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Featured researches published by Hideaki Kitajima.


Life Sciences | 2002

Effect of taurine on cholesterol metabolism in hamsters: up-regulation of low density lipoprotein (LDL) receptor by taurine.

Shigeru Murakami; Yukiko Kondo; Yoshihisa Toda; Hideaki Kitajima; Kazuya Kameo; Masanobu Sakono; Nobuhiro Fukuda

The effects of taurine on hepatic cholesterol metabolism were investigated in hamsters fed a high-fat diet or normal chow. Two weeks-treatment of taurine at 1% in drinking water prevented high-fat diet-induced increase in cholesterol levels of serum and liver. The decrease in serum cholesterol by taurine was due to decrease in non-HDL cholesterols. A similar tendency was noted in serum and liver cholesterol levels of hamsters fed a normal diet. In hamsters fed a high-fat diet, taurine prevented elevation in hepatic activity of acyl-CoA:cholesterol acyltransferase (ACAT) and increased the activity of cholesterol 7alpha-hydroxylase. Taurine also increased cholesterol 7alpha-hydroxylase activity in hamsters fed normal chow. Studies on liver membranes revealed that taurine increased 125I-labeled LDL binding by 52% and 58% in hamsters fed either a normal chow or high-fat diet, respectively. Furthermore, LDL kinetic analysis showed that taurine intake resulted in significant faster plasma LDL fractional catabolic rates (FCR). These results suggest that taurine elevates hepatic LDL receptor and thereby decreases serum cholesterol levels, an event which may be the result of hepatic cholesterol depletion as a consequence of increased bile acid synthesis via enhancement of cholesterol 7alpha-hydroxylase activity. Thus, up-regulation of the LDL receptor and subsequent increase in receptor- mediated LDL turnover may be a key event in the cholesterol-lowering effects of taurine in hamsters.


Atherosclerosis | 2002

Taurine suppresses development of atherosclerosis in Watanabe heritable hyperlipidemic (WHHL) rabbits

Shigeru Murakami; Yukiko Kondo; Takanobu Sakurai; Hideaki Kitajima; Takatoshi Nagate

While the hypocholesterolemic effects of taurine have extensively been studied using experimental animals, the anti-atherosclerotic effects of taurine have been given less attention. We examined the effect of taurine on atherosclerotic lesions in Watanabe heritable hyperlipidemic (WHHL) rabbits. Treatment of WHHL rabbits with taurine (0.3% in drinking tap water) for 24 weeks decreased aortic lesions by 31%, estimated as intimal thickening. Taurine significantly decreased cholesteryl ester content of aortic arch, thoracic aorta, and abdominal aorta by 35, 43, and 54%, respectively. Concomitantly, activity of acyl-CoA:cholesterol acyltransferase (ACAT), an enzyme responsible for cholesterol esterification, was also significantly decreased. Immunohistochemical analysis revealed decreased macrophages in the intima of taurine-treated rabbits. Taurine had no apparent effect on blood pressure and serum cholesterol levels. Contents of thiobarbituric acid reactive substances (TBARS), a marker of lipid peroxidation, was reduced in serum and aorta by 29 and 50%, respectively, when taurine was ingested. In addition, LDL from taurine-treated rabbits was resistant to copper-induced oxidative modification. These results revealed that taurine prevents development of atherosclerosis and that the anti-atherosclerotic effects of taurine are independent of serum cholesterol levels. The anti-oxidant action of taurine may be involved in inhibiting atherosclerosis in these rabbits.


Lipids in Health and Disease | 2008

Taurine reduces the secretion of apolipoprotein B100 and lipids in HepG2 cells

Teruyoshi Yanagita; Seo-Young Han; Ying Hu; Koji Nagao; Hideaki Kitajima; Shigeru Murakami

BackgroundHigher concentrations of serum lipids and apolipoprotein B100 (apoB) are major individual risk factors of atherosclerosis and coronary heart disease. Therefore ameliorative effects of food components against the diseases are being paid attention in the affluent countries. The present study was undertaken to investigate the effect of taurine on apoB secretion and lipid metabolism in human liver model HepG2 cells.ResultsThe results demonstrated that an addition of taurine to the culture media reduces triacylglycerol (TG)-mass in the cells and the medium. Similarly, cellular cholesterol-mass was decreased. Taurine inhibited the incorporation of [14C] oleate into cellular and medium TG, suggesting the inhibition of TG synthesis. In addition, taurine reduced the synthesis of cellular cholesterol ester and its secretion, suggesting the inhibition of acyl-coenzyme A:cholesterol acyltransferase activity. Furthermore, taurine reduced the secretion of apoB, which is a major protein component of very low-density lipoprotein.ConclusionThis is a first report to demonstrate that taurine inhibits the secretion of apoB from HepG2 cells.


