• Toxicological Research
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• 제23권4호
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• pp.405-413
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• 2007

This study was to investigate single and repeated-dose toxicities of Tensolin-$F^{(R)}$, an anti-wrinkle agent, in Sprague-Dawley (SD) rats or ICR mice. In single-dose oral toxicity study, the test materials were administered once by gavage to male and female SD rats at dose levels of 0 and 2,000 mg/kg. No dead animals and abnormal necropsy findings were found in control and Tensolin-$F^{(R)}$ treated group. Therefore, the approximate lethal dose of Tensolin-$F^{(R)}$ was considered to be higher than 2,000 mg/kg in rats. In the 4-week repeated oral toxicity study, the test material was administered once daily by gavage to male and female ICR mice at dose levels of 0, 25, 50 and 100 mg/kg/day for 4-weeks. In the results, no abnormality was observed in mortality, clinical findings, body weight changes, food and water consumptions, opthalmoscopic findings, necropsy findings, histopathological findings. In hematological analysis, there was a trend of increase in reticulocyte at male 25 mg/kg, although such changes were in normal ranges. On the other hand, there was a trend of decrease in hemoglobin at female 50, 100 mg/kg, such changes were in normal ranges. In addition, serum biochemical parameters including sodium, BUN and chloride increased at 25, 50 and 100 mg/kg. Relative organ weights of right testis, brain, lung and left epididymis were increased in 100 mg/kg groups of male rats in contrast to not change in female groups. However, these changes of relative organ weights, hematological and serum biochemical parameters were not accompanied with related signs such as histopathological changes or clinical findings. In conclusion, 4-week repeated oral dose of Tensolin-$F^{(R)}$ to ICR mice did not cause apparent toxicological change at the dose of 25, 50, 100 mg/kg body weight. Consequently the no-observed-adverse-effect level (NOAEL) for Tensolin-$F^{(R)}$ in ICR mice following gavage for at least 4-week is higher than 100 mg/kg/day.

• 한국어병학회지
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• 제21권1호
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• pp.35-43
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• 2008

남해안 일원의 양식 대상종인 참돔의 월동기간중의 폐사발생 원인구명을 위해 병리학적, 혈액생화학적 성상 및 장단기간 양식장의 수온조사를 종합비교하였다. 1. 월동 기간중에 폐사한 참돔의 병리학적조사결과, 육안적으로 녹간증, 장내 복수 증상을 나타내었으며, 경증의 아가미흡충 감염을 제외한 세균, 바이러스 질병은 확인하지 못하였다.2. 혈액생화학적 분석결과, 폐사시기에 혈중의 AST, ALT는 폐사시기에 급격히 높아졌으며, 단백질, 지방 성분값은 저하된 것으로 나타났다. 3. 실시간 양식어장 환경정보제공시스템의 수온 분석에 의하면, 참돔의 폐사가 가장 먼저 시작된 해역인 사량도 해역은 참돔의 저온 한계수온인 8℃ 이하의 수온이 42일간 지속된 것으로 나타나 저수온에 장기간 노출된 것으로 판단되었다. 4. 폐사가 많았던 사량도 양지와 미륵도 명지해역의 2003년에서 2006년까지 3년간 장기수온변화를 보면, 월동기간인 2005년 12월에서 2006년 2월까지의 수온이 2003, 2004년에 비해 낮은 수온 분포를 보였다.5. 참돔의 폐사발생해역은 비폐사해역에 비해 수심이 얕으며, 수층별 수온변화가 큰 것이 특징이었다.

