• 한국응용곤충학회지
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• 제23권4호
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• pp.221-232
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• 1984

Padan (Cartap) 4G의 벼멸구에 대한 살충효과, 방제효과 및 이들에 관여하는 몇가지 요인을 구명하기 위하여 실내시험, 폿트시험을 수행하여 아래와 같은 결과를 얻었다. 1. 벼멸구에 대한 Padan의 $LD_{50}$치는 암컷은 $0.2021\;{\mu}g$(24시간)$\~$$0.0032\;{\mu}g$(48시간)/충이었고, 수컷은 $0.215\;{\mu}g$(24시간)$\~$$0.0008\;{\mu}g$ (48시간)충/ 이었다. 2. 벼멸구 암컷에 대한 Padan의 $LD_{50}$치는 온도수준에 따라서 현저한 차이가 있었다. 즉 $25^{\circ}C$에서는 $0.1076\;{\mu}g$/충, $30^{\circ}C$에서는 $0.0072\;{\mu}g$/충, $35^{\circ}C$에서는 $0.0031\;{\mu}g$/충 이었다. 3. 벼멸구 암컷에 대한 Padan의 $LC_{50}$치(ppm)는 칩엽처리에서는 낮았다. 즉, 침근처리에서 살충효과가 훨씬 높았다. 4. Padan의 처리를 받은 벼멸구의 감로배치량은 $458mm^2$로서 $LD_{30}$ 약량수준에서는 무처리 $935mm^2$에 비하며 낮았으나 $LD_{50}$ 약량수준에서는 무처리와 비등하였다. 5. 벼멸구에 대한 Padan 4G의 살충효과는 성충에 대해서는 낮았고 약충에 대해서는 높았다. 6. 폿트시험에 있어서 벼멸구에 대한 Padan 4G의 살충효과는 Broadcasting와 Top-dressing 처리간에 별 차이를 인정할 수 없었다. 7. 폿트시험에 있어서 Padan 4G의 벼멸구에 대한 살충효과는 담수상태에 비하여 배수상태에서 높았다. 8. Padan의 처리를 받은 벼멸구의 차세대의 밀도는 총 513마리로서 무처리구 550마리에 비하여 차이가 없었으나 Furadan 처리구의 3.0마리에 비하여는 현저히 높았다. 그리고 Diazinon 처리에서 370.7 마리 비해서는 높은 경향을 나타내었다. 9. 수원지방에 있어서 Padan 4 G의 벼멸구 방제효과는 $94.3\~100\%$인데 비하여 Diazinon $47.0\~99.8\%$, Furadan $63.3\~99.8\%$로서 월등히 높았다. 그리고 담수상태에 비하여 배수상태에서 벼멸구 방제효과가 높았는데 그 현상은 Diazinon, Furadan 처리에서 더욱 뚜렷하다. 10. 해남지방에 있어서 Padan 4G의 벼멸구 방제효과는 $62.3\~94.1\%$ 인데 비하여 Diazinon처리구 $3.5\~80.4\%$. Furadan 처리구 $0\~50.6\%$로서 월등히 높았다. 그러나 수원의 방제효과에 비하면 좀 낮은 편이었다. 담수조건과 배수조건에 따른 방제효과의 차이는 나타나지 않았다. 이와 같은 현상은 Diazinon과 Furadan 처리에서도 마찬가지였다. 11. 포장시험결과 Padan 4G는 4kg/10a 수준에서 벼멸구 방제효과 발현은 충분하였다. 12. 폿트시험과 포장시험 결과가 일치하지 않았던 이유에 대해서는 금후에 연구검토가 요망된다.

