フルテキストURL fulltext.pdf
著者 Fukushima, Kazuhiko| Uchida, Haruhito A.| Fuchimoto, Yasuko| Mifune, Tomoyo| Watanabe, Mayu| Tsuji, Kenji| Tanabe, Katsuyuki| Kinomura, Masaru| Kitamura, Shinji| Miyamoto, Yosuke| Wada, Sae| Koyanagi, Taisaku| Sugiyama, Hitoshi| Kishimoto, Takumi| Wada, Jun|
キーワード lupus nephritis lupus pneumonitis silicosis SLE
発行日 2022-02-18
出版物タイトル Medicine
101巻
7号
出版者 Lippincott Williams & Wilkins
開始ページ e28872
ISSN 0025-7974
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2022 the Author(s).
論文のバージョン publisher
PubMed ID 35363197
DOI 10.1097/MD.0000000000028872
Web of Science KeyUT 000776738500059
関連URL isVersionOf https://doi.org/10.1097/MD.0000000000028872
フルテキストURL fulltext20220413-7.pdf
著者 Mifune, Tomoyo| Tanabe, Katsuyuki| Nakashima, Yuri| Tanimura, Satoshi| Sugiyama, Hitoshi| Sato, Yasufumi| Wada, Jun|
キーワード Vasohibin-1 Microtubules Detyrosination Podocytes
備考 © 2022 Elsevier Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.bbrc.2022.02.047] . |
発行日 2022-4
出版物タイトル Biochemical and Biophysical Research Communications
599巻
出版者 Elsevier BV
開始ページ 93
終了ページ 99
ISSN 0006-291X
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2022 Elsevier Inc.
論文のバージョン author
PubMed ID 35180473
DOI 10.1016/j.bbrc.2022.02.047
Web of Science KeyUT 000759467800001
関連URL isVersionOf https://doi.org/10.1016/j.bbrc.2022.02.047
フルテキストURL fulltext.pdf
著者 Tanabe, Katsuyuki| Matsuoka-Uchiyama, Natsumi| Mifune, Tomoyo| Kawakita, Chieko| Sugiyama, Hitoshi| Wada, Jun|
キーワード corticosteroid drug-induced interstitial nephritis eosinophils mycophenolate mofetil polypharmacy
発行日 2021-12-17
出版物タイトル Medicine
100巻
50号
出版者 Lippincott Williams & Wilkins
開始ページ e28252
ISSN 0025-7974
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2021 the Author(s).
論文のバージョン publisher
PubMed ID 34918693
DOI 10.1097/MD.0000000000028252
Web of Science KeyUT 000731129100044
関連URL isVersionOf https://doi.org/10.1097/MD.0000000000028252
フルテキストURL fulltext20210721-2.pdf figure20210721-2.pdf
著者 Watari, Shogo| Araki, Motoo| Wada, Koichiro| Yoshinaga, Kasumi| Maruyama, Yuki| Mitsui, Yosuke| Sadahira, Takuya| Kubota, Risa| Nishimura, Shingo| Kobayashi, Yasuyuki| Takeuchi, Hidemi| Tanabe, Katsuyuki| Kitagawa, Masashi| Morinaga, Hiroshi| Kitamura, Shinji| Sugiyama, Hitoshi| Wada, Jun| Watanabe, Masami| Watanabe, Toyohiko| Nasu, Yasutomo|
備考 © 2021 Published by Elsevier Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.transproceed.2021.03.043] . |
発行日 2021-4-28
出版物タイトル Transplantation Proceedings
53巻
5号
出版者 Elsevier BV
開始ページ 1494
終了ページ 1500
ISSN 0041-1345
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
論文のバージョン author
PubMed ID 33931247
DOI 10.1016/j.transproceed.2021.03.043
Web of Science KeyUT 000668604400017
関連URL isVersionOf https://doi.org/10.1016/j.transproceed.2021.03.043
フルテキストURL fulltext.pdf
著者 Yoshinaga, Kasumi| Araki, Motoo| Wada, Koichiro| Sekito, Takanori| Watari, Shogo| Maruyama, Yuki| Mitsui, Yosuke| Sadahira, Takuya| Kubota, Risa| Nishimura, Shingo| Edamura, Kohei| Kobayashi, Yasuyuki| Tanabe, Katsuyuki| Takeuchi, Hidemi| Kitagawa, Masashi| Kitamura, Shinji| Wada, Jun| Watanabe, Masami| Watanabe, Toyohiko| Nasu, Yasutomo|
キーワード diabetes mellitus kidney function kidney transplantation marginal donor
発行日 2021-06-08
出版物タイトル Immunity Inflammation and Disease
出版者 Wiley
ISSN 2050-4527
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2021 The Authors.
