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1.
Food Funct ; 15(9): 5088-5102, 2024 May 07.
Article in English | MEDLINE | ID: mdl-38666497

ABSTRACT

Diets rich in taurine can increase the production of taurine-conjugated bile acids, which are known to exert antihypertensive effects. Despite their benefits to the heart, kidney and arteries, their role in the central nervous system during the antihypertensive process remains unclear. Since hypothalamic paraventricular nucleus (PVN) plays a key role in blood pressure regulation, we aimed to investigate the function of bile acids in the PVN. The concentration of bile acids in the PVN of spontaneously hypertensive rats (SHRs) and normotensive Wistar-Kyoto rats (WKY) fed with normal chow was measured using LC-MS/MS, which identified taurocholic acid (TCA) as the most down-regulated bile acid. To fully understand the mechanism of TCA's functions in the PVN, bi-lateral PVN micro-infusion of TCA was carried out. TCA treatment in the PVN led to a significant reduction in the blood pressure of SHRs, with decreased plasma levels of norepinephrine and improved morphology of cardiomyocytes. It also decreased the number of c-fos+ neurons, reduced the inflammatory response, and suppressed oxidative stress in the PVN of the SHRs. Most importantly, the TGR5 receptors in neurons and microglia were activated. PVN infusion of SBI-115, a TGR5 specific antagonist, was able to counteract with TCA in the blood pressure regulation of SHRs. In conclusion, TCA supplementation in the PVN of SHRs can activate TGR5 in neurons and microglia, reduce the inflammatory response and oxidative stress, suppress activated neurons, and attenuate hypertension.


Subject(s)
Hypertension , Paraventricular Hypothalamic Nucleus , Receptors, G-Protein-Coupled , Taurocholic Acid , Animals , Male , Rats , Antihypertensive Agents/pharmacology , Blood Pressure/drug effects , Hypertension/drug therapy , Hypertension/metabolism , Neurons/drug effects , Neurons/metabolism , Paraventricular Hypothalamic Nucleus/metabolism , Paraventricular Hypothalamic Nucleus/drug effects , Rats, Inbred SHR , Rats, Inbred WKY , Receptors, G-Protein-Coupled/metabolism , Receptors, G-Protein-Coupled/genetics
2.
Polymers (Basel) ; 14(15)2022 Aug 02.
Article in English | MEDLINE | ID: mdl-35956659

ABSTRACT

The results of studies on the corrosion protectiveness and thermal conductivity of reduced graphene oxide-BaSO4 epoxy composites are reported here. A commercial epoxy resin and reduced graphene oxide (rGO) were blended with a hardening reagent and then mixed with prepared BaSO4-epoxy resin (B-epoxy). The reduced graphene oxide-BaSO4-epoxy composite (rGO-B-epoxy) paste was used to coat the surfaces of Al 7205 alloy and the corrosion and thermal properties were investigated. A corrosion test in a 3.5 wt% synthetic sea water solution showed that the composite coating containing BaSO4 had the best corrosion resistance. Moreover, the rGO-B-epoxy composite showed better protection against corrosion than the epoxy alone. The rGO-B-epoxy composite with 5 wt% BaSO4 had an in-plane coefficient of thermal conductivity of approximately 165.0 W/m K, and the in-plane thermal diffusivity was 71.38 mm2/s. In standard thermal conductivity tests, all three samples had values below 40 W/m K. The rGO-B-epoxy composites showed good surface corrosion protection and in-plane thermal conductivity.

3.
Materials (Basel) ; 15(9)2022 Apr 20.
Article in English | MEDLINE | ID: mdl-35591331

ABSTRACT

This study simulated the after-burned zirconium cladding oxidation in air at temperatures between 500 and 800 °C. The weight changes of Zircaloy-4 cladding with hydrogen contents of 100-1000 ppm continuously measured through thermogravimetric analysis (TGA) during oxidation tests at different temperatures in an air atmosphere. The TGA results indicate a transition of oxidation kinetics from a parabolic rate law to a linear rate law for as-received and hydrided Zircaloy-4 cladding. The hydrogen concentration of Zircaloy-4 had a marked effect on its pre-transition oxidation in air between 500 and 800 °C. For all samples, the linear oxidation (post transition stage) at 650 °C, which is the critical oxidation temperature, displays a similar trend. In addition, scanning electron microscopy and transmission electron micros-copy examinations indicated the presence of a few and numerous discontinuous micro-cracks in the oxide layer in the pre-transition and post-transition stages, respectively.

4.
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
5.
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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