• 한국동물위생학회지
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• 제44권4호
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• pp.271-281
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• 2021

Pathogenic Escherichia coli (E. coli) is one among the most important agents of diarrhea in calves. From January to December 2021, 108 isolates from feces of calves with diarrhea were investigated for enterotoxigenic E. coli (ETEC), enteropathogenic E. coli (EPEC), shiga toxin-producing E. coli (STEC), enteroaggregative E. coli (EAEC), and enteroinvasive E. coli (EIEC) using real-time PCR. In addition, the genes for F5, F17 and F41 fimbriae were detected by PCR. The most frequently isolated pathotypes were EPEC/STEC (29 isolates), and ETEC/EPEC/STEC (29 isolates). ETEC/EPEC, and ETEC/STEC were also found in 10 isolates. EPEC, STEC, and ETEC were detected in 13, 11, and 6 respectively. EAEC, and EIEC was not detected. Antimicrobial resistance test was carried out by agar disc diffusion method with 14 antimicrobials. Among 108 pathogenic E. coli isolates, 107 isolates were resistant to at least one of 14 antibiotics used in this study, 99 (91.7%) were resistant to two or more antimicrobials, and a single remarkable isolate was resistant to 14 antimicrobials. The isolates were primarily resistant to penicillins, streptomycin, tetracycline, ceftiofur, Trimethoprim/sulfamethoxazole, Kanamycin, and Ciprofloxacin. The high rate of resistance in pathogenic E. coli, sometimes to multiple drugs, may complicate future options for treating human infections. These results may bu used for diagnosis and therpeitic purposes in calves with diarrhea.

• Journal of Preventive Medicine and Public Health
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• 제3권1호
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• pp.1-16
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• 1970

