• 제목/요약/키워드: safety in vivo

검색결과 317건 처리시간 0.028초

건강기능성 수산식품소재의 개발 (Development of functional food products with natural materials derived from marine resources)

  • 류보미;전유진
    • 식품과학과 산업
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    • 제51권2호
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    • pp.157-164
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    • 2018
  • Recently demand for safer and healthier food has augmented with advancements in health conditions. Food ingredients with yet to be known safety and functionality, are being investigated for their safety or detrimental effects. The Ministry of Food and Drug Safety has introduced "health functional food" by the "Health Functional Food Act" to evaluate bio-functional and safety properties of raw materials using standard methods including in-vitro and in-vivo testing before human consumption. Despite recent growth in net worth of domestic functional food market, most of the raw materials are not from local Korean industries with own research and development, and mostly terrestrial not marine resources. Geographically, Korea has access to diverse marine bio-resources that need to be managed and utilized sustainably. Recently, diverse novel physiologically active substances have been reported from marine organisms. Hence, the development of functional foods from marine bio-resources is considered as an inevitably important task.

Effect of Arsenic on Acetylcholine-Induced Relaxation in Blood Vessels in vitro cad in vivo

  • Lee, M.Y.;Chung, S.M.;Bae, O.N.;Chung, J.H.
    • 한국식품위생안전성학회:학술대회논문집
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    • 한국식품위생안전성학회 2002년도 춘계학술발표대회 및 심포지움
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    • pp.137-137
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    • 2002
  • Several epidemiologidal studies suggested that arsenic exposure was strongly correlated with the development of cardiovascular disease such as hypertension. In order to examine whether arsenic affects vasomotor tone in blood vessels, we investigated the effect of arsenic on agonist-induced vasorelaxation using the isolated rat aortic ring in in vitro organ bath system. Treatment with arsenite inhibited acetylcholine-induced relaxation of aortic rings in a concentration- dependent manner. The inhibitory effects by arsenic were also observed in the relaxation induced by sodium nitroprusside, a NO-donor. Consistent with these findings, the cGMP levels stimulated by acetylcholine in blood vessels were reduced significantly by arsenite treatment. In addition, higher concentration of arsenite decreased the relaxation by 8-Br-cGMP, a cGMP analog, in aortic rings without endothelium. These in vitro results indicated that arsenite that arsenite was capable of suppressing acetylcholine-induced relaxation in blood vessels by inhibiting production of nitric oxide in endothelial cells and by impairing the relaxation machinary in smooth muscle cells. In vivo studies revealed that the reduction of blood pressure by acetylcholine infusion was signigicantly suppressed after arsenite was administered intravenously to rate. These data suggest that vasomotor tone impaired by arsenite exposure may be one of the contrbuting factors in development of cardiovascular disease.

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개비자나무 유효성분인 homoharringtonine의 in vitro 항암활성 및 in vivo 만성 독성 (in vitro Anticancer Activity and in vivo Chronic Toxicity of Homoharringtonine)

  • 유귀재;조철희;이건순;류재웅;채희정
    • Applied Biological Chemistry
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    • 제51권2호
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    • pp.124-128
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    • 2008
  • 개비자나무의 유효성분으로 알려진 homoharringtonine의 암세포주 K562에 대한 세포증식 저해 활성을 분석하였고, 마우스를 이용한 만성독성시험을 수행하였다. 총 약물처리 시간에 따른 최적 투여조건 결정 실험에서는 HHT를 9일, 6일, 3일 동안 매일 처리할 경우 각각 0.27, 0.37, 1.10mM의 농도에서 K562세포의 성장을 50% 감소시킴을 확인하였다. 기존 백혈병 치료제로 사용되고 있는 adriamycin과의 비교실험 결과 HHT는 K562 세포주에 대하여 adriamycin보다 낮은 저해율을 나타냈으나 비교적 근사한 값을 가졌다. HHT의 만성독성 실험 결과 혈액학적 지표 측정 실험에서 적혈구수(RBC)는 대조군과 HHT 투여군 사이에 유의적인 차이가 없었고, 간 기능 관련 효소의 혈액을 분석한 결과, 간 손상과 관련된 효소glutamate-oxalate-transferase, glutamate-pyruvate- transferase, cholesterol 및 alkaline phosphatase 모두 정상 범위에 있었다. 그러나 간 조직학적 검사에서는 HHT를 투여한 마우스의 간 조직에서 밴드형의 호중구를 침착시키는 것이 확인되었다.