論文のバージョン publisher
PubMed ID 34102025
NAID 120007053366
DOI 10.1002/iid3.470
Web of Science KeyUT 000658836600001
関連URL isVersionOf https://doi.org/10.1002/iid3.470
フルテキストURL fulltext.pdf
著者 Matsuoka, Natsumi| Watanabe, Haruki| Kurooka, Naoko| Kato, Sumari| Higashi, Chika| Tanabe, Katsuyuki| Kinomura, Masaru| Fujii, Nobuharu| Sada, Ken-Ei| Sugiyama, Hitoshi| Wada, Jun|
キーワード acute kidney injury Evans syndrome autoimmune hemolytic anemia
発行日 2021-04-01
出版物タイトル Internal Medicine
60巻
7号
出版者 Japanese Society of Internal Medicine
開始ページ 1055
終了ページ 1060
ISSN 0918-2918
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2021 The Japanese Society of Internal Medicine
論文のバージョン publisher
PubMed ID 33116016
NAID 120007042384
DOI 10.2169/internalmedicine.5976-20
Web of Science KeyUT 000637009100013
関連URL isVersionOf https://doi.org/10.2169/internalmedicine.5976-20
フルテキストURL fulltext.pdf
著者 Tanabe, Katsuyuki| Kanzaki, Hiromitsu| Wada, Takahira| Nakashima, Yuri| Sugiyama, Hitoshi| Okada, Hiroyuki| Wada, Jun|
キーワード case report gastric cancer IgA nephropathy nivolumab steroid
発行日 2020-05-22
出版物タイトル Medicine
99巻
21号
出版者 Lippincott, Williams & Wilkins
開始ページ e20464
ISSN 0025-7974
NCID AA00728867
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2020 the Author(s).
論文のバージョン publisher
PubMed ID 32481351
DOI 10.1097/MD.0000000000020464
Web of Science KeyUT 000551508200106
関連URL isVersionOf https://doi.org/10.1097/MD.0000000000020464
フルテキストURL fulltext.pdf
著者 Miyake, Hiromasa| Tanabe, Katsuyuki| Tanimura, Satoshi| Nakashima, Yuri| Morioka, Tomoyo| Masuda, Kana| Sugiyama, Hitoshi| Sato, Yasufumi| Wada, Jun|
キーワード acute kidney injury ischemia-reperfusion oxidative stress vasohibin-2 peritubular capillaries
発行日 2020-06-26
出版物タイトル International Journal of Molecular Sciences
21巻
12号
出版者 MDPI
開始ページ 4545
ISSN 1422-0067
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2020 by the authors.
論文のバージョン publisher
PubMed ID 32604722
DOI 10.3390/ijms21124545
Web of Science KeyUT 000549478900001
関連URL isVersionOf https://doi.org/10.3390/ijms21124545
フルテキストURL fulltext.pdf
著者 Ogawa-Akiyama, Ayu| Sugiyama, Hitoshi| Kitagawa, Masashi| Tanaka, Keiko| Kano, Yuzuki| Mise, Koki| Otaka, Nozomu| Tanabe, Katsuyuki| Morinaga, Hiroshi| Kinomura, Masaru| Uchida, Haruhito A.| Wada, Jun|
発行日 2020-01-24
出版物タイトル PLoS ONE
15巻
1号
出版者 Public Library of Science
ISSN 1932-6203
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2020 Ogawa-Akiyama et al.
