• 한국양식학회지
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• 제11권3호
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• pp.311-317
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• 1998

Estradiol-17${\beta}$($E_2$)에 의한 Vitellogenin (VTG) 함성에 미치는 Cu 및 Zn의 영향을 무지개송어의 배양 간세포를 이용하여 조사하였다. 간세포는 2일간 배양 한 후, E하(2) ($2{\times}10^6$ M)와 동시에 Cu ($2{\times}10^{-5}$~$10^{-4}$M) 또는 Zn ($10^{-5}$~$10^{-3}$M)을 배양액에 첨가하여 5일간 배양하였다. VTG 합성률은 총 단백질에 대한 VTG의 배율로 나타내었다. CU 및 Zn의 첨가는 배양 간세포의 생존율에는 영향을 미치지 않았다. 그러나, Cu의 첨가에 사용된 모든 농도에서, Zn의 첨가에는 농도 의존적으로 감소하여(10^{-3}$M에서 유의하게 감소하였다. 이러한 감소는, Zn의 제거시에는 회복되었으나, Cu에서는 회복되지 않았다. 그리고, Cu (10^{-4}$M의 첨가 시에 Ca (1.8 mM) 농도를 2.5 및 5.0 mM로 증가시켜도 Cu의 작용을 저해하지 못하였다. 이러한 결과로 보아, Cu 및 Zn은 간세포에서 합성되는 다른 단백질 보다 VTG 합성에 더 깊이 관여하는 것으로 추정된다.

• Asian Pacific Journal of Cancer Prevention
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• 제17권4호
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• pp.1649-1654
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• 2016

Tea derived from the leaves and buds of Camellia sinensis (Theaceae) is consumed worldwide. Green tea contains various components with specific health-promoting effects, and is believed to exert protective effects against diseases including cancer, diabetes and hepatitis, as well as obesity. Of the various tea components, the polyphenol catechins have been the subject of extensive investigation and among the catechins, (-)-epigallocatechin gallate has the strongest bioactivity in most cases. Our research group has postulated that hepatocyte nuclear factor-$4{\alpha}$, sterol regulatory element-binding proteins, and tumor necrosis factor-${\alpha}$ are targets of green tea constituents including (-)-epigallocatechin gallate for their anti-diabetes, anti-obesity, and anti-hepatitis effects, respectively. Published papers were reviewed to determine whether the observed changes in these factors can be correlated with anti-cancer effects of green tea. Two major action mechanisms of (-)-epigallocatechin gallate have been proposed; one associated with its anti-oxidative properties and the other with its pro-oxidative activity. When reactive oxygen species are assumed to be involved, our findings that (-)-epigallocatechin gallate downregulated hepatocyte nuclear factor-$4{\alpha}$, sterol regulatory element-binding proteins, and tumor necrosis factor-${\alpha}$ may explain the anti-cancer effect of green tea as well. However, further studies are required to elucidate which determinant directs (-)-epigallocatechin gallate action as an anti-oxidant or a pro-oxidant for favorable activity.

• International Journal of Industrial Entomology and Biomaterials
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• 제2권1호
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• pp.15-18
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• 2001

Silk fibroin (SF) derided from the domestic silk worm, bombyx mori, is the natural protein and widely used as bio-functional materials as well as apparels. We studied the livers protective effect of SF from alcohol-induced hepatotoxicity in the alcohol preference mouse. To increase more absorption of SF in experimental animals, molecular weight of SF was lowered by 2N of HCI aqueous solution at 10$0^{\circ}C$ for 48 hrs. SF was added to liquid diet with alcohol and fed to the alcohol preference mice for 4 weeks. To assess the liver function, the concentration of alanine aminotransferase (AlT), aspartate aminotransferase (AST) and cholesterol present in either blood or liver tissue were measured. As compared with non-SF treated groups the SF-treated showed significantly low concentrations of ALT, AST, cholesterol and triacylglycerol values, respectively. Histopathological examination revealed that the extent of hepatocyte injury in the SF-treated group was reduced when it was compared with non SF-treated group. These results suggest that SF may have liver protective effects against alcohol-induced hepatotoxicity.

