JP2014043406A - Agent having blood pressure elevation-suppressing action from post-fermented tea, and drink or food product and medicament comprising the same - Google Patents

Agent having blood pressure elevation-suppressing action from post-fermented tea, and drink or food product and medicament comprising the same Download PDF

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JP2014043406A
JP2014043406A JP2012185874A JP2012185874A JP2014043406A JP 2014043406 A JP2014043406 A JP 2014043406A JP 2012185874 A JP2012185874 A JP 2012185874A JP 2012185874 A JP2012185874 A JP 2012185874A JP 2014043406 A JP2014043406 A JP 2014043406A
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tea
blood pressure
ethyl acetate
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smooth muscle
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Akio Nakamura
彰男 中村
Shinji Yoshiyama
伸司 吉山
Natsume Tanaka
夏女 田中
Ritsuko Kawarada
律子 河原田
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Gunma University NUC
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Abstract

PROBLEM TO BE SOLVED: To provide an agent allowing inhibition of angiotensin-converting enzyme action for indirect relaxation of vascular smooth muscle, having an action of suppressing blood pressure elevation by direct action on the vascular smooth muscle for relaxation of the vascular smooth muscle, permitting daily administration due to its safety, and being capable of continuously suppressing blood pressure elevation.SOLUTION: A blood pressure elevation-suppressing agent has, as an active ingredient, an ethyl acetate extract of a substance obtained by extracting a post-fermented tea with hot water.

Description

本発明は、血圧上昇抑制作用を有する剤並びに当該剤を含有する飲食品及び医薬に関するものである。   The present invention relates to an agent having an antihypertensive action, a food and drink containing the agent, and a medicine.

近年、我が国は深刻な高齢化社会を迎えており、また、食生活の欧米化などによる高血圧性疾患を伴う生活習慣病患者が増加する傾向にある。高血圧患者は、また治療を開始していない人を含めると、およそ4000万人に上ると推定されている(高血圧治療ガイドライン2009、日本高血圧学会高血圧治療ガイドライン作成委員会編、日本高血圧学会発行)。
現在、高血圧の治療薬として、利尿剤、カルシウム拮抗剤、交感神経抑制剤、血管拡張剤及びアンギオテンシン変換酵素阻害剤といった降圧剤が広く用いられているが、腎機能悪化、血管浮腫、糖・脂質代謝への悪影響及び心臓への負担といった副作用を起こすことが少なからず報告されている。
一方、健康志向、そして安全志向の高まりとともに、健康によい影響を与えるとされる食品や特定保健用食品(いわゆる「特保」)が、注目を集めるようになってきた。古くから飲用されるお茶には、さまざまな有効成分が含まれているとされ、血管内皮由来の血管弛緩因子(NO及びEDHF等)を活性化することにより血管平滑筋を弛緩させて血圧を低下させる杜仲茶配糖体、血圧上昇に関わるアンギオテンシン変換酵素を阻害するペプチド類、及び血圧低下作用を示すアミノ酪酸(GABA)といったお茶由来の成分が血圧の低下に効果的であることが認められている。また、お茶はこの他にも体脂肪低下や動脈硬化予防など多様な効果・効能を持つことも知られている。
例えば、発酵した茶の利用として、特許文献1には、茶を好気的発酵した後に嫌気的発酵して得られたものの水系溶媒抽出物を有効成分とする酸化抑制及びコレステロール抑制組成物が開示されている。
また、特許文献2には、発酵茶を水性液体で抽出し、得られた抽出物をさらに有機溶媒で抽出して得た発酵茶抽出残渣を有効成分とする糖尿病用組成物が開示されている。
しかしながら、後発酵茶を熱水で抽出したものの有機溶媒抽出物を有効成分とする血圧上昇抑制のための剤及び当該剤を含有する飲食品や医薬については知られていなかった。
In recent years, Japan is facing a serious aging society, and there is a tendency to increase the number of patients with lifestyle-related diseases associated with hypertensive diseases due to westernization of dietary habits. It is estimated that the number of hypertensive patients, including those who have not started treatment, is approximately 40 million (edited by the Japanese Society for Hypertension 2009, edited by the Japanese Society of Hypertension, Hypertension Treatment Guidelines, published by the Japanese Society of Hypertension).
Currently, antihypertensive drugs such as diuretics, calcium antagonists, sympathetic nerve inhibitors, vasodilators and angiotensin converting enzyme inhibitors are widely used as antihypertensive drugs, but renal function deterioration, angioedema, sugars and lipids Adverse effects such as adverse metabolic effects and burden on the heart have been reported.
On the other hand, with an increase in health-oriented and safety-oriented, foods that are said to have a positive effect on health and foods for specified health use (so-called “special insurance”) have attracted attention. Teas that have been drunk for a long time are said to contain various active ingredients. By activating vascular relaxation factors (NO, EDHF, etc.) derived from vascular endothelium, blood vessel smooth muscles are relaxed to lower blood pressure. It has been recognized that tea-derived components such as tochu tea glycosides, peptides that inhibit angiotensin-converting enzymes involved in increasing blood pressure, and aminobutyric acid (GABA) that exhibit blood pressure lowering effects are effective in lowering blood pressure. Yes. In addition to this, tea is also known to have various effects such as body fat reduction and arteriosclerosis prevention.
For example, as a utilization of fermented tea, Patent Document 1 discloses an oxidation-inhibiting and cholesterol-inhibiting composition comprising, as an active ingredient, an aqueous solvent extract obtained by anaerobic fermentation after aerobic fermentation of tea. Has been.
Patent Document 2 discloses a composition for diabetes containing fermented tea extract residue obtained by extracting fermented tea with an aqueous liquid and further extracting the obtained extract with an organic solvent as an active ingredient. .
However, an agent for suppressing blood pressure elevation using an organic solvent extract as an active ingredient of post-fermented tea extracted with hot water, and a food and drink or a medicine containing the agent have not been known.

特開2007−314508号公報JP 2007-314508 A 特開2012−31078号公報JP 2012-31078 A

上述したように、高血圧治療に広く用いられている降圧剤には、腎機能悪化、血管浮腫、血糖・代謝脂質への悪影響及び心臓への負担といった副作用の報告が少なからずされていることから、副作用を引き起こすことのない安全な、血圧上昇抑制作用を有する組成物が求められている。   As mentioned above, the antihypertensive agent widely used in the treatment of hypertension has many reports of adverse effects such as kidney function deterioration, angioedema, adverse effects on blood glucose and metabolic lipids and burden on the heart, There is a need for a safe composition that does not cause side effects and has an antihypertensive action.