論文のバージョン publisher
PubMed ID 31978139
DOI 10.1371/journal.pone.0228337
Web of Science KeyUT 000534599100142
関連URL isVersionOf https://doi.org/10.1371/journal.pone.0228337
JaLCDOI 10.18926/AMO/57953
フルテキストURL 74_1_53.pdf
著者 Kubota, Risa| Araki, Motoo| Wada, Koichiro| Kawamura, Kasumi| Maruyama, Yuki| Mitsui, Yosuke| Sadahira, Takuya| Ariyoshi, Yuichi| Iwata, Takehiro| Nishimura, Shingo| Takamoto, Atsushi| Sako, Tomoko| Edamura, Kohei| Kobayashi, Yasuyuki| Kano, Yuzuki| Kitagawa, Masashi| Tanabe, Katsuyuki| Sugiyama, Hitoshi| Wada, Jun| Watanabe, Masami| Watanabe, Toyohiko| Nasu, Yasutomo|
抄録 We investigated the feasibility of robotic renal autotransplantation (RAT) in a porcine model to reduce invasiveness of RAT. Five pigs underwent robotic RAT using the da Vinci® robotic system. A robotic left nephrectomy was performed in all cases. Robotic RAT was performed on the left side in all but one case. Four ports were used. In 3 cases, the kidney was taken out through the GelPort® and irrigated on ice with Ringer’s solution. In 2 cases, a complete intracorporeal robotic RAT was performed. An end-to-side anastomosis was performed between the renal vein and the external iliac vein and between the renal artery and the external iliac artery. Ureteroneocystostomy was also performed in 2 cases. All cases were performed robotically without open conversion. The median (IQR) console time was 3.1 (0.7) h, and the operative time was 3.8 (1.1) h. The estimated blood loss was 30 (0) ml. The warm ischemia time was 4.0 (0.2) min, and the cold ischemia time was 97 (17) min. Intracorporeal transarterial hypothermic renal perfusion was feasible in the 2 complete intracorporeal robotic RAT cases by using a perfusion catheter through a laparoscopic port. Robotic RAT has the potential to be a new minimally invasive substitute for conventional open surgery.
キーワード renal autotransplantation robotic porcine model transplantation
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2020-02
74巻
1号
出版者 Okayama University Medical School
開始ページ 53
終了ページ 58
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2020 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 32099249
Web of Science KeyUT 000516606200008
NAID 120006795620
JaLCDOI 10.18926/AMO/55434
フルテキストURL 71_5_369.pdf
著者 Arata, Yuka| Tanabe, Katsuyuki| Hinamoto, Norikazu| Yamasaki, Hiroko| Sugiyama, Hitoshi| Maeshima, Yohei| Kanomata, Naoki| Sato, Yasufumi| Wada, Jun|
抄録 Several angiogenesis-related factors are known to play important roles in the pathogenesis of kidney disease. Vasohibin-2 (VASH-2) was recently reported as a novel proangiogenic factor. Although VASH-2 was demonstrated to accelerate tumor angiogenesis, its roles in non-tumor processes including renal disease have not been well elucidated yet. Here, we performed a retrospective study including an immunohistochemical analysis of human kidney biopsy specimens from 82 Japanese patients with a variety of kidney diseases, and we evaluated the correlations between the immunoreactivity of VASH-2 and the patients’ clinicopathological parameters. VASH-2 immunoreactivity was detected in varying degrees in renal tubules as well as in peritubular capillaries and vasa recta. The cortical and medullary tubule VASH-2+ scores were correlated with the presence of hypertension, and the medullary tubule VASH-2+ score was significantly correlated with the blood glucose (p=0.029, r=0.35) and hemoglobin A1c levels (p=0.0066, r=0.39). Moreover, decreased VASH-2+ scores in the vasa recta were associated with reduced renal function (p=0.0003). These results suggest that VASH-2 could play an important role in the pathogenesis of renal diseases, and that VASH-2 is closely associated with hypertension and impaired glucose tolerance.
キーワード vasohibin-2 kidney disease vasa recta medullary tubules
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2017-10
71巻
5号
出版者 Okayama University Medical School
開始ページ 369
終了ページ 380
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2017 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 29042694
JaLCDOI 10.18926/AMO/54507
フルテキストURL 70_4_295.pdf
著者 Araki, Motoo| Wada, Koichiro| Mitsui, Yosuke| Kubota, Risa| Yoshioka, Takashi| Ariyoshi, Yuichi| Kobayashi, Yasuyuki| Kitagawa, Masashi| Tanabe, Katsuyuki| Sugiyama, Hiroshi| Wada, Jun| Watanabe, Masami| Watanabe, Toyohiko| Hotta, Katsuyuki| Nasu, Yasutomo|
抄録 Although graft survival following renal transplantation (RTx) has improved, outcomes following highrisk RTx are variable. Preexisting antibodies, including donor-specific antibodies (DSA), play an important role in graft dysfunction and survival. We have designed a study to investigate the safety and efficacy of anti-CD20 monoclonal antibodies (rituximab) in high-risk RTx recipients. Major eligibility criteria include: 1) major and minor ABO blood group mismatch, 2) positive DSA. Thirty-five patients will receive 200 mg/body of rituximab. The primary endpoint is the incidence of B cell depletion. This study will clarify whether rituximab is efficacious in improving graft survival in high-risk RTx recipients.
