• Title/Summary/Keyword: human toxicity

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Current Progress of Next Generation Battery of Toxicology-Cellular and Molecular Toxicology

  • Ryu, Jae-Chun;Kim, Youn-Jung
    • Molecular & Cellular Toxicology
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    • v.1 no.1
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    • pp.26-31
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    • 2005
  • The detection and the regulation of man-made synthetic chemicals and the establishment of toxicity that may pose a genetic hazard in our environment are subjects of great concern because of its close correlation between environmental contamination and human health. Since the tens of thousands of man-made chemicals that have been introduced into the environment in the last few decades must also be tested for their damaging effect on DNA, the agents that cause this damage must be identified.

Thioredoxin System and Redox Signaling; Defence against Stress and Toxicity

  • Yodoi, Junji;Masutani, Hiroshi;Nakamura, Hajime
    • Proceedings of the Korean Society of Toxicology Conference
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    • 2001.05a
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    • pp.84-88
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    • 2001
  • Human Thioredoxin (TRX) with with redox-active dithiol (C-C-Y-C-) in the active site has been cloned as adult T cell leukemia derived factor produced by HTLV-I transformed cells. Thioredoxin (TRX) is one of the major components of the thiol-reducing system and plays multiple roles in cellular processes such as proliferation, apoptosis and gene expression.(omitted)

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Identification of Differentially Expressed Genes by Methylmercury in Neuroblastoma cell line using suppression subtractive hybridization (SSH) and cDNA Microarray

  • Kim, Youn-Jung;Chang, Suk-Tai;Yun, Hye-Jung;Ryu, Jae-Chun
    • Proceedings of the PSK Conference
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    • 2003.04a
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    • pp.189.2-190
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    • 2003
  • Methylmercury (MeHg), one of the heavy metal compounds. can cause severe damage to the central nervous system in humans. Many reports have shown that MeHg is poisonous to human body through contaminated foods and has released into the environment. Despite many studies on the pathogenesis of MeHg-induced central neuropathy, no useful mechanism of toxicity has been established so far. (omitted)

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Application of Calux Bioassay for Determining Dioxin Toxicity Equivalents

  • Joung, Ki-Eun;An, Jin-Young;Sheen, Yhun-Yhong
    • Proceedings of the Korean Society of Toxicology Conference
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    • 2003.10b
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    • pp.172-173
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    • 2003
  • There are growing concerns about human health effects of dioxin and dioxin like compounds such as polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and polychlorinated biphenyls (PCBs). Earlier studies recognized that 2.3.7.8-tetrachloro dibenzo-p-dioxin (TCDD) and structually related dioxin like compounds invoke a number of common toxic responses that are mediated through a high-affinity cytosolic receptor protein, the AhR.(omitted)

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Identification and Characterization of Genes that are Induced after Cadmium Exposure

  • Lee, Mi-Ock
    • Proceedings of the PSK Conference
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    • 2003.10a
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    • pp.73-73
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    • 2003
  • The heavy metal cadmium is a xenobiotic toxicant of environmental and occupational concern and it has been classified as a human carcinogen. Inhalation of cadmium has been implicated in the development of emphysema and pulmonary fibrosis, but, the detailed mechanism by which cadmium induces adverse biological effects is not yet known. Therefore, we undertook the investigation of genes that are induced after cadmium exposure to illustrate the mechanism of cadmium toxicity. (omitted)

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Differential Role of Solvents on Human Cytochrome P450 2El Activity in Intact HepG2 Cells (HepG2 세포에서 용매에 의한 차별적인 사람 싸이토크롬 P450 2E1활성 변화)

  • 최달웅
    • Journal of Environmental Health Sciences
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    • v.29 no.3
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    • pp.9-15
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    • 2003
  • The modification of CYP2El activity is a matter of considerable interest because of its role in the metabolic activation of a variety of environmental toxicants. In the present study, the time-course of changes in human CYP2El activities was determined following treatment with solvents (acetone, dimethylsulphoxide or pyridine) using intact HepG2 cells transfected by human CYP2El. Hydroxylation of chlorzoxazone was used for the measurement of CYP2El activity. CYP2E1 protein level was increased upon cultivation of cells in the presence of the solvents for 24 hr. Determination of CYP2El activities after 24 ht cultivation with the solvents demonstrated that acetone or dimethylsulphoxide increased, whereas pyridine inhibited the activities. This differential effect of the solvents on CYP2El activities persisted to subsequent 24 ht. Competitive inhibition study suggested that pyridine has stronger binding affinity to CYP2E1 than acetone or dimethylsulphoxide. These results demonstrate that different binding affinity of the solvents to CYP2El plays important role in determining real CYP2El activity in intact cells after exposure to the solvents. Present study would be helpful in precise understanding of human CYP2El-mediated toxicity.

