JPH10327766A - Feed composition for treatment of urolithiasis and its production - Google Patents
Feed composition for treatment of urolithiasis and its productionInfo
- Publication number
- JPH10327766A JPH10327766A JP9142299A JP14229997A JPH10327766A JP H10327766 A JPH10327766 A JP H10327766A JP 9142299 A JP9142299 A JP 9142299A JP 14229997 A JP14229997 A JP 14229997A JP H10327766 A JPH10327766 A JP H10327766A
- Authority
- JP
- Japan
- Prior art keywords
- urolithiasis
- weight
- pts
- parts
- water
- 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
- 206010007027 Calculus urinary Diseases 0.000 title claims abstract description 45
- 208000008281 urolithiasis Diseases 0.000 title claims abstract description 44
- 239000000203 mixture Substances 0.000 title claims abstract description 30
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims abstract description 26
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims abstract description 24
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 20
- 239000000194 fatty acid Substances 0.000 claims abstract description 20
- 229930195729 fatty acid Natural products 0.000 claims abstract description 20
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 17
- 229930003231 vitamin Natural products 0.000 claims abstract description 15
- 235000013343 vitamin Nutrition 0.000 claims abstract description 15
- 239000011782 vitamin Substances 0.000 claims abstract description 15
- 229940088594 vitamin Drugs 0.000 claims abstract description 15
- 239000011780 sodium chloride Substances 0.000 claims abstract description 13
- 239000001103 potassium chloride Substances 0.000 claims abstract description 12
- 235000011164 potassium chloride Nutrition 0.000 claims abstract description 12
- 150000003722 vitamin derivatives Chemical class 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011575 calcium Substances 0.000 claims description 11
- 229910052791 calcium Inorganic materials 0.000 claims description 11
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 235000002639 sodium chloride Nutrition 0.000 abstract description 13
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 abstract description 8
- 239000000292 calcium oxide Substances 0.000 abstract description 7
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 abstract description 6
- 230000001225 therapeutic effect Effects 0.000 abstract description 6
- -1 fatty acid calcium salt Chemical class 0.000 abstract description 3
- 235000018343 nutrient deficiency Nutrition 0.000 abstract description 2
- 208000002720 Malnutrition Diseases 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 description 14
- 235000021317 phosphate Nutrition 0.000 description 14
- 241000283690 Bos taurus Species 0.000 description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 13
- 239000010452 phosphate Substances 0.000 description 13
- 210000002700 urine Anatomy 0.000 description 13
- 239000003814 drug Substances 0.000 description 11
- 230000037396 body weight Effects 0.000 description 9
- 239000013078 crystal Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000004575 stone Substances 0.000 description 9
- 229940124597 therapeutic agent Drugs 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 7
- 210000004767 rumen Anatomy 0.000 description 7
- 235000019786 weight gain Nutrition 0.000 description 7
- 235000012255 calcium oxide Nutrition 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 238000009395 breeding Methods 0.000 description 4
- 235000015097 nutrients Nutrition 0.000 description 4
- 230000004584 weight gain Effects 0.000 description 4
- 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 3
- 208000009911 Urinary Calculi Diseases 0.000 description 3
- 230000001488 breeding effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000027939 micturition Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- JZRWCGZRTZMZEH-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 3
- 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 2
- RBCOYOYDYNXAFA-UHFFFAOYSA-L (5-hydroxy-4,6-dimethylpyridin-3-yl)methyl phosphate Chemical compound CC1=NC=C(COP([O-])([O-])=O)C(C)=C1O RBCOYOYDYNXAFA-UHFFFAOYSA-L 0.000 description 2
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 230000004596 appetite loss Effects 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019197 fats Nutrition 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
- 238000010438 heat treatment Methods 0.000 description 2
- 235000021266 loss of appetite Nutrition 0.000 description 2
- 208000019017 loss of appetite Diseases 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000010902 straw Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 230000002485 urinary effect Effects 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 208000010444 Acidosis Diseases 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 208000037157 Azotemia Diseases 0.000 description 1
- 208000008035 Back Pain Diseases 0.000 description 1
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 208000007882 Gastritis Diseases 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 206010020649 Hyperkeratosis Diseases 0.000 description 1
- 208000001126 Keratosis Diseases 0.000 description 1
- FFEARJCKVFRZRR-UHFFFAOYSA-N L-Methionine Natural products CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
- XVOYSCVBGLVSOL-UHFFFAOYSA-N L-cysteine sulfonic acid Natural products OC(=O)C(N)CS(O)(=O)=O XVOYSCVBGLVSOL-UHFFFAOYSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- 229930195722 L-methionine Natural products 0.000 description 1
- 206010024652 Liver abscess Diseases 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
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 241000282849 Ruminantia Species 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 241001125046 Sardina pilchardus Species 0.000 description 1
