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Dive into the research topics where Madoka Nakajima is active.

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Featured researches published by Madoka Nakajima.


Mutation Research-genetic Toxicology and Environmental Mutagenesis | 2015

JaCVAM-organized international validation study of the in vivo rodent alkaline comet assay for the detection of genotoxic carcinogens: I. Summary of pre-validation study results.

Yoshifumi Uno; Hajime Kojima; Takashi Omori; Raffaella Corvi; Masamistu Honma; Leonard M. Schechtman; Raymond R. Tice; Brian Burlinson; Patricia A. Escobar; Andrew R. Kraynak; Yuzuki Nakagawa; Madoka Nakajima; Kamala Pant; Norihide Asano; David P. Lovell; Takeshi Morita; Yasuo Ohno; Makoto Hayashi

The in vivo rodent alkaline comet assay (comet assay) is used internationally to investigate the in vivo genotoxic potential of test chemicals. This assay, however, has not previously been formally validated. The Japanese Center for the Validation of Alternative Methods (JaCVAM), with the cooperation of the U.S. NTP Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM)/the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM), the European Centre for the Validation of Alternative Methods (ECVAM), and the Japanese Environmental Mutagen Society/Mammalian Mutagenesis Study Group (JEMS/MMS), organized an international validation study to evaluate the reliability and relevance of the assay for identifying genotoxic carcinogens, using liver and stomach as target organs. The ultimate goal of this exercise was to establish an Organisation for Economic Co-operation and Development (OECD) test guideline. The study protocol was optimized in the pre-validation studies, and then the definitive (4th phase) validation study was conducted in two steps. In the 1st step, assay reproducibility was confirmed among laboratories using four coded reference chemicals and the positive control ethyl methanesulfonate. In the 2nd step, the predictive capability was investigated using 40 coded chemicals with known genotoxic and carcinogenic activity (i.e., genotoxic carcinogens, genotoxic non-carcinogens, non-genotoxic carcinogens, and non-genotoxic non-carcinogens). Based on the results obtained, the in vivo comet assay is concluded to be highly capable of identifying genotoxic chemicals and therefore can serve as a reliable predictor of rodent carcinogenicity.


Mutation Research\/dnaging | 1995

Effect of aging on spontaneous micronucleus frequencies in peripheral blood of nine mouse strains: the results of the 7th collaborative study organized by CSGMT/JEMS · MMS*

Sci-ichi Sato; Masako Taketomi; Madoka Nakajima; Michiyo Kitazawa; Hiroyasu Shimada; Satoru Itoh; Miyuki Igarashi; Naohiko Higashikuni; Shizuyo Sutou; Yu F. Sasaki; Makoto Hayashi; Toshio Sofuni; Takafumi Higashiguchi; Shinji Nito; Yasushi Kondo; Sachiko Honda; M. Hayashi; Yasuhiro Shinagawa; Eiichi Nakajima; Yoshie Oka; Kayoko Shimoi; Yumiko Hokabe; Akira Morita; Naohide Kinae; Masaki Takeuchi; Haruyoshi Hirono; Eiji Yamamura; Koichi Tamai

The spontaneous frequencies of micronucleated reticulocytes (MNRETs) were examined monthly over the life spans of animals belonging to nine mouse strains for the 7th collaborative study organized by the CSGMT/JEMS.MMS. Both sexes of the BDF1 strain and females of the A/J strain showed a statistically significant increase in mean spontaneous MNRET frequency in their last month of life, suggesting the possibility of strain-specific, age-dependent chromosomal instability. SAMP6/Tan, an accelerated senescence-prone strain, showed the same tendency, although it was not statistically significant. The other strains studied, ddY, CD-1, B6C3F1, SAMR1, and MS/Ae, did not show significant age-related differences in mean of MNRET frequencies. More extensive statistical analyses are underway, and the outcomes will be reported separately.


Regulatory Toxicology and Pharmacology | 2009

Practical issues on the application of the GHS classification criteria for germ cell mutagens

Takeshi Morita; Makoto Hayashi; Madoka Nakajima; Noriho Tanaka; David Tweats; Kaoru Morikawa; T. Sofuni

The Globally Harmonized System of Classification and Labeling of Chemicals (GHS) requires classification of chemicals on germ cell mutagenicity. The Japanese government has conducted GHS classification on about 1400 chemicals in a 2-year project (J-GHS) for implementing GHS domestically. Prior to the classification work, the technical guidance for classification of germ cell mutagens was prepared. This guidance introduces the concept of heritable mutagenicity, and presents detailed criteria for germ cell mutagens, test data to be used, and a practical decision tree for classification. These practical guidance and supporting explanations are useful for non-expert Classifiers (scientists applying the classification criteria). Several issues, however, were identified during the course of J-GHS and in re-evaluating the classification results. These include: (1) the information sources when available data are limited; (2) lack of understanding GHS classification criteria or insufficient review of the information by Classifiers; (3) varying opinions of experts on data quality and weight of evidence, and; (4) decision tree approaches, e.g., inadequacy for use in overall evaluation in some cases. Ideally, classification should be performed by Classifiers with high expertise using high quality information sources. Genetic toxicologists as experts should consider data quality and reliability, and give a critical review of all available information for support of classification. A weight of evidence approach is also required to assess mutagenic potential of chemicals. Critical points for suitable classification for GHS are discussed.


