• 제목/요약/키워드: Gerbil

검색결과 76건 처리시간 0.021초

Molecular Characterization of Ischemia-Responsive Protein 94 (irp94) Response to Unfolded Protein Responses in the Neuron

  • ;;;;권오유
    • 대한의생명과학회지
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    • 제12권2호
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    • pp.81-89
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    • 2006
  • The ischemia-responsive 94 gene (irp94) encoding a 94 kDa endoplasmic reticulum resident protein was investigated its molecular properties associated with unfoled protein responses. First, the expression of irp94 mRNA was tested after the reperfusion of the transient forebrain ischemia induction at the central nervous system in three Mongolian gerbils. Second, irp94 expression in PC12 cells, which are derived from transplantable rat pheochromocytoma cultured in the DMEM media, was tested at transcriptional and translational levels. The half life of irp94 mRNA was also determined In PC12 cells. Last, the changes of irp94 mRNA expression were investigated by the addition of various ER stress inducible chemicals (A23187, BFA, tunicamycin, DTT and $H_2O_2$) and proteasome inhibitors, and heat shock. High level expression of irp94 mRNA was detected after 3 hours reperfusion in the both sites of the cerebral cortex and hippocampus of the gerbil brain. The main regulation of irp94 mRNA expression in PC 12 cells was determined at the transcriptional level. The half life of irp94 mRNA in PC12 cells was approximately 5 hours after the initial translation. The remarkable expression of irp94 mRNA was detected by the treatment of tunicamycin, which blocks glycosylation of newly synthesized polypeptides, and $H_2O_2$, which induces apoptosis. When PC12 cells were treated with the cytosol proteasome inhibitors such as ALLN (N-acetyl-leucyl-norleucinal) and MG 132 (methylguanidine), irp94 mRNA expression was increased. These results indicate that expression of irp94 was induced by ER stress including oxidation condition and glycosylation blocking in proteins. Expression of irp94 was increased when the cells were chased after heat shock, suggesting that irp94 may be involved in recovery rather than protection against ER stresses. In addition, irp94 expression was remarkably increased when cytosol proteasomes were inhibited by ALLN and MG 132, suggesting that irp94 plays an important role for maintaining the ERAD (endoplasmic reticulum associated degradation) function.

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Immunohistochemical Studies of Human Ribosomal Protein S3 (rpS3)

  • Choi, Soo-Hyun;Kim, So-Young;An, Jae-Jin;Lee, Sun-Hwa;Kim, Dae-Won;Won, Moo-Ho;Kang, Tae-Cheon;Park, Jin-Seu;Eum, Won-Sik;Kim, Joon;Choi, Soo-Young
    • BMB Reports
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    • 제39권2호
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    • pp.208-215
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    • 2006
  • The human ribosomal protein S3 (rpS3) was expressed in E. coli using the pET-I5b vector and the monoclonal antibodies (mAbs) were produced and characterized. A total of five hybridoma cell lines were established and the antibodies recognized a single band of molecular weight of 33 kDa on immunoblot with purified rpS3. When the purified rpS3 was incubated with the mAbs, the UV endonuclease activity of rpS3 was inhibited up to a maximum of 49%. The binding affinity of mAbs to rpS3 determined by using a biosensor technology showed that they have similar binding affinities. Using the anti-rpS3 antibodies as probes, we investigated the cross-reactivities of various other mammalian brain tissues and cell lines, including human. The immunoreactive bands on Western blots appeared to be the same molecular mass of 33 kDa in all animal species tested. They also appear to be extensively cross-reactive among different organs in rat. These results demonstrated that only one type of immunologically similar rpS3 protein is present in all of the mammalian brain tissues including human. Furthermore, these antibodies were successfully applied in immunohistochemistry in order to detect rpS3 in the gerbil brain tissues. Among the various regions in the brain tissues, the rpS3 positive neurons were predominantly observed in the ependymal cells, hippocampus and substantia nigra pars compacta. The different distributions of rpS3 in brain tissues reply that rpS3 protein may play an important second function in the neuronal cells.

