JP2004242567A - Digestion absorption suppressant, food gi value diminishing agent, and food containing the suppressant and the diminishing agent - Google Patents

Digestion absorption suppressant, food gi value diminishing agent, and food containing the suppressant and the diminishing agent Download PDF

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JP2004242567A
JP2004242567A JP2003035143A JP2003035143A JP2004242567A JP 2004242567 A JP2004242567 A JP 2004242567A JP 2003035143 A JP2003035143 A JP 2003035143A JP 2003035143 A JP2003035143 A JP 2003035143A JP 2004242567 A JP2004242567 A JP 2004242567A
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gum
food
value
digestion
water
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Yuji Uzuhashi
祐二 埋橋
Kazumi Akeo
一美 明尾
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INA Food Industry Co Ltd
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INA Food Industry Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a digestion absorption suppressant and a food GI value diminishing agent inhibiting digestion absorption and diminishing GI value for food made from various carbohydrate, and to provide food containing the suppressant and the diminishing agent. <P>SOLUTION: This digestion absorption suppressant has as the main ingredient a water-soluble high polymer and suppresses digestion absorption of food through being added to the food. The food GI value diminishing agent has as the main ingredient a water-soluble high polymer and diminishes GI value of food through being added to the food. The food containing the digestion absorption suppressant and the GI value diminishing agent is also provided. <P>COPYRIGHT: (C)2004,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
本発明は、食品に加えることによりその消化吸収を抑制する消化吸収抑制剤及び食品に加えることによりそのGI値を低減する食品のGI値低減剤、並びにこれらが含まれた食品に関する。
【0002】
【従来の技術】
人間は、食事により栄養素を得て、その栄養素をエネルギーに変え、又は体内にグリコーゲンや蛋白質として蓄積することによって、体を維持し、健康を保っている。人間にとって生命を維持していくための重要な栄養素も、第二次世界大戦頃の日本においては、極度の栄養不足が続き、その後の高度成長期前までは、総エネルギー量を確保することしかできず、炭水化物に頼り蛋白質・脂質が少なく栄養バランスの不適正な時代があった。このため、国民の栄養に関し、積極的に動物性蛋白を摂取する欧米型の食生活が推奨されてきた。その結果、肉食で柔らかい噛むことが少ない出来合い食品や加工食品が多く出回るようになってきた。このような出来合い食品や加工食品は、容易に摂食することができるため、逆に栄養バランスを崩してしまい、このため肥満からくる糖尿病及びその合併症や心筋梗塞など生活習慣病と呼ばれる現代病が増加している。このため、総カロリーを抑えた食事制限による改善をしながら生活習慣病の予防や治療が行われている。しかしながら、一度覚えた栄養過剰の贅沢な食事をやめることは難しく、我が国においては、1割以上の糖尿病予備軍の病状が進行してしまうという問題がある。
【0003】
このような現状の中、最近食品のGI値(グリセミックインデックス値)を考えて食事を組み立てるという考え方が出てきている。GI値は、食品中の糖質の量は、同じでも血糖値の上昇が食品の質によって異なるということを数値で表したものであり、ブドウ糖を飲んだときの血糖値を100として色々な食品について数値化している。具体的には、GI値50の玄米ご飯は、GI値70の白米ご飯に比べて低く、ブドウ糖の吸収が遅いことになる。GI値が高い食品ばかり摂取すると、血糖値を一定に保つためにインシュリンが吸収過剰により余った血液中のブドウ糖を脂肪に変換・合成し脂肪細胞に取り込まれ肥満になる。しかし、GI値が低い食品を摂取すると、正常に筋肉や肝臓などでグリコーゲンや蛋白質の合成を促進しエネルギー代謝に使われることになる。
【0004】
このような背景から、物理的処理又は化学的処理を施し、酵素耐性が付加されたGI値の低い澱粉を作り、そのGI値の低い澱粉を含有させた消化性の悪い食品が考案されている(特許文献1)。
【0005】
【特許文献1】
特開2001−231469号公報
【0006】
【発明が解決しようとする課題】
しかしながら、特許文献1に記載のものは、特殊な澱粉のみのGI値を下げるものであるので、米飯のように添加できない食品も存在し、様々な炭水化物から作られる食品に対応できるものではない。このような難消化性の澱粉を既存の澱粉と一部置き換えで添加した場合、消化吸収をより少なくするためには多くの澱粉を置き換える必要があり、食感や味が本来の食品と大きく異なってしまう場合がある。
【0007】
そこで、本発明は、様々な炭水化物から作られる食品に対して消化吸収を抑制する消化吸収抑制剤、及びGI値を低減することができる食品のGI値低減剤、並びにこれが含まれた食品を提供することを目的とする。
【0008】
【課題を解決するための手段】
以上の目的を達成するため、本発明者らは、鋭意検討を重ねた結果、水溶性高分子を食品に加えることにより、食品の消化吸収を抑制したり、GI値を低減することを見出した。すなわち、本発明は、水溶性高分子を主成分とし、食品に加えることによりその消化吸収を抑制する消化吸収抑制剤、及び水溶性高分子を主成分とし、食品に加えることによりそのGI値を低減する食品のGI値低減剤、並びにこれらが含まれた食品である。
【0009】
【発明の実施の形態】
