• 생명과학회지
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• 제19권8호
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• pp.1152-1158
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• 2009

본 연구는 우리나라에 분포하는 광대버섯인 amanita muscaria로 단회투여독성시험과 반복투여독성시험을 하였을 때 SD 랫드의 독성병리학적 변화를 알아보고자 수행하였다. 단회투여독성시험은 강경증, 경사판법, 정압자극법을 이용하여 측정하였다. 강경증은 33 mg/kg의 농도에서 투여 2${\sim}$3 시간 후 강경증 시간이 감소하였다. 경사판법의 경우 33 mg/kg의 농도에서 투여 2시간 후 대조군과 비교하였을 때 낮은 경사 각도에서도 쉽게 미끄러졌으며, 앞다리 보다는 뒷다리 쪽에서의 움직임 감소를 보였다. 정압자극법의 경우 대조군, 저용량군, 중간용량군에서 SD 랫드가 자극을 인지하는 시간이 1${\sim}$2초 정도로 짧고 매우 공격적인 반응을 보였지만, 고용량군에서는 자극인지 시간이 대략 3${\sim}$5초로 증가하였으며, 대부분 공격적인 반응을 보이지 않는 것이 관찰되었다. 강경증, 경사판법, 정압자극법 모두 투여 4시간 후 대조군과 비슷한 수치로 회복되었으며 이것으로 보아 섭취 4시간 전후에는 amanita muscaria의 독성이 현저히 감소하는 것으로 확인되었다. 반복투여독성시험은 혈액, 혈청분석, 조직 병리학적 검사를 실시하였다. 혈청 분석에서 투여군과 대조군을 비교하였을 때 BUN과 creatinine의 변화는 없었지만 ALT와 LDH는 투여군에서 증가하였다. 이러한 결과를 바탕으로 표적장기인 간과 신장의 손상을 의심하였고 조직 병리학적 검사를 통해 간과 신장의 손상을 확인할 수 있었다.

• 대한방사선치료학회지
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• 제17권2호
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• pp.133-140
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• 2005

목 적 : 3차원치료계획 (3D plan)과 대향2문조사(POP plan)의 선량 계획시 치료표적 (Planning Target Volume, PTV)와 정상조직(Organ at Risk, OAR)에 실제 흡수되는 선량을 반도체검출기를 이용하여 실시간선량측정(Real- time dosimetry)을 시행함으로써 치료계획의 타당성을 확인하고자 한다. 대상 및 방법 : 실제 치료할 환자의 구강안을 채워줄 Aquaplaste를 Simulation과정에서 제작하며 측정하고자 하는 부위에 Aquaplaste를 성형하여 반도체 검출기가 자리할 공간을 확보한다. 치료시 반도체검출기를 측정부위에 위치시키고 치료가 진행중 각 Port에 해당하는 Electrometer의 지시치를 얻는다. 얻은 지시치에 선량변환계수(Diode Calibration Factor, DCF)를 이용하여 실제 선량으로 환원하여 Exp. Dose와 실제 Dose를 비교하며 오차를 구한다. 실험의 수를 증가시켜 보다 정확한 결과를 얻기 위하여 Alderson Rando phantom(Huestis, USA)을 이용하여 같은 실험을 반복한다. 결 과 : 대향2문조사를 한 A환자의 경우 Exp. value와 측정선량의 비(exp.D/eff.D)가 197.5/199로 -1.2%, 3차원치료계획을 한 B환자는 exp.D/eff.D가 199.9/198.7로 +0.6%, C환자의 경우 exp.D/eff.D가 196/200으로 -1.5%가 차이 남을 알 수 있었다. 또 Target dose 외에 방어하고자 하는 부위의 측정도 병행한 C환자의 결과치는 96/200으로 47%의 선량이 측정되어 방어의 목적을 달성했음을 알 수 있었다. Phantom을 이용한 측정에서는 A환자와 같이 (a) point(target), (b) point(protect)로 나뉘어 측정하여 다음의 결과치를 얻었다. Phantom 1 (a): 190.6/198.4=-3.9%, (b): 119.6/124.2=-3.7%, Phantom 2 (a): 185.4/191.3=-3%, (b): 109.6/113.8=-3.7%의 결과치를 얻어 목적한 선량에 ${\pm}5%$이내로 만족함을 알 수 있었다. 결 론 : 반도체검출기를 이용한 치료전 선량 측정의 유용성을 알아본 이번 실험은 Target dose 뿐만 아니라 방어하고자 하는 영역 또한 알아봄으로써 치료의 타당성을 확인하는데 매우 유용했고 단순선량계산에 의한 확인되지 않는 Target dose를 확인하는 데에도 큰 이점이 있다고 생각된다. 치료 전 L-gram과 같이 이런 측정은 매우 효과적으로 치료방법의 타당성과 이후의 치료계획에도 많은 이득을 가져다 줄 것이라고 생각된다.

