JPS6361906B2 - - Google Patents
Info
- Publication number
- JPS6361906B2 JPS6361906B2 JP56079587A JP7958781A JPS6361906B2 JP S6361906 B2 JPS6361906 B2 JP S6361906B2 JP 56079587 A JP56079587 A JP 56079587A JP 7958781 A JP7958781 A JP 7958781A JP S6361906 B2 JPS6361906 B2 JP S6361906B2
- Authority
- JP
- Japan
- Prior art keywords
- thiamine
- fish
- hydrochloride
- dbt
- feed
- 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.)
- Expired
Links
- 241000251468 Actinopterygii Species 0.000 claims description 16
- AZJUFRDUYTYIHV-NKFKGCMQSA-N Dibenzoyl Thiamine Chemical compound C=1C=CC=CC=1C(=O)OCC\C(SC(=O)C=1C=CC=CC=1)=C(/C)N(C=O)CC1=CN=C(C)N=C1N AZJUFRDUYTYIHV-NKFKGCMQSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 235000019688 fish Nutrition 0.000 description 15
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 13
- 229960003495 thiamine Drugs 0.000 description 13
- 235000019157 thiamine Nutrition 0.000 description 13
- 239000011721 thiamine Substances 0.000 description 13
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 241001600434 Plectroglyphidodon lacrymatus Species 0.000 description 5
- 238000009372 pisciculture Methods 0.000 description 4
- UIERGBJEBXXIGO-UHFFFAOYSA-N thiamine mononitrate Chemical compound [O-][N+]([O-])=O.CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N UIERGBJEBXXIGO-UHFFFAOYSA-N 0.000 description 4
- GTQXMAIXVFLYKF-UHFFFAOYSA-N thiochrome Chemical compound CC1=NC=C2CN3C(C)=C(CCO)SC3=NC2=N1 GTQXMAIXVFLYKF-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241001454694 Clupeiformes Species 0.000 description 3
- 235000019513 anchovy Nutrition 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- IWXAZSAGYJHXPX-BCEWYCLDSA-N Bisbentiamine Chemical compound C=1C=CC=CC=1C(=O)OCC/C(SS\C(CCOC(=O)C=1C=CC=CC=1)=C(/C)N(CC=1C(=NC(C)=NC=1)N)C=O)=C(/C)N(C=O)CC1=CN=C(C)N=C1N IWXAZSAGYJHXPX-BCEWYCLDSA-N 0.000 description 2
- 241001149724 Cololabis adocetus Species 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 2
- 241001125048 Sardina Species 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- RMRCNWBMXRMIRW-BYFNXCQMSA-M cyanocobalamin Chemical compound N#C[Co+]N([C@]1([H])[C@H](CC(N)=O)[C@]\2(CCC(=O)NC[C@H](C)OP(O)(=O)OC3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)C)C/2=C(C)\C([C@H](C/2(C)C)CCC(N)=O)=N\C\2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O RMRCNWBMXRMIRW-BYFNXCQMSA-M 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- GFEGEDUIIYDMOX-BMJUYKDLSA-N n-[(4-amino-2-methylpyrimidin-5-yl)methyl]-n-[(z)-3-[[(z)-2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl]disulfanyl]-5-hydroxypent-2-en-2-yl]formamide Chemical compound C=1N=C(C)N=C(N)C=1CN(C=O)C(\C)=C(CCO)/SSC(/CCO)=C(/C)N(C=O)CC1=CN=C(C)N=C1N GFEGEDUIIYDMOX-BMJUYKDLSA-N 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000019512 sardine Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 1
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 description 1
- 241001310494 Ammodytes marinus Species 0.000 description 1
- 241000473391 Archosargus rhomboidalis Species 0.000 description 1
- 235000019743 Choline chloride Nutrition 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- 239000004470 DL Methionine Substances 0.000 description 1
- 239000011627 DL-alpha-tocopherol Substances 0.000 description 1
- 235000001815 DL-alpha-tocopherol Nutrition 0.000 description 1
- 235000019733 Fish meal Nutrition 0.000 description 1
- 108010068370 Glutens Proteins 0.000 description 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- 241000269821 Scombridae Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 208000005428 Thiamine Deficiency Diseases 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- ISIPQAHMLLFSFR-GDNBJRDFSA-N [(z)-3-acetylsulfanyl-4-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]pent-3-enyl] acetate Chemical compound CC(=O)OCC\C(SC(C)=O)=C(/C)N(C=O)CC1=CN=C(C)N=C1N ISIPQAHMLLFSFR-GDNBJRDFSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 239000003674 animal food additive Substances 0.000 description 1
