• Title/Summary/Keyword: BALB/C mouse

검색결과 467건 처리시간 0.024초

카드뮴이 BALB/c 마우스의 면역반응 및 효소활성에 미치는 영향 3. 효소활성 (Effect of cadmium on immune responses and enzyme activities in BALB/c mice 3. Enzyme activities)

  • 윤창용;김태중;조정곤;송희종
    • 대한수의학회지
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    • 제37권2호
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    • pp.383-388
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    • 1997
  • 카드뮴이 마우스의 효소활성에 미치는 영향을 평가하고자 BALB/c 마우스를 대상으로 0, 25, 50, 100 및 200 ppm의 $CdCl_2$가 첨가된 음료를 7주동안 자유급식한 후 간 및 신장에서 카드뮴(Cd)의 축적정도 및 효소(LDH 및 SOD)활성 변화를 조사하여 다음과 같은 결과를 얻었다. 1. 간 및 신장에서의 Cd축적도는 투여량이 증가될 수록 높았으며 특히 신장에서 더욱 높았다. 2. 간장과 신장의 lactate dehydrogenase(LDH)활성치는 신장의 경우 농도가 증가할 수록 활성치도 증가(25 ppm ; p<0.05, 50, 100 및 200 ppm; p<0.01)하는 경향을 보였으나 간에서는 100 ppm까지는 농도에 비례하여 활성치도 증가(50 및 100 ppm; p<0.05)하였다가 200ppm 투여군에서는 25 ppm 투여군 수준으로 감소되었다. 3. Superoxide dismutase(SOD)활성은 25 ppm 투여군의 간장에서 유의한 상승치(p<0.05)를 보인 것을 제외하고는 대조군의 간 및 신장의 활성치와 유사한 결과를 보였다. 이상의 결과는 카드뮴이 농도에 따라서 생체내의 LDH 및 SOD와 같은 효소계의 활성에 영향을 미칠 수 있음을 시사한다.

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PD-1 유전자 제거 마우스에서 홍역바이러스 감염 (Measles Viral Infection in PD-1 Gene Knockout Mice)

  • 전진경;김규연;허지애;강동원;김기환;김동수
    • Pediatric Infection and Vaccine
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    • 제20권3호
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    • pp.123-130
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    • 2013
  • 목적: 아급성경화범뇌염은 퇴행성 신경질환으로 홍역바이러스의 지속적 중추신경계 감염으로 나타난다. 저자들은 마우스 모델을 통해 아급성경화범뇌염 발병에서 만성 바이러스 감염에 관여하는 PD-1 유전자의 역할을 알아보고자 하였다. 방법: 3주령의 동형 PD-1 유전자 제거 마우스, 이형 PD-1 유전자 제거 마우스, 야생 BALB/c 마우스를 대상으로 측뇌실내 홍역바이러스를 주입하여 동물 모델로 하였다. 바이러스 주입 3개월 후, 마우스의 뇌 조직학적 소견을 관찰하고 혈청을 분리하여 IL-21의 혈청 농도를 ELISA kit을 통해 측정하였다. 결과: 야생 BALB/c 마우스에서 가장 많은 국소적 뇌백질의 괴사 및 성상세포의 증가가 관찰되었다. 이형 마우스에서 뇌실질의 병변은 적었으며 동형 마우스는 거의 보이지 않았다. 세 그룹에서 모두 혈청 IL-21의 증가는 보이지 않았다. 결론: 이 결과는 PD-1 유전자가 만성 바이러스 감염에 중요한 역할을 함을 시사한다.

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BALB/c mice에서 quercetin의 경구투여가 picryl chloride로 유발된 접촉성 피부 알레르기의 예방에 미치는 영향 (Allergy Prevention Effect of Oral Administration of Quercetin on Picryl Chloride-induced Contact Dermatitis in BALB/c Mice)