• 사상체질의학회지
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• 제9권2호
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• pp.203-225
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• 1997

Jihwangbakhotang(地黃白虎楊) is made by Li Je Ma, the creator of the Four Constitutional Medicine. Single and 13 weeks oral repeated dose toxicity studies were conducted in Sprague Dawley rats of both sexes to elucidate the potential acute and subchronic toxicity of JBT extract and reversibility of any effects. In the single dose study, JBT extract was administered orally to rats with the dose of 2 g/kg and 8 g/kg. In the long term administration of 13 weeks, the JBT extract of 125 mg/kg/day, 500 mg/kg/day, 2000 mg/kg/day was administered to rats. The change of blood weight, urine volume, electrolyte in urine, hematological change, the change of blood chemistry, autopsy finding, and histological observation were researched, the results were as follows; 1. The lethal dose of JBT extract seems to be over 10 g/kg, the single administration of JBT extract 8 g/kg showed no toxical signs except little increase of urine volume. 2. The change of body weight had the trend of decrease in the group of, but has no significance, and also the consumption of food and water had no changes. 3. The hematological changes induced by the 13 weeks administration of JBT extract showed the significance in the item of Hb, MCH, MCV, WBC in the group of 125 mg/kg/day. 4. In the test of blood chemistry, total cholesterol showed little decrease and A/G ratio showed little increase, but the change was not clear, and the standard error was large. So the result was obtained insignificantly and the toxicity of JBT extract was not observed. 5. In the male group after recovery period, the level of cholesterol and triglyceride decreased slightly, but the result was not significant. 6. In the urine test, the little change of electrolyte was appeared, but it seemed not to be the result induced by the toxicity of JBT extract. 7. In each group of male and female rats, the weight change of organ and the serum histological changes was observed, but the result did not showed the dose dependent toxicity. So the toxicity of JBT extract was not regarded. In the conclusion, the toxicity of JBT extract was not observed in the single dose treatment and long term repetitive administration of JBT extract.

• 대한한방내과학회지
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• 제27권1호
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• pp.102-113
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• 2006

Objectives & Methods : To obtain the 50% lethal dose(LD50), approximated lethal dose(ALD) and approximated target organs of 'Mahwangyounpae-tang' for further study into such things as repeated dose toxicity, genotoxicity and reproductive toxicity, single dose toxicity was tested in male SD rats according to KFDA Guideline 1999-61[KFDA, 1999] at dosage levels of 2,000, 1,000, 500, 250 and 125 mg/kg/$10m{\ell}$. In this study, mortalities, clinical signs, body weight changes and body weight gains, gross findings and weight of principal organs were detected during and/or after 14 days of single dosing. Results & Conclusions : After 2 or 3 days of dosing, 1 or 2 animals in 2,000 mg/kg-dosing groups died. Excitation and leaping response were observed as test article-treatment related clinical signs. These abnormal signs were restricted to 2,000 and 1,000 mg/kg-dosing groups and survivors recovered to normal within 3 or 4 days after dosing. Significant decrease in body weight were observed in some periods of observation in 2,000 and 1,000 mg/kg-dosing group, from 1 days after dosing compared to those of vehicle control group. Significantly diminished body weight gains were observed in observation periods in 2,000 and 1,000 mg/kg-dosing group compared to those of vehicle control group. Hypertrophy and hemorrhage of heart and decoloration of kidney were observed as test article-treatment related gross findings. These abnormal findings were restricted to 2,000 and 1,000 mg/kg-dosing groups. A significant increase of absolute and relative heart and kidney weight were demonstrated in 2,000 mg/kg-dosing groups. The value for LD50 found in this study was 2,218.57 mg/kg. ALD in this study was 2,000 mg/kg, and the target organs are considered to be the heart and the kidney.