우리나라에서 공중보건상(公衆保健上) 중요(重要)한 연충류감염에 대(對)하여 1969년(年) 현재(現在) 실시(實施)한 관리(管理) 현황(現況)을 조사(調査)하였으며, 그 결과(結果)를 보면 1966년(年)부터 1969년(年)까지의 학생기생충검사 및 회충구충 사업(事業)에 있어서 그 간(間) 회충감염률의 저하(低下)를 별(別)로 가져오지 못하였음이 나타났으며 따라서 앞으로 본(本) 사업(事業)의 개선(改善) 또는 보다 적극적인 사업(事業)의 추진(推進)이 요망(要望)된다. 보건사회부(保健社會部)에서 지정(指定)한 지역(地域)에서 $1965{\sim}1968$년(年)의 4년간(年間)에 실시(實施)한 폐(肺) 및 간(肝) 디스토마 집단치료사업(集團治療事業)에 있어서는 추정환자수(推定患者數)의 감소(減少)를 크게 가져오지 못하여 사업(事業)의 부진(不振)함을 나타내었다. 구충제제조에 있어서 너무 많은 제조회사(製造會社)에서 많은 종류(種類)의 상품(商品)이 제조(製造)되어 난맥(亂脈)을 이루고 있었으며 따라서 구충제 제조허가(製造許可)에 있어서의 재고(再考)가 요구(要求)된다. 인분처리(人糞處理) 상황(狀況)에 있어서 도시지역(都市地域)에 있어서는 위생적(衛生的)인 하수도(下水道)가 미비(未備)되고 하수종말처리장(下水終末處理場)이 전연(全然) 없고 수거처리(收去處理)되고 있으며 한편 농촌지역(農村地域)의 인분처리(人糞處理)는 거의 수임상태(收任狀態)로 비위생적(非衛生的)이어서 기생충 전파(傳播)의 가장 큰 요인(要因)의 하나가 된다. 인분사용금지구역(人糞使用禁止區域)으로 지정된 전국(全國) 55개(個) 지역중(地域中) 34개(個) 지역(地域)에서 총(總) 170건(件)의 토양(土壤)(밭흙)을 채취하여 검사(檢査)한바 그중(中) 44%에서 회충난이 검출(檢出)되었다. 청정채소보급소(淸淨菜蔬補給所)와 일반시장(一般市場)에서 판매하는 각종 채소(菜蔬) 각(各) 64건(件)씩을 구입하여 검사(檢査)한바 회충난검출률은 보급소(補給所)의 것이 25%, 일반시장(一般市場)의 것이 36%로 나타났다. 전국(全國) 보건소(保建所)에서의 기생충병관리사업 실적(實績)과 기생충 검사능력(檢査能力)은 저조(低調)하였다. 보건사회부(保健社會部)의 기생충병 관리(管理) 예산(豫算)은 아주 적으며, 세로판후층도말법(厚層塗抹法)에 소요(所要)되는 실비(實費)를 산출(算出)한바 1건당(件當) 8원이었다. 기생충병 관리원칙(管理原則)은 기생충 자체(自體)의 생활사(生活史)를 중심(中心)으로 하는 요인(要因)과 이에 영향을 주는 제환경적(諸環境的) 요인(要因), 그리고 감염(感染)과 관계되는 인간숙주측(人間宿主側) 요인(要因)등의 여러가지 요인(要因)에 의(依)해서 발생(發生)되는 기생충감염의 생성과정중(生成過程中)의 어느 한 부분(部分) 또는 그 이상(以上)을 제거하는 방향으로 이루어지며, 그 방법에는 다음과 같은 사항들을 들수 있다. (1) 감염자(感染者)에 대(對)한 집단치료(集團治療)로서 감염(感染)의 근원(根源)이 되는 병원소(病原巢)를 제거(除去)한다. (2) 보충동물을 제거(除去)함으로써 인체감염(人體感染)과 관계되는 동물병원소(動物病原巢)를 제거(除去)한다. (3) 보충숙주의 배설물(排泄物)에 대(對)한 위생적(衛生的) 처리(處理)인바 여기에서 주요(主要)한 것은 도시지역(都市地域)에서의 완비(完備)된 하수도(下水道)와 하수종말처리장(下水終末處理場), 그리고 농촌지역(農村地域)에서의 비흡취식(非吸取式)인 위생적편소(衛生的便所)의 설치(設置) 등이며 이것은 우리나라에서의 인분비료사용(人糞肥料使用)의 폐지(廢止)와 국가경제(國家經濟)의 향상(向上)으로서 그 목적(目的)을 달성(達成)할 수 있게 된다. (4) 매개체(媒介體) 및 중간숙주(中間宿主)의 관리(管理)로서 토양(土壤)의 기생충오염방지, 식품위생(食品衛生), 곤충관리 그리고 패류관리(貝類管理) 등을 들 수 있다. (5) 비위생적(非衛生的) 태도(態度)와 폐습(弊習)의 개선(改善)으로서 기생충감염과 관계 있는 입분비료(入糞肥料)의 사용(使用), 식습관(食習慣) 및 개인위생(個人衛生) 등이 문제된다. (6) 화학예방(化學豫防) 및 예방접종(豫防接種)은 전술(前述)한 바와같은 전파예방(傳播豫防) 조치(措置)가 실패(失敗)하는 경우 체내(體內)에 침입(侵入)되는 기생충체를 체내(體內)의 방어력(防禦力)에 의(依)하여 그 감염(感染)의 성립(成立)과 성충에의 발육(發育)을 방지(防止)하려는 조치(措置)로서 이에 대(對)한 앞으로의 보다 적극적인 연구(硏究) 개발(開發)이 요망(要望)된다.