• Asian-Australasian Journal of Animal Sciences
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• 제26권6호
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• pp.772-779
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• 2013

Linkage disequilibrium (LD) plays an important role in genomic selection and mapping quantitative trait loci (QTL). In this study, the pattern of LD and effective population size ($N_e$) were investigated in Chinese beef Simmental cattle. A total of 640 bulls were genotyped with IlluminaBovinSNP50BeadChip and IlluminaBovinHDBeadChip. We estimated LD for each autosomal chromosome at the distance between two random SNPs of <0 to 25 kb, 25 to 50 kb, 50 to 100 kb, 100 to 500 kb, 0.5 to 1 Mb, 1 to 5 Mb and 5 to 10 Mb. The mean values of $r^2$ were 0.30, 0.16 and 0.08, when the separation between SNPs ranged from 0 to 25 kb to 50 to 100 kb and then to 0.5 to 1 Mb, respectively. The LD estimates decreased as the distance increased in SNP pairs, and increased with the increase of minor allelic frequency (MAF) and with the decrease of sample sizes. Estimates of effective population size for Chinese beef Simmental cattle decreased in the past generations and $N_e$ was 73 at five generations ago.

• 농약과학회지
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• 제16권4호
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• pp.376-382
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• 2012

식물추출물 함유(마늘추출액, 잔톡실럼오일, 레몬그라스오일 30%) 유제의 물벼룩급성독성 결과 마늘추출액 함유 30% 유제의 $EC_{50}$은 $3.3mg\;L^{-1}$로 EPA 기준으로 보통독성정도이었고, 레몬그라스오일, 잔톡실럼(Zanthoxylum)오일 함유 30% 유제의 $EC_{50}$는 $10mg\;L^{-1}$ 이상으로 저독성이었다. 송사리급성독성 시험의 경우, 마늘추출액 함유 30% 유제의 $LC_{50}$ 값이 $3.0mg\;L^{-1}$으로 나타났으며 나머지 두 유제는 모두 $10mg\;L^{-1}$ 이상으로 확인되었다. 꿀벌급성독성시험은 접촉과 섭식 시험으로 나누어서 실시하였고, 접촉독성의 경우 모두 100 a.i ${\mu}g\;bee^{-1}$ 이상으로 확인되었다. 섭식독성의 경우 마늘추출액 함유 30% 유제의 $LD_{50}$ 값이 44.3 a.i ${\mu}g\;bee^{-1}$ 이었으며 잔톡실럼(Zanthoxylum)오일과 레몬그라스오일 함유 30% 유제의 경우 $LD_{50}$ 값이 100 a.i ${\mu}g\;bee^{-1}$ 이상으로 나타나 독성이 낮은 것으로 판단되었다. 지렁이급성독성시험의 경우, 마늘추출액, 잔톡실럼(Zanthoxylum)오일, 레몬그라스오일 함유 30% 유제의 $LC_{50}$ 값이 각각 267, 592, $430mg\;kg^{-1}$ 로 나타났는데 이는 제품살포물량을 확정한 뒤 환경추정농도를 이용한 위해성평가를 통해 안전성을 확보한다면 친환경 농자재로서 활용이 가능할 것으로 판단하였다.

• 한국식품위생안전성학회지
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• 제11권4호
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• pp.299-306
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• 1996

6-[(N-3,4-Dibromophenyl)amino]-7-chloro-5,8-quinolinedione(FCK13) was tested for antifungal activities. The MIC values were determined by the two-fold dilution method. The therapeutic potential of RCK13 had been assessed in comparison with ketoconazole and fluconazole against systemic infections with candida albicans in normal mice. RCK13 had ED50,0.80$\pm$0.21 mg/kg but ketoconazole had ED50, 8.00$\pm$0.73 mg/kg respectively. And administered RCK13 at the ED50 for 14 days improved survival rates as well as ketoconazole. Acute oral toxicity studies of RCK13 were carried out in ICR mice of both sexes. These acute oral toxicities of RCK13 were low and LD50 values were over 2,850 mg/kg in ICR mice. The genotoxicities of RCK13 had been evaluated. RCK13 was negative in Ames test with Salmonella typhimurium and chromosomal aberration test in CHL cells. The clastogenicity was tested on the RCK13 with in vivo mouse micronucleus assay. RCK13 did not show any clastogenic effect in mouse peripheral blood and was negative in mouse micronucleus assay. These results indicate that RCK13 has no genotoxic potential under these experimental conditions.

