JPS6232726B2 - - Google Patents
Info
- Publication number
- JPS6232726B2 JPS6232726B2 JP4982080A JP4982080A JPS6232726B2 JP S6232726 B2 JPS6232726 B2 JP S6232726B2 JP 4982080 A JP4982080 A JP 4982080A JP 4982080 A JP4982080 A JP 4982080A JP S6232726 B2 JPS6232726 B2 JP S6232726B2
- Authority
- JP
- Japan
- Prior art keywords
- hdl
- ldl
- trapidil
- cholesterol
- hyperlipidemia
- 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
- 108010010234 HDL Lipoproteins Proteins 0.000 claims description 37
- 102000015779 HDL Lipoproteins Human genes 0.000 claims description 37
- 230000000694 effects Effects 0.000 claims description 24
- 230000001965 increasing effect Effects 0.000 claims description 21
- 210000002966 serum Anatomy 0.000 claims description 18
- 230000037356 lipid metabolism Effects 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims 1
- GSNOZLZNQMLSKJ-UHFFFAOYSA-N Trapidil Chemical compound CCN(CC)C1=CC(C)=NC2=NC=NN12 GSNOZLZNQMLSKJ-UHFFFAOYSA-N 0.000 description 44
- 229960000363 trapidil Drugs 0.000 description 43
- 108010007622 LDL Lipoproteins Proteins 0.000 description 29
- 102000007330 LDL Lipoproteins Human genes 0.000 description 29
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 28
- 108010023302 HDL Cholesterol Proteins 0.000 description 26
- 208000031226 Hyperlipidaemia Diseases 0.000 description 26
- 108010028554 LDL Cholesterol Proteins 0.000 description 22
- 239000002960 lipid emulsion Substances 0.000 description 17
- 206010003210 Arteriosclerosis Diseases 0.000 description 15
- 208000011775 arteriosclerosis disease Diseases 0.000 description 15
- 241000700159 Rattus Species 0.000 description 13
- 235000012000 cholesterol Nutrition 0.000 description 13
- 235000009200 high fat diet Nutrition 0.000 description 13
- 241000283973 Oryctolagus cuniculus Species 0.000 description 12
- 150000002632 lipids Chemical class 0.000 description 12
- 238000000034 method Methods 0.000 description 10
- 241000699670 Mus sp. Species 0.000 description 9
- 210000004369 blood Anatomy 0.000 description 9
- 239000008280 blood Substances 0.000 description 9
- 230000003247 decreasing effect Effects 0.000 description 9
- 150000003626 triacylglycerols Chemical class 0.000 description 9
- 241000286209 Phasianidae Species 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- 238000011161 development Methods 0.000 description 6
- 235000005911 diet Nutrition 0.000 description 6
- 230000037213 diet Effects 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 108010013563 Lipoprotein Lipase Proteins 0.000 description 5
- 102000043296 Lipoprotein lipases Human genes 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 238000008214 LDL Cholesterol Methods 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000004006 olive oil Substances 0.000 description 4
- 235000008390 olive oil Nutrition 0.000 description 4
- 150000003904 phospholipids Chemical class 0.000 description 4
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241000699800 Cricetinae Species 0.000 description 3
- 206010020772 Hypertension Diseases 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- KNAHARQHSZJURB-UHFFFAOYSA-N Propylthiouracile Chemical compound CCCC1=CC(=O)NC(=S)N1 KNAHARQHSZJURB-UHFFFAOYSA-N 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- 150000001840 cholesterol esters Chemical class 0.000 description 3
- 238000006911 enzymatic reaction Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 235000019626 lipase activity Nutrition 0.000 description 3
- 235000019359 magnesium stearate Nutrition 0.000 description 3
- 208000031225 myocardial ischemia Diseases 0.000 description 3
- 229920001592 potato starch Polymers 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- ZEMGGZBWXRYJHK-UHFFFAOYSA-N thiouracil Chemical compound O=C1C=CNC(=S)N1 ZEMGGZBWXRYJHK-UHFFFAOYSA-N 0.000 description 3
- 201000001320 Atherosclerosis Diseases 0.000 description 2
- 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 2
- 102000004895 Lipoproteins Human genes 0.000 description 2
- 108090001030 Lipoproteins Proteins 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 208000008589 Obesity Diseases 0.000 description 2
- MZUSCVCCMHDHDF-UHFFFAOYSA-N P(=O)(=O)[W] Chemical compound P(=O)(=O)[W] MZUSCVCCMHDHDF-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000007059 acute toxicity Effects 0.000 description 2
- 231100000403 acute toxicity Toxicity 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
- 235000021240 caseins Nutrition 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 235000021588 free fatty acids Nutrition 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000010253 intravenous injection Methods 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000020824 obesity Nutrition 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000000391 smoking effect Effects 0.000 description 2
