• 생물정신의학
• /
• 제4권2호
• /
• pp.237-245
• /
• 1997

The study was designed to evaluate the significant roles of SSRI in rat of depression model. Chronic exposure to mild unpredictable stress has been found to depress the consumption of sweet 1% sucrose solutions in the Sprague-Dawley rats. We applied the variety of 11 types of stress regimens and identified depressive behaviours(developed by Willner) in 70 Sprague-Dawley rats. Rats in experiments were stratified into 6 groups, ie ; 3 kinds of SSRI(paroxetine, fluoxetine, sertraline), clomipramine, choline and saline control. Memory function was evaluated by passive avoidance learning and retention test. The authors determined how long memory retention would remain improved with 24 hour, 1 week, 2 weeks, 3 weeks, and 4 weeks at training-testing interval in depressive states of the Sprague-Dawley rats. The results were as follows ; 1) There were no significant differences between the 6 groups at the 24 hour training-testing interval. 2) The paroxetine treated group showed significant differences from the control group at the 1 week and 2 weeks training-testing interval. 3) The paroxetine and the fluoxetine treated groups showed singificant differences from the control group at 3 week training-testing interval. 4) The paroxetine and the choline treated groups showed significant differences from the control group at 4 week training-testing interval. In summary, paroxetine had an effect on long term memory processing from 1st week to 4th week. Also, fluoxetine(at 3rd week) and choline(at 4th week) had effect on long term memory processing. Sertraline, clomipramine were ineffective on memory processing during 4 weeks observation. Possible explanations why paroxetine had early effect on memory processing than the other selective serotonin reuptake inhibitors are rapid bioavailability, which is the characteristics of pharmacokinetics of paroxetine. In clinical situation, author carefully suggest that SSRI would be beneficial to improve the memory function caused by depressive neurochemical changes.

• 한국작물학회:학술대회논문집
• /
• 한국작물학회 2006년도 한국약용작물학회 공동춘계학술발표회
• /
• pp.656-657
• /
• 2006

• The Journal of Korean Physical Therapy
• /
• 제2권1호
• /
• pp.47-63
• /
• 1990

The purpose of this study was to determined the effect of low-frequency electrical stimulation on the denervated gastrocnemius muscles of the albino rats, Sprague-Dawley. Fifteen Sprague-Dawley adult male albino rats were divided into non-treated (normal) group, denervated (control) group, denervated and electrical stimulated (experiments). The gastrocnemius muscles of the right leg were submaximally stimulated with 30 Hz electrical stimulation. After 4-week period, the animals were sacrificed, and muscle were removed, fixed by immersion, and processed for light and electron microscopy. The numbers of Ag-NOR increased significantly (p<0.001), but significant reductions of girth(p<0.01), wet muscle weight (p<0.001), high glycogen content fiber (p<0.01), and mitochondrial number (p<0.05) were found in denervated control group. In comparison with control group, significant increase of right leg girth (p<0.05), wet muscle weight (p<0.001), high glycogen content fiber (p<0.05), numbers of Ag-NOR(p<0.001), number of mitochondria (p<0.01), mitochondrial volume found in electrical stimulated experimental group. The results suggest that the electrical stimulation of the muscle partially prevented the denervated atrophy in the rat gastrocnemius muscles.

• 한방재활의학과학회지
• /
• 제25권2호
• /
• pp.73-80
• /
• 2015

Objectives To assess the safety of Shinbaro3 Pharmacopuncture by analyzing the potential single-dose intramuscular toxicity of Shinbaro3 Pharmacopuncture at various dose levels in SD (Spraque-Dawley) rats and Beagle dogs. Methods For evaluation of single-dose intramuscular toxicity of Shinbaro3 Pharmacopuncture, 40 SD rats (20 male and 20 famale) and 4 Beagle dogs (2 male and 2 female) were used. The rats were divided in four groups of 10 each, and treated intramuscularly with Shinbaro3 Pharmacopuncture at doses of 0.3, 0.6 and 1.2 mg/kg in distilled water, and distilled water as a vehicle control group, respectively. The Beagle dogs were divided into two groups of 2 each, and treated intramuscularly with Shinbaro3 Pharmacopuncture at doses of 0.15, and 0.3 mg/kg in distilled water, respectively, and signs of toxicity were observed. After a wash-out period of 3 days, the procedure was repeated with Shinbaro3 Pharmacopuncture at doses of 0.6, and 1.2 mg/kg in distilled water, respectively. Mortality, body weight changes, and necropsy findings were examined during the study period. Results There were no mortalities in either the SD rats or Beagle dogs. There were also no significant differences in adverse effects, body weight, or necropsy findings between the Shinbaro3 Pharmacopuncture and control groups. Conclusions There results suggest that the lethal dose 50 ($LD_{50}$) and approximate lethal dose (ALD) value of the test substance Shinbaro3 Pharmacopuncture are higher than 1.2 mg/kg in SD rats and Beagle dogs.

