ログイン
Language:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. G. 附属病院
  2. g 10. 学術雑誌掲載論文
  3. 1. 査読済論文

TAK-603, an anti-inflammatory compound, reduces crescentic glomerulonephritis and preserves renal function in WKY rats

http://hdl.handle.net/2297/2862
http://hdl.handle.net/2297/2862
2e5b0412-5bf3-4ee5-86b3-7eb15a77abec
名前 / ファイル ライセンス アクション
HO-PR-WADA-T-02.pdf HO-PR-WADA-T-02.pdf (63.1 kB)
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2017-10-05
タイトル
タイトル TAK-603, an anti-inflammatory compound, reduces crescentic glomerulonephritis and preserves renal function in WKY rats
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Yamahana, Junya

× Yamahana, Junya

WEKO 45079

Yamahana, Junya

Search repository
Wada, Takashi

× Wada, Takashi

WEKO 118
e-Rad 40334784
金沢大学研究者情報 40334784
研究者番号 40334784

Wada, Takashi

Search repository
Yokoyama, Hitoshi

× Yokoyama, Hitoshi

WEKO 20313
e-Rad 50191531
研究者番号 50191531

Yokoyama, Hitoshi

Search repository
Kaneko, Shuichi

× Kaneko, Shuichi

WEKO 62
e-Rad 60185923
金沢大学研究者情報 60185923
研究者番号 60185923

Kaneko, Shuichi

Search repository
Furuichi, Kengo

× Furuichi, Kengo

WEKO 330
e-Rad 50432125
金沢大学研究者情報 50432125
研究者番号 50432125

Furuichi, Kengo

Search repository
提供者所属
内容記述タイプ Other
内容記述 金沢大学医学部附属病院血液浄化療法部
書誌情報 Nephrology Dialysis Transplantation

巻 21, 号 10, p. 2736-2744, 発行日 2006-10-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0931-0509
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1093/ndt/gfl431
出版者
出版者 Oxford University Press
抄録
内容記述タイプ Abstract
内容記述 Background. The therapeutic efficacy of the regulation of T helper (Th)-1-predominant immune responses remains to be investigated. Therefore, the effects of the anti-inflammatory compound TAK-603 were investigated in a model of crescentic glomerulonephritis induced by a small dose of nephrotoxic serum in Wistar-Kyoto rats. Methods. TAK-603 (50 mg/kg body weight) was administered orally, starting at the time of induction of glomerulonephritis. In group 1, the drug was administered daily for the initial 6 days. TAK-603 was administered on day 0 only in group 2, and from day 3 to 5 in group 3. In each group, nephritic rats were killed on days 6 and 56. Results. In group 1 consisting of rats treated with TAK-603 daily from day 0 to 5, glomerular damage, including crescent formation, was improved on day 6, with reductions in the numbers of CD4, CD8 and ED-1 positive cells, as well as in urinary protein excretion. Protein and transcript levels of Th1 cytokines in the diseased kidneys were markedly decreased by TAK-603 treatment. Renal pathology, including glomerulosclerosis and interstitial fibrosis, was ameliorated and proteinuria was markedly decreased. Elevated levels of serum creatinine showed concomitant improvement. In group 3, in which treatment was initiated shortly after the appearance of glomerular abnormalities, glomerular damage was also diminished, resulting in a decrease in urinary protein excretion. Treatment only on the first day in group 2, partially rescued renal dysfunction. Conclusions. These results suggest the possible therapeutic application of inhibition of Th1-predominant immune responses in progressive crescentic glomerulosclerosis. © 2006 Oxford University Press.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
戻る
0
views
See details
Views

Versions

Ver.1 2023-07-27 12:23:34.787446
Show All versions

Share

Share
tweet

Cite as

Other

print

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX
  • ZIP

コミュニティ

確認

確認

確認


Powered by WEKO3


Powered by WEKO3