• Asian Journal of Atmospheric Environment
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• 제9권4호
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• pp.247-258
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• 2015

Exposure of high concentration of ground-level ozone (GLO) can trigger a variety of health problems including chest pain, coughing, throat irritation, asthma, bronchitis and congestion. There are substantial human and animal toxicological data that support health effects associated with exposure to ozone and associations have been observed with a wide range of outcomes in epidemiological studies. The aim of the present study is to estimate the spatial distributions of GLO using geostatistical method (ordinary kriging) for assessing the exposure level of ozone in the eastern part of Texas, U.S.A. GLO data were obtained from 63 U.S. EPA's monitoring stations distributed in the region of study during the period January, 2012 to December, 2012. The descriptive statistics indicate that the spatial monthly mean of daily maximum 8 hour ozone concentrations ranged from 30.33 ppb (in January) to 48.05 (in June). The monthly mean of daily maximum 8 hour ozone concentrations was relatively low during the winter months (December, January, and February) and the higher values observed during the summer months (April, May, and June). The higher level of spatial variations observed in the months of July (Standard Deviation: 10.33) and August (Standard Deviation: 10.02). This indicates the existence of regional variations in climatic conditions in the study area. The range of the semivariogram models varied from 0.372 (in November) to 15.59 (in April). The value of the range represents the spatial patterns of ozone concentrations. Kriging maps revealed that the spatial patterns of ozone concentration were not uniform in each month. This may be due to uneven fluctuation in the local climatic conditions from one region to another. Thus, the formation and dispersion processes of ozone also change unevenly from one region to another. The ozone maps clearly indicate that the concentration values found maximum in the north-east region of the study area in most of the months. Part of the coastal area also showed maximum concentrations during the months of October, November, December, and January.

• 생태와환경
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• 제42권3호
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• pp.271-279
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• 2009

VC는 국제적인 발암등급 체계인 IRIS, IARC, ESIS에 의해 인체발암물질로 평가되고 있으며, 경구, 호흡, 경피 노출 경로를 통해 간세포 다형성 등을 유발하는 것으로 보고된 바 있다. 또한 VC는 자연계에서 쉽게 분해되지 않는 유기 염소계용제로서, 대기, 지표수, 지하수, 먹는물, 토양으로 유출되어 인체를 포함한 환경을 오염시킬 가능성이 높은 것으로 나타났다. 현재 우리나라의 수질환경기준과 먹는물 기준에서는 VC에 대한 규제 항목 및 기준치가 제시되어 있지 않으나, 인체 및 수생태계 위해 우려가 있어 특정수질유해물질 및 수질오염물질로 지정된 바 있다. US EPA, 일본, WHO 등 선진국에서는 법적 항목 및 기준치로 VC를 제도적으로 관리하고 있다. 특히 우리나라에서는 2004년 한강 및 낙동강 유역에서 $0.8\sim4.7{\mu}g\;L^{-1}$ (검출한계 $0.1{\mu}g\;L^{-1}$),개별배출업소 유출수에서 $10.6\sim668{\mu}g\;L^{-1}$의 농도로 VC가 검출된 사례가 있으며, 독일, 일본, 미국 등의 국외에서 검출된 $0.03\sim566{\mu}g\;L^{-1}$ 농도보다 국내 수계 내 VC의 분포 수준이 높은 것으로 나타났다. 국내 인체 위해성 평가 결과 VC에 대한 위해 우려가 높은 것으로 평가된 바 있으며, 생태 위해성 평가는 자료 부족으로 보류된 바 있다. 이 때 활용된 모니터링 자료는 일부 지점 및 단회 기반의 신뢰성 다소 낮은 자료에 국한되므로 지속적인 모니터링 사업을 통해 신뢰성 높은 자료로 대체될 필요가 있다. 또한 물 환경 내 생태독성연구는 일부 시험증에 국한되어 있고, 실험 설계도 VC의 수체 내 농도 감소를 고려하지 않아 결과치가 과다 산정되었을 가능성이 높다. 따라서 지속적으로 다양한 수서생물을 활용한 VC의 생태 독성 자료가 생성되어야 추후 VC에 대한 신뢰도가 높은 생태 위해성 평가가 수행될 것으로 사료된다.