• Tuberculosis and Respiratory Diseases
• /
• 제48권1호
• /
• pp.33-44
• /
• 2000

연구배경: 기관지천식은 기도의 과민성을 특징을 지닌 기도의 염증성 질환이며, 기관지천식에서의 기도 염종의 특성에 관한 연구는 기관지천식의 병인과 병태생리를 이해하는데 필수적이다. 본 연구의 목적은 백서에서 국내에서 개발된 일실 체용적 변동기록기을 이용하여 항원에 의한 반응을 관찰하여 기관지천식의 모델을 확립하고, 사람 기관지 천식과의 유사성을 알아보고자 백서의 기관지천식 모텔에서 기도의 염증을 관찰하여 항원에 의한 기도의 반응 양상에 따른 차이를 비교하고자 하였다. 대상 및 방법: 백서 30마리에 0.1mg의 난황을 피하로 주입하여 감작시키고, 감작후 14-16일 항원유발시험을 시행하여 각 10마리씩 3군으로 나누어 기도의 반응을 관찰하면서 1시간, 6-8시간, 24시간 후에 사망시켜 폐조직의 변화를 관찰하였다. 대조군 10마리는 감작군과 동일한 방법으로 항원을 흡입하고 1일 후에 사망시켰다. 기도반응은 동물용 일실 체용적 변동기록기를 사용하여 enhanced pause(Penh)를 지표로 측정하였다. 병리소견은 백서를 사망시켜 폐와 기관지를 절제한 후 Hematoxylin Eosin으로 염색하여 기관, 대기관지 및 소기관지 및 혈관주위에서 염증반응과 호산구 침윤을 관찰하였다. 결 과: 항원 유발시험을 시행한 20마리중 총 17마리(85%)에서 항원에 의한 기도의 수축반응을 보였다. 이들중 15 마리(75%)에서 조기반응을, 5 마리(25%)는 이중반응을 보였고 2마리(10%)는 후기반응만을 보였다. 항원 유발 후 기관, 대기관지, 소기관지와 혈관주 위에서의 염증반응은 1시간군, 6시간군, 1일군모두에서 대조군과 유의한 차이는 없었다(p>0.05). 항원유발시험후 호산구의 침윤은 1시간군과 대조군에서는 호산구의 침윤을 전혀 관찰할 수 없었으나, 6시간군은 5마리(50%)에서 호산구의 침윤을 관찰하였으며, 대조군과 유의한 호산구의 침윤을 관찰할 수 있었다(p<0.05). 조기반응과 후기반응을 관찰할 수 있었던 6시간군과 1일군에서 조기반응군(조기반응만을 보인 백서, n=10)과 후기반응군(이중반응과 후기반응만을 보인 백서, n=7) 에서 염증의 침윤은 모든 부위에서 유의한 차이는 없었다. 호산구의 침윤은 조기반응군에는 10마리중 4마리(40%)에서 $0.7{\pm}1.1$등급이었으며, 후기반응군은 7마리중 4 마리(57.1%)에서 $1.0{\pm}1.0$으로 높았으나, 통계적으로 유의하지는 않았다(p>0.05). 결 론: 백서의 기관지천식 모델에서 항원에 의한 기도의 수축 반응은 높고 반응률을 보였으나 기도의 염증 반응을 유발하지는 않으며, 호산구의 침윤도 미약하다고 생각된다. 그러므로 백서 기관지 천식모델은 항원에 의한 기도 반응의 연구에는 좋으나, 사랑의 만성 기관지 천식을 연구하기에는 적당치 못하다고 생각된다.

• Journal of Acupuncture Research
• /
• 제37권3호
• /
• pp.167-172
• /
• 2020

Background: This study aimed to assess the toxicity of capsaicin (CP) pharmacopunture in an animal model. Methods: The toxicity of a single-muscular dose of CP (45.45 mg/mL) was evaluated in 6-week-old male and female Sprague-Dawley rats. A total of 20 rats were assigned to 2 groups which were sex and weight matched. All rats acclimatized for 1 week before receiving 1.0 mL of CP (45.45 mg/mL) or normal saline solution (control) intramuscularly. The general condition and mortality of the animals were observed. The rats were sacrificed 2 weeks after CP was administered and histopathology was performed. Results: No abnormal symptoms or deaths were observed, and there was no difference in body weights between the CP and control groups throughout the study. No significant differences in histopathology were observed between the groups. Conclusion: No toxicological changes related to the administration of CP were observed. This study indicated that the safe dose of CP in Sprague-Dawley rats was 1.0 mL of CP (45.45 mg/mL) or less. Further studies are needed to confirm the safety of CP in the human body.

