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FullText URL Int_J_Med_Microbiol_306_8_657.pdf
Author Chourashi, Rhishita| Mondal, Moumita| Sinha, Ritam| Debnath, Anusuya| Das, Suman| Koley, Hemanta| Sekhar Chatterjeea, Nabendu|
Keywords ChiS Mucin Vibrio cholerae Virulence
Note This is an Accepted Manuscript of an article published by Elsevier GmbH|
Published Date 2016-12
Publication Title International Journal of Medical Microbiology
Volume volume306
Issue issue8
Publisher ELSEVIER GMBH
Start Page 657
End Page 665
ISSN 14384221
NCID AA11427330
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 27670078
DOI 10.1016/j.ijmm.2016.09.003
Web of Science KeyUT 000390824600008
Related Url isVersionf https://doi.org/10.1016/j.ijmm.2016.09.003
Title Alternative Transcription factor Runx3 in the mouse hypothalamo-pituitary-gonadal system
FullText URL poalas_034_002.pdf
Author Takahashi, Sumio|
Abstract Runx3 is a transcription factor that belongs to the Runx family. Female Runx3 knockout (Runx3−⁄−) mouse was anovulatory and infertile. Ovarian transplantation experiment suggested that lack of ovulation in Runx3−⁄− mice was caused by alteration of gonadotropin secretion in Runx3−⁄− mice. Cyp11a1 mRNA expression was less in Runx3−⁄− mouse ovaries than in wt ones. Hypothalamic Gnrh1 mRNA was increased, and Kiss1 mRNA expression in the anteroventral periventricular nucleus was decreased, but Kisspeptin mRNA in the arcuate nucleus was increased in Runx3-/- mice. Pituitary Fshb mRNA levels were increased in Runx3−⁄− mice. Cholesterol side-chain cleavage enzyme gene (Cyp11a1) expression was decreased in ovaries of Runx3−⁄− mice. These findings suggest that anovulation in Runx3−⁄− mice was partly due to the alterations in hypothalamus-pituitary-ovary system. Runx3 plays a key role in female reproduction through alteration of gonadotropin secretion.
Publication Title Proceedings of Okayama Association for Laboratory Animal Science
Published Date 2018-04
Volume volume34
Start Page 2
End Page 4
language Japanese
File Version publisher
FullText URL Reprod_Fertil_Dev_29_7_1280.pdf fig.pdf
Author Horihata, Kei| Yoshioka, Shin| Sano, Masahiro| Yamamoto, Yuki| Kimura, Koji| Skarzynski, Dariusz J.| Okuda, Kiyoshi|
Keywords luteal phase ovary progesterone prostaglandin reproduction
Note This is an Accepted Manuscript of an article published by CSIRO Publishing|
Published Date 2016-05-17
Publication Title Reproduction, Fertility and Development
Volume volume29
Issue issue7
Publisher CSIRO Publishing
Start Page 1280
End Page 1286
ISSN 10313613
NCID AA10718189
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version author
PubMed ID 27185011
DOI 10.1071/RD15538
Web of Science KeyUT 000403550200002
Related Url https://doi.org/10.1071/RD15538
FullText URL Reprod_Fertil_Dev_28_6_673.pdf
Author Yamamoto, Yuki| Kohka, Misa| Kobayashi, Yoshihiko| Woclawek-Potocka, Izabela| Okuda, Kiyoshi|
Keywords endothelin converting enzyme endothelin receptor epithelial cell ovarian steroids oviductal contraction and relaxation
Note This is an Accepted Manuscript of an article published by CSIRO Publishing|
Published Date 2014-11
Publication Title Reproduction, Fertility and Development
Volume volume28
Issue issue6
Publisher CSIRO Publishing
Start Page 673
End Page 681
ISSN 1031-3613
NCID AA10718189
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version author
PubMed ID 25370848
DOI 10.1071/RD14076
Web of Science KeyUT 000374546100003
Related Url isVersionOf https://doi.org/10.1071/RD14076
FullText URL Reprod_Fertil_Dev_29_10_1902.pdf
Author Bui, Tra M. T.| Nguyễn, Khánh X.| Karata, Asako| Ferré, Pilar| Trần, Minh T.| Wakai, Takuya| Funahashi, Hiroaki|
Keywords pig
Note This is an Accepted Manuscript of an article published by CSIRO Publishing|
Published Date 2016-12-12
Publication Title Reproduction, Fertility and Development
Volume volume29
