본 연구에서는 삼칠화 에탄올 추출물의 항산화 및 피부 세포 독성, 항염증을 확인하고, 삼칠화 함유 화장품을 여드름 피부에 적용하여 수분, 홍반, 모공, 블랙헤드에 미치는 영향을 분석하여 화장품 소재로서의 가능성을 규명하고자 하였다. 연구 결과, 삼칠화 에탄올 추출물의 DPPH radicial 소거능을 확인하였고, 높은 폴리페놀 함량과 플라보노이드 함량을 나타내었다. 삼칠화 에탄올 추출물은 RAW 264.7 세포에 대한 독성이 적었고, LPS에 의해 유도된 NO 생성을 유의하게 억제하는 것을 확인하였다. 4주간 삼칠화 에탄올 추출물이 3% 함유된 스킨 토너와 스팟 솔루션을 여드름 피부에 적용한 결과, 수분 증가와 홍반지수, 눈에 띄는 모공수, 블랙헤드 감소가 유의하게 나타났고, 사용 후 만족도 조사에서 피지량 감소, 붉음증 완화에 대한 만족도가 높은 것을 확인하였다. 따라서 삼칠화는 항산화 및 항염증 효과가 있으며, 여드름 관리용 화장품 소재로서 활용 가능할 것으로 사료된다.

본 연구는 정향추출물의 E. coli O157:H7에 대한 항균 효과와 E. coli O157:H7 감염 마우스에 대한 치료효과를 평가하기 위해 수행되었다. 정향 메탄올 추출물(FSAE)을 이용하여 E. coli O157:H7 에 대한 항균효과 확인 시험을 수행한 결과, 배양 후 24 시간째에, FSAE를 첨가한 모든 군들에서 E. coli O157:H7 의 생존율이 무투여 대조군에 비해 통계적으로 유의성 있게 감소하는 결과를 보여(0.269 mg/ml, p < 0.05; 0.538과 1.075 mg/ml, p < 0.001), FSAE가 E. coli O157:H7의 증식 억제 효과가 뛰어난 것으로 확인되었다. 또한, E. coli O157:H7을 감염시킨 마우스에 FSAE를 경구로 투여한 결과, 투여 후 3일째에, FSAE를 1.075 (p < 0.05)와 2.15 mg/ ml (p < 0.01)로 투여한 군들에서 대조군과 비교하여 분변 내 E. coli O157:H7의 균수가 유의성 있게 감소하였으며, 투여 7일째에는, 모든 FSAE 투여군들에서 대조군과 비교 하여 E. coli O157:H7의 균수가 통계적으로 유의성 있게 감소하였다(0.538 mg/ml, p < 0.05; 1.075와 2.15 mg/ml, p < 0.001). 이상의 연구결과로부터, FSAE를 E. coli O157: H7에 감염된 마우스에 경구로 투여할 경우, 감염증상을 완화 시킬 수 있을 것으로 기대된다.

The identity of toxin producers remains only hypothesis unless there were identified by strain isolation and analytical confirmation of both the cyanotoxin production and the genetic identity of the monoculture. The purposes of this study were to identify a morphologic and phylogenetic classification in Aphanizomenon flos-aquae strains isolated from the Nakdong River and to investigate the potential ability of the strains to produce toxins such as saxitoxin and cylindrospermopsin using target genes. The 16S rRNA and sxtA, sxtI, cyrA, cyrJ genes were analyzed on two strains (DGUC001, DGUC003) isolated from the Nakdong River. Morphological features of the strains were observed a shape of aggregated trichomes in parallel fascicles which can reach up to macroscopic size and a hyaline terminal cell without aerotope. In addition, the 16S rRNA phylogenetic analyses showed that the strains were identified as the same species with high genetic similarity of 98.4% and grouped within a monospecific andsupported cluster I of Aphanizomenon flosaquae selected from GenBank of the NCBI. The cyrA and cyrJ genes encoding for the cylindrospermopsinbiosynthesis were not detected in the present study. The sxtA gene was in detected both the two strains, whereas the sxtI gene which had been suggested as a suitable molecular marker to detect saxitoxin-producing cyanobacteria was not found both the strains. Thus, the two strains isolated from Nakdong River were identified as the same species of Aphanizomenon flos-aquae Ralfs ex Bornet et Flahault 1888, the two strains were confirmed as potential non-producing strains of the saxitoxin and cylindrospermopsin.