• 한국식품영양과학회지
• /
• 제22권4호
• /
• pp.374-380
• /
• 1993

녹차추출액을 사용하여 Sprague Dawley 휜쥐를 63일간 사육한 뒤 십이지장궤양 유발제 cysteamineㆍHCI(400mg/1kg b.w.)을 투여하면 수도물에 의해 같은 기간 사육한 대조군 (TW군) 보다 cysteamine에 대한 감수성은 유의하게 저하되어 십이지장궤양 발병율이 TW군의 50%를 나타냈다. 또한 TW군은 cysteamine투여에 의해 십이지장점막 극재 효소인 alkaline phosphatase (ALP) 활성을 상부십이지장 점막에 있어서 현저하게 저하시켰으나 GT군은 유의하게 활성이 유지되고 ALP 분자종에 있어서도 TW군과 상이한 양상을 나타내 녹차 추출액이 cysteamine 궤양에 있어서 항 궤양적 생리활성을 발휘하고 있는 사실이 밝혀졌다.

• Biomolecules & Therapeutics
• /
• 제11권3호
• /
• pp.200-203
• /
• 2003

The present study was carried out to investigate the potential acute toxicity of bamboo leaf water extract by a single oral dose in Sprague-Dawley rats. Twenty male and female rats aged 5 weeks were randomly assigned to four groups of 5 rats each and were administered singly by gavage at dose levels of 0, 1250, 2500, or 5000 mg/kg body weight. Mortalities, clinical findings, and body weight changes were monitored for the l4-day period following the administration. At the end of 14-day observation period, all animals were sacrificed and complete gross postmortem examinations were performed. Throughout the study period, no treatment-related deaths were observed. There were no adverse effects on clinical signs, body weight, and gross finding at any dose tested. The results showed that the single oral administration of bamboo leaf water extract did not induce any toxic effect at a dose level of below 5000 mg/kg in rats and that the minimal lethal dose were considered to be over 5000 mg/kg body weight for both sexes.

• 대한약침학회지
• /
• 제26권1호
• /
• pp.86-93
• /
• 2023

Objectives: This study aimed to evaluate the potential toxicity of a recently developed and clinically used No-Pain pharmacopuncture (NPP) solution. We also assessed the lethal dose of the NPP agent following a single intramuscular injection in Sprague-Dawley (SD) rats. Methods: Animals were divided into two groups: the NPP test material group and the normal saline control group. A single intramuscular injection of the NPP agent (1.0 mL/animal) was administered to rats of the NPP test material group. The control group rats received the same volume of normal saline. Both female and male rats were included in each group. All rats were monitored for clinical signs and body weight changes for 14 days after administration of the test substance or saline. At the end of the observation period, a gross necropsy was conducted and localized tolerance at the injection site was analyzed. Results: No mortality was observed in the NPP test material and control groups. Moreover, no test substance-related effects were observed on clinical signs, body weight, necropsy findings, and localized tolerance at the injection site. Conclusion: The approximate lethal dose of the NPP agent is greater than 1.0 mL/animal under the conditions used in this study. Additional toxicity evaluations and clinical studies are needed to confirm the safety of NPP use in clinical practice.

• 한국식생활문화학회지
• /
• 제22권5호
• /
• pp.645-651
• /
• 2007

Male weanling Sprague Dawley rats were used to evaluate the effect of dietary rice starch with different particle size on growth performance, intestinal function and proliferation. There were two dietary treatment: rice starch (RS), ultra finely pulverized rice starch with less than $15{\mu}m$ size (PRS). They were eight rats per treatment. In vitro digestibility, body weight change and organs weight were evaluated. Serum GPT, GOT and blood urea nitrogen were analyzed. Transit time, short chain fatty acid contents of cecum, and cell proliferation of duodenum and jejunum were measured. In vitro digestibility of PRS was higher than that of RS. Rats fed ultra finely pulverized rice starch for 3 weeks grew faster than rats fed rice starch. PRS group has higher weights of liver, kidney, spleen and epididymal fat pad, perhaps as a result of increased digestibility. GPT and GOT were not different between two groups. Blood urea nitrogen was higher in RS-fed rats than that of PRS-fed rats. Feeding ultra finely pulverized rice starch resulted in a proliferation of duodenum significantly. These results suggest that ultra finely pulverized rice starch increases the growth performance in weanling animals with reduced number of cells in the cell cycle of small intestine.