• 대한본초학회지
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• 제38권4호
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• pp.31-43
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• 2023

Objectives : The objective of this study was to investigate the phytochemistry and pharmacological activities of Cirsium setidens. Methods : Domestic and international articles about Cirsium setidens were investigated. A review was perfoemed via DB searching engine such as Sci.Direct, Springer, DBpia, KISS, Google scholar, Kipris, and so on. Total 73 listed literature were classified by compound analysis and pharmacological efficacy. Results : C. setidens contains pectolinarin and its glycoside, pectolinarigenin as index compounds, and linarin, apigenin, diosmetin, scopoletin, acacetin, cirsimarin, cirsimaritin, setidenosides A and B, silymarin, hispidulin, 92 volatile compounds, and 15 fatty acids. The Pharmacological activities of C. setidens has been reported to inhibit of platelet aggregation and fat accumulation in the liver, inhibit to hepatitis, anti-cancer, antibacterial, skin improvement, hair growth, liver protection, anti-diabetic, anti-inflammatory, sedative. Also, It has been reported the effect of cholesterol-lowering and anti-obesity, neuroprotective effects, increasing human stem cell viability, inhibiting osteoclast formation and osteogenic differentiation. Conclusion : This reviews showed that C. setidens which has been traditionally used for the treatment of inflammation and hypertension, has anticancer and river protective effect, as well as hair loss and diet. In order to maximize the efficacy of C. setidens, research has also begun on the effect of processing processes such as fermentation or fine powdering and combining natural plant resources.

• 생명과학회지
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• 제25권7호
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• pp.801-809
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• 2015

활성화된 단핵구의 동형성 세포 부착(동형성 응집)은 염증반응, 분화, 이동과 같은 생리학적, 병리학적 과정에서 중요한 역할을 한다. 매실 추출물은 항바이러스, 항균, 항암작용과 같은 효과를 보인다고 알려 져있다. 따라서, 매실 추출물은 단핵구의 동형성 응집 억제를 통해 염증반응을 조절할 가능성을 가진다. 본 연구에서는, 염증성 질환에서 매실 추출물의 치료효능을 뒷받침할 수 있는 분자적 기전을 조사하였다. 매실 추출물이 지질다당질(LPS)로 활성화된 단핵구의 동형성 응집을 억제함을 확인하였다. 이러한 효과는 LPS로 활성화된 THP-1 세포의 iNOS 단백질 발현 억제를 통해, 산화질소(NO) 생산의 감소로 조절되는 것을 발견하였다. 또한 NO 생성물질인 SNAP 처리 실험을 통해 단핵구 동형성 응집을 억제하는데 매실에 의한 NO 억제가 필수적인 기작임을 확인하였다. 게다가, 매실 추출물은 LPS로 유도된 IκB-α 의 인산화와 NF-κB의 핵내로의 이동을 현저하게 감소시키는 것을 확인하였다. 매실 추출물은 NO생성과 NF-κB 활성 억제를 통해 LPS로 활성화된 단핵구의 동형성 응집을 저해하고 이를 통해 항염증 효과를 유도할 수 있다는 결론으로부터 만성 염증성 질환의 치료와 예방에 매실 추출물의 효능을 제시하고자 한다.

• 대한한방부인과학회지
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• 제21권2호
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• pp.125-151
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• 2008

Purpose: In this study, we investigated the anti-thrombotic efficacy of "Eungapbang-gagam(EGB)" currently used in clinical treatment of PID Methods: We studied inhibitory effect of platelet cohesion, suppressive effect of GPIIb/IIIa activity, inhibitory effect of $TXB_2$ and $PGE_2$ biosynthesis, and oxidative damage suppression effects of "EGB" in vitro. Also, suppression of pulmonary embolism and changes of related factors in dextran coagulation condition model were studied in vivo. Results: In this study, EGB extract showed dose-dependent inhibitory effect on platelet coagulation induced by ADP, epinephrine, collagen, arachidonic acid. Also it showed dose-dependent inhibition effect on GPIIb/IIIa activities compared to the control group. EGB extract significantly suppressed the decrease of speed of bloodstream caused by blood coagulation in dextran coagulation condition model and increased the number of platelets and amount of fibrinogen, and decreased the APTT in dextran coagulation condition model compared to the control group. EGB extract showed dose-dependent decrease of oxidative damages caused by DPPH and superoxide anion radicals, whereas dose-dependent increase of superoxide dismutase like activity was observed compared to the control group. Conclusion: We confirmed the anti-thrombosis and anti-oxidative efficacy of "Eungapbang-gagam". Various clinical applications of "Eungapbang-gagam" as well as use of data for the construction of EBM is anticipated.

