The caterpillar-shaped Chinese medicinal mushroom (DongChongXiaCao) looks like a worm in the winter and likes a grass in the summer. The fruiting bodies of Cordyceps species have demonstrated various biological activities and used as traditional medicines in Asian countries. The price of wild Cordyceps have been ascending every year as their demand increase. Recently, the artificial cultivation of these fungi has been successfully established and they are currently produced on a rice or pupae media. This study was carried out to investigate the soluble sugar, amino acid and fatty acid profiles in the fruiting-bodies of Cordyceps militaris, C. pruinosa and Paecilomyces. tenuipes formed on the living silkworm (Bombyx mori) host. Soluble sugars such as glycerol, glucose, mannitol and sucrose were found in the fruiting bodies of Cordyceps militaris, C. pruinosa and P. tenuipes. Total soluble sugar content was 29.23 ㎎g-1in C. militaris, 8.61㎎g-1 in C. pruinosa and 24.00 ㎎g-1in P. tenuipes on dry weight basis. Total free amino acid content was 14.09 ㎎g-1in C. militaris, 34.60㎎g-1 in C. pruinosa and 17.09 ㎎g-1 in P. tenuipes. The content of oleic acid in fatty acids was above high more than 30% regardless of species.

This study was carried out to investigate amino acid contents of golden mushroom and pink mushroom. The amino acid analysis was followed by AccQ-Tag method and HPLC on gradient conditions. Seventeen amino acids were analyzed and sixteen amino acids were found in golden mushroom ; fifteen amino acids in pink mushroom respectively. Among total amino acid in golden mushroom, cystein content was the highest and glycine, glutamic acid, proline were followed. Among total amino acid in pink mushroom, cystein was the highest and glycine, lysine, methionine were followed. As shown in Fig.1, 2, concerning amino acids, cystein was dominant. and alanine was detectied in golden mushroom but pink mushroom.

Treponema denticola is the best studied oral spirochete and numerous studies have shown that it is strongly associated with periodontitis and expresses several putative virulence factors. In this study, we report on a surface protein of T. denticola, Td92, which is homologous to Tp92 of Treponema pallidum, an agent of syphilis. Immunofluorescence assay and immunogold labeling with anti-Td92 Ab revealed that Td92 had surface-exposed epitopes. And Td92 was capable of binding to fibronectin and KB cells, an oral epithelial cell line. In addition, Td92 could enter the KB cells. These results indicate that Td92 is a fibronectin-binding protein which can bind to and internalize into the host cells, facilitating the virulence of T. denticola.

Phytic acid (PA) is a naturallu occurring polyphosphorylated carbohydrate that is present in substantial amounts in almost all plants and mammalian cells. Recently PA has received much attention for its role in anticancer activity. We investigated the preventive effect of PA on the formation of colonic aberrant crypt foci (ACF), a preneoplastic lesion, induced by azoxymethane (AOM). After acclimation for one week, six-week old male ICR mice were fed on the AIN-93G purified diet and PA (0.5% or 2% PA in water) for 8 weeks. The animals were treated with azoxymethane (AOM, 10 mg/kg b.w.) three times (0, 1, and 2 weeks) to induce colonic aberrant crypt foci (ACF). After sacrifice, the total numbers of aberrant crypts (AC) and ACF in colonic mucosa were counted after staining with methylene blue. Blood and serum were analyzed with a blood cell differential counter and an automatic serum analyzer. AOM treatment without PA induced the total numbers of 85.7 ± 12.9 and 115.2 ± 19.9, respectively. PA at the dose of 2% AC/colon by PA at the dose of 0.5% were 73.4 ± 12.9 and 115.2 ± 19.9, respectively. PA at the dose of 2% significantly decreased the ACF and AC numbers to 56.5 ± 14.6 and 95.4 ± 17.2, respectively (p＜0.01). PA at the doses of 0.5 and 2% decreased the numbers of ACF and AC/colon in a dose-dependent manner. Although some parameters in blood counts and serum chemistry were changed compared with the control, no specific toxicity was found. Theses findings suggest that phytic acid can be a chemopreventive agent for colon carcinogenesis resulting from inhibition of the development of ACF in ICR mice.

Developmental periods of sweet potato whitefly, Bemisia tabaci(Gennaius) Q-biotype, were investigated on three host plants- sweet bell pepper (Capsicum annuum L.), eggplant(Solanum melongena L.) and oriental melon(Cucumis melo L. var. makuwa MAKINO). Egg and nymph development of B. tabaci were studied within temperature ranging of 15℃-35℃ by 2.5℃ under photoperiod 16:8(L:D). Egg period of B. tabaci was the shortest at 32.5℃ and nymphal period was shortest at 27.5℃ on sweet bell pepper. Nymphal period of B. tabaci on eggplant was the shortest at 27.5℃ as well. On the other hand, nymphal period of B. tabaci was shortest at 30℃ and 32.5℃. Lower temperature threshold and effective degree-day for completing egg development on sweet bell pepper were estimated as 13.11, 91.95, respectively. Lower threshold temperature of nymphal stage on sweet bell pepper, eggplant, oriental melon were estimated as 13.01, 13.39, 12.31,respectively. Degree-days required to complete nymphal stage on sweet bell pepper, eggplant, oriental melon were estimated as 191.22, 164.41, 190.34, respectively. The relationships between development rates of egg and nymph were well described by poikilothermal rate function and weibull function. The fitted curves will be used as input for a simulation model of the population dynamics of B. tabaci.