• Journal of Microbiology and Biotechnology
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• 제18권2호
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• pp.314-321
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• 2008

Acaricidal effects of materials derived from Diospyros kaki roots against Dermatophagoides farinae and D. pteronyssinus were assessed using impregnated fabric disk bioassay and compared with that of the commercial benzyl benzoate. The observed responses varied according to dosage and mite species. The $LD_{50}$ values of the chloroform extract of Diospyros kaki roots were 1.66 and $0.96{\mu}g/cm^2$ against D. farinae and D. pteronyssinus. The chloroform extract of Diospyros kaki roots was approximately 15.2 more toxic than benzyl benzoate against D. farinae, and 7.6 times more toxic against D. pteronyssinus. Purification of the biologically active constituent from D. kaki roots was done by using silica gel chromatography and high-performance liquid chromatography. The structure of the acaricidal component was analyzed by GC-MS, $^1H-NMR,\;^{13}C-NMR,\;^1H-^{13}C$ COSY-NMR, and DEPT-NMR spectra, and identified as plumbagin. The acaricidal activity of plumbagin and its derivatives (naphthazarin, dichlon, 2,3-dibromo-1,4-naphthoquinone, and 2-bromo-1,4-naphthoquinone) was examined. On the basis of $LD_{50}$ values, the most toxic compound against D. farinae was naphthazarin $(0.011{\mu}g/cm^2)$ followed by plumbagin $(0.019{\mu}g/cm^2),$ 2-bromo-1,4-naphthoquinone $(0.079{\mu}g/cm^2)$, dichlon $(0.422{\mu}g/cm^2)$, and benzyl benzoate $(9.14{\mu}g/cm^2)$. Additionally, the skin color of the dust mites was changed from colorless-transparent to dark brown-black by the treatment of plumbagin. Similar results have been exhibited in its derivatives (naphthazarin, dichlon, and 2-bromo-1,4-naphthoquinone). In contrast, little or no discoloration was observed for benzyl benzoate. From this point of view, plumbagin and its derivatives can be very useful for the potential control agents, lead compounds, and indicator of house dust mites.

• 약학회지
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• 제34권2호
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• pp.126-132
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• 1990

To enhance the activity of ibuprofen, amides of ibuprofen, 1-piperazinyl-2-(4-isobutylphenyl)propionamide(Ibu-P.A.) and 1-(4-methylpiperazinyl)-2-(4-isobutylphenyl)propionamide (Ibu-M.P.), were synthesized and the pharmaceutical properties and the pharmacological activities of the amides were studied. The lipid:water partition coefficients and pKa values were examined in vitro, and the antiinflammatory effect, analgesic effects, acute toxicity, and intestinal absorption were studied for the amides and compared with ibuprofen in vivo. The results are summarized as belows; 1) The lipid:water partition coefficients of Ibu-M.P. were higher than those of ibuprofen. 2) The calculated pKa values of ibuprofen and Ibu-M.P. were 5.49 and 8.66, respectively. 3) The antiinflammatory effects of ibuprofen, Ibu-P.A., and Ibu-M.P. were same intensity, but the duration of the effects of Ibu-P.A. and Ibu-M.P. were longer than that of ibuprofen. 4) The analgesic effect of Ibu-M.P. was more potent than those of ibuprofen and Ibu-P.A. in the acetic acid-induced writhing test. 5) The $LD_{50}$ was 495 mg/kg for ibuprofen, 187 mg/kg for Ibu-M.P., and over 1250 mg/kg for Ibu-P.A.. 6) The absorption rate constants(k) and half-life($t_{1/2}$) were 0.74($hr^{-1}$) and 0.94(hr) for ibuprofen, and 0.72 ($hr^{-1}$) and 0.96 (hr) respectively for Ibu-M.P..

• Journal of Microbiology and Biotechnology
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• 제16권10호
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• pp.1591-1596
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• 2006

