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        Antiarrhythmic effects of ginsenoside Rg2 on calcium chloride-induced arrhythmias without oral toxicity

        Dongxia Gou,Xuejing Pei,Jiao Wang,Yue Wang,Chenxing Hu,Chengcheng Song,Sisi Cui,Yifa Zhou 고려인삼학회 2020 Journal of Ginseng Research Vol.44 No.5

        Background: Malignant arrhythmias require drug therapy. However, most of the currently available antiarrhythmic drugs have significant side effects. Ginsenoside Rg2 exhibits excellent cardioprotective effects and appears to be a promising candidate for cardiovascular drug development. So far, the oral toxicity and antiarrhythmic effects of Rg2 have not been evaluated. Methods: Acute oral toxicity of Rg2 was assessed by the Limit Test method in mice. Subchronic oral toxicity was determined by repeated dose 28-day toxicity study in rats. Antiarrhythmic activities of Rg2 were evaluated in calcium chloride-induced arrhythmic rats. Antiarrhythmic mechanism of Rg2 was investigated in arrhythmic rats and H9c2 cardiomyocytes. Results: The results of toxicity studies indicated that Rg2 exhibited no single-dose (10 g/kg) acute oral toxicity. And 28-day repeated dose treatment with Rg2 (1.75, 3.5 and 5 g/kg/d) demonstrated minimal, if any, subchronic toxicity. Serum biochemical examination showed that total cholesterol in the high-dose cohort was dramatically decreased, whereas prothrombin time was increased at Day 28, suggesting that Rg2 might regulate lipid metabolism and have a potential anticoagulant effect. Moreover, pretreatment with Rg2 showed antiarrhythmic effects on the rat model of calcium chloride induced arrhythmia, in terms of the reduced duration time, mortality, and incidence of malignant arrhythmias. The antiarrhythmic mechanism of Rg2 might be the inhibition of calcium influx through L-type calcium channels by suppressing the phosphorylation of Ca<SUP>2+</SUP>/calmodulin-dependent protein kinase II. Conclusion: Our findings support the development of Rg2 as a promising antiarrhythmic drug with fewer side effects for clinical use.

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        Deep dechlorination of hydrocarbon oil by reactive adsorption on TiO2-based metal oxides

        Hui Niu,Yuyu Feng,Jie Ding,Wei Zhang,Chenxing Hu,Qingxiang Zhang,Chen Zhang,Cuiqing Li 한국화학공학회 2022 Korean Journal of Chemical Engineering Vol.39 No.7

        This study reports reactive adsorptive dechlorination of hydrocarbon oil over TiO2-based metal oxides atthe temperatures of 20-150 oC. TiO2 and a series of TiO2-CeO2 were prepared by precipitation method and characterizedby N2 adsorption, XRD, FT-IR, pyridine-IR, NH3-TPD and CO2-TPD. The characterization results showed thatboth the acidity and basicity of the adsorbent had a significant impact on its dechlorination capacity. TiO2-U precipitatedby urea exhibited higher dechlorination capacity than TiO2-A precipitated by ammonia due to the higher surfacearea, more acid and base amounts of the former. Among various Ti(1x)CexO2 (x=0.1, 0.3, 0.5, 0.7, 0.9, 1) oxides,Ti0.7Ce0.3O2 and Ti0.3Ce0.7O2 bimetallic oxides showed higher dechlorination capacity than TiO2-U, and the chlorineremoval over Ti0.7Ce0.3O2 reached 82.8% after adsorption at 150 oC for 3 h. Mixing 5 wt% of alkali earth metal oxideinto Ti0.7Ce0.3O2 mechanically enhanced its dechlorination capacity, and the chlorine removal over Ti0.7Ce0.3O2-BaOreached as high as 92.1%. The chlorine removal increased with increasing the adsorption temperature. Ion chromatographyand GC-MS analysis revealed that organochlorine compound was converted into Cl and its corresponding alcoholover the adsorbent at 150 oC. Finally, the mechanism of reactive adsorption dechlorination was proposed.

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