• IMMUNE NETWORK
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• 제1권3호
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• pp.213-220
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• 2001

Background: A previous study has shown that Euonymus alatus (EA) has an antidotic activities against inflammation, suggesting possibility that EA can exert this beneficial effects to liver injury by an initial protection against drug-induced hepatocyte demage. The present study was undertaken to evaluate the protective effect of EA-extract on experimentally induced hepatitis in ICR mice and to investigate some mechanisms responsible for its action. Methods: Water EA extract was used in this experiments. The mice received i.p. a dose of 700 mg/kg galactosamine (GalN) together with $5{\mu}g/kg$ of endotoxin (LPS), or received i.v. 12 mg/kg of concanavalin A (Con A). EA (4 mg/mouse) was administrated on day -2, -1 and 0 before induction of liver injury. Liver injury was assessed by measurement of serum alanin amino-transferase (SGPT) levels on 9 hr after GaIN.LPS, or 8 hr after con A administration. Results: Treatment with either GaIN or LPS alone did not cause hepatitis. However, simultaneous administration of GalN and LPS to mice resulted in LPS-dose dependent fulminant hepatitis. GaLN/LPS-induced liver injury was reduced when mice were given EA for 3 days before induction. This preventive effect of Ea was more prominent when EA was given by intraperitoneal route rather then by oral route. Pretreatment of EA or dexamethasone inhibited significantly $TNF{\alpha}$ production in GalL/LPS-injured mice. However, EA-treatment did not influence $TNF{\alpha}$-induced hepatitis in GalN-sensitized mice, suggesting that $TNF{\alpha}$ is likely to act as one of final mediators of endotoxin action and the protective effect of EA might be manifested chiefly by inhibition of endotoxin-induced $TNF{\alpha}$ production, not by blocking the $TNF{\alpha}$-action. Injection of Con A into mice evoked remarkable liver injury in a dose dependent fashion. This liver damage was reduced by EA-pretreatment. Dexamethasone significantly reduced both GalL/LPS-induced and Con A-induced liver damages, showing synergism with EA. However, indomethacin reduced only GalN/ LPS-induced hepatitis, not for Con A-induced hepatitis. Conclusion: These results led to the conclusion that EA may be able to contribute at least in part to prevent the drug-induced hepatotoxicity, and that its anti-hepatitis effects might be manifested directly by modulation of endogenous mediators, such as leukotriese D4, $TNF{\alpha}$ and free radical, and indirectly by regulation of immune mediated responses. Also these results suggested that EA could be developed as a potential antidotic agent.

• 대한한의학회지
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• 제21권3호
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• pp.174-185
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• 2000

Objectives : This study was carried out to evaluate the effects of five fractions on cell viability, cell cycle progression and apoptosis. Methods : This study employed MTT assay, Cell cycle analysis, Cpp32 protease assay, DNA fragmentation assay and Quantitative RT-PCR analysis. Results : In MTT assay, the butanol fraction of Injinsaryung-San has showed magnificent viability, while the $H_2O$ fraction and ethylacetate fraction also showed higher viability than the control group. The $H_2O$ fraction of Injinsaryung-San has showed magnificent viability, and butanol fraction and ethylacetate fraction of Injinsaryung-San with etoposide have also showed higher viability than the only etoposide group. Cell cycle analysis showed that each fraction of Injinsaryung-San had no significant effect on the cell cycle. DNA fragmentation assay showed that the butanol fraction, $H_2O$ fraction and ethylacetate fraction carried inhibitory effects on apoptosis induction. Cpp32 protease activity assay showed that the butanol fraction, $H_2O$ fraction and ethylacetate fraction decreased Cpp32 protease activity, with the butanol fraction displaying greater effects. Quantitative RT-PCR showed that the butanol fraction, $H_2O$ fraction and ethylacetate fraction suppressed Fas and Bax genes, the butanol fraction increased BcI-2 gene, however no effect on Cpp32. Conclusions : The data shows that the butanol fraction of Injinsaryung-San increases the hepatocyte viability and has the heptocelluar protective effect by the suppression of apoptosis through gene regulation.