本発明に係る消化吸収抑制剤及び食品のGI値低減剤において、前記水溶性高分子は、アラビアガム、プルラン、デキストリン、タマリンドガム、寒天、カラギナン、ファーセレラン、ローカストビーンガム、タラガム、グアーガム、グアー分解物、コンニャクマンナン、ジェランガム、フノリ抽出物、サイリュームシードガム、カードラン、カシアガム、カラヤガム、アルギン酸およびその塩、キサンタンガム、大豆多糖類、ペクチン、ゼラチン、CMCナトリウム、メチルセルロース、セルロース、難消化性デキストリン、及びポリデキストロースのうち少なくとも1以上であることが好ましい。
【0010】
前記グアー分解物とは、グアーガムを酸や加熱処理、または酵素により加水分解したものである。前記フノリ抽出物とは、フノリを熱水抽出することにより得られたものである。アルギン酸塩としては、アルギン酸ナトリウム、アルギン酸カルシウムなどがある。また、難消化性デキストリンとは、デキストリンを焙焼することにより得られるものである。
【0011】
また、本発明に係る消化吸収阻害剤及び食品のGI値低減剤は、食品の加熱処理前に加えられることにより消化吸収を抑制し、又はGI値を低減するよう構成されていることが好ましい。
【0012】
【実施例】
次に、本発明に係る消化吸収抑制剤及び食品のGI値低減剤の実施例について説明する。
実施例1乃至28
先ず、本発明に係る消化吸収抑制剤及び食品のGI値低減剤の実施例1乃至28として、表1に示すようにアラビアガム(CNI社製)、プルラン(林原商事社製)、デキストリン(松谷化学社製)、タマリンドガム(大日本製薬社製)、タラガム(伊那食品工業社製)、グアー分解物(伊那食品工業社製)、コンニャクマンナン(伊那食品工業社製)、フノリ抽出物(伊那食品工業社製)、カラヤガム(ソマール社製)、アルギン酸ナトリウム(キミカ製)、大豆多糖類(不二製油社製)、HMペクチン(CPケルコ社製)、ゼラチン(新田ゼラチン社製)、乳化でんぷん(松谷化学工業社製)、LMペクチン(CPケルコ社製)、CMCナトリウム(第一化学薬品社製)、寒天(伊那食品工業社製)、κ―カラギナン(伊那食品工業社製)、λ―カラギナン(伊那食品工業社製)、ローカストビーンガム(伊那食品工業社製)、グアーガム(伊那食品工業社製)、ジェランガム(CPケルコ社製)、サイリュームシードガム(五協産業社製)、カードラン(武田薬品工業製)、カシアガム(伊那食品工業社製)、キサンタンガム(伊那食品工業社製)、セルロース(旭化成社製)、難消化性デキストリン(松谷化学工業社製)を用意した。
【0013】
【表1】

Figure 2004242567
【0014】
実験例1
これら実施例1乃至28に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gを小麦粉(日清製粉製)10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表1に示すようにサンプル1a乃至28aを得た。
【0015】
同様に小麦粉10gと水200gでスラリーを作り、これを100℃まで加熱し、完全に小麦粉を糊化させた後、実施例1乃至28に係る消化吸収抑制剤(食品のGI値低減剤)を添加することによって表1に示すようにサンプル1b乃至28bを得た。
【0016】
また、小麦粉10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。
【0017】
これらサンプル1a乃至28a、サンプル1b乃至28b、比較例それぞれについてα−アミラーゼの消化性試験を行った。α−アミラーゼの消化性試験は、サンプル1a乃至28a、サンプル1b乃至28b及び比較例それぞれにα−アミラーゼ50unitを添加後30分後、60分後、及び120分後にサンプリングを行い、直ちに蒸留水で任意に希釈を行い、Park−Johnson法にてα−アミラーゼの消化作用によって生じた還元末端の定量を行った。比較例の120分後の還元末端数を100としてその割合を%で示した。その結果を図1に示す。サンプル1a乃至28aは、図1から明らかなようにサンプル1b乃至28b及び比較例に比し消化率が低い値を示した。
【0018】
実験例2
次に、実施例1乃至16に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gを餅粉10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表2に示すようにサンプル1c乃至16cを得た。また、餅粉10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。これらサンプル1c乃至16c及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図2に示す。サンプル1c乃至16cは、図2から明らかなように比較例に比し消化率が低い値を示した。
【0019】
【表2】
Figure 2004242567
【0020】
実験例3
次に、実施例1乃至16に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gを米粉10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表2に示すようにサンプル1d乃至16dを得た。また、米粉10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。これらサンプル1d乃至16d及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図3に示す。サンプル1d乃至16dは、図3から明らかなように比較例に比し消化率が低い値を示した。
【0021】
実験例4
次に、実施例1乃至16に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gを馬鈴薯澱粉10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表2に示すようにサンプル1e乃至16eを得た。また、馬鈴薯澱粉10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。これらサンプル1e乃至16e及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図4に示す。サンプル1e乃至16eは、図4から明らかなように比較例に比し消化率が低い値を示した。
【0022】
実験例5
次に、実施例1乃至16に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gをタピオカ澱粉10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表2に示すようにサンプル1f乃至16fを得た。また、タピオカ澱粉10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。これらサンプル1f乃至16f及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図5に示す。サンプル1f乃至16fは、図5から明らかなように比較例に比し消化率が低い値を示した。
【0023】
実験例6
次に、実施例1乃至16に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gをコーンスターチ10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表2に示すようにサンプル1g乃至16gを得た。また、コーンスターチ10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。これらサンプル1g乃至16g及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図6に示す。サンプル1g乃至16gは、図6から明らかなように比較例に比し消化率が低い値を示した。
【0024】
実験例7
