• Title/Summary/Keyword: TOXICITY TEST

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Oxygen Toxicity: Behavioral Assessment by Swim Test in Mouse Exposed to Hypoxia and Hyperoxia (수영 시험 모델에서 산소 농도에 따른 운동성 변화와 독성 평가)

  • 김동희;강문철;김재일;이근호;김광열;김형건
    • Toxicological Research
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    • v.19 no.2
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    • pp.99-104
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    • 2003
  • This study was aimed to evaluate the effect of oxygen on motor activity and toxicity in male mice. The modified Porsolt forced swim test (FST) was used and the distance and time of movement by mice were analyzed in 15。C water bath for 20 minutes using the automatic Ethovision videotracking system. Analyses were carried out before and after 20 minutes of exposure to 10%-70% concentration of normobaric oxygen. The effects of inspired oxygen tension on the distance and time of movement showed the similar trends, but changes in distance were more prominent. Both the distance and time of movement increased after exposure to 30% and 40% oxygen concentration. The distance and time of movement also increased upon exposure to 50% and 60% oxygen. In contrast, increases En movement and time under exposure to 21% oxygen concentration were suppressed when exposed to over 50% oxygen concentration. With exposure to 10% oxygen, there was a significant decrease in the distance of movement and a slight suppression of movement time. During the swim test, 12.5%, 37.5%, and 87.5% of the mice drowned after exposure to 10%, 60%, and 70% oxygen concentration, respectively. These results suggest that motor activity can be enhanced by inspired oxygen up to 40% concentration. When hypoxic and hyperoxic oxygen exposure over 50%, motor activity is reduced and toxicity may be induced.

Effect of Cynanchi wilfordii Radix Extract on the Acute Toxicity in Mice and Subacute Toxicity in Rats (백수오(白首烏) 엑스의 마우스 급성독성(急性毒性) 및 흰쥐 아급성독성(亞急性毒性)에 미치는 영향(影響))

  • Chung, Eun-Jin;Lee, Byung-Joo;Chung, Myung- Hyun
    • Korean Journal of Pharmacognosy
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    • v.24 no.2
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    • pp.166-176
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    • 1993
  • This study was attempted to investigate the acute toxicity in mice, the subacute toxicity in rats of Cynanchi wilfordii Radix extract, the effect on transaminase activities, hematological parameters, leukocyte parameters in serum of subacute-toxicated rats. In acute toxicity test, the death rate was not observed in 50, 100, 200, 300 mg/kg(i.p.), one tenths to two tenths in 300, 500, 1000, 1500 mg/kg(p.o.) for two weeks. In subacute test, rats were all died in 300 mg/kg(p.o.) during 4 weeks, in 500, 1000 mg/kg(p.o.) during three weeks. The cause of death believed to be stomach ulcer. The activities of S-GOT and S-GPT were significantly increased in all sample-treated groups, when compared with the normal groups. A number of WBC and neutrophil belong to hematological parameter were significantly increased, lymphocyte was decreased in all sample-treated group, when compared with normal group. The hemolytic action on water extract, saponin and alcohol extract showed very low activities.

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Evaluation and Comparison with Standard 48 hr Acute Bioassay and High Temperature Rapid Toxicity Test for Sewage Toxicity Test (하수의 독성평가를 위한 표준독성시험법과 온도증가 단기독성평가법의 비교 평가)