• Biomolecules & Therapeutics
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• 제25권5호
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• pp.545-552
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• 2017

Increasing concern is being given to the association between risk of cancer and exposure to low-dose bisphenol A (BPA), especially in young-aged population. In this study, we investigated the effects of repeated oral treatment of low to high dose BPA in juvenile Sprague-Dawley rats. Exposing juvenile rats to BPA (0, 0.5, 5, 50, and 250 mg/kg oral gavage) from post-natal day 9 for 90 days resulted in higher food intakes and increased body weights in biphasic dose-effect relationship. Male mammary glands were atrophied at high dose, which coincided with sexual pre-maturation of females. Notably, proliferative changes with altered cell foci and focal inflammation were observed around bile ducts in the liver of all BPA-dosed groups in males, which achieved statistical significance from 0.5 mg/kg (ANOVA, Dunnett's test, p<0.05). Toxicokinetic analysis revealed that systemic exposure to BPA was greater at early age (e.g., 210-fold in $C_{max}$, and 26-fold in AUC at 50 mg/kg in male on day 1 over day 90) and in females (e.g., 4-fold in $C_{max}$ and 1.6-fold in AUC at 50 mg/kg vs. male on day 1), which might have stemmed from either age- or gender-dependent differences in metabolic capacity. These results may serve as evidence for the association between risk of cancer and exposure to low-dose BPA, especially in young children, as well as for varying toxicity of xenobiotics in different age and gender groups.

• 생명과학회지
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• 제15권1호
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• pp.1-8
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• 2005

이황화메틸의 반복 흡입노출에 의한 아급성 독성 잠재력을 평가하기 위해 암수 랫드에게 0, 5, 25 및 125 ppm용량으로 21일간 반복 흡입노출하고, 일반증상과 체중, 사료섭취 량, 혈액치, 혈청생화학치 및 부검소견을 관찰하였다. 시험결과, 랫드에게 이황화메틸을 3주간 반복 흡입노출하면 125 ppm의 농도에서 체중증가의 억제와 사료섭취 량의 감소를 유발하나, 혈액 및 혈청생화학치에는 어떠한 이상도 유발하지 않는 것으로 나타났다. 본 시험 조건 하에서 이황화메틸의 표적 장기는 관찰되지 않았으며, 무해용량은 암수 모두 25 ppm으로 사료된다.

• 대한디지털의료영상학회논문지
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• 제14권2호
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• pp.1-8
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• 2012

Purpose : We aim at presenting the optimum radiologic factor through the evaluation of dose variation and of image quality through the use of a grid in Humerus examination and the change of dose because of the change of radiologic factor. Materials and Methods : We divided it in 3 cases: when using a grid or not and when using IP(Image Plate) in a digital system. Also, as fixing kVp to 70kVp it changed mAs, and fixing mAs to 10 it changed kVp, we put up resolution chart and Burger rose phantom on the acrylic phantom of 7cm (the same level of Humerus) to evaluate the dose and image. We used Image J program to evaluate the quantitative resolution of the obtained image, and made the qualitative evaluation and statistical analysis of the image saved in PACS for 20 radiologic technologist with more than 10 years of experience in order of evaluate its contrast. We used SPSS10(SPSS Inc. Chicago, Illinois) for statistical analysis. Results : We observed the analytic result of resolution by the change of kVp that it was $4.539dGycm^2$ in 60kVp and $757.472dGycm^2$ in 75kVp, which increased about 64.6% of dose, while for the resolution it had the pixel value 30.7% better with 851 in 60kVp than 651 in 75kVp. Also, we analyzed the result of resolution by the change of mAs that it was $3.106dGycm^2$ in 5mAs, and $12.470dGycm^2$ in 20mAs, which increased about 400% of dose, while for the resolution DR had 678 in 5mAs, and 724 in 20mAs that increased about 6.8% of resolution. We made the qualitative evaluation of contrast by the change of kVp that DR showed the higher quality than CR, but the contrast by the change of kVp had no special different at the moment of visual evaluation, nor statistically significant difference(P>0.05). We observed the qualitative evaluation of contraste by the change of mAs that the contrast increased as DR increased mAs, and had statistically significant difference(P<0.05). On the other hand, CR had no significant difference for more than 10mAs nor statistically significant difference(P>0.05). Conclusion : In case of some patients with radiographic exposure by the repeated examination such as emergent patient or Follow up patient, they are considered to try to limit the use of a grid, to set kVp under 65kVp in fixed mode, to select less than 10mAs and to reduce the possibility of patient being bombed.

