JPH06199696A - Carcinostatic anticancer agent - Google Patents
Carcinostatic anticancer agentInfo
- Publication number
- JPH06199696A JPH06199696A JP4084860A JP8486092A JPH06199696A JP H06199696 A JPH06199696 A JP H06199696A JP 4084860 A JP4084860 A JP 4084860A JP 8486092 A JP8486092 A JP 8486092A JP H06199696 A JPH06199696 A JP H06199696A
- Authority
- JP
- Japan
- Prior art keywords
- anticancer agent
- carcinostatic
- activity
- compound
- sod
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、制癌剤・抗癌剤に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an anticancer agent / anticancer agent.
【0002】[0002]
【従来の技術】従来より、癌腫あるいは肉腫などの悪性
腫瘍に対しては、癌細胞を破壊する等の多くの治療剤
や、ステロイド等の免疫抑制剤が知られている。2. Description of the Related Art Conventionally, many therapeutic agents for destroying cancer cells and immunosuppressive agents such as steroids have been known for malignant tumors such as carcinoma and sarcoma.
【0003】[0003]
【発明が解決しようとする課題】しかし、これらの治療
剤は癌細胞を殺すだけでなく正常な細胞にも作用する為
に、副作用が強かった。However, these therapeutic agents have strong side effects because they not only kill cancer cells but also act on normal cells.
【0004】また、ステロイド剤などの免疫抑制剤も副
作用が強く、十分な効果を得ることが難しく、さらに、
これらの薬剤は経口的に利用することが困難で、おもに
点滴や静脈注射による摂取がなされており患者への負担
が大きかった。Immunosuppressive agents such as steroids also have strong side effects, making it difficult to obtain sufficient effects.
These drugs were difficult to use orally, and were ingested mainly by drip or intravenous injection, which placed a heavy burden on patients.
【0005】本発明は、前記課題を解決し、悪性腫瘍を
日常経口的に摂取でき、かつ、副作用がなく有効な制癌
・抗癌剤を提供することを目的とする。An object of the present invention is to solve the above-mentioned problems and to provide an effective anti-cancer / anti-cancer agent which can orally take a malignant tumor daily and has no side effect.
【0006】そこで、本発明者らは、前記目的を解決す
るために鋭意研究を重ねた結果、体内の活性酸素を除去
するスーパーオキシドジスムターゼ(SOD)様活性お
よび/または抗酸化能(スーパーオキシドラジカルなど
の活性酸素を捕捉するスカベンジャー機能を含む)を有
する物質、かつ、フェノール化合物、及び、糖蛋白質、
糖化フラボノイド等の糖化合物を含有する組成物が、悪
性腫瘍に対し優れた効果を有し、かつ副作用がなく安全
に制癌・抗癌機能を発揮するとの知見を得て本発明を完
成した。Therefore, as a result of intensive studies to solve the above-mentioned object, the present inventors have found that superoxide dismutase (SOD) -like activity for removing active oxygen in the body and / or antioxidant ability (superoxide radical). (Including a scavenger function of capturing active oxygen) such as, and a phenol compound and glycoprotein,
The present invention has been completed based on the finding that a composition containing a sugar compound such as a glycated flavonoid has an excellent effect on a malignant tumor and has a safe anticancer / anticancer function without side effects.
【0007】SOD様活性とは、スーパーオキシドラジ
カルを過酸化水素に変換するSOD活性に類似の活性
(生理機能)を有するものを示し、SOD様活性を有す
る物質として、アミノ酸やペプチドの銅(II)錯体、
マンガン錯体、脂溶性アスコルビン酸、ポリフィリン金
属錯体、ポリアミン金属錯体等の低分子化合物が挙げら
れ、また抗酸化能を有するものとしてビタミンC、ビタ
ミンE、尿酸、グルタチオン、βカロチン、カラター
ゼ、グルタチオンパーオキシンダーゼ等が挙げられる。[0007] SOD-like activity refers to a substance having an activity (physiological function) similar to the SOD activity for converting superoxide radicals into hydrogen peroxide, and as a substance having SOD-like activity, amino acids and peptides such as copper (II) are used. ) Complex,
Low molecular weight compounds such as manganese complex, fat-soluble ascorbic acid, porphyrin metal complex, polyamine metal complex, etc. are mentioned, and those having antioxidant ability are vitamin C, vitamin E, uric acid, glutathione, β-carotene, calatase, glutathione peroxin. Examples include dase.