  • Lee, Sang-Ill;Jun, Byong-Hee;Weon, Seung-Yeon;Kim, Yi-Jung;Kim, Keum-Yong
    • Journal of Korean Society of Environmental Engineers
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    • v.27 no.2
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    • pp.191-197
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    • 2005
  • A new method, ToxTemp (TOXcity test based on TEMPerature control) using Ceridaphnia dubia was applied to evaluate the toxicity of insecticide materials and compared with the standard 48 hr acute bioassay. BPMC, diazinon and fenitrothion may cause the inhibition to the biological process in sewage treatment plant and need to detect toxicity within short contact time. The ToxTemp method showed sensitive detection with more shorter contact of 1-1.5 hr time than that of the standard 48 hr acute bioassay. To evaluate toxicity of real wastewater/sewage, the inhibition rate of nitrification and oxygen uptake rate (OUR) using activated sludge, the standard 48hr acute bioassay and ToxTemp method using C. dubia were compared, respectively. On the basis of the inhibition rate of nitrification, the OUR test showed the less sensitive results at the relatively strong toxic sewage. On the other hands, the standard 48hr acute bioassay and ToxTemp method using C. dubia represented the toxicity of each wastewater/sewage with high sensitivity. Even the slightly low (about 1.5%) sensitivity, the ToxTemp method showed the high applicability to the real site of sewage treatment plant.

Acute and Subacute Oral Toxicity of $HELIKIT^{TM}$ in Rats (흰주에서 $HELIKIT^{TM}$의 급성 및 아급성 경구독성시험)

  • 김창종;조철형;최현호;심상수;김정례
    • YAKHAK HOEJI
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    • v.43 no.2
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    • pp.180-197
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    • 1999
  • Acute and subacute oral toxicity of $HELIKIT^{TM}$ ($^{13}C-urea$) were carried out in Sprague-Dawley rats of both sex. The toxicity of $HELIKIT^{TM}$ was compared with urea($^{12}C-urea$ which is used for control). In acute toxicity studies, we daily examined number of deaths, clinical signs, body weights and pathological examination for 14 days after single oral administration of HELIKIT or urea($^{12}C-urea$) at a dose of 5000 mg/kg. The subacute oral toxicity was investigated in Sprague-Dawley rats treated with $HELIKIT^{TM}$ at a dose of 40, 200 and 1,000 mg/kg/day or $^{12}C-urea$ at a dose of 1,000 mg/kg/day for 4 weeks. In acute toxicity studies, $HELIKIT^{TM}$ and urea did not show any toxic effect in rats and oral LD50 value was over 5,000 mg/kg rats. In subacute toxicity studies, no death occured and no drug-related changes were found in clinical observations; body weight, food consumption, opthalmoscopy. auditory test, urinalysis, hematology, blood chemistry, gross pathological examination or organ weight between $HELIKIT^{TM}$, urea and control groups. In histopathological examinations, the slight thickening of mucosa of the limiting ridge in the stomach was noted in the animals treated with $HELIKIT^{TM}$ at a dose of 1,000 mg/kg/day and also the changes in urea group at a dose of 1,000 mg/kg/day was found, but all of these changes in the changes in ures group at a dose of 1,000 mg/kg/days was found, but all of these changes in the stomach regressed after withdrawal of the test article for 2 weeks and reversibility of the effect was revealed. These results indicate that the non toxic dose level of $HELIKIT^{TM}$ was 1,000 mg/kg/day in the 4 weeks-repeated dose study, suggesting that the substitution of $^{13}C$ for carbon in urea molecule has no effect on the toxicity of urea and changes in stomach are reversible.

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Comparative Study on Acute Toxicity of Treated Effluent Containing Salt using Daphnia magna and Vibrio fischeri (염 함유 폐수처리수에 대한 Daphnia magna 및 Vibrio fischeri 급성독성 비교연구)