- 238000009360 aquaculture Methods 0.000 description 1
- 244000144974 aquaculture Species 0.000 description 1
- 208000002894 beriberi Diseases 0.000 description 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- BLORRZQTHNGFTI-ZZMNMWMASA-L calcium-L-ascorbate Chemical compound [Ca+2].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] BLORRZQTHNGFTI-ZZMNMWMASA-L 0.000 description 1
- 239000002967 calcium-L-ascorbate Substances 0.000 description 1
- 235000005937 calcium-L-ascorbate Nutrition 0.000 description 1
- SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 description 1
- 229960003178 choline chloride Drugs 0.000 description 1
- 229960002104 cyanocobalamin Drugs 0.000 description 1
- 235000000639 cyanocobalamin Nutrition 0.000 description 1
- 239000011666 cyanocobalamin Substances 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 239000004467 fishmeal Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 235000021312 gluten Nutrition 0.000 description 1
- 229960000367 inositol Drugs 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 235000020640 mackerel Nutrition 0.000 description 1
- WIXFIQKTHUVFDI-UHFFFAOYSA-N menadione sulfonic acid Chemical compound C1=CC=C2C(=O)C(C)(S(O)(=O)=O)CC(=O)C2=C1 WIXFIQKTHUVFDI-UHFFFAOYSA-N 0.000 description 1
- FFEARJCKVFRZRR-UHFFFAOYSA-N methionine Chemical compound CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 235000006109 methionine Nutrition 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004172 pyridoxine hydrochloride Drugs 0.000 description 1
- 235000019171 pyridoxine hydrochloride Nutrition 0.000 description 1
- 239000011764 pyridoxine hydrochloride Substances 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 108010093489 thiaminase II Proteins 0.000 description 1
- 229940101691 thiamine 10 mg Drugs 0.000 description 1
- 229960001385 thiamine disulfide Drugs 0.000 description 1
- 229960000344 thiamine hydrochloride Drugs 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- 235000019190 thiamine hydrochloride Nutrition 0.000 description 1
- 239000011747 thiamine hydrochloride Substances 0.000 description 1
- 150000003544 thiamines Chemical class 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 235000019195 vitamin supplement Nutrition 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Landscapes
- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
本発明は、生餌用養魚組成物に関する。
ハマチ、ブリ、タイなどの養殖には、飼料とし
てしばしばサンマ、サバ、カタクチイワシ、マイ
ワシ、イカナゴ、オオナゴなどの生魚を丸のまゝ
あるいはブツ切り、ミンチ状にしたものなど生餌
が用いられ、これに魚の栄養補給、疾病予防など
を目的として各種のビタミン剤を添加して投与さ
れている。
しかしながら、これらの生餌の中には強いチア
ミナーゼ活性を示す場合があり、さらに耐熱性還
元因子その他の分解性因子によつて生餌中のおよ
び(または)添加されたサイアミンが分解される
ためにサイアミン欠乏症になることが知られてい
る。特にミンチ状にした生餌中ではサイアミンが
急速に分解されるためにきわめて多量のサイアミ
ンを添加する必要がある〔Green、R.Gら、「ジ
ヤーナル・オブ・ニユートリシヨン」、21巻243頁
(1941年);Sealock、R.Rら、「ジヤーナル・オ
ブ・アメリカン・ケミカル・ソサエテイ」、65巻、
935頁(1943年);Krampitz、L.Oら、「ジヤーナ
ル・オブ・バイオロジカル・ケミストリイ」152
巻、9頁(1944)〕。
かかる欠点を補う目的はサイアミンを油脂等に
よる被覆化を行なつて生餌中でのサイアミンの分
解を防止することが提唱されている〔特公昭50−
13192号〕が、高コストであるのみならずその防
止効果も完全なものとはいえない。
本発明者らは、かかる従来技術とは全く視点を
変えて鋭意研究した結果、O,S−ジベンゾイル
サイアミンが、養魚用生餌中できわめて安定であ
りしかも魚体中への吸収が特異的にすぐれかつ持
続時間も長いという意外な知見を得、さらに研究
を進めて本発明を完成するに至つた。
すなわち、本発明は、O,S−ジベンゾイルサ
イアミンまたはその塩を含有してなる生餌用養魚
組成物である。
本発明において、O,S−ジベンゾイルサイア
ミンは、遊離塩基として用いてもよく、生理学的
に許容されうる塩たとえば鉱酸塩(塩酸塩、硝酸
塩、硫酸塩など)として用いてもよい。かかる
O,S−ジベンゾイルサイアミンおよびその塩は
単体のまま生餌に添加してもよいが、一般にあら
かじめ小麦粉などの澱粉質、グルテン、ビール酵
母、魚粉、配合飼料などの賦形剤で希釈してプレ
ミツクスとして使用するのが好ましい。また、他
のビタミン類およびミネラル類などと混合した総
合ビタミン剤として用いるようにしてもよい。通
常、O,S−ジベンゾイルサイアミンまたはその
塩は、魚体重1Kg当り約1〜20mg(1日量)摂取
させるのが好ましく、このためには生餌1Kgに対
して約0.5〜1000mgとりわけ約2〜200mgの割合で
添加するのがよい。
このようにして生餌中に添加されたO,S−ジ
ベンゾイルサイアミンおよびその塩は、後記実験
例からも明らかなように、各種サイアミン誘導体
のうちでも特異的に養魚用生餌中で長時間分解さ
れず、しかも魚体中への吸収がよく長時間接続す
