ABSTRACT
The tested drug cramizol exhibits lipid-lowering and anti-atherogenic effects. Cramizol reduces blood cholesterol and triglycerides. It also increases HDL and reduces the atherogenic index in rats with the chronic dyslipidemia model induced by a hypercholesterol diet. Cramizol is effective as a hypolipidemic agent and its efficiency is comparable with the reference drug, phenofibrate. Cramizol increases expression of the ApoA1 and ApoC2 genes, and also reduces expression of the Scarb1 gene in rats with experimentally induced hyperlipidemia. These mechanisms could be the basis of its hypolipidemic and anti-atherogenic actions.
Subject(s)
Dyslipidemias , Fenofibrate , Hyperlipidemias , Animals , Cholesterol, HDL , Dyslipidemias/drug therapy , Dyslipidemias/genetics , Hyperlipidemias/drug therapy , Hypolipidemic Agents/pharmacology , Hypolipidemic Agents/therapeutic use , Rats , Triglycerides/metabolismABSTRACT
An imidazole derivative cramizol, has lipid-lowering and anti-atherogenic effects. Cramizol reduces blood levels of cholesterol and triglycerides, and also reduces the atherogenic index in animals with acute hyperlipidemia induced by Triton WR-1339. Cramizol and the lipid-lowering drug fenofibrate exhibited similar effectiveness as hypolipidemic agents. Cramizol also restores the expression of the Apoa1 gene in rats with experimentally induced hyperlipidemia to normal values. This may be a basis of its hypolipidemic and anti-atherogenic action.
Subject(s)
Apolipoprotein A-I/genetics , Hyperlipidemias/drug therapy , Hypolipidemic Agents/pharmacology , Imidazoles/pharmacology , Animals , Cholesterol/blood , Fenofibrate , Hyperlipidemias/genetics , Rats , Triglycerides/bloodABSTRACT
The experimental study in vivo was aimed at evaluation of hypolipidemic action of the original natural microbial enzyme preparation of cholesterol oxidase (CHO). In preliminary chronic experiments in rats, rabbits, dogs, low toxicity, good tolerability, and anti-atherosclerotic activity of the CHO preparation were established. To assess the effect of CHO under conditions of moderate, nutritional, atherogenic dyslipoproteinemia, experiments were carried out in rats, guinea pigs, and rabbits. It was shown that administration of CHO had the pronounced lipid-lowering effect in models of atherogenic dyslipoproteinemia induced in these animals.
Subject(s)
Atherosclerosis/drug therapy , Cholesterol Oxidase/pharmacology , Hypolipidemic Agents/pharmacology , Lipids/blood , Animals , Dogs , Guinea Pigs , Rabbits , RatsABSTRACT
Methods: Experiments were carried out on outbred albino male rats (n = 150, 230-250 g). For modeling dislipoproteinemia (DLP) we used 3 models: single intraperitoneal injection of the detergent triton WR-1339; administration of ethanol; maintenance on a special hypercholesterolaemic diet (HD) during 21 days. Animals were divided into four groups: normal control, model group, gemfibrozil (Gfb) group, benzohexonium (Benz) group. Rats received per os benzohexonium (20mg/kg), reference drug gemfibrozil (50 mg/kg). We determined content of total cholesterol (TCh), triglycerides (TG) in samples of blood serum and liver, TCh in aorta. TCh, TG and Ch-HDL were analyzed spectrophotometrically using of standardized methods. Results: Compared with model group the contents of TCh, TG in serum and liver were significantly decreased in model + Benz group, whereas Ch-HDL was raised in rats fed special HD (P<0.05). Calculated index of atherogenity (TCh - Ch-HDL) / (Ch-HDL) showed the positive effect. Conclusion: The results obtained were shown the hypolipidemic activity of N-cholinergic antagonist Benzohexonium (20 mg/kg) lowered the content of lipids in blood, liver, and aorta.
Subject(s)
Cholinergic Agonists , Dyslipidemias , Hexamethonium Compounds , Hypolipidemic Agents , Animals , Cholinergic Agonists/pharmacokinetics , Cholinergic Agonists/pharmacology , Dyslipidemias/blood , Dyslipidemias/drug therapy , Hexamethonium Compounds/pharmacokinetics , Hexamethonium Compounds/pharmacology , Hypolipidemic Agents/pharmacokinetics , Hypolipidemic Agents/pharmacology , Male , RatsABSTRACT
We have found that N-cholinolytic drug benzohexonium produces a hypolipidemic effect: it reduces dyslipoproteinemia, fatty infiltration of the liver, and risk of atherosclerotic lesions.