- 229950000329 thiouracil Drugs 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- RWJRFPUNLXBCML-UHFFFAOYSA-N 5-propyl-2-sulfanylidene-1h-pyrimidin-4-one Chemical compound CCCC1=CNC(=S)NC1=O RWJRFPUNLXBCML-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- YEKQSSHBERGOJK-UHFFFAOYSA-N Pyricarbate Chemical compound CNC(=O)OCC1=CC=CC(COC(=O)NC)=N1 YEKQSSHBERGOJK-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 102000000019 Sterol Esterase Human genes 0.000 description 1
- 108010055297 Sterol Esterase Proteins 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- -1 and mannitrate Substances 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 239000000935 antidepressant agent Substances 0.000 description 1
- 229940005513 antidepressants Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000003143 atherosclerotic effect Effects 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000731 choleretic agent Substances 0.000 description 1
- 150000001841 cholesterols Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000019700 dicalcium phosphate Nutrition 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 210000001723 extracellular space Anatomy 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 230000001404 mediated effect Effects 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
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229940070851 pyridinolcarbamate Drugs 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 1
- 150000003872 salicylic acid derivatives Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000003270 steroid hormone Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 230000000304 vasodilatating effect Effects 0.000 description 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4982080A JPS56147717A (en) | 1980-04-15 | 1980-04-15 | Lipid-metabolism improver |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4982080A JPS56147717A (en) | 1980-04-15 | 1980-04-15 | Lipid-metabolism improver |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56147717A JPS56147717A (en) | 1981-11-16 |
JPS6232726B2 true JPS6232726B2 (cs) | 1987-07-16 |
Family
ID=12841737
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4982080A Granted JPS56147717A (en) | 1980-04-15 | 1980-04-15 | Lipid-metabolism improver |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56147717A (cs) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS645734A (en) * | 1987-06-30 | 1989-01-10 | Besuto Eng Kk | Method and device for electrolytic burr removal |
JPH0627020U (ja) * | 1992-09-08 | 1994-04-12 | 西山ステンレスケミカル株式会社 | 複合電解研磨装置 |
-
1980
- 1980-04-15 JP JP4982080A patent/JPS56147717A/ja active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS645734A (en) * | 1987-06-30 | 1989-01-10 | Besuto Eng Kk | Method and device for electrolytic burr removal |
JPH0627020U (ja) * | 1992-09-08 | 1994-04-12 | 西山ステンレスケミカル株式会社 | 複合電解研磨装置 |
Also Published As
Publication number | Publication date |
---|---|
JPS56147717A (en) | 1981-11-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2328730C (en) | Treatment of iatrogenic and age-related hypertension and pharmaceutical compositions useful therein | |
JPH05503508A (ja) | アルギニンを用いる血中コレステロールを減少させる方法 | |
US6329361B1 (en) | High-dose chromic picolinate treatment of type II diabetes | |
SK10802001A3 (sk) | Esenciálne mastné kyseliny na prevenciu kardiovaskulárnych príhod | |
EP0019423A1 (en) | Pharmaceutical and dietary composition comprising gamma-linolenic acids | |
EP0087864B1 (en) | Pharmaceutical composition | |
WO2009089093A1 (en) | Thyroid hormone receptor agonists | |
US20010044469A1 (en) | Methods and pharmaceutical preparations for normalizing blood pressure with (-)-hydroxycitric acid | |
US5627172A (en) | Method for reduction of serum blood lipids or lipoprotein fraction | |
US20100323031A1 (en) | Synergistic combination to enhance blood glucose and insulin metabolism | |
US6441041B1 (en) | (-)-hydroxycitric acid for the prevention of osteoporosis | |
JPS6299323A (ja) | 高脂血症剤 | |
JPS6232726B2 (cs) | ||
US4861784A (en) | Use of oxoquinazoline derivatives in the treatment of hyperuricaemia | |
KR930001809B1 (ko) | 항 고지방 혈증제 | |
AU2019315823A1 (en) | New use of carbamate beta phenylethanolamine analogues for enhancing intracellular clearance of ldl cholesterol and for combining therapy with statins to enhance the efficacy and reduce adverse effects | |
Stamler et al. | The status of hormonal therapy for the primary and secondary prevention of atherosclerotic coronary heart disease | |
EP1156795A1 (en) | Use of succinic acid or salts thereof and method of treating insulin resistance | |
EP1648438A1 (en) | (-)-hydroxycitric acid for controlling inflammation | |
JP2616845B2 (ja) | システノール酸又はその胆汁酸抱合体を含有する血中コレステロール低下剤 | |
US20050182036A1 (en) | Medicinal composition containing an HMG-CoA reductase inhibitor | |
US20050009919A1 (en) | Treating cachexia and excessive catabolism with (-)-hydroxycitric acid | |
TWI322687B (en) | Combination of antidiabetic drugs | |
JP3035328B2 (ja) | 血中脂質低下剤 | |
ULC | Aldosterone Antagonist |