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Noh, Jung-Ran,Kim, Yong-Hoon,Gang, Gil-Tae,Yang, Keum-Jin,Kim, Sang-Kyum,Ryu, Shi-Yong,Kim, Young-Sup,Lee, Chul-Ho,Lee, Hyun-Sun Pharmaceutical Society of Japan 2010 Biological & pharmaceutical bulletin Vol.33 No.3
<P><I>Platycodon grandiflorum</I> (PG) (Korean name, <I>Doraji</I>; Chinese name, <I>Jiegeng</I>; and Japanese name, <I>Kikyo</I>) is a perennial plant in the Campanulaceae family that contains triterpenoid saponins, carbohydrates, and fibers. This study was carried out to investigate effects of root of PG on fatty liver inhibition in high fat diet (HFD)-fed C57BL/6 mice. C57BL/6 mice were divided into control, total extract of PG (T-PG, 500 mg/kg) and saponin fraction (S-PG, 50 mg/kg)-treated groups. Significant decreases in body weight, associated with fat mass reduction, were observed in PG-treated groups (<I>p</I><0.05). Hepatic lipid content and score index calculated from morphometric observations on fatty liver were significantly decreased in the PG-treated groups (<I>p</I><0.05). Moreover, activities of fatty acid synthase (FAS) and carnitine palmitoyl-transferase (CPT) were significantly suppressed and increased as compared with the control group, respectively (<I>p</I><0.05). mRNA expressions of the sterol regulatory element binding protein (SREBP1c) and stearoyl-CoA desaturase (SCD1) gene were suppressed in the T-PG and S-PG groups (<I>p</I><0.05). From these findings, we speculate that fatty liver inhibition effects of PG extract and its saponins appear to be conferred by hepatic lipogenesis and acceleration of energy expenditure, along with modulation of liver FAS and CPT activities in HFD-fed C57BL/6 mice.</P>
Jung-Ran Noh,이인경,이선영,양금진,Gil-Tae Gang,Yong-Hoon Kim,황정환,윤봉식,이철호 한국식품영양과학회 2011 Journal of medicinal food Vol.14 No.3
This study evaluated the anti-obesity effects of Phellinus baumii extract (PBE) in high-fat diet (HFD)-fed mice. Male 8-week-old C57BL/6 mice were randomly divided into four groups: control, normal chow diet plus vehicle; HFD-control, high-fat plus vehicle; HFD plus orlistat (Xenical®, Roche, Basel, Switzerland) (50 mg/kg); and HFD plus PBE (500 mg/kg). PBE was administered daily by oral gavage for 12 weeks. Oral administration of PBE (500 mg/kg) significantly reduced body weight gain, hepatic lipid concentrations, and fat accumulation in epididymal adipocytes compared with mice fed HFD alone (P < .05). mRNA expression of genes related to triglyceride (TG) synthesis was suppressed in the PBE groups, and fatty acid synthase activity was also significantly inhibited (P < .05). Furthermore, we evaluated the effect of PBE on TG absorption and detected marked reduction in TG absorption in Xenical- and PBE-treated mice compared with the control group (P < .05). To determine the active compound of PBE, fractionation was conducted, and interfungin A, davallialactone, and hypholomine B were identified as the main compounds. Among the three identified compounds, as a representative compound, davallialactone was also shown to suppress fat accumulation in an in vitro model system. These anti-obesity and hypolipidemic effects appear to be partly mediated by suppressing plasma and hepatic fat accumulation through the inhibition of enzymes associated with hepatic and intestinal lipid absorption and synthesis.
Ran, Weiguang,Noh, Hyeon Mi,Park, Sung Heum,Lee, Bo Ram,Kim, Jung Hwan,Jeong, Jung Hyun,Shi, Jinsheng Elsevier 2019 Materials research bulletin Vol.117 No.-
<P><B>Abstract</B></P> <P>Er<SUP>3+</SUP>-activated CdMoO<SUB>4</SUB> phosphors were prepared by a traditional high-temperature solid-state method. The crystal structure, photoluminescence (PL) characteristics and performance in non-contact thermometry of as-prepared phosphors were studied in detail. Benefiting from the 3D network structure of CdMoO<SUB>4</SUB> host, the desirable green emission of Er<SUP>3+</SUP>-based phosphors were observed. Especially, based on the thermally coupled energy levels, the obtained phosphors show enhanced emission intensity in high temperatures. When applied to the temperature sensor based on the fluorescence intensity ratio (FIR), the prepared CdMoO<SUB>4</SUB>:0.02Er<SUP>3+</SUP> phosphor show an excellent sensitivity (0.875% K<SUP>−1</SUP>) at 483 K. Therefore, it is demonstrated that the as-prepared Er<SUP>3+</SUP>-activated CdMoO<SUB>4</SUB> phosphors have a promising potential application in both solid-state lighting and non-contact thermometry.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Enhanced emission intensity in high temperatures has been achieved. </LI> <LI> Er<SUP>3+</SUP> doped CdMoO<SUB>4</SUB> phosphor has a potential application in solid-state lighting. </LI> <LI> High sensitivity indicates that CdMoO<SUB>4</SUB>: 0.02Er<SUP>3+</SUP> phosphor can be used in non-contact thermometer. </LI> <LI> Excellent water stability of Er<SUP>3+</SUP> doped CdMoO<SUB>4</SUB> can be used in a complex condition. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Jung-Ran Noh,Gil-Tae Gang,Yong-Hoon Kim,Keum-Jin Yang,Chul-Ho Lee,O-Su Na,Gi-Ju Kim,Won-Keun Oh,Young-Don Lee 한국영양학회 2010 Nutrition Research and Practice Vol.4 No.1
This study was performed to investigate the effect of desalinated underground seawater (named as ‘magma seawater’, MSW) of Jeju Island in Korea on lipid metabolism and antioxidant activity. MSW was collected from underground of Han-Dong in Jeju Island, and freely given to high fat diet (HFD)-fed C57BL/6 mice for 10 weeks. Although there were no significant differences in the body weight changes and plasma lipid levels, hepatic triglyceride levels were significantly lower in the MSW group than in the normal tap water (TW)-drunken control group. Furthermore, the activity of fatty acid synthase (FAS) was significantly decreased and carnitine palmitoyltransferase (CPT) activity was increased in MSW group compared to TW group. Similarly, real-time PCR analysis revealed that mRNA expressions of lipogenic genes were lowered in MSW groups compared to the control group. In a morphometric observation on the liver tissue, accumulation of fats was remarkably reduced in MSW group. Meanwhile, in vitro assay, free radical scavenging activity measured by using diphenylpicrylhydrazyl (DPPH) was increased in MSW group. The 2'-7'-dichlorofluorescein diacetate (DCF-DA) staining followed with fluorescent microscopy showed a low intensity of fluorescence in MSW-treated HepG2 cells, compared to TW-treated HepG2 cells, which indicated that the production of reactive oxygen species by tert-butyl hydroperoxide (t-BHP) in HepG2 cells was decreased by MSW treatment. The antioxidant effect of MSW on t-BHP-induced oxidative stress in HepG2 cells was supported by the increased activities of intracellular antioxidant enzymes such as catalase and glutathione reductase. From these results, we speculate that MSW has an inhibitory effect on lipogenesis in liver and might play a protective role against cell damage by t-BHP-induced oxidative stress.