• Toxicological Research
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• 제26권2호
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• pp.157-162
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• 2010

In this study, we investigated the atmospheric heavy metal concentrations in the particulate matter inside the subway stations of Seoul. In particular, we examined the correlation between the heavy metals and studied the effect of the heavy metals on cell proliferation. In six selected subway stations in Seoul, particulate matter was captured at the platforms and 11 types of heavy metals were analyzed. The results showed that the mean concentration of iron was the highest out of the heavy metals in particulate matter, followed by copper, potassium, calcium, zinc, nickel, sodium, manganese, magnesium, chromium and cadmium in that order. The correlation analysis showed that the correlations between the heavy metals was highest in the following order: (Cu vs Zn), (Ca vs Na), (Ca vs Mn), (Ni vs Cr), (Na vs Mn), (Cr vs Cd), (Zn vs Cd), (Cu vs Cd), (Ni vs Cd), (Cu vs Ni), (K vs Zn), (Cu vs K), (Cu vs Cr), (K vs Cd), (Zn vs Cr), (K vs Ni), (Zn vs Ni), (K vs Cr), and (Fe vs Cu). The correlation coefficient between zinc and copper was 0.937, indicating the highest correlation. Copper, zinc, nickel, chromium and cadmium, which are generated from artificial sources in general, showed correlations with many of the other metals and the correlation coefficients were also relatively high. The effect of the heavy metals on cell proliferation was also investigated in this study. Cultured cell was exposed to 10 mg/l or 100 mg/l of iron, copper, calcium, zinc, nickel, manganese, magnesium, chromium and cadmium for 24 hours. The cell proliferation in all the heavy metal-treated groups was not inhibited at 10 mg/l of the heavy metal concentration. The only exception to this was with the cadmium-treated group which showed a strong cell proliferation inhibition. This study provides the fundamental data for the understanding of simultaneous heavy metal exposure tendency at the time of particulate matter exposure in subway stations and the identification of heavy metal sources. Moreover, this study can be used as the fundamental data for the cell toxicity study of the subway-oriented heavy metal-containing particulate matter.

• 한국식품위생안전성학회지
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• 제26권1호
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• pp.49-56
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• 2011

전통적으로 사용되어온 ${\beta}$-glucan에 대한 기초적 연구로서 본 실험은 ${\beta}$-glucan의 영양학적 성분을 분석하고 이를 투여했을 때 흰쥐의 발육에 미치는 영향에 대하여 고찰하였다. SD종 5주령의 어린 쥐를 각각 5마리씩 배치하였고, ${\beta}$-glucan을 급여하지않은 대조군, ${\beta}$-glucan을 D.W-(distilled water)에 용해시켜 저용량 (하루 사료섭취량의 0.2%의 ${\beta}$-glucan), 중간용량 (하루 사료섭취량의 1%의 ${\beta}$-glucan), 고용량 (하루 사료섭취량의 5%의 ${\beta}$-glucan) 으로 구분하여 6주간 사육하였으며, 실험쥐의 체중, 식이섭취량, 식이효율, 장기발육 및 혈액 형상에 대하여 조사하였다. 실험군 모두에서 실험쥐의 시험 종료시 평균체중과 식이섭취량의 통계적 유의차는 발견되지않았다. 그리고 간, 심장, 선장, 및 위장 등의 장기무게와 백혈구, 적혈구, 혈색소, 헤마토크릿 및 혈소판 등의 혈액학적 지수에 있어서도 통계적 유의차가 발견되지 않았다. 즉 ${\beta}$-glucan식이로 이상적으로 장기가 비대해지거나 억제됨 없이 정상적 발육이 이루어졌으며, 이상현상없이 정상적 혈액학적 지수를 나타내었다. 따라서 본 연구의 결과는 ${\beta}$-glucan이 생리대사에 무해하고 안전하며, 면역력증진 효능에 대한 세부적 및 과학적 규명과 함께 면역력증강 사료첨가제로 개발 필요성 및 가능성을 시사한다.