次に、実施例1乃至16に係る消化吸収抑制剤(食品のGI値低減剤)それぞれ0.5gと水200gをワキシコーンスターチ10gに加えてスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表2に示すようにサンプル1h乃至16hを得た。また、ワキシコーンスターチ10gと水200gでスラリーを作り、これを100℃まで加熱し完全に糊化させることによって比較例を得た。これらサンプル1h乃至16h及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図7に示す。サンプル1h乃至16hは、図7から明らかなように比較例に比し消化率が低い値を示した。
【0025】
実験例8乃至10
次に、サンプル1a乃至16aについて、消化酵素としてαーアミラーゼの代わりにβ−アミラーゼ、グルコアミラーゼとプルラナーゼを用いて実験例1と同様の消化性試験を行った。これらの結果を図8乃至10に示す。サンプル1a乃至16aは、図8乃至10から明らかなように、消化酵素を変えた場合であっても、比較例に比し消化率が低い値を示した。
【0026】
実験例11
次に、実施例1に係るアラビアガムの添加量を変化させて水と小麦粉(日清製粉製)に加えて小麦粉に対して1%、2%、5%、10%、25%のスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表3に示すようにサンプル1i乃至1mを得た。これらサンプル1i乃至1m及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図11に示す。サンプル1i乃至1mは、図11から明らかなように濃度を上げると消化率が抑制されることを示した。
【0027】
【表3】
Figure 2004242567
【0028】
実験例12
次に、実施例に係る大豆多糖類の添加量を変化させて水と小麦粉(日清製粉製)に加えて小麦粉に対して1%、2%、5%、10%、25%のスラリー状にした後、100℃まで加熱し見かけ上十分な位糊化させることによって表4に示すようにサンプル11i乃至11mを得た。これらサンプル11i乃至11m及び比較例について実験例1と同様にそれぞれについてα−アミラーゼの消化性試験を行った。その結果を図12に示す。サンプル11i乃至11mは、図12から明らかなように濃度を上げると消化率が抑制されることを示した。
【0029】
【表4】
Figure 2004242567
【0030】
実験例13
中力粉500gに対し、実施例1に係るアラビアガム及び実施例4に係るタマリンドガムをそれぞれ15gずつ加え混合後、12ボーメの食塩水230gを添加し、混合器で15分間練り上げ、30分静置した後ローリングプレス機でさらに練り上げ、3時間室温にねかし、ローリングプレス機で生地を長方形に薄く延ばし、切断機で切断することによって、実施例1に係るアラビアガム及び実施例4に係るタマリンドガムそれぞれが含まれている生麺(うどん)をそれぞれ作製した。また、消化吸収抑制剤を加えないこと以外は同様の処方で生麺(うどん)を比較例として作成した。
【0031】
作製したそれぞれのうどんを10倍量の水で一定時間茹で上げ、10meshの篩に通し、そのうちの100gを1Lの50mMリン酸緩衝液(pH6.0)の入った溶出試験機に分散させ、α−アミラーゼを100unit添加し、0〜120分までのサンプリングを行い、各サンプルについて酵素反応により生じる還元末端の定量をPark−Johnson法によって行った。その結果を図13に示す。実施例1に係るアラビアガム及び実施例4に係るタマリンドガムが含まれているうどんは、図13から明らかなように比較例に係るうどんに比し消化率が抑制されることを示した。
【0032】
実験例14
小豆500gを3倍量の水に一晩浸漬後、実施例1に係るアラビアガム5g、15g及び実施例12に係るHMペクチン15gをそれぞれ溶解した水1Lでかご炊きを行い、水切りをして灰汁を洗い流した後、実施例1に係るアラビアガム5g、15g及び実施例12に係るHMペクチン15gをそれぞれ溶解した水1.5Lで30分間茹で上げ、20分間蒸らし、茹で小豆を作製した。出来上がった茹で小豆をそれぞれ潰し、皮と“ゴ”を分離し、“ゴ”を流水にさらして灰汁抜きをした後、さらしで絞り、生餡を作成した。次に、実施例1に係るアラビアガムから1%及び3%のアラビアガム水溶液を作り、これら水溶液それぞれと生餡を1:2の割合で混ぜ合わせ、次いで生餡の1/2重量のエリスリトールと、生餡に対し0.01%のアスパルテームを加えて練り餡を作成した。また、消化吸収抑制剤を加えないこと以外は同様の処方で練り餡を比較例として作成した。
【0033】
作製した練り餡それぞれを5%濃度になるように50℃のリン酸緩衝液(pH6.0)に懸濁し、α−アミラーゼ50unitを添加し、0〜120分までのサンプリングを行い、各サンプルについて酵素反応により生じる還元末端の定量をPark−Johnson法によって行った。その結果を図14に示す。実施例1に係るアラビアガム及び実施例12に係るHMペクチンが含まれている練り餡は、図14から明らかなように比較例に係る練り餡に比し消化率が抑制されることを示した。
【0034】
【発明の効果】
以上のように本発明によれば、水溶性高分子を主成分とすることにより、様々な炭水化物から作られる食品に対して消化吸収を阻害し、またGI値を低減することができる消化吸収阻害剤及び食品のGI値低減剤、並びにこれらが含まれた食品を提供することができる。
【図面の簡単な説明】
【図1】水溶性高分子を加えた場合の小麦粉に対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図2】水溶性高分子を加えた場合の餅粉に対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図3】水溶性高分子を加えた場合の米粉に対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図4】水溶性高分子を加えた場合の馬鈴薯澱粉に対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図5】水溶性高分子を加えた場合のタピオカ澱粉に対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図6】水溶性高分子を加えた場合のコーンスターチに対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図7】水溶性高分子を加えた場合のワキシーコーンスターチに対するα―アミラーゼ消化率の測定結果を示すグラフである。
【図8】水溶性高分子を加えた場合の小麦粉に対するβ―アミラーゼ消化率の測定結果を示すグラフである。
【図9】水溶性高分子を加えた場合の小麦粉に対するグルコアミラーゼ消化率の測定結果を示すグラフである。
【図10】水溶性高分子を加えた場合の小麦粉に対するプルラナーゼ消化率の結果を示すグラフである。
【図11】アラビアガムの濃度を変えた場合の小麦粉に対するα―アミラーゼ消化率の結果を示すグラフである。
【図12】大豆多糖類の濃度を変えた場合の小麦粉に対するα―アミラーゼ消化率の結果を示すグラフである。
【図13】アラビアガム及びタマリンドガムを加えた生麺(うどん)に対するα―アミラーゼ消化率の結果を示すグラフである。
【図14】アラビアガム及びペクチンを加えた練り餡に対するα―アミラーゼ消化率の結果を示すグラフである。[0001]
TECHNICAL FIELD OF THE INVENTION
TECHNICAL FIELD The present invention relates to a digestion / absorption inhibitor that suppresses digestion and absorption when added to food, a GI value reducing agent for food that reduces its GI value when added to food, and a food containing these.