• Archives of Pharmacal Research
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• 제21권1호
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• pp.17-23
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• 1998

Flavonoid glycosides were metabolized to phenolic acids via aglycones by human intestinal microflora producing ${\alpha}$-rhamnosidase, exo-${\beta}$-glucosidase, endo- ${\beta}$-glucosidase and/or ${\beta}$-glucuronidase. Rutin, hesperidin, naringin and poncirin were transformed to their aglycones by the bacteria producing ${\alpha}$-rhamnosidase and ${\beta}$-glucosidase or endo- ${\beta}$-glucosidase, and baicatin, puerarin and daidzin were transformed to their aglycones by the bacteria producing ${\beta}$glucuronidase, C-glycosidase and ${\beta}$-glycosidase, respectively. Anti-platelet activity and cytotoxicity of the metabolites of flavonoid glycosides by human intestinal bacteria were more effective than those of the parental compounds. 3,4-Dihydroxyphenylacetic acid and 4-hydroxyl-phenylacetic acid were more effective than rutin and quercetin on anti-platelet aggregation activity. 2,4,6-Trihydroxybenzaidehyde, quercetin and ponciretin were more effective than rutin and ponciretin on the cytotoxicity for tumor cell lines. We insist that these flavonoid glycosides should be natural prodrugs.

• Journal of Ginseng Research
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• 제37권3호
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• pp.300-307
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• 2013

20S-dihydroprotopanaxatriol (2H-PPT) is a derivative of protopanaxatrol from ginseng. Unlike other components from Panax ginseng, the pharmacological activity of this compound has not been fully elucidated. In this study, we investigated the modulatory activity of 2H-PPT on the cellular responses of monocytes and macrophages to understand its immunoregulatory actions. 2H-PPT strongly upregulated the release of radicals in sodium nitroprusside-treated RAW264.7 cells and the surface levels of costimulatory molecule CD86. More importantly, this compound remarkably suppressed nitric oxide production, morphological changes, phagocytic uptake, cell-cell aggregation, and cell-matrix adhesion in RAW264.7 and U937 cells in the presence or absence of lipopolysaccharide, anti-CD43 antibody, fibronectin, and phorbal 12-myristate 13-acetate. Therefore, our results suggest that 2H-PPT can be applied as a novel functional immunoregulator of macrophages and monocytes.

• 고려인삼학회:학술대회논문집
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• 고려인삼학회 1998년도 Advances in Ginseng Research - Proceedings of the 7th International Symposium on Ginseng -
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• pp.146-159
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• 1998

A new processed ginseng with fortified activity is developed. The process comprise with the heat treatment of fresh or white ginseng at higher temperature and pressure than those used for the preparation of red ginseng. This new processed ginseng showed 7 times higher antioxidant activity and more than 30 times stronger vasodilating activity than those shown in raw ginseng. Other activities found in the new processed ginseng include cancer chemoprevention, antinephrotoxic, and antineurotoxic activities. Less polar ginsenosides isolated from processed ginseng exhibited anti-platelet aggregation activity and anti-cancer activity. Many ginsenosides were isolated from this new processed ginseng, namely 20(S)-$Rg_3$,20(R)-$Rg_3$, $Rg_5$, $Rg_6$, $F_4$, $Rh_4$,20(S)-$Rg_3$,20(R)-$Rg_3$ and $Rg_4$. In addition to these known compounds, seven new ginsenosides, named as gisenoside $Rk_1$, $Rk_2$, $Rk_3$, $Rs_4$, $Rs_5$, $Rs_6$, and $Rs_7$ were isolated. The major constituents of new processed ginseng were 20(S)-$Rg_3$,20(R)-$Rg_3$, $Rk_1$ and $Rg_5$ which are minors in red ginseng. Since the chemical constituents and biological activities of this new processed ginseng are quite different from those of white or red ginseng, we designated it as $'$sun ginseng (仙蔘)$'$.s;$.

• 생명과학회지
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• 제30권5호
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• pp.443-451
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• 2020

현대사회는 고지방의 서구화된 식사, 과도한 스트레스 등으로 비정상적인 혈액응고 및 과다한 혈소판 응집이 증가되고 있으며, 이로 인한 다양한 혈전성 질환 위험성도 증가되고 있다. 본 연구에서는 제주 특용식물인 상동나무(Sageretia thea) 지상부의 항혈전 활성을 평가하기 위해 잎(ST-L), 줄기(ST-B), 열매(ST-F) 에탄올 추출물을 조제하고 이의 항혈전 활성, 인간 적혈구 용혈활성 및 flavonoids·phenolic acids 조성을 검토하였다. ST-B 추출물은 식용으로 이용되고 있는 ST-F 추출물보다 6.7배의 총 폴리페놀 함량을 보였으며, ST-L 추출물은 ST-F 추출물보다 2.7배 높은 총 플라보노이드 함량을 보였다. 혈액응고 저해활성 평가 결과, ST-F 추출물은 aPTT에서만 혈액응고시간 연장이 미약하게 나타났으나, ST-L 및 ST-B 추출물은 기존 항혈전제인 aspirin 및 베리류 및 한방 약재 추출물보다 트롬빈, 프로트롬빈, 응고인자들에 대해 강력한 저해활성을 나타내었다. 혈소판 응집저해 역시 ST-L 및 ST-B 추출물은 aspirin보다 우수한 응집저해 활성을 나타내었으며, 인간 적혈구에 대한 용혈활성은 1 mg/ml 농도까지 전혀 나타나지 않았다. ST-L 및 ST-B 추출물의 phenolic acid 및 flavonoids 분석결과, rutin, isoquercitrin 및 astragalin이 주요 활성물질로 확인되었다. 본 연구결과는 상동나무 잎과 줄기의 강력한 항혈전 활성의 최초 보고이며, 상동나무를 이용한 항혈전제 개발이 가능함을 제시하고 있다. 향후 상동나무에서 처음으로 확인된 isoquercitrin의 항혈전 기전에 대한 연구가 필요하다.