る。このように、本発明の養魚組成物は、魚類
B1欠乏症の予防治療剤、養魚用飼料添加剤など
として顕著な効果を奏するものである。
以下に、本発明を実験例、実施例によりさらに
具体的に説明するが、これらは本発明をなんら制
限するものではない。
実験例 1
サンマおよびカタクチイワシをそれぞれミンチ
にして生餌100g当りサイアミンとして5mgのO,
S−ジベンゾイルサイアミン(以下、DBT)、サ
イアミン硝酸塩、ベンゾイルサイアミンジスルフ
イド(以下、BTDS)塩酸塩またはサイアミンジ
スルフイド(以下TDS)硝酸塩を添加、混合し、
30℃で保存して一定時間毎に取出し、残存サイア
ミン量をチオクローム法で定量した。結果は第1
表、第2表に示されるとおりであつた。数値は添
加したサイアミン量に対する残存量のパーセント
である。
The present invention relates to a fish culture composition for live bait. For aquaculture of yellowtail, yellowtail, sea bream, etc., raw fish such as saury, mackerel, anchovy, sardine, sand eel, and giant eel are often used as feed, such as whole, cut into chunks, or minced raw fish. Various vitamin supplements are added to fish and administered for the purpose of nutritional supplementation and disease prevention. However, some of these live feeds may exhibit strong thiaminase activity, and furthermore, the thiamine in the live feed and/or added to it is degraded by heat-stable reducing factors and other degradable factors. It is known to cause thiamine deficiency. Particularly in minced raw feed, thiamine is rapidly decomposed, so it is necessary to add a very large amount of thiamine [Green, RG et al., Journal of Nutrition, Vol. 21, p. 243 (1941 ); Sealock, RR et al., Journal of the American Chemical Society, vol. 65,
Page 935 (1943); Krampitz, LO et al., Journal of Biological Chemistry 152
Volume, page 9 (1944)]. In order to compensate for this drawback, it has been proposed that thiamine be coated with oil or the like to prevent it from decomposing in live bait [Special Publication No. 1973-
No. 13192] is not only expensive, but also cannot be said to be completely effective in preventing it. As a result of intensive research from a completely different perspective from the conventional technology, the present inventors found that O,S-dibenzoylthiamine is extremely stable in live feed for fish farming and is uniquely absorbed into the fish body. They obtained the unexpected finding that it was excellent in water and lasted for a long time, and proceeded with further research and completed the present invention. That is, the present invention is a fish culture composition for live bait containing O,S-dibenzoylthiamine or a salt thereof. In the present invention, O,S-dibenzoylthiamine may be used as a free base or as a physiologically acceptable salt, such as a mineral salt (hydrochloride, nitrate, sulfate, etc.). Such O,S-dibenzoylthiamine and its salts may be added to live feed as a single substance, but generally they are diluted in advance with excipients such as starchy substances such as wheat flour, gluten, brewer's yeast, fish meal, and compound feed. Preferably, it is used as a premix. It may also be used as a multivitamin mixed with other vitamins and minerals. Normally, it is preferable to ingest O,S-dibenzoylthiamine or its salt at about 1 to 20 mg per 1 kg of fish body weight (daily dose), and for this purpose, about 0.5 to 1000 mg, especially about 100 mg per 1 kg of live feed. It is best to add it at a rate of 2 to 200 mg. O,S-dibenzoylthiamine and its salts added to the live feed in this way are unique among various thiamine derivatives for a long time in the live feed for fish farming, as is clear from the experimental examples below. It is not time-resolved, is absorbed well into the fish body, and remains connected for a long time. In this way, the fish farming composition of the present invention
It has remarkable effects as a preventive treatment for B1 deficiency and as a feed additive for fish farming. The present invention will be explained in more detail below using experimental examples and examples, but these are not intended to limit the present invention in any way. Experimental example 1 Mince saury and anchovy and add 5mg of O as thiamine per 100g of raw bait.