[0002]
[Prior art]
Humans maintain their body and maintain their health by obtaining nutrients through diet and converting the nutrients into energy or accumulating them as glycogen and proteins in the body. Important nutrients for sustaining human life are also extremely undernourished in Japan around World War II, and until the high growth period, it was only possible to secure total energy. There was a time when they couldn't do so and relied on carbohydrates, had little protein and fat, and had an improper nutritional balance. For this reason, regarding the nutrition of the people, a Western-style dietary habit of actively ingesting animal protein has been recommended. As a result, many ready-made foods and processed foods that are carnivorous and have less soft chewing have come to market. Such ready-made foods and processed foods can easily be eaten, and conversely cause a loss of nutritional balance, which leads to obesity-related diabetes and its complications, and modern diseases called lifestyle-related diseases such as myocardial infarction. Is increasing. For this reason, prevention and treatment of lifestyle-related diseases are being carried out while improving by dietary restriction that suppresses total calories. However, it is difficult to stop a once-measured luxurious diet that is overnutrition, and there is a problem in Japan that more than 10% of diabetic reserve medical conditions progress.
[0003]
Under such circumstances, there has recently been an idea of assembling a meal in consideration of a GI value (glycemic index value) of a food. The GI value is a numerical value indicating that the increase in blood sugar level differs depending on the quality of food even if the amount of carbohydrate in the food is the same. Is quantified. Specifically, brown rice with a GI value of 50 is lower than white rice with a GI value of 70, and the absorption of glucose is slow. When only foods with a high GI value are ingested, insulin converts excess glucose into blood into fat and synthesizes it into fat to keep the blood sugar level constant. However, when a food with a low GI value is ingested, it normally promotes the synthesis of glycogen and protein in muscle and liver and is used for energy metabolism.
[0004]
From such a background, a starch having a low GI value to which an enzyme resistance has been added by performing a physical treatment or a chemical treatment to produce a starch having a low GI value has been devised. (Patent Document 1).
[0005]
[Patent Document 1]
JP 2001-231469 A
[Problems to be solved by the invention]
However, the one described in Patent Literature 1 lowers the GI value of only special starch, so that there are foods such as cooked rice that cannot be added, and cannot cope with foods made from various carbohydrates. When such indigestible starch is partially replaced with existing starch, it is necessary to replace a large amount of starch in order to reduce digestion and absorption, and the texture and taste differ greatly from the original food. In some cases.
[0007]
Accordingly, the present invention provides a digestion and absorption inhibitor that suppresses digestion and absorption of foods made from various carbohydrates, a GI value reducing agent for foods that can reduce GI values, and a food containing the same. The purpose is to do.
[0008]
[Means for Solving the Problems]
In order to achieve the above object, the present inventors have conducted intensive studies and, as a result, have found that by adding a water-soluble polymer to food, the digestion and absorption of food can be suppressed or the GI value can be reduced. . That is, the present invention comprises a water-soluble polymer as a main component, a digestion-absorption inhibitor that suppresses digestion and absorption by adding it to food, and a water-soluble polymer as a main component, the GI value of which is added to food, GI value reducing agents for foods to be reduced, and foods containing these.
[0009]
BEST MODE FOR CARRYING OUT THE INVENTION
In the digestion absorption inhibitor and the food GI value reducing agent according to the present invention, the water-soluble polymer is gum arabic, pullulan, dextrin, tamarind gum, agar, carrageenan, furceleran, locust bean gum, tara gum, guar gum, guar decomposition. Products, konjac mannan, gellan gum, funori extract, silium seed gum, curdlan, cassia gum, karaya gum, alginic acid and its salts, xanthan gum, soy polysaccharides, pectin, gelatin, CMC sodium, methylcellulose, cellulose, resistant dextrin, and Preferably, at least one of polydextrose is used.
