• 대한수의학회지
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• 제30권4호
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• pp.487-497
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• 1990

This study was carried out to observe in vitro effect of praziquantel on the tegumental changes of Heterophyopsis continua with scanning electron microscope. Metacercariae were collected from the perch, Lateolabrax japonicus, by artificial digestion technique and fed to 2-week old chickens. Adult worms were recovered from small intestine of chickens 8 days after infection. For working solutions, praziquantel was diluted with TC199 medium at concentration of 0.01, 0.1. 1 and $10{\mu}g/ml$. To each petri dish containing 10ml of solution, 5~10 worms were introduced and incubated at $37^{\circ}C$. For the scanning electron microscopy(SEM), the worms were fixed in cold 2.5% glutaraldehyde, dehydrated in a series of graded ethanol and freeze-dried. Dried specimen was mounted on stub and coated with gold and observed in an SEM. The results were as follows: 1. Severe tegumental alterations were recognized by scanning electron microscope. Bleb formation of tegument was observed in 5 minute group and most pronounced on anterior tegument of worms. The number and size of blebs increased as incubation time prolonged. 2. The surface destruction was more pronounced at ventral margin between the oral and the ventral suckers. 3. The sensory papillae were slightly affected, but destruction of tegumental spine was not recognized. 4. The effect of praziquantel on the worm was found dependent on the concentration and incubation time, however, the effect was more dependent upon the incubation time.

• Asian-Australasian Journal of Animal Sciences
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• 제20권2호
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• pp.208-213
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• 2007

The objective of the experiment was to determine the optimum cultural [moisture levels (55, 60 and 70%), days of fermentation (7, 14 and 21), temperature (25 and $35^{\circ}C$) of incubation)] and nutritional parameters (urea addition (0 and 2%) and variable levels of single super phosphate (0.25 and 0.50% SSP)) for bio-processing of the mustard (Brassica campestris) straw (MS) under solid-state fermentation (SSF) system. The performance of SSF was assessed in terms of favorable changes in cell wall constituents, protein content and in vitro DM digestibility of the MS. Sorghum based inoculum (seed culture) of Ganoderma lucidum to treat the MS was prepared. The 50 g DM of MS taken in autoclavable polypropylene bags was mixed with a pre-calculated amount of water and the particular nutrient in the straw to attained the desired levels of water and nutrient concentration in the substrate. A significant progressive increase in biodegradation of DM (p<0.001), NDF (p<0.01) and ADF (p<0.05) was observed with increasing levels of moisture. Among the cell wall constituents the loss of ADF fraction was greatest compared to that of NDF. The loss of DM increased progressively as the fermentation proceeded and maximum DM losses occurred at 28 days after incubation. The protein content of the treated MS samples increased linearly up to the day $21^{th}$ of the incubation and thereafter declined at day $28^{th}$, whereas the improvement in in vitro DM digestibility were apparent only up to the day $14^{th}$ of the incubation under SSF and there after it declined. The acid detergent lignin (ADL) degradation was slower during the first 7 days of SSF and thereafter increased progressively and maximum ADL losses were observed at the day $28^{th}$ of the SSF. The biodegradation of DM and ADL was not affected by the variation in incubation temperature. Addition of urea was found to have inhibitory effect on fungal growth. The effect of both the levels (0.25 and 0.50) of SSP addition in the substrate, on DM, NDF, ADF, cellulose and ADL biodegradation was similar. Similarly, the protein content and the in vitro DM digestibility remain unaffected affected due to variable levels of the SSP inclusion in the substrate. From the results it may be concluded that the incubation of MS with 60 percent moisture for 21 days at $35^{\circ}C$ with 0.25 percent SSP was most suitable for MS treatment with Ganoderma lucidum. Maximum delignification, enrichment in the protein content and improvement in in vitro DM digestibility were achieved by adopting this protocol of bioprocessing of MS.

• Asian-Australasian Journal of Animal Sciences
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• 제18권9호
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• pp.1249-1254
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• 2005

