• Natural Product Sciences
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• 제16권1호
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• pp.39-42
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• 2010

The content of hyperin in Acanthopanax species was determined by high performance liquid chromatography (HPLC). Hyperin was quantified by a reverse-phase column with elution program [initially gradient solvent (acetonitrile : water = 85 : 15 to 80 : 20 for 20 min), then isocratic solvent (acetonitrile : water = 80 : 20 for 20 min), and finally gradient solvent (acetonitrile : water = 80 : 20 to 65 : 35 for 20 min)]. UV detection was conducted at 210 nm. The content of hyperin in the fruits of Acanthopanax was measured in the species A. chiisanensis (2.04 mg/g), A. sessiliflorus (1.13 mg/g), A. divaricatus (0.98 mg/g), A. koreanum (0.75 mg/g) and A. senticosus (0.05 mg/g). The content of hyperin in A. chiisanensis was higher than that of other Acanthopanax species.

• Current Research on Agriculture and Life Sciences
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• 제1권
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• pp.101-111
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• 1983

연습림(演習林)에 분포(分布)된 식물(植物)은 79과(科) 188속(屬) 248종(種) 16변종(變種), 1아종(亞種), 3품종(品種)으로서 총계(總計) 298종류(種類)였다. 목본식물(木本植物)은 39과(科), 67속(屬)112종(種), 7변종(變種) 3품종(品種)이었으며 이중에서 교목(喬木)이 50종류(種類) 관목(灌木)이 46종류(種類), 만목(蔓木)이 16종류(種類)였다. 참취, 더덕, 지치등의 식용식물(食用植物)이 118종류(種類) 오미자, 오갈피나무등의 약용식물(藥用植物)이 48종류(種類)였다. 이 지역일대(地域一帶)에서 아직 보고(報告)되지 않았던 특기할 수 있는 군락(群落)은 왕느릅나무(Ulmus macrocarpa), 오미자(Schizandra chinensis), 오갈피나무(Acanthopanax sessiliflorus), 지치(Lithospermum erythrorhizon)등이었다.

• 산업식품공학
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• 제14권1호
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• pp.1-6
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• 2010

본 연구에서는 오가피(Acanthopanax sessiliflorus)의 열매 발효주를 제조하였고 발효 중 생리활성 성분의 함량 변화를 측정함으로써 그 특징을 규명하였다. 열매의 일반성분 조성은 수분75.74${\pm}$0.49%(w/w), 조단백질 12.51${\pm}$1.23%(w/w), 조지방 4.20${\pm}$0.51.%(w/w), 조회분 5.21${\pm}$1.64%(w/w)이었으며 주된 미네랄 성분은 칼륨(12.94${\pm}$0.08 mg/g), 칼슘 (1.53${\pm}$0.06 mg/g), 마그네슘(1.12${\pm}$0.05 mg/g) 등 이었다. 발효주 제조를 위해 설탕으로 24, 26, 28, 30, 32$^{\circ}$Brix가 되도록 가당하고 발효 한 결과 30$^{\circ}$Brix 이상 가당 하였을 경우 알콜 발효가 저해되었으므로 목적하는 최종 알콜 농도와 잔당에 따라 24-30$^{\circ}$Brix가 되도록 조절하는 것이 바람직하였다. 발효가 진행되면서 총 폴리페놀의 함량은 증가하는 경향을 보였고 20${^{\circ}C}$로 발효한 경우가 125.24${\pm}$1.86 mg/mL로 25${^{\circ}C}$(99.69${\pm}$2.11 mg/mL), 30${^{\circ}C}$(95.55${\pm}$1.54 mg/mL)에서 발효한 경우보다 더 많은 총 폴리페놀 함량을 보였다. 또한 전자공여능을 측정 한 결과 20, 25, 30${^{\circ}C}$에서 발효시 각각 85.9${\pm}$2.3, 55.7${\pm}$2.5, 55.2${\pm}$3.4%로 20${^{\circ}C}$에서 발효하였을 경우 가장 높은 전자공여능을 보였는데 이는 1%(w/v) $\alpha$-tocopherol의 전자공여능과 비슷한 수준이었다. 오가피 열매의 주된 생리활성 물질인 eleutheroside B 함량은 발효가 진행됨에 따라 증가하여 최대 146.58${\pm}$4.10 $\mu$g/mL에 이르렀다. 그러나 발효 온도에 따라 eleutheroside B 함량은 차이가 없음을 알 수 있었다. 본 연구를 통해 착색료나 동물사료로 사용되거나 폐기되는 오가피 열매가 생리활성물질을 다량 함유한 고부가가치 기능성 식품 소재로 활용될 수 있는 가능성을 제시하였다.