[0010]
The guar decomposition product is obtained by hydrolyzing guar gum with an acid, heat treatment, or an enzyme. The Funori extract is obtained by extracting Funori with hot water. Alginate includes sodium alginate, calcium alginate and the like. Indigestible dextrin is obtained by roasting dextrin.
[0011]
Moreover, it is preferable that the digestion-absorption inhibitor and the food GI value reducing agent according to the present invention are configured to suppress digestion and absorption or reduce the GI value by being added before the heat treatment of the food.
[0012]
【Example】
Next, examples of the digestion absorption inhibitor and the food GI value reducing agent according to the present invention will be described.
Examples 1 to 28
First, as Examples 1 to 28 of the digestion absorption inhibitor and the food GI value reducing agent according to the present invention, as shown in Table 1, gum arabic (manufactured by CNI), pullulan (manufactured by Hayashibara Shoji), dextrin (Matsutani) Chemicals), Tamarind Gum (Dainippon Pharmaceutical Co., Ltd.), Tara Gum (Ina Food Industry Co., Ltd.), Guar Decomposed Product (Ina Food Industry Co., Ltd.), Konjac Mannan (Ina Food Industry Co., Ltd.), Funori Extract (Ina Food Industry Co., Ltd., Karaya Gum (Somar), Sodium Alginate (Kimika), Soybean Polysaccharide (Fuji Oil), HM Pectin (CP Kelco), Gelatin (Nitta Gelatin), Emulsification Starch (Matsuya Chemical Industries), LM pectin (CP Kelco), CMC sodium (Daiichi Pure Chemicals), agar (Ina Food Industry), κ-carrageenan (Ina Food Industry) , Λ-carrageenan (manufactured by Ina Food Industry Co., Ltd.), locust bean gum (manufactured by Ina Food Industry Co., Ltd.), guar gum (manufactured by Ina Food Industry Co., Ltd.), gellan gum (manufactured by CP Kelco), silium seed gum (manufactured by Gokyo Industry Co., Ltd.) Curdlan (manufactured by Takeda Pharmaceutical Co., Ltd.), Cassia gum (manufactured by Ina Food Industry Co., Ltd.), xanthan gum (manufactured by Ina Food Industry Co., Ltd.), cellulose (manufactured by Asahi Kasei Corporation), and indigestible dextrin (manufactured by Matsutani Chemical Industry Co., Ltd.) were prepared.
[0013]
[Table 1]
Figure 2004242567
[0014]
Experimental example 1
0.5 g of each of the digestion and absorption inhibitors (GI food value reducing agents) according to Examples 1 to 28 and 200 g of water were added to 10 g of flour (manufactured by Nisshin Flour Milling Co., Ltd.) to form a slurry, and then heated to 100 ° C. Samples 1a to 28a were obtained as shown in Table 1 by performing gelatinization to a sufficient degree.
[0015]
Similarly, a slurry was prepared from 10 g of flour and 200 g of water, and heated to 100 ° C. to completely gelatinize the flour. Then, the digestion and absorption inhibitors (GI value reducing agents for food) according to Examples 1 to 28 were added. By adding, samples 1b to 28b were obtained as shown in Table 1.
[0016]
Also, a comparative example was obtained by preparing a slurry from 10 g of flour and 200 g of water and heating the slurry to 100 ° C. to completely gelatinize.
[0017]
Each of Samples 1a to 28a, Samples 1b to 28b, and Comparative Example was subjected to α-amylase digestibility test. In the digestibility test of α-amylase, samples were taken 30 minutes, 60 minutes, and 120 minutes after adding 50 units of α-amylase to each of Samples 1a to 28a, Samples 1b to 28b, and Comparative Example, and immediately sampled with distilled water. The dilution was arbitrarily performed, and the reducing end generated by the digestion of α-amylase was quantified by the Park-Johnson method. The number of reducing terminals after 120 minutes in the comparative example was taken as 100, and the ratio was shown in%. The result is shown in FIG. As is clear from FIG. 1, Samples 1a to 28a exhibited lower digestibility than Samples 1b to 28b and Comparative Example.
[0018]
Experimental example 2
Next, 0.5 g of each of the digestion and absorption inhibitors (GI food value reducing agents) according to Examples 1 to 16 and 200 g of water were added to 10 g of rice cake flour to form a slurry, which was then heated to 100 ° C. and seemed to be sufficiently satisfactory. Samples 1c to 16c were obtained as shown in Table 2 by performing gelatinization. In addition, a comparative example was obtained by preparing a slurry from 10 g of rice cake flour and 200 g of water, heating the slurry to 100 ° C., and completely gelatinizing. For each of the samples 1c to 16c and the comparative example, an α-amylase digestibility test was performed in the same manner as in Experimental Example 1. The result is shown in FIG. As is clear from FIG. 2, the samples 1c to 16c exhibited lower digestibility than the comparative example.
[0019]
[Table 2]
Figure 2004242567
[0020]
Experimental example 3
Next, after adding 0.5 g of each of the digestion absorption inhibitors (GI food value reducing agents) according to Examples 1 to 16 and 200 g of water to 10 g of rice flour to form a slurry, the mixture was heated to 100 ° C. and seemingly sufficient. Samples 1d to 16d were obtained as shown in Table 2 by gelatinizing. Further, a slurry was prepared from 10 g of rice flour and 200 g of water, and the slurry was heated to 100 ° C. and completely gelatinized to obtain a comparative example. For each of the samples 1d to 16d and the comparative example, an α-amylase digestibility test was performed in the same manner as in Experimental Example 1. The result is shown in FIG. Samples 1d to 16d exhibited lower digestibility than the comparative example, as is clear from FIG.