• 대한핵의학회지
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• 제32권3호
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• pp.298-304
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• 1998

목적 : Re-188 황 교질을 제조하여 관절염 활액막절제술, 복강내 암전이 치료제로서의 사용 가능성을 알아보았다. 대상 및 방법: Re-188 황 교질의 표지에 EDTA $Na_2.2H_2O$의 양, $KReO_4$의 존재유무, pH의 영향을 관찰하였다. Re-188 황 교질의 안정성을 실온에서 24 시간, 사람혈청과 활액에서 72 시간동안 관찰하였다. Re-188 황 교질의 입자 크기 분포는 여러 가지 크기의 필터를 사용하여 측정하였다. Re-188 황 교질을 실험 동물에 투여하여 생체내 분포와 체외 대사량을 관찰하였다. 결과: Re-188 황교질은 sodium thiosufate 40 mg, EDTA $Na_2.2H_2O$ 0.8 mg, $KReO_4$ 0.8 mg, pH 1의 조건에서 60분 동안 가열시 표지효율이 $64.5{\pm}5.8%$ (n=5)로 가장 높았고, 이를 정제하였을때 방사화학적 순도는 99%이상이었다. Re-188 황 교질은 실온에서 24 시간, 혈청과 활액에서 72시간 동안 모두 방사화학적 순도가 99%이상으로 매우 안정하였다. Re-188 황 교질의 입자크기 분포는 $1{\mu}m$ 이하가 0.3%, $1{\sim}5{\mu}m$ 11.2%, $5{\sim}10{\mu}m$ 35.8%, $10{\mu}m$ 이상은 52.8%으로 나타났다. 마우스의 꼬리정맥으로 Re-188 황 교질을 주사한 후 1 시간에 폐와 간의 섭취율($37.30{\pm}5.36$, $32.33{\pm}5.79%$ ID/organ)이 가장 높았으며, 근육의 섭취율은 $6.60{\pm}0.02 %$ID/organ였다. 마우스복강내에 Re-188 황 교질을 주사한 후 1, 24 시간에 복강외 장기의 섭취율은 $0.1{\pm}0.1$, $0.4{\pm}0.1%$ ID/organ으로 매우 낮았으며, 주사 후 70 시간까지 뇨와 대변으로 배설된 양은 $2.68{\pm}0.50%$와 $0.95{\pm}0.17%$였다. 토끼 무릎관절에 Re-188 황 교질을 주사한 후 24 시간에 무릎을 제외한 모든 장기에서의 섭취율은 0.07% ID/g 이하로 매우 낮았다. 결론: 이실험에서 표지한 Re-188 황 교질은 표지효율과 안정성이 높고 임상적으로 방사선 활액막 절제술 등에 사용할 수 있을 것으로 생각한다.

• 미생물학회지
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• 제40권4호
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• pp.286-294
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• 2004

1997년과 1998년 사이에 설사 증상을 보이는 돼지의 분변으로부터 총56균주의 Escherichia coli를 분리하여 이중 용혈성을 나타내는 38균주의 항생제 내성과 독소 생산능을 확인하였다. 항생제 한천 희석법으로 최소억제농도(minimal inhibitory concentration)를 측정한 결과 36균주$(94.7\%)$가 tetracycline에 대해 내성을 나타내었고, 27주$(71.0\%)$는 ampicillin에 내성, 26균주$(68.4\%)$는 chloramphenicol에 내성, 그리고 21균주$(55.2\%)$는 tri-methoprim에 내성을 나타내었으나, aztreonam, amikacin, norfloxacin에 내성을 나타낸 균주는 발견되지 않았다. 이중 4가지 이상의 항생제에 대해 내성을 가지는 다제내성(multiple drug resistance, MDR)을 보인 균주는 총 38 균주 중 21균주$(55.3\%)$였다. 또한 이중 디스크 시험법(Double Disk Synergy Test)을 수행한 결과 extended spectrum $\beta-lactamase$를 생산하는 균주는 없는 것으로 나타났다. 이들 중 가장 많은 수의 균주가 내열성 독소$(ST,89.5\%)$를 생산하였고, 다음으로 베로 독소(VT와 VTe, 각각$47.4\%$)와 이열성 독소$(LT,31.6\%)$를 생산하는 것으로 나타났다. 이 중에서 8균주$(21.0\%)$는 57만을 생산하였던 반면에 12균주$(31.6\%)$는 LT와 ST를 동시에 생산하였고, 13균주$(34.2\%)$는 ST, VT, VTe를 동시에 생산하였으며, 5균주$(13.2\%)$는 VT와 VTe를 동시에 생산하는 것으로 나타났다. 그러나 네 가지 독소를 동시에 생산하는 균주는 없었다. 또한 이 균주들은 매우 다양한 혈청형(serotype)을 가지고 있음이 확인되었다. 사람에 직접적인 유해성을 가지고 있는 지 확인하기 위해 사람 방광 유래의 T-24세포와 장내 표피 유래의 Caco-2세포에 대한 부착능을 시험하였을 때, 16균주$(42.1\%)$가 T-24방광 세포에, 그리고 17균주$(44.7\%)$가 Caco-2장세포에 대해 강한 부착능을 나타내었다. 특히 11균주$(28.9\%)$는 두 세포 모두에 강한 부착능을 가지고 있었다. Filter mating method를 수행하여 이들 균주들의 독소 생산 유전자와 항생제 내성 유전자가 사람에서 분리된 균주로 전달되는 것을 확인할 수 있었다. 본 실험의 결과는 설사 중상을 나타내는 돼지로부터 분리된 용혈성 E. coli의 독성과 세포 부착능력, 그리고 항생제 내성간의 상호 연관성을 보여주지 않았으나 동물 분리 세균의 항생제 내성과 독소 생산 능력이 유전자 전달을 통해서 뿐만 아니라 세균의 직접 접촉에 의해서도 인체로 전달될 수 있는 것을 보여주는 것이다.

