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Featured researches published by Yoshihiko Ohashi.
Toxicology Letters | 1995
Takashi Yamoto; Yoshihiko Ohashi; Munehiro Teranishi; Masaya Takaoka; Sunao Manabe; Naochika Matsunuma; Takashi Makita
Age-related changes in the susceptibility to clofibric acid were investigated in male F344 rats of 8, 52, and 117 weeks old. Hepatomegaly, decrease of serum total cholesterol and triglyceride, increase of the total cytochrome P-450 contents, induction of the activities of microsomal omega-hydroxylation and peroxisomal beta-oxidation, proliferation of smooth endoplasmic reticulum and peroxisomes were detected in 8- and 52-week-old rats. In 117-week-old rats clofibric acid treatment resulted in decrease of serum total cholesterol, elevation of the activities of microsomal and peroxisomal enzymes, and slight proliferation of peroxisomes. These results suggest that the susceptibility of the male F344 rat liver to clofibric acid decreases in 117-week-old rats, though the effect is still recognizable.
Toxicology Letters | 1999
Tadashi Furukawa; Sunao Manabe; Yoshihiko Ohashi; Satoru Sharyo; Kunio Kimura; Yuji Mori
It has been reported that drug metabolizing enzyme activities in the liver fluctuate daily, though the daily fluctuation of 7-alkoxycoumarin O-dealkylase (ACD) activities catalyzed by P450 has not been examined. The ACD activities are known to be useful to clarify the extensive induction of P450-dependent oxygenases. In the present study, the hepatic ACD activities, as well as P450 content, were investigated periodically in male F344 rats under ad libitum-feeding or fasting condition. The ACD activities in ad libitum-fed rats were found to follow obvious daily fluctuations with high values during dark periods and with low values during light periods. This agreed with the other previous results of drug metabolizing enzyme activities measured with other substrates. Because the daily fluctuation was also observed in fasted rats, the fluctuation in ACD activities was clearly not affected by feeding, an external factor. P450 content, however, showed different fluctuation patterns from the ACD activities. This suggests that the fluctuation of ACD activities might not be related to the quantitative variation of P450 proteins.
Toxicology Letters | 1996
Takashi Yamoto; Yoshihiko Ohashi; Tadashi Furukawa; Munehiro Teranishi; Sunao Manabe; Takashi Makita
Although it has been reported that male rats are more responsive than females to peroxisome proliferation induced by clofibrate, these sex differences have been confirmed in young adult rats. Using 4-, 8-, and 12-week-old F344 rats, postnatal change of the sex-dependent response to clofibrate was investigated. These animals were administered 200 mg/kg body wt./day clofibrate by gavage for 7 days. In 4-week-old rats clofibrate-dependent changes (hepatomegaly, induction of hepatic microsomal and peroxisomal enzymes, proliferation of smooth endoplasmic reticulum and peroxisomes of hepatocytes) were slight in both sexes. In 8- and 12-week-old rats clofibrate-induced changes of males were moderate, whereas those of females were slight. These results suggest that the responsiveness of immature rat to clofibrate is weak and in males the susceptibility is gradually strong during postnatal development.
Pathophysiology | 1996
Takashi Yamoto; Yoshihiko Ohashi; Nobuhiro Miyakoshi; Naochika Matsunuma; Sunao Manabe; Takashi Makita
Abstract Difference among strains in the susceptibility to clofibrate in male rats was clarified. Males of three rat strains (F344, Sprague Dawley (SD), and Wistar Lewis) were treated with clofibrate mixed in the diet for 14 days. Both biochemical analysis (measurement of cytochrome P450 content, alkoxycoumarin O-dealkylation, carnitine acetyltransferase activity, peroxisomal β-oxidation, and catalase activity) and morphological analysis (electron microscopy and morphometry of peroxisomes) proved the strain difference. Although the changes caused by clofibrate administration were detected in all strains, the degree of these changes was variable among different strains. The most responsive rat strain was Wistar Lewis, while SD was the least responsive.
Archives of Toxicology | 2004
Toshiyuki Watanabe; Tomomi Sugiura; Sunao Manabe; Wataru Takasaki; Yoshihiko Ohashi
Journal of Toxicological Sciences | 2000
Toshiyuki Watanabe; Tadashi Furukawa; Satoru Sharyo; Yoshihiko Ohashi; Mitsuya Yasuda; Masaya Takaoka; Sunao Manabe
Journal of Toxicologic Pathology | 1998
Toshiyuki Watanabe; Sunao Manabe; Yoshihiko Ohashi; Hideaki Okamiya; Hiroshi Onodera; Kunitoshi Mitsumori
Archives of Toxicology | 2006
Toshiyuki Watanabe; Yoshihiko Ohashi; Toshiyuki Kosaka; Shingo Arakawa; Yukari Shibaya; Takashi Yamoto; Sunao Manabe; Wataru Takasaki
Journal of Toxicologic Pathology | 1998
Toshihiko Makino; Shinya Sehata; Isao Igarashi; Toshiyuki Watanabe; Yoshihiko Ohashi; Sunao Manabe; Takashi Yamoto
Journal of Toxicological Sciences | 1992
Isao Igarashi; Sunao Manabe; Yoshihiko Ohashi; Masaya Takaoka; Takashi Yamoto; Munehiro Teranishi; Naochika Matsunuma