Issue issue10
Publisher CSIRO Publishing
Start Page 1902
End Page 1909
ISSN 1031-3613
NCID AA10718189
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version author
PubMed ID 27938625
DOI 10.1071/RD16321
Web of Science KeyUT 000409376900003
Related Url https://doi.org/10.1071/RD16321
FullText URL K0005439_other2.pdf
Author Onoda, Satoshi| Kimata, Yoshihiro| Matsumoto, Kumiko| Yamada, Kiyoshi|
Note 学位審査副論文|
Published Date 2016-01
Publication Title Plastic and Reconstructive Surgery
Volume volume137
Issue issue1
Publisher Lippincott Williams & Wilkins
Start Page 83e
End Page 91e
ISSN 00321052
NCID AA00775696
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version author
PubMed ID 26710064
DOI 10.1097/PRS.0000000000001884
Web of Science KeyUT 000367333300001
Related Url https://doi.org/10.1097/PRS.0000000000001884
Title Alternative Dissecting the hierarchy and lineage of mesenchymal stem cells by mouse genetics
FullText URL poalas_033_015_017.pdf
Author Takarada, Takeshi|
Abstract Determination of stem cell hierarchy/lineage is indispensable for a better understanding and augmentation of many aspects of medical sciences, including the mechanisms of tissue development and maintenance of tissue homeostasis, as well as disease development. It also has implications in the field of tissue regeneration for medical treatments and disease modeling for drug discovery using iPS technology. Mesenchymal stem cells are multipotent stem cell that can differentiate into various type of cells including osteoblasts, adipocytes, myocytes and chondrocytes. Runt-related transcription factor 2 (Runx2) is an essential transcriptional regulator of osteoblast differentiation. Runx2 deficiency in Prx1+-derived cells (Runx2prx1−/− mice) resulted in defective intramembranous ossification. Double-positive cells for Prx1-GFP and stem cell antigen-1 (Sca1) (Prx1+Sca1+ cells) in the calvaria expressed Runx2 at lower levels and were more homogeneous and primitive as compared with Prx1+Sca1− cells. Our results suggest that osteoblast differentiation in vivo may begin at the Prx1+Sca1+ MSC stage with sequential progression to Prx1+Sca1−cells, then Osx+Prx1−Sca1− osteoblast precursors, which eventually form mature α1(I)-collagen+ osteoblasts.
Publication Title Proceedings of Okayama Association for Laboratory Animal Science
Published Date 2017-04
Volume volume33
Start Page 15
End Page 17
language Japanese
File Version publisher
JaLCDOI 10.18926/AMO/54499
FullText URL 70_4_243.pdf
Author Osawa, Masahiro| Ohashi, Kadoaki| Kubo, Toshio| Ichihara, Eiki| Takata, Saburo| Takigawa, Nagio| Takata , Minoru| Tanimoto, Mitsune| Kiura, Katsuyuki|
Abstract Vandetanib (ZactimaTM) is a novel, orally available inhibitor of both vascular endothelial growth factor receptor-2 (VEGFR-2) and epidermal growth factor receptor (EGFR) tyrosine kinase. In the present study, a line of transgenic mice with a mouse Egfr gene mutation (delE748-A752) corresponding to a human EGFR mutation (delE746-A750) was established. The transgenic mice developed atypical adenomatous hyperplasia to adenocarcinoma of the lung at around 5 weeks of age and died of lung tumors at approximately 17 weeks of age. In the mice treated with vandetanib (6mg/kg/day), these lung tumors disappeared and the phosphorylations of EGFR and VEGFR-2 were reduced in lung tissues to levels comparable to those of non-transgenic control mice. The median overall survival time of the transgenic mice was 28 weeks in the vandetanib-treated group and 17 weeks in the vehicle-treated group. Vandetanib significantly prolonged the survival of the transgenic mice (log-rank test, p<0.01); resistance to vandetanib occurred at 20 weeks of age and the animals died from their lung tumors at about 28 weeks of age. These data suggest that vandetanib could suppress the progression of tumors harboring an activating EGFR mutation.