- 241000269821 Scombridae Species 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
- 206010046530 Urinary bladder rupture Diseases 0.000 description 1
- 206010046555 Urinary retention Diseases 0.000 description 1
- 210000003165 abomasum Anatomy 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 230000007950 acidosis Effects 0.000 description 1
- 208000026545 acidosis disease Diseases 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- MXZRMHIULZDAKC-UHFFFAOYSA-L ammonium magnesium phosphate Chemical compound [NH4+].[Mg+2].[O-]P([O-])([O-])=O MXZRMHIULZDAKC-UHFFFAOYSA-L 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003674 animal food additive Substances 0.000 description 1
- 208000022531 anorexia Diseases 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- FDJOLVPMNUYSCM-UVKKECPRSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2,7, Chemical compound [Co+3].N#[C-].C1([C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)[N-]\C2=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 FDJOLVPMNUYSCM-UVKKECPRSA-L 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 206010061428 decreased appetite Diseases 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 235000013325 dietary fiber Nutrition 0.000 description 1
- 235000012888 dietary physiology Nutrition 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000002651 drug therapy Methods 0.000 description 1
- 230000002349 favourable effect Effects 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
- 235000013305 food Nutrition 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 238000005534 hematocrit Methods 0.000 description 1
- 208000027701 hepatic abscess Diseases 0.000 description 1
- 244000038280 herbivores Species 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 235000020640 mackerel Nutrition 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- 229960004452 methionine Drugs 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000035935 pregnancy Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 239000010686 shark liver oil Substances 0.000 description 1
- 229940069764 shark liver oil Drugs 0.000 description 1
- GJPYYNMJTJNYTO-UHFFFAOYSA-J sodium aluminium sulfate Chemical compound [Na+].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GJPYYNMJTJNYTO-UHFFFAOYSA-J 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052567 struvite Inorganic materials 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 208000009852 uremia Diseases 0.000 description 1
- 208000014001 urinary system disease Diseases 0.000 description 1
- 210000001635 urinary tract Anatomy 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
Landscapes
- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、脂肪酸カルシウ
ム、水溶性ビタミン群ならびに塩化ナトリウムおよび/
または塩化カリウムを併用した尿石症治療効果を有する
飼料組成物、ならびにその製造方法に関し、詳しくはル
ーメン微生物に影響を与えず、かつエネルギー源を効率
的に供給できる尿石症治療用飼料組成物およびその製造
方法に関する。TECHNICAL FIELD The present invention relates to a fatty acid calcium, a water-soluble vitamin group, and sodium chloride and / or sodium chloride.
Or a feed composition having a therapeutic effect on urolithiasis combined with potassium chloride, and a method for producing the same, in particular, a feed composition for treating urolithiasis which does not affect rumen microorganisms and can efficiently supply an energy source And its manufacturing method.
【0002】[0002]
【従来の技術】近年、牛の肥育に関して、単位面積当た
りの生産力向上および飼育管理の効率化を行うため、高
密度飼育方式が追究されており、これに伴う濃厚飼料多
給によって肥育効率を上げたり、大麦の多給によって肉
質の改善を図るなどの集約化が進んでいる。このように
非草食動物的な飼育が行われるようになって以来、ルー
メンアシドーシス、第一胃角化不全症、第一胃炎、鼓張
症、第四胃変位、肝膿症などの消化器疾患が増え、また
蹄葉炎その他の四肢疾患が報告されている。2. Description of the Related Art In recent years, with regard to fattening of cattle, a high-density breeding method has been pursued in order to improve productivity per unit area and to improve the efficiency of breeding management. Increasing the number of barleys and increasing barley to improve meat quality are being concentrated. Since such non-herbivore breeding has started, digestive disorders such as rumen acidosis, rumen keratosis, rumen gastritis, bloat, abomasum displacement, and hepatic abscess Have been reported, and laminitis and other limb disorders have been reported.
【0003】濃厚飼料は、セルロース含量が少なく消化
が良いことから、泌尿、妊娠、肥育といった生産に必要
なエネルギー源として、粗飼料に適量添加して家畜に与
えるのが望ましい使用方法であるが、多頭飼育、省力管
理が追究されると、濃厚飼料に依存しすぎ、その過剰給
与による弊害が現れやすい。尿石症もそのひとつと考え
られている。[0003] Since concentrated feed has a low cellulose content and is easily digested, it is a desirable method to use it as a source of energy necessary for production such as urination, pregnancy, and fattening, and to give it to livestock by adding an appropriate amount to roughage. When breeding and labor-saving management are pursued, reliance on concentrated feed is excessive, and the adverse effects of overfeeding are likely to appear. Urolithiasis is also considered one of them.
【0004】我が国の肥育牛に多発している尿石症は、
リン酸マグネシウム・アンモニウムを主成分とするリン
酸型であり、結石の沈着による尿路系の障害である。初
期には、雄牛で陰毛に微細な灰白色の結石の付着を認
め、重症では排尿が困難になり食欲不振、元気消失、食
欲廃絶、腰部疼痛、尿閉等を訴え、膀胱破裂、尿毒症な
どにより死亡することがある。尿中には多量の結石沈殿
がみられる。尿石症は、通常雄去勢牛の18〜30か月
齢の若齢牛での発生が多く、尿石症の発生に月齢差はな
くなってきている。Urolithiasis, which frequently occurs in fattening cattle in Japan,
It is a phosphoric acid type containing magnesium ammonium phosphate as a main component, and is a disorder of the urinary system due to the deposition of stones. In the early stage, fine grayish white stones were observed on the pubic hair of bulls, and in severe cases, urination was difficult, complaining of anorexia, loss of appetite, loss of appetite, lumbar pain, urinary retention, etc., bladder rupture, uremia, etc. May cause death. A large amount of calculus precipitate is seen in urine. Urolithiasis usually occurs more often in young steers of 18 to 30 months of steers, and there is no difference in the age at which urolithiasis occurs.