Clinical and Experimental Pharmacology and Physiology | 2001

Taurine Inhibits Development Of Atherosclerotic Lesions In apolipoprotein E-Deficient Mice‡

Yukiko Kondo; Yoshihisa Toda; Hideaki Kitajima; Hiroaki Oda; Takatoshi Nagate; Kazuya Kameo; Shigeru Murakami

1. The effects of taurine on the development of atherosclerotic lesions were investigated in apolipoprotein (apo) E‐deficient mice, an animal model with severe hypercholesterolaemia and extensive atherosclerosis. These mice were fed a normal laboratory chow containing 2% taurine for 12 weeks.


Journal of The American College of Nutrition | 2004

Balance of Magnesium Positively Correlates with That of Calcium

Mamoru Nishimuta; Naoko Kodama; Eiko Morikuni; Yayoi H. Yoshioka; Hideaki Yamada; Hideaki Kitajima; Hidemaro Takeyama; Kazumasa Suzuki

Background and Objective: In a prior study [1], we showed no significant relationship between intake and balance of magnesium (Mg). Subsequent further investigation [2] disclosed that intakes of both Ca and P were positively correlated with their respective balances, whereas intake of Mg did not show any significant correlation with Mg balance. In this paper, we show positive correlations between intake of Mg and balances of both Ca and P. Methods and Results: Using these correlations, the mean value and upper limit of the 95% confidence interval (from the regression equation between Mg intake and either the balances of Ca or that of P, when each balance is equal to zero) were 4.584 and 4.802 (against Ca balance), 4.554 and 4.785 (against P balance) mg/kg BW/d, respectively. Balances of Mg and Ca correlated with each other.


Archive | 2007

Magnesium Requirement and Affecting Factors

Mamoru Nishimuta; Naoko Kodama; Eiko Morikuni; Nobue Matsuzaki; Yayoi H. Yoshioka; Hideaki Yamada; Hideaki Kitajima; Hidemaro Takeyama

We performed 11 balance studies to learn the estimated average requirement (EAR) of magnesium (Mg). Magnesium intake was not correlated with Mg balance when all data was used (n = 109). However, Mg intake was correlated with calcium (Ca) and phosphorus (P) balances. During the analysis, we found a correlation between sodium intake and Ca and Mg balances. After excluding the data of the highest sodium (Na) intake study, Mg intake turned out to be correlated with Mg balance.


Journal of Nutritional Science and Vitaminology | 2004

Balances of calcium, magnesium and phosphorus in Japanese young adults.

Mamoru Nishimuta; Naoko Kodama; Eiko Morikuni; Yayoi H. Yoshioka; Hidemaro Takeyama; Hideaki Yamada; Hideaki Kitajima; Kazumasa Suzuki


Archive | 1996

Remedy for dermatitis

Akiko Yoneda; Hideaki Kitajima; Kenji Tsunoda; Kazuo Hasegawa; Takako Ishii


Journal of Nutritional Science and Vitaminology | 2005

Sodium and Potassium Balances in Japanese Young Adults

Naoko Kodama; Eiko Morikuni; Nobue Matsuzaki; Yayoi H. Yoshioka; Hidemaro Takeyama; Hideaki Yamada; Hideaki Kitajima; Mamoru Nishimuta


Archive | 1996

Pharmaceutical preparation comprising crude drug for nourishment and robust

Hideaki Kitajima; Kenji Tsunoda; Akiko Yoneda; 秀明 北島; 晶子 米田; 健司 角田

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Kenji Tsunoda

Taisho Pharmaceutical Co.

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Eiko Morikuni

Chiba College of Health Science

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Naoko Kodama

University of Yamanashi

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Shigeru Murakami

Fukui Prefectural University

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Akiko Yoneda

Taisho Pharmaceutical Co.

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Nobue Matsuzaki

Chiba College of Health Science

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Kazuo Hasegawa

Taisho Pharmaceutical Co.

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Yukiko Kondo

Taisho Pharmaceutical Co.

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