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Dive into the research topics where Miki Hiemori is active.

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Featured researches published by Miki Hiemori.


Bioscience, Biotechnology, and Biochemistry | 2007

Improvement of obesity and glucose tolerance by acetate in Type 2 diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) rats.

Hiromi Yamashita; Katsuhiko Fujisawa; Erina Ito; Seika Idei; Nobuyo Kawaguchi; Masumi Kimoto; Miki Hiemori; Hideaki Tsuji

Acetate has been found to have an inhibitory effect on the activity of carbohydrate-responsive element-binding protein (ChREBP) in cultured hepatocytes, this being a transcription factor that regulates several genes required for the conversion of glucose to fatty acids in the liver. The aim of this study was to investigate whether an oral administration of acetate would contribute to reducing lypogenic genes and protecting against obesity. We orally injected 5.2 mg/kg BW of acetate to obesity-linked type 2 diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) rats. The treatment with acetate showed a marked reduction in lipid accumulation in the adipose tissue, protection against accumulation of fat in the liver, and improved glucose tolerance. An analysis by Northern blotting revealed that the transcripts of several lipogenic genes in the liver of OLETF rats were decreased by the acetate treatment. On the basis of those results, it was indicated that acetate was a potential compound to improve obesity and obesity-linked type 2 diabetes.


Journal of Agricultural and Food Chemistry | 2009

Influence of Cooking on Anthocyanins in Black Rice (Oryza sativa L. japonica var. SBR)

Miki Hiemori; Eunmi Koh; Alyson E. Mitchell

The composition and thermal stability of anthocyanins in black rice (Oryza sativa L. japonica var. SBR) produced in California were investigated. Six anthocyanin pigments were identified and quantified by high performance liquid chromatography using photo diode-array detection (HPLC-PDA) and electrospray ionization mass spectrometry [LC-(ESI)MS/MS]. The predominant anthocyanins are cyanidin-3-glucoside (572.47 microg/g; 91.13% of total) and peonidin-3-glucoside (29.78 microg/g; 4.74% of total). Minor constituents included three cyanidin-dihexoside isomers and one cyanidin hexoside. Thermal stability of anthocyanins was assessed in rice cooked using a rice cooker, pressure cooker, or on a gas range. All cooking methods caused significant (P < 0.001) decreases in the anthocyanins identified. Pressure cooking resulted in the greatest loss of cyanidin-3-glucoside (79.8%) followed by the rice cooker (74.2%) and gas range (65.4%). Conversely, levels of protocatechuic acid increased 2.7 to 3.4 times in response to all cooking methods. These findings indicate that cooking black rice results in the thermal degradation of cyanidin-3-glucoside and concomitant production of protocatechuic acid.


Bioscience, Biotechnology, and Biochemistry | 2002

Identification of a Wheat Allergen, Tri a Bd 36K, as a Peroxidase

Hiromi Yamashita; Yoko Nanba; Miki Onishi; Masumi Kimoto; Miki Hiemori; Hideaki Tsuji

A 36-kDa allergen, Tri a Bd 36K, was purified from wheat albumin and characterized. The protein was similar to barley peroxidase BP-1 both in its amino acid sequence and peroxidase activity. The enzyme seemed to contain L-fucose and D-mannose and the glycan moiety reacted with IgE antibodies in a patients serum.


Bioscience, Biotechnology, and Biochemistry | 2007

Effect of a hypolipidemic drug, Di (2-ethylhexyl) phthalate, on mRNA-expression associated fatty acid and acetate metabolism in rat tissues.