Developmental Toxicity Study in the Embryos/Fetuses with a Recombinant Human Granulocyte Colony-Stimulating Factor (YHB6211) in Pregnant Rabbits (임신토끼에 있어서 새로운 Recombinant Human Granulocyte Colony-Stimulating Factor(YHB6211)의 배.태자 발생독성평가)

  • 황재식;장호송;정은용;이수해;신지순;서동석;신장우;남상윤;김대중
    • Biomolecules & Therapeutics
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    • v.9 no.4
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    • pp.311-317
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    • 2001
  • YHB6211, a newly developed recombinant human granulocyte colonystimulating factor, was administered at dose levels of 0, 3, 15, and 75 $\mu$g/kg/day intravenously to the pregnant New Zealand White rabbits (20 rabbits per group) during the organogenetic period, days 6 to 18 of gestation. All dams were subjected to Caesarian section on day 28 of gestation and their fetuses were examined for external, visceral, and skeletal abnormalities. No abnormalities in clinical signs, body weight changes, gross findings, mortality, and external appearance were found in all dams and fetuses exposed to 0, 3, and 15 $\mu$g/kg/day of YHB6211. However, in the group treated with 75 $\mu\textrm{g}$/kg/day of YHB6211, maternal body and uterine weights, fetal body weights and length, and the number of live fetuses were significantly decreased and further fetal mortality was remarkably increased. It is suggested that YHB6211 may have no side effect up to the dose level of 15 $\mu$g/kg/day, and there would be no teratogenicity for fetuses of rabbits up to 75 $\mu\textrm{g}$/kg/day even if it may have some toxic effects over 75$\mu\textrm{g}$/kg/day for dams and fetuses of rabbits.

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Potential Risk to Human Health by Arsenic and Its Metabolite (환경 오염물질 비소의 체내 대사 및 인체 위해성)

  • Bae Ok-Nam;Lee Moo-Yeol;Chung Seung-Min;Ha Ji-Hye;Chung Jin-Ho
    • Environmental Analysis Health and Toxicology
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    • v.21 no.1 s.52
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    • pp.1-11
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    • 2006
  • Arsenic is a ubiquitous element found in several forms in environment. Although certain foods, such as marine fish, contain substantial levels of organic arsenic forms, they are relatively low in toxicity compared to inorganic forms. In contrast, arsenic in drinking water is predominantly inorganic and very toxic. Chronic ingestion of arsenic-contaminated drinking water is therefore the major pathway posing potential risk to human health. World populations are exposed to low to moderate levels of arsenic of parts per billion (ppb) to thousands of ppb. When exposed to human, it could metabolize into monomethylarsonous acid ($MMA^{III}$) and dimethylarsinous acid ($DMA^{III}$) which are highly toxic. Lots of stuides have been recently focused how $MMA^{III}\;and\;DMA^{III}$ induce toxic insults in various target tissues. Epidemiological studies revealed that chronic arsenic exposure caused cancer, cardiovascular diseases, and diabetes etc. In this review, the current understanding of arsenic on health effects will be discussed.

The Optimization of Method for Prediction of Drug-Induced Liver Injury Using HepG2 Cells Cultured with Human Liver Microsomes (Human Liver Microsomes과 HepG2 세포를 이용한 약물유래 간독성 평가 방법의 최적화)

  • Choi, Jong Min;Jeon, Jang Su;Kim, Sang Kyum
    • YAKHAK HOEJI
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    • v.59 no.5
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    • pp.201-206
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    • 2015
  • The aim of the present study was to optimize in vitro method for the prediction of drug-induced liver injury using human liver microsomes (HLM). Cytotoxicity test of cyclophosphamide and acetaminophen in HepG2 cells cultured with HLM showed that the newly established condition using 0.375 mg/ml HLM for 24 hr incubation was comparable or more sensitive than the previously established condition using 0.75 mg/ml HLM for 12 hr incubation. Although the cytotoxic effect of troglitazone was completely attenuated by 0.75 mg/ml HLM, it was augmented by 0.375 mg/ml HLM in the presence of the NADPH-generating system. The cytotoxic effect of chlormezanone, a withdrawn drug due to hepatotoxicity in human, was increased by HLM in the presence of the NADPH-generating system. In contrast, the cytotoxic effect of methapyrilene, a withdrawn drug due to hepatotoxicity in rats, was decreased by HLM in the presence of the NADPH-generating system. The present study suggests that the optimized in vitro method using HLM can be useful for the prediction of drug-induced hepatotoxicity.

Analysis of Toxicity and Bias of ChatGPT within Korean Social Context (한국의 사회적 맥락에서의 ChatGPT의 독성 및 편향성 분석)

  • Seungyoon Lee;Chanjun Park;Gyeongmin Kim;Heuiseok Lim
    • Annual Conference on Human and Language Technology
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    • 2023.10a
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    • pp.539-545
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    • 2023
  • 초거대 언어모델은 심화된 언어적 이해를 요구하는 여러 분야에 높은 영향력을 미치고 있으나, 그에 수반되는 편향성과 윤리성에 대한 우려 또한 함께 증대되었다. 특히 편향된 언어모델은 인종, 성적 지향 등과 같은 다양한 속성을 가진 개인들에 대한 편견을 강화시킬 수 있다. 그러나 이러한 편향성에 관한 연구는 대부분 영어 문화권에 한정적이며 한국어에 관한 연구 또한 한국에서 발생하는 지역 갈등, 젠더 갈등 등의 사회적 문제를 반영하지 못한다. 이에 본 연구에서는 ChatGPT의 내재된 편향성을 도출하기 위해 의도적으로 다양한 페르소나를 부여하고 한국의 사회적 쟁점들을 기반으로 프롬프트 집합을 구성하여 생성된 문장의 독성을 분석하였다. 실험 결과, 특정 페르소나 또는 프롬프트에 관해서는 지속적으로 유해한 문장을 생성하는 경향성이 나타났다. 또한 각 페르소나-쟁점에 대해 사회가 갖는 편향된 시각이 모델에 그대로 반영되어, 각 조합에 따라 생성된 문장의 독성 분포에 유의미한 차이를 보이는 것을 확인했다.

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