• 산업식품공학
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• 제15권2호
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• pp.130-135
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• 2011

오가피는 다양한 생리활성을 가진 약재로 사용되어왔다. 본 연구에서는 오가피 부위별 열수 추출액의 기능적 특징을 규명하기위해 추출부위별 총 폴리페놀 함량, 항산화활성, 아질산염 소거능 및 항암활성을 알아보았다. 오가피의 생리활성 표준물질인 eleutheroside E는 줄기(542.50 $\mu$g/g) >뿌리(343.35 $\mu$g/g) >열매(30.78 $\mu$g/g) 순으로 함유되어 있었고 eleutheroside B는 열매(372.01 $\mu$g/g) >뿌리(289.33 $\mu$g/g) >줄기(125.05 $\mu$g/g) 순으로 많이 함유되어 있었다. 총 폴리페놀은 뿌리(227.21 mg/100 g)와 줄기(131.22 mg/100 g)에 많이 함유되어 있었다. 전자공여능은 줄기에서 79.87%, 뿌리에서 77.27%를 보여 총 폴리페놀 함량과 상관관계가 있었다. 산성 환경에서 nitrosoamine을 생성하는 아질산염에 대한 오가피의 제거 효과는 추출부위와 관계없이 pH 1.2에서 76-81.5%로 높게 나타났다. pH가 높아짐에따라 아질산염제거효과는 대개 소실되었으나 열매 추출액의 경우 pH 6.0에서도 43.1%의 아질산염제거효과를 유지하고 있었다. 오가피 부위별 열수 추출액은 정상세포인 DC2.4의 생육 억제 효과는 관찰되지 않았고 오히려 뿌리추출액의 경우는 DC2.4의 생육을 유의미하게 촉진하는 것으로 밝혀져 세포독성은 없는것으로 판단되었다. 위암 세포주인 SNU-719와 간암세포인 Hep3B에 대해서는 뿌리 추출액과 줄기 추출액에서 20-23%의 억제효과를 보였다. 따라서 오가피 부위별 추출액은 항산화활성, 식육에서의 nitrosoamine 생성 억제 등 다양한 기능성을 가진 식품소재로 활용이 가능 할 것으로 판단되었다.

• Food Science and Biotechnology
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• 제15권5호
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• pp.778-780
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• 2006

High performance liquid chromatography (HPLC) was used for the analysis of the lignans eleutheroside B and eleutheroside E in the fruits of Acanthopanax species. A reverse-phase system using a gradient of $H_2O$ and acetonitrile as the mobile phase was developed and detection was at 210 nm. The analysis was successfully carried out within 20 min. The content of eleutheroside B and eleutheroside E in Acanthopanax species was measured in the fruits of A. senticosus (0.58 and $1.66\;{\mu}g/mg$, respectively), A. sessiliflorus (1.15 and $8.49\;{\mu}g/mg$, respectively), A. koreanum (2.16 and $1.80\;{\mu}g/mg$, respectively), and A. divaricatus (1.06 and $7.08\;{\mu}g/mg$, respectively).

