T
Takashi Ochiai
Researcher at Fukuoka University
Publications - 19
Citations - 1149
Takashi Ochiai is an academic researcher from Fukuoka University. The author has contributed to research in topics: Ceramide & Crocin. The author has an hindex of 13, co-authored 19 publications receiving 1055 citations.
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Journal ArticleDOI
Crocin prevents the death of rat pheochromyctoma (PC-12) cells by its antioxidant effects stronger than those of α-tocopherol
TL;DR: It is reported that crocin is a unique and potent antioxidant that combats oxidative stress in neurons and was more effective than those of alpha-tocopherol at the same concentration.
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Protective effects of carotenoids from saffron on neuronal injury in vitro and in vivo.
Takashi Ochiai,Hiroshi Shimeno,Kenichi Mishima,Katsunori Iwasaki,Michihiro Fujiwara,Hiroyuki Tanaka,Yukihiro Shoyama,Akihisa Toda,Reiko Eyanagi,Shinji Soeda +9 more
TL;DR: Among these saffron's constituents, crocin most effectively promotes mRNA expression of gamma-glutamylcysteinyl synthase (gamma-GCS), which contributes to GSH synthesis as the rate-limiting enzyme, and that the carotenoid can significantly reduce infarcted areas caused by occlusion of the middle cerebral artery (MCA) in mice.
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Crocin suppresses tumor necrosis factor-α-induced cell death of neuronally differentiated PC-12 cells
Shinji Soeda,Takashi Ochiai,Loungratana Paopong,Hiroyuki Tanaka,Yukihiro Shoyama,Hiroshi Shimeno +5 more
TL;DR: It is demonstrated that crocin suppresses the effect of tumor necrosis factor (TNF)-alpha on neuronally differentiated PC-12 cells and inhibits neuronal cell death induced by both internal and external apoptotic stimuli.
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Crocin prevents the death of PC-12 cells through sphingomyelinase-ceramide signaling by increasing glutathione synthesis
TL;DR: The data suggest that crocin combats the serum/glucose deprivation-induced ceramide formation in PC-12 cells by increasing GSH levels and prevents the activation of JNK pathway, which is reported to have a role of the signaling cascade downstream ceramide for neuronal cell death.
Journal ArticleDOI
Acid sphingomyelinase inhibition suppresses lipopolysaccharide-mediated release of inflammatory cytokines from macrophages and protects against disease pathology in dextran sulphate sodium-induced colitis in mice.
Akira Sakata,Takashi Ochiai,Hiroshi Shimeno,Sadao Hikishima,Tsutomu Yokomatsu,Shiroshi Shibuya,Akihisa Toda,Reiko Eyanagi,Shinji Soeda +8 more
TL;DR: A central role for acid SMase/ceramide signalling in the pathology of DSS‐induced colitis in mice is suggested, indicating a possible preventive or therapeutic role for SMase inhibitor in inflammatory bowel disease.