  • Kim, Jongmin;Shin, Kisik;Yu, Soonju;Lee, Jungseo;Kim, Woongki
    • Journal of Korean Society on Water Environment
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    • v.31 no.5
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    • pp.453-459
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    • 2015
  • This paper aims to evaluate the results of acute toxicity testing with Daphnia mag$Na^+$ and Vibrio fischeri and characteristics of ionic substance of treated effluent which contained salt. Acute toxicity with Daphnia mag$Na^+$ and Vibrio fischeri and salinity of 19 samples (4 business categories) were a$Na^+$lysed. Salinity of effluent could explain the fluctuation of toxicity with D. mag$Na^+$ about 66% ~ 91% ($r^2=0.66{\sim}0.91$). The results of acute toxicity testing with V. fischeri of treated effluent (aggregate manufacture facilities) did not indicate toxicity (TU = 0), whereas that of chemical manufacture facilities indicated toxicity. V. fischeri, a candidate test organism, seemed suitable test organism for acute toxicity testing of effluent except high salinity (above 65‰ ~ 70‰) in aggregate manufacture facilities (nonmetalic minerals facilities). The performance of ion composition about treated effluent of surveyed facilities indicated that ion concentration of $Na^+$ (5,740 mg/L) and $Cl^-$ (9,727 mg/L) showed high level among 6 major ions ($Na^+$, $K^+$, $Ca^{2+}$, $Mg^{2+}$, $SO_4{^{2-}}$, $Cl^-$) in effluent of nonmetalic minerals facilities. In addition, Clion seemed to influence the D. magna survival rather than $Na^+$ ion.

Toxicity Assessment of Photorhabdus temperata Isolated from Heterorhabditis megidis Gwangju Strain (Nematoda: Heterorhabditidae) in Fish and Rat (Heterorhabditis megidis Gwangju Strain (Nematoda: Heterorhabditidae)으로부터 분리한 Photorhabdus temperata의 어류 및 쥐 독성평가)

  • Park, Sun-Han;Chung, Nam-Jun;Choo, Young-Moo;Kim, Young-Joon;Kim, Jin-Ho
    • Korean Journal of Organic Agriculture
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    • v.30 no.1
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    • pp.103-118
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    • 2022
  • Photorhabdus is a bacterial symbiont of entomopathogenic nematodes of the genus Heterorhabditis in the family Heterorhabditidae. Photorhabdus is known to have nematicidal activity in addition to insecticidal activity. P. temperata isolated from Korean indigenous H. megidis Gwangju strain also produced high control efficacy against root-knot nematode Meloidogyne incognita and root-lesion nematode Pratylenchus penetrans. P. temperata has drawn interest as a potential bionematicide for the control of root-knot nematodes thereby. For the registration as an organic agricultural material, the toxicity of P. temperata was assessed by the acute toxicity test in carp (Cyprinus carpio) and acute oral and dermal toxicity tests in Sprague-Dawley rat (Rattus norvegicus) in compliance with the guidelines of the Rural Development Administration (RDA). In the acute toxicity test in fish, neither lethality nor abnormal responses of carp were observed. Body length and weight of carp and changes in DO concentrations and pH values were not significantly different between the treated group and the untreated control. In the acute oral and dermal toxicity tests, clinical signs, abnormal behavior, mortality, and pathological findings were not observed in all the experimental rats. The weight increment of all rats was normal. Acute toxicity results of P. temperata in fish and rats belonged to categories III, IV, and IV of RDA, respectively. Toxicity results of the present study indicated that P. temperata could be a safe and promising bionematicide against root-knot nematodes and root lesion nematode.

Acute and Repeated 28-Day Oral Dose Toxicity Studies of Thymus vulgaris L. Essential Oil in Rats