[0021]
Experimental example 4
Next, 0.5 g of each of the digestion and absorption inhibitors (GI agent of food) according to Examples 1 to 16 and 200 g of water were added to 10 g of potato starch to form a slurry, which was then heated to 100 ° C. and seemingly sufficient. As shown in Table 2, samples 1e to 16e were obtained by performing gelatinization. Further, a slurry was prepared from 10 g of potato starch and 200 g of water, and this was heated to 100 ° C. to completely gelatinize, thereby obtaining a comparative example. The digestibility test of α-amylase was performed on each of the samples 1e to 16e and the comparative example in the same manner as in Experimental Example 1. The result is shown in FIG. As is clear from FIG. 4, the samples 1e to 16e exhibited lower digestibility than the comparative example.
[0022]
Experimental example 5
Next, 0.5 g of each of the digestion and absorption inhibitors (GI value reducing agents for food) according to Examples 1 to 16 and 200 g of water were added to 10 g of tapioca starch to form a slurry, which was then heated to 100 ° C. and seemed to be sufficiently satisfactory. As shown in Table 2, samples 1f to 16f were obtained by performing gelatinization. Further, a comparative example was obtained by preparing a slurry from 10 g of tapioca starch and 200 g of water and heating the slurry to 100 ° C. to completely gelatinize. The digestibility test of α-amylase was performed on each of the samples 1f to 16f and the comparative example in the same manner as in Experimental Example 1. The result is shown in FIG. As is clear from FIG. 5, the samples 1f to 16f exhibited lower digestibility than the comparative example.
[0023]
Experimental example 6
Next, after adding 0.5 g of each of the digestion and absorption inhibitors (the GI value reducing agents of food) according to Examples 1 to 16 and 200 g of water to 10 g of corn starch to form a slurry, the mixture was heated to 100 ° C. and seemingly sufficient. As shown in Table 2, 1 g to 16 g of samples were obtained by gelatinization. Further, a slurry was prepared from 10 g of corn starch and 200 g of water, and the slurry was heated to 100 ° C. and completely gelatinized to obtain a comparative example. The digestibility test of α-amylase was performed on each of the samples 1 g to 16 g and the comparative example in the same manner as in Experimental Example 1. FIG. 6 shows the result. Samples 1g to 16g showed lower digestibility than the comparative example, as is apparent from FIG.
[0024]
Experimental example 7
Next, 0.5 g of each of the digestion absorption inhibitors (GI food value reducing agents) according to Examples 1 to 16 and 200 g of water were added to 10 g of waxy corn starch to form a slurry, which was then heated to 100 ° C. and apparently. Samples 1h to 16h were obtained by sufficient gelatinization as shown in Table 2. Further, a comparative example was obtained by preparing a slurry from 10 g of waxy corn starch and 200 g of water, heating the slurry to 100 ° C., and completely gelatinizing. The digestibility test of α-amylase was performed on each of the samples 1h to 16h and the comparative example in the same manner as in Experimental Example 1. FIG. 7 shows the result. Samples 1h to 16h exhibited lower digestibility than the comparative example, as is clear from FIG.
[0025]
Experimental Examples 8 to 10
Next, samples 1a to 16a were subjected to the same digestibility test as in Experimental Example 1 using β-amylase, glucoamylase and pullulanase instead of α-amylase as digestive enzymes. These results are shown in FIGS. As is clear from FIGS. 8 to 10, Samples 1a to 16a showed lower digestibility than the Comparative Example even when the digestive enzymes were changed.
[0026]
Experimental Example 11
Next, the amount of the gum arabic according to Example 1 was changed to add water, flour (manufactured by Nisshin Flour Milling Co., Ltd.), and 1%, 2%, 5%, 10%, 25% slurry based on flour. Then, the mixture was heated to 100 ° C. and gelatinized to a sufficient degree to obtain samples 1i to 1m as shown in Table 3. The digestibility test of α-amylase was performed on each of the samples 1i to 1m and the comparative example in the same manner as in Experimental Example 1. The result is shown in FIG. Samples 1i to 1m showed that increasing the concentration suppressed digestibility, as is evident from FIG.
[0027]
[Table 3]
Figure 2004242567
[0028]
Experimental Example 12
Next, the amount of the soybean polysaccharide according to the example was changed to add 1%, 2%, 5%, 10%, and 25% slurry to the flour in addition to water and flour (manufactured by Nisshin Seifun KK). Then, the mixture was heated to 100 ° C. and gelatinized to a sufficient degree to obtain samples 11i to 11m as shown in Table 4. The digestibility test of α-amylase was performed on each of these samples 11i to 11m and the comparative example in the same manner as in Experimental Example 1. FIG. 12 shows the result. Samples 11i to 11m showed that the digestibility was suppressed when the concentration was increased, as is clear from FIG.
[0029]
[Table 4]
Figure 2004242567
[0030]
Experimental Example 13
15 g each of gum arabic according to Example 1 and tamarind gum according to Example 4 were added to and mixed with 500 g of all-purpose flour, and then 230 g of 12 Baume salt solution was added, kneaded with a mixer for 15 minutes, and allowed to stand for 30 minutes. After placing, the mixture was further kneaded with a rolling press, aged at room temperature for 3 hours, the dough was spread thinly into a rectangle with a rolling press, and cut with a cutter to cut the gum arabic according to Example 1 and the tamarind gum according to Example 4. Raw noodles (udon) containing each of them were produced. In addition, raw noodles (udon) were prepared as a comparative example with the same formulation except that no digestion absorption inhibitor was added.