【0005】このような問題を解決するため、この治療
剤として、特開平4−208227号には、塩化アンモ
ニウムとウラジロガシエキスを主成分とする尿石症予防
治療剤、特開昭63−87948号には、ウラジロガシ
エキスおよびサイクロデキストリンを含有する家畜用の
尿石症予防治療剤、特開昭62−61921号には、硝
酸アンモニウムを含有する尿石症治療剤が記載されてい
る。[0005] In order to solve such problems, Japanese Patent Application Laid-Open No. 4-208227 discloses a therapeutic agent for preventing and treating urolithiasis comprising ammonium chloride and Virginia oak extract as main components. Discloses a preventive and therapeutic agent for urolithiasis for domestic animals containing a vulgaris extract and cyclodextrin, and JP-A-62-61921 describes a therapeutic agent for urolithiasis containing ammonium nitrate.
【0006】また、これ以外にも尿石症予防治療剤とし
て特開平6−298641号には可食性カルボン酸およ
び可食性オキシカルボン酸またはその塩を利用したペッ
トの尿石症治療剤および予防剤、特開平7−33678
号には尿石症予防および治療効果を有する茶葉抽出エキ
ス、特開昭58−67624号には尿酸性化剤としてD
L−メチオニンを使用した猫泌尿器系症候群の予防方
法、特開昭64−66123号には尿石症の治療のため
のコロイド状水溶性重合アルカンカルボン酸を含有する
非経口薬学的組成物、特開昭61−140522号には
リン酸塩結石を抑制するL−システイン酸付加塩、特開
昭61−17517号には非イオン系界面活性剤を有効
成分とする尿酸塩、混合尿酸塩結合症用薬剤が記載され
ている。また特開昭62−19153号には、膨張剤と
してセメントコンクリート、生石灰などを利用して水和
反応を起こし、膨張圧を発現する結石破壊剤が記載さ
れ、特開昭54−22993号には、カテーテル内部に
尿結石分解作用を及ぼす超音波による作動素子を含んだ
尿結石分解装置が記載されている。[0006] In addition, as a prophylactic / therapeutic agent for urolithiasis, Japanese Patent Application Laid-Open No. 6-298641 discloses a therapeutic and prophylactic agent for pet urolithiasis using edible carboxylic acid and edible oxycarboxylic acid or a salt thereof. JP-A-7-33678
JP-A-58-67624 discloses D as a urine acidifying agent.
A method for preventing cat urinary system syndrome using L-methionine, JP-A-64-66123 discloses a parenteral pharmaceutical composition containing a colloidal water-soluble polymerized alkanecarboxylic acid for treating urolithiasis. JP-A-61-140522 discloses an L-cysteic acid addition salt which inhibits phosphate stones, and JP-A-61-17517 discloses a urate containing a nonionic surfactant as an active ingredient. Drugs are described. JP-A-62-19153 describes a calculus breaking agent which causes a hydration reaction by using cement concrete, quick lime or the like as an expanding agent and develops an expanding pressure. A urinary stone disintegrating device including an ultrasonic operating element that exerts a urinary stone decomposing action inside a catheter is described.
【0007】[0007]
【発明が解決しようとする課題】しかし、尿石症の治療
のための薬物療法として従来行われてきた塩化アンモニ
ウム単独あるいはビタミンB1、ビタミンB2などとの混
合剤の投与は、結石の症状やその効果にバラツキがあり
治療効果が思わしくない。これはこれらの薬剤を用いる
と牛の栄養生理にとって極めて重要な役割を担っている
ルーメン微生物が減少するため菌体由来の栄養供給が減
少したり、牛自体の採食量が減少するので、結果的にエ
ネルギー不足となり、充分な効果が得られないものと考
えられている。またエネルギー、その他の栄養素が不足
すると結果的に肥育期間が延長され、生産性が大幅に低
下するという問題も起こっている。[SUMMARY OF THE INVENTION] However, ammonium chloride has been conventionally performed as a drug therapy alone or in vitamin B 1 for the treatment of urolithiasis, administration of admixture with such as vitamin B 2, symptoms of stones And its effects vary, and the therapeutic effect is poor. This is because the use of these drugs reduces the number of rumen microorganisms, which play an extremely important role in the nutritional physiology of cattle, thereby reducing nutrient supply from bacterial cells and reducing the amount of food consumed by the cow itself. It is considered that the energy becomes insufficient and the effect cannot be obtained sufficiently. Insufficient energy and other nutrients also result in a prolonged fattening period and a significant decrease in productivity.