すなわち、本発明の課題は、アンギオテンシン変換酵素(ACE)作用阻害のような、血管内皮細胞又はそれに由来する他の因子を介した間接的な血管平滑筋の弛緩作用に加え、血管平滑筋に直接働きかけて血管平滑筋を弛緩させる作用を有し、副作用を引き起こす
ことのない安全な、血圧上昇抑制作用を有する剤並びに当該剤を含む飲食品及び医薬を提供することにある。
That is, the object of the present invention is to directly relax the vascular smooth muscle via vascular endothelial cells or other factors derived therefrom, such as inhibition of angiotensin converting enzyme (ACE) action. An object of the present invention is to provide a safe agent that has an action of relaxing vascular smooth muscle by working and has no side effects, and a food and drink and a medicine containing the agent.

本発明者らは、上記課題を解決すべく上記特性を有する物質を探索したところ、後発酵茶を熱水で抽出したものの酢酸エチル抽出物が上記特性を示すことを見出した。後発酵茶とは、茶(Camellia sinensis)を殺青し、微生物を用いた後発酵工程を経て得られた茶
のことを言い、例えば、生の茶葉を炒るあるいは蒸した後に好気的に発酵させたプーアル茶や、生の茶を蒸した後に好気的に発酵させ、その後さらに嫌気的に発酵させた碁石茶などが挙げられる。
他にも日本古来の好気発酵のバタバタ茶(富山)、碁石茶と同じ製法の天狗黒茶(愛媛)、嫌気発酵のみの阿波番茶(徳島)などが伝承されて残っている。
The present inventors searched for a substance having the above characteristics to solve the above problems, and found that an ethyl acetate extract obtained by extracting post-fermented tea with hot water exhibits the above characteristics. Post-fermented tea refers to tea obtained by killing tea (Camellia sinensis) and undergoing a post-fermentation process using microorganisms. For example, raw tea leaves are roasted or steamed and then aerobically fermented. Pu-eru tea, and ganishi tea that has been aerated aerobically after steaming raw tea and then anaerobically fermented.
In addition, traditional Japanese aerobic fermented batterbatter tea (Toyama), Tengu black tea (Ehime), which has the same manufacturing method as Soseki tea, and Awabancha (Tokushima), which has only anaerobic fermentation, have been passed down.

すなわち、本発明の血圧上昇抑制のための剤は、後発酵茶を熱水により抽出したものの酢酸エチル抽出物を有効成分とする。   That is, the agent for suppressing blood pressure elevation according to the present invention contains, as an active ingredient, an ethyl acetate extract obtained by extracting post-fermented tea with hot water.

抽出に用いる有機溶媒として、酢酸エチルを用いることにより、有効成分をより多く抽出することができ、血圧上昇抑制効果がより高くなる。   By using ethyl acetate as the organic solvent used for extraction, more active ingredients can be extracted, and the blood pressure increase suppressing effect is further enhanced.

また、本発明の飲食品及び医薬は、上記血圧上昇抑制剤を含有するものである。   Moreover, the food / beverage products and medicine of this invention contain the said blood pressure rise inhibitor.

本発明の剤は、蒸した後に、好気的に発酵させた茶、又は、好気的に発酵させたのちに嫌気的に発酵させた茶の抽出物であるため、安全性に優れ、毎日の摂取も可能である。その上、ACEの作用を阻害して間接的に血管平滑筋を弛緩させるだけではなく、血管平滑筋に直接的に作用して血管平滑筋を弛緩させることができるため、優れた血圧上昇抑制効果を示し、脳卒中や脳梗塞といった脳血管障害、心不全や心筋梗塞といった心臓疾患、及び、腎硬化症や腎不全といった腎臓疾患などの予防、進行抑制及び治療などに有効である。従って、本発明の剤、飲食品及び医薬は、近年の健康志向に適合するものとして極めて有効なものである。   The agent of the present invention is an extract of tea that has been aerobically fermented after steaming, or tea that has been aerobically fermented and then anaerobically fermented. Ingestion is also possible. In addition, it not only inhibits the action of ACE and indirectly relaxes vascular smooth muscle, but also acts directly on vascular smooth muscle to relax vascular smooth muscle, so it has an excellent blood pressure rise inhibiting effect It is effective for prevention, progression inhibition and treatment of cerebrovascular disorders such as stroke and cerebral infarction, heart diseases such as heart failure and myocardial infarction, and kidney diseases such as nephrosclerosis and renal failure. Therefore, the agent, food / beverage product, and medicine of the present invention are extremely effective for adapting to the recent health orientation.

張力測定実験のチャート模式図を示す。The chart schematic diagram of a tension measurement experiment is shown. ラット大腿動脈の内皮除去血管平滑筋における、プーアル茶及び碁石茶の各有機溶媒抽出物の血管平滑筋弛緩作用を測定した結果を示す。The result of having measured the vascular smooth muscle relaxation effect | action of each organic solvent extract of Puer tea and garnet tea in the endothelium removal vascular smooth muscle of a rat femoral artery is shown. ラット大腿動脈の内皮除去血管平滑筋標本における、プーアル茶及び碁石茶の酢酸エチル分画エキス、及びGABA含有緑茶を添加した張力測定実験の代表チャートを示す。The representative chart of the tension | tensile_strength measurement experiment which added the ethyl acetate fraction extract of puer tea and garnet tea, and GABA containing green tea in the endothelium removal blood-vessel smooth muscle sample of a rat femoral artery is shown. ラット大腿動脈の内皮除去血管平滑筋標本における、塩酸ヒドララジン、GABA含有緑茶及び碁石茶の酢酸エチル分画エキスの血管平滑筋弛緩作用を比較した結果を示す。The result of comparing the vascular smooth muscle relaxation effect of ethyl acetate fraction extracts of hydralazine hydrochloride, GABA-containing green tea, and meteorite tea in the endothelium-removed vascular smooth muscle preparation of rat femoral artery is shown. 非観血式血圧測定による雄性高血圧自然発症ラット(SHR)に対する、プーアル茶及び碁石茶の酢酸エチル分画エキスの連続投与による血圧降下作用を示す。The blood pressure lowering effect by the continuous administration of the ethyl acetate fraction extract of Pu'er tea and Soseki tea to the male hypertensive rat (SHR) by noninvasive blood pressure measurement is shown. 非観血式血圧測定による雄性高血圧自然発症ラット(SHR)に対する、プーアル茶及び碁石茶の酢酸エチル分画エキスの単回投与による経時的な血圧降下作用を示す。The blood pressure-lowering effect | action with time by the single administration of the ethyl acetate fraction extract of Pu'er tea and agate stone tea with respect to the male hypertensive rat (SHR) by noninvasive blood pressure measurement is shown. 観血式血圧測定による正常ウィスターラットに対する、碁石茶酢酸エチル分画エキスの血圧降下作用を示す。The blood pressure lowering effect of Soseki tea ethyl acetate fraction extract on normal Wistar rats by open blood pressure measurement is shown. ラット大腿動脈の内皮除去血管平滑筋標本における、様々な後発酵茶酢酸エチル分画エキスの血管平滑筋弛緩作用を比較した結果を示す。The result of having compared the vascular smooth muscle relaxation effect of various post-fermented tea ethyl acetate fraction extracts in the endothelium removal vascular smooth muscle preparation of a rat femoral artery is shown. 様々な後発酵茶酢酸エチル分画エキスのACE作用阻害能を比較した結果を示す。The result of having compared the ACE action inhibitory ability of various post-fermented tea ethyl acetate fraction extracts is shown.