The aim of this study was to determine the effect of maturity stage on the nutritive value of wild mustard straw in terms of chemical composition, in situ, in vitro dry matter degradability and calculated ME. The nutritive values of wild mustard, Sinapsis arvensis hays harvested at three stages were evaluated by chemical composition, in vitro gas production and in situ dry matter degradation methods. Gas production or dry matter (DM) degradation were determined at 0, 3, 6, 12, 24, 48, 72 and 96 h and their kinetics were described using the equation p = a+b(1-e$^{-ct}$). Maturity had a significant effect on both the chemical composition and degradability of wild mustard. Neutral detergent fibre (NDF) and acid detergent fibre (ADF) (p<0.001) increased with increasing maturity whereas the crude protein (CP) (p<0.001) decreased. The gas produced after 96 h incubation ranged between 64.7 and 81.5 ml per 0.200 g of dry matter. The gas production (ml) at all incubation times and estimated parameters decreased with increasing maturity of wild mustard. The gas production at all incubation times and estimated parameters (a, b (a+b), metabolizable energy (ME) and organic matter digestibility (OMD)) were negatively correlated with NDF and ADF. The DM disappearance after 96 h incubation ranged between 50.8 and 76.1%. The in situ DM disappearance at all incubation times and estimated parameters decreased with increasing maturity of wild mustard. The in situ dry matter disappearance at all incubation times and some estimated parameters (c, a, b and effective dry matter degradability (EDMD)) were negatively correlated with NDF and ADF but positively correlated with CP. The nutritive value of wild mustard continually changed as it matured. Wild mustard, harvested at the proper stage of maturity offers considerable potential as a high quality forage for ruminants during the winter feeding period. The present study showed that if higher quality forage is an objective, wild mustard should be harvested at the early flowering stage.

• 한국동물위생학회지
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• 제18권1호
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• pp.41-56
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• 1995

The present study was conducted to investigate results of B. anthracis isolated from Anthrax in the Kyong-Ju of Feb. 12. 1994. 1. In biochemical feature, B. anthracis was a gram-positive rod, non-motility, sporulation, capsulation. It was positive in gelatinase, starch hydrolysis, glucose. But negative in urease, arabinose, mannitol, xylose. 2. B. anthracis grew well on B4 Br A TSA after incubation for 24 hours. The organisim grew well on BA, Br. A, NA, TSA after incubation for 72 hours. The media grew well on Br A instead of BA. 3. On 5% blood agar by laboratory animal, ${\beta}$ -hemolysis was produced from 36 hours to 48 hours incubation. There was perfect ${\beta}$-hemolysis after incubation for 48 hours. On the other side ${\beta}$-hemolysis was begun on 5% goat blood agar after incubation for 60 hours. 4. In the test of antimicrobial susceptibility, B. anthracis was very sensitive to AM, CF, TE, ENR, GM, AN, DFX, S, P, TYLO, N, KM, C, E, Lins＋Sp, NN, CC, CFP, CB were sensitive one by one. B. anthracis was no-sensitive to L, XNL, TIA, CL, SXT 5. B. anthracis had never sensitivity to direct inoculation of rat and chicken, after subcutanous inj. It was very sensitive to mouse and goat, hamster, guinea pig, rabbit had a sensibility one by one. 6. The dead laboratory animal which had been inoculated with B. anthracis preserved at $37^{\circ}C$ incubation, B. anthracis didn't cultivate on non-dissected animal after 80 hours but cultivate on dissected animal after 360 hours. 7. The rapidly death could cause high concentration, died from 420 after S. C. 8. The blood smeared samples of hamster from inoculation with B. anthracis, spore germinated In 37$^{\circ}C$ after 5 hours, in $32^{\circ}C$ after 6 hours, in room temperature after 9 hours, in $-4^{\circ}C$ to $-20^{\circ}C$ after 10 hours. 9. B, anthracis inoculated to laboratory animal after SC or PO. Mice and rats feces didn't cultivated with B. anthracis after SC, but did cultivated with B. anthracis after PO. 10. In the test of disinfectant, B. anthracis was high effective to $HgC1_2$, formalin, effect phenol, cresol, but non-effect NaOH, ethanol.

• Journal of Periodontal and Implant Science
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• 제30권1호
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• pp.145-157
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• 2000

Cytotoxic substances in dental calculus and root cementum of periodontally diseased teeth inhibit new attachment and regeneration. The purpose of scaling and root planing is to remove pathologic structures harboring these cytotoxic substances in order to create a biologically acceptable root surface. However, these procedures inevitably leave a non-biocompatible smear layer. Conventionally, the smear layer has been removed with low pH etching agents such as citric acid, phosphoric acid and tetracycline hydrochloride(TC). Lately, a supersaturated neutral pH etching solution of ethylene diamine tetraacetic acid(EDTA) has been found to be as effective as low pH etchants with respect to smear removal and to be superior in exposing root surfaceassociated collagen. The aim of the present study was to determine the effect of root surface treatment using EDTA on the initial attachment of human gingival fibroblasts. 27 human teeth, extracted due to severe periodontitis, were cut into dentin slices after root planing. The specimens were divided into TC group(treated with $50㎎/m{\ell}$ tetracycline-HCl, pH 1.52), EDTA group(treated with 17% EDTA, pH 7.4), and non-treated control group. After sterilization, 5th subcultured human gingival fibroblasts were seeded in each culture well containing a prepared root slice and incubated for 15 min., 60 min., and 4 hours in 5% $CO_2$ incubator at $37^{\circ}C$. At each incubation time, the number of attached fibroblasts were counted on the microphotographs taken at a magnification of x100. The difference of the number of attached cells between groups was statistically analyzed by the ANOVA followed by Duncan test in SPSS/PC＋programs. The results were as follows : 1. After incubation for 15 min, the attached cells were significantly more in EDTA group and TC group than non-treated control group(p<0.05), but there was no significance in the difference between EDTA group and TC group(p>0.1). 2. After incubation for 60 min and 4 hours, there was no significant difference in the number of attached cells between all groups(p>0.1). 3. In both EDTA group and TC group, there was no significant difference in the number of attached cells between different incubation(p>0.1). But in control group, the number of attached cells was significantly increased after incubation for 60 min, compared with incubation for 15 min(p<0.05). The above results suggest that root surface treatment using EDTA could enhance the initial attachment of gingival fibroblasts to root surface as effective as tetracycline-HCl.