• Journal of Ginseng Research
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• 제42권4호
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• pp.419-428
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• 2018

Background: Despite the large number of studies on ginseng, pharmacological activities of ginseng seed oil (GSO) have not been established. GSO is rich in unsaturated fatty acids, mostly oleic and linoleic acids. Unsaturated fatty acids are known to exert a therapeutic effect in nonalcoholic fatty liver disease (NAFLD). In this study, we investigated the protective effect and underlying mechanisms of GSO against NAFLD using in vitro and in vivo models. Methods: In vitro lipid accumulation was induced by free fatty acid mixture in HepG2 cells and by 3 wk of high fat diet (HFD)-feeding in Sprague-Dawley rats prior to hepatocyte isolation. The effects of GSO against diet-induced hepatic steatosis were further examined in C57BL/6J mice fed a HFD for 12 wk. Results: Oil Red O staining and intracellular triglyceride levels showed marked accumulation of lipid droplets in both HepG2 cells and rat hepatocytes, and these were attenuated by GSO treatment. In HFD-fed mice, GSO improved HFD-induced dyslipidemia and hepatic insulin resistance. Increased hepatic lipid contents were observed in HFD-fed mice and it was lowered in GSO (500 mg/kg)-treated mice by 26.4% which was evident in histological analysis. Pathway analysis of hepatic global gene expression indicated that GSO increased the expression of genes associated with ${\beta}$-oxidation (Ppara, Ppargc1a, Sirt1, and Cpt1a) and decreased the expression of lipogenic genes (Srebf1 and Mlxipl), and these were confirmed with reverse transcription and quantitative polymerase-chain reaction. Conclusion: These findings suggest that GSO has a beneficial effect on NAFLD through the suppression of lipogenesis and stimulation of fatty acid degradation pathway.

• 생명과학회지
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• 제18권10호
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• pp.1342-1347
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• 2008

알코올 급여 흰쥐에서 알코올성 간독성에 대한 누에배설물(silkworm excrement powder)의 영향을 검토하기 위하여 반합성 식이에 누에배설물을 3% (w/w) 수준으로 첨가하여 30일간 급여한 후 혈중 알코올 및 지질 농도, 간 기능 지표 효소 활성 및 간 조직 검사를 실시하였다. 임상생화학적으로 중요한 간 기능 지표 효소인 alanine aminotransferase (ALT), aspartate aminotransferase (AST), $\gamma$-glutamyl transpeptidase ($\gamma$-GTP) 및 lactate dehydrogenase (LDH) 활성이 알코올 대조군에서 증가하였다. 또한 혈중 알코올 농도도 알코올 섭취에 의해 증가하였다. 그러나 누에배설물 투여에 의해 혈중 ALT 및 LDH 활성은 현저하게 감소하였다. 혈중 중성지질, 콜레스테롤 농도는 알코올 대조군에 비해 누에배설물 투여에 의해 현저히 감소하였다. 또한 간 조직 검사에서 알코올 대조군에서 많은 지방적이 나타나 지방간이 확인되었으나 누에배설물 투여에 의해서는 지방적의 크기와 수가 많이 줄어드는 결과를 얻었다. 이상의 결과에서 누에배설물에 의한 알코올-유발 간독성의 개선효과는 간 조직의 임상생화학적 지표 효소의 활성 감소에 기인하는 것으로 나타났다.

• 한국식품영양과학회지
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• 제45권7호
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• pp.973-979
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• 2016

본 연구에서는 렌틸을 이용한 새로운 기능성 소재의 개발에 우선하여 세계적으로 소비량이 비교적 많은 벨루가, 레드, 그린, 프렌치 렌틸을 연구 소재로 선정하고, 0.2% HCl을 함유한 메탄올을 이용하여 추출물을 제조한 후 이들의 항산화 활성을 조사하였다. 총폴리페놀과 플라보노이드 함량은 각각 27.3~30.3 mg TAE/g과 13.14~16.29 mg QUE/g으로 다양하게 나타났으며, 그중 벨루가와 레드 렌틸이 상대적으로 높은 총폴리페놀 함량을 보였다. DPPH와 ABTS 라디칼 소거 활성 및 $H_2O_2$ 소거 활성은 총폴리페놀 함량이 상대적으로 높았던 벨루가와 레드 렌틸이 다른 품종에 비해 유의적으로 높은 활성을 보였으며, 항산화 활성 및 폴리페놀함량과의 비례적 상관관계가 있음을 확인할 수 있었다. ROS 소거 활성이 가장 높았던 벨루가 렌틸을 이용하여 linoleic acid에 대한 과산화 억제 효과를 FTC법으로 조사한 결과, $62.5{\sim}500{\mu}g/mL$에서 농도 의존적으로 유의적인 산화억제효과를 보였으며 $RC_{50}$은 $222.76{\mu}g/mL$로 확인되었다. 또한, 벨루가 및 레드 렌틸 추출물은 산화적 스트레스 발생을 통해 간세포 손상을 유발하는 것으로 알려진 알코올의 세포독성으로부터 우수한 간세포 보호 효과를 나타내었다. 따라서 향후 추가적인 세포실험과 동물실험을 통한 렌틸의 항산화 활성 검정 및 항산화 기전에 관한 연구가 필요할 것으로 생각되며, 이를 비롯한 다양한 생리활성에 대한 연구들이 이루어진다면 기능성 소재로서 렌틸의 산업적 응용이 활발해질 것으로 기대된다.