Ai Itsuki-Yoneda; Masumi Kimoto; Hideaki Tsuji; Miki Hiemori; Hiromi Yamashita

Di (2-ehtylhexyl) phthalate (DEHP) is a peroxisome proliferator and a drug having a hypolipidemic effect. The body-weight change of rats treated with DEHP was lower than that of rats in an untreated control group. Expressions of long-chain acyl-CoA dehydrogenase and 3-ketoacyl-CoA thiolase, which are involved in fatty acid oxidation and acetate formation in mitochondria, showed an increase in the liver and testes of rats treated with DEHP. The expression of acetyl-CoA synthetase 1 was significantly decreased in the testes and relatively decreased in the liver, while the expression of acetyl-CoA synthetase 2 was significantly increased in the heart. Furthermore, the expressions of acetyl-CoA carboxylase in heart and testes showed a tendency to decrease. From these results, it is suggested that DEHP-treatment increased fatty acid oxidation and acetate formation in liver and testes, and that acetate utilization was increased in peripheral tissues such as the heart.


Bioscience, Biotechnology, and Biochemistry | 2009

Effects of Acetate on Lipid Metabolism in Muscles and Adipose Tissues of Type 2 Diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) Rats

Hiromi Yamashita; Hitomi Maruta; Michiyo Jozuka; Rie Kimura; Hiromi Iwabuchi; Makiko Yamato; Tsukasa Saito; Katsuhiko Fujisawa; Yoshitaka Takahashi; Masumi Kimoto; Miki Hiemori; Hideaki Tsuji

We have reported that orally administrated acetate contributed to suppression of lipogenesis in the liver and to reduction of lipid accumulation in the adipose tissue of Otsuka Long-Evans Tokushima Fatty (OLETF) rats. The aim of this study was to investigate the effect of acetate on skeletal muscle and adipose tissues. Treatment with acetate showed a higher rate of oxygen consumption and a smaller size of lipid droplets in white adipose and brown adipose tissues. An analysis by Northern blotting revealed that the transcripts of myoglobin and Glut4 genes in the abdominal muscle of the OLETF rats were increased by acetate treatment, while the transcripts of lipolytic genes increased in the white adipose and brown adipose tissues. It is possible that acetate has effects on lipid metabolism in the skeletal muscles and the adipose tissues, and has functions that work against obesity and obesity-linked type 2 diabetes.


Bioscience, Biotechnology, and Biochemistry | 2009

Isolation and Molecular Cloning of a Major Wheat Allergen, Tri a Bd 27K

Masumi Kimoto; Makiko Suzuki; Nobuko Komiyama; Ayumi Kunimoto; Hiromi Yamashita; Miki Hiemori; Kyoko Takahashi; Hideaki Tsuji

Tri a Bd 27K is the predominant allergen in wheat. In the present study, this allergen was purified to homogeneity from wheat flour. The N-terminal amino acid sequences of the purified allergen and the peptides obtained by its digestion, with trypsin were determined, and the allergen was shown to be a glycoprotein with an Asn-linked sugar moiety containing fucose residues. A cDNA encoding the allergen was obtained by polymerase chain reaction (PCR). The cDNA codes for a protein of 203 amino acid residues, with a molecular mass of 22,803 Da, that has two tentative sites glycosylated at Asn residues. Homology analysis suggested that the allergen might belong to a family of γ-interferon-inducible thiol reductases. The cDNA was expressed as a fusion protein with glutathione S-transferase in Escherichia coli. However, unlike the allergen purified from wheat, recombinant Tri a Bd 27K was not immunoblotted with IgE antibodies in the serum of a wheat-sensitive patient.


Bioscience, Biotechnology, and Biochemistry | 2009

Molecular Cloning and Allergenicity of Pen j 1, a Major Allergen of Kuruma Prawn, Penaeus japonicus

Ayumi Kunimoto; Takako Sisino; Kentaro Sakai; Tomoaki Matsumoto; Kyoko Takahashi; Hiromi Yamashita; Miki Hiemori; Hideaki Tsuji; Masumi Kimoto

Tropomyosins have been identified as a common allergen in crustaceans, but their allergenicity is not well understood. In the present study, we isolated an allergen, Pen j 1, a tropomyosin from kuruma prawn Penaeus japonicus, and determined its N-terminal amino acid sequence. The cDNA encoding the allergen was cloned by 5′- and 3′-rapid amplification of cDNA ends (RACE), and was found to code for a protein which consists of 284 amino acid residues. Sequencing analyses indicated for the first time that mature tropomyosin is formed by the elimination of a leader peptide of nine amino acid residues. To elucidate the binding sites of IgE antibodies in the sera of shrimp-sensitive patients, various recombinant peptides were expressed in Escherichia coli as fusion proteins with glutathione S-transferase (GST), and the examined with regard to reactivity with IgE antibodies. The IgE-binding epitopes were found to locate over the whole sequence of the allergen, and the IgE antibodies in the sera were found to recognize strongly its C-terminal region.