• 미생물학회지
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• 제55권3호
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• pp.274-277
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• 2019

본 연구에서는 건강한 한국인 분변으로부터 Ruminococcus sp. KGMB03662 균주를 분리하고 유전체서열을 PacBio Sequel 플랫폼을 사용하여 분석하였다. 염색체의 크기는 2,707,502 bp로 G + C 구성 비율은 43.09%, 총 유전자수는 2,484개, 단백질 코딩 유전자는 2,367개, rRNA는 14개 및 tRNA는 53개로 구성되었다. 본 유전체로부터 가수분해효소, 지방산생합성 및 대사와 항생제생합성 및 내성 관련 유전자를 확인하였다. 이러한 유전체의 분석은 KGMB03662 균주가 사람의 건강 및 질병에 관여할 것으로 여겨진다.

• Journal of Nutrition and Health
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• 제8권1호
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• pp.15-37
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• 1975

I. Subject of the study A study on the nutritive value and utilization of powdered seaweeds. II. Purpose and Importance of the study A. In Korea the shortage of food will be inevitable by the rapidly growing population. It will be very important study to develop a new food from the seaweeds which were not used hitherto for human consumption. B. The several kinds of seaweeds have been used by man in Korea mainly as side-dishes. However, a properly powdered seaweed will enable itself to be a good supplement or mixture to certain cereal flours. C. By adding the powdered seaweed to any cereals which have long been staple foods in this country the two fold benefits; saving of cereals and change of dietary pattern, will be secured. III. Objects and scope of the study A. Objects of the study The objects will come under four items. 1. To develop a powdered seaweed as a new food from the seaweeds which have been not used for human consumption. 2. To evaluate the nutritional quality of the products the analysis for chemical composition and animal feeding experiment will be conducted. 3. Experimental cocking and accepability test will be conducted for the powdered products to evaluate the value as food stuff. 4. Sanitary test and also economical analysis will be conducted for the powdered products. B. Scope of the study 1. Production of seaweed powders Sargassum fulvellum growing in eastern coast and Sargassum patens C.A. in southern coast were used as the material for the powders. These algae, which have been not used for human consumption, were pulverized through the processes of washing, drying, pulverization, etc. 2. Nutritional experiments a. Chemical composition Proximate components (water, protein, fat, cellulose, sugar, ash, salt), minerals (calcium, phosphorus, iron, iodine), vitamins (A, $B_1,\;B_2$ niacin, C) and amino acids were analyzed for the seaweed powders. b. Animal feeding experiment Weaning 160 rats (80 male and 80 female rats) were used as experimental animals, dividing them into 16 groups, 10 rats each group. Each group was fed for 12 weeks on cereal diet (Wheat flour, rice powder, barley powder, potato powder, corn flour) with the supplementary levels of 5%, 10%, 15%, 20% and 30% of the seaweed powder. After the feeding the growth, feed efficiency ratio, protain efficiency ratio and ,organs weights were checked and urine analysis, feces analysis and serum analysis were also conducted. 3. Experimental cooking and acceptability test a. Several basic studies were conducted to find the characteristics of the seaweed powder. b. 17 kinds of Korean dishes and 9 kinds of foreign dishes were prepared with cereal flours (wheat, rice, barley, potato, corn) with the supplementary levels of 5%, 10%, 15%, 20% and 30% of the seaweed powder. c. Acceptability test for the dishes was conducted according to plank's Form. 4. Sanitary test The heavy metals (Cd, Pb, As, Hg) in the seaweed powders were determined. 