • 제39권3호
    • /
    • pp.221-229
    • /
    • 2015
  • Background: Minor ginsenosides, those having low content in ginseng, have higher pharmacological activities. To obtain minor ginsenosides, the biotransformation of American ginseng protopanaxadiol (PPD)-ginsenoside was studied using special ginsenosidase type-I from Aspergillus niger g.848. Methods: DEAE (diethylaminoethyl)-cellulose and polyacrylamide gel electrophoresis were used in enzyme purification, thin-layer chromatography and high performance liquid chromatography (HPLC) were used in enzyme hydrolysis and kinetics; crude enzyme was used in minor ginsenoside preparation from PPD-ginsenoside; the products were separated with silica-gel-column, and recognized by HPLC and NMR (Nuclear Magnetic Resonance). Results: The enzyme molecular weight was 75 kDa; the enzyme firstly hydrolyzed the C-20 position 20-O-${\beta}$-D-Glc of ginsenoside Rb1, then the C-3 position 3-O-${\beta}$-D-Glc with the pathway $Rb1{\rightarrow}Rd{\rightarrow}F2{\rightarrow}C-K$. However, the enzyme firstly hydrolyzed C-3 position 3-O-${\beta}$-D-Glc of ginsenoside Rb2 and Rc, finally hydrolyzed 20-O-L-Ara with the pathway $Rb2{\rightarrow}C-O{\rightarrow}C-Y{\rightarrow}C-K$, and $Rc{\rightarrow}C-Mc1{\rightarrow}C-Mc{\rightarrow}C-K$. According to enzyme kinetics, $K_m$ and $V_{max}$ of Michaelis-Menten equation, the enzyme reaction velocities on ginsenosides were Rb1 > Rb2 > Rc > Rd. However, the pure enzyme yield was only 3.1%, so crude enzyme was used for minor ginsenoside preparation. When the crude enzyme was reacted in 3% American ginseng PPD-ginsenoside (containing Rb1, Rb2, Rc, and Rd) at $45^{\circ}C$ and pH 5.0 for 18 h, the main products were minor ginsenosides C-Mc, C-Y, F2, and C-K; average molar yields were 43.7% for C-Mc from Rc, 42.4% for C-Y from Rb2, and 69.5% for F2 and C-K from Rb1 and Rd. Conclusion: Four monomer minor ginsenosides were successfully produced (at low-cost) from the PPD-ginsenosides using crude enzyme.

인삼모상근 배양에서 Ginsenoside R $b_2$ 및 Rc 생성과 무기이온 흡수 (Ginsenoside R $b_2$ and Rc Formation and Inorganic Elements Uptake in Ginseng Hairy Roots Cultures)

  • 양덕조;윤길영;최규명;유승희
    • 식물조직배양학회지
    • /
    • 제27권6호
    • /
    • pp.461-468
    • /
    • 2000
  • 인삼 (Panax ginseng C.A. Meyer)의 뿌리로부터 유도 인삼모상근을 이용한 무기이온 흡수과정의 상승 및 길항작용에서 phosphorus (P $O_{4}$$^{-}$)와 nitrogen source (N $H_{4}$$^{+}$, N $O_{3}$$^{-}$)의 증가는 조직 내에 $Mg^{2+}$ 및 F $e^{2+}$ 의 흡수를 증가시키는 원인으로 확인되었다 특히, ammonium의 농도를 4배 높일 경우 F $e^{2+}$의 흡수는 13 mg/L, C $u^{2+}$의 흡수는 0.32mg/L이 증가하여 각각 47.5%와 123.1%로 현저한 이온흡수의 상승효과를 초래하였다. 이러한 결과는 인삼포장에서 인산과 질소원의 과도한 시비는 생장을 다소 증가시키고 뿌리의 철이온과 2가 무기이온 흡수도 증가시킴을 알 수 있다 유리당의 함량은 유리당의 종류에 따라 인산과 질소원의 최적 농도가 다르게 나타났다. 반면에 ginsenoside함량은 인산과 질소원 모두 가장 낮은 농도에서 가장 높았다. 인산의 경우에는 1/2 MS배지의 농도 (0.62 mM)보다 낮은 0.31 mM에서 R $b_2$는 44.7%, Rc는 29.9%가 높았다. Ammonium은 1/2 MS 배지 (10.30 mM)보다 낮은 5.15 mM에서 R $b_2$와 Rc를 각각 21.7%와 31.9% 그리고 nitrate 역시 1/2 MS배지 (9.4mM)보다 낮은 4.70 mM 에서 각각 17.6%와 25.5%의 뚜렷한 함량증가를 나타냈다. 질소원에 따른 ginsenoside 함량 증가에서는 N $H_{4}$$^{+}$가 N $O_{3}$$^{-}$보다 다소 효과적이었다. 따라서 인삼모상근의 ginsenoside생산을 높이기 위해서는 인산과 질소원의 농도를 조절한 새로운 배지가 적합한 것으로 확인되었다.

  • PDF

Ginsenoside Rc from Panax ginseng exerts anti-inflammatory activity by targeting TANK-binding kinase 1/interferon regulatory factor-3 and p38/ATF-2

  • Yu, Tao;Yang, Yanyan;Kwak, Yi-Seong;Song, Gwan Gyu;Kim, Mi-Yeon;Rhee, Man Hee;Cho, Jae Youl
    • Journal of Ginseng Research
    • /
    • 제41권2호
    • /
    • pp.127-133
    • /
    • 2017
  • Background: Ginsenoside Rc (G-Rc) is one of the major protopanaxadiol-type saponins isolated from Panax ginseng, a well-known medicinal herb with many beneficial properties including anticancer, anti-inflammatory, antiobesity, and antidiabetic effects. In this study, we investigated the effects of G-Rc on inflammatory responses in vitro and examined the mechanisms of these effects. Methods: The in vitro inflammation system used lipopolysaccharide-treated macrophages, tumor necrosis $factor-{\alpha}/interferon-{\gamma}-treated$ synovial cells, and HEK293 cells transfected with various inducers of inflammation. Results: G-Rc significantly inhibited the expression of macrophage-derived cytokines, such as tumor necrosis $factor-{\alpha}$ and $interleukin-1{\beta}$. G-Rc also markedly suppressed the activation of TANK-binding kinase $1/I{\kappa}B$ kinase ${\varepsilon}/interferon$ regulatory factor-3 and p38/ATF-2 signaling in activated RAW264.7 macrophages, human synovial cells, and HEK293 cells. Conclusion: G-Rc exerts its anti-inflammatory actions by suppressing TANK-binding kinase $1/I{\kappa}B$ kinase ${\varepsilon}/interferon$ regulatory factor-3 and p38/ATF-2 signaling.