Safety and Efficacy Assessment of Isoflavones from Pueraria (Kudzu) Flower Extract in Ovariectomised Mice: A Comparison with Soy Isoflavones

Numerous Foods with Function Claims that contain the extract of flower (kudzu) isoflavones (PFI) are available in the Japanese market. These are labelled with function claims of reducing visceral fat. However, these foods have not undergone proper safety assessment such as the evaluation of their oe...

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Veröffentlicht in:International journal of molecular sciences 2019-06, Vol.20 (12), p.2867
Hauptverfasser: Tousen, Yuko, Takebayashi, Jun, Kondo, Takashi, Fuchino, Hiroyuki, Kawano, Noriaki, Inui, Takayuki, Yoshimatsu, Kayo, Kawahara, Nobuo, Ishimi, Yoshiko
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container_issue 12
container_start_page 2867
container_title International journal of molecular sciences
container_volume 20
creator Tousen, Yuko
Takebayashi, Jun
Kondo, Takashi
Fuchino, Hiroyuki
Kawano, Noriaki
Inui, Takayuki
Yoshimatsu, Kayo
Kawahara, Nobuo
Ishimi, Yoshiko
description Numerous Foods with Function Claims that contain the extract of flower (kudzu) isoflavones (PFI) are available in the Japanese market. These are labelled with function claims of reducing visceral fat. However, these foods have not undergone proper safety assessment such as the evaluation of their oestrogenic activity and effects on drug-metabolising enzymes (cytochrome P-450: CYP) in the liver. This study evaluated the estrogenic effect and the hepatic CYP activity and mRNA expression in normal female mice as a safety assessment of PFI (Experiment 1). In addition, the bone mineral density and visceral fat weight in ovariectomised mice (OVX) compared to soy isoflavones (SI) was evaluated to assess the efficacy of PFI (Experiment 2). OVX control fed a control diet, OVX fed a PFI diet (the recommended human intake of PFI), OVX fed a PFI20 diet (20- times the recommended PFI), OVX fed an SI diet (the recommended human intake of SI), and OVX fed an SI20 diet (20 -times the recommended intake of SI) for 28 days in Experiment 2. Body, liver, and visceral fat weights were not affected by the PFI, PFI20, SI, or SI20 diets. The hepatic CYP1A and CYP3A activities were elevated by the SI20 treatment. Ovariectomy-induced bone loss was inhibited by the SI20 treatment, but not by the PFI20 treatment. These results suggest that (1) PFI intake in human doses had no oestrogenic properties and did not affect CYP activity in the liver; (2) there was no evidence that PFI affects the amount of visceral fat in OVX mice.
doi_str_mv 10.3390/ijms20122867
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These are labelled with function claims of reducing visceral fat. However, these foods have not undergone proper safety assessment such as the evaluation of their oestrogenic activity and effects on drug-metabolising enzymes (cytochrome P-450: CYP) in the liver. This study evaluated the estrogenic effect and the hepatic CYP activity and mRNA expression in normal female mice as a safety assessment of PFI (Experiment 1). In addition, the bone mineral density and visceral fat weight in ovariectomised mice (OVX) compared to soy isoflavones (SI) was evaluated to assess the efficacy of PFI (Experiment 2). OVX control fed a control diet, OVX fed a PFI diet (the recommended human intake of PFI), OVX fed a PFI20 diet (20- times the recommended PFI), OVX fed an SI diet (the recommended human intake of SI), and OVX fed an SI20 diet (20 -times the recommended intake of SI) for 28 days in Experiment 2. Body, liver, and visceral fat weights were not affected by the PFI, PFI20, SI, or SI20 diets. The hepatic CYP1A and CYP3A activities were elevated by the SI20 treatment. Ovariectomy-induced bone loss was inhibited by the SI20 treatment, but not by the PFI20 treatment. These results suggest that (1) PFI intake in human doses had no oestrogenic properties and did not affect CYP activity in the liver; (2) there was no evidence that PFI affects the amount of visceral fat in OVX mice.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20122867</identifier><identifier>PMID: 31212773</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abdomen ; Abdominal Fat - drug effects ; Abdominal Fat - metabolism ; Age ; Animals ; Biomarkers ; Bone Density - drug effects ; Consumption ; Cytochrome P-450 Enzyme System - metabolism ; Dietary supplements ; Drug metabolism ; Enzyme Activation - drug effects ; Estrogens ; Female ; Flowers - chemistry ; Food ; Functional foods &amp; nutraceuticals ; Gene Expression Regulation - drug effects ; Isoflavones ; Isoflavones - chemistry ; Isoflavones - pharmacology ; Liver ; Liver - drug effects ; Liver - metabolism ; Menopause ; Metabolism ; Mice ; Models, Animal ; Natural &amp; organic foods ; Osteogenesis - drug effects ; Ovariectomy ; Pharmaceuticals ; Phytoestrogens ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Post-menopause ; Pueraria ; Pueraria - chemistry ; Safety ; Sex hormones</subject><ispartof>International journal of molecular sciences, 2019-06, Vol.20 (12), p.2867</ispartof><rights>2019. 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These are labelled with function claims of reducing visceral fat. However, these foods have not undergone proper safety assessment such as the evaluation of their oestrogenic activity and effects on drug-metabolising enzymes (cytochrome P-450: CYP) in the liver. This study evaluated the estrogenic effect and the hepatic CYP activity and mRNA expression in normal female mice as a safety assessment of PFI (Experiment 1). In addition, the bone mineral density and visceral fat weight in ovariectomised mice (OVX) compared to soy isoflavones (SI) was evaluated to assess the efficacy of PFI (Experiment 2). OVX control fed a control diet, OVX fed a PFI diet (the recommended human intake of PFI), OVX fed a PFI20 diet (20- times the recommended PFI), OVX fed an SI diet (the recommended human intake of SI), and OVX fed an SI20 diet (20 -times the recommended intake of SI) for 28 days in Experiment 2. Body, liver, and visceral fat weights were not affected by the PFI, PFI20, SI, or SI20 diets. The hepatic CYP1A and CYP3A activities were elevated by the SI20 treatment. Ovariectomy-induced bone loss was inhibited by the SI20 treatment, but not by the PFI20 treatment. These results suggest that (1) PFI intake in human doses had no oestrogenic properties and did not affect CYP activity in the liver; (2) there was no evidence that PFI affects the amount of visceral fat in OVX mice.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31212773</pmid><doi>10.3390/ijms20122867</doi><orcidid>https://orcid.org/0000-0002-6302-4507</orcidid><oa>free_for_read</oa></addata></record>
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source MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Abdomen
Abdominal Fat - drug effects
Abdominal Fat - metabolism
Age
Animals
Biomarkers
Bone Density - drug effects
Consumption
Cytochrome P-450 Enzyme System - metabolism
Dietary supplements
Drug metabolism
Enzyme Activation - drug effects
Estrogens
Female
Flowers - chemistry
Food
Functional foods & nutraceuticals
Gene Expression Regulation - drug effects
Isoflavones
Isoflavones - chemistry
Isoflavones - pharmacology
Liver
Liver - drug effects
Liver - metabolism
Menopause
Metabolism
Mice
Models, Animal
Natural & organic foods
Osteogenesis - drug effects
Ovariectomy
Pharmaceuticals
Phytoestrogens
Plant Extracts - chemistry
Plant Extracts - pharmacology
Post-menopause
Pueraria
Pueraria - chemistry
Safety
Sex hormones
title Safety and Efficacy Assessment of Isoflavones from Pueraria (Kudzu) Flower Extract in Ovariectomised Mice: A Comparison with Soy Isoflavones
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