Acaricidal effects of materials derived from Caesalpinia sappan heartwoods against Dermatophagoides farinae and D. pteronyssinus were assessed and compared with those evidenced by commercial benzyl benzoate and DEET. The observed responses varied according to dosage and mite species. The $LD_{50}$ values of the methanol extracts derived from C. sappan heartwoods were 6.13 and $5.44{\mu}g/cm^3$ against D. farinae and D. pteronyssinus, respectively. Furthermore, the ethyl acetate fraction derived from the methanol extract was approximately 8.71 more toxic than DEET against D. farinae, and 4.73 times more toxic against D. pteronyssinus. The biologically active constituent from the ethyl acetate fraction of C. sappan heartwood extract was purified via silica gel chromatography and high-performance liquid chromatography. The structure of the acaricidal component was analyzed by $GC-MS,\;^1H-NMR,\;^{13}C-NMR,\;^1H-^{13}C\;COSY-NMR$, and DEPT-NMR spectroscopy, and identified as juglone (5-hydroxy-l,4-naphthoquinone). Based on the $LD_{50}$ values of juglone and its derivatives, the most toxic compound against D. farinae was juglone ($0.076{\mu}g/cm^3$), followed by benzyl benzoate ($9.143{\mu}g/cm^3$) and 2methyl-l,4-naphthoquinone ($40.0{\mu}g/cm^3$). These results indicate that the acaricidal activity of C. sappan heartwoods is likely to be the result of the effects of juglone. Additionally, juglone treatment was shown to effect a change in the color of the cuticles of house dust mites, from colorless-transparent to dark brownish-black. Accordingly, as a naturally occurring acaricidal agent, C. sappan heartwood-derived juglone should prove to be quite 'useful as a potential control agent, lead compound, and house dust mite indicator.

• 대한약침학회지
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• 제5권1호
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• pp.7-26
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• 2002

Objective: The purpose of this study was to investigate acute and subacute toxicity and sarcoma-180 anti-cancer effects of herbal acupuncture with Carthami- Tinctorii fructus (CF) in mice and rats. Method: Balb/c mice were injected intraperitoneally with Carthami - Tinctorii fructus (CF) for $LD_{50}$ and acute toxicity test. Sprague Dawley rats were injected intraperitoneally with Carthami- Tinctorii fructus (CF) for subacute toxicity test. The Carthami- Tinctorii fructus herbal-acupuncture was injected on Chung-wan (CV12) of mice with Sarcoma-180 cancer cell line. Results: 1. $LD_{50}$ was uncountable as none of the subjects expired during the test. 2. In acute toxicity test, toxic symptoms were not detected, but the body weight of mice was increased in treatment Ⅰ, treatment Ⅱ groups, compared to the normal group.(p<0.05) 3. In acute toxicity test of serum biochemical values of mice, glucose was increased in treatment Ⅰ and treatment Ⅱ groups, total cholesterol was increased in treatment I group, GOT was decreased in treatment Ⅱ group, and GPT was decreased in treatment Ⅰ group, compared to the normal group.(p<0.05) 4. The clinical signs and the body weight of mice treated with 0.1 cc, 0.2cc Carthami- Tinctorii fructus (CF) were not affected during the subacute toxicity test. 5. In subacute toxicity test, treatment groups didn't show significant changes in complete blood count test (CBC) of rats, compared to the nonnal group.(p<0.05) 6. In subacute toxicity test of serum biochemical values of rats, uric acid was decreased in treatment Ⅰ and treatment Ⅱ groups, compared to the nonnal group, triglyceride was decreased in treatment I group, compared to the normal group, GOT and GPT were decreased in treatment I and treatment Ⅱ groups, and alkaline phosphatase was decreased in treatment Ⅰ and treatment Ⅱ groups, compared to the normal group.(p<0.05) 7. Median survival time was increased in all the treatment groups for Sarcoma-180 cancer cell treated with Carthmni- Tinctorii fructus (CF).(p<0.05) 8. Natural killer cell activity was significantly increased in all the treatment groups compared to the normal group.(p<0.05) 9. Interleukin-2 productivity was decreased in treatment Ⅰ and treatment Ⅱ groups.(p<0.05) Conclusion: According to the results, we can conclude herbal-acupuncture of Carthami-Tinctoriifructus (CF) caused negligible toxkity, and had anti-tumor effects in mice.