The characteristic of implant s llrface is the most i mportant factor in osseointegra t ion procesR , Prol i fera tion and rli ffel' entiat ion of osteoblast, a nd local factors concerning bone forma tion a l'e inflllenced by sUl' face cha racteri s tic and it al so con t l'ols bone reactlOn The purpose of this reseal'ch was to s tlldy a boll t ini t ial adhesion. prolife ration and acti vation of osteo blast to titanium surface treated wi th mac hined‘ hydroxyapat ite coating, resorba ble blast materi al blasting and a n odi zing method To attach and culture osteobl ast‘ titanium cylinder block wi th 5mm in di ameter and 5mm in height was mad e , After t l'eating the titanium surface of each bl ock with machined, hydroxyapatite coating, I'esorhable blast ma teri al blasting and anodi zed coating, i.mpllrities wel'e I'emoved and stenllzed The number of cells attached from cultul'ed osteobl ast of I'espective expel’imental groups were measured at 1, 4, 7. and 14day, Al ka line phosphatase, calcium. and inorganic phosphate concen tra ti on 0 1' cultured solution was measul'ed, Anodi zing group showed the hi ghest. and RBM treated grollp was foll owed, Machined grollp was the worst ra te of cell a ttachment and pl 미 ife ra ti o n activity, RBM t l'eated grollp s howed the high est in creasi ng on theil‘ alkaline phosphatase activi ty of 1 and " days in cultllred osteobJast to compnrc wi th othcr groups. Thc rc was no significant differe nce among other grollps , stati stically, RBM trea ted grollp showed the hi ghest rate 0 1' increa s ing on the ca lcillm apposition of 1 a nd 4 days in cllltured osteobl ast to compa re wi th other groups , The re was no s ignificant differ ence among other groups ‘ statistica lly, RBM t reated g roup showed the highest rate of inorganic phospha te apposi t ion to compare with other groups , The re was no s ignifi cant diffe rence among other groups‘ s tati stically, It suggested tha t surface modi fï cation of titani um would be profoundly effected on the attachment. proliferation and activation 0 1' osteoblast in init ial stage osseolll tegrat lOn

The aims 0 1' t his study we re to evaluate proliferative and apoptotic cell distribution pattern in condylar articu lar and pl'oliferative layer as two types of diet(soft and ha rd) we1'e supplied to growing 1'a ts, 30 male Sprague Dawley g1'owing l'ats(twenty-one c1ays fl'om bi l'th) were c1ivided into two group, Each 15 rats were supplied by soft and hal'd di et , After c1 iluted Bl'du solution(5mg/ Kg)was injected into pel'itoneum befol'c sacrificc. rats wel'e sacl'i f iced at 1. 2. 3 week llltel'vals St1'eptoavidin-Biotin method for Brdu was used to evaluate celluJar proliferative activity. ancl fluol'escent TUNEL method was used to estima te the apoptotic activity, The results about this expe riment wel'e recorded about ante1'io1' and posterior condyle separateJy, In anteriol' portion of condyle, soft diet group showed inc1'eased p1'olife1'ative celluJar activity tha n hal'd diet group dw'ing 1, 2 week but decl'eased than hal'd diet g1'oup at 3 weeks. while hal'd diet group showed constant p1'oliferative cellular activity during all experimenta l period , ln posterior pOl'tion of condyl e、soft diet group showed increased activity than hard diet group at 3 weeks, while ha rd di et gl'oup showed constant proliferative cellular activity during exper‘ imental period , In a nterior pOl'tion of condyle‘ soft c1 iet group showed increased apoptotic activity with time progress, but hard diet group showed continuous low level of activity during experimental period , In posterio1' porti on 0 1' condyle, hard diet group showed cons tant low level apoptotic activity, plthough showed the lowes t leveJ at 1 week, On the con trary soft diet g1'oup showed c1ecl'eased apoptotic activity wi th time progress, ConcJusively, in soft diet group an teroposterior direction was reduced in condyJar morphologic dimension because of decreased prol iferative cellular and increased apoptotic activity on anterior portion and vertical dimension 0 1' condyle was increased because of increased proliferative cellular and decreased apoptotic activity on posterior portion. but in hard di et group proli ferative cellular and apoptotic activity were comparatively constant. and thus harcl diet group s howed antet'opos teriorJy broad and flat condylar morphoJogy

The present study investigated the effects of follicle stimulating hormone (FSH) and human chorionic gonadotrophin (hCG) on the nuclear maturation of canine oocytes. Oocytes were recovered from mongrel female ovaries in various reproductive states; follicular, luteal or anestrous stage. Oocytes were cultured in serum-free tissue culture medium (TCM)-199 supplemented with various concentrations of FSH (Exp. 1: 0, 0.5, 1.0 or 10 IU) or hCG (Exp. 2: 0, 0.5, 1.0 or 10 IU) or both (Exp. 3: 1 IU FSH + 1 IU hCG) for 72 hr to determine the effective concentration of these hormones, and to examine their combined effect. After maturation culture, oocytes were denuded in PBS containing 0.1% (w/v) hyaluronidase by gentle pipetting. The denuded oocytes were stained with 1.9 μM. Hoechst 33342 in glycerol and the nuclear state of oocytes was evaluated under UV light. More (p<0.05) oocytes matured to MII stage when follicular stage oocytes were supplemented with 1 IU FSH (6.2%) compared with the control, 0.1 or 10.0 IU FSH (0 to 1.2%). Significantly higher (p<0.05) maturation rate to MII stage was observed in follicular stage oocytes supplemented with 1.0 IU hCG (7.2%) compared with the control or other hCG supplemented groups (0 to 1.5%). However, the combination of FSH and hCG did not improve the nuclear maturation rate of canine oocyte (2.4 %) compared with FSH (6.2%) and hCG alone (7.2%). In conclusion, FSH or hCG alone significantly increased the maturation of canine oocytes to MII stage.