Genotoxicity Evaluation of Capsaicin-Containing (CP) Pharmacopuncture, in an In Vivo Micronucleus Test

  • Hwang, Ji Hye;Ku, Jaseung;Jung, Chul
    • 대한약침학회지
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    • 제23권4호
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    • pp.237-246
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    • 2020
  • Objectives: Capsaicin-containing (CP) pharmacopuncture was developed to treat neuropathic pain. This study was conducted to assess the toxicity of CP extract for pharmacopuncture, using a micronucleus test. Methods: First, a dose range finding study was conducted. Then an in vivo micronucleus test was performed to determine the induction of micronuclei in mouse bone marrow cells after intramuscular administration of CP twice with a 24-hour interval to 8-week-old ICR mice. A high dose of 0.2 mL/animal was selected, and this was sequentially diluted by applying a geometric ratio of 2 to produce two lower dose levels (0.1 and 0.05 mL/animal). In addition, negative and positive control groups were set up, and an HPLC analysis was conducted to confirm the capsaicin content of CP. Results: The incidence of micro-nucleated polychromatic erythrocytes in polychromatic erythrocytes in the CP-treated group was similar to that in the negative-control group, while that in the positive-control group was significantly greater. In addition, the ratio of polychromatic erythrocytes to total erythrocytes in the CP treatment group and the positive control group was not significantly different from the negative control group. In the HPLC analysis, capsaicin in the CP was identified through a comparison with the retention time of the capsaicin standard of 27 min. Conclusion: CP did not show any indication of any potential to induce micronuclei formation in bone marrow cells of ICR mice under the conditions of this study. Further toxicity studies are necessary to ensure the safety of the use of CP in clinical practice.

ICR 마우스를 이용한 소핵시험을 통한 TA 약침의 안전성 평가 (Toxicity Evaluation of TA, a Pharmacopuncture Medicine, in an in Vivo Micronucleus Test)

  • 황지혜;정효원;정철
    • Korean Journal of Acupuncture
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    • 제36권1호
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    • pp.74-80
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    • 2019
  • Objectives : TA, a polyherbal extract, typically is used for pharmacopuncture therapy on patients with traffic accident-related injuries and musculoskeletal diseases. This study was performed to evaluate the safety of the TA extract, using a micronucleus test. Methods : The dose range and sampling time were first established. An in vivo micronucleus test was then performed to determine the induction of micronuclei in mouse bone marrow cells after a single intramuscular administration of TA to 7-week-old ICR mice (0.2 ml/animal, at 24 hours post-dosing). Results : The incidence of micro-nucleated polychromatic erythrocytes (PCEs) in PCEs in the TA group was similar to that in the negative-control group, while that in the positive-control group was significantly greater. The positive- and negative-control groups did not differ in the ratio of PCEs to total erythrocytes. Conclusions : Our toxicity study indicates that the TA extract does not induce micronucleus formation in mouse bone marrow cells.