【0008】フェノール化合物としては、グアイアコー
ル、フェノール、オイゲノール、フェニルエタノール等
の群より選ばれた1種またはこれらの混合物が上げられ
る。Examples of the phenol compound include one selected from the group of guaiacol, phenol, eugenol, phenylethanol and the like, or a mixture thereof.
【0009】糖蛋白質、糖化フラボノイド等の糖化合物
としては、アスパラチン、オリエンチン(ルテキシ
ン)、シスオリエンチン(ルトナレチン)、イソクエル
シチン、ルチン等の群より選ばれた1種またはこれらの
混合物が挙げられる。Examples of sugar compounds such as glycoproteins and glycated flavonoids include one selected from the group consisting of aspalathin, orientin (lutexin), cis-orientin (lutonaretin), isoquercitin, rutin or a mixture thereof.
【0010】また、本発明は、リン、鉄、カルシウム、
ナトリウム、カリウム、マグネシウム、銅、亜鉛、マン
ガン、ケルセチン、セレン等の1種またはこれらの混合
物であるミネラルを混合すればより効果が優れる。The present invention also provides phosphorus, iron, calcium,
The effect is more excellent if one or more kinds of minerals such as sodium, potassium, magnesium, copper, zinc, manganese, quercetin, selenium, etc. or a mixture thereof is mixed.
【0011】本発明の構成物質はいずれも無毒性のもの
で薬理基準にも合致したもので、ラットに対する急性毒
性試験で死亡例は皆無であり、生化学血液検査および病
理組織学的検査においても異常が認められなかった。All of the constituents of the present invention are non-toxic and meet the pharmacological criteria. There are no deaths in the acute toxicity test for rats, and no biochemical blood test or histopathological test is performed. No abnormality was found.
【0012】本発明は、SOD様活性を有する物質およ
び/または抗酸化能、糖化フラボノイド及びフェノール
化合物、また必要に応じて添加されるミネラルを含有す
ることによって初めて優れた効果を示すのであり、その
構成は、SOD様活性および/または抗酸化能の力価が
10,000〜100,000単位/g、糖化合物2〜
20mg/g、蛋白性物質1〜30mg/g、及びフェ
ノール化合物を1〜20%、またミネラルを添加すると
きは、10〜500mg/g含有することが必要であ
る。The present invention exhibits an excellent effect for the first time by containing a substance having SOD-like activity and / or antioxidant ability, a glycated flavonoid and a phenol compound, and a mineral added as necessary. The composition has a titer of SOD-like activity and / or antioxidant ability of 10,000 to 100,000 units / g, sugar compound 2 to
20 mg / g, 1 to 30 mg / g of a proteinaceous substance, 1 to 20% of a phenol compound, and when adding minerals, it is necessary to contain 10 to 500 mg / g.
【0013】本発明に用いる、SOD様活性および/ま
たは抗酸化能を有する物質、糖成分、フェノール化合物
は、混合してそのまま溶液、粉末顆粒、錠剤、乳剤、ゼ
リー状など任意の形態で単独投与、または、他の飲食物
に混合して飲食することもできる。The substance having an SOD-like activity and / or antioxidant ability, the sugar component and the phenol compound used in the present invention are mixed alone and directly administered in any form such as solution, powder granules, tablets, emulsions and jellies. Alternatively, it can be mixed with other foods and drinks.
【0014】投与量は、対象となる疾患の種類、程度に
より異なるが、2〜40mg/kg/日の範囲で用いる
のが好ましく、飲料として常用する場合には、0.1〜
3.0%溶液を100ml〜500ml/日飲食するの
が好ましい。Although the dose varies depending on the kind and degree of the target disease, it is preferably used within the range of 2 to 40 mg / kg / day, and when used as a beverage, 0.1 to
It is preferable to eat and drink the 3.0% solution at 100 ml to 500 ml / day.
【0015】[0015]
【作用】癌の発症要因は複雑で不明な点が多いが、体内
の活性酸素が深く関わっている可能性がある。本発明
は、スーパーオキシドラジカルなどの活性酸素の除去作
用を有するスーパーオキシドジスムターゼ(SOD)様
活性を有する物質および糖化合物などの抗酸化作用を有
する物質が、組み合わさって作用していると考えられ
る。[Function] Although the factors that cause cancer are complex and unclear, there are possibilities that active oxygen in the body is deeply involved. In the present invention, it is considered that a substance having a superoxide dismutase (SOD) -like activity having an action of removing active oxygen such as a superoxide radical and a substance having an antioxidant action such as a sugar compound act in combination. .