• Radiation Oncology Journal
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• 제15권1호
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• pp.65-69
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• 1997

목적 : 전리함의 크기로 인한 공간 분해능의 문제로 나타나는 전리함 반응함수를 제거하여 실제 선량분포를 얻고자 하였다. 대상 및 방법 : 내경 5mm, 6.4mm 등 2개의 서로 다른 크기를 갖는 전리함들과 다이오드, 필름의 반응함수를 구하고, 동일한 방사선 조사면$(10\times20cm^2)$의 선량분포 프로파일을 측정하여, 각각 deconvolution 기법으로 보정한 후, 보절된 격과가 일치하는지 비교하였다. 결과 : 원통형 전리함의 반응함수와 선량분포를 측정하였고, 측정한 선량분포에서 반응 함수의 효과를 deconvolution방법으로 제거하여 실제 선량분포를 찾아내었다. 사용한 에너지는 최대 광자선 에너지 4MV, 6MV, 15MV였으며, 전 에너지 영역에 걸쳐 보정 된 결과가 일치하는 방향으로 변화하였으며, 분해능 증가 효과가 있었다. 결론 : deconvolution 방법으로 전리함 반응 함수의 효과를 제거했을 때, 여러 측정기를 이용하여 측정한 선량 프로파일의 결과가 일치하는 경향을 볼 수 있어서 deconvolution 방법을 통해 얻은 선량 프로파일을 임상적으로 응용할 수 있음을 알았다.

• Journal of Dental Anesthesia and Pain Medicine
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• 제24권1호
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• pp.19-35
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• 2024

Background: This study investigated a safe and effective bolus dose and lockout time for patient-controlled sedation (PCS) with dexmedetomidine for dental treatments. The depth of sedation, vital signs, and patient satisfaction were investigated to demonstrate safety. Methods: Thirty patients requiring dental scaling were enrolled and randomly divided into three groups based on bolus doses and lockout times: group 1 (low dose group, bolus dose 0.05 ㎍/kg, 1-minute lockout time), group 2 (middle dose group, 0.1 ㎍/kg, 1-minute), and group 3 (high dose group, 0.2 ㎍/kg, 3-minute) (n = 10 each). ECG, pulse, oxygen saturation, blood pressure, end-tidal CO₂, respiratory rate, and bispectral index scores (BIS) were measured and recorded. The study was conducted in two stages: the first involved sedation without dental treatment and the second included sedation with dental scaling. Patients were instructed to press the drug demand button every 10 s, and the process of falling asleep and waking up was repeated 1-5 times. In the second stage, during dental scaling, patients were instructed to press the drug demand button. Loss of responsiveness (LOR) was defined as failure to respond to auditory stimuli six times, determining sleep onset. Patient and dentist satisfaction were assessed before and after experimentation. Results: Thirty patients (22 males) participated in the study. Scaling was performed in 29 patients after excluding one who experienced dizziness during the first stage. The average number of drug administrations until first LOR was significantly lower in group 3 (2.8 times) than groups 1 and 2 (8.0 and 6.5 times, respectively). The time taken to reach the LOR showed no difference between groups. During the second stage, the average time required to reach the LOR during scaling was 583.4 seconds. The effect site concentrations (Ce) was significantly lower in group 1 than groups 2 and 3. In the participant survey on PCS, 8/10 in group 3 reported partial memory loss, whereas 17/20 in groups 1 and 2 recalled the procedure fully or partially. Conclusion: PCS with dexmedetomidine can provide a rapid onset of sedation, safe vital sign management, and minimal side effects, thus facilitating smooth dental sedation.

• BMB Reports
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• 제36권5호
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• pp.499-504
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• 2003

There has been increasing interest in studying the various effects of organophosphate insecticides in humans and experimental animals. Only a few data are available on the effect of the organophosphate insecticide, diazinon, on lipid metabolism. The aim of this study was to evaluate the effect of diazinon on plasma lipid constituents in mammalian animals. The plasma levels of total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), triglycerides (TG), and phospholipids (PL) were measured in albino rats that were orally treated with a single dose of diazinon at a level of $LD_{50}$ or with repeated daily doses at the levels of $\frac{1}{2}$, $\frac{1}{8}$, and $\frac{1}{32}$ $LD_{50}$ for 2, 8, and 32 days, respectively. After a 24 h post-treatment with a single $LD_{50}$ dose of diazinon, TC was not significantly changed, the HDL-C and PL levels were significantly decreased, but the LDL-C and TG levels were significantly increased. Separate daily oral administrations of diazinon at $\frac{1}{2}$ $LD_{50}$, $\frac{1}{8}$ $LD_{50}$, and $\frac{1}{32}$ $LD_{50}$ doses resulted in a significant decrease in HDL-C and PL, with no significant change in TG. The LDL-C levels were significantly increased and TC showed no significant change with $\frac{1}{2}$ $LD_{50}$ and $\frac{1}{32}$$LD_{50}$ doses of diazinon, whereas a significant decrease in the levels of TC, HDL-C, as well as LDL-C, was observed with the $\frac{1}{8}$ $LD_{50}$ dose. These data suggest that diazinon may interfere with lipid metabolism in mammals.