Bioscience, Biotechnology, and Biochemistry | 2011

Gastrointestinal Digestion and Absorption of Pen j 1, a Major Allergen from Kuruma Prawn, Penaeus japonicus

Ayumi Kunimoto; Miyuki Yokoro; Kaeko Murota; Rintaro Yamanishi; Toshiko Suzuki-Yamamoto; Makiko Suzuki; Chikao Yutani; Shinobu Doi; Miki Hiemori; Hiromi Yamashita; Yoshitaka Takahashi; Hideaki Tsuji; Masumi Kimoto

Tropomyosin had been identified as a major allergen in shrimp. The digestion and absorption of tropomyosin (Pen j 1) from kuruma prawn were investigated by ex vivo, in vitro, and in vivo techniques in order to elucidate the relationship between the allergenicity of the allergen and its gastrointestinal behavior. Pen j 1 transported the Caco-2 monolayer in a dose-dependent manner, and also enhanced the permeability of lucifer yellow, a marker of paracellular transportation, at high concentrations of the allergen. Studies with everted sacs revealed that Pen j 1 was rapidly degraded to small peptides (MW<3.5 kDa) and amino acids by intestinal proteases and absorbed from enterocytes. Furthermore, Pen j 1 orally administered to rats tended to remain in the stomach rather than in the small intestine, after which the allergen moved to the epithelial cells. These observations suggest that Pen j 1 may be absorbed via the gastric mucosa prior to its digestion in the intestines.


Bioscience, Biotechnology, and Biochemistry | 2010

Investigation of Multiple Forms of Tri a Bd 27K, a Major Wheat Allergen, by Immunoblotting Analysis

Miki Hiemori; Yukari Yosida; Masumi Kimoto; Hiromi Yamashita; Kyoko Takahashi; Kiyoshi Takahashi; Nobuko Komiyama; Hideaki Tsuji

Tri a Bd 27K, a major wheat allergen, is a glycoprotein. Tri a Bd 27K was found to occur in multiple forms by two-dimensional polyacrylamide gel electrophoresis and immunoblotting with a monoclonal antibody against the allergen. Furthermore, it was found that only Tri a Bd 27K components, which have N-linked glycan moieties with fucose residues, bound to IgE antibodies in the sera of wheat-sensitive patients.


Bioscience, Biotechnology, and Biochemistry | 2008

Characterization of New 18-kDa IgE-Binding Proteins in Beer

Miki Hiemori; Yuka Eguchi; Masumi Kimoto; Hiromi Yamasita; Kyoko Takahashi; Kiyoshi Takahashi; Hideaki Tsuji

The IgE-binding proteins in beer were examined by immunoblotting analysis with sera of patients sensitive to beer. Several proteins were immunoblotted with the sera, and among these, 18-kDa proteins were identified as new IgE-binding proteins in beer. Perhaps they originated from barley as a raw material.

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Hideaki Tsuji

Okayama Prefectural University

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Masumi Kimoto

Okayama Prefectural University

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Hiromi Yamashita

Okayama Prefectural University

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Kyoko Takahashi

Mukogawa Women's University

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Akiko Ishikawa

Okayama Prefectural University

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Ayumi Kunimoto

Okayama Prefectural University

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Makiko Suzuki

Okayama Prefectural University

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Misako Okita

Okayama Prefectural University

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Nobuko Komiyama

Okayama Prefectural University

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