【0008】ウラジロガシエキスによる尿石症治療にお
いては、主原料のウラジロガシエキスの大量入手が困難
であり、またこの混合飼料を牛が激しく忌避するなどの
理由により実用的ではない。外科手術による結石の除去
は、生産性の低下につながり、また再発の可能性が高
く、適当な治療方法とはいえない。このように、肥育農
家が国際的な競争力を培うため、生産性や肉質の向上を
目ざし、安定した経営を営む上で尿石症の治療方法の改
良および確立が急務となっている。[0008] In the treatment of urolithiasis with the urajirogashi extract, it is difficult to obtain a large amount of the urajirogashi extract as a main raw material, and it is not practical because cattle violently avoid this mixed feed. Removal of stones by surgery leads to reduced productivity and a high likelihood of recurrence, and is not an appropriate treatment. As described above, fattening farmers aim to improve productivity and meat quality in order to cultivate international competitiveness, and to carry out stable management, there is an urgent need to improve and establish treatment methods for urolithiasis.
【0009】従って、本発明が解決しようとする課題
は、短期間で尿石症治療の効果が得られ、かつ尿石症治
療用飼料組成物投与に起因する栄養素不足を防止して、
肥育期間および生産効率を維持することができる尿石症
治療用飼料組成物およびその製造方法を提供することで
ある。Accordingly, an object of the present invention is to provide an effect of treating urolithiasis in a short period of time and prevent nutrient deficiency caused by administration of a feed composition for treating urolithiasis.
An object of the present invention is to provide a feed composition for treating urolithiasis which can maintain a fattening period and production efficiency, and a method for producing the same.
【0010】[0010]
【課題を解決するための手段】本発明は次の尿石症治療
用飼料組成物およびその製造方法である。 (1) 脂肪酸カルシウム100重量部に対して、水溶
性ビタミン0.1〜20重量部、ならびに塩化ナトリウ
ムおよび/または塩化カリウム1〜80重量部を含有す
ることを特徴とする尿石症治療用飼料組成物。 (2) 加熱して溶融させた脂肪酸80重量部に対し
て、水溶性ビタミン0.1〜20重量部、ならびに塩化
ナトリウムおよび/または塩化カリウム1〜80重量部
を添加した後、酸化カルシウム5〜40重量部を添加し
て混合し、次に水5〜50重量部を加えて混合すること
を特徴とする上記(1)記載の尿石症治療用飼料組成物
の製造方法。The present invention provides the following feed composition for treating urolithiasis and a method for producing the same. (1) A feed for treating urolithiasis, comprising 0.1 to 20 parts by weight of a water-soluble vitamin and 1 to 80 parts by weight of sodium chloride and / or potassium chloride with respect to 100 parts by weight of fatty acid calcium. Composition. (2) 0.1 to 20 parts by weight of a water-soluble vitamin and 1 to 80 parts by weight of sodium chloride and / or potassium chloride are added to 80 parts by weight of a fatty acid melted by heating, and then calcium oxide 5 to 20 parts by weight is added. A method for producing a feed composition for treating urolithiasis according to the above (1), wherein 40 parts by weight are added and mixed, and then 5 to 50 parts by weight of water are added and mixed.
【0011】本発明で使用する脂肪酸カルシウムは特に
限定はなく、例えば牛脂、豚脂などの動物性油脂;鰯
油、鯖油、鮫肝油、鱈肝油、鯨油などの水産動物油脂;
キリ油、菜種油、大豆油、ひまわり油、サフラワー油、
アマニ油、パーム油、パーム核油等の植物性油脂などを
加水分解して製造した脂肪酸を出発原料とし、直接法や
複分解法によって製造される脂肪酸カルシウムである。
この脂肪酸カルシウムの粒径としては、通常3mm以下
であるのが好ましく、これより大きなものは、成形する
前に粉砕しておくのが好ましい。また、この脂肪酸カル
シウムは常温で固体であるため、液体油に比べて配合、
給与時の作業性がよい。The fatty acid calcium used in the present invention is not particularly limited. For example, animal fats and oils such as beef tallow and lard; marine animal fats such as sardine oil, mackerel oil, shark liver oil, cod liver oil and whale oil;
Kiri oil, rapeseed oil, soybean oil, sunflower oil, safflower oil,
Fatty acid calcium produced by a direct method or a metathesis method using a fatty acid produced by hydrolyzing vegetable oils such as linseed oil, palm oil and palm kernel oil as a starting material.
The particle size of the fatty acid calcium is generally preferably 3 mm or less, and the larger one is preferably ground before molding. Also, since this fatty acid calcium is solid at normal temperature, it is blended compared to liquid oil,
Good workability at the time of salary.