Aphanizomenon flos-aquae는 시아노박테리아 일종이며 anatoxin-a, saxitoxin, neosaxitoxin 등의 독소를 생산할 수 있어 국내에서는 식품원료로 사용이 금지되어있다. 전통적으로 시아노박테리아는 사상체 넓이, 세포 크기, 분열방법, 세포형태, 가스주머니의 존재유무 등의 형태학적 특징에 의한 분류가 가능하다. 그러나 가스주머니 혹은 무성 포자와 같은 특징은 주변 환경 또는 생장조건에 따라 차이가 있으며 경우에 따라 소실되기도 한다. 따라서 PCR에 의한 Aph. flos-aquae를 함유하는 기능식품을 검출할 수 있는 분석법을 개발하였다. 프라이머를 설계하기 위하여 유전자은행(www.ncbi.nlm.nih.gov)에 등록되어있는 Aph. flos-aquae, 스피루리나의 16S rRNA 염기서열을 이용하였으며, 비교 및 분석에는 BioEdit ver. 7.0.9.0 프로그램을 사용하였다. 최종적으로 클로렐라, 스피루리나, 녹차, 시금치로부터 Aph. flos-aquae를 검출할 수 있는 AFA-F1/AFAR1 (363 bp) 프라이머를 최종 선정하였다. 그리고 상기 프라이머는 Aph. flos-aquae가 각각 1% 함유 되도록 제조된 클로렐라, 스피루리나 제품에서 모두 혼입여부의 확인이 가능함을 확인하였다.

The present study was undertaken to estimate the antibacterial effect of a combination of C. rhizoma,L. Flos, and P. japonica (1:1:1) extracts (CLP1000) and a combination of the herbal extract mixture and dioctahedral smectite (CLPS1000) against murine salmonellosis. At the concentration of CLP1000 and CLPS10000.5 mg/ml, the antibacterial effect was not showed on Salmonella typhimurium (S. typhimurium). On the other hand,the antibacterial effect against S. typhimurium was observed at the concentration of CLP1000 and CLPS1000 1.0 mg/ml. Oral administration of Smectite, CLP1000, and CLPS1000 at the dose of 10 mg/ml showed a therapeutic effect for S. typhimurium infected BALB/c mice. The mortality of Smectite, CLP1000 and CLPS1000-treated mice was 90%,90%, and 70% at 12 days, respectively, while that of untreated mice was 100% at 9 days after a lethal dose of S. typhimurium infection. The results of our study strongly indicate that CLPS1000 has potential as an effective of salmonellosis.

This experimental study was designed to investigate the effects of Chrysanthemi Flos extract (CFE) on the change of cerebral hemodynamics〔regional cerebral blood flow (rCBF) and mean arterial blood pressure(MABP)〕in normal and cerebral ischemic rats, and to determine the mechanism of action of CFE. This study was also designed to investigate whether CFE inhibit lactate dehydrogenase (LDH) activity in neuronal cells and cytokines production in serum of cerebral ischemic rats. The results were as follows ; 1. CFE increased rCBF and increased MABP significantly in a dose-dependent manner. 2. The CFE-induced increase in rCBF was significnatly inhibited by pretreatment with indometh acin(IDN), an inhibitor of cyclooxygenase and methylene blue(MTB), an inhibitor of guanylate cyclase. 3. The CFE-induced increase in MABP was significnatly inhibited by pretreatment with IDN and MTB. 4. CFE 100㎍/㎖ significantly inhibited lactate dehydrogenase(LDH) activity in neuronal cells. 5. rCBF was significantly and stably increased by CFE (1㎎/㎏, i.p.) during the period of cerebral reperfusion, which contrasted with the findings of rapid and marked increase in control group. 6. In serum, by drawing from femoral arterial blood after middle cerebral arterial occlusion (MCAO) 1 hr and reperfusion 1 hr, sample group was significantly decreased IL-1β production compared to that of the control group. 7. In serum, by drawing from femoral arterial blood after MCAO 1 hr and reperfusion 1 hr, sample group was significantly decreased TNF-α production compared to that of the control group. 8. In serum, by drawing from femoral arterial blood after reperfusion 1 hr, sample group significantly increased TGF-β production compared to that of the control group. 9. In serum, by drawing from femoral arterial blood after reperfusion 1 hr, sample group increased IL-10 production compared to that of the control group. These results suggested that the mechanism of CFE was mediated by cyclooxygenase and guanylate cyclase, and CFE had inhibitive effect on the brain damage by inhibited LDH activity, IL-1β and TNF-α production, but accelerated TGF-β production and IL-10 production.thought that CFE should have an anti-ischemic effect on the improvement of cerebral hemodynamics and inhibitive effect on the brain damage.

