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1.
Bioorg Med Chem Lett ; 28(23-24): 3787-3792, 2018 12 15.
Article in English | MEDLINE | ID: mdl-30337230

ABSTRACT

Hypolipidemic effects of the newly synthesized 5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thione-based fibrates were evaluated in Triton WR-1339 and high-fat diet (HFD)-induced hyperlipidemic mice. Preliminary screening of all the synthesized compounds was done by using an acute model (Triton WR-1339 model), in which compound 6 shown more significant antidyslipidemic activity than fenofibrate (FF). The compound 6 was also found to reduce serum triglyceride (TG), total cholesterol (TC) and low density lipoprotein cholesterin (LDL) in HFD-induced hyperlipidemic mice. Moreover, compound 6 displayed hepatoprotective effect, a significant amelioration in hepatic indices (AST and ALT) toxicity was observed and the histological examination showed that compound 6 inhibited the development of hepatic lipid accumulation and ameliorated the damage in hepatic tissue compared to model mice. Additional effects such as the potent antioxidant and anti-inflammatory action confirmed and reinforced the efficacy of compound 6 as a new agent of dual-effect hypolipidemic and hepatoprotective activities.


Subject(s)
Fibric Acids/chemistry , Fibric Acids/therapeutic use , Hyperlipidemias/drug therapy , Hypolipidemic Agents/chemistry , Hypolipidemic Agents/therapeutic use , Thiones/chemistry , Thiones/therapeutic use , Thiophenes/chemistry , Thiophenes/therapeutic use , Animals , Diet, High-Fat/adverse effects , Fibric Acids/pharmacology , Hyperlipidemias/blood , Hyperlipidemias/etiology , Hyperlipidemias/metabolism , Hypolipidemic Agents/pharmacology , Lipid Metabolism/drug effects , Liver/drug effects , Liver/metabolism , Liver/pathology , Male , Mice , Protective Agents/chemistry , Protective Agents/pharmacology , Protective Agents/therapeutic use , Thiones/pharmacology , Thiophenes/pharmacology
2.
Bioorg Med Chem Lett ; 28(18): 3119-3122, 2018 10 01.
Article in English | MEDLINE | ID: mdl-30119959

ABSTRACT

Oxidative stress has been regarded as the leading mechanism of the hepatotoxicity of clofibrate (CF). To achieve multifunctional novel hypolipidemic agents with hypolipidemia, antioxidant, and ameliorating liver injury, clofibric acid derivative hydroxytyrosol-clofibrate (CF-HT) was synthesized by molecular hybridization. CF-HT exhibited significant hypolipidemia, reducing serum triglyceride (TG), total cholesterol (TC), and malonaldehyde (MDA) by 30%, 33%, and 29% in hyperlipidemic mice induced by Triton WR 1339. CF-HT also shown hepatoprotective effect, a significant decrease in hepatic indices toxicity was observed, i.e. aspartate and lactate transaminases (AST and ALT) activities, alkalines phosphatases (ALP), and total bilirubin (TBIL) levels. The liver weight and liver coefficient were also ameliorated. Serum superoxide dismutase (SOD) was significantly elevated, and serum catalase (CAT) and malondialdehyde (MDA) content were remarkably restored. The hepatic glutathione (GSH) content was obviously increased and hepatic oxidized glutathione (GSSG) content was reduced dramatically by CF-HT, as compared to the CF treated mice (p < 0.05). Moreover, the histopathological damage that hepatocyte hyperplasia and hypertrophy was also significantly ameliorated by treatment with CF-HT. Therefore, the results indicated that CF-HT exerted more potent hypolipidemic activity and definite hepatoprotective effect which may mainly be associated with its antioxidative property in mice.


Subject(s)
Antioxidants/pharmacology , Clofibrate/pharmacology , Hepatocytes/drug effects , Hypolipidemic Agents/pharmacology , Phenylethyl Alcohol/analogs & derivatives , Animals , Antioxidants/administration & dosage , Antioxidants/chemistry , Body Weight/drug effects , Clofibrate/administration & dosage , Clofibrate/chemistry , Dose-Response Relationship, Drug , Hepatocytes/metabolism , Hypolipidemic Agents/administration & dosage , Hypolipidemic Agents/chemistry , Male , Mice , Mice, Inbred ICR , Molecular Structure , Organ Size/drug effects , Phenylethyl Alcohol/administration & dosage , Phenylethyl Alcohol/chemistry , Phenylethyl Alcohol/pharmacology , Polyethylene Glycols/pharmacology , Structure-Activity Relationship
3.
Biomed Pharmacother ; 99: 715-724, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29710469

ABSTRACT

Hydroxytyrosol (HT) is a natural polyphenol antioxidant that exists in olive oil. In the study of multifunctional hypolipidemic of nicotinic derivatives, we found that hydroxytyrosol nicotinate (HT-N) incorporation of niacin with HT displayed ?-glucosidase inhibitory activities in vitro, such as yeast ?-glucosidase (IC50?=?117.72??M) and rat intestinal ?-glucosidases maltase (IC50?=?31.86??M) and sucrase (IC50?=?22.99??M), and had a good control of postprandial blood glucose (PBG). HT-N shown significantly hypoglycemic action by 16.9% and protection of pancreatic tissue in type 2 diabetic mellitus (T2DM) mouse model. HT-N also shown a potent antioxidant activity and property of anti-glycation in vitro, which were benefit for ameliorating diabetic complications. Moreover, HT-N exhibited much significant hypolipidemia, lowering plasma triglyceride (TG), total cholesterol (TC), and malonaldehyde (MDA) by 34.6%, 45.8% and 32.1% respectively, in hyperlipidemic mice induced by Triton WR 1339. The results indicated that HT-N has hypolipidemic, hypoglycemic and antioxidant actions. All these properties could be conducive to amelioration of oxidative stress, hyperlipidemia, and diabetes that HT-N may serve as a multifunctional potential therapeutic strategy in diabetic patients with hyperlipidemia.


Subject(s)
Hypoglycemic Agents/pharmacology , Hypolipidemic Agents/pharmacology , Niacin/pharmacology , Phenylethyl Alcohol/analogs & derivatives , Animals , Antioxidants/administration & dosage , Antioxidants/chemistry , Antioxidants/pharmacology , Blood Glucose/drug effects , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Type 2/drug therapy , Hyperlipidemias/drug therapy , Hypoglycemic Agents/administration & dosage , Hypoglycemic Agents/chemistry , Hypolipidemic Agents/administration & dosage , Hypolipidemic Agents/chemistry , Inhibitory Concentration 50 , Lipids/blood , Male , Mice , Niacin/administration & dosage , Niacin/chemistry , Oxidative Stress/drug effects , Phenylethyl Alcohol/administration & dosage , Phenylethyl Alcohol/chemistry , Phenylethyl Alcohol/pharmacology , Rats
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