• 제목/요약/키워드: Small body size mice

검색결과 13건 처리시간 0.033초

Studies on the Small Body Size Mouse Developed by Mutagen N-Ethyl-N-nitrosourea

  • Zhang, Qian-Kun;Cho, Kyu-Hyuk;Cho, Jae-Woo;Cha, Dal-Sun;Park, Han-Jin;Yoon, Seok-Joo;Zhang, ShouFa;Song, Chang-Woo
    • Toxicological Research
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    • 제24권1호
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    • pp.69-78
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    • 2008
  • Mutant mouse which show dwarfism has been developed by N-ethyl-N-nitrosourea (ENU) mutagenesis using BALB/c mice. The mutant mouse was inherited as autosomal recessive trait and named Small Body Size (SBS) mouse. The phenotype of SBS mouse was not apparent at birth, but it was possible to distinguish mutant phenotype from normal mice 1 week after birth. In this study, we examined body weight changes and bone mineral density (BMD), and we also carried out genetic linkage analysis to map the causative gene(s) of SBS mouse. Body weight changes were observed from birth to 14 weeks of age in both affected (n = 30) and normal mice (n = 24). BMD was examined in each five SBS and normal mice between 3 and 6 weeks of age, respectively. For the linkage analysis, we produced backcross progeny [(SBS${\times}$C57BL/6J) $F_1{\times}$ SBS] $N_2$ mice (n = 142), and seventy-four microsatellite markers were used for primary linkage analysis. Body weight of affected mice was consistently lower than that of the normal mice, and was 43.7% less than that of normal mice at 3 weeks of age (P < 0.001). As compared with normal mice at 3 and 6 weeks of age, BMD of the SBS mice was significantly low. The results showed 15.5% and 14.1 % lower in total body BMD, 15.3% and 8.7% lower in forearm BMD, and 29.7% and 20.1% lower in femur BMD, respectively. The causative gene was mapped on chromosome 10. The map order and the distance between markers were D10Mit248 - 2.1 cM - D10Mit51 - 4.2 cM - sbs - 0.7 cM - D10Mit283 - 1.4cM - D10Mit106 - 11.2cM - D10Mit170.

Heterosis Effects of Body Weight and Jumping Height in Rotational Crossing of Two-Subspecies of Mice

  • Kurnianto, E.;Shinjo, A.;Suga, D.
    • Asian-Australasian Journal of Animal Sciences
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    • 제13권7호
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    • pp.888-893
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    • 2000
  • The present study was conducted to evaluate heterosis effects of body weight and jumping height for successive generations of rotational crossing using two subspecies of mice which are very different in body weight and in genetic relationship from each other. Domesticated laboratory mouse $CF_{{\sharp}1}$ (C) and Yonakuni wild mouse (Y) were used as materials. Two groups of rotational crossing was made according to the parent used at the beginning of crosses, C male$\times$Y female and Y male$\times$C female. These crosses were done to produce the first ($G_1$ and $G_1{^{\prime}}$), second ($G_2$ and $G_2{^{\prime}}$) and third generations ($G_3$ and $G_3{^{\prime}}$) with sire used was alternated. Individual body weights were weighed at 1 (wk1), 3 (wk3), 6 (wk6) and 10 weeks of age (wk10) and jumping heights were measured at six weeks of age (wk6). Only the first litter used. For body weight, results of this study showed that genetic group effects were significant (p<0.01) source of variation at all ages studied. Sex effects were significant (p<0.01) at wk3, wk6 and wk10, but not at wk1. Significant interaction effects (p<0.01) between genetic group and sex were found at wk6 and wk10. The C mice with large maternal effects produced heavier offspring body weight and crosses using sire of this subspecies maintained heavy weight compared to wild Y mouse sire that has small body size. Heterosis tended to exist at the rotational crossing started from Y male C female. For jumping height, effects of genetic group and sex were significant, sire and dam effects (heterosis) exhibited from the first to third generations, and no maternal effects were observed.

