Rchr
J-GLOBAL ID:200901040904172928
Update date: Sep. 23, 2024
Nishinaka Toru
ニシナカ トオル | Nishinaka Toru
Affiliation and department:
Job title:
Associate Professor
Research field (4):
Pharmacology
, Cell biology
, Molecular biology
, Functional biochemistry
Research keywords (5):
転写調節
, 生活習慣病
, 発癌
, 酸化的ストレス
, カルボニル代謝
Research theme for competitive and other funds (8):
- 2006 - 2007 Study on aldo-keto reductases as potential targets of antitumor agents : its involvement in the drug resistance of cancer cells
- 2002 - 2004 転写因子Nrf2による薬物代謝酵素の発現調節と薬物相互作用に及ぼす効果の解析
- 1999 - 2000 酸化的ストレスによる糖尿病合併症発症因子の発現誘導と病態モデルでの解析
- 薬物代謝酵素の発現および活性の調節機構
- 酸化的ストレス、化学ストレスによって活性化される情報伝達機構に関する研究
- Regulation of Drug Metabolizing Enzyme Expression and Activity
- Study on the signal pathways activated by oxidative stress and chemical stress
- 糖尿病合併症発症因子の遺伝子発現調節機序の解明と治療への応用
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Papers (80):
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Kahori Shimizu, Moe Ono, Takenari Mikamoto, Yuya Urayama, Sena Yoshida, Tomomi Hase, Shotaro Michinaga, Hiroki Nakanishi, Miho Iwasaki, Tomoyuki Terada, et al. Overexpression of lysophospholipid acyltransferase, LPLAT10/LPCAT4/LPEAT2, in the mouse liver increases glucose-stimulated insulin secretion. The FASEB Journal. 2024. 38. 2
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Kahori Shimizu, Syogo Nishimuta, Yuri Fukumura, Shotaro Michinaga, Yuka Egusa, Tomomi Hase, Tomoyuki Terada, Fuminori Sakurai, Hiroyuki Mizuguchi, Koji Tomita, et al. Liver-specific overexpression of lipoprotein lipase improves glucose metabolism in high-fat diet-fed mice. PLOS ONE. 2022. 17. 9. e0274297-e0274297
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Satoshi Endo, Yoshifumi Morikawa, Toshiyuki Matsunaga, Akira Hara, Toru Nishinaka. Porcine aldo-keto reductase 1C subfamily members AKR1C1 and AKR1C4: Substrate specificity, inhibitor sensitivity and activators. The Journal of steroid biochemistry and molecular biology. 2022. 221. 106113-106113
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Satoshi Endo, Tsubasa Nishiyama, Tomoe Matuoka, Takeshi Miura, Toru Nishinaka, Toshiyuki Matsunaga, Akira Ikari. Loxoprofen enhances intestinal barrier function via generation of its active metabolite by carbonyl reductase 1 in differentiated Caco-2 cells. Chemico-biological interactions. 2021. 348. 109634-109634
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Satoshi Endo, Toshiyuki Matsunaga, Toru Nishinaka. The Role of AKR1B10 in Physiology and Pathophysiology. Metabolites. 2021. 11. 6
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MISC (10):
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K. Shimizu, Y. Ogiya, T. Nishinaka, F. Sakurai, H. Mizuguchi, K. Tomita, T. Terada. Study of zinc finger AN1-type domain gene transduction by a novel adenovirus vector with lower hepatotoxicity for treatment of diabetes mellitus. HUMAN GENE THERAPY. 2016. 27. 11. A179-A179
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Takeshi Miura, Toru Nishinaka, Tomoyuki Terada. Potential Targeting Region for the Specific Inhibition of Human Monomeric Carbonyl Reductases of the Short-Chain Dehydrogenase/Reductase Superfamily. DRUG METABOLISM REVIEWS. 2009. 41. 54-55
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Takeshi Miura, Toru Nishinaka, Tomoyuki Terada. COMPARATIVE STUDY OF HUMAN MONOMERIC CARBONYL REDUCTASES IN TISSUE DISTRIBUTION, REDUCTASE ACTIVITY, AND COENZYME SPECIFICITY. DRUG METABOLISM REVIEWS. 2007. 39. 191-192
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Takeshi Miura, Toru Nishinaka, Tomoyuki Terada. COMPARATIVE STUDY OF HUMAN MONOMERIC CARBONYL REDUCTASES IN TISSUE DISTRIBUTION, REDUCTASE ACTIVITY, AND COENZYME SPECIFICITY. DRUG METABOLISM REVIEWS. 2007. 39. 263-263
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K Iwata, K Matsuno, T Nishinaka, C Yabe-Nishimura. Inhibition of aldose reductase improves myocardial reperfusion injury by a dual mechanism. JOURNAL OF PHARMACOLOGICAL SCIENCES. 2006. 100. 86P-86P
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Education (2):
- 1988 - 1993 大阪大学大学院 薬学研究科 応用薬学専攻
- 1984 - 1988 Osaka University School of Pharmaceutical Sciences
Professional career (1):
- Doctor of Pharmaceutical Science (Osaka University)
Work history (6):
- 2019 - 現在 Osaka Ohtani University Faculty of Phamacy
- 2007 - 2019 Osaka Ohtani University Faculty of Phamacy
- 2006 - 2007 Osaka Ohtani University Faculty of Phamacy
- 2002 - 2006 Kyoto Prefectural University of Medicine
- 1997 - 2002 Kyoto Prefectural University of Medicine
- 1993 - 1997 University of California, Los Angeles
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Association Membership(s) (3):
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