• 생약학회지
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• 제18권2호
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• pp.127-135
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• 1987

In vitro sensitivity testing was performed for 21 kinds putative anticancer drugs selected from references and information. Cellular damage of P815 mastocytoma cells following exposure to water extracts of drugs was evaluated by colony formation assay. Highly effective drugs with more than 50% inhibition of colony formation were seven (Houttuyniae Herba, Sanguisorbae Radix, Nepetae Herba, Manitis Squama, Lonicerae Flos, Amomi Semen, Polyporus), though not more effective than BCNU. According to the results of $^3H-thymidine$ incorporation assay for determination of selective cytotoxicity, 3 of these drugs (Houttuyniae Herba, Polyporus, Manitis Squama) were found to be low cytotoxic to normal mouse lymphoid cells. These findings suggest that the above 3 drugs may be used for effective anticancer drugs in vivo.

• 한국식품영양과학회지
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• 제33권3호
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• pp.475-479
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• 2004

저령 버섯으로부터 추출된 다당체는 78.2%의 당류, 16.8%의 단백질 및 4%의 회분으로 구성되었다. 저령다당체는 20-160 mg/kg/day로 ,3주간 투여 시 ICR mouse에서 유발된 sarcoma-180에 대하여 항종양효능을 나타내었다. 또한 저령다당체를 50-400$\mu\textrm{g}$/mL의 농도로 투여시 백혈암세포인 L-1210와 K-562세포에서 대조군에 비하여 52.6%, 55.0%로 각각 성장하였다. 그러나 이들 세포에서 세포사멸의 생화학적인 증거가 되는 DNA 분절현상은 나타나지 아니하였다. 2.5-10.0%의 농도의 저령다당체는 Salmonella typhimurium TA 100과 TA 98에서 2-nitrofluorene과 sodium azide에 의해 유발된 돌연변이를56%까지 억제하였다 이 결과로 저령다당체는 항종양효능, 암세포성장 억제효능 및 항돌연변이 효능을 갖는 것으로 사료되며, 이 항종양 및 암세포 성장억제효능은 세포사멸(apoptosis)에 기인하지 않는 것으로 사료된다.

• 생약학회지
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• 제41권2호
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• pp.141-146
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• 2010

A simple and reliable reverse phase HPLC method was developed to determine pharmacologically active marker compounds of Ephedrae Herba, Phytolaccae Radix and Polyporus. The stability test of water-extract of three natural medicines were examined for six months. However, no significant change in the content of the marker compounds of each extract observed during the time of investigation.

• Journal of the Korean Wood Science and Technology
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• 제44권2호
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• pp.253-263
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• 2016

Fungi, such as the wood-rotting Polyporus brumalis, are excellent sources of pharmaceutically interesting natural products such as sesquiterpenoids. In this study, we investigated the biosynthesis of P. brumalis sesquiterpenoids on modified medium. Ten additional species of white rot fungi were inoculated in medium containing nutrients such as $C_6H_{12}O_6$, $C_4H_{12}N_2O_6$, $KH_2PO_4$, $MgSO_4$, and $CaCl_2$ at $28^{\circ}C$ for 25 days. After 10 days of incubation, eudesmane-type sesquiterpenes, ${\beta}$-eudesmane and ${\beta}$-eudesmol, were only synthesized during the growth phase of P. brumalis. Experiments excluding one nutrient at a time were conducted to determine the effects of inorganic nutrients on sesquiterpene biosynthesis. In conclusion, GC-MS analysis showed that biosynthesis of sesquiterpenes was differentially regulated by inorganic nutrients such as $MgSO_4$, $C_4H_{12}N_2O_6$, and $KH_2PO_4$. We found $MgSO_4$ supplementation to be vital for eudesmane-type sesquiterpene biosynthesis in P. brumalis; nitrogen ($C_4H_{12}N_2O_6$) and phosphate ($KH_2PO_4$) inhibited the synthesis of P. brumalis metabolites. Magnesium is a known cofactor of sesquiterpene synthase, which promotes ${\beta}$-eudesmol synthesis. To mechanistically understand eudesmane-type sesquiterpene biosynthesis in P. brumalis, further research into the genes regulating the dynamics of such biosynthesis is warranted.