Animal Models for Echinostoma malayanum Infection: Worm Recovery and Some Pathology

  • Songsri, Jiraporn;Aukkanimart, Ratchadawan;Boonmars, Thidarut;Ratanasuwan, Panaratana;Laummaunwai, Porntip;Sriraj, Pranee;Sripan, Panupan
    • Parasites, Hosts and Diseases
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    • 제54권1호
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    • pp.47-53
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    • 2016
  • Echinostomes are intestinal trematodes that infect a wide range of vertebrate hosts, including humans, in their adult stage and also parasitize numerous invertebrate and cold-blooded vertebrate hosts in their larval stages. The purpose of this study was to compare Echinostoma malayanum parasite growth, including worm recovery, body size of adult worms, eggs per worm, eggs per gram of feces, and pathological changes in the small intestine of experimental animals. In this study, 6-8-week-old male hamsters, rats, mice, and gerbils were infected with echinostome metacercariae and then sacrificed at day 60 post-infection. The small intestine and feces of each infected animal were collected and then processed for analysis. The results showed that worm recovery, eggs per worm, and eggs per gram of feces from all infected hamsters were higher compared with infected rats and mice. However, in infected gerbils, no parasites were observed in the small intestine, and there were no parasite eggs in the feces. The volume of eggs per gram of feces and eggs per worm were related to parasite size. The results of histopathological changes in the small intestine of infected groups showed abnormal villi and goblet cells, as evidenced by short villi and an increase in the number and size of goblet cells compared with the normal control group.

Peroxisome Proliferator-activated Receptor ${\gamma}$ Is Not Associated with Adipogenesis in Female Mice

  • Yoon, Mi-Chung;Jeong, Sun-Hyo
    • 대한의생명과학회지
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    • 제14권3호
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    • pp.139-146
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    • 2008
  • The peroxisome proliferator-activated receptor ${\gamma}$ $(PPAR{\gamma})$ plays a central role in adipogenesis and lipid storage. The $(PPAR{\gamma})$ ligands, thiazolidinediones (TZDs), enhance in vitro adipogenesis in several cell types, but the role of the TZDs on in vivo adipogenesis is still poorly understood. To investigate how $PPAR{\gamma}$ ligand troglitazone regulates adipogenesis in female mice, we examined the effects of the troglitazone on adipose tissue mass, morphological changes of adipocytes, and the expression of $PPAR{\gamma}$ target and adipocyte-specific genes in low fat diet-fed female C57BL/6 mice. Administration of troglitazone for 13 weeks did not change body and total white adipose tissue weights compared with control mice. Troglitazone treatment also did not cause a significant decrease in the average size of adipocytes in parametrial adipose tissue although it is reported to increase the number of small adipocytes in male animals. Troglitazone did not affect the mRNA expression of $PPAR{\gamma}$ and its target genes as well as adipocyte-specific genes in parametrial adipose tissue. These results suggest that $PPAR{\gamma}$ does not seem to be associated with adipogenesis in females with functioning ovaries and that its inability to induce adipogenesis may be due to sex-related factors.

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소형 동물의 생체 촬영을 위한 고해상도 Micro-CT 시스템의 개발 (Development of High Resolution Micro-CT System for In Vivo Small Animal Imaging)