• 한국식품영양과학회지
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• 제39권12호
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• pp.1761-1768
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• 2010

오갈피나무 속의 가시오갈피(Eleutherococcus senticosu), 섬오갈피나무(Eleutherococcus gracilistylus), 오가나무(Eleutherococcus sieboldianus), 오갈피나무(Eleutherococcus sessiliflorus)의 잎 부위를 이용하여 $\alpha$-glucosidase와 $\alpha$-amylase 활성 저해 효과를 통한 혈당강하 효과를 평가 하였다. $\alpha$-Glucosidase 활성 저해 효과를 비교한 결과 섬오갈피 잎 추출물이 acarbose 대비 약 43.38%의 활성 저해 효과를 나타내었고, 가시오갈피 잎 추출물이 41.24%의 저해 효과를 보였다. $\alpha$-Amylase 활성 저해 효과를 측정한 결과 acarbose가 10 mg/mL의 농도에서 73.25%의 활성 저해 효과를 보였으며, 가시오갈피 잎 추출물이 acarbose 대비 91.90%의 높은 활성 저해 효과를 나타내었다. 또한 streptozotocin (STZ)으로 당뇨를 유도한 모델에 2주간 오갈피나무 속 식물 추출물을 섭취시킨 후 혈당과 지질 개선 효과를 탐색한 결과 STZ 투여로 인하여 모든 당뇨 유발군은 정상군에 비하여 혈당 수준이 유의적으로 증가하였다. 당뇨 유발 대조군(C)과 대비하여 시료 투여군인 가시오갈피(T1), 섬오갈피나무(T2), 오가나무(T3), 오갈피나무(T4)군 모두 혈당이 크게 감소하였다. 혈중 지질 농도 변화 실험 중 총 콜레스테롤의 함량은 정상군에 비하여 당뇨 유발 대조군은 증가하는 경향을 나타내는 반면 약물 투여군인 가시오갈피(T1), 오가나무 (T3), 오갈피나무(T4)군에서는 대조군에 비하여 유의적으로 감소하였다. HDL-cholesterol은 오가나무군에서 대조군에 비하여 55.61% 가장 크게 유의적으로 증가하였다. LDLcholesterol의 경우 정상군과 대조군과의 큰 차이가 관찰되지 않았으나 섬오갈피나무, 오가나무에서는 유의적으로 증가하였고, 가시오갈피와 오갈피나무 투여군에서는 대조군에 비하여 유의적으로 감소하였다. 혈중 중성지방의 경우 또한 총 콜레스테롤과 유사하게 대조군의 경우 혈중 농도가 증가하였다. 약물 투여군인 오가나무군은 60.16%, 오갈피군은 60.80%, 가시오갈피군은 50.16% 대조군 대비 유의적으로 감소하였다. 적출한 간 내의 중성지방의 농도를 측정한 결과 대조군의 경우 정상군에 비교하여 유의적인 증가를 보였으며, 가시오갈피군, 섬오갈피나무군은 각각 대조군 대비 유의적으로 감소하였다. 이상의 결과들에서 오갈피나무 속 추출물들은 혈당강하 및 당뇨대사 이상으로 인한 지질대사의 개선에 효과적인 것으로 나타났다.

• 동의생리병리학회지
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• 제20권2호
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• pp.352-357
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• 2006