[0031]
Each produced udon is boiled with 10 times the volume of water for a certain time, passed through a 10 mesh sieve, and 100 g of the noodles is dispersed in a dissolution tester containing 1 L of 50 mM phosphate buffer (pH 6.0). Amylase was added in an amount of 100 units, sampling was performed from 0 to 120 minutes, and the amount of the reducing end generated by the enzyme reaction in each sample was determined by the Park-Johnson method. The result is shown in FIG. The udon containing the gum arabic according to Example 1 and the tamarind gum according to Example 4 showed that the digestibility was suppressed as compared to the udon according to the comparative example, as is apparent from FIG.
[0032]
Experimental Example 14
After immersing 500 g of red beans in three times the amount of water overnight, cook the basket with 1 L of water in which 5 g and 15 g of gum arabic according to Example 1 and 15 g of HM pectin according to Example 12 are dissolved, drain, and drain lye After washing off, 5 g and 15 g of gum arabic according to Example 1 and 15 g of HM pectin according to Example 12 were respectively dissolved and boiled in 1.5 L of water for 30 minutes and steamed for 20 minutes to prepare boiled red beans. The finished boiled red beans were each crushed, the skin and “go” were separated, and “go” was exposed to running water to remove lye, and then squeezed with blister to prepare raw bean jam. Next, 1% and 3% aqueous solutions of gum arabic were prepared from the gum arabic according to Example 1, and each of these aqueous solutions and raw bean jam were mixed at a ratio of 1: 2. Then, 0.01% aspartame was added to the raw bean paste to prepare a kneaded bean paste. In addition, kneaded bean paste was prepared as a comparative example with the same formulation except that the digestion absorption inhibitor was not added.
[0033]
Each prepared dough was suspended in a phosphate buffer (pH 6.0) at 50 ° C. so as to have a concentration of 5%, 50 units of α-amylase was added, and sampling was performed for 0 to 120 minutes. Quantification of the reducing end generated by the enzymatic reaction was performed by the Park-Johnson method. FIG. 14 shows the result. The paste containing the gum arabic according to Example 1 and the HM pectin according to Example 12 showed a lower digestibility than the paste according to the comparative example, as is apparent from FIG. .
[0034]
【The invention's effect】
As described above, according to the present invention, a water-soluble polymer as a main component inhibits digestion and absorption of foods made from various carbohydrates, and can also reduce GI value. Agent and a GI value reducing agent for food, and a food containing these.
[Brief description of the drawings]
FIG. 1 is a graph showing the measurement results of α-amylase digestibility of wheat flour when a water-soluble polymer is added.
FIG. 2 is a graph showing measurement results of α-amylase digestibility of rice cake flour when a water-soluble polymer is added.
FIG. 3 is a graph showing the measurement results of α-amylase digestibility of rice flour when a water-soluble polymer is added.
FIG. 4 is a graph showing the results of measuring the α-amylase digestibility of potato starch when a water-soluble polymer was added.
FIG. 5 is a graph showing the results of measuring the α-amylase digestibility of tapioca starch when a water-soluble polymer was added.
FIG. 6 is a graph showing the results of measuring the α-amylase digestibility of corn starch when a water-soluble polymer was added.
FIG. 7 is a graph showing the results of measuring the α-amylase digestibility of waxy corn starch when a water-soluble polymer was added.
FIG. 8 is a graph showing the measurement results of β-amylase digestibility of wheat flour when a water-soluble polymer was added.
FIG. 9 is a graph showing the results of measuring the glucoamylase digestibility of wheat flour when a water-soluble polymer was added.
FIG. 10 is a graph showing results of pullulanase digestibility of wheat flour when a water-soluble polymer was added.
FIG. 11 is a graph showing the results of α-amylase digestibility of wheat flour when the concentration of gum arabic was changed.
FIG. 12 is a graph showing the results of α-amylase digestibility of wheat flour when the concentration of soybean polysaccharide was changed.
FIG. 13 is a graph showing the results of α-amylase digestibility of raw noodles (udon) to which gum arabic and tamarind gum have been added.
FIG. 14 is a graph showing the results of α-amylase digestibility of dough with gum arabic and pectin added.