  • 김형진;정지윤
    • 생명과학회지
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    • 제19권10호
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    • pp.1444-1450
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    • 2009
  • 본 연구를 통해 BALB/c 마우스에서 quercetin의 경구투여가 PCL로 유도된 접촉성 피부 알레르기의 예방에 미치는 효과에 대해 알아보았다. Quercetin을 투여 농도에 따라 대조군(0 mg/kg), 저용량군(50 mg/kg), 고용량군(100 mg/kg)으로 나누고 8일에 걸쳐 총 8번 경구투여를 실시한 후 알레르기 유발물질인 PCL을 마우스의 양쪽 귀에 감작시켜 접촉성 피부 알레르기를 유발 시켰다. Quercetin의 투여 농도별 ear swelling 변화를 확인한 결과 quercetin을 투여하지 않은 대조군에 비해 quercetin을 투여한 군의 ear swelling 증가폭이 낮게 나타났고, 100 mg/kg (고용량군)에서 농도 유의적으로 ear swelling의 증가폭이 현저히 낮게 나타났다. Quercetin의 투여 농도에 따른 혈청 내 염증성 매개 물질의 농도 변화를 알아보기 위한 IgE 및 histamine level 측정 결과에서 quercetin을 투여하지 않은 대조군에 비해 quercetin을 투여한 50 mg/kg (저용량군), 100 mg/kg (고용량군)에서 낮은 수준의 IgE, histamine 수치가 나왔다. H&E염색과 Toluidine blue stain을 통한 조직병리학적 검사결과에서 quercetin을 투여한 고용량군의 귀 두께가 대조군에 비해 얇게 관찰되었고, 비만세포의 유무를 알아보기 위한 Toluidine blue stain의 결과 대조군에 비해 고용량군에서 적은 수의 비만세포들이 관찰되었다. 따라서 ear swelling과 IgE, histamine level, 조직병리학적 결과를 종합해 봤을 때 식물성 flavonoid 성분인 quercetin은 접촉성 피부 알레르기의 예방에 상당한 효과가 있다고 판단되며, 부작용이 발생하는 기존의 치료제를 대체할 수 있는 후보 물질로써 중요한 가치가 있다고 사료된다.

Fine localization of a new cataract locus, Kec, on mouse chromosome 14 and exclusion of candidate genes as the gene that causes cataract in the Kec mouse

  • Kang, Min-Ji;Cho, Jae-Woo;Kim, Jeong-Ki;Kim, Eun-Min;Kim, Jae-Young;Cho, Kyu-Hyuk;Song, Chang-Woo;KimYoon, Sun-Joo
    • BMB Reports
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    • 제41권9호
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    • pp.651-656
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    • 2008
  • A mouse with cataract, Kec, was generated from N-ethyl-N-nitrosourea (ENU) mutagenesis. Cataract in the Kec mouse was observable at about 5 weeks after birth and this gradually progressed to become completely opaque by 12 weeks. Dissection microscopy revealed that vacuoles with a radial or irregular shape were located primarily in the cortex of the posterior and equatorial regions of the lens. At the late stage, the lens structure was distorted, but not ruptured. This cataract phenotype was inherited in an autosomal recessive manner. We performed a genetic linkage analysis using 133 mutant and 67 normal mice produced by mating Kec mutant (BALB/c) and F1 (C57BL/6 $\times$ Kec) mice. The Kec locus was mapped to the 3 cM region encompassed by D14Mit34 and D14Mit69. In addition we excluded coding sequences of 9 genes including Rcbtb2, P2ry5, Itm2b, Med4, Nudt15, Esd, Lcp1, Slc25a30, and 2810032E02Rik as the candidate gene that causes cataract in the Kec mouse.

Inhibition of Eosinophil Infiltration and Humoral Immune Reaction by Ketotifen in BALB/c Mice Infected with Echinostoma hortense

  • Lim Byung-Hyuk;Im Jee-Aee;Jo Yoon-Kyung;Kim In-Sik;Lee Kyu-Jae;Yang Eun-Ju;Lim Su-Joung;Ryang Yong-Suk
    • 대한의생명과학회지
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    • 제10권4호
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    • pp.353-360
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    • 2004
  • Eosinophils play an essential role in allergy reaction after parasite infection. To examine the immune reaction induced by eosinophils, we investigated the allergy reaction in BALB/c mice infected with Echinostoma hortense's metacercariae, as well as the effect of ketotifen, an anti-allergy drug, on eosinophil immune reaction in the villi of host intestine. The worm recovery rate was higher in ketotifen-treated mice than in untreated mice and the worms in ketotifen-treated mice survived longer than those in untreated mice. The antibody titer in the serum of ketotifen-treated mice was very low. Especially, Echinostoma hortense infection strongly increased serum IgE level and eosinophil infiltration into the villi of the mouse intestine. Ketotifen treatment suppressed eosinophil infiltration into the infected areas and inhibited IL-4 production. The reduced IL-4 production may be related with the reduction of IgE, IgG1 and IgG2 production. In conclusion, ketotifen inhibited eosinophil infiltration functioning in the allergy reaction induced by parasite infection and the expression of immunoglobulins and cytokines.