A study on the antitoxic effects of Flos Carthami against Cadmium Chloride Toxicity in Live and Kidney of Rats. This study was performed to find out the effect of Flos Carthami against Cadmium toxicity. The experimental rats were divided into 5 groups such as control group, Cadmium alone treatment group, three simultaneous treatment groups of Flos Carthami and cadmium. Rat were given pellets administration with three dosage of Flos Carthami such as 4mg/kg body weight for four weeks. The results were summarized as follows on: 1. The simultaneously administration of Flos Carthami and cadmium significantly more decreased cadmium concentration in liver and kidney tissues compared to the administration of cadmium alone. (p<0.05) 2. The simultaneously administration of Flos Carthami and cadmium significantly more increased metallothionein concentration in liver and kidney tissues compared to administration alone (p<0.05)

Background : Stevia rebaudiana (Asteraceae), a perennial plant, has been used as a low caloric sweetener and therapeutic agent for diabetes, hypertension, myocardial, and antimicrobial infections. It has been commonly used leaves and stems because of their high anti-oxidative potential. The present research was carried out to explore anti-oxidative and anti-melanogenic effects of aqueous extract of Stevia rebaudiana Bertoni flos in B16F10 cells. Methods and Results : Anti-oxidant activity of Stevia flos extract (SFE) was determined by using 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical scavenging assay, nitric oxide (NO) radical scavenging method, and reducing power method. The results showed that the total phenolic content of SFE was 63.154 ± 0.0002 ㎍·QE/100㎎ and the total flavonoid was 8.64 1 ± 0.002 ㎍·GAE/100㎎. SFE exhibited a big significant effect on NO radical scavenging activity (IC50: 179.6 ㎍/㎖) comparing with standard ascorbic acid (IC50: 368.6 ㎍/㎖), and showed concentration dependent DPPH radical scavenging activity (IC50: 131.8 ㎍/㎖). Anti-melanogenic effect of SFE was also examined with B16F10 melanocytes. The amount of melanin synthesis followed by α-melanocyte stimulating hormone on B16F10 cells were significantly reduced in the presence of SFE treatment (p < 0.05). SFE also suppressed the tyrosinase activity (p < 0.05) and α-glucosidase activity (p < 0.05). Conclusion : These results provide evidence Stevia rebaudiana flos has an antioxidant potency and can be used as an anti-melanogenic agent.

Background : Chrysanthemi Indici Flos (甘菊) is listed in 「The Korea Herbal Pharmacopoeia (KHP)」as the original plant of Chrysanthemum indicum L. C. indicum was one of the most representative medicinal plants in Asteraceae, Dried flowers of this plant have been valid chemical composition such as flavonoids, phenylpropanoids, terpenoids, and polysaccharides, possessing broad spectrum antibacterial, antiviral, antihypertensive and anti-oxidation functions. Meanwhile, C. indicum was a polymorphic species, its morphological characteristics showed great diversity due to the different geographical and environmental factors. For this reason, there was conducted to develop molecular markers to distinguishing these C. indicum with C. morifolium, C. zawadskii var. latilobum and Aster spathulifolius by using conventional polymerase chain reaction (PCR). Methods and Results : In this study, In order to clearly identify origin of Chrysanthemi Indici Flos, these samples (C. indicum, C. morifolium, C. zawadskii var. latilobum and A. spathulifolius) were analyzed from five barcoding regions of chloroplast DNA (rbcL, matK, rpoB, atpF-atpH) and nuclear ribosomal DNA (ITS2) to evaluate the ability of discrimination for each barcoding region. Based on genetic distance, the percent of variable sites were provided the highest ITS2 value (56.9%), followed by atpF-atpH (48.18%), matK (27.2%), psbK (8.2%), and rbcL (2.9%). Comparative analysis based on the complete genome sequence of the petL-petG region INDEL (insertion/deletion) that the gene annotations were registered to the GenBank (accession number: JN-867592.1, NC-020092.1, MF-034027.1, NF-279514.1). Conclusion : From the above results, we may suggest that the petL-petG region INDEL analysis were conducted for molecular authentication of four plants (C. indicum, C. morifolium, C. zawadskii var. latilobum and A. spathulifolius). The findings of results indicated that petL-petG region might be established INDEL analysis systems and hence were proved to be an effective tools for molecular evaluation and comparison of “Chrysanthemi Indici Flos” with other plants.