• Toxicological Research
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• 제21권2호
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• pp.179-186
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• 2005

Dimethylamine (DMA) is a widely used commodity chemical with few toxicity data. Groups of 10 male and female F-344 rats were exposed by inhalation to 0, 5, 10, 20, 40 and 80 ppm of DMA for 6 hrs/day, 5 days/week for 90 days. The changes of body weight, organ weight, hematology, clinical chemistry, and histopathological changes were evaluated after the exposure. As the results, the body weight was significantly decreased at 80 ppm in male and female rats (p<0.05). The absolute lung weight showed no statistically significant changes in any group. In contrast, the relative lung weight significantly increased at 80 ppm in male and female rats (p<0.05). Erythrocytes, mean cell hemoglobin, leukocytes, neutrophil, and platelet numbers were significantly increased in male and female at 40 or 80 ppm of DMA (p<0.05, p<0.01). In addition, the serum values of total protein, urea nitrogen were increased in male and creatine kinase, total protein were increased in female rats at 40 or 80 ppm (p<0.05, p<0.01). Histopathological examinations of the male and female lung samples showed slight hyperplasia and congestion at 80 ppm. Taken together, our study revealed that maximum tolerated dose of DMA would be over 40 ppm.

• Toxicological Research
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• 제18권1호
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• pp.87-98
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• 2002

This study was conducted to evaluate the safety of a recombinant human Factor VIII(GC-$\gamma$ AHF) manufactured by Korea Green Cross Company with different technology according to the Regulation of Korean Food and Drug Administration (l 998. 12. 3). In acute toxicity test, both genders of Sprague-Dawley rats and Beagle dogs were administered intravenously with GC-$\gamma$ AHF of three doses (3,125, 625 and 125 IU/kg), and single dose of 3,125 IU/kg, respectively. No dead animal and abnormal autopsy findings were found in Control and GC-$\gamma$ AHF treated group. Therefore, the 50% lethal dose ($LD_{50}$) of GC-$\gamma$ AHF was conidered to be higher than 3,125 IU/kg in rats and dogs. In the four weeks repeated intravenous toxicity study, GC-$\gamma$ AHF was administrated intravenosly to both genders of rats and dogs with 3 doses (500, 150, 50 IU/kg). There were neither dead animals nor significant changes of body weights during the experimental Period. In addition, no significant GC-$\gamma$ AHF related changes were found in clinical sign, urinalysis and other finding. Statistically changes were observed in hematological, biochemical and organ weight parameters of treated groups: however these changes were not dose dependent. No histopathological lesion were observed in both control and treated animals. Above data suggest that no observed adverse effect level of test materials in rats and dogs might be over 500 IU/kg/day in this study. In ocular irritation test, any injury on iris, conjunctiva and cornea in rabbits were not observed. The acute ocular irritation index (A.O.I.), mean ocular irritation index (M.O.I.) and Day-7 individual ocular irritation Index (I.O.I.) of GC-$\gamma$ AHF were 0. In the primary skin Irritation test, the primary irritation index (P.I.I.) oj GC-$\gamma$ AHF were 0. Therefore, the GC-$\gamma$ AHF is considered not to have the primary skin and eye toxicity in rabbits. In active systemic anaphylaxis (ASA) test, GC-$\gamma$ AHF and GC-$\gamma$ AHF emulsified with Freund's complete adjuvant (FCA) did not induce any symptom of anaphylactic shock in guinea pigs. In passive cutaneous anaphylxis (PCA) test, after sensitization with antisera of GC-$\gamma$ AHF sensitized mice, blue spots were observed on the hypodermis of back of rats, but diameter of each spot was smaller than 5 mm in each test groups except the positive control group. Based on the results of this study, GC-$\gamma$ AHF is not conidered to have any antigenic potential. In conclusion, at levels of up to 500 IU/kg, GC-$\gamma$ AHF did not produce treatment-related toxicity under the conditions of these acute-, four week repeated-toxicity, primary skin and eye toxicity, and antigenicity test.