전갈(全蝎) 약침액(藥鍼液)의 항돌연변이(抗突然變異) 및 항암(抗癌) 효과(效果) (The antimutagenic effect and genetic safety of Buthus martensi Karsch aqua-acupuncture solution (BMKAS))

  • 김소형;김갑성
    • Journal of Acupuncture Research
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    • 제17권3호
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    • pp.151-167
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    • 2000
  • Objective : The aim of this study is to determine the antimutagenic effect and genetic safety of Buthus martensi Karsch aqua-acupuncture solution(BMKAS) against various chemical carcinogens. Method : Ames(Salmonella typhimurium) test and Rec assay(Bacillus subtilis) were used as indicators for DNA damage and antimutagenesis. Furthermore, the levels of umu operon expression by measuring the ${\beta}$-galactosidase activity wete monitored with the SOS umu test using S. typhimurium 1535 containing plasmid pSK1002. And the host-mediated assay was used to investigate the mutagenicity and antimutagenicity of BMKAS inducing various chemical carcinogens after the activation with in vivo metabolic systems. Results : From the results, BMKAS did not atfect DNA of S. typhimurium and B. subtilis strains and showed no mutagenicity at the all concentrations of tested solution. Furthermore BMKAS dose-dependently protected the mutagenecity by AF-2, 2-AA and B[a]P. These phenomena was also similar to that after metabolic activation of BMKAS in in vivo system. Conclusion : These results suggested that BMKAS did not show the mutagenicity and protected the mutagenesis against various chemical carcinogens by four different methods used in this study.

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Genotoxicity Assessment of Erythritol by Using Short-term Assay

  • Chung, Young-Shin;Lee, Michael
    • Toxicological Research
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    • 제29권4호
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    • pp.249-255
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    • 2013
  • Erythritol is a sugar alcohol that is widely used as a natural sugar substitute. Thus, the safety of its usage is very important. In the present study, short-term genotoxicity assays were conducted to evaluate the potential genotoxic effects of erythritol. According to the OECD test guidelines, the maximum test dose was 5,000 ${\mu}g$/plate in bacterial reverse mutation tests, 5,000 ${\mu}g/ml$ in cell-based assays, and 5,000 mg/kg for in vivo testing. An Ames test did not reveal any positive results. No clastogenicity was observed in a chromosomal aberration test with CHL cells or an in vitro micronucleus test with L5178Y $tk^{+/-}$ cells. Erythritol induced a marginal increase of DNA damage at two high doses by 24 hr of exposure in a comet assay using L5178Y $tk^{+/-}$ cells. Additionally, in vivo micronucleus tests clearly demonstrated that oral administration of erythritol did not induce micronuclei formation of the bone marrow cells of male ICR mice. Taken together, our results indicate that erythritol is not mutagenic to bacterial cells and does not cause chromosomal damage in mammalian cells either in vitro or in vivo.

자외선 차단 제품의 SPF 측정과 안전성 (SPF Evaluation and Safety of Sunscreen Products)

  • 김종일;이병곤;고재숙
    • 대한화장품학회:학술대회논문집
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    • 대한화장품학회 1992년도 자외선 차단 화장품의 SPF에 관한 심포지움(대한화장품학회)
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    • pp.5-26
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    • 1992
  • Many methods of in vitro SPF evaluation have been developed in order to measure SPF of sunscreen products. In this study, we compared two spectrophotometric in vitro measurements using the skin cast made of Luviset CAP- $X^{R}$ resin and Transpor $e^{R}$ tape as substrate with two in vivo measurements using guinea pig and human. And we also observed the radiation reaching on the earth's surface in Seoul for one year and the change of the primary skin irritancy along the change of SPF value. According to the our research, the first, in vivo measurement using guinea pig had the close agreement with SPF measurement using human and showed the tendancy that guinea pig SPF was lower than human SPF. The second, there was the good relationship between in vitro SPF by using Transpor $e^{R}$ tape and in vivo SPF, and it is possible to predict human SPF from Protection Index(PI) by using tape. The third, it is thought that SPE 20 is reasonable value because of UV intensity in Seoul and the primary skin irritancy of higher SPF than 25. So we propose that it is important to distinguish the sunscreen product having higher than approximate 25 from the category of general cosmetics including lower SPF sunscreen product.oduct.

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