• 생명과학회지
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• 제27권11호
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• pp.1376-1380
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• 2017

본 연구에서는, 만삼(Codonopsis pilosula)의 뿌리를 말린 한약재인 당삼을 마우스에 매일 장기간 투여할 경우 실험 동물의 체중 변화에 어떠한 영향을 미치는지 알아보고자 하였다. 당삼 열수 추출물(CP-W) 1 g/kg을 매일 1회씩 10주 동안 마우스에 경구 투여하였으며, 전체 실험 기간 동안 체중 및 사료 섭취량을 측정하였다. 실험 종료시점에서 마우스로부터 채혈하여 각종 혈액학적/혈청 생화학적 지표들을 분석하였으며, 안락사 후 부검을 실시하고 복부 내 장기들의 무게를 측정하였다. 그 결과, CP-W 투여군의 체중이 대조군에 비해 약 10% 가벼웠던 반면, 사료 섭취량은 군 간의 유의적인 차이가 없었다. 실험 기간 내내 어느 개체에서도 임상적으로 이상 징후가 관찰되지 않았으며, 부검 시 어떠한 이상 증상도 발견되지 않았다. 혈액 시료 분석 및 장기 무게 측정 결과 역시 어느 지표에서도 군 간의 차이를 보이지 않았다. 이상의 연구 결과들을 요약하면, CP-W 1 g/kg을 마우스에 매일 1회씩 10주 동안 경구 투여한 결과, 사료 섭취량의 변화 없이 체중 증가가 유의적으로 억제되었으며, 장기간 투여에 따른 뚜렷한 독성 증상은 발견되지 않았다.

• 환경생물
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• 제39권3호
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• pp.344-353
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• 2021

본 실험에서 미세플라스틱의 노출은 넙치의 혈액학적 성상인 hemoglobin 및 hematocrit 수치의 유의적인 감소를 유발하였다. 또한 미세플라스틱의 노출은 넙치 혈장 무기성분인 calcium, 유기성분인 glucose 및 cholesterol, 효소성분인 AST의 유의적인 변화를 나타냈다. 본 연구에서 바이오플락 환경에서 미세플라스틱의 노출이 어류의 혈액생리에 영향을 주며 독성으로 작용하는 것을 확인할 수 있었다. 향후, 일반 해수와 바이오플락 환경으로 각각 양성한 넙치를 이용하여 사육환경의 변화에 의한 미세플라스틱 노출영향의 차이에 대해서도 추가적인 연구가 이루어져야 할 것이다. 본 연구는 다양한 어종에서 종별 미세플라스틱의 농도 연구에서 미세플라스틱 노출에 따른 종별 독성영향비교평가를 위한 기본 자료로 활용될 수 있을 것이다. 하지만, 바이오플락 환경에서 미세플라스틱의 응집은 미세플라스틱의 독성에 영향을 미치는 중요한 요소이기 때문에(Choi et al. 2020), 향후 연구에서 철저한 모니터링과 함께 다양한 미세플라스틱 독성에 미치는 요소에 대한 추가연구가 필요할 것이다.

• 한국해양생명과학회지
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• 제8권2호
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• pp.150-159
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• 2023

수인성 질산 노출에 대한 향어의 독성 영향을 확인하기 위해 96시간 동안 0, 4, 20, 100, 500 및 2,500 mg NO₃^-/L의 수인성 질산에 노출을 실시하였다. 질산 96시간 급성 노출에 의한 향어의 반수치사농도(LC50)는 1,433.54 mg NO₃^-/L로 나타났다. 혈액학적 성상을 통해 수인성 질산 노출이 향어에게 미치는 생리학적 변화를 평가하였으며, RBC count는 유의적인 감소를 나타내었다(p < 0.05). 혈장 무기성분을 통해 수인성 질산 노출에 따른 향어의 이온 조절 능력 변화를 평가하였으며, 혈장 무기성분에서 calcium과 magnesium은 유의적으로 감소하였다(p < 0.05). 혈장 유기성분을 통해 수인성 질산 노출로 인한 향어의 건강도와 스트레스 상태를 평가하였으며, 혈장 유기성분인 glucose는 유의적인 증가를 나타내었다(p < 0.05). 혈장 효소성분을 통해 수인성 질산 노출로 인한 간 손상도 및 효소 활성의 변화를 평가하였으며, 혈장 효소성분인 AST, ALT 및 ALP는 높은 수준의 수인성 질산 노출에서 유의적으로 감소하였다(p < 0.05). 본 연구의 결과는 C. carpio nudus에 대한 수인성 질산 노출이 생존율, 혈액학적 성상 및 혈장성분에 독성으로 영향을 미칠 수 있음을 의미한다.