本発明の血圧上昇抑制剤は、後発酵茶を熱水で抽出したものの酢酸エチル抽出物を有効成分とする。
以下、本発明の剤の製造方法について説明する。
The antihypertensive agent of the present invention comprises, as an active ingredient, an ethyl acetate extract obtained by extracting post-fermented tea with hot water.
Hereinafter, the manufacturing method of the agent of this invention is demonstrated.

本発明の組成物の原料となる茶の種類等は特に制限されず、一般的なものを使用することができる。例えば、茶としては主に低木のもの(学名:Camellia sinensis)と高木の
もの(学名:C. sinensis var. assamica)があるが、何れを使用してもよい。中でも、
日本で一般的な低木の茶を特に制限なく用いることができる。
The kind etc. of the tea used as the raw material of the composition of this invention are not restrict | limited, A general thing can be used. For example, tea mainly includes shrubs (scientific name: Camellia sinensis) and teas (scientific name: C. sinensis var. Assamica), either of which may be used. Above all,
Shrub tea common in Japan can be used without particular limitation.

本発明では、茶を蒸した(蒸煮)後に一段階又は二段階で発酵する。蒸煮は、葉のみで行ってもよいが枝ごとに行ってもよい。蒸煮後には葉を枝からとり易くなるため、採取直後に分離するよりも手間がかからないためである。   In the present invention, the tea is steamed (steamed) and then fermented in one or two stages. Steaming may be performed only with leaves, but may be performed for each branch. This is because it becomes easier to remove the leaves from the branches after cooking, and it takes less time than separating them immediately after collection.

蒸煮は一般的な条件に従って行えばよく、茶の層へ水蒸気又は湯気を通じればよい。例えば、蒸し器など、底面から水蒸気を通じることができる容器に茶葉あるいは茶葉と枝を密に詰め、その下方で水を沸騰させ、当該容器へ水蒸気又は湯気を通じることにより行われる。蒸煮の時間は、続いてそのまま発酵させることができる程度とすればよいが、例えば、水が沸騰してから1〜4時間とすることができ、好ましくは2〜3時間とする。実際には、茶葉の状態や蒸汁の色等を確認しつつ、時間を調節する。   Steaming may be performed according to general conditions, and steam or steam may be passed through the tea layer. For example, it is carried out by closely packing tea leaves or tea leaves and branches into a container such as a steamer that can pass water vapor from the bottom, boiling water underneath, and passing water vapor or steam through the container. The steaming time may be set to such an extent that it can be subsequently fermented as it is, but for example, it can be 1 to 4 hours, preferably 2 to 3 hours, after the water boils. In practice, the time is adjusted while checking the state of the tea leaves and the color of the juice.

なお、蒸煮した場合には、その蒸汁にも有効成分が含まれていると考えられるため、これを発酵工程で必要な水分として用いてもよい。   In addition, since it is thought that the active ingredient is also contained in the steamed steam, you may use this as a water | moisture content required in a fermentation process.

上記前処理を行った茶は、続いて発酵処理を行う。
一段階目の発酵処理としては好気的発酵を行う。具体的には、茶葉を高湿下で静置することにより行われる。例えば、茶葉を容器に入れ、湿度を保つために水や蒸汁を散布した上でカバーをかけ、常温で5〜10日間程度静置することにより行われる。その間、適度な温度や湿度を保つことが必要であり、茶葉の状態等を確認しつつ、発酵条件を適宜調節する。また、好気的発酵を行う際に、手で押さえたり、又は、足で踏むなどして適度な圧力をかけてもよい。さらに、好気的発酵に適する好気的細菌又は真菌を添加してもよいが、これらを添加しない場合においても、茶葉自身の酸化酵素や自然に存在する細菌等により発酵は進行する。
The tea that has been subjected to the pretreatment is then subjected to a fermentation treatment.
Aerobic fermentation is performed as the first stage fermentation process. Specifically, it is carried out by leaving tea leaves under high humidity. For example, it is carried out by putting tea leaves in a container, spraying water or steam to maintain the humidity, applying a cover, and allowing to stand at room temperature for about 5 to 10 days. Meanwhile, it is necessary to maintain an appropriate temperature and humidity, and the fermentation conditions are appropriately adjusted while confirming the state of the tea leaves. In addition, when aerobic fermentation is performed, an appropriate pressure may be applied by pressing with hands or by stepping with feet. Further, aerobic bacteria or fungi suitable for aerobic fermentation may be added, but even when these are not added, the fermentation proceeds by the tea leaf oxidase, naturally occurring bacteria, and the like.

このように、茶葉を一段階の好気的発酵を行うことで製造される後発酵茶としては、プーアル茶を挙げることができる。   Thus, Pu'er tea can be mentioned as post-fermented tea produced by performing one-stage aerobic fermentation of tea leaves.