  • 박정진;이수열;조민형
    • 대한의용생체공학회:의공학회지
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    • 제28권1호
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    • pp.95-101
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    • 2007
  • Recently, small-animal imaging technology has been rapidly developed for longitudinal screening of laboratory animals such as mice and rats. One of newly developed imaging modalities for small animals is an x-ray micro-CT (computed tomography). We have developed two types of x-ray micro-CT systems for small animal imaging. Both systems use flat-panel x-ray detectors and micro-focus x-ray sources to obtain high spatial resolution of $10{\mu}m$. In spite of the relatively large field-of-view (FOV) of flat-panel detectors, the spatial resolution in the whole-body imaging of rats should be sacrificed down to the order of $100{\mu}m$ due to the limited number of x-ray detector pixels. Though the spatial resolution of cone-beam CTs can be improved by moving an object toward an x-ray source, the FOV should be reduced and the object size is also limited. To overcome the limitation of the object size and resolution, we introduce zoom-in micro-tomography for high-resolution imaging of a local region-of-interest (ROI) inside a large object. For zoom-in imaging, we use two kinds of projection data in combination, one from a full FOV scan of the whole object and the other from a limited FOV scan of the ROI. Both of our micro-CT systems have zoom-in micro-tomography capability. One of both is a micro-CT system with a fixed gantry mounted with an x-ray source and a detector. An imaged object is laid on a rotating table between a source and a detector. The other micro-CT system has a rotating gantry with a fixed object table, which makes whole scans without rotating an object. In this paper, we report the results of in vivo small animal study using the developed micro-CTs.

참붕어(Pseudorasbora parva)에서 분리한 Echinochasmus japonicus 피낭유충 및 마우스 실험감염 (Metarercariae of Echinochusmus japonicus Encysted in a Fresh Water Fibh, Pseudorasboru purva, and Their Development in Experimental Mice)

  • 제종일;홍성종
    • Parasites, Hosts and Diseases
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    • 제23권2호
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    • pp.221-229
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    • 1985
  • 우리나라 참붕어의 아가미에서 검출되는 Echinochasmus속 피낭유충을 마우스에서 실험감염 시킨 후 성충을 얻어 종을 동안하고 마우스내에서의 간단한 발육상황을 관찰하였다. 1. 참붕어에서 수집한 Echinochasmus속 피낭유충은 타원형으로 $0.073~0.078{\times}0.054~0.065{\;}mm$의 크기이었고 탈낭시킨 표본에서 두관(head crown) 및 두극(collar spine)이 뚜렷하며 두극은 좌우 12개씩 총 24개가 구흡반 주위를 일열로 둘러싸고 있었으나 구흡반배측에서 연결이 끊어져 있었다. 2. 마우스로부터의 충체회수율은 감염 1일부터 21일까지 평균 19.5%이었고 감염기간 경과에 따른 감소는 관찰되지 않았다. 충체는 주로 마우스의 소양하부에서 회수되었다. 3. 마우스 체내에서 충체는 5일후면 모든 생식기관이 성숙되었고 충체 길이는 7일에 최대에 달한 후 21일까지 큰 변화가 없었다. 생식기관의 감염 7일까지 성장은 비생생기관과는 달리 {$\ulcorner}S자{\Ircorner}$형 곡선을 보였다. 감염 5~6일 후 마우스의 대변에서 크기 평균 $0.0865{\times}0.0608mm$인 충란이 검출되었고 감염 5일에 회수된 충체 자궁에서 1~2개의 충란이 발견되었다. 4. 감염 7일째의 성충을 관찰한 바 충체외형은 란원형으로 크기 $0.54~0.69{\times}0.29~0.34{\;}mm$이었고 잘 발달된 두관과 좌우 12개씩 총 24개의 두극을 가지고 있므려, 란황선이 복흡반 부위에서 충체 후단까지 분포하는 점 등으로 Echinochasmus japonicus Tanabe, 1926으로 동정되었다. 이상의 결과로 참붕어가 우리나라에서 E. japonicus 중간숙주 중 하나임이 확증되었다.