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 2015

The Japan Flavour and Fragrance Materials Association’s (JFFMA) safety assessment of acetal food flavouring substances uniquely used in Japan

Hiroyuki Okamura; Hajime Abe; Yasuko Hasegawa-Baba; Kenji Saito; Fumiko Sekiya; Shim mo Hayashi; Yoshiharu Mirokuji; Shinpei Maruyama; Atsushi Ono; Madoka Nakajima; Masakuni Degawa; Shogo Ozawa; Makoto Shibutani; Tamio Maitani

Using the procedure devised by the Joint FAO/WHO Expert Committee on Food Additives (JECFA), we performed safety evaluations on five acetal flavouring substances uniquely used in Japan: acetaldehyde 2,3-butanediol acetal, acetoin dimethyl acetal, hexanal dibutyl acetal, hexanal glyceryl acetal and 4-methyl-2-pentanone propyleneglycol acetal. As no genotoxicity study data were available in the literature, all five substances had no chemical structural alerts predicting genotoxicity. Using Cramer’s classification, acetoin dimethyl acetal and hexanal dibutyl acetal were categorised as class I, and acetaldehyde 2,3-butanediol acetal, hexanal glyceryl acetal and 4-methyl-2-pentanone propyleneglycol acetal as class III. The estimated daily intakes for all five substances were within the range of 1.45–6.53 µg/person/day using the method of maximised survey-derived intake based on the annual production data in Japan from 2001, 2005, 2008 and 2010, and 156–720 µg/person/day using the single-portion exposure technique (SPET), based on the average use levels in standard portion sizes of flavoured foods. The daily intakes of the two class I substances were below the threshold of toxicological concern (TTC) – 1800 μg/person/day. The daily intakes of the three class III substances exceeded the TTC (90 μg/person/day). Two of these, acetaldehyde 2,3-butanediol acetal and hexanal glyceryl acetal, were expected to be metabolised into endogenous products after ingestion. For 4-methyl-2-pentanone propyleneglycol acetal, one of its metabolites was not expected to be metabolised into endogenous products. However, its daily intake level, based on the estimated intake calculated by the SPET method, was about 1/15 000th of the no observed effect level. It was thus concluded that all five substances raised no safety concerns when used for flavouring foods at the currently estimated intake levels. While no information on in vitro and in vivo toxicity for all five substances was available, their metabolites were judged as raising no safety concerns at the current levels of intake. Graphical Abstract


Food and Chemical Toxicology | 2014

The JFFMA assessment of flavoring substances structurally related to menthol and uniquely used in Japan

Yoshiharu Mirokuji; Hajime Abe; Hiroyuki Okamura; Kenji Saito; Fumiko Sekiya; Shim mo Hayashi; Shinpei Maruyama; Atsushi Ono; Madoka Nakajima; Masakuni Degawa; Shogo Ozawa; Makoto Shibutani; Tamio Maitani

Using the procedure devised by the Joint FAO/WHO Expert Committee on Food Additives (JECFA), we performed safety evaluations on four flavoring substances structurally related to menthol (L-menthyl 2-methylbutyrate, DL-menthyl octanoate, DL-menthyl palmitate, and DL-menthyl stearate) uniquely used in Japan. While no genotoxicity study data were available in the literature, all four substances had no chemical structural alerts predictive of genotoxicity. Moreover, they all four are esters consisting of menthol and simple carboxylic acids that were assumed to be immediately hydrolyzed after ingestion and metabolized into innocuous substances for excretion. As menthol and carboxylic acids have no known genotoxicity, it was judged that the JECFA procedure could be applied to these four substances. According to Cramers classification, these substances were categorized as class I based on their chemical structures. The estimated daily intakes for all four substances were within the range of 1.54-4.71 μg/person/day and 60-1250 μg/person/day, using the methods of Maximized Survey-Derived Intake and Single Portion Exposure Technique, respectively, based on the annual usage data of 2001, 2005, and 2010 in Japan. As the daily intakes of these substances were below the threshold of concern applied to class I substances viz., 1800 μg/person/day, it was concluded that all four substances raise no safety concerns when used for flavoring foods under the currently estimated intake levels.