【0012】本発明で使用する水溶性ビタミンには食品
添加物用、飼料添加物用に市販されている水溶性ビタミ
ン類が使用でき、ビタミンB1、ビタミンB2、ビタミン
B6、ビタミンB12、ナイアシン、パントテン酸、葉
酸、ビオチンおよびコリンなどがあげられる。これらは
1種単独で使用することもできるし、2種以上を組合せ
て使用することもできる。これらの中ではビタミン
B1、ビタミンB2、ビタミンB6からなる群より選ばれ
た1種以上のビタミンを用いるのが好ましい。これらの
ビタミンの使用量は、脂肪酸カルシウム100重量部に
対して、0.1〜20重量部、好ましくは1〜15重量
部である。0.1重量部未満の場合は、尿石症治療剤と
しての効果が小さい。また20重量部を越えて給与して
も、尿石症治療剤としての効果向上は小さい。As the water-soluble vitamin used in the present invention, commercially available water-soluble vitamins for food additives and feed additives can be used, and vitamin B 1 , vitamin B 2 , vitamin B 6 and vitamin B 12 , Niacin, pantothenic acid, folic acid, biotin and choline. These can be used alone or in combination of two or more. Among these, it is preferable to use at least one vitamin selected from the group consisting of vitamin B 1 , vitamin B 2 and vitamin B 6 . The use amount of these vitamins is 0.1 to 20 parts by weight, preferably 1 to 15 parts by weight, based on 100 parts by weight of fatty acid calcium. When the amount is less than 0.1 part by weight, the effect as a therapeutic agent for urolithiasis is small. Further, even if the amount is more than 20 parts by weight, the improvement in the effect as a therapeutic agent for urolithiasis is small.
【0013】本発明で用いる塩化ナトリウムまたは塩化
カリウムは特に限定はなく、一般に市販されているもの
を用いることができる。これらの使用量は、脂肪酸カル
シウム100重量部に対して、1〜80重量部、好まし
くは30〜70重量部である。1重量部未満の場合は、
尿石症治療剤としての効果が小さい。また80重量部を
越えて給与しても、尿石症治療剤としての効果は小さ
い。The sodium chloride or potassium chloride used in the present invention is not particularly limited, and generally commercially available ones can be used. These are used in an amount of 1 to 80 parts by weight, preferably 30 to 70 parts by weight, based on 100 parts by weight of the fatty acid calcium. If less than 1 part by weight,
The effect as a therapeutic agent for urolithiasis is small. Further, even if the amount is more than 80 parts by weight, the effect as a therapeutic agent for urolithiasis is small.
【0014】本発明の尿石症治療用飼料組成物は、牛な
どの反芻動物に経口投与することにより、尿石症の予防
および治療を効果的に行うことができる。この場合、投
与された動物の体重増加は順調であり、肥育期間および
生産効率は低下しない。体重増加が順調な理由は、ルー
メン微生物菌体数が減少せず、菌体由来の栄養供給が十
分に行われるためであると推測される。The feed composition for treating urolithiasis of the present invention can effectively prevent and treat urolithiasis by orally administering it to ruminants such as cattle. In this case, the weight gain of the administered animals is smooth and the fattening period and production efficiency do not decrease. It is presumed that the reason why the weight increase is favorable is that the number of rumen microbial cells does not decrease and nutrients derived from the cells are sufficiently supplied.
【0015】本発明の尿石症治療用飼料組成物の製造方
法は、加熱して溶融させた脂肪酸80重量部に対して、
前記水溶性ビタミン0.1〜20重量部、好ましくは1
〜15重量部、ならびに塩化ナトリウムおよび/または
塩化カリウム1〜80重量部、好ましくは30〜70重
量部を添加した後、酸化カルシウム5〜40重量部、好
ましくは10〜35重量部を添加して良く攪拌する。さ
らに水5〜50重量部、好ましくは10〜45重量部を
加えよく攪拌して脂肪酸と酸化カルシウムを反応させて
脂肪酸カルシウムを生成させることにより、尿石症治療
用飼料組成物が得られる。反応後は1〜2時間後に70
〜80℃で3〜4時間熱風乾燥するのが好ましい。The method for producing a feed composition for treating urolithiasis of the present invention comprises the steps of:
0.1 to 20 parts by weight of the water-soluble vitamin, preferably 1
-15 parts by weight, and 1-80 parts by weight of sodium chloride and / or potassium chloride, preferably 30-70 parts by weight, and then 5-40 parts by weight of calcium oxide, preferably 10-35 parts by weight. Stir well. Further, 5 to 50 parts by weight, preferably 10 to 45 parts by weight of water is added, and the mixture is stirred well to cause the fatty acid and calcium oxide to react to generate fatty acid calcium, whereby a feed composition for treating urolithiasis can be obtained. After 1-2 hours, 70
It is preferable to dry with hot air at 8080 ° C. for 3 to 4 hours.
【0016】尿石症治療剤としての使用に際しては、尿
石症の症状を呈する初中期あるいは後期までに本発明の
飼料組成物を体重100kg当たり5〜300g/日、
好ましくは10〜250g/日の範囲内で、7〜21日
間経口投与するのが好ましい。なお本発明で用いる基礎
飼料には特に限定はなく、一般に市販されている肉牛用
配合飼料などを用いる。使用量は8〜12kg/日/頭
の範囲である。When used as a therapeutic agent for urolithiasis, the feed composition of the present invention is administered in an amount of 5 to 300 g / day per 100 kg of body weight by the first or middle stage showing symptoms of urolithiasis.