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은나노 입자의 입경 크기 및 형태에 따른 체내 동태 및 염증 반응 (Comparison of Distribution and Inflammatory Response by Diameter and Shape of Silver Nanoparticles)

  • 김수남;노진규;강민성;한영아;이병석;김영훈;박광식;최경희;박은정
    • Environmental Analysis Health and Toxicology
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    • 제25권3호
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    • pp.215-222
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    • 2010
  • The market size of engineered nanoparticles is rapidly increasing due to the fast application of nanotechnologies into different industries and consumer products. The development of new technology and materials has improved human's quality of life, but it also entails the possibility of exposure to new materials. In this study, we compared the distribution in the body by the inflow of silver nanoparticles having another diameter and shape at 1 h or 24 h after injection via the tail vein. And, we compared the cell composition and cytokine concentration in BAL fluid, and histopathological changes. As results, discharge of silver nanoparticles having small diameter and sphere shape was more rapid than that of big diameter or plate shape. It is estimated that the toxicity in liver and lung was proportional to accumulation level. The persistence of inflammation was also longer in mice treated with plate shape. Consequently, we suggest that the first choice of silver nanoparticles having small diameter and sphere shape in applying is desirable.

VPS26b-VPS29-VPS35 리트로머 복합체 결여가 마우스 뇌조직에 미치는 영향 (Deletion of the VPS26b-VPS29-VPS35 Retromer Complex Results in Learning Disabilities and Neurodegeneration)

  • 김익균
    • 생명과학회지
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    • 제30권8호
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    • pp.708-712
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    • 2020
  • 리트로머(retromer)는 VPS26, VPS29, VPS35 분자로 구성된 복합체로, 세포막에 존재하는 특정 단백질을 엔도솜에서 트렌스골지망으로 리사이클에 관여하는 단백질 복합체이다. 2000년대 초반 콜롬비아대학의 Scott A, Small 팀에 의해서, 알츠하이머 환자에서 리트로머 분자의 발현량이 저하된다는 것을 발견하였으며, 리트로머를 구성하는 VPS35 발현을 저하시킨 마우스를 이용한 Morris Water Maze (MWM) 실험에서 인지능력이 떨어진다는 것을 보고 하였다. 본 연구진은 리트로머를 구성하는 VPS26 분자에 대한 서브타입인 VPS26b를 발견하였고, 낙아웃 마우스를 제작하였다. VPS26b 낙아웃 마우스 뇌조직을 이용한 웨스턴 블롯 결과, 낙아웃 마우스 뇌조직에서 VPS29와 VPS35의 발현량의 50% 정도로 감소되는 것을 확인하였다. 또한, VPS29 낙아웃 마우스를 이용하여 MWM실험은 한 결과 인지능력이 저하되는 것을 확인하였으며 뇌조직의 해마 CA3영역의 세포 분포도가 정상마우스에 비해 감소되는 것을 확인하였다. 결과적으로 이번 연구를 통하여 VPS26b 낙아웃 마우스는 뇌질환 연구에 대한 실험 동물로서 기초 자료를 제공할 수 있을 것임을 보여준다.

소동물영상을 위한 마이크로 컴퓨터단층촬영장치 (Micro-CT System for Small Animal Imaging)

  • 남기용;김경우;김재희;손현화;유종현;강성훈;천권수;박성훈;윤권하
    • 한국의학물리학회지:의학물리
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    • 제19권2호
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    • pp.102-112
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    • 2008
  • 살아있는 마우스 영상화를 목적으로 겐트리 회전형과 평판영상검출기를 기반으로 한 고분해능 마이크로 컴퓨터단층촬영 장치를 개발하였다. 이 장치는 주로, 마이크로 크기 광원사이즈를 갖는 X-선 광원, Csl (TI)과 결합된 평판형 상보성 금속산화 반도체 영상검출기(CMOS), 선형이송 카우치, 위치정보 엔코더와 결합된 겐트리, 그리고 영상데이터 처리를 위한 병렬처리 시스템으로 구성되었다. 본 장치는 겐트리 회전형으로 설계되었는데, 이는 살아있는 마우스를 CT 영상을 얻는데 있어서 마우스 움직임에 기인한 영상결점의 최소화에 유리하고 촬영하는 동안 쥐의 호흡마취시행에 여러 가지 장점을 갖기 때문이다. CT팬텀을 이용하여 개발한 CT장치의 공간해상도, 영상대비도 그리고 영상균일도를 평가하였다. 결과로써, 본 장치의 공간해상도는 MTF 곡선으로부터 10%에 해당하는 약 11.3 cycles/mm을 얻었으며, 마우스에 대한 방사선 피폭선량은 81.5 mGy의 결과를 얻었다. 저대비 영상팬텀을 이용한 영상실험에서 분해가능 최소영상대비차는 약 46 CT였다. $55{\times}55{\times}X100\;{\mu}^3$의 복셀(voxel) 크기에서 영상의 불균일도는 약 70 CT 임을 얻었다. 또한 본 연구에서는 살아있는 마우스의 몸체, 뼈, 그리고 간에 대한 영상 테스트 결과를 제시하였다.