  • Rojas-Armas, Juan;Arroyo-Acevedo, Jorge;Ortiz-Sanchez, Manuel;Palomino-Pacheco, Miriam;Castro-Luna, Americo;Ramos-Cevallos, Norma;Justil-Guerrero, Hugo;Hilario-Vargas, Julio;Herrera-Calderon, Oscar
    • Toxicological Research
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    • v.35 no.3
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    • pp.225-232
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    • 2019
  • Thymus vulgaris L. is widely used as an ingredient in cooking and in herbal medicine. However, there is little information about its toxicity. The present study was performed to evaluate the acute and repeated 28-day oral dose toxicity of thyme essential oil in rats. For the acute toxicity test, two groups of three rats were used. The rats received a single dose of essential oil: 300 or 2,000 mg/kg of body weight (bw). The rats were observed individually during the first four hours, and then daily until day 14. For the toxicity test with repeated doses, four groups of 10 rats were used. Doses of 100, 250, and 500 mg/kg/day were tested for 28 days. At the end of the experiment, blood was collected and the animals were sacrificed. Histopathological examination showed that in the lungs of rats given the 2,000 mg/kg bw dose, polymorph nuclear infiltrates, hemosiderin macrophages, and interstitial space thickening were present. In the repeated dose study, all rats survived the 28-day treatment period and apparently showed no signs of toxicity. The hematological and biochemical parameters were not altered. The histopathological study of the organs showed severe changes in the lung, with the dose of 500 mg/kg/day; in the other organs, no alterations were observed or the changes were slight. The body weight was only altered in male rats given the 500 mg/kg dose. The relative weight of the organs did not show any significant changes. Our studies revealed that the essential oil of Thymus vulgaris has moderate oral toxicity according to the results of the acute test, whereas the results of the 28-day oral toxicity test suggest that the no-observed-adverse effect level (NOAEL) is greater than 250 mg/kg/day.

Experimental studies on the Acute Toxicity of Bos taurus.Ursus thibetanus.Moschus extrct solution(BUM) for Herbal-acupuncture (우황(牛黃).태담(態膽).사향약침액(麝香藥鍼液)(BUM)의 급성독성(急性毒性)에 관한 실험적(實驗的) 연구(硏究))

  • Lee, Sang-Woon;Kang, Dae-In;Jeong, Chan-Gil;Kim, Kwang-Ho;Soh, Kyung-Sun
    • Journal of Pharmacopuncture
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    • v.5 no.2
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    • pp.6-24
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    • 2002
  • This experiment was carried out to study on the safety assessment of Bos tures$^{\circ}{\S}Ursus thibetanus^{\circ}{\S}$Moschus extract solution(BUM) for Herbal-acupuncture. SD rats and ICR mice were used for acute toxicity test. the results were summerized as follows; 1. In rats and mice, LD50 value could not be measured. 2. There were no abnormal finding in acute toxicity test treated BUM for Herbal-acupuncture

The Experimental Study on Toxicity Effects of Pinus Densiflora Siebold et Zuccarini Herbal-acupuncture (송엽약침액(松葉藥鍼液)의 독성시험에 관한 실험적(實驗的) 연구(硏究))

  • Kim, Dae-Hyun;Soh, Kyung-Sun
    • Journal of Society of Preventive Korean Medicine
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    • v.10 no.1
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    • pp.123-140
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    • 2006
  • This experiment was carried out to study on the safety assessment of Pinus densiflora Siebold et Zuccarini for Hebal-acupuncture. SD rats and ICR mice were used for acute toxicity test, the results were summerized as follows; 1. In rats and mice, $LD_{50}$ value could not be measured. 2. There were no abnormal finding in acute toxicity test treated Pinus densiflora Siebold et Zuccarini for Hebal-acupuncture.

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Evaluation of the Single-Dose Toxicity of TA Pharmacopuncture in Rats

  • Hwang, Ji Hye;Jung, Hyo Won;Jung, Chul
    • Journal of Pharmacopuncture
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    • v.22 no.3
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    • pp.171-175
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    • 2019
  • Objectives: TA is a polyherbal extract comprising seven herbs, typically used for the pharmacopuncture treatment of patients with traffic accident- related injuries and musculoskeletal diseases. This animal study was conducted to evaluate the safety of the TA extract, using a single-dose toxicity test. Methods: The dose range and sampling time were first established. Six- week-old Sprague-Dawley rats were administered 1.0 mL of TA or normal saline (control), intramuscularly, for the single-dose toxicity test. The general condition, mortality, and histology of all rats were observed for 2 weeks. Results: No abnormal symptoms or deaths were observed in any group. The body weights of the rats in the TA and control groups were similar. No significant differences in histopathology were observed between the groups. Conclusion : Our study indicates that 1.0 mL of TA extract may be safely administered for pharmacopuncture for treatment of patients in traditional medicine clinics.