Oral administration is preferably performed within a range of 10 to 250 g / day for 7 to 21 days. The basic feed used in the present invention is not particularly limited, and a commercially available mixed feed for beef cattle or the like is used. The amount used ranges from 8 to 12 kg / day / head.
【0017】[0017]
【発明の実施の形態】以下に、配合例、比較例、実施例
を用いてより具体的に説明する。 《基礎飼料》表1に示す組成で肥育牛用飼料の基礎飼料
を配合した。DETAILED DESCRIPTION OF THE INVENTION The present invention will be described more specifically with reference to formulation examples, comparative examples, and examples. << Basic feed >> A basic feed for fattening cattle was blended with the composition shown in Table 1.
【表1】 [Table 1]
【0018】《比較例用試料》対照区用試料として下記
の表2に示す組成で飼料組成物を調製し、これをそれぞ
れ試料1〜6とした。<< Samples for Comparative Examples >> Feed compositions were prepared with the compositions shown in Table 2 below as samples for the control, and these were designated as Samples 1 to 6, respectively.
【表2】 [Table 2]
【0019】《実施例用試料》表3に示した組成で試料
を調製した。得られたものを試料7〜9とした。<< Samples for Examples >> Samples having the compositions shown in Table 3 were prepared. The obtained ones were designated as Samples 7 to 9.
【表3】 [Table 3]
【0020】《実施例用試料》下記の表4または表5に
示す組成で飼料組成物を調製し、これをそれぞれ試料1
0〜18とした。調製方法は加熱して溶融させた脂肪酸
80重量部に水溶性ビタミン、ならびに塩化ナトリウム
および/または塩化カリウムを添加した後、酸化カルシ
ウム30重量部を添加して良く攪拌した。さらに水40
重量部を加えてよく攪拌して脂肪酸と酸化カルシウムを
反応させた。1時間後に80℃、3時間熱風乾燥して飼
料組成物を得た。<< Samples for Examples >> A feed composition was prepared with the composition shown in Table 4 or Table 5 below, and
0 to 18. The method of preparation was such that after adding a water-soluble vitamin and sodium chloride and / or potassium chloride to 80 parts by weight of the fatty acid melted by heating, 30 parts by weight of calcium oxide was added, followed by thorough stirring. More water 40
The fatty acid and calcium oxide were allowed to react with each other by adding parts by weight and stirring well. One hour later, the mixture was dried with hot air at 80 ° C. for 3 hours to obtain a feed composition.
【0021】[0021]
【表4】 [Table 4]
【0022】[0022]
【表5】 [Table 5]
【0023】実施例1および比較例1《尿石症牛への投
与による治療効果試験》 試料1〜18を用いて以下の方法で尿石症治療効果試験
を行った。まず、尿石症と診断された10か月齢ホルス
タイン種去勢牛54頭を供試し、各3頭の18群に分け
た。試料1〜18をそれぞれ体重100kg当たり20
0gとなるように各群に2週間にわたって強制経口投与
し、それぞれ投与前、投与開始から4日後、8日後、1
4日後(製剤投与終了)、21日後(基礎飼料のみ)の
尿を採取した。なお、表1に示した基礎飼料4kgと稲
わら(2cmにカット)4kgを1日の給餌分とし、試
験期間中給与を行った。尿石症の程度の診断法として、
尿のpHおよび尿中のリン酸塩結晶値(UPV:Urinay
Phosphate Volume)を測定した。これはリン酸塩類
(カルシウム塩、マグネシウム塩)を主成分とする尿路
結石の排出量を尿中のリン酸塩結晶値(UPV)をもと
に判断する方法である。得られた結果を下記の表6およ
び表7に示す。Example 1 and Comparative Example 1 << Therapeutic effect test by administration to urolithiasis cattle >> Using Specimens 1 to 18, a therapeutic effect test for urolithiasis was performed in the following manner. First, 54 10-month-old Holstein steers diagnosed with urolithiasis were tested and divided into 18 groups of 3 each. Samples 1 to 18 were each added to 20
Each group was gavage-administered orally to each group for 2 weeks before administration, and 4 days and 8 days after the start of administration, respectively.
Urine was collected after 4 days (end of preparation administration) and 21 days after (basal feed only). In addition, 4 kg of the basic feed shown in Table 1 and 4 kg of rice straw (cut to 2 cm) were used as a daily feed, and were fed during the test period. As a diagnostic method for the degree of urolithiasis,
Urine pH and urinary phosphate crystal level (UPV: Urinay)
Phosphate Volume) was measured. This is a method of judging the amount of urinary calculus mainly composed of phosphates (calcium salt and magnesium salt) based on the phosphate crystal value (UPV) in urine. The obtained results are shown in Tables 6 and 7 below.
