Mariko Uehara

Prof. Mariko Uehara

Department of Nutritional Science and Food Safety, Faculty of Applied Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2009 in Journal of Clinical Biochemistry and Nutrition
Verified
Journal Article
Open access
SASatoko Akiyama
Satoko Akiyama
SKShin-Ichi Katsumata
Shin-Ichi Katsumata
KSKazuharu Suzuki
Kazuharu Suzuki
YIYoshiko Ishimi
Yoshiko Ishimi
JWJian Wu
Jian Wu
MUMariko Uehara
Mariko Uehara
Citrus bioflavonoids may offer some protection against the early stage of diabetes mellitus and the development of complications. We investigated the effect of hesperidin on blood glucose levels, hepatic glucose-regulating enzyme activities, serum insulin and adiponectin levels, serum and hepatic lipid levels, and parameters of bone loss in streptozotocin (STZ)-induced marginal type 1 diabetic rats. Weanling male rats were randomly assigned to experimental 3 groups: a control (C) group, a STZ induced marginal type 1 diabetes (S) group, and a diabetes and hesperidin group, and fed their respective diets for 4 weeks. STZ injection increased blood glucose in rats, but the increase was marginal. Serum and hepatic lipids, serum adiponectin and insulin levels were significantly changed by STZ injection. Dietary hesperidin (10 g/kg diet) decreased blood glucose by altering the activity of glucose-regulating enzymes, and normalized the lipids and adiponectin levels, but did not change bone parameters in the marginal type 1 diabetic rats. Hesperidin showed both hypoglycemic and hypolipidemic effects but did not affect bone tissue and bone metabolic makers in STZ-injected marginal diabetic weanling rats without any body weight loss due to STZ injection.

1 June 2023 in Free Radical Biology and Medicine
Verified
Journal Article
Closed access
MTMiori Tanaka
Miori Tanaka
HIHirofumi Inoue
Hirofumi Inoue
NTNobuyuki Takahashi
Nobuyuki Takahashi
MUMariko Uehara
Mariko Uehara

1 January 2013 in Journal of Clinical Biochemistry and Nutrition
Verified
Journal Article
Open access
MUMariko Uehara
Mariko Uehara
Several dietary phytochemicals exhibit anti-oxidative, anti-inflammatory and anti-osteoporotic activities relevant to prevention of chronic diseases, including lifestyle-related diseases. Soybean isoflavones are similar in structure to estrogen and have received considerable attention as potential alternatives to hormone replacement therapy. Daidzein, a major isoflavone found in soybean, is metabolized to equol by intestinal microflora; this metabolite exhibits stronger estrogenic activity than daidzein. Recent studies suggest that the clinical effectiveness of isoflavones might be due to their ability to produce equol in the gut. This review focused on the metabolic pathway of equol and possible bioactivities of equol and O-desmethylangolensin, another metabolite of daidzein, with regard to bone metabolism and the status of intestinal microflora. Furthermore, we considered risk-benefit analyses of isoflavones and their metabolites.

15 May 2013 in Phytotherapy Research
Verified
Journal Article
Closed access
PDF file
HCHiroshige Chiba
Hiroshige Chiba
HKHyounju Kim
Hyounju Kim
AMAkiyo Matsumoto
Akiyo Matsumoto
SASatoko Akiyama
Satoko Akiyama
YIYoshiko Ishimi
Yoshiko Ishimi
MUMariko Uehara
Mariko Uehara

13 September 2013 in Nutrition Journal
Verified
Journal Article
Open access
PDF file
YTYuko Tousen
Yuko Tousen
MUMariko Uehara
Mariko Uehara
FAFumiko Abe
Fumiko Abe
YKYoshifumi Kimira
Yoshifumi Kimira
YIYoshiko Ishimi
Yoshiko Ishimi
Background: Recent studies suggest that some of the clinical effectiveness of soy or daidzein, which is a type of isoflavone, may be attributed to a person’s ability to produce equol from daidzein. Equol, which is a metabolite of one of the major soybean isoflavones called daidzein, is produced in the gastrointestinal tract by certain intestinal microbiota where present. Habitual dietary patterns may alter the intestinal bacterial profile, and influence the metabolism of isoflavones and the production of equol. Fructooligosaccharides (FOS) have a prebiotic activity as well as being a dietary fibre. The purpose of the present study was to determine whether FOS supplementation increases equol production in equol producers and stimulates equol production in equol non-producers in Japanese postmenopausal women. Methods: A soy challenge was used to assess equol-producer status prior to the start of the study in healthy postmenopausal Japanese women. The study involved 4 separate groups in randomised crossover design. First, subjects were classified as equol producers (n = 25) or non-producers (n = 18), and then they were randomly assigned to the FOS or control group. All subjects received a daily dose of 37 mg isoflavone conjugates in the capsule (21 mg aglycone form) and either FOS (5g/day) or sucrose as control, in a randomised crossover study design. Equol -production was assessed by testing the serum and urine before and after the 2-week supplementation period. Results: The analyses were conducted on 34 subjects completed the study, 21 (61.8%) were classified as equol producers, and 13 (38.2%) as non-producers. Significant differences were observed in the interaction effect of time × equol state after 1 week of intervention (p = 0.006). However there were no effects after 2 weeks of intervention (p = 0.516). Finally, in both equol producers and non-producers, FOS supplementation did not affect the serum equol concentration or the urinary equol to daidzein concentration ratios. Conclusions: We have reported that FOS intervention (5 g/day for 2 weeks) does not significantly modulate the capacity of intestinal microbiota to produce equol in postmenopausal Japanese women, in either equol producers or non-producers in this pilot study. Further larger investigations that explore the roles of specific intestinal microbiota in equol production will enable the establishment of dietary conditions that are required to enhance equol production.

3 August 2015 in Bioscience, Biotechnology, and Biochemistry
Verified
Journal Article
Open access
PDF file
HIHirofumi Inoue
Hirofumi Inoue
KKKen-Ichi Kobayashi
Ken-Ichi Kobayashi
MNMoussa Ndong
Moussa Ndong
YYYuji Yamamoto
Yuji Yamamoto
SKShin-Ichi Katsumata
Shin-Ichi Katsumata
MUMariko Uehara
Mariko Uehara
We investigated the effects of dietary iron deficiency on the redox system in the heart. Dietary iron deficiency increased heart weight and accumulation of carbonylated proteins. However, expression levels of heme oxygenase-1 and LC3-II, an antioxidant enzyme and an autophagic marker, respectively, in iron-deficient mice were upregulated compared to the control group, resulting in a surrogate phenomenon against oxidative stress.