【0016】[0016]
【効果】本発明は、ヒトを含む哺乳動物の悪性腫瘍を日
常経口的に摂取でき、かつ、副作用がなく、迅速に改善
治療することができる。[Effects] The present invention allows daily orally ingestion of malignant tumors of mammals including humans, has no side effects, and can be rapidly treated for improvement.
【0017】[0017]
製造例 糖化合物として糖化フラボノイド1〜50mg/g、蛋
白質2〜20%、フェノール3〜15%を溶液状のまま
混合し、SOD様活性および/または抗酸化能として力
価20,000単位/g以上となるように調製した。得
られた組成物に蒸留水を添加し、組成物が0.25%含
有する溶液を得た。Production Example Glycated flavonoids 1 to 50 mg / g, protein 2 to 20%, and phenol 3 to 15% as a sugar compound are mixed in a solution state, and a titer of 20,000 units / g as SOD-like activity and / or antioxidant ability is mixed. It was prepared as described above. Distilled water was added to the obtained composition to obtain a solution containing 0.25% of the composition.
【0018】[動物]実験には、F344系(チャール
ス・リバー)およびウィスター系ラット(SRL)を用
いた。動物は、入手後すべて12時間明暗サイクル(午
前7時から午後7時まで明期)の室温24±1℃、相対
湿度55±5%の飼育室で餌(オリエンタル酵母、固形
飼料)を自由摂取下で飼育した。[Animal] In the experiment, F344 strain (Charles River) and Wistar strain rat (SRL) were used. All animals have free access to food (Oriental yeast, solid feed) in a breeding room with a room temperature of 24 ± 1 ° C and a relative humidity of 55 ± 5% under a 12-hour light-dark cycle (light period from 7 am to 7 pm) after acquisition. Raised below.
【0019】実施例1 製造例で得た溶液をラットに日常摂取する水のかわりに
本組成物を飲ませた該溶液投与群と、通常の水を飲ませ
たラット(コントロール群)との膵臓癌の変化を調べ、
その結果を表1に示した。この結果、投与群では膵臓癌
の発生頻度が低く、また悪性腫瘍の程度も軽くなってい
た。Example 1 Pancreas of a solution-administered group in which the composition obtained by drinking the solution obtained in the Production Example in place of water for daily intake to rats and a rat (control group) in which normal water was ingested To investigate changes in cancer,
The results are shown in Table 1. As a result, the incidence of pancreatic cancer was low and the degree of malignant tumor was low in the administration group.
【表1】 [Table 1]
【0020】実施例2 製造例で得た溶液をC3HIOT/2細胞に混ぜて発癌
抑制効果を調べた(AB)。さらに、放射線を照射して
発癌を誘発し、本発明の発癌抑制効果を調べた(CD
E)。その結果を図1に示す。Example 2 The solution obtained in Production Example was mixed with C3HIOT / 2 cells to examine the carcinogenic inhibitory effect (AB). Furthermore, irradiation was conducted to induce carcinogenesis, and the carcinogenic inhibitory effect of the present invention was investigated (CD
E). The result is shown in FIG.
【0021】実施例3 製造例で得た溶液を用いて、試験管内における溶液の添
加量による活性酸素除去・消去作用を調べた。その結果
を図2に示す。図2によれば、試験管内におけるESR
のシグナル(波形)の大きなものは活性酸素の存在を示
しており、溶液の添加量を増加することによって活性酸
素量が減少していくことがわかる。Example 3 Using the solution obtained in the production example, the active oxygen removing / eliminating action depending on the addition amount of the solution in a test tube was examined. The result is shown in FIG. According to FIG. 2, ESR in the test tube
A large signal (waveform) indicates the presence of active oxygen, and it can be seen that the amount of active oxygen decreases as the amount of solution added increases.
【0022】ついで、ラットに製造例で得た溶液を水の
代わりに8週間にわたり与えて脂肪組織における活性酸
素量を調べた。その結果を図3に示す。Then, the solution obtained in the production example was fed to rats instead of water for 8 weeks to examine the amount of active oxygen in adipose tissue. The result is shown in FIG.
【図1】発癌抑制効果を示す図。FIG. 1 is a diagram showing a carcinogenesis suppressing effect.
【図2】試験管内における溶液の添加量による活性酸素
の変化を示す図。FIG. 2 is a diagram showing changes in active oxygen according to the amount of solution added in a test tube.
【図3】腹腔内脂肪組織におけるESRシグナルの変動
を示す図。FIG. 3 shows changes in ESR signal in abdominal adipose tissue.