Background: Inula japonica Thunb. is a plant belonging to the family compositae. Inulae flos (flower of I. britannica var. chinensis Regal.) is the dried flower of I. japonica Thunb. and contains various flavonoids (patulitrin, nepitrin and kaempferol), which have been utilized in traditional oriental medicine to treat nausea, phlegm, and coughs. However, ethanol extract of I. britannica (IJE) has not been previously studied for its use in cancer treatment, and its effects on oxidative stress, or inflammation. Thus, the present study investigated the anti-oxidant, anti-inflammatory, and anti-colorectal cancer effects of IJE using RAW264.7 and HCT- 116 cells, which are human colorectal cancer cell line. Methods and Results: IJE contained flavonoids (80.95 ± 5.3 ㎎/g) and polyphenols (310.53 ± 10.6 ㎎/g). Moreover, it reduced lipopolysaccharide (LPS)-induced nitric oxide (NO) production and H2O2-induced oxidative stress by decreasing reactive oxygen species (ROS) levels. Additionally, the 500 ㎍/㎖ IJE treatment increased caspase-3 activity and apoptotic cell death in HCT-116 cells. Conclusions: These results demonstrate that the anti-cancer effect of IJE against human colorectal cancer cells involves caspase-3 activation and apoptotic cell death. IJE also inhibited LPS-induced NO production, and H2O2-induced oxidative stress in RAW264.7 cells. However, further studies are required to explore how IJE treatment regulates signal transduction in NO and ROS production.

Although Sophorae Flos (SF) has been reported to exert an anti-cancer activity, molecular targets and mechanisms associated with anti-cancer activity of SF have been unclear. Because cyclin D1 has been regarded as an important regulator in the cell proliferation, we focused cyclin D1 and investigated the effect of SF on the cyclin D1 regulation in light of elucidating the molecular mechanism for SF’s anti-cancer activity. The treatment of SF decreased cellular accumulation of cyclin D1 protein. However, SF did not change the level of cyclin D1 mRNA. Inhibition of proteasomal degradation by MG132 attenuated SF-mediated cyclin D1 downregulation and the half-life of cyclin D1 was decreased in the cells treated with SF. In addition, a point mutation of threonine-286 to alanine attenuated SF-mediated cyclin D1 downregulation. Inhibition of ERK1/2 by a selective inhibitor, PD98059 suppressed cyclin D1 downregulation by SF. From these results, we suggest that SF-mediated cyclin D1 downregulation may result from proteasomal degradation through its threonine-286 phosphorylation via ERK1/2. SF-induced proteasomal degradation of cyclin D1 might inhibit proliferation in human colorectal cancer cells. The current study provides information on molecular events for an anti-cancer activity of SF

Magnoliae Flos (Sini in Korean) is one of the most important oriental medicinal plants. In the Korean Herbal Pharmacopeia, the bud of the all species in Manolia denudate and Manolia genus were regarded as the botanical sources for ‘Sini’. Most the dried bud of Manolia denudata, Manolia biondii and Manolia sprengeri were used as ‘Xin-yi’ in China. Therefore, the purpose of this study was to determine and compare the ‘Magnolia’ species, four species including Manolia denudata, M. biondii, M. liliiflora and M. Kobus were analysis of sequencing data revealed DNA polymorphisms. The based on tRNA coding leucine/phenylalanine (trnL-F) and NADH-plastoquinone oxidoreductase subunit 5 (ndhF) sequences in chloroplast DNA. For the identification of ‘Magnolia’ species, polymerase chain reaction (PCR) analysis of chloroplast DNA regions such as ndhF have proven an appropriate method. A single nucleotide polymorphism (SNP) has been identified between genuine “Sini” and their fraudulent and misuse. Specific PCR primers were designed from this polymorphic site within the sequence data, and were used to detect true plants via multiplex PCR.