5. Economical analysis The retail price of the seaweed powder was compared with those of other cereals in the market. And also economical analysis was made from the nutritional point of view, calculating the body weight gained in grams per unit price of each feeding diet. IV. Results of the study and the suggestion for application A. Chemical composition 1. There is no any big difference in proximate components between powders of Sargassum fulvellum in eastern coast and Sargassum patens C.A. in southern coast. Seasonal difference is also not significant. Higher levels of protein, cellulose, ash and salt were found in the powders compared with common cereal foods. 2. The levels of calcium (Ca) and iron (Fe) in the powders were significantly higher than common cereal foods and also rich in iodine (I). Existence of vitamin A and vitamin C in the Powders is different point from cereal foods. Vitamin $B_1\;and\;B_2$ are also relatively rich in the powders.'Vitamin A in ·Sargassum fulvellum is high and the levels of some minerals and vitamins are seemed4 to be some influenced by seasons. 3. In the amino acid composition methionine, isoleucine, Iysine and valine are limiting amino acids. The protein qualities of Sargassum fulvellum and Sargassum patens C.A. are seemed to be .almost same and generally ·good. Seasonal difference in amino acid composition was found. B. Animal feeding experiment 1. The best growth was found at.10% supplemental level of the seaweed Powder and lower growth rate was shown at 30% level. 2. It was shown that 15% supplemental level of the Seaweed powder seems to fulfil, to some extent the mineral requirement of the animals. 3. No any changes were found in organs development except that, in kidney, there found decreasing in weight by increasing the supplemental level of the seaweed powder. 4. There is no any significant changes in nitrogen retention, serum cholesterol, serum calcium and urinary calcium in each supplemental level of the seaweed powder. 5. In animal feeding experiment it was concluded that $5%{\sim}15%$ levels supplementation of the seaweed powder are possible. C. Experimental cooking and acceptability test 1. The seaweed powder showed to be utilized more excellently in foreign cookings than in Korean cookings. Higher supplemental level of seaweed was passible in foreign cookings. 2. Hae-Jo-Kang and Jeon-Byung were more excellent than Song-Pyun, wheat cake, Soo-Je-Bee and wheat noodle. Hae-Je-Kang was excellent in its quality even as high as 5% supplemental level. 3. The higher levels of supplementation were used the more sticky cooking products were obtained. Song-Pyun and wheat cake were palatable and lustrous in 2% supplementation level. 4. In drop cookie the higher levels of supplementation, the more crisp product was obtained, compared with other cookies. 5. Corn cake, thin rice gruel, rice gruel and potato Jeon-Byung were more excellent in their quality than potato Man-Doo and potato noodle. Corn cake, thin rice gruel and rice gruel were excellent even as high as 5% supplementation level. 6. In several cooking Porducts some seaweed-oder was perceived in case of 3% or more levels of supplementation. This may be much diminished by the use of proper condiments. D. Sanitary test It seems that there is no any heavy metals (Cd, Pb, As, Hg) problem in these seaweed Powders in case these Powders are used as supplements to any cereal flours E. Economical analysis The price of the seaweed powder is lower than those of other cereals and that may be more lowered when mass production of the seaweed powder is made in future. The supplement of the seaweed powder to any cereals is also economical with the criterion of animal growth rate. F. It is recommended that these seaweed powders should be developed and used as supplement to any cereal flours or used as other food material. By doing so, both saving of cereals and improvement of individual's nutrition will greatly be achieved. It is also recommended that the feeding experiment for men would be conducted in future.