キーワード end-stage renal disease immunosuppression kidney transplantation
Amo Type Clinical Study Protocols
出版物タイトル Acta Medica Okayama
発行日 2016-08
70巻
4号
出版者 Okayama University Medical School
開始ページ 295
終了ページ 297
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2016 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 27549676
Web of Science KeyUT 000384748600011
JaLCDOI 10.18926/AMO/53117
フルテキストURL 69_1_1.pdf
著者 Watatani, Hiroyuki| Yamasaki, Hiroko| Maeshima, Yohei| Nasu, Tatsuyo| Hinamoto, Norikazu| Ujike, Haruyo| Sugiyama, Hitoshi| Sakai, Yoshiki| Tanabe, Katsuyuki| Makino, Hirofumi|
抄録 Diabetic nephropathy is the most common pathological disorder predisposing patients to end-stage renal disease. Considering the increasing prevalence of type 2 diabetes mellitus worldwide, novel therapeutic approaches are urgently needed. ONO-1301 is a novel sustained-release prostacyclin analog that inhibits thromboxane A2 synthase. Here we examined the therapeutic effects of the intermittent administration of slow-release ONO-1301 (SR-ONO) on diabetic nephropathy in obese type 2 diabetes mice, as well as its direct effects on mesangial cells. The subcutaneous injection of SR-ONO (3mg/kg) every 3 wks did not affect the obesity or hyperglycemia in the db/db obese mice used as a model of type 2 diabetes, but it significantly ameliorated their albuminuria, glomerular hypertrophy, glomerular accumulation of type IV collagen, and monocyte/macrophage infiltration, and also the increase of TGF-β1, α-smooth muscle actin (α-SMA) and MCP-1 compared to vehicle treatment. In cultured mouse mesangial cells, ONO-1301 concentration-dependently suppressed the increases in TGF-β, type IV collagen, α-SMA, MCP-1 and fibronectin induced by high ambient glucose, at least partly through prostacyclin (PGI2) receptor-mediated signaling. Taken together, these results suggest the potential therapeutic efficacy of the intermittent administration of SR-ONO against type 2 diabetic nephropathy, possibly through protective effects on mesangial cells.
キーワード prostacyclin ONO-1301 diabetic nephropathy TGF-β1 diabetes mellitus
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2015-02
69巻
1号
出版者 Okayama University Medical School
開始ページ 1
終了ページ 15
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2015 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 25703166
Web of Science KeyUT 000349740300001
関連URL http://ousar.lib.okayama-u.ac.jp/metadata/53128
JaLCDOI 10.18926/AMO/52788
フルテキストURL 68_4_219.pdf
著者 Hinamoto, Norikazu| Maeshima, Yohei| Saito, Daisuke| Yamasaki, Hiroko| Tanabe, Katsuyuki| Nasu, Tatsuyo| Watatani, Hiroyuki| Ujike, Haruyo| Kinomura, Masaru| Sugiyama, Hitoshi| Sonoda, Hikaru| Kanomata, Naoki| Sato, Yasufumi| Makino, Hirofumi|
抄録 Experimental studies have demonstrated the involvement of angiogenesis-related factors in the progression of chronic kidney disease (CKD). There have so far been no reports investigating the distribution and clinical roles of Vasohibin-1 (VASH-1), a negative feedback regulator of angiogenesis, in CKD. We recruited 54 Japanese CKD patients and 6 patients who had normal renal tissues excised due to localized renal cell carcinoma. We evaluated the correlations between the renal expression level of VASH-1 and the clinical/histological parameters. VASH-1 was observed in renal endothelial/mesangial cells, crescentic lesions and interstitial inflammatory cells. Significant positive correlations were observed between 1) crescent formation and the number of VASH-1+ cells in the glomerulus (r=0.48, p=0.001) or cortex (r=0.64, p<0.0001), 2) interstitial cell infiltration and the number of VASH-1+ cells in the cortex (r=0.34, p=0.02), 3) the glomerular VEGFR-2+ area and the number of VASH-1+ cells in the glomerulus (r=0.44, p=0.01) or medulla (r=0.63, p=0.01). These results suggest that the renal levels of VASH-1 may be affected by local inflammation, crescentic lesions and VEGFR-2.
キーワード chronic kidney disease inflammation Vasohibin-1 VEGF-A VEGFR-2
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2014-08
68巻
4号
出版者 Okayama University Medical School
開始ページ 219
終了ページ 233
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2014 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 25145408
Web of Science KeyUT 000340687500004
関連URL http://ousar.lib.okayama-u.ac.jp/metadata/52824