【0024】なお、尿中のリン酸塩結晶値(UPV)
は、ヘマトクリット測定法に準じて次のようにして測定
した。採取した尿の上清2mLに1Mアンモニア水2m
Lを加え、30分間放置後、これを5000rpmで5
分間遠心分離した。上澄みの10分の9量を除去し、残
留分をよく振った後、ヘマトクリック用毛細管に入れ、
3000rpmで10分間遠心分離した。ヘマトクリッ
ク用毛細管中の試料全体の高さに対する結晶の高さを測
定し、これを尿中のリン酸塩結晶値(UPV)として
「%」で表示した。この分析値は、数値が高いほど尿路
系中の結石がより多く溶解し、排尿時にリン酸塩として
溶出していることを示している。従って、リン酸塩結晶
値が高いほど尿石症治療効果が高いことを意味してい
る。The phosphate crystal value in urine (UPV)
Was measured as follows according to a hematocrit measurement method. 2M of 1M ammonia water is added to 2mL of the collected urine supernatant.
L and left for 30 minutes.
Centrifuged for minutes. After removing 9/10 volume of the supernatant and shaking the residue well, put into a hematoctic capillary,
Centrifuged at 3000 rpm for 10 minutes. The crystal height relative to the height of the entire sample in the hematoctic capillary was measured, and this was expressed as "%" as a phosphate crystal value (UPV) in urine. This analysis indicates that the higher the number, the more the stones in the urinary tract are dissolved and elute as phosphate during urination. Therefore, it means that the higher the phosphate crystal value, the higher the effect of treating urolithiasis.
【0025】[0025]
【表6】 ※3頭の平均値[Table 6] * Average value of three animals
【0026】[0026]
【表7】 ※3頭の平均値[Table 7] * Average value of three animals
【0027】結果は表6および表7に示す通り、リン酸
塩を核とした結石を有する尿石症の牛の尿は投与前には
pHがアルカリ性を呈しているが実施例の製剤を投与す
ることにより投与開始から4日後、8日後、14日後、
21日後に採取した尿はpHがアルカリ性から中性、弱
酸性域に移行している。また比較例の製剤を投与するよ
りも実施例の製剤投与によりpHがアルカリ性から中
性、弱酸性域に移行するまでの日数が短くなった。As shown in Tables 6 and 7, the urine of urolithic cattle having a stone with phosphate as a nucleus had an alkaline pH before administration. 4 days, 8 days, 14 days,
The urine collected after 21 days has shifted its pH from alkaline to neutral and weakly acidic. The administration of the preparation of the example shortened the number of days required for the pH to shift from an alkaline to a neutral or weakly acidic range, compared to the administration of the preparation of the comparative example.
【0028】実施例の製剤を投与することによりリン酸
塩結晶値(UPV)は、投与前と比較し増加傾向を示し
た。また、比較例の製剤を投与するよりも短期間でリン
酸塩結晶値が増加した。以上の結果より尿石症の牛に本
発明の製剤を投与すると尿中のリン酸塩を核とした結石
が溶解し、尿中に溶出したことからリン酸塩結晶値が上
昇したものと考えられる。また、それに伴ない、尿のp
Hが正常範囲となり、結石ができにくい状態に改善され
たものと考えられる。By administering the preparations of the examples, the phosphate crystal value (UPV) showed an increasing tendency as compared with that before the administration. In addition, the phosphate crystal value increased in a shorter period of time than when the preparation of the comparative example was administered. From the above results, it is considered that the administration of the preparation of the present invention to cattle with urolithiasis caused phosphate stones in the urine to dissolve and eluted in the urine, indicating that phosphate crystal values increased. Can be In addition, the urine p
It is considered that H was in the normal range, and the stone was improved to a state where calculus was hardly formed.
【0029】実施例2および比較例2《尿石症牛への投
与による増体量試験》 体重約500kgのホルスタイン種去勢牛54頭を3頭
ずつ18区に分け試料1〜18を体重100kg当たり
10gを3週間にわたって強制経口投与し、それぞれ投
与前、投与開始から14日後、投与21日後(製剤投与
終了)、投与28日後(基礎飼料のみ)の体重を測定し
た。また、試験中の増体量についても測定を行った。な
お試験期間中に基礎飼料を8kg/日、稲わらを4kg
/日給与した。得られた結果を表8に示した。Example 2 and Comparative Example 2 << Tissue Weight Gain Test by Administration to Urolithiatous Cattle >> 54 Holstein steers with a body weight of about 500 kg were divided into 3 groups of 18 cows, and Samples 1 to 18 were weighed per 100 kg of body weight. 10 g was orally administered by gavage for 3 weeks, and the body weight was measured before administration, 14 days after administration, 21 days after administration (end of preparation administration), and 28 days after administration (basal feed only). The weight gain during the test was also measured. During the test period, 8 kg / day of basal feed and 4 kg of rice straw
/ Day salary. Table 8 shows the obtained results.
【0030】[0030]
【表8】 ※3頭の平均値を記載 ※増体量(kg/日)=(28日目の体重−0日目の体重)/28日[Table 8] * Average value of three animals is described. * Weight gain (kg / day) = (weight on day 28-weight on day 0) / 28 days
【0031】表8より比較例に比べて試料10〜18を
給与した実施例は給与期間も順調に体重の増加がみられ
た。また、比較例に比べて増体量も高いことから本発明
の製剤投与による増体低下はないものと考えられる。順
調な体重の増加が認められる理由は、ルーメン微生物菌
体数が減少せず、菌体由来の栄養供給が十分に行われて
いるためと推測される。As can be seen from Table 8, in Examples in which Samples 10 to 18 were fed as compared with Comparative Examples, the body weight increased smoothly during the feeding period. In addition, since the body weight gain was higher than that of the comparative example, it is considered that the body weight gain was not reduced by administration of the preparation of the present invention. The reason why a steady increase in body weight is observed is presumed to be because the number of rumen microbial cells did not decrease and nutrients derived from the cells were sufficiently supplied.