• 대한임상독성학회지
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• 제14권2호
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• pp.136-143
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• 2016

Purpose: In patients with altered mentality caused by drugs or unknown causes, ammonia is checked to facilitate differential diagnosis or diagnose hepatic coma. This helps early prevention and treatment of brain damage due to hyperammonemia. This study was conducted to evaluate clinical characteristics of intoxicated adult patients with hyperammonemia. Methods: We evaluated 95 patients with hyperammonemia among intoxicated patients above the age of 15 who visited our ED from January 2013 to December 2015. We analyzed the demographic characteristics and type of poisoning substance, reason for ingestion, toxicological characteristics such as elapsed time from ingestion to hospital visit, lab, clinical progression and complications. Data were evaluated using the student's t test or Mann-Whitney U test for continuous variables, and Chi-square test and Fisher's exact test for frequency analysis of categorical variables. Results: When compared to healthy individuals, patients with hyperammonemia showed statistical significance on their SOFA score (p=0.016) and poison severity score (p<0.001). Additionally, patients with hyperammonemia showed significantly different initial serum AST level (p=0.012) and maximum serum AST level during the hospital stay (p=0.026) when compared to healthy individuals. Moreover, individuals with sustained hyperammonemia compared to transient hyperammonemia showed clinically significant SOFA scores (p<0.001), poison severity scores (p=0.007), mortality rates in the ICU (p=0.021), as well as different duration of hospital stay (p=0.037), serum creatinine level (p=0.002), erythrocyte sedimentation rate (p=0.025), and serum myoglobin (p=0.015). Conclusion: Most poisoning-induced hyperammonemia cases were transient and recovered without special treatment. Therefore, hyperammonemia is almost non-specific among poisoning patients.

• 환경생물
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• 제27권4호
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• pp.323-333
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• 2009

파라벤은 p-하이드록시 벤조산(p-hydroxybenzoic acid)의 알킬에스테르로, 비교적 빠르게 흡수, 대사 및 배설되는 살균성 보존제로 식품, 화장품, 약품 등에 널리 사용되고 있다. 실제 인체는 파라벤 복합물에 노출된다. 파라벤의 안전성에 관한 연구결과들에 대한 고찰 결과 파라벤 종류에 따라 다양한 독성종말점을 대상으로 파라벤의 급성, 아급성 및 만성독성 영향은 비교적 적은 것으로 나타났다. 파라벤은 에스트로젠 유사활성을 가지며 화장품을 통한 경피흡수를 통해 유방암과의 상관성이 보고되었으나, 이와 상반된 견해도 있다. 파라벤의 항안드로젠성은 남성생식기계의 장애를 유발할 수 있으나 이와 상반된 견해도 있다. 파라벤은 정자의 미토콘드리아 기능 및 남성호르몬 생성을 저해할 수 있으나 이와 상반된 견해도 있다. 배아발달에는 독성이 없는 것으로 나타났다. 세포독성으로는 세포용혈, 미토콘드리아 막투과성 변화, 세포사멸 등을 유발할 수 있다. 수환경에서 파라벤은 환경에스트로젠으로 작동하여 어류에서 내분비장애 효과를 발휘한다. 결론적으로 파라벤은 저독성물질로 분류할 수 있으나, 인체 및 수생동물들에서 파라벤의 노출경로 및 농도, 사용기간 등에 따른 독성과 내분비계장애 효과에 대하여는 다양한 종말점을 대상으로 좀 더 구체적인 독성자료들이 요구된다.