• Asian-Australasian Journal of Animal Sciences
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• 제20권9호
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• pp.1462-1467
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• 2007

This study investigated the effect of chemical treatments on tannins (condensed and hydrolysable) and on the trypsin inhibitor (TI) activity in salseed meal. Triplicate samples of ground salseed meal (1 kg) were mixed with 820 ml of either distilled water (pH 5.3), 0.67 M acetic acid (pH 2.4), 0.67 M sodium bicarbonate (pH 8.2) or 2% polyvinyl-pyrrolidone (PVP) solution. The material was placed in airtight plastic containers and incubated at $37^{\circ}C$ for 0, 3, 6, 12, 24, 48 and 72 h. Samples of untreated salseed meal which had not been subjected to soaking or incubation were run through the analysis to serve as control. Addition of water, acetic acid, sodium bicarbonate and PVP solutions to salseed meal and subsequent anaerobic incubation at $37^{\circ}C$ significantly reduced chemically detectable tannins. At each incubation time, alkali solution was more effective than its counterparts. The effect of acidic solution on hydrolysable tannin was least among the treatments. All the treatments reduced TI activity of salseed meal. The reduction in TI activity by these treatments was similar and ranged between 80-84%. Treatment time effected a decrease in the contents of antinutritional substances. However, the effect of the treatment with the reagents, even for zero incubation time, was quite pronounced. It may be concluded from the present results that the treatment of salseed meal with sodium bicarbonate (0.67 M) is more effective in reducing hydrolysable and condensed tannin contents than PVP, water and acid solutions. Treatment with sodium bicarbonate solution is more economical and easier to handle than acid and PVP treatments. Incubation of the treated material for 12 h is reasonably effective, economical and safe from any mould growth.

• Parasites, Hosts and Diseases
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• 제28권2호
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• pp.91-100
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• 1990

폐흡충(Paragonimus Tuestermani) 피낭유충을 흰쥐(Wistar) 및 고양이에 감염시키고 감염 힐청이나 분회분리된 IgG또는 보체가 정상 또는 감염 흰쥐 복강 대식세포의 폐흡충 유충 살충에 어떠한 영향을 미치는지 부착 실험 (adherence assay) 및 세포독성을 통하여 관찰하였다. 폐흡충 감염은 복강 대식세포를 비특이적으로 활성화시퍼 대식세포의 유충에 대한 부착률 및 세포독성을 증가시켰으며, 감염 혈청을 첨가하였을 때 항체-의존 세포매개성 세포독성에 의해 배양 6시간 후에 세포 부착률 및 세포독성이 가장 강하였다. 감염 혈청을 56℃에서 30분간 가열하였을 때 IgG 항체 변성에 의해 세포독성이 저하되었다. IgG 및 보체를 첨가한 경우 세포 부착률은 낮았으나 24시간 후에는 유충이 사멸하였다. 그러나 보체의 단독적인 역할은 이 실험에서 알 수 없었다.

• 한국식품영양과학회지
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• 제31권3호
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• pp.521-526
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• 2002