• 대한한의학회지
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• 제36권3호
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• pp.73-83
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• 2015

Objectives: The purpose of this study was to evaluate the effects of Polyporus Herbal-acupuncture(PO-HA) at KI10 (Umgok) on nephritis induced by lipopolysaccharide(LPS) in rats. Methods: Rats were allocated into normal, control, and 2 experimental groups. The rats in the control group were intra-peritoneally injected with LPS for nephritis induction. The rats in the groups of experiment 1 and experiment 2 were treated with Saline injection, and PO-HA, respectively at KI10 three times for a week and then intra-peritoneally injected with LPS. To evaluate the effects of PO-HA at KI10, WBC count in blood, creatine, tumor necrosis factor-alpha (TNF-${\alpha}$), cytokine-induced neutrophil chemoattractant 1(CINC-1) in serum, urinary volume, creatinine, total protein in urine, myeloperoxidase(MPO) in kidney were measured. Results: PO-HA at KI10 significantly suppressed the increase of WBC in blood, TNF-${\alpha}$, CINC-1 in serum, MPO in kidney of LPS-stimulated rats. PO-HA at KI10 significantly suppressed the increase creatinine, total protein in urine of LPS-stimulated rats. Conclusions: According to these results, it is postulated that PO-HA at KI10 has an anti-inflammatory and renal-protective effects on LPS-induced nephritis in rats. Therefore, it is suggested that PO-HA at KI10 may be an useful therapeutics for nephritis in clinical field after further researches.

• 대한한방내과학회지
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• 제39권6호
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• pp.1181-1190
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• 2018

Objective: This study investigated the effect of purified medical herb extracts such as Alisma canaliculatum and Polyporus umbellatuson adipogenic differentiation of human bone marrow derived mesenchymal stromal stem cells (hBMSCs). Methods: Two different medical herb were extracted using hot distilled water. The optimal concentration of extracts were fixed at 100 ng/ml by means of cell viability and cytotoxic assay. To test the adipogenic differentiation ability of extracts, we induced the adipogenesis of hBMSCs for 21 days. At day 5, the cell was harvested to check mRNA and protein expression level of adipogenic related factors. The efficacy of lipid droplet formation was evaluated using the oil-red O staining method at days 21. Results: Two different medical herb extracts have no toxicity on hBMSCs. And two different medical herb extracts significantly decreased formation of lipid droplet compared with control groups in hBMSCs. The A. canaliculatum extract group showed the lowest mRNA and protein expression level of adipossgenic related transcription factors. This data suggests that extract of A. canaliculatum and P. umbellata decrease the adipogenic differentiation of hBMSCs. Conclusions: Our findings indicate that water-extract of A. canaliculatum and P. umbellata will be useful therapeutic reagents for prevention of obesity related disease such as diabetes, hyperlipidemia, coronary artery disease, and osteoporosis.

• Journal of the Korean Wood Science and Technology
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• 제40권6호
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• pp.424-430
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• 2012

본 연구에서는 국내에서 자생하는 백색부후균인 겨울우산버섯(Polyporus brumalis)을 소나무 시편에 배양하여 목재 처리에 의한 리그닌 분해효소의 활성변화를 조사하고 목재의 분해가 일어나는 동안 중량감소율 및 리그닌 감소율을 통해 분해능을 확인하고 여기에 관여하는 유전자의 발현을 조사하였다. SSC (Shallow Stationary Culture) 액체배지에 목재 시편을 넣고 겨울우산버섯을 배양하였을 때 무처리구에서는 laccase의 활성이 20일 이후 감소하는 반면, 시편 처리구에서는 활성이 계속 증가되었다. 특히, 60일 전후의 처리구에서 무처리구에 비해 10배 이상 높은 활성을 나타내었다. 또한, 겨울우산버섯에 의한 소나무칩의 중량 감소율과 리그닌 감소율은 80일 후 각각 23.4%와 6.3%로 나타났다. 40일 배양한 목질칩에서 분리한 겨울우산버섯의 pblac1의 유전자 발현은 무처리구에 비해 소나무 칩 처리구에서 약 3배 정도 높게 나타났다. 이상의 결과로 백색부후균에 의한 목재칩 처리에 의해 리그닌 분해효소의 활성이 증가되며 pblac1이 리그닌 분해에 중요한 역할을 하는 것으로 보여진다. 따라서 백색부후균의 리그닌분해효소 유전자 발현을 조절함으로써 리그닌 분해능이 우수한 균주 개발이 가능하고 목질에탄올 생산 전처리에 효율적으로 이용할 것으로 기대된다.