• 한국식품과학회지
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• 제52권5호
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• pp.555-559
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• 2020

본 연구에서는 팔라티노스 시럽 Pal-L을 반복 투여하였을 때 나타나는 독성을 확인하기 위하여 암수 SD rat에 1,000 mg/kg의 용량으로 14일간 1일 1회 경구 투여한 후 사망률, 일반 증상, 체중 및 사료/음수 섭취량 변화, 장기 중량의 변화, 혈액 및 혈액 생화학적 변화, 뇨 분석 및 간과 신장의 조직학적 검사에 대한 변화를 관찰하였다. 실험 결과 투여 기간 중 암수 대조군 및 Pal-L을 투여한 군 모두 사망 동물은 발견되지 않았으며, 팔라티노스의 반복 투여에 의한 일반 증상의 변화 역시 관찰되지 않았다. 또한 체중 및 사료/음수 섭취량에 대한 변화, 장기 중량의 변화에 대한 이상 변화 역시 관찰되지 않았다. 부검 후 채취한 전혈의 혈액학적 분석 결과, 암컷 Pal-L 투여군에서 Hgb, MCHC, PLT의 수치가 유의적인 차이를 보였으나 정상 범위 내에서의 차이로 팔라티노스에 의한 독성이라고 판단하기는 어려웠으며, 혈액의 생화학적 분석 결과 암수 대조군 및 시험군에서 모든 항목이 정상 수치를 나타냈다. 부검 전 채취한 뇨를 분석한 결과 암컷 시험군에서 glucose, 수컷 시험군에서 total protein 수치가 유의적으로 감소하였지만 정상 범위 내에서의 차이로 팔라티노스에 의한 독성이라고 판단하기 또한 어려웠다. 혈액, 혈청 및 뇨에서 일부 유의적인 차이가 나타난 것을 바탕으로 간 및 신장에 대한 조직병리학적 검사를 진행한 결과 대조군과 시험군 모두 조직학적 이상은 관찰되지 않았다. 이상의 결과를 종합해보면 SD rat을 이용하여 팔라티노스(Palatinose-L)를 1,000 mg/kg/day의 용량으로 14일간 반복 경구투여하고 사망 여부, 체중 변화, 혈액학적 검사, 혈액 생화학적 검사, 뇨 분석 및 조직학적 검사 등을 통해 독성 평가를 진행하고자 하였다. 그 결과 2주간의 투여 기간 동안 시험 동물에게 어떠한 독성도 관찰되지 않았음을 확인하였고, 이에 따라 팔라티노스(Pal-L)는 1,000 mg/kg/day 용량까지는 독성이 없는 안전한 물질이라는 것이 최종 확인되었다.

• Toxicological Research
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• 제32권2호
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• pp.159-173
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• 2016

Crickets have been attracting considerable interest in the field of nutrition and toxicology due to the global exhaustion of food resulting from a growing population. The cricket is normally eaten in several countries after roasting, similar to the grasshopper; however, safety evaluation data on cricket powder is limited. Here, we performed general toxicity studies of cricket powder including a single, 2-week repeated dose range evaluation test, a 13-week repeated oral dose toxicity test in Sprague-Dawley rats, a single oral dose toxicity test in Beagle dogs, and a skin sensitization test in guinea pigs following the Organization for Economic Cooperation and Development test guidelines 406 and 408 in addition to Good Laboratory Practice. To investigate the NOAEL and target organs of cricket powder, Sprague-Dawley rats were allocated to 4 groups: vehicle control, 1,250 mg/kg, 2,500 mg/kg, 5,000 mg/kg dose test groups and cricket powder was administered over 13 weeks after single dose and dose range finding studies in rats based on the results of the single oral administration toxicity study in rats and Beagle dogs. The results of the study showed that the NOAEL of cricket powder was over 5,000 mg/kg for both sexes of rats without adverse effects in a 13-week repeated oral toxicity study and there was no skin hypersensitivity reaction. Therefore, our results reveal that crickets can be widely used as a new substitute food or nutrient resource.