Helicobacter pylori의 in vivo 연구를 위한 ethanol-pretreating animal model의 개발 (Establishment of ethanol-pretreating animal model to study Helicobacter pylori infection)

  • 이진욱;김승희;박탄우;김옥진
    • 대한수의학회지
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    • 제46권4호
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    • pp.327-335
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    • 2006
  • A stable and reliable Helicobacter pylori (H. pylori) infection animal model would be necessary for evaluating vaccine efficacy and helpful for understanding the pathological mechanism of the organism. The aim of the present study is to investigate the effect of ethanol treatment prior to H. pylori inoculation on associated gastric mucosal injury and to establish ethanol-pretreating animal model to study H. pylori infection. Male Mongolian gerbils were used for the study. H. pylori was orally inoculated after 12 h fasting. 3 h prior to H. pylori inoculation, a group of gerbils was orally treated with absolute ethanol, 60% and 40% ethanol respectively. Another group of animals was treated either with H. pylori culture media alone or with different concentrations of ethanol plus culture media. Gerbils were killed 4 or 8 weeks after H. pylori inoculation. The colonization of H. pylori was confirmed by both histological examination and rapid urease test. Mucosal damage was evaluated grossly and histologically according to the criteria. The colonization of H. pylori and pathological changes in gastric mucosa of the animals were also observed. Although no significant change to the gastric mucose was observed in the animals treated either with H. pylori culture media alone or with different concentrations of ethanol plus culture media, persistent H. pylori infection was seen in the mucosa and mucosal leucocyte infiltration and severe epithelial damage was observed in the Helicobacter and ethanol + Helicobacter groups after 4 weeks. The gross and histological scores were higher in the ethanol + Helicobacter than in the Helicobacter alone group. As the results, ethanol-pretreatment with 60% concentration induced severe pathogenic changes by H. pylori infection in 5 weeks-old Mongolian gerbils. These results suggested that ethanol-pretreatment before H. pylori inoculation could increase the severity of gastric mucosal inflammation and enhance the colonization of H. pylori. The established ethanol-pretreating animal model would contribute to screen new drugs against H. pylori and be used as an useful tool for various animal experiments with H. pylori strains.

Helicobacter pylori에 대한 항균활성을 나타내는 Pediococcus pentosaceus CBT SL4 배양물의 감염방어 및 제균활성 (Protection of Infection and Eradication Activity of Culture Product by Pediococcus pentosaceus CBT SL4 Showing Antimicrobial Activity against Helicobacter pylori)

  • 홍운표;정명준;김수동;오은택;소재성;정충일
    • 한국식품과학회지
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    • 제36권5호
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    • pp.779-783
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    • 2004
  • P. pentosaceus CBT SL4균이 생산하는 항균물질 농축건조물은 H. pylori균에 대하여 평판 및 액상배양 조건에서 생육억제 활성이 확인되었고, 사막모래쥐를 사용한 감염실험에서는 감염방어 및 제균작용이, 보균자 인체실험에서는 제균작용이 확인되었다. 최근 3제 요법이나 신규 약물 등에 의하여 자각증세가 있는 위염증 환자에서의 제균율은 크게 향상되었으나, 국내의 경우에는 전체국민의 감염율이 매우 높은 것과 식습관 등의 요인에 의하여 단체 및 사회생활을 통한 신규감염이나 재감염을 방어할 효과적 수단은 없는 상태에 있다. 따라서, 일상적인 섭취가 가능하고, 병원균의 내성개발 우려나 인체에 대한 부작용이 없으며, H. pylori균에 대한 감염방어 및 제균작용을 동시에 지닌 유산균 및 그 항균활성물질을 이용한 식품소재는 국민전체의 H. pylori 감염율을 낮추고, 신규감염과 재감염의 악순환을 방지하기 위한 유용한 방어수단이 될 수 있을 것으로 판단된다. 한편, 유산균 배양액에 의한 H. pylori균에 대한 생육억제 현상은 모든 유산균에서 보편적인 현상은 아닌 것으로서 특정한 균주의 배양액에서만 관찰되고 있어 단순히 젖산 등 유기산에 의한 효과로 보기에는 어려움이 있으며 Gram 음성의 병원균들은 외막의 보호작용에 의하여 분자량이 큰 박테리오신 성분에 의해서는 생육이 억제되지 않는 것으로 판단되고 있다. 저자들은 당 균주가 생성하는 H. pylori 생육 억제 물질을 산성의 저분자 물질로 추정하고, 물질 및 작용기작 규명을 위하여 활성물질의 분리 및 구조분석 작업을 진행 중에 있으며, 이러한 연구가 완료되면 분리정제 물질을 활용한 추가적인 산업화 용도 개발이 가능할 것으로 기대하고 있다.