• Asian-Australasian Journal of Animal Sciences
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• 제25권9호
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• pp.1262-1268
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• 2012

The present investigation was designed to determine whether supplementation of different level of vitamin E for 12 months to arsenic exposed goats (50 ppm as sodium arsenite) affords protection against the blood hemato-biochemical parameters caused by the metalloid. A total of 24 crossbred (Alpine${\times}$Beetal) lactating goats were assigned randomly into 4 equal groups (control, $T_1$, $T_2$ and $T_3$) of 6 in each, on the basis of average body weight ($36.10{\pm}0.11$ kg) and milk yield ($1.61{\pm}0.04$ kg/d). The animals in $T_1$, $T_2$ and $T_3$ were given 50 ppm arsenic, while in $T_2$ and $T_3$, additionally; vitamin E at the rate of 100 IU and 150 IU/kg dry matter (DM) respectively was additionally supplemented for the period of 12 months. Hemoglobin (Hb), total leukocyte (TLC) and blood lymphocyte % were decreased (p<0.05) in arsenic fed groups and vitamin E supplementation in the experimental group showed a protective potential. Significant increases (p<0.05) in aspertate transaminase (AST) and alanine transaminase (ALT) activities among arsenic supplemented groups were recorded, however vitamin E supplementation at higher doses showed a protective effect (p<0.05) against AST but in the case of ALT no ameliorating effect was found in either of the doses. Plasma total protein was decreased (p>0.05) but creatinine level was periodically increased in all As supplemented groups and vitamin E supplementation did not produce any protective effect. It can be concluded that arsenic exposure resulted in varying degree of changes in hemato-biochemical parameters and activities of antioxidant enzymes in goats but concomitant treatment with Vitamin E is partially helpful in reducing the burden of arsenic induced effect.

• Asian-Australasian Journal of Animal Sciences
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• 제24권7호
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• pp.1001-1006
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• 2011

To determine the efficiency of copper (Cu) supplementation, a feeding experiment was carried out with 240 day old broiler chicks (vencobb-100). Birds were divided into four dietary treatments: i) C - no additives, ii) $T_1$-75 mg inclusion of Cu/kg diet, iii) $T_2$-150 mg inclusion of Cu/kg diet, iv) $T_3$-250 mg inclusion of Cu/kg diet. The present study was carried out in the Department of Animal Physiology, West Bengal University of Animal and Fishery Sciences, Kolkata, India for a period of 42 days (6 weeks). Growth performance was measured in terms of live weight gain, cumulative feed intake and feed conversion ratio at the end of $21^{st}$ and $42^{nd}$ day of the experiment and the result was found to be encouraging for commercial enterprises when the chickens were fed at 150 mg Cu/kg ($T_2$) of their diet. Excess dietary copper more than 150 mg/kg reduced the haemoglobin (Hb) concentration in blood and resulted in the accumulation of copper in the liver with decreased blood Hb concentration and packed cell volumes (PCV). Copper supplementation increased the total erythrocyte count (TEC) as copper is involved in erythropoiesis. But, from the result it is indicated that the dietary copper concentration could not alter the total leukocyte count (TLC). In case of different leucocytes count (DLC), there were no significant differences observed among the different treated groups. Statistical analysis showed significant (p<0.01) difference in plasma concentration of copper, zinc, ferrous and cholesterol among the different copper treated groups. The result indicates that supplementation of copper is an effective way of improving the production performance and haematological parameters in broiler chicken.