• 대한약침학회지
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• 제6권1호
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• pp.76-94
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• 2003

Objectives : The purpose of this study was to investigate Acute$\cdot$Subacute Toxicity and Anti-cancer Effect of K-Herbal-acupuncture in mice and rats. Methods : Balb/c mice were injected intraperitoneally with K-herbal-acupuncture for $LD_{50}$ and acute toxicity test. Sprague-Dawley rats were injected intraperitoneally with K-herbal-acupuncture for subacute toxicity test. K-Herbal-acupuncture was injected on abdomen of mice with S-180 cancer cell line. Result : 1. $LD_{50}$ of K-Herbal-acupuncture was limited $4{\times}10^{-3}$ml/kg~$2{\times}10^{-3}$ml/kg by the test. 2. In acute toxicity test, all of mice were down to the moving reflex, but the weight of mice was increased in treatment group, compared with the normal group. (P<0.05) 3. In acute toxicity test of serum biochemical values of mice, glucose was increased in treatment II group, total cholesterol was increased both treatments.(P<0.05) 4. In subacute toxicity test, the clinical signs of toxication was down to the moving reflex, but it is not severe like acute toxicity test, and observed weight loss at the treatments. 5. In subacute toxicity test, liver weight was decreased compared with the normal group. (P<0.05) 6. In subacute toxicity test of complete blood count test (CBC) of rat, HCT was decreased in treatments, compared with the normal group.(P<0.05) 7. In subacute toxicity test of serum biochemical values of rat, uric acid and triglyceride were decreased, and glucose was increased in treatment groups compared with the control group. (P<0.05) 8. Median survival time was increased about $45\%$ in treatment groups compared with the control group.(P<0.05) 9. Natural killer cell activity was increased in B16F10 lung cancer model, but it was not in sarcoma-180 abdomen cancer. 10. In interleukin-2 productivity test, treatment groups didn't show significant change in lung cancer and abdomen cancer, compared with the normal group.(P<0.005) 11. In making an examination of metastatic cancer with the naked eye, melanoma metastasized in the Lung of C57BL/6 mice. The treated group showed more Melanoma than the control in the numbers and volume. Conclusion : According to the result, K-herbal-acupuncture need further study to know the function and effect in cancer.

• 한국환경농학회지
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• 제7권1호
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• pp.58-64
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• 1988

살충제 Monocrotophos의 독성평가(毒性評價)를 위하여 흰쥐에 $1{\sim}4$주동안 투여후 급성(急性) 및 아급성(亞急性) 독성검정(毒性檢定) 그리고 혈액성상(血液性狀) 및 혈장중(血漿中) Cholinesterase(ChE)를 측정(測定)하여 그 변화(變化)를 구명(究明) 하므로서 농약중독(農藥中毒)에 대(對)한 기초자료(基礎資料)를 얻고자 본(本) 시험(試驗)을 실시(實施)한 결과(結果)는 다음과 같다. 1. Monocrotophos의 급성경구(急性經口) 반수치사(半數致死) 약량(藥量)$LD_{50}$은 흰쥐에서 암, 수 각각(各各) 5.1, 8.7mg/kg이었고 복강내(腹腔內) 투여시(投與時)에는 암컷이 4.9mg/kg 수컷이 6.0mg/kg 이었다. 2. Monocrotophos는 경구(經口)에 6.4mg/kg, 복강내(腹腔內) 4.0mg/kg 투여시(投與時)에 4시간(時間)이 지난후 암, 수 모두의 혈장(血漿) ChE 활성도(活性度)를 최대(最大)로 억제(抑制) 시켰고 투여(投與) 24시간(時間) 이후(以後)부터는 점차 회부(回復) 되었다. 3. Monocrotophos를 흰쥐에 4주간(週間) 경구투여(經口投與) 할 때 3.5mg/kg/day 투여군(投與群)에서는 대조군(對照群)에 비(比)해 암, 수 모두 체중증체량(體重增體量)과 수컷에서 사료섭취량이 현저하게 감소(減少) 되었다. 4. 약제 투여시(投與時)에는 혈장(血漿) ChE 활성도(活性度)를 크게 억제(抑制)시켰으나 투여(投與) 중단(中斷)후에는 2주(週)가 지나면서 거의 회부(回復)되었다. 5. 약제투여(藥劑投與)된 쥐의 적혈구(赤血球), 백혈구(白血球), Ht치(値), Hb량(量)에 대(對)한 혈액상(血液狀) 변화(變化)는 거의 없었다.