Mongolian gerbil의 뇌허혈에 대한 현삼의 신경보호효과 (Neuroprotective Effects of Scrophulariae Radix on Cerebral Ischemia in Mongolian Gerbils)

  • 이준환;송미연;이종수;김성수;신현대;정석희
    • 한방재활의학과학회지
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    • 제18권4호
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    • pp.1-11
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    • 2008
  • 목적 : 뇌허혈은 일시적 혹은, 영구적 뇌동맥 폐색에 의한 뇌혈류의 감소로 유발되며, 허혈 부위에서는 복잡한 병태 생리적 과정을 통하여 신경 세포사가 초래되어 비가역적인 신경학적 손상을 일으킨다. 본 연구에서는 모래쥐를 대상으로 일시적인 전뇌허혈을 유발 시킨 후 해마 치상회에서 허혈로 인한 세포사멸을 관찰하고, 현삼(玄蔘)의 투여가 허혈로 유발된 해마 치상회에서 세포사멸에 미치는 영향과 단기 기억에 미치는 효과를 규명하고자 실험하였다. 연구방법 : 세포사멸은 DNA 분절을 나타내는 terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) 염색법과 단백분해 과정의 마지막 단계에 발현되는 caspase-3에 대한 면역조직화학법을 이용하였고, 단기기억은 step-down avoidance task를 실시하여 평가하였다. 결과 : 본 실험의 결과 일시적인 전뇌허혈은 해마 치상회의 세포사멸을 유의하게 증가시켰으며 단기기억을 감소시켰다. 현삼의 투여는 허혈로 증가된 해마 치상회의 세포사멸을 유의하게 억제하였고, 허혈로 인한 단기 기억의 감소를 유의하게 억제시켰다. 결론 : 본 실험을 통하여 현삼은 뇌허혈로 증가된 세포사멸을 억제하고 단기 기억을 향상시킴을 알 수 있었고, 따라서 현삼은 뇌허혈로 인한 뇌손상을 보호할 수 있는 효과가 있음을 제시하는 바이다.

Effect of Acupuncture at ST36 on Ischemia-induced Learning and Memory Deficits in Gerbils

  • Chung, Jin-Yong;Park, Hyun-Jung;Shim, Hyun-Soo;Hahm, Dae-Hyun;Kim, Hee-Young;Lee, Hye-Jung;Kim, Kyung-Soo;Shim, In-Sop
    • 동의생리병리학회지
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    • 제25권2호
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    • pp.300-305
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    • 2011
  • The present study was investigated the neuroprotective effects of acupuncture at ST36 on learning and memory deficits after transient cerebral ischemia in a gerbil model. The animals were randomly divided into three groups (n=7 in each group): the sham operation group (SHAM), ischemia-induced and ST36 acupuncture group (ISC + ST36), and the ischemia-induced and Tail-acupuncture group (ISC + TAIL). For the acupuncture stimulation, stainless steel needles, 0.3 mm in diameter, were inserted bilaterally into the ST36 locus or the tail and stimulated for 1 min/day for 14 days. Using the Morris water maze test, the animals were tested on spatial learning and memory. In addition, the effects of acupuncture on memory storage and the choline acetyltransferase (ChAT) activity, in the hippocampal CA1 area, were investigated by ChAT immunohistochemistry. Transient cerebral ischemia produced impaired performance on the MWM test (DAY 5: p<0.01 and retention test: p<0.05) and severely decreased ChAT immunoreactivity in the CA1 hippocampal area compared to the SHAM group (p<0.05). However, improved learning and memory were observed (DAY 5: p<0.05 and retention test: p<0.01) as well as a significantly reduced loss of ChAT immunoactivity in the hippocampal CA1 region (p<0.001) after acupuncture stimulation at ST36 were observed. These results show that acupuncture at ST36 ameliorated the learning and memory deficits at least in part through the cholinergic system. The findings of this study provide potential data that acupuncture is useful for the treatment of some of the behavioral impairs of transient cerebral ischemia.