• 대한약리학회지
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• 제16권2호
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• pp.55-70
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• 1980

The pharmacological and microbiological studies of Cefoperazone (T-1551, Toyama Chemical Co., Japan) were conducted in vitro and in vivo. The studies included stability and physicochemical characteristics, antimicrobial activity, animal and human pharmacokinetics, animal pharmacodynamics and safety evaluation of Cefoperazone sodium for injection. 1) Stability and physicochemical characteristics. Sodium salt of cefoperazone for injection had a general appearance of white crystalline powder which contained 0.5% water, and of which melting point was $187.2^{\circ}C$. The pH's of 10% and 25% aqueous solutions were 5.03 ana 5.16 at $25^{\circ}C$. The preparations of cefoperazone did not contain any pyrogenic substances and did not liberate histamine in cats. The drug was highly compatible with common infusion solutions including 5% Dextrose solution and no significant potency decrease was observed in 5 hours after mixing. Powdered cefoperazone sodium contained in hermetically sealed and ligt-shielded container was highly stable at $4^circ}C{\sim}37^{\circ}C$ for 12 weeks. When stored at $4^{\circ}C$ the potency was retained almost completely for up to one year. 2) Antimicrobial activity against clinical isolates. Among the 230 clinical isolates included, Salmonella typhi was the most susceptible to cefoperazone, with 100% inhibition at MIC of ${\leq}0.5{\mu}g/ml$. Cefoperazone was also highly active against Streptococcus pyogenes(group A), Kletsiella pneumoniae, Staphylococcus aureus and Shigella flexneri, with 100% inhibition at $16{\mu}g/ml$ or less. More than 80% of Escherichia coli, Enterobacter aerogenes and Salmonella paratyphi was inhibited at ${\leq}16{\mu}/ml$, while Enterobacter cloaceae, Serratia marcescens and Pseudomonas aerogenosa were somewhat less sensitive to cefoperagone, with inhibitions of 60%, 55% and 35% respectively at the same MIC. 3) Animal pharmacokinetics Serum concentration, organ distritution and excretion of cefoperazone in rats were observed after single intramuscular injections at doses of 20 mg/kg and 50 mg/kg. The extent of protein binding to human plasma protein was also measured in vitro br equilibrium dialysis method. The mean Peak serum concentrations of $7.4{\mu}g/ml$ and $16.4{\mu}/ml$ were obtained at 30 min. after administration of cefoperazone at doses of 20 mg/kg and 50 mg/kg respectively. The tissue concentrations of cefoperazone measured at 30 and 60 min. were highest in kidney. And the concentrations of the drug in kidney, liver and small intestine were much higher than in blood. Urinary and fecal excretion over 24 hours after injetcion ranged form 12.5% to 15.0% in urine and from 19.6% to 25.0% in feces, indicating that the gastrointestinal system is more important than renal system for the excretion of cefoperazone. The extent of binding to human plasma protein measured by equilibrium dialysis was $76.3%{\sim}76.9%$, which was somewhat lower than the others utilizing centrifugal ultrafiltration method. 4) Animal pharmacodynamics Central nervous system : Effects of cefoperazone on the spontaneous movement and general behavioral patterns of rats, the pentobarbital sleeping time in mice and the body temperature in rabbits were observed. Single intraperitoneal injections at doses of $500{\sim}2,000mg/kg$ in rats did not affect the spontaneous movement ana the general behavioral patterns of the animal. Doses of $125{\sim}500mg/kg$ of cefoperazone injected intraperitonealy in mice neither increased nor decreased the pentobarbital-induced sleeping time. In rabbits the normal body temperature was maintained following the single intravenous injections of $125{\sim}2,000mg/kg$ dose. Respiratory and circulatory system: Respiration rate, blood pressure, heart rate and ECG of anesthetized rabbits were monitored for 3 hours following single intravenous injections of cefoperazone