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마우스의 비장에 미치는 7,12-Dimethylbenz[a]anthracene의 면역병리학적 연구 (Immunopathology of Spleen following 7,12-Dimethylbenz[a]anthracene Treatment in BALB/C Mice)

  • 이덕윤;한상섭;이상목
    • Toxicological Research
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    • 제8권2호
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    • pp.179-189
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    • 1992
  • This study was carried out to investigate the immunopathological effects of 7,12-Dimethylbenz[a]anthracene(DMBA) on spleen in mice. DMBA was administered subcutaneously to BALB/C mice by interscapular single injection of 50 or 100${\mu}g/g$ of body weight. Each DMBA treatment group and additional corn oil control group of mice were studied on day 1,3,7,14 and 21 following the injection of DMBA. DMBA treatment resulted in marked decrease in weights and cellularity of spleen. Spleen weights showed the greatest decrease at 14days after 50${\mu}g/g$ DMBA treatment, and at 21days after 100${\mu}g/g$ DMBA treatment. Spleen cellularity was similarly deceased in comparison with spleen weights. Spleen showed morphologically no typical changes throughout the experiment after 50${\mu}g/g$ DMBA treatment. Following the treatment of 100${\mu}g/g$ DMBA the spleen showed severe fibrosis, hemosiderin precipitation, and megakaryocytes decrease in red pulp at 14 days, while hemopoietic function was partly restored in addition to the appearance of a few megakaryocytes at 21 days. In spleen sections treated with antibodies to IgM or Thy1.2, lymphocytes strongly stained with IgM antibody were infiltrated around the central artery within the white pulp, and T-lymphocytes of periarterial lymphatic sheath (PALS) were diminished and destructed in sections treated with Thy1.2 antibody, at 14 days after the treatment of 100${\mu}g/g$ DMBA. By the electron microscopy phagocytic epithelial cells or macrophages were remarkably increased in spleen at 14and 21days following the treatment of 100${\mu}g/g$ DMBA.

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서울주걱흡충 감염 마우스의 IgA 반응 (IgA response in mice infected with Neodiplostomum seoulensis)

  • Sun HUH;Soo-Ung LEE;Moo-Ho WON;Young-Gil JEONG;Young-Hyun KWON;Chang sig CHOI
    • Parasites, Hosts and Diseases
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    • 제33권1호
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    • pp.55-60
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    • 1995
  • 서울주걱흡충감염 마우스의 혈청내 IgA와 소장의 IgA의 반응을 알아보려고 하였다 서울주걱흡충 의 피낭유충 200마리씩을 Balb/c 마우스에 경구 감염시킨 뒤 3. 7 14, 28일에 희생시켜, 혈청에 서의 서울주걱홉충 특이 IgA를 면역효소법으로 측정하였다. 또한 소장에서의 IgA를 면역조직화학법으로 반응을 관찰하였다. 감염 7일째부터 혈청내 특이 IgA의 역가가 증가하기 시작하여 28일째도 지속되었다. 소장 상피세포에서의 IgA 반응은 감염 14일에 가장 강하였다. 이 결과로 보아 서울주걱흡충 감염 Balb/c 마우스에서 감염후 혈청내 특이 IgA가 증가하고 소장에서 국소반응이 나타나나 충체 배출에는 큰 영향을 미치지 못하는 것으로 생각한다.

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Effects of Pre-conditioning dose on the Immune Kinetics and Cytokine Production in the Leukocytes Infiltrating GVHD Tissues after MHC-matched Transplantation