Add and mix S-dibenzoyl thiamine (hereinafter referred to as DBT), thiamine nitrate, benzoyl thiamine disulfide (hereinafter referred to as BTDS) hydrochloride or thiamine disulfide (hereinafter referred to as TDS) nitrate,
It was stored at 30°C, taken out at regular intervals, and the amount of remaining thiamine was determined by the thiochrome method. The result is the first
The results were as shown in Table 2. The numerical value is the percentage of the amount remaining relative to the amount of thiamine added.
【表】【table】
【表】
実験例 2
ブリ(体重1Kg)にDBT塩酸塩またはサイア
ミン硝酸塩をサイアミンとして10mg/Kg魚体重の
投与量で強制経口投与し、水温25℃にて消化管か
らの吸収性を比較した。一定時間毎に、魚をとり
あげ、心臓より採取した血液2mlを用い、以下実
験例1と同様還元操作を行なわずに操作して血中
のサイアミン量を定量した。その結果を第3表に
示す。[Table] Experimental Example 2 DBT hydrochloride or thiamine nitrate was forcibly administered orally as thiamine to yellowtail (1 kg body weight) at a dose of 10 mg/kg fish body weight, and the absorbability from the gastrointestinal tract was compared at a water temperature of 25°C. At regular intervals, fish were taken and 2 ml of blood collected from the heart was used to quantify the amount of thiamine in the blood in the same manner as in Experimental Example 1 without performing the reduction operation. The results are shown in Table 3.
【表】
実験例 3
DBT塩酸塩を乳糖でサイアミンとして10mg/
gの含量となるように調整した散剤10gを市販の
ハマチ用配合飼料4Kgに添加混合した後、カタク
チイワシミンチ16Kgと混合して、体重約25gのハ
マチ(開始時3000尾、15日後2000尾、30日後1500
尾、60日後1000尾)に1日量として毎日投餌して
60日後までの成長性、生存率をDBT塩酸塩の代
りにサイアミンとして同量のサイアミン硝酸塩添
加区と比較したところ、第4表の通り、DBT塩
酸塩の効果サイアミン塩酸塩よりはるかにすぐれ
ていた。[Table] Experimental example 3 DBT hydrochloride with lactose as thiamine 10mg/
After adding and mixing 10g of the powder adjusted to have a content of 10g to 4Kg of commercially available compound feed for yellowtail, it was mixed with 16Kg of anchovy mince to produce yellowtail weighing about 25g (3000 fish at the start, 2000 fish after 15 days, 30 1500 days later
1,000 fish after 60 days).
When the growth rate and survival rate up to 60 days were compared with the same amount of thiamine nitrate as thiamine instead of DBT hydrochloride, as shown in Table 4, the effect of DBT hydrochloride was far superior to that of thiamine hydrochloride. .