at doses of $125{\sim}2,000mg/kg$. The respiration rate decreased by $3{\sim}l7%$ at all the doses of cefoperazone administered. Blood pressure did not show any changes but slight decrease from 130/113 to 125/107 by the highest dose(2,000 mg/kg) injected in this experiment. The dosages of 1,000 and 2,000 mg/kg seemed to slightly decrease the heart rate, but it was not significantly different from the normal control. All the doses of cefoperazone injected were not associated with any abnormal changes in ECG findings throughout the monitering period. Autonomic nervous system and smooth muscle: Effects of cefoperazone on the automatic movement of rabbit isolated small intestine, large intestine, stomach and uterus were observed in vitro. The autonomic movement and tonus of intestinal smooth muscle increased at dose of $40{\mu}g/ml$ in small intestine and at 0.4 mg/ml in large intestine. However, in stomach and uterine smooth muscle the autonomic movement was slightly increased by the much higher doses of 5-10 mg/ml. Blood: In vitro osmotic fragility of rabbit RBC suspension was not affected by cefoperazone of $1{\sim}10mg/ml$. Doses of 7.5 and 10 mg/ml were associated with 11.8% and 15.3% prolongation of whole blood coagulation time. Liver and kidney function: When measured at 3 hours after single intravenous injections of cefoperaonze in rabbits, the values of serum GOT, GPT, Bilirubin, TTT, BUN and creatine were not significantly different from the normal control. 5) Safety evaluation Acute toxicity: The acute toxicity of cefoperazone was studied following intraperitoneal and intravenous injections to mice(A strain, 4 week old) and rats(Sprague-Dawler, 6 week old). The LD_(50)'s of intraperitonealy injected cefoperazone were 9.7g/kg in male mice, 9.6g/kg in female mice and over 15g/kg in both male and female rats. And when administered intravenously in rats, LD_(50)'s were 5.1g/kg in male and 5.0g/kg in female. Administrations of the high doses of the drug were associated with slight inhibition of spontaneous movement and convulsion. Atdominal transudate and intestinal hyperemia were observed in animals administered intraperitonealy. In rats receiving high doses of the drug intravenously rhinorrhea and pulmonary congestion and edema were also observed. Renal proximal tubular epithelial degeneration was found in animals dosing in high concentrations of cefoperazone. Subacute toxicity: Rats(Sprague-Dawley, 6 week old) dosing 0.5, 1.0 and 2.0 g/kg/day of cefoperazone intraperitonealy were observed for one month and sacrificed at 24 hours after the last dose. In animals with a high dose, slight inhibition of spontaneous movement was observed during the experimental period. Soft stool or diarrhea appeared at first or second week of the administration in rats receiving 2.0g/kg. Daily food consumption and weekly weight gain were similar to control during the administration. Urinalysis, blood chemistry and hematology after one month administration were not different from control either. Cecal enlargement, which is an expected effect of broad spectrum antibiotic altering the normal intestinal microbial flora, was observed. Intestinal or peritoneal congestion and peritonitis were found. These findings seemed to be attributed to the local irritation following prolonged intraperitoneal injections of hypertonic and acidic cefoperazone solution. Among the histopathologic findings renal proximal tubular epithelial degeneration was characteristic in rats receiving 1 and 2g/kg/day, which were 10 and 20 times higher than the maximal clinical dose (100 mg/kg) of the drug. 6) Human pharmacokinetics Serum concentrations and urinary excretion were determined following a single intravenous injection of 1g cefoperazone in eight healthy, male volunteers. Mean serum concentrations of 89.3, 61.3, 26.6, 12.3, 2.3, and $1.8{\mu}g/ml$ occured at 1,2,4,6,8 and 12 hours after injection respectively, and the biological half-life was 108 minutes. Urinary excretion over 24 hours after injection was up to 43.5% of administered dose.