続いて、必要に応じて二段階目の発酵処理として嫌気的発酵を行う。嫌気的発酵の条件も特に制限されず、公知の方法を用いて行うことができる。例えば、伝統的には、好気的発酵させた茶葉を、圧力をかけながら容器へ密に詰めていき、最終的には容器に蓋をした上でさらに圧力をかけ、外気との接触を遮断することにより嫌気的発酵を行う。このとき、上記蒸汁を散布したり、または茶葉が浸かる程度に添加してしてもよい。さらに、嫌気的発酵を行うための細菌等を添加してもよいが、添加せずに自然に嫌気的発酵を進行させてもよい。   Subsequently, anaerobic fermentation is performed as a second stage fermentation process as necessary. The conditions for anaerobic fermentation are not particularly limited, and can be performed using a known method. For example, traditionally, aerobically fermented tea leaves are packed tightly into a container while applying pressure, and finally the container is covered with pressure to block contact with outside air. To do anaerobic fermentation. At this time, the above-mentioned steam may be sprayed or added to such an extent that the tea leaves are immersed. Furthermore, although bacteria for performing anaerobic fermentation may be added, anaerobic fermentation may be allowed to proceed without being added.

嫌気的発酵の後は、茶葉は圧力のために一塊になっているため、適度な大きさに切断することが好ましい。続いて行う茶葉の乾燥が円滑に進むからである。   After anaerobic fermentation, the tea leaves are agglomerated due to pressure, so it is preferable to cut them to a suitable size. This is because the subsequent drying of the tea leaves proceeds smoothly.

茶葉の乾燥は機械的に行ってもよいが、天日干しでも行うこともできる。また、乾燥の程度も特に制限されるものではないが、少なくとも保管時に腐敗等しない程度には乾燥させる必要がある。   Tea leaves may be dried mechanically, but can also be dried in the sun. Also, the degree of drying is not particularly limited, but it is necessary to dry to the extent that it does not rot at least during storage.

このように、好気的発酵を行った後に嫌気的発酵を行うことで製造される後発酵茶としては、高知県で伝統的に製造されている碁石茶を挙げることができる。碁石茶については、これまでにその抗酸化活性が研究されており、その他の機能性の解明や健康増進作用についてさらなる研究が行われている。   Thus, as a post-fermented tea manufactured by performing anaerobic fermentation after performing an aerobic fermentation, the garnet tea traditionally manufactured in Kochi Prefecture can be mentioned. Soseki tea has been studied for its antioxidant activity so far, and further research has been conducted on elucidation of other functions and health promotion effects.

本発明の組成物の一態様では、上記のとおり発酵した茶葉を熱水により抽出し、得られた熱水抽出物をさらに酢酸エチルで抽出したものを有効成分とする。   In one aspect of the composition of the present invention, the tea leaves fermented as described above are extracted with hot water, and the obtained hot water extract is further extracted with ethyl acetate as an active ingredient.

熱水による抽出方法としては、例えば、500mLのDDWに対して発酵工程を経た茶葉を50g加え、100〜120℃の熱水で1分間〜1時間程度抽出する。かかる抽出中、混合物は撹拌しても静置してもよく、また、継続的に加熱したり、加熱還流してもよい。   As an extraction method using hot water, for example, 50 g of tea leaves that have undergone the fermentation process are added to 500 mL of DDW, and extracted with hot water at 100 to 120 ° C. for about 1 minute to 1 hour. During such extraction, the mixture may be stirred or allowed to stand, or may be continuously heated or heated to reflux.

酢酸エチルによる抽出方法も特に限定されず、常法により行うことができる。例えば、上記熱水抽出により得られた抽出物に酢酸エチルを加えて撹拌しながら酢酸エチル相と水相に分離して酢酸エチル抽出物を得る。なお、酢酸エチル抽出を行う前に、熱水抽出物についてヘキサン処理を行い、ヘキサン抽出画分を除去してから酢酸エチル抽出を行ってもよい。   The extraction method using ethyl acetate is not particularly limited, and can be performed by a conventional method. For example, ethyl acetate is added to the extract obtained by the hot water extraction, and the mixture is separated into an ethyl acetate phase and an aqueous phase with stirring to obtain an ethyl acetate extract. Before performing the ethyl acetate extraction, the hot water extract may be treated with hexane to remove the hexane extraction fraction and then the ethyl acetate extraction.

得られた酢酸エチル抽出物については、酢酸エチルを除去する操作を行うことが望ましい。そして、血圧上昇抑制作用を損なわない限り、さらなる抽出・精製を行ってもよい。   The obtained ethyl acetate extract is preferably subjected to an operation for removing ethyl acetate. Further, further extraction / purification may be performed as long as the blood pressure increase suppressing action is not impaired.

また、抽出物は、そのまま服用してもよいが、凍結乾燥等した後に服用してもよい。   The extract may be taken as it is, but may be taken after lyophilization or the like.

本発明の剤は、血圧上昇抑制作用を示すことから、高血圧、並びに、高血圧に起因して引き起こされる合併症、例えば、脳卒中や脳梗塞といった脳血管障害、心不全や心筋梗塞といった心臓疾患、及び、腎硬化症や腎不全といった腎臓疾患などの予防、進行抑制及び治療などに有効である。   Since the agent of the present invention exhibits an antihypertensive action, hypertension and complications caused by hypertension, for example, cerebrovascular disorders such as stroke and cerebral infarction, heart diseases such as heart failure and myocardial infarction, and It is effective for prevention, progression inhibition and treatment of kidney diseases such as nephrosclerosis and renal failure.

本発明の剤は、飲食品(健康食品及び機能性食品など)に配合することもできる。本発明の剤は、茶を一段発酵又は二段発酵したものから得られる抽出物を含有するものであり、安全で副作用もないと考えられるため、毎日の摂取も可能だからである。飲食品として使用する場合には、通常の飲食品(茶、ジュース、ヨーグルトなど)に、抽出物を添加してもよい。さらに、賦形剤、増量剤、結合剤、増粘剤(安定化剤)、乳化剤、着色料、香料、食品添加物、調味料、栄養補助剤(ビタミン類、カルシウム類、プロテイン、キトサン及びレシチンなど)及び甘味料などを添加してもよい。   The agent of this invention can also be mix | blended with food-drinks (health food, functional food, etc.). This is because the agent of the present invention contains an extract obtained from one-stage fermentation or two-stage fermentation of tea and is considered safe and free from side effects. When used as a food or drink, the extract may be added to a normal food or drink (tea, juice, yogurt, etc.). In addition, excipients, extenders, binders, thickeners (stabilizers), emulsifiers, colorants, fragrances, food additives, seasonings, nutritional supplements (vitamins, calciums, proteins, chitosan and lecithin Etc.) and sweeteners may be added.

また、飲食品に含有させる酢酸エチル抽出物の量は、0.001〜5重量%であることが好ましく、0.01〜1重量%であることがより好ましい。   Moreover, it is preferable that it is 0.001 to 5 weight%, and, as for the quantity of the ethyl acetate extract contained in food-drinks, it is more preferable that it is 0.01 to 1 weight%.