  • Choi, Jung-Hwa;Yoon, Hye-Won;Min, Chang-Ki;Choi, Eun-Young
    • IMMUNE NETWORK
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    • 제11권1호
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    • pp.68-78
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    • 2011
  • Background: Graft-versus-host disease (GVHD) is a huddle for success of hematopoietic stem cell transplantation. In this study, effects of irradiation dose on immune kinetics of GVHD were investigated using B6 ${\rightarrow}$ BALB.B system, a mouse model for GVHD after MHC-matched allogeneic transplantation. Methods: BALB.B mice were transplanted with bone marrow and spleen cells from C57BL/6 mice after irradiation with different doses. Leukocytes residing in the peripheral blood and target organs were collected periodically from the GVHD hosts for analysis of chimerism formation and immune kinetics along the GVHD development via flow cytometry. Myeloid cells were tested for production of IL-17 via flow cytometry. Results: Pre-conditioning of BALB.B hosts with 900 cGy and 400 cGy resulted in different chimerism of leukocytes from the blood and affected survival of GVHD hosts. Profiles of leukocytes infiltrating GVHD target organs, rather than profiles of peripheral blood leukocytes (PBLs), were significantly influenced by irradiation dose. Proportions of IL-17 producing cells in the infiltrating $Gr-1^+$ or $Mac-1^+$ cells were higher in the GVHD hosts with high does irradiation than those with low dose irradiation. Conclusion: Pre-conditioning dose affected tissue infiltration of leukocytes and cytokine production by myeloid cells in the target organs.

Hisrological Alterations and Immune Response Induced by Pet Toxin During Colonization with Enteroaggregative Escherichia coil (EAEC) in a Mouse Model Infection

  • Eslava, Carlos;Sainz, Teresita;Perez, Julia;Fresan, Ma.Cristina;Flores, Veronica;Jimenez, Luis;Hernandez, Ulises;Herrera, Ismael
    • Journal of Microbiology
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    • 제40권2호
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    • pp.91-97
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    • 2002
  • Enteroaggregative E. coil (EAEC) is an important aethiological causal agent of diarrhea in people of developed and undeveloped countries. Different in vitro and in vivo models have been proposed to study the pathdgenic and immune mechanisms of EAEC infaction. The aim of this study was to analyze whether BALB/c mice could be used as an animal model to study EAEC pathogenesis Six-week-old BALB/c mice were inoculated with EAEC strain 042 (044:H88) nalidixic acid resistant, and re-inoc-ulated ten days after. Mice feces were monitored for the presence of the EAEC strain over a period of 20 days . Bacteria were enumerated on MacConkey agar containing 100$\mu$g of nalidixic acid per ml. Results showed that 35% of the animals were colonized for 3 days, 15% for 5 and 10% for more than 7 days . After re-inoculation only 16% of the animals remained colonized for more than 3 days. During the necropsy, the intestinal fluid of same of the infected animals presented mucus and blood. Six of these fluids showed the presence of IgA antibodies againset Pet toxin and IgG natibodies raised against the toxin were also detected in the animal serum. Histopathologic evidence confirms the stimulation of mucus hypersecretion, an increased amount of goblet cells and the presence of bacterial aggregates in the apical surfaces of intestinal epithelial cells. Edema was present in the submucosa. These results suggest that BALB/c mice could be used as an animal model for in vivo study of EAEC infection.

DNCB로 유도한 아토피 유사 피부염에 지모 추출물이 미치는 영향 (Effects of Anemarrhena asphodeloides Extract on Atopic-Dermatitis like Skin Lesions in DNCB-induced Balb/c Mice)

  • 장유미;김용웅;김미려;임혜선;박건혁
    • 한국환경과학회지
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    • 제32권1호
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    • pp.67-76
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    • 2023
  • Under constant environmental pollution, the incidence of Atopic Dermatitis (AD) caused by air pollutants and allergens has increased. AD is an allergy inflammatory skin disease characterized by pruritus, eczema, and skin dryness. In herbal medicine, Anemarrhena asphodeloides (Anemarrhenae Rhizoma; AR) has been utilized to treat Alzheimer's disease, osteoporosis, hypertension, and inflammation. The purpose of study evaluated the effect of AR in a mouse model of 2,4-dinitrochlorobenzene (DNCB)-induced AD-like skin lesions. After acclimatization for 5 days, the mice (6-week-old, male Balb/c) were divided into five groups (n=6/group): NC (normal control), DNCB (control), Dex (5 mg·kg-1, p.o.), AR100 (100 mg·kg-1, p.o.), and AR300 (300 mg·kg-1, p.o.). On days 1 and 3, 1% DNCB was applied to the skin and ears. After 4 days, 0.5% DNCB was applied once every 2 days for 2 weeks. Then, skin and ears eczema area and severity index (EASI); skin nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2) levels; and plasma immunoglobulin E (IgE) levels were examined. The AR groups showed lower EASI, skin and ear thickness, mast cell count, and IgE levels than the control groups. Moreover, AR reduced iNOS, COX-2, and PGE2 levels. Therefore, AR possesses anti-inflammatory properties and can improve skin damage, indicating its therapeutic potential against AD.