Claims (7)

水溶性高分子を主成分とし、食品に加えることによりその消化吸収を抑制する消化吸収抑制剤。A digestion and absorption inhibitor that contains a water-soluble polymer as a main component and suppresses digestion and absorption when added to food. 前記水溶性高分子は、アラビアガム、プルラン、デキストリン、タマリンドガム、寒天、カラギナン、ファーセレラン、ローカストビーンガム、タラガム、グアーガム、グアー分解物、コンニャクマンナン、ジェランガム、フノリ抽出物、サイリュームシードガム、カードラン、カシアガム、カラヤガム、アルギン酸およびその塩、キサンタンガム、大豆多糖類、ペクチン、ゼラチン、CMCナトリウム、メチルセルロース、セルロース、難消化性デキストリン、及びポリデキストロースのうち少なくとも1以上であることを特徴とする請求項1記載の消化吸収抑制剤。The water-soluble polymer includes gum arabic, pullulan, dextrin, tamarind gum, agar, carrageenan, furceleran, locust bean gum, tara gum, guar gum, guar decomposition product, konjac mannan, gellan gum, funori extract, silium seed gum, curdlan And at least one of cassia gum, karaya gum, alginic acid and salts thereof, xanthan gum, soybean polysaccharide, pectin, gelatin, sodium CMC, methylcellulose, cellulose, indigestible dextrin, and polydextrose. The digestion and absorption inhibitor according to the above. 食品の加熱処理前に加えられることによりその消化吸収を抑制することを特徴とする請求項1又は2記載の消化吸収抑制剤。The digestion and absorption inhibitor according to claim 1 or 2, wherein the digestion and absorption of the food is suppressed by being added before the heat treatment. 水溶性高分子を主成分とし、食品に加えることによりそのGI値を低減するする食品のGI値低減剤。An agent for reducing the GI value of food, which contains a water-soluble polymer as a main component and reduces the GI value by adding it to food. 前記水溶性高分子は、アラビアガム、プルラン、デキストリン、タマリンドガム、寒天、カラギナン、ファーセレラン、ローカストビーンガム、タラガム、グアーガム、グアー分解物、コンニャクマンナン、ジェランガム、フノリ抽出物、サイリュームシードガム、カードラン、カシアガム、カラヤガム、アルギン酸およびその塩、キサンタンガム、大豆多糖類、ペクチン、ゼラチン、CMCナトリウム、メチルセルロース、セルロース、難消化性デキストリン、及びポリデキストロースのうち少なくとも1以上であることを特徴とする請求項4記載の食品のGI値低減剤。The water-soluble polymer includes gum arabic, pullulan, dextrin, tamarind gum, agar, carrageenan, furceleran, locust bean gum, tara gum, guar gum, guar decomposition product, konjac mannan, gellan gum, funori extract, silium seed gum, curdlan 5. At least one selected from the group consisting of cassia gum, karaya gum, alginic acid and salts thereof, xanthan gum, soybean polysaccharide, pectin, gelatin, sodium CMC, methylcellulose, cellulose, indigestible dextrin and polydextrose. A GI value reducing agent for the food according to the above. 食品の加熱処理前に加えられることによりそのGI値を低減することを特徴とする請求項4又は5記載の食品のGI値低減剤。The GI value reducing agent for food according to claim 4 or 5, wherein the GI value is reduced by being added before the heat treatment of the food. 請求項1乃至3いずれか記載の消化吸収抑制剤又は請求項4乃至6いずれか記載のGI値低減剤を含むことを特徴とする食品。A food comprising the digestion and absorption inhibitor according to any one of claims 1 to 3 or the GI value reducing agent according to any one of claims 4 to 6.
JP2003035143A 2003-02-13 2003-02-13 Digestion absorption suppressant, food gi value diminishing agent, and food containing the suppressant and the diminishing agent Pending JP2004242567A (en)

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Cited By (7)

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JP2007259801A (en) * 2006-03-29 2007-10-11 Kaneka Corp Cooked rice-like food
WO2008001800A1 (en) * 2006-06-28 2008-01-03 Otsuka Pharmaceutical Co., Ltd. Tooth enamel dissolution inhibitor
JP2008303175A (en) * 2007-06-07 2008-12-18 Otsuka Pharmaceut Co Ltd Gi value-reducing agent and method for producing foodstuff reduced with gi value
JP2009034031A (en) * 2007-08-01 2009-02-19 Fancl Corp Functional food
KR100921665B1 (en) * 2007-04-03 2009-10-15 고려대학교 산학협력단 A preparation method of boiled rice which glycemic index is controlled by adding hydrocolloids to rice during cooking
CN112438363A (en) * 2019-09-05 2021-03-05 四川农业大学 Bait block quality improver and preparation method thereof
CN114507295A (en) * 2021-12-22 2022-05-17 云南猫哆哩集团食品有限责任公司 Preparation method of tamarind seed polysaccharide glue solution

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007259801A (en) * 2006-03-29 2007-10-11 Kaneka Corp Cooked rice-like food
JP4687533B2 (en) * 2006-03-29 2011-05-25 株式会社カネカ Cooked rice-like food
WO2008001800A1 (en) * 2006-06-28 2008-01-03 Otsuka Pharmaceutical Co., Ltd. Tooth enamel dissolution inhibitor
EP2039362A1 (en) * 2006-06-28 2009-03-25 Otsuka Pharmaceutical Co., Ltd. Tooth enamel dissolution inhibitor
EP2039362A4 (en) * 2006-06-28 2011-06-29 Otsuka Pharma Co Ltd Tooth enamel dissolution inhibitor
JP5419451B2 (en) * 2006-06-28 2014-02-19 アース製薬株式会社 Tooth enamel dissolution inhibitor
KR100921665B1 (en) * 2007-04-03 2009-10-15 고려대학교 산학협력단 A preparation method of boiled rice which glycemic index is controlled by adding hydrocolloids to rice during cooking
JP2008303175A (en) * 2007-06-07 2008-12-18 Otsuka Pharmaceut Co Ltd Gi value-reducing agent and method for producing foodstuff reduced with gi value
JP2009034031A (en) * 2007-08-01 2009-02-19 Fancl Corp Functional food
CN112438363A (en) * 2019-09-05 2021-03-05 四川农业大学 Bait block quality improver and preparation method thereof
CN114507295A (en) * 2021-12-22 2022-05-17 云南猫哆哩集团食品有限责任公司 Preparation method of tamarind seed polysaccharide glue solution

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