また、本発明の剤は、血圧上昇を抑制するための医薬として使用することもできる。医薬として使用する場合には、上記酢酸エチル抽出物をそのまま用いてもよいが、製剤学的に許容される製剤担体と組み合わせて用いてもよい。製剤学的に許容される製剤担体としては、賦形剤、結合剤、崩壊剤、滑沢剤、安定剤、矯味矯臭剤、希釈剤、界面活性剤、注射剤用溶剤等の添加剤が挙げられる。また、本発明の効果を損なわない限り、本発明の剤
と、血圧上昇を抑制するための他の剤等とを併用してもよい。
Moreover, the agent of this invention can also be used as a pharmaceutical for suppressing a blood pressure rise. When used as a medicine, the ethyl acetate extract may be used as it is, or may be used in combination with a pharmaceutically acceptable pharmaceutical carrier. Pharmaceutically acceptable pharmaceutical carriers include excipients, binders, disintegrants, lubricants, stabilizers, flavoring agents, diluents, surfactants, solvents for injections, etc. It is done. Moreover, unless the effect of this invention is impaired, you may use together the agent of this invention, the other agent for suppressing a blood pressure rise, etc. together.

医薬として使用する場合、投与量は血圧上昇の抑制に有効な量である限り特に制限されず、過剰の摂取や体質的な問題等から異常が生じない程度の量とすればよいが、具体的な投与量としては、茶葉1gより得られた酢酸エチル抽出物の量を1として、0.00001〜1/kg体重/日であることが好ましく、0.0001〜0.5/kg体重/日であることがより好ましく、0.001〜0.1/kg体重/日であることが特に好ましい。1日1回又は複数回に分けて摂取することができる。   When used as a medicine, the dosage is not particularly limited as long as it is an effective amount for suppressing an increase in blood pressure, and may be an amount that does not cause abnormalities due to excessive intake or constitutional problems. The preferred dosage is 0.00001 to 1 / kg body weight / day, with the amount of ethyl acetate extract obtained from 1 g of tea leaves being 1, preferably 0.0001 to 0.5 / kg body weight / day. It is more preferable that it is 0.001-0.1 / kg body weight / day. Can be taken once a day or divided into multiple doses.

以下、実施例を挙げて本発明をより具体的に説明するが、本発明は下記実施例により制限されるものではなく、本発明の趣旨に適合し得る範囲内で適宜変更を加えて実施することも可能であり、それらはいずれも本発明の技術的範囲内に含まれる。   Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples, and may be implemented with appropriate modifications within a range that can meet the gist of the present invention. All of which are within the scope of the present invention.

[製造例1]本発明の抽出物の製造
抽出物原料である後発酵茶の酢酸エチルエキスは、以下の通り製造した。
50gの碁石茶茶葉を500mLのDDWに加え、120℃で20分間加熱し、茶葉をろ過して抽出液を得た。得られた抽出液に等量のヘキサンを加え、室温で3時間撹拌した。分液ロートを用いてヘキサン相と水相を分離し、水相に等量の酢酸エチルを加えて室温で12時間撹拌した。分液ロートを用いて酢酸エチル相と水相を分離し、酢酸エチル相をエバポレーターで完全に乾燥させた。酢酸エチル相の乾燥重量を測定後、10mg/mlとなるようにDDWに溶解して酢酸エチルエキスとした。
また、プーアル茶茶葉についても同様の条件及び工程で酢酸エチルエキスを得た。
[Production Example 1] Production of extract of the present invention An ethyl acetate extract of post-fermented tea as an extract raw material was produced as follows.
50 g of Soseki tea leaves were added to 500 mL of DDW, heated at 120 ° C. for 20 minutes, and the tea leaves were filtered to obtain an extract. An equal amount of hexane was added to the resulting extract and stirred at room temperature for 3 hours. A hexane phase and an aqueous phase were separated using a separatory funnel, an equal amount of ethyl acetate was added to the aqueous phase, and the mixture was stirred at room temperature for 12 hours. The ethyl acetate phase and the aqueous phase were separated using a separatory funnel, and the ethyl acetate phase was completely dried by an evaporator. After measuring the dry weight of the ethyl acetate phase, it was dissolved in DDW so as to be 10 mg / ml to obtain an ethyl acetate extract.
Moreover, the ethyl acetate extract was obtained also about puer tea tea leaves on the same conditions and processes.

[試験例1]プーアル茶及び碁石茶の各溶媒分画エキスの血管平滑筋弛緩作用の測定
ラット大腿動脈の内皮細胞を除去した血管平滑筋標本を用いて、血管平滑筋の微細張力を測定する飯塚らの方法(Iizuka et al., InsP3, but not novel Ca2+ releasers, contributes to agonist-initiated contraction in rabbit airway smooth muscle, J. Physiol., 1998 Sep 15; 511(Pt 3): 915-33)により、プーアル茶(一段発酵茶)及び碁石茶(二段発酵茶)の各溶媒分画エキスの血管平滑筋弛緩作用の測定を行った。
まず、血管平滑筋組織としてラット大腿動脈平滑筋を使用した。摘出した大腿動脈を短冊状に切り出し、血管内皮細胞と結合組織を取り除き張力測定装置にセットした。血管平滑筋組織の弛緩には正常細胞外液(NES)を用いた。また、収縮には155mMのカリウムを含む高カリウム細胞外液(KES)を用いた。以下の手順で血管平滑筋組織を弛緩・収縮させ、図1に示すチャートの1〜4の各時点における張力を測定した。
(1)平滑筋組織の張力を安定させるために、細胞外液をKESに交換し3分間収縮させ、その後NESに交換し弛緩させた。この操作を3回繰り返して完全に弛緩させた。この時点の張力を「1.基準」とする。
(2)細胞外液をKESに交換し、平滑筋の持続性の収縮が安定したら、細胞外液に各溶媒分画エキス(10mg/ml)を4μL又は12μL添加して張力の変化を観察した。持続性の収縮が安定した時点の張力を「2.前収縮」とし、各溶媒分画エキス添加後の張力を「3.弛緩」とする。
(3)細胞外液を各溶媒分画エキスが添加されていない別のKESに交換し、張力の変化を観察した。この時点での張力を「4.後収縮」とする。
(4)各溶媒分画エキスについて(2)及び(3)を行い、張力の変化を観察した。
平滑筋組織の張力変化を表すT値は以下の計算式に基づき計算した。