Mutation Research\/dnaging | 1996

Effect of aging on spontaneous micronucleus frequencies in peripheral blood of nine mouse strains: the results of the 7th collaborative study organized by CSGMT/JEMS · MMS: Mutation Res. 338 (1995) 51–57☆☆☆

Sei-ichi Sato; Masako Taketomi; Madoka Nakajima; Michiyo Kitazawa; Hiroyasu Shimada; Satoru Itoh; Miyuki Igarashi; Naohiko Higashikuni; Shizuyo Sotou; Yu F. Sasaki; Makoto Hayashi; Toshio Sofuni; Takafumi Higashiguchi; Shinji Nito; Yasushi Kondo; Sachiko Honda; M. Hayashi; Yasuhiro Shinagawa; Eiichi Nakajima; Yoshie Oka; Kayoko Shimoi; Yumiko Hokabe; Akira Morita; Naohide Kinae; Masaki Takeuchi; Haruyoshi Hirono; Eiji Yamamura; Koichi Tamai

Abstract The spontaneous frequencies of micronucleated reticulocytes (MNRETs) were examined monthly over the life spans of animals beloning to nine mouse strains for the 7th collaborative study organized by the CSGMT/JEMS · MMS. Both sexes of the BDF1 strain and females of the A/J strain showed a statistically significant increase ni mean spontaneous MNRET frequency in their last month of life, suggesting the possibility of strain-specific, age-dependent chromosomal instability. SAMP6/Tan, an accelerated senescence-prone strain, showed the same tendency, although it was not statistically significant. The other strains studied, ddY, CD-1, B6C3F1, SAMR1, and MS/Ae, did not show significant age-related differences in mean of MNRET frequencies. More extensive statistical analyses are underway, and the outcomes will be reported separately.


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 2017

Japan Flavour and Fragrance Materials Association’s (JFFMA) safety assessment of food-flavouring substances uniquely used in Japan that belong to the class of aliphatic primary alcohols, aldehydes, carboxylic acids, acetals and esters containing additional oxygenated functional groups

Kenji Saito; Yasuko Hasegawa-Baba; Fumiko Sekiya; Shim mo Hayashi; Yoshiharu Mirokuji; Hiroyuki Okamura; Shinpei Maruyama; Atsushi Ono; Madoka Nakajima; Masakuni Degawa; Shogo Ozawa; Makoto Shibutani; Tamio Maitani

ABSTRACT We performed a safety evaluation using the procedure devised by the Joint FAO/WHO Expert Committee on Food Additives (JECFA) of the following four flavouring substances that belong to the class of ‘aliphatic primary alcohols, aldehydes, carboxylic acids, acetals, and esters containing additional oxygenated functional groups’ and are uniquely used in Japan: butyl butyrylacetate, ethyl 2-hydroxy-4-methylpentanoate, 3-hydroxyhexanoic acid and methyl hydroxyacetate. Although no genotoxicity study data were found in the published literature, none of the four substances had chemical structural alerts predicting genotoxicity. All four substances were categorised as class I by using Cramer’s classification. The estimated daily intake of each of the four substances was determined to be 0.007–2.9 μg/person/day by using the maximised survey-derived intake method and based on the annual production data in Japan in 2001, 2005 and 2010, and was determined to be 0.250–600.0 μg/person/day by using the single-portion exposure technique and based on average-use levels in standard portion sizes of flavoured foods. Both of these estimated daily intake ranges were below the threshold of toxicological concern for class I substances, which is 1800 μg/person/day. Although no information from in vitro and in vivo toxicity studies for the four substances was available, these substances were judged to raise no safety concerns at the current levels of intake. Graphical Abstract


Environmental and Molecular Mutagenesis | 2001

Evaluation of the rodent micronucleus assay by a 28‐day treatment protocol: Summary of the 13th Collaborative Study by the Collaborative Study Group for the Micronucleus Test (CSGMT)/Environmental Mutagen Society of Japan (JEMS)–Mammalian Mutagenicity Study Group (MMS)

Shuichi Hamada; Sizuyo Sutou; Takeshi Morita; Akihiro Wakata; Shougo Asanami; Satoko Hosoya; Shigenari Ozawa; Koji Kondo; Madoka Nakajima; Hiroyasu Shimada; Koichi Osawa; Yasushi Kondo; Norihide Asano; Sei-ichi Sato; Hironobu Tamura; Nobuhiro Yajima; Richard Marshall; Catherine Moore; David H. Blakey; Leonard M. Schechtman; James L. Weaver; Dorothea K. Torous; Ray Proudlock; Seiichi Ito; Chiaki Namiki; Makoto Hayashi


Environmental and Molecular Mutagenesis | 2006

MX, a by-product of water chlorination, lacks in vivo genotoxicity in gpt delta mice but inhibits gap junctional intercellular communication in rat WB cells

Akiyoshi Nishikawa; Kimie Sai; Kazushi Okazaki; Hwa-Young Son; Keita Kanki; Madoka Nakajima; Naohide Kinae; Takehiko Nohmi; James E. Trosko; Tohru Inoue; Masao Hirose


Genes and Environment | 2007

New Method of Specimen Preparation as Cell Suspension for a Micronucleus Test

Masayoshi Kawabata; Hironao Takasawa; Shigenori Minowa; Hitoshi Saitou; Munehiro Nakagawa; Madoka Nakajima; Shuichi Hamada

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Makoto Shibutani

Tokyo University of Agriculture and Technology

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Shogo Ozawa

Iwate Medical University

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