• BMB Reports
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• 제42권12호
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• pp.812-816
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• 2009

To screen chaperone proteins from Schizosaccharomyce pombe (S. pombe), we prepared recombinant citrate synthase of the fission yeast as a substrate of anti-aggregation assay. Purified recombinant citrate synthase showed citrate synthase activity and was suitable for the substrate of chaperone assay. Several heat stable proteins including aspartyl aminopeptidase (AAP) for candidates of chaperone were screened from the supernatant fraction of heat-treated crude extract of S. pombe. The purified AAP migrated as a single band of 47 kDa on SDS-polyacrylamide gel electrophoresis. The native size of AAP was estimated as 200 kDa by a HPLC gel permeation chromatography. This enzyme can remove the aspartyl residue at N-terminus of angiotensin I. In addition, AAP showed the heat stability and protected the aggregation of citrate synthase caused by thermal denaturation. This study showed that S. pombe AAP is a moonlight protein that has aspartyl aminopeptidase and chaperone activities.

• 한국식품저장유통학회지
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• 제24권5호
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• pp.658-665
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• 2017

식용 및 약용으로 이용되고 있는 함초를 이용한 고부가가치 제품개발을 위해, 동결건조, 열풍건조, 음건한 함초의 ethanol추출물을 조제하여 건조방법에 따른 성분 변화, 항산화 및 항혈전 활성 변화를 평가하였다. 동결건조, 열풍건조 및 음건 시료의 ethanol 추출효율은 각각 14.4, 13.2, 11.9%를 나타내어 동결건조시 수율이 음건에 비해 1.2배 높았다. 성분 분석결과, 동결건조 시료의 total polyphenol 함량은 4.6 mg/g으로 열풍건조 및 음건 시료보다 높았으며, total flavonoid 함량은 건조방법과 무관하게 4.2-4.4 mg/g을 나타내었다. 반면 총당 함량은 동결건조에서 가장 높게 나타났으며, 음건 시료는 동결건조 시료에 비해 53% 수준을 나타내었다. 환원당의 경우 열풍건조시료에서 가장 높게 나타났으며, 음건시료에 비해 3.3배 높게 나타났다. 항산화 활성 평가결과, 동결건조, 열풍건조 시료에서는 유사한 항산화 활성이 나타났으나, 음건 시료의 경우 환원력과 nitrite 소거능은 유의적으로 감소되었다. 항응고 활성의 경우, 모든 건조 시료에서 농도 의존적인 우수한 항응고 활성을 나타내었으며, 특히 열풍건조 시료에서 강력한 TT 및 aPTT 연장 활성을 나타내었다. 인간 혈소판에 대한 응집저해 활성과 적혈구 용혈활성은 건조방법에 따른 유의적인 변화는 나타나지 않았다. 본 연구결과는 함초의 유용 기능성 유지를 위해 열풍건조 및 동결건조가 필요하며, 특히 함초의 항혈전 활성을 이용하는 기능성 식품을 제조하고자 하는 경우 열풍건조를 이용하는 것이 경제적이면서 효과적임을 제시하고 있다.

• 대한한방부인과학회지
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• 제22권1호
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• pp.53-78
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• 2009

Purpose: In this study, we investigated the anti-thrombotic and antiinflammatory efficacy of "Gamijoukyungtang(GJKT)". Methods: We studied inhibitory effects of platelet aggregation, FXa activation, $TXB_2$ and $PGE_2$ biosynthesis and suppressive effects of GPIIb/IIIa activity and oxidative damage, pro-inflammatory cytokine reduction effects of 'GJKT(by press extractor)/GJKT-1(by pressless extractor)' in vitro. Also, we studied suppression of pulmonary embolism, AV shunt model in rats and shortening of Rat tail bleeding time in vivo. Results: GJKT/GJKT-1 extract showed inhibitory effects on GPIIb/IIIaactivities and platelet aggregation induced by ADP, epinephrine, collagen and arachidonic acid. They suppressed biosynthesis of $PGE_2$ but GJKT-1 only supressed biosynthesis of $TXB_2$. In FXa assay, they inhibited activation of FXa. they suppressed pulmonary embolism triggered by collagen and epinephrine. In AV shunt model, they decreased the weights of AV shunt thrombus. they inhibited pro-inflammatory cytokines and decreased oxidative damages caused by DPPH. Conclusion: We confirmed the anti-thrombosis, and ant-inflammatory efficacy of 'GJKT(by press extractor)/GJKT-1(by pressless extractor)'.