T値=([3.弛緩]−[1.基準値])/{([2.前収縮]+[4.後収縮])/2−[1.基準値]}

T値が1以上の場合には収縮効果があることを意味し、1以下の場合には弛緩効果があることを意味する。
結果を図2に示す。
[Test Example 1] Measurement of vascular smooth muscle relaxant action of each solvent fraction extract of Puer tea and Meteorite tea Using a vascular smooth muscle specimen from which the endothelial cells of rat femoral artery were removed, the fine tension of vascular smooth muscle was measured. Iizuka et al. (Iizuka et al., InsP3, but not novel Ca 2+ releasers, contributes to agonist-initiated contraction in rabbit airway smooth muscle, J. Physiol., 1998 Sep 15; 511 (Pt 3): 915-33 ), The vascular smooth muscle relaxation action of each solvent fraction extract of Puer tea (one-stage fermented tea) and Goseki tea (two-stage fermented tea) was measured.
First, rat femoral artery smooth muscle was used as vascular smooth muscle tissue. The excised femoral artery was cut into strips, vascular endothelial cells and connective tissue were removed, and the femoral artery was set in a tension measuring device. Normal extracellular fluid (NES) was used to relax vascular smooth muscle tissue. In addition, high potassium extracellular fluid (KES) containing 155 mM potassium was used for contraction. The vascular smooth muscle tissue was relaxed and contracted by the following procedure, and the tension at each time point 1 to 4 in the chart shown in FIG. 1 was measured.
(1) In order to stabilize the tension of the smooth muscle tissue, the extracellular fluid was changed to KES and contracted for 3 minutes, and then changed to NES and relaxed. This operation was repeated three times for complete relaxation. The tension at this point is defined as “1. Reference”.
(2) When the extracellular fluid was replaced with KES and the sustained contraction of smooth muscle was stabilized, 4 μL or 12 μL of each solvent fraction extract (10 mg / ml) was added to the extracellular fluid, and the change in tension was observed. . The tension at the time when the sustained shrinkage is stabilized is defined as “2. Pre-shrinkage”, and the tension after addition of each solvent fraction extract is defined as “3. Relaxation”.
(3) The extracellular fluid was replaced with another KES to which each solvent fraction extract was not added, and the change in tension was observed. The tension at this point is referred to as “4.
(4) (2) and (3) were performed on each solvent fraction extract, and the change in tension was observed.
The T value representing the change in the tension of the smooth muscle tissue was calculated based on the following formula.

T value = ([3. Relaxation] − [1. Reference value]) / {([2. Pre-contraction] + [4. Post-contraction]) / 2− [1. Reference value]}

When the T value is 1 or more, it means that there is a contraction effect, and when it is 1 or less, it means that there is a relaxation effect.
The results are shown in FIG.

図2から明らかなように、本発明の抽出物は、他の茶葉又は他の溶媒を用いて得た抽出物に比して優れた血管平滑筋弛緩作用を有していることが明らかとなった。特に、抽出溶媒として酢酸エチルを用いて得た抽出物(酢酸エチル分画エキス)は、他の溶媒を用いて得た抽出物に比して特に優れた血管平滑筋弛緩作用を有していることが明らかとなった。   As is apparent from FIG. 2, the extract of the present invention has an excellent vascular smooth muscle relaxing action as compared with extracts obtained using other tea leaves or other solvents. It was. In particular, an extract obtained by using ethyl acetate as an extraction solvent (ethyl acetate fraction extract) has a particularly excellent vascular smooth muscle relaxation action compared to extracts obtained using other solvents. It became clear.

[試験例2]プーアル茶及び碁石茶の酢酸エチル分画エキスの血管平滑筋弛緩作用の測定
ラット大腿動脈の内皮除去血管平滑筋を用いて、プーアル茶の酢酸エチル分画エキス、碁石茶の酢酸エチル分画エキス及びGABA含有緑茶(製品名:ナチュラルケア、大正製薬)を累積的に添加した場合の血管平滑筋弛緩作用を飯塚らの方法により測定した具体的には、血管内皮を除去したラットの大腿動脈の血管平滑筋に、プーアル茶と碁石茶の酢酸エチル分画エキス(10mg/ml)をそれぞれ4μlずつ5分おきに累積添加した。一方で、GABA含有緑茶(ナチュラルケア)を4μlずつ加算投与した。結果を図3に示す。
[Test Example 2] Measurement of vascular smooth muscle relaxing action of ethyl acetate fraction extract of Pu'er tea and meteorite tea Using the endothelium-removed vascular smooth muscle of rat femoral artery, ethyl acetate fraction extract of Pu'er tea, acetic acid of meteorite tea Specifically, the vascular smooth muscle relaxing action when accumulating ethyl fraction extract and GABA-containing green tea (product name: Natural Care, Taisho Pharmaceutical Co., Ltd.) was measured by the method of Iizuka et al. To the vascular smooth muscle of the femoral artery, 4 μl each of puer tea and meteorite tea ethyl acetate extract (10 mg / ml) was added cumulatively every 5 minutes. Meanwhile, 4 μl of GABA-containing green tea (natural care) was added and administered. The results are shown in FIG.

図3から明らかなように、プーアル茶と碁石茶の酢酸エチル分画エキスを投与した場合には、それぞれ濃度依存的に血管平滑筋は弛緩するが、GABA含有緑茶を投与した場合には血管平滑筋の弛緩は見られなかった。この結果から、プーアル茶と碁石茶の酢酸エチル分画エキスは、血管平滑筋に直接作用してその弛緩作用を示すと考えられる。   As can be seen from FIG. 3, vascular smooth muscle relaxes in a concentration-dependent manner when puer tea and garnet tea ethyl acetate fraction extracts are administered, but vascular smoothness occurs when GABA-containing green tea is administered. There was no muscle relaxation. From these results, it is considered that the ethyl acetate fraction extract of Pu'er tea and Soseki tea acts directly on the vascular smooth muscle and exhibits its relaxing action.

[試験例3]塩酸ヒドララジンとの血管平滑筋弛緩作用の比較
末梢血管に直接作用する降圧剤である塩酸ヒドララジンと碁石茶の酢酸エチル分画エキスの血管平滑筋弛緩作用を試験例1と同様の手順で測定し、比較を行った。塩酸ヒドララジンは、作用機序は不明であるが、臨床において動脈の平滑筋を弛緩することにより、末梢の血管を拡張させ、血圧を下げる降圧剤として知られている。
[Test Example 3] Comparison of vascular smooth muscle relaxing action with hydralazine hydrochloride The vascular smooth muscle relaxing action of hydralazine hydrochloride, which is an antihypertensive agent acting directly on peripheral blood vessels, and ethyl acetate fraction extract of Meishiishi tea is the same as in Test Example 1. Measurements were made according to the procedure and compared. Although the mechanism of action of hydralazine hydrochloride is unknown, it is known as a hypotensive agent that lowers blood pressure by dilating peripheral blood vessels by relaxing arterial smooth muscle in the clinic.