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미세 혈관 접합술에서 봉합적 수기와 비봉합적 수기의 실험적 비교 연구 (Experimental Study of the Anastomosis with Suture vs Non-suture Techinique)

  • 정덕환;한정수;유명철;남기운;선승덕
    • Archives of Reconstructive Microsurgery
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    • 제3권1호
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    • pp.45-53
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    • 1994
  • Suture microvascular anastomosis is time-consuming and tedious and demands long and continuous training. Techinique of anastomosis of microvessel was presented interrupted suture and continuous suture. Recently the unilink instrument system is created as a fast and simple method to achieve high patency rates without long and continuous training in the anastomosis of small vessels. The author experimentally studied the femoral artery of 20 mice(0.5-1.0mm, av. 0.7mm), the femoral vein of 20 mice(0.8-1.6mm, av. 1.2mm) after anastomosis with interrupted suture in 20 cases and continuous sutre in 20 cases. For the unilink apparatus we used the carotid arteries of 15 cases in 14 rabbits(1.0-1.6mm, av. 1.3mm) and facial veins of 12 cases in 14 rabbits(0.9mm-2.2mm, av. 1.5mm). A total of 27 arterial and venous anastomoses were performed. We examined the postoperative patency at immediate, 2 weeks, and 8 weeks. The results were as followings, 1. In the arterial anastomosis the rate of patency was 90%(18/20) in interrupted suture, 90%(18/20) in continuous suture and 93%(13/15) in unilink apparatus. In the venous anastomosis the rate of patency was 90%(18/20) in interrupted suture, 80%(16/20) in continuous suture and 100%(9/9) in unilink apparatus. 2. The mean time for completion of the arterial anastomosis were 12.2 minutes in interrupted suture group, 10.3 minutes in continouous suture group and 8.5 minutes in unillnk apparatus group. The mean time for completion of the venous anastomosis were 13.6 minutes in interrupted suture group, 11.0 minutes in continuous suture group and 6.2 minutes in unilink apparatus group. 3. At the histological examination of suture group, hyperplastic reaction of middle layer and subintimal hyperplasia were observed. In unilink apparatus group, the endothelium layer was continued and the thickness of vessel wall was decreased due to moderate atrophy of the media and mild degree of nonspecific chronic inflammation were seen around the unilink apparatus. 4. No significants was noticied in foreign body reaction among the interrupted, continuous and unilink apparatus group. 5. A case of the arterial anastomosis was released with acting out at 15 minutes after operation. 6. The important factors in the technical problems were accurate apposition of the cut vessel edges in suture group and the proper selection of the ring size and optimal fitting between two rings in unilink apparatus group. Even though the outer diamater of vessel in suture group was different from that in unilink apparatus group the unilink method provides a very safe, fast, and simple way to perform microvascular anastomoses especially in anastomosis of vein. But howerver suture was needed in vessels below 1 mm outer diamater. In that situation continuous suture was benefit than the interrupted suture in operation time.

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