• 한국식품영양과학회지
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• 제37권4호
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• pp.428-436
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• 2008

본 연구에서는 고지방식으로 유도한 식이성 비만 모델 수컷 흰쥐에게 고지방식이와 함께 유청단백질 및 유청단백질 가수분해물을 급여하였을 때, 유청단백질 가수분해물의 섭취에 따른 체중, 장기 및 체지방, 지질 농도 및 식욕 조절호르몬에 대한 영향을 살펴보았다. 즉, 실험동물 흰쥐에게 18% 우지를 첨가한 고지방식을 기본으로 하여 질소원으로 유청단백질(whey protein concentrate 80: WPC80, 매일유업(주)) 10%를 4주간 공급한 후(control period), 4군으로 나누어서 고지방식을 기본으로 유청단백질, 유청단백질 가수분해물(whey protein hydrolysate), 유청 macropeptide fraction(whey macropeptide fraction; WH중 MW${\geq}$10,000)의 3종을 함유한 실험식이를 각각 6주 동안 급여하였다. 그 결과는 다음과 같다. 체중증가량 및 식이섭취량은 유청단백질 수준이나 가수분해물 섭취에 따른 실험군간 유의적 차이가 없었다. 간의 무게는 가수분해물 섭취에 의해 감소하였으나, 신장, 고환 및 비장의 무게는 실험군간 유의적 차이가 없었다. 한편, 신장의 무게는 고단백 식이에 의해 유의적으로 증가하였다(p<0.05). 지방조직의 무게는 신장 주변 지방과 부고환 주변 지방 모두 유청단백질 수준이나 가수분해물 섭취에 따른 차이를 보이지 않았다. 혈청의 총 지질과 중성지방은 가수분해물 섭취에 의해 유의적으로 낮게 나타났다(p<0.05). 반면, 혈청의 총 콜레스테롤과 HDL 콜레스테롤은 유청단백질 수준과 가수분해물 섭취에 따른 차이를 보이지 않았다. 간 조직의 총 지질, 중성지방과 총 콜레스테롤은 가수분해물 섭취에 따라 차이가 없었으며, 고단백식이에 의해 유의적으로 감소하였다(p<0.05). 일일 분 배설량은 고단백식이에 의해 유의적으로 증가하였다(p<0.05). 분 중 총 지질함량과 중성지방 함량은 가수분해물 섭취 시 그 함량이 유의적으로 증가하였다(p<0.05). 반면, 분 중 총 콜레스테롤 함량은 유청단백질 수준이나 가수분해물 섭취에 따른 영향을 받지 않았다. 혈청 중 glucose와 insulin 농도는 가수분해물 섭취 시 유의적으로 감소하였다(p<0.05). 혈청 중 leptin 농도는 유청단백질 수준이나 가수분해물 섭취에 따른 유의적인 차이를 보이지 않았다. 혈청 중 ghrelin 농도는 고단백 식이에 의해 유의적으로 감소하였으며(p<0.05), 특히, 가수분해물 섭취 시 감소하는 경향을 보였다. 이상의 결과로부터 유청단백질 가수분해물의 섭취는 intact 유청단백질보다 흰쥐의 혈청과 간의 지질 농도를 저하시키고, 분 중으로의 지질배설량을 증가시키는 것으로 나타났다. 또한 혈중 glucose 농도와 insulin 농도를 감소시킴으로서 인슐린 저항성을 개선시켰으며, ghrelin 감소를 통한 식욕조절 효과를 보였다. 한편, 본 연구에서 유청단백질 가수분해물이 체중감소나 조직의 지방량에는 영향을 미치지 않았는데, 이것은 본 연구에서 사용된 25% 단백질 수준이 체중감소나 조직 지방량에 영향을 미치기에는 부족한 수준이라 사료되며, 단백질 수준에서의 증가 또는 보다 장기간 동안의 섭취가 수행되어진다면 식욕 촉진 호르몬 분비 감소를 통해 체중 감소에 있어서 더 유의적인 효과가 나타날 것으로 사료된다.