【表】
実験例 4
冷凍マイワシを解凍後ミンチにしてこの100g
当たりサイアミンとして3mgのO,S−ジベンゾ
イルサイアミン(以下、DBT)塩酸塩、O,S
−ジアセチルサイアミン(以下、DAT)塩酸塩、
O,S−ジフロイルサイアミン(以下、DFT)
またはサイアミン硝酸塩を添加、混合し、30℃で
180分間保存した後に取出し、残存サイアミン量
をチオクローム法で定量した。
結果は第5表に示されるとおりであつた。数値
は添加したサイアミン量に対する残存量のパーセ
ントである。
第5表からDBTが最も高い残存量を示し、特
にO,S−ジアシルサイアミンのなかでも、
DBTが生餌中で特異的かつ顕著に安定であるこ
とが明らかである。[Table] Experimental example 4 100g of frozen sardine thawed and minced
3 mg of O,S-dibenzoylthiamine (hereinafter referred to as DBT) hydrochloride as thiamine, O,S
- diacetylthiamine (hereinafter referred to as DAT) hydrochloride,
O,S-difluorylthiamine (hereinafter referred to as DFT)
Or add thiamine nitrate, mix and at 30℃
After being stored for 180 minutes, it was taken out and the amount of remaining thiamine was determined by the thiochrome method. The results were as shown in Table 5. The numerical value is the percentage of the amount remaining relative to the amount of thiamine added. From Table 5, DBT shows the highest residual amount, especially among O,S-diacylthiamines.
It is clear that DBT is uniquely and significantly stable in live feed.
【表】
実施例 1
DBT塩酸塩が10mg/gとなるよう飼料用ビー
ル酵母で調製した散剤。本品は1日当り魚体重1
Kgにつき0.3g摂取するような割合に生餌に混和
又は展着して投与するのがよい。
実施例 2
1Kg中DBT塩酸塩1.5gのほかにビタミンA油
100万単位、ビタミンD3油20万単位、酢酸dl−α
−トコフエロール3.0g、メナジオン亜硫酸水素
ジメチルピリミジノール0.1g、リボフラビン1.8
g、ニコチン酸アミド3.0g、塩酸ピリドキシン
2.2g、D−パントテン酸カルシウム20.0g、d
−ビオチン2.0mg、パラアミノ安息香酸0.3g、イ
ノシトール1.0g、塩化コリン10.0g、葉酸0.3g、
シアノコバラミン2.0mg、L−アスコルビン酸カ
ルシウム14.5g、DL−メチオニン3.0g、残余賦
形物質からなる組成物。本品を0.5%の割合で混
和した生餌を1日当り魚体重1Kgにつき200g投
与する。[Table] Example 1 Powder prepared using feed brewer's yeast so that DBT hydrochloride was 10 mg/g. This product is 1 fish weight per day.
It is best to administer it by mixing or spreading it into live feed at a rate of 0.3g per kg. Example 2 Vitamin A oil in addition to 1.5g of DBT hydrochloride per 1Kg
1 million units, vitamin D 3 oil 200,000 units, acetic acid DL-α
-Tocopherol 3.0g, Menadione bisulfite dimethylpyrimidinol 0.1g, Riboflavin 1.8
g, nicotinamide 3.0g, pyridoxine hydrochloride
2.2g, D-calcium pantothenate 20.0g, d
-Biotin 2.0mg, para-aminobenzoic acid 0.3g, inositol 1.0g, choline chloride 10.0g, folic acid 0.3g,
Composition consisting of 2.0 mg of cyanocobalamin, 14.5 g of calcium L-ascorbate, 3.0 g of DL-methionine, and residual excipients. Administer 200g of live bait mixed with this product at a rate of 0.5% per 1kg of fish weight per day.
Claims (1)
塩を含有してなる生餌用養魚組成物。1 A fish culture composition for live bait containing O,S-dibenzoylthiamine or a salt thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56079587A JPS57194755A (en) | 1981-05-25 | 1981-05-25 | Composition for pisciculture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56079587A JPS57194755A (en) | 1981-05-25 | 1981-05-25 | Composition for pisciculture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57194755A JPS57194755A (en) | 1982-11-30 |
| JPS6361906B2 true JPS6361906B2 (en) | 1988-11-30 |
Family
ID=13694116
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56079587A Granted JPS57194755A (en) | 1981-05-25 | 1981-05-25 | Composition for pisciculture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57194755A (en) |
-
1981
- 1981-05-25 JP JP56079587A patent/JPS57194755A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57194755A (en) | 1982-11-30 |
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