Subject(s)
Cholinergic Antagonists/pharmacology , Disease Models, Animal , Dyslipidemias/drug therapy , Fatty Liver/drug therapy , Hexamethonium Compounds/pharmacology , Hypolipidemic Agents/pharmacology , Plaque, Atherosclerotic/prevention & control , Analysis of Variance , Animals , Cholinergic Antagonists/therapeutic use , Guinea Pigs , Hexamethonium Compounds/therapeutic use , Hypolipidemic Agents/therapeutic use , Lipid Metabolism/drug effects , Male , RatsABSTRACT
Hypolipidemic properties of a native trimethyl derivative of glycine, trimethylglycine (TMGl), were studied in hyperlipidemic rats and guinea pigs. The administration of TMGl to the hyperlipidemic rats and guinea pigs produced a pronounced hypolipidemic effect. A positive action of TMGl on the lipid profile of blood serum of the experimental animals was observed as manifested by a decrease in the level of cholesterol of low density lipoproteins (LDL) and an increase in the cholesterol level of high density lipoproteins (HDL).
Subject(s)
Anticholesteremic Agents/therapeutic use , Betaine/therapeutic use , Hyperlipidemias/drug therapy , Animals , Cholesterol/blood , Guinea Pigs , Hyperlipidemias/blood , Lipoproteins, HDL/blood , Lipoproteins, LDL/blood , Liver/chemistry , Male , Mice , RatsABSTRACT
Experiments on rats with myocardial ischemia modeled by occlusion of the left coronary artery aggravated by alimentary dislipoproteinemia showed that therapy with taurepar (50 mg/kg), a taurine derivative, decreased blood corticosterone concentration and increased the level of endogenous testosterone, which attests to normalization of the compensatory-adaptive and gonadotropic functions of the organism.
Subject(s)
Myocardial Ischemia/physiopathology , Taurine/analogs & derivatives , Testosterone/deficiency , Animals , Corticosterone/blood , Dietary Fats/administration & dosage , Dyslipidemias/drug therapy , Male , Myocardial Ischemia/complications , Rats , Taurine/therapeutic use , Testosterone/bloodABSTRACT
Taurine derivatives taurepar, tauritman and IEM-1702 exhibit a significant hypolipidemic activity. The most pronounced effect was observed for taurepar, which effectively prevented the experimental dislipoproteinemia in albino rats and guinea pigs.
Subject(s)
Hypolipidemic Agents/therapeutic use , Lipid Metabolism/drug effects , Taurine/analogs & derivatives , Animals , Diet , Dyslipidemias/drug therapy , Guinea Pigs , Male , Rats , Species Specificity , Taurine/therapeutic useABSTRACT
Diabetes mellitus (DM) is often combined with arterial hypertension, which increases the risk of serious complications. The purpose of this review was analysis of the peculiarities of pharmacotherapy with drugs belonging to different groups (ACE inhibitors, calcium channel blockers, alpha- and beta-adrenoblockers, diuretics, angiotensin II blockers, and imidazoline receptor agonists) as a part of combined therapy of compensated DM.
Subject(s)
Antihypertensive Agents/therapeutic use , Diabetes Mellitus/physiopathology , Hypertension/drug therapy , Blood Pressure/drug effects , Diabetes Mellitus/drug therapy , Drug Therapy, Combination , Humans , Hypertension/complications , Hypertension/physiopathology , Hypoglycemic Agents/therapeutic use , Treatment OutcomeABSTRACT
Mildronate is a new antiischemic drug which inhibits biosynthesis of carnitine from butyrobetaine. We studied antiatherosclerotic and antiinflammatory effects of mildronate in guinea-pigs, rats and rabbits. We found a hypolipidemic action of this substance in rats with triton WR-1339 hyperlipidemia. A protective antiatherosclerotic effect of mildronate was observed in rabbits kept on the atherogenic diet for 3 months. Antiinflammatory efficiency of mildronate in rats was demonstrated after injection of bradykinin, carragenine or implantation of a small cotton-wool pad.
Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Arteriosclerosis/drug therapy , Cardiovascular Agents/pharmacology , Methylhydrazines/pharmacology , Animals , Anti-Inflammatory Agents, Non-Steroidal/toxicity , Bradykinin , Cardiovascular Agents/toxicity , Guinea Pigs , Hyperlipidemias/chemically induced , Hyperlipidemias/drug therapy , Inflammation/chemically induced , Inflammation/drug therapy , Lethal Dose 50 , Lipids/blood , Liver/drug effects , Liver/metabolism , Methylhydrazines/toxicity , Polyethylene Glycols/toxicity , Rabbits , RatsABSTRACT
In experiments on hyperlipidemic rats it was observed the hypolipidemic effect of new sulfated polisaccharides-chitosan, lutelan and krilan sulfates, More pronounced decrease was established in VLDL and increase of HDL after sulfated polysaccharides treatment. The most distinct efficiency exhibites preparation with moledular mass of 20-40 x 10(3) D and the rate of sulfation 9-14%.
Subject(s)
Hyperlipidemias/prevention & control , Hypolipidemic Agents/pharmacology , Lipoproteins/blood , Polysaccharides/pharmacology , Animals , Chitin/analogs & derivatives , Chitin/pharmacology , Chitin/toxicity , Chitosan , Detergents/toxicity , Hyperlipidemias/chemically induced , Hypolipidemic Agents/toxicity , Lethal Dose 50 , Male , Mice , Polyethylene Glycols/toxicity , Polysaccharides/toxicity , Rats , Sulfates/pharmacology , Sulfates/toxicity , UltracentrifugationABSTRACT
In vitro experiments were shown that native ecologically pure non-starch polysaccharide crylan bind the bile acid. Crylan was found to decrease hyperlipidemia induced in rats by means of diet enriched with cholesterol and 6-methylthiouracil. This effect of crylan was more pronounced as compare with the action of native nonspecific enterosorbent polyfepan.
Subject(s)
Hyperlipidemias/drug therapy , Hypolipidemic Agents/therapeutic use , Polysaccharides/therapeutic use , Animals , Antithyroid Agents/administration & dosage , Cholesterol, Dietary/administration & dosage , Diet, Atherogenic , Enterosorption , Hyperlipidemias/etiology , Lignin/administration & dosage , Lipids/analysis , Lipids/blood , Liver/chemistry , Male , Methylthiouracil/administration & dosage , RatsABSTRACT
New Russian phospholipid compounds (PLC) made of plants rich in vitamins were tested for effects on induced rat hyperlipidemia in comparison with those of lipostabil (essentiale). Administration of PLC gave rise to a marked hypolipidemic effect, decreased hepatic lipid infiltration and aortic cholesterol. Some novel PLC are much more effective than lipostabil.
Subject(s)
Hyperlipidemias/drug therapy , Hypolipidemic Agents/therapeutic use , Phospholipids/therapeutic use , Animals , Aorta/chemistry , Cholesterol/analysis , Evaluation Studies as Topic , Fat Emulsions, Intravenous , Hyperlipidemias/blood , Hyperlipidemias/diet therapy , Lipids/analysis , Lipids/blood , Liver/chemistry , Male , Phosphatidylcholines/therapeutic use , RatsABSTRACT
Experiments on guinea pigs and rats have revealed that thiazole derivatives of isoflavone has a beneficial effects on disturbed lipid and lipoprotein metabolism. New phospholipid complexes enriched with vitamins have been demonstrated to produce a hypolipidemic effect. Sulfated chitosans decrease lipid infiltration of the liver and elevate serum high density lipoprotein levels in rats.
Subject(s)
Chitin/analogs & derivatives , Hypolipidemic Agents/therapeutic use , Isoflavones/therapeutic use , Phospholipids/therapeutic use , Animals , Chitin/therapeutic use , Chitosan , Cholesterol, Dietary/administration & dosage , Drug Evaluation, Preclinical , Guinea Pigs , Hyperlipidemias/drug therapy , Hyperlipidemias/etiology , Hyperlipidemias/metabolism , Lipid Metabolism , Male , RatsABSTRACT
Hypolipidemic effect of the polyphenol compound triophen possessing antihypoxic activity was demonstrated in chronic experiments on rabbits. It was also shown that a new derivative of methylxanthine, which does not penetrate the blood--brain barrier, produces a hypolipidemic and antiatherosclerotic effect. Experiments on rats, guinea pigs, and rabbits with induced hyperlipidemia revealed a hypolipidemic effect of new complex compounds which are not absorbed in the intestine--steroid glycosides digitonin and tomatonin immobilized on a polymer. These substances resemble cholesteramine in activity but are distinguished by solubility, low toxicity, and a mechanism of action which is more physiological.