Keywords vandetanib VEGFR EGFR nonsmall cell lung cancer transgenic mouse
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2016-08
Volume volume70
Issue issue4
Publisher Okayama University Medical School
Start Page 243
End Page 253
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2016 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 27549668
Web of Science KeyUT 000384748600003
Author Yamamoto, Yuki|
Published Date 2016-02-01
Publication Title 岡山大学農学部学術報告
Volume volume105
Content Type Departmental Bulletin Paper
Author Sakaguchi, Ei|
Published Date 2015-02-01
Publication Title 岡山大学農学部学術報告
Volume volume104
Content Type Departmental Bulletin Paper
Author Takayama, Hiroki| Miyake, Yasuhiro| Nouso, Kazuhiro| Ikeda, Fusao| Shiraha, Hidenori| Takaki, Akinobu| Kobashi, Haruhiko| Yamamoto, Kazuhide|
Published Date 2011-01
Publication Title Journal of Gastroenterology and Hepatology
Volume volume26
Issue issue1
Content Type Journal Article
Author Narita, Yuichi| Kajari Karmakar| Sébastien Ducret| Filippo M. Rijli|
Published Date 2014-04
Publication Title 岡山実験動物研究会報
Volume volume30
Content Type Others
Author Kosaka, Junko| Morimatsu, Hiroshi| Takahashi, Toru| Shimizu, Hiroko| Kawanishi, Susumu| Omori, Emiko| Endo, Yasumasa| Tamaki, Naofumi| Morita, Manabu| Morita, Kiyoshi|
Published Date 2013-05-07
Publication Title PLoS ONE
Volume volume8
Issue issue5
Content Type Journal Article
Author Ohuchi, Hideyo|
Published Date 2013-12-02
Publication Title 岡山医学会雑誌
Volume volume125
Issue issue3
Content Type Journal Article
Author Nishikawa, Toshio| Takaoka, Munenori| Ohara, Toshiaki| Tomono, Yasuko| Hao, Huifang| Bao, Xiaohong| Fukazawa, Takuya| Wang, Zhigang| Sakurama, Kazufumi| Fujiwara, Yasuhiro| Motoki, Takayuki| Shirakawa, Yasuhiro| Yamatsuji, Tomoki| Tanaka, Noriaki| Fujiwara, Toshiyoshi| Naomoto, Yoshio|
Published Date 2013-03
Publication Title Cancer Biology & Therapy
Volume volume14
Issue issue3
Content Type Journal Article
Author Shimzu, K.| Takahashi, T.| Iwasaki, T.| Shimizu, H.| Inoue, K.| Morimatsu, H.| Omori, E.| Matsumi, M.| Akagi, R.| Morita, K.|
Published Date 2008-11
Publication Title Medicinal Chemistry
Volume volume4
Issue issue6
Content Type Journal Article
Author Endo, Yasumasa| Tomofuji, Takaaki| Ekuni, Daisuke| Azuma, Tetsuji| Irie, Koichiro| Kasuyama, Kenta| Morita, Manabu|
Published Date 2013-01
Publication Title Journal of Clinical Periodontology
Volume volume40
Issue issue1
Content Type Journal Article
Author Yashiro, Masato| Tsukahara, Hirokazu| Matsukawa, Akihiro| Yamada, Mutsuko| Fujii, Yosuke| Nagaoka, Yoshiharu| Tsuge, Mitsuru| Yamashita, Nobuko| Ito, Toshihiro| Yamada, Masao| Masutani, Hiroshi|
Published Date 2013-01
Publication Title Critical Care Medicine
Volume volume41
Issue issue1
Content Type Journal Article
Author Kondo, Yasuhiro|
Published Date 2013-02-01
Publication Title 岡山大学農学部学術報告
Volume volume102
Content Type Departmental Bulletin Paper
JaLCDOI 10.18926/AMO/48686
FullText URL 66_4_317.pdf
Author Pak, Wing| Takayama, Fusako| Hasegawa, Azusa| Mankura, Mitsumasa| Egashira, Toru| Ueki, Keiji| Nakamoto, Kazuo| Kawasaki, Hiromu| Mori, Akitane|
Abstract This study aimed to investigate the therapeutic effects of the water extract of leaves of Vitis coignetiae Pulliat (VCPL) on nonalcoholic steatohepatitis (NASH) with advanced fibrosis, as our previous study exhibited its preventive effect on NASH. The NASH animal model [PCT/JP2007/52477] was prepared by loading recurrent and intermittent hypoxemia stress to a rat with fatty liver, which resembled the condition occurring in patients with obstructive sleep apnea (OSA) and fatty liver, who have a high incidence of NASH. Intermittent hypoxemia stress is regarded as a condition similar to warm ischemia followed by re-oxygenation, which induces oxidative stress (OS). The daily 100 or 300mg/kg VCPL administrations were performed for 3 weeks perorally beginning at the time of detection of advanced liver fibrosis. The therapeutic efficacy of VCPL on NASH was demonstrated by the reduction of the leakage of hepato-biliary enzymes and the amelioration of liver fibrosis. The OS elevation in NASH rats was measured based on the derivation of reactive oxygen species from liver mitochondrial energy metabolism and on the decrease in plasma SOD-like activity. The aggravation of inflammatory responses was demonstrated by the neutrophil infiltration (elevated myeloperoxidase activity) and the progression of fibrosis in the livers of NASH rats. In addition, the NASH rats without VCPL treatment also exhibited activation of nuclear factor-κB, a key factor in the link between oxidative stress and inflammation. All of these changes were reduced dose-dependently by the VCPL administration. These findings indicate that VCPL may improve hepatic fibrosis or at least suppress the progression of NASH, by breaking the crosstalk between OS and inflammation.
Keywords non-alcoholic steatohepatitis antioxidative oxidative stress anti-inflammation Vitis coignetiae Pulliat
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2012-08
Volume volume66
Issue issue4
Publisher Okayama University Medical School
Start Page 317
End Page 327
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2012 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 22918204
Web of Science KeyUT 000307918900004