図4から明らかなように、本発明の碁石茶の酢酸エチル分画エキスは、塩酸ヒドララジン及びGABA含有緑茶(製品名:ナチュラルケア、大正製薬)に比して優れた血管平滑筋弛緩作用を有していることが明らかとなった。   As is apparent from FIG. 4, the ethyl acetate fraction extract of the meteorite tea of the present invention has an excellent vascular smooth muscle relaxing action compared to hydralazine hydrochloride and GABA-containing green tea (product name: Natural Care, Taisho Pharmaceutical). It became clear that

[試験例4]連続投与試験による非観血式血圧測定
動物における血圧上昇抑制作用を検証するために、雄性高血圧自然発症ラット(SHR)を用いた連続投与試験による非観血式血圧測定を行った。具体的には、試料として、プーアル茶(一段発酵茶)及び碁石茶(二段発酵茶)の酢酸エチル分画エキス、GABA含有緑茶(製品名:ナチュラルケア、大正製薬)を用い、コントロールとしてDDWを用いて、以下の方法により行った。それぞれ一群につき6匹のSHRに対し、6週齢目より胃ゾンデを用いて熱水抽出物エキス(10mg)を経口投与し、さらに13週齢目よりプーアル茶と碁石茶それぞれの酢酸エチル分画エキス、GABA含有緑茶及びDDWをそれぞれ1mgずつ経口投与した。血圧測定は、午前中に非観血式自動血圧測定装置BP−98A(株式会社Softron製)を用いて、保定温度38℃でtail-cuff法にて収縮期及び拡張期血圧を各群1匹につき3回ずつ測定した。結果を図5に示す。
[Test Example 4] Non-invasive blood pressure measurement by continuous administration test In order to verify the blood pressure increase-inhibiting action in animals, non-invasive blood pressure measurement by a continuous administration test using male hypertensive rats (SHR) was performed. It was. Specifically, the sample used was a puer tea (one-stage fermented tea) and garnet tea (two-stage fermented tea) ethyl acetate fraction extract, GABA-containing green tea (product name: Natural Care, Taisho Pharmaceutical), and DDW as a control. Was carried out by the following method. Each group of 6 SHR was orally administered with hot water extract (10 mg) using a gastric sonde from the 6th week of age, and from the 13th week of age, each of the ethyl acetate fractions of Puer tea and Soseki tea. 1 mg each of extract, GABA-containing green tea and DDW was orally administered. Blood pressure measurement was performed in the morning using a non-invasive automatic blood pressure measurement device BP-98A (manufactured by Softron Co., Ltd.) with a tail-cuff method at a holding temperature of 38 ° C. for each systolic and diastolic blood pressure per group The measurement was performed three times per time. The results are shown in FIG.

図5から明らかなように、13週齢目よりプーアル茶又は碁石茶の酢酸エチル分画エキスを投与した群において、収縮期血圧がコントロール及びGABA含有緑茶に対して有意に減少した。   As is clear from FIG. 5, systolic blood pressure was significantly decreased with respect to the control and GABA-containing green tea in the group to which the ethyl acetate fraction extract of Puer tea or Soseki tea was administered from the 13th week.

[試験例5]単回投与試験による非観血式血圧測定
動物における血圧上昇抑制作用を検証するために、雄性高血圧自然発症ラット(SHR)を用いた単回投与試験による非観血式血圧測定を行った。具体的には、試料として、プーアル茶(一段発酵茶)及び碁石茶(二段発酵茶)の酢酸エチル分画エキスを用いて、以下の方法により行った。それぞれ一群につき4匹の21週齢SHRにおいて、試料投与前の収縮期及び拡張期血圧をBP−98A血圧計(株式会社Softron製)にて各6回測定し
た。続いて、胃ゾンデによりプーアル茶と碁石茶の酢酸エチル分画エキスをそれぞれ1mgずつ経口投与し、投与後4、8、24及び28時間目の収縮期血圧を測定した。結果を図6に示す。
[Test Example 5] Non-invasive blood pressure measurement by single-dose test Non-invasive blood pressure measurement by single-dose test using spontaneously hypertensive rats (SHR) in order to verify the blood pressure increase inhibitory effect in animals Went. Specifically, using the ethyl acetate fraction extract of puer tea (one-stage fermented tea) and ganishi tea (two-stage fermented tea) as samples, the following method was used. In each group of 4 21-week-old SHR, systolic and diastolic blood pressure before sample administration were measured 6 times each with a BP-98A sphygmomanometer (manufactured by Softron Co., Ltd.). Subsequently, 1 mg each of ethyl acetate fraction extract of Pu'er tea and Soseki tea was orally administered by stomach sonde, and systolic blood pressures at 4, 8, 24 and 28 hours after the administration were measured. The results are shown in FIG.

図6から明らかなように、プーアル茶の酢酸エチル分画エキスを投与した場合には、4時間後に投与前に比べて約10mmHg血圧が低下し、さらにその後約8時間にわたり血圧低下作用が持続した。また、碁石茶の酢酸エチル分画エキスを投与した場合には、8時間後に投与前に比べて約30mmHg近く血圧が低下し、さらにその後20時間以上にわたり血圧低下作用が持続した。   As is apparent from FIG. 6, when the Puer tea ethyl acetate fraction extract was administered, the blood pressure decreased about 10 mmHg after 4 hours compared to before administration, and the blood pressure lowering effect continued for about 8 hours thereafter. . In addition, when the ethyl acetate fraction extract of Goishi tea was administered, the blood pressure decreased by about 30 mmHg after 8 hours compared to before administration, and the blood pressure lowering action continued for more than 20 hours thereafter.