• 한국식품과학회지
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• 제30권3호
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• pp.688-692
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• 1998

천연생리활성물질의 개발과 미이용자원의 효율적 재이용방안을 모색하기 위하여 13여종의 한국산 야생 버섯류를 에탄올과 물로 추출하여 각 시료추출물의 항변이원성 물질 검색을 시도하였다. B(a)P과 MNNG의 돌연변이 유발성에 미치는 야생버섯류의 에탄올 추출물과 물추출물의 항돌연변이 효과의 검토는 Salmonella typhimurium TA98과 TA100을 이용한 Ames 실험계를 이용하였으며 B(a)P에 대해 꽃구멍장이버섯(Polyporus dispansus), 깔때기꾀꼬리버섯(Cantharellus infundibuliformis), 진갈색주름버섯(Agaricus subrutilescens), 테미로버섯(Daedalea dickinsii), 목장말똥버섯 (Panaeolus papilionaceus) 및 턱수염버섯(Hydnum repandum) 등의 에탄올추출물에서 비교적 강한 항변이 원성을 나타내었다. 물추출물의 경우는 B(a)P에 대해서 턱수염버섯(Hydnum repandum)이 TA100에서 가장 강한 저해효과를 나타내었고 대부분의 시료는 낮거나 저해활성이 보이지 않았다. 직접변이원인 MNNG에 대해서는 야생버섯류의 에탄올추출물중 5종만 항변이원성이 관찰되었고, 물추출물의 경우는 꽃구멍장이버섯(Polyporus dispansus)이 가장 강한 저해효과를 보였으나 대부분의 버섯류는 낮거나 저해 효과를 거의 나타내지 않았다. 그중 직, 간접 변이원에 대해 가장 강한 저해 효과를 나타낸 꽃구멍장이 버섯의 에탄올추출물은 농도가 높을수록 항변이원성 효과가 증가하는 경향을 보였다.

• 대한한방내과학회지
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• 제40권3호
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• pp.551-556
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• 2019

Objectives: This study aimed to introduce a clinical case of asymptomatic microhematuria due to suspicion of kidney trauma following a motor vehicle accident. Methods: A 19-year-old male was hospitalized with the chief complaint of back pain after a motor vehicle accident. He showed an elevated urine red blood cell (RBC) level in the laboratory test, although no specific traumatic lesions were present on the body. He was assessed to have asymptomatic microhematuria, and Zhu Ling Tang (polyporus decoction) was given to him to be taken three times daily. Results: After the treatment, the level of urine red blood cells returned to normal range. Adverse events were not observed. Conclusions: Zhu Ling Tang caused a short-term improvement in the urinalysis levels of a patient with asymptomatic hematuria. However, further studies are needed, as this study is only a single-case report.

• 한국버섯학회지
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• 제11권4호
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• pp.194-200
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• 2013

Polyporus umbellatus (Syn. Grifola umbellata) is a sclerotium forming mushroom belongs to family Polyporaceae of Polyphorales, Basidiomycota. The sclerotia of P. umbellatus have long been used for traditional medicines in China, Korea and Japan. This study was initiated to obtain the basic data for artificial sclerotial production of P. umbellatus. Here, we investigated the favorable conditions for mycelial growth of P. umbellatus and its symbiotic fungus Armillaria mellea. We also evaluate the favorable carbon and nitrogen sources for sclerotial formation in dual culture between P. umbellatus and A. mellea. The favorable conditions for mycelial growth of P. umbellatus were $20^{\circ}C$ and pH 4, while optimal conditions for mycelial growth of A. mellea were $25^{\circ}C$ and pH 6. The carbon sources for optimal mycelial growth of P. umbellatus were fructose and glucose, while carbon sources for favorable mycelial growth of A. mellea were also fructose and glucose. The nitrogen sources for favorable mycelial growth P. umbellatus were peptone and yeast extract, while optimal mycelial growth of A. mellea were obtained in peptone and yeast extract. When P. umbellatus and A. mellea were dual cultured on carbon sources, sclerotia were induced on basal media supplemented with glucose, fructose and maltose at pH 4~6, while nitrogen sources inducing sclerotia were basal media supplemented with peptone and yeast extract for 60 days at $20^{\circ}C$ under dark condition.