Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Kazuta Oguri"'
Autor:
Yasushi Yamazoe, Peter I. Mackenzie, Shuso Takeda, Yuji Ito, Megumi Iwanaga, Kiyoshi Nagata, Yuji Ishii, Arief Nurrochmad, Hideyuki Yamada, Kazuta Oguri
Publikováno v:
Flinders University PURE
We have reported that the protein-protein interaction between UDP-glucuronosyltransferase (UGT) 2B7 and cytochrome P450 3A4 (CYP3A4) alters UGT2B7 function. However, the domain(s) involved in the interaction are largely unknown. To address this issue
Autor:
Yurie Kitajima, Hideyuki Yamada, Kazuta Oguri, Peter I. Mackenzie, Yoshio Nishimura, Shuso Takeda, Yuji Ishii
Publikováno v:
Flinders University PURE
Glucuronidation of morphine in humans is predominantly catalyzed by UDP-glucuronosyltransferase 2B7 (UGT2B7). Since our recent research suggested that cytochrome P450s (P450s) interact with UGT2B7 to affect its function [Takeda S et al. (2005) Mol Ph
Publikováno v:
福岡醫學雜誌. 96(5):204-213
This review deals with the three candidate compounds which may combat with dioxins' toxicity. Geranylgeranylacetone (GGA), an antiulcer drug, counteracts suppression of body weight gain and lethality produced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (T
Publikováno v:
Journal of Dermatological Science Supplement. 1:S105-S112
Summary Background: Dioxins and related compounds, exemplified by 2,3,7,8-tetrachlorodibenzo-p-dioxin, are recognized as widespread, persistent and highly toxic environmental pollutants. Although numerous studies have been performed to clarify the me
Publikováno v:
Biological and Pharmaceutical Bulletin. 28:1087-1090
The effect of an aryl hydrocarbon receptor (AhR) ligand on the carbonic anhydrase III (CAIII) mRNA level was studied using primary cultured hepatocytes of rats. CAIII gene which is highly suppressible by dioxins in vivo, was also suppressible in prim
Publikováno v:
Journal of Health Science. 51:1-7
Abuse of drugs remains a serious and world-wide problem. As exemplified by opioids, there are large inter-individual differences in the effects and toxicity of drugs. However, the mechanism underlying such inter-individual differences remains largely
Publikováno v:
Biological and Pharmaceutical Bulletin. 27:56-60
The effects of cytochrome P450 (P450, CYP) ligands and permeabilization of microsomes on 3-hydroxybenzo(a)pyrene [3-OH-B(a)P] glucuronidation mediated by rat hepatic microsomes were studied. While the UDP-glucuronosyltransferase (UGT) activity with n
Publikováno v:
Drug Metabolism and Pharmacokinetics. 19:290-296
The role of selenium-binding protein (SeBP), which has a high ability to associate with acetaminophen (AAP), on the cytotoxicity of AAP was studied. To clarify this issue, we examined the cytotoxic effect of AAP using COS cells stably expressing SeBP
Autor:
Satoru Ishida, Hideyuki Yamada, Midori Yamamoto, Sanae Matsumoto, Noriko Gohyama, Kazuta Oguri, Masashi Mise, Curtis J. Omiecinski, Shoich Ito, Yasuhiro Sagara
Publikováno v:
Journal of Biochemical and Molecular Toxicology. 18:124-130
Potential mechanisms were investigated whereby CYP2B18, a cytochrome P450 gene exhibiting high constitutive expression but only low levels of phenobarbital-inducibility in the guinea pig liver, may be differentially regulated versus the highly induci
Autor:
Akifumi Akamine, Junpei Mutoh, Yuji Ishii, Takumi Ishida, Hideyuki Yamada, Isao Hashiguchi, Tomomi Oshimo, Kazuta Oguri, Akihisa Nishimura, Nobuyuki Koga
Publikováno v:
Biological and Pharmaceutical Bulletin. 27:1397-1402
The protective effect of geranylgeranylacetone (GGA), an antiulcer drug, against the acute toxicity and teratogenicity produced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) was examined in C57BL/6J mice. When mice were co-treated, GGA reduced the lo