대두(백태,흑태)와 현미의 메탄올과 아세톤 추출물이 호르몬 의존형 유방암세포(MCF-7)와 호르몬 비의존형세포(MDA-MB-231)의 세포독성과 apoptosis에 미치는 영향을 살펴보았다 각 추출물별 25, 50, 100 ug/well의 농도로 24, 48, 72시간 배양 시 배양시간과 사용된 시료 모두 농도 의존적으로 유방암 세포생존율을 억제하는 것으로 나타났다. 특히 호르몬 의존형 세포인 MCF-7 에서는 현미의 아세톤 추출물이 낮은 농도에서 짧은 배양시간에도 그 효과가 나타났고 호르몬 비의존형 세포주 MDA-MB-231에서는 현미의 아세톤 및 메탄올 추출물의 효과가 다른 시료들에 비해 높게 나타났다. Apoptosis에 미치는 영향에서는 호르몬 비의존형 세포(MDA-MB-231)에서 메탄올추출물 처리군이 대조군에 비해 apoptosis된 세포가 유의적으로 증가한 것을 관찰할 수 있었다. 그러나 세포생존율 결과와는 다르게 호르몬의존형 세포와 호르몬비의존형 세포 모두에서 아세톤 처리군은 대조군에 비해 apptosis에 유의차를 나타내지 않았다. 이상의 결과에 의하면 이들 화합물이 소유한 암세포 성장억제 기전은 추출물내 함유된 화합물의 종류와 세포성장의 호르몬 의존도에 따라 다양한 것으로 사료된다.

• 식물병연구
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• 제29권1호
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• pp.11-22
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• 2023

Resazurin 기반 호흡 측정법으로 strobilurin계 살균제에 대해서 감수성인 고추탄저병균 Colletotrichum acutatum s. lat. 20JDS8에 대한 살균제의 호흡 억제 효과를 조사하였다. Potato dextrose broth에 병원균의 포자를 접종하고 배양하면서 시간별로 상대 형광값(relative fluorescence unit)을 조사한 결과, 12시간 후부터 상승하기 시작하여 24시간 후의 1×10⁴, 1×10⁵, 1×10⁶ spores/ml의 포자 접종구에서 상대 형광값은 1,965.5, 5,412.5, 10,061.0이었다. 병원균을 0, 6, 12, 24시간씩 배양 후에 공시한 살균제를 처리하고, 24시간 후에 상대 형광값을 조사하였다. Dithianon, isopyrazam, pyraclostrobin, fluazinam을 병원균의 포자(0시간), 포자 발아(6시간), 균사 생장(12시간) 단계에 처리할 경우, 각 살균제의 고농도에서 호흡을 90-100% 억제하였다. 하지만 병원균을 24시간 배양한 후에 살균제를 처리할 경우에는 호흡 억제 효과가 크게 감소하였다. Pyraclostrobin 저항성인 C. acutatum s. lat. 20CDJ6에 대해서 pyraclostrobin, azxoystrobin, trifloxystrobin, kresoxim-methyl을 병원균의 모든 생장 단계에 각각 처리하였을 때, 호흡에 대한 억제 효과는 매우 미미하거나, 나타나지 않았다.

• 대한환경공학회지
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• 제39권5호
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• pp.288-302
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• 2017

퇴적물이 수층의 영양염 분포에 미치는 영향을 평가하기 위해서 퇴적물의 용출률을 정확하게 측정할 필요가 있다. 이에 본 연구에서 퇴적물 용출률 측정 방법 중 퇴적물 코어 배양법을 대상으로 용출률의 측정 조건과 실험 절차를 제시하였다. 낙동강 수계 중류에서 2015년 7월에 표층이 교란되지 않은 퇴적물 코어 시료를 채취하여, pre-incubation 시간(6, 12, 24시간), 초기 산소농도(포화도 90, 70 50%), 확산경계층의 두께(0, 0.6-0.8, 1.2-1.4 mm), 배양 온도(10, 17, 20, $25^{\circ}C$) 등을 여러 가지 조건으로 조성하여 측정한 영양염 용출률의 결과를 그 바탕으로 하였다. 네 가지 주요 환경 조건이 달라지면, 안정화 시간 동안 유기물 분해 및 산화 과정에 의한 화학 조성 변화, 퇴적층의 산화-환원 환경 변화에 따른 흡착 및 탈착, 퇴적물-수층 경계면에서의 수리역학적 상황 변동에 의한 물질 교환 증감, 퇴적물 내 미생물의 활성 증가 등을 야기하여 퇴적물의 영양염용출률에 영향을 미친다. 따라서, 퇴적물 코어 배양법으로 실제 현장값과 유사한 결과를 생산하기 위해서는 현장 심수층의 수온 및 용존산소 농도, 유속을 자연 상태와 가깝게 재현하고 퇴적물 시료 채집 후 되도록 빠른 시간 안에 배양 실험을 수행해야 한다. 두 개의 반복구에 대하여 퇴적물 코어 배양법으로 영양염 용출률을 측정하였을 때 대부분의 실험 조건에서 상대백분율차가 20% 이하였다. 측정 조건과 절차를 엄밀히 준수하여 실험하였을 때 정밀도를 확보할 수 있는 것으로 사료되며, 향후 측정 결과의 정확도를 확인하기 위하여 현장 측정법과 비교할 예정이다.