접촉성 피부염 유발제인 크롬(Cr)의 세포독성을 조사하기 위하여 chromium trioxide(CrO3)가 배양 인체피부 섬유모세포(Detroit 551)에 미치는 영향을 알아보았으며, 이와 동시에 CrO3에 대한 금은화(Lonicerae Flos, LF) 추출물의 영향을 항산화 측면에서 조사하였다. 본 연구에서 CrO3는 처리 농도에 의존적으로 배양 Detroit 551세포의 생존률을 유의하게 감소시킴으로서 세포독성을 나타냈으며 XTT50값인 midcytotoxicity value(MCV)는 29.4μM로 나타났다. 한편, CrO3의 세포독성에 대한 항산화제의 영향에 있어서, 항산화제의 일종인 vitamin E는 CrO3에 의하여 유도된 세포독성을 유의하게 방어하였다. CrO3의 세포독성에 대한 금은화 추출물의 영향에 있어서는, 금은화 추출물이 CrO3에 의하여 감소된 세포생존률을 유의하게 증가시킴으로서 CrO3의 독성을 효과적으로 방어하였다. 이와 동시에 금은화 추출물은 SOD-유사 활성을 비롯하여 지질과산화(lipid peroxidation, LP)억제 및 lactate dehydrogenase(LDH) 활성감소를 보임으로서 항산화능을 나타냈다. 이상의 결과로부터 CrO3는 배양 Deroit 551 세포에 고독성을 나타냈으며, CrO3의 세포독성에 산화적 손상이 관여하고 있는 것으로 나타났다. 한편, 금은화 추출물은 이의 항산화능에 의하여 CrO3의 산화적 손상과 관련된 세포독성을 효과적으로 방어하였다. 따라서 금은화 추출물과 같은 식물의 천연물은 크롬처럼 산화적 손상과 관련된 중금속들에 의하여 유도되는 알러지성 접촉성 피부염(contact dermatitis, CD)의 예방이나 치료적 접근을 위한 소재로서의 개발적 가치가 클 것으로 생각된다.

신이는 전통적으로 비염 등의 치료에 사용되어 왔는데, 신이 에탄올 추출물은 그람 양성균인 Staphylococcus aureus 그람 음성균인 Pseudomonas fluorescens균 및 곰팡이균인 Aspergillus niger에 대하여 모두 항균활성을 보였으며, proteinase로 활성화된 receptor-2에 의한 흰쥐 뒷발바닥 부종모델에서 신이 에탄올 추출물을 경구투여한 경우 typsin이나 tc-NH2로 유발된 발바닥 부종, 혈관투과성, myoloperoxidase 활성도에서 유의성 있는 억제율을 보여 항염증 활성이 뚜렷함을 나타냈다.

잇꽃 재배시 홍화수확적기 및 이에 따른 종실 (홍화자) 수확적기를 구명하고자 홍화를 개화성기 후 2, 4, 6일, 종설을 개화 성기후 10, 15, 20, 25일에 수확하여 시험한 결과를 요약하면 다음과 같다. 1. 건홍화의 수확적기는 개화후 4일로 수량은 개화 후 2일(28.1kg/10a)에 비하여 유의차가 없었고 색채색차 (δEab) 로 본 품질도 개화 후 6일에 비하여 1.07로 차이가 작았던 개화 후 4일로 판단되었다. 2. 홍화의 수확유무 및 수확시기에 따른 종실수량은 유의차가 인정되지 않았다. 3. 수확시기에 따른 ha당 종실수량은 개화성기 후 10일 수확 284.8kg에 비하여 수확이 늦추어짐에 따라 백립중이 증가하여 20일 수확시 17%, 25일 수확은 8% 증수되어 홍화의 종실수확적기는 개화후 20일 전후로 판단되었다.