[試験例6]正常ウィスターラットを用いた観血式血圧測定
正常ウィスターラットを用いた観血式血圧測定を行った。具体的には、24週齢の正常ウィスターラットをウレタン麻酔し、気道確保後、頸動脈に留置したカニューレを動物用ディスポ血圧トランスジューサに接続し、Quad Bridgeアンプを介することで、血圧変化
を電圧変化に変換した。血圧の測定及び記録はADINSTRUMENTS社のPowerLabシステムを使
用した。変換された電圧はADコンバーターPowerLab 4/25により1/100秒間隔でデジ
タルデータとしてコンピューターに記録した。記録されたデータは、水銀血圧計を用いて測定した圧力の実測値を基準としてmmHgに校正した。碁石茶の酢酸エチル分画エキス(10mg/ml)を生理食塩水にて1/1000倍希釈、1/100倍希釈、1/10倍希釈したもの、及び原液をそれぞれ30分おきに0.1 ml大腿静脈に投与し、投与
後、10分の収縮期及び拡張期血圧を測定した。測定したチャートとデータを図7に示す。
[Test Example 6] Open blood pressure measurement using normal Wistar rats Open blood pressure measurement using normal Wistar rats was performed. Specifically, a 24-week-old normal Wistar rat was anesthetized with urethane, and after securing the airway, a cannula placed in the carotid artery was connected to a disposable blood pressure transducer for animals, and the blood pressure change was changed to a voltage via a Quad Bridge amplifier. Converted to. Blood pressure was measured and recorded using the PowerLab system from ADINSTRUMENTS. The converted voltage was recorded on a computer as digital data at 1/100 second intervals by an AD converter PowerLab 4/25. The recorded data was calibrated to mmHg with reference to the actual pressure measured using a mercury sphygmomanometer. Soseki Tea's ethyl acetate fraction extract (10 mg / ml) diluted 1/1000 times, 1/100 times and 1/10 times with physiological saline, and the stock solution every 0.1 min. After administration, the systolic and diastolic blood pressure was measured for 10 minutes. The measured chart and data are shown in FIG.

図7から明らかなように、最も薄い濃度の1/1000倍希釈のエキスを投与した場合には、投与後10分で収縮期血圧が約12mmHg低下し、1/100倍希釈のエキスでは約16mmHg、1/10倍希釈のエキスでは約18mmHg低下し、エキスの濃度が高くなるに従い血圧は低下した。なお、原液を投与した場合には、1/10倍希釈のエキスを投与した場合に比してさらなる血圧の低下は観察されなかった。これは、エキスの濃度が1/100〜1/10程度で血圧低下作用が頭打ちになるためであると考えられる。   As can be seen from FIG. 7, when the extract with a dilution of 1/1000 times the lowest concentration was administered, the systolic blood pressure decreased by about 12 mmHg 10 minutes after administration, and with the extract diluted 1/100 times, about 16 mmHg. In the extract diluted 1/10, the blood pressure decreased by about 18 mmHg, and the blood pressure decreased as the extract concentration increased. In addition, when the stock solution was administered, a further decrease in blood pressure was not observed as compared with the case where the extract diluted 1/10 was administered. This is considered to be because the blood pressure lowering action reaches its peak when the concentration of the extract is about 1/100 to 1/10.

[試験例7]後発酵茶の平滑筋弛緩作用の比較
碁石茶(高知県)、天狗黒茶(愛媛県)、阿波番茶(徳島県)、バタバタ茶(富山県)及びプーアル茶の酢酸エチル分画エキスを製造例1と同様の方法で調製し、それぞれの血管平滑筋弛緩作用を試験例1と同様の手順で測定し、比較を行った。
[Test Example 7] Comparison of smooth muscle relaxant action of post-fermented tea Soseki tea (Kochi Prefecture), Tengu black tea (Ehime Prefecture), Awaban tea (Tokushima Prefecture), Batabata tea (Toyama Prefecture) and Puer tea ethyl acetate content The extract was prepared in the same manner as in Production Example 1, and each vascular smooth muscle relaxing action was measured in the same procedure as in Test Example 1 for comparison.

図8から明らかなように、碁石茶やプーアル茶以外の後発酵茶の酢酸エチル分画エキスも、碁石茶やプーアル茶と同様に血管平滑筋に直接作用して血管を弛緩させる作用を有していることが明らかとなった。   As is clear from FIG. 8, the ethyl acetate fraction extract of post-fermented teas other than meteorite tea and puer tea has the effect of relaxing the blood vessels by acting directly on vascular smooth muscle, as is the case with meteorite tea and puer tea. It became clear that.

[試験例8]後発酵茶のアンギオテンシン変換酵素(ACE)阻害能の比較
碁石茶、プーアル茶、阿波番茶、バタバタ茶及び天狗黒茶のそれぞれの酢酸エチル分画エキスについて、ACE kit-WST(同仁化学)を用いてACE阻害活性測定を行った。ポジ
ティブコントロールとしては臨床で使用されているAlaceprilを用い、同時に測定した。
[Test Example 8] Comparison of the ability of post-fermented tea to inhibit angiotensin converting enzyme (ACE) For each ethyl acetate fraction extract of Goishi tea, Puaru tea, Awaban tea, Batabata tea and Tengu black tea, ACE kit-WST (Dojin) The ACE inhibitory activity was measured using Chem. As a positive control, Alacepril used clinically was used, and the measurement was performed simultaneously.

図9から明らかなように、後発酵茶の酢酸エチル分画エキスにはACEに対する阻害活
性がある事がわかった。特にプーアル茶、バタバタ茶及び天狗黒茶の酢酸エチル分画エキスには比較的強いACE阻害効果があることがわかった。
As is clear from FIG. 9, it was found that the ethyl acetate fraction extract of post-fermented tea has inhibitory activity against ACE. In particular, it was found that ethyl acetate fraction extracts of Pu'er tea, Batabata tea and Tengu black tea have a relatively strong ACE inhibitory effect.

以上の結果の通り、本発明の抽出物の投与により血圧上昇を抑制することができる。   As described above, an increase in blood pressure can be suppressed by administration of the extract of the present invention.

Claims (4)

後発酵茶を熱水抽出したものの酢酸エチル抽出物を有効成分とする血圧上昇抑制剤。   An antihypertensive agent comprising, as an active ingredient, an ethyl acetate extract of post-fermented tea extracted with hot water. 前記後発酵茶が碁石茶またはプーアル茶であることを特徴とする、請求項1に記載の血圧上昇抑制剤。   The antihypertensive agent according to claim 1, wherein the post-fermented tea is Goishi tea or Pu'er tea. 請求項1又は2に記載の血圧上昇抑制剤を含有する飲食品。   Food / beverage products containing the blood pressure rise inhibitor of Claim 1 or 2. 請求項1又は2に記載の血圧上昇抑制剤を含有する医薬。   A medicament comprising the blood pressure increase inhibitor according to claim 1 or 2.
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