This experimental study was designed to investigate the effects of Acanthopanax sessiliflorus $S_{EEM}$ leaves, stems, roots (ACL, ACS, ACR) on the change of weight and the serum total cholesterol, HDL-cholesterol, LDL-cholesterol, triglyceride, free fatty acid, total lipid and phospholipid level in obese mice induced Dy high fat diet. Experimental groups were as follows ; Normal group was fed with normal diet and administered with distilled water during 7 weeks, Control group was fed with high fat diet and administered with distilled water during 7 weeks, Sample A group was fed with high fat diet and administered with ACL of 500 mg/kg/mouse/day during 7 weeks, Sample B group was fed with high fat diet and administered with ACS of 500 mg/kg/mouse/day during 7 weeks, Sample C group was fed with high fat diet and administered with ACR of 500 mg/kg/mouse/day during 7 weeks. The results were as follows ; 1. Sample A group, Sample B group and Sample C group were significantly decreased the serum total lipid level in comparison with Control group. 2. Sample A group was decreased the body weight (4 weeks, 7 weeks), the serum total cholesterol level, the serum LDL-cholesterol level, the serum triglyceride level, the serum free fatty acid and phospholipid level but increased the serum HDL-cholesterol level in comparison with Control group. 3. Sample B group was increased the serum HDL-cholesterol level but decreased the body weight (4weeks), the serum total cholesterol level, the serum free fatty acid and triglyceride level in comparison with Control group. 4. Sample B group was significantly decreased the body weight (7 weeks), the serum LDL-cholesterol and phospholipid level in comparison with Control group. 5. Sample C group was increased the serum HDL-cholesterol level but decreased the body weight (4 weeks) and the serum free fatty acid level in comparison with Control group. 6. Sample C group was significantly decreased the body weight (7 weeks), the serum total cholesterol level, the serum LDL-cholesterol and triglyceride level in comparison with Control group. According to above results, I suggest ACR is able to be used for the obesity.

• Asian-Australasian Journal of Animal Sciences
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• 제32권11호
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• pp.1776-1788
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• 2019

Objective: The demands for measures to improve disease resistance and productivity of livestock are increasing, as most countries prohibit the addition of antibiotics to feed. This study therefore aimed to uncover functional feed additives to help enhance livestock immunity and disease resistance, using Acanthopanax sessiliflorus fruit extract (ASF). Methods: ASF was extracted with 70% EtOH, and total polyphenolic and catechin contents were measured by the Folin-Ciocalteu and vanillin assay, respectively. The 3D4/31 porcine macrophage cells ($M{\Phi}$) were activated by phorbol 12-myristate 13-acetate (PMA), and cell survival and growth rate were measured with or without ASF treatment. Flow-cytometric analysis determined the lysosomal activity, reactive oxygen species levels (ROS), and cell cycle distribution. Nuclear factor kappa B ($NF-{\kappa}B$) and superoxide dismutase (SOD) protein expression levels were quantified by western blotting and densitometry analysis. Quantitative polymerase chain reaction was applied to measure the lipid metabolism-related genes expression level. Lastly, the antibacterial activity of 3D4/31 $M{\Phi}$ cells was evaluated by the colony forming unit assay. Results: ASF upregulated the cell viability and growth rate of 3D4/31 $M{\Phi}$, with or without PMA activation. Moreover, lysosomal activity and intracellular ROS levels were increased after ASF exposure. In addition, the antioxidant enzyme SOD2 expression levels were proportionately increased with ROS levels. Both ASF and PMA treatment resulted in upregulation of $NF-{\kappa}B$ protein, tumor necrosis factor $(TNF){\alpha}$ mRNA expression levels, lipid synthesis, and fatty acid oxidation metabolism. Interestingly, co-treatment of ASF with PMA resulted in recovery of $NF-{\kappa}B$, $TNF{\alpha}$, and lipid metabolism levels. Finally, ASF pretreatment enhanced the in vitro bactericidal activity of 3D4/31 $M{\Phi}$ against Escherichia coli. Conclusion: This study provides a novel insight into the regulation of $NF-{\kappa}B$ activity and lipid metabolism in $M{\Phi}$, and we anticipate that ASF has the potential to be effective as a feed additive to enhance livestock immunity.