A:通常のもの B:溶液を10%加えたもの C:通常のものに放射線を照射したもの D:溶液を2%加え放射線を照射したもの E:溶液を10%加え放射線を照射したもの A: Normal product B: 10% solution added C: Normal product irradiated with radiation D: 2% solution added with irradiation E: 10% solution added with irradiation
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 31/375 7431−4C 31/70 8314−4C (72)発明者 中野 昌俊 愛知県知立市新林町茶野36−16 (72)発明者 奥村 寛 長崎県諫早市白岩町2−13 西諫早ハイツ D−301 (72)発明者 小松 賢志 長崎県西彼杵郡時津町浜田郷561−20─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI Technical indication location A61K 31/375 7431-4C 31/70 8314-4C (72) Inventor Masatoshi Nakano New Chiryu City, Aichi Prefecture 36-16 Chano, Hayashi-cho (72) Inventor Hiroshi Okumura 2-13 Shiraiwa-cho, Isahaya-shi, Nagasaki Nishi-isahaya Heights D-301 (72) Inventor Kenji Komatsu 561-20 Hamada-go, Togitsu-cho, Nishisonogi-gun, Nagasaki Prefecture
Claims (3)
D)様活性および/または抗酸化能(スカベンジャー機
能を含む)を有する物質、フェノール化合物、及び、糖
蛋白質、糖化フラボノイド等の糖化合物を含有してなる
制癌・抗癌剤。1. Superoxide dismutase (SO
D) An anti-cancer / anti-cancer agent containing a substance having a similar activity and / or an antioxidant ability (including a scavenger function), a phenol compound, and a glyco compound such as a glycoprotein and a glycated flavonoid.
ェノール、オイゲノール、フェニルエタノール等の群よ
り選ばれた1種またはこれらの混合物であることを特徴
とする請求項1記載の制癌・抗癌剤。2. The antitumor / anticancer agent according to claim 1, wherein the phenol compound is one selected from the group consisting of guaiacol, phenol, eugenol, phenylethanol and the like, or a mixture thereof.
物がアスパラチン、オリエンチン(ルテキシン)、シス
オリエンチン(ルトナレチン)、イソクエルシチン、ル
チン等の群より選ばれた1種またはこれらの混合物であ
ることを特徴とする請求項1記載の制癌・抗癌剤。3. The glyco compound such as glycoprotein and glycated flavonoid is one or a mixture thereof selected from the group consisting of aspalathin, orientin (lutexin), cis-orientin (lutonaretin), isoquercitin, rutin and the like. The anticancer / anticancer agent according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4084860A JPH06199696A (en) | 1992-03-06 | 1992-03-06 | Carcinostatic anticancer agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4084860A JPH06199696A (en) | 1992-03-06 | 1992-03-06 | Carcinostatic anticancer agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06199696A true JPH06199696A (en) | 1994-07-19 |
Family
ID=13842568
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4084860A Pending JPH06199696A (en) | 1992-03-06 | 1992-03-06 | Carcinostatic anticancer agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06199696A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003080093A1 (en) * | 2002-03-27 | 2003-10-02 | Prasanta Banerji | A process for the preparation of a new medicinal combination for regression of intracranial tumors and other tumors occurring in the human body |
WO2003080094A1 (en) * | 2002-03-27 | 2003-10-02 | Prasanta Banerji | Product for regression of tumors occuring in the human body |
JP2010059200A (en) * | 2002-05-22 | 2010-03-18 | Fushimi Pharm Co Ltd | Use for utilizing of physiological activity action of d-allose |
CN116056761A (en) * | 2020-08-31 | 2023-05-02 | 建国大学全球本土化产学合作基金会 | Pharmaceutical composition for treating androgen receptor related diseases comprising extract of fructus forsythiae as active ingredient |
-
1992
- 1992-03-06 JP JP4084860A patent/JPH06199696A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003080093A1 (en) * | 2002-03-27 | 2003-10-02 | Prasanta Banerji | A process for the preparation of a new medicinal combination for regression of intracranial tumors and other tumors occurring in the human body |
WO2003080094A1 (en) * | 2002-03-27 | 2003-10-02 | Prasanta Banerji | Product for regression of tumors occuring in the human body |
JP2010059200A (en) * | 2002-05-22 | 2010-03-18 | Fushimi Pharm Co Ltd | Use for utilizing of physiological activity action of d-allose |
CN116056761A (en) * | 2020-08-31 | 2023-05-02 | 建国大学全球本土化产学合作基金会 | Pharmaceutical composition for treating androgen receptor related diseases comprising extract of fructus forsythiae as active ingredient |
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