【0032】[0032]
【発明の効果】本発明の尿石症治療用飼料組成物は、脂
肪酸カルシウム、ビタミン群ならびに塩化ナトリウムお
よび/または塩化カリウムを併用しているので、尿石症
の治療に効果を有している。また、増体量の低下も抑え
られ、健全な肥育が行える。本発明の尿石症治療用飼料
組成物の製造方法は、上記飼料組成物を容易に効率よく
製造することができる。The feed composition for the treatment of urolithiasis according to the present invention is effective for the treatment of urolithiasis since it uses calcium fatty acids, vitamins and sodium chloride and / or potassium chloride in combination. . In addition, a decrease in the body weight gain is suppressed, and healthy fattening can be performed. The method for producing a feed composition for treating urolithiasis of the present invention can easily and efficiently produce the above feed composition.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 深山 雅彦 兵庫県神戸市北区山田町小部字南山2− 545−302 (72)発明者 吉田 恒典 福島県福島市下鳥渡字扇田17番地1 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Masahiko Miyama 2-545-302 Minamiyama, Kobe, Yamada-cho, Kita-ku, Kobe-shi, Hyogo (72) Inventor Tsuneori Yoshida 17-1 Ogita, Shimodori-Watari, Fukushima-shi, Fukushima
Claims (2)
て、水溶性ビタミン0.1〜20重量部、ならびに塩化
ナトリウムおよび/または塩化カリウム1〜80重量部
を含有することを特徴とする尿石症治療用飼料組成物。1. A treatment for urolithiasis, comprising 0.1 to 20 parts by weight of a water-soluble vitamin and 1 to 80 parts by weight of sodium chloride and / or potassium chloride with respect to 100 parts by weight of a fatty acid calcium. Feed composition.
対して、水溶性ビタミン0.1〜20重量部、ならびに
塩化ナトリウムおよび/または塩化カリウム1〜80重
量部を添加した後、酸化カルシウム5〜40重量部を添
加して混合し、次に水5〜50重量部を加えて混合する
ことを特徴とする請求項1記載の尿石症治療用飼料組成
物の製造方法。2. A method according to claim 1, wherein 0.1 to 20 parts by weight of a water-soluble vitamin and 1 to 80 parts by weight of sodium chloride and / or potassium chloride are added to 80 parts by weight of the molten fatty acid. The method for producing a feed composition for treating urolithiasis according to claim 1, wherein 5 to 40 parts by weight are added and mixed, and then 5 to 50 parts by weight of water are added and mixed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9142299A JPH10327766A (en) | 1997-05-30 | 1997-05-30 | Feed composition for treatment of urolithiasis and its production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9142299A JPH10327766A (en) | 1997-05-30 | 1997-05-30 | Feed composition for treatment of urolithiasis and its production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH10327766A true JPH10327766A (en) | 1998-12-15 |
Family
ID=15312156
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9142299A Pending JPH10327766A (en) | 1997-05-30 | 1997-05-30 | Feed composition for treatment of urolithiasis and its production |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH10327766A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6924382B2 (en) | 2003-05-06 | 2005-08-02 | Nusci Laboratories Llc | Rumen bypass calcium salts of C18:1 and C18:2 fatty acids |
| WO2007065097A1 (en) * | 2005-11-29 | 2007-06-07 | Hill's Pet Nutrition, Inc. | Composition and method for preventing or treating urolithiasis |
| US8093415B2 (en) | 2001-11-16 | 2012-01-10 | Virtus Nutrition Llc | Polyunsaturated fatty acid monovalent and divalent metal salt synthesis |
| US8278354B2 (en) | 2001-11-14 | 2012-10-02 | Virtus Nutrition Llc | Method for increasing ruminant fertility |
-
1997
- 1997-05-30 JP JP9142299A patent/JPH10327766A/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8278354B2 (en) | 2001-11-14 | 2012-10-02 | Virtus Nutrition Llc | Method for increasing ruminant fertility |
| US8093415B2 (en) | 2001-11-16 | 2012-01-10 | Virtus Nutrition Llc | Polyunsaturated fatty acid monovalent and divalent metal salt synthesis |
| US6924382B2 (en) | 2003-05-06 | 2005-08-02 | Nusci Laboratories Llc | Rumen bypass calcium salts of C18:1 and C18:2 fatty acids |
| WO2007065097A1 (en) * | 2005-11-29 | 2007-06-07 | Hill's Pet Nutrition, Inc. | Composition and method for preventing or treating urolithiasis |
| JP2009517484A (en) * | 2005-11-29 | 2009-04-30 | ヒルズ・ペット・ニュートリシャン・インコーポレーテッド | Compositions and methods for preventing or treating urolithiasis |
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