• 한국응용과학기술학회지
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• 제22권4호
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• pp.323-331
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• 2005

Fatty acid compositions of the seed oils of P. schinseng, A. continentalis and A. sessiliflorus, were analyzed by gas chromatography (GC) equipped with a capillary column. A large unusual peak was observed just before the peak corresponding to oleic acid $(cis-9-C_{18:1})$. This unknown fatty acid was isolated by silver ion chromatography and then derivatized into the picolinyl ester. The mass spectrum of the picolinyl ester showed molecular ion at m/z=373 with other diagnostic ions such as m/z=178, 218, 232, 246, 274, 288, 302 and 344. Characteristic absorption peaks at $720\;cm^{-1}$, $1640\;cm^{-1}$ and $3010\;cm^{-1}$ in IR spectrum indicated the presence of cis-configurational double bond in the molecule. The $^1H-NMR$ spectrum of this acid gave two quintets centered at ${\delta}1.638$ (2H, C-3) and ${\delta}1.377$ (2H, C-4), and two multiplets centered at ${\delta}2.022{\sim}2.047$ (2H, C-5) and ${\delta}2.000{\sim}2.022$ (2H, C-8), and multiplet signals of olefinic protons centered at ${\delta}5.3015{\sim}5.3426$ (C-6, J=9.5 Hz) and ${\delta}\;5.3465{\sim}5.3877$ (C-7, J=9.5 Hz). The $^13C-NMR$ spectrum showed 18 carbon resonance signals including an overlapped signal at ${\delta}29.7002$ for C-12 and ${\delta}29.6520$ for C-13 (or they can be reversed), and other highly resolved signals at ${\delta}33.950$, ${\delta}24.558$, ${\delta}26.773$ and ${\delta}27.205$ due to C-2, C-3, C-5 and C-8 of a ${\Delta}^6-octadecenoic$ acid, respectively. From analysis results this unknown fatty acid could be identified as cis-6-octadecenoic acid. The seed oils of P. schinseng and A. sessiliflorus contained petroselinic acid (59.7%, 56.0%), oleic acid (18.3%, 6.1%) and linoleic acid (16.2%, 30.4%) with small amount of palmitic acid (3.0%, 3.1%) while the seed oil of A. continentalis comprised mainly oleic acid (30.2%), petroselinic acid (29.0%), linoleic acid (24.1%) and palmitic acid (13.1%).

• 한국응용과학기술학회지
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• 제22권4호
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• pp.339-348
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• 2005

On the analysis of triacylglycerol (TG) from the kernels of Acanthopanax sessiliflorus by reversed phase-HPLC, it was separated into three main fractions of PN 44, 46 and 48, according to partition number (PN). On the contrary, it could be clearly classified into seven fractions of SMM, MMM, SMD, MMD, SDD, MDD and MDT by silver ion-HPLC by the number of double bond in the acyl chains of TG species. But resolution of so-called critical pairs of TG molecular species such as molecular pairs of $P_eLL$ $[C_{18:1{\omega}12}/(C_{18:2{\omega}6)2}]$ and OLL $[C_{18:1{\omega}9}/(C_{18:2{\omega}6)2}]$ and OOL $[(C_{18:1{\omega}9)2}/C_{18:2{\omega}6]$, and $P_eP_eL$ $[(C_{18:2{\omega}12)2}/C_{18:1{\omega}6]$ was not achieved $(P_e;$ petroselinic acid, L; linoleic acid, O; oleic acid). On the other hand, TG extracted from Aralia continentalis kernels were also fractionated into seven groups of SSM, SMM, MMM, SMD, MMD, SDD and MDD (S; saturated acid, M; monoenoic acid, D; dienoic acid) by silver ion-HPLC, although it's were classified into three groups of PN 44, 46 and 48 by reversed phase-HPLC. The fractions of SMM, MMM, MMD and MDD were divided into two subfractions, respectively; the fractions of SMM, MMM, MMD and MDD were resolved into the subfraction of $PP_e/P_e$ and POO (critical pairs from each other), that of $P_e/P_e/P_e$ and OOO, that of $P_e/P_e/L$ and OOL, and that of $P_e/L/L$ and OLL.