• Fisheries and Aquatic Sciences
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• 제18권4호
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• pp.379-385
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• 2015

We studied the effects of the proprietary prebiotic Immunogen$^{(R)}$ on the growth, hematology and gut microbiota of common carp fingerlings. A basal diet was formulated using common feed ingredients and supplemented with Immunogen$^{(R)}$ at concentrations of 0, 5, 10, 20 and $40g\;kg^{-1}$, each of which was tested experimentally on replicated groups of fish. The trials ran for 8 weeks. Common carp fingerlings with an initial weight of $4.82{\pm}0.05g$ were randomly distributed among the experimental tanks at a stocking density of 25 fish per tank. The experimental diets were provided thrice per day; on each occasion the fingerlings were given a weight of feed that amounted to 4% of fish biomass. At the end of the experimental period, we determined the growth performance, feed conversion ratio, hematological parameters, body composition and gut micro-flora parameters of the test fish. Inclusion of $5g\;kg^{-1}$Immunogen$^{(R)}$ in the diet significantly improved growth performance and feed utilization in comparison with controls. However, the whole-body composition of the fish was not significantly influenced by prebiotic inclusion. Inclusion of $5g\;kg^{-1}$ Immunogen$^{(R)}$ significantly increased the total bacterial and Lactobacillus counts in fish intestines, but these bacterial parameters were significantly negatively impacted by higher concentrations of the prebiotic. Red blood cells counts were increased by prebiotic dietary supplementation at concentrations of 5 and $10g\;kg^{-1}$ prebiotic. Glucose and cholesterol levels were elevated by administration of Immunogen$^{(R)}$. Thus, dietary supplementation with $5g\;kg^{-1}$ Immunogen$^{(R)}$ improved fingerling common carp growth performance and feed utilization, and beneficially influenced the gut microflora

• 대한한의학방제학회지
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• 제20권2호
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• pp.55-63
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• 2012

Objectives : This study was conducted to investigate the safety of Bangpungtongsung-san in rats. Methods : The safety of this prescription on acute toxicity was evaluated by single dose toxicity study. Rats were orally administrated in a single dose of 0 and 2,000 mg/kg(limited dose) Bangpungtongsung-san. There were 7 rats in each groups. All animals were sacrificed after 14 days of treatment. After single administration, mortality, clinical signs, and body weight changes were observed for 14 days. Three parameters(autopsy finding, clinical chemistry, and hematology) were tested on the last day. Results : In this study with rats, Bangpungtongsung-san treatment did not show any acute toxicity. No mortality was noted for 14 days of treatment. There were no adverse effects on clinical signs, body weight changes, and autopsy finding at all treatment groups. The clinical chemistry parameters attesting to liver and kidney functions as well as the hematological parameters were within the normal ranges. Conclusions : It is considered that $LD_{50}$ of Bangpungtongsung-san is over 2,000 mg/kg in oral administration by rats. This finding of the safety of Bangpungtongsung-san is expected to strengthen the position of this prescription as nontoxic medicine.

• Journal of Ginseng Research
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• 제35권1호
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• pp.39-44
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• 2011

We studied the acute oral toxicity of black ginseng (BG) produced by heat process in rats. Single acute BG extract doses of 0, 5, 10, and 15 g/kg dissolved in saline were administered by oral gavage and the animals were kept under observation for 14 days. The single administration of BG extract up to 15 g/kg did not produce mortality, behavioral change or abnormal clinical signs in the rats. These results indicated that the oral $LD_{50}$ of the BG extract in the rats is higher than 15 g/kg. Compared to the control group, no treatment-related biologically significant effects of BG extract were noted in the measurements of the body weight or food intake. At the end of the period, the biochemical parameters and hematological parameters were analyzed in the plasma and blood. A histopathological examination of the liver and kidney was also conducted. Only the blood nitrogen urea and potassium levels in the biochemical indices showed significant differences at 10 and 15 g/kg doses of BG extract compared to the control group. These changes were not considered to be due to the toxicity. None of the other clinical chemistry parameters were affected. Therefore, these results indicate that the BG by heat processing is virtually nontoxic.