• 대한한의학방제학회지
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• 제32권1호
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• pp.63-82
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• 2024

Objective : Saengkankunbi-tang (SKT) is used as a traditional Korean herbal formula for treatment of liver diseases. We investigated the hepatoprotective effects of SKT plus Epimedium koreanum Nakai (EKE) against arachidonic acid (AA) + iron-mediated cytotoxicity in HepG2 cells and carbon tetrachloride (CCl₄)-mediated acute liver damage in mice. Methods : The cyto-protective effects of SKT + EKE were determined by MTT assay, western blot and fluorescence activated cell sorting analysis. In mice, blood biochemistry and western blot were assessed in CCl₄-induced acute hepatic damage. The animal groups included vehicle-treated control, CCl₄, SKT (200 mg/kg/day), EKE (100 mg/kg/day), SKT (200 mg/kg/day) + EKE (100 mg/kg/day) and silymarin (200 mg/kg/day). Results : In HepG2 cells, pretreatment with SKT + EKE significantly suppressed cytotoxicity induced by AA + iron and reduced the expression of proteins related to apoptosis. In addition, pretreatment with SKT + EKE significantly prevented the increase in H₂O₂ production, GSH depletion, and lower mitochondrial membrane potential induced by AA + iron. In CCl₄-induced liver damage mice, the administration of SKT + EKE prevented the liver damage by inhibition of hepatocyte damage and expression of apoptosis proteins in liver. More importantly, in vitro and in vivo assay, SKT + EKE showed significant effect compare with SKT alone or EKE alone in all parameters. Conclusions : These results indicated that SKT + EKE could protect against oxidative stress-induced liver damage, and SKT + EKE is more effective than SKT alone or EKE alone.

• 한국식품위생안전성학회지
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• 제28권2호
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• pp.146-151
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• 2013

t-BHP는 대표적인 산화스트레스에 의한 간 손상 모델이며, 본 연구자는 랫드에 기능성이 강화된 기능성 들깻잎 추출물(P. frutescens leaf extract, PLE)을 250, 500 또는 1000 mg/kg body weight (b.w.)으로 6일간 경구 투여하고 t-BHP의 복강 주사로 간 손상을 일으킨 후 기능성 들깻잎 추출물이 간에서 산화스트레스를 얼마나 억제하여 주는지를 혈액의 간 손상 지표인 lactate dehydrogenase (LDH), aspartate aminotransferase (AST) 그리고 alanine aminotransferase (ALT)를 측정하였으며, 간 조직에서 항산화 바이오 마커인 reduced glutathione (GSH), 지질과산화물의 척도인 malondialdehyde (MDA)를 통해서 측정하였다. 산화스트레스에 의한 간 손상시 GSH는 아무것도 처리하지 않은 정상 대조군($146.0{\pm}5.4$ mM GSH/g protein)에 비해 t-BHP로 산화스트레스를 유발한 그룹에서 $128.6{\pm}6.8$ mM GSH/g protein로 감소하였다. 반면 기능성 들깻잎 추출물을 250, 500 그리고 1000 mg/kg b.w. 을 투여한 그룹에서는 $129.3{\pm}2.6$ mM GSH/g protein, $151.9{\pm}6.8$ mM GSH/g protein, $171.9{\pm}5.2$ mM GSH/g protein로 농도 의존적으로 GSH 함량이 회복되는 경향을 나타내며, 500 mg/kg b.w. 투여군부터 정상 대조군의 GSH 함량과 비슷한 수준을 나타내었다. 또한, 간 조직에서 산화스트레스에 의하여 발생된 지질과산화물을 측정하였을 때 t-BHP에 의하여 산화스트레스만 유발한 그룹은 $834.0{\pm}154.7{\mu}M/g$ protein 로 정상 대조군의 $385.6{\pm}39.7{\mu}M/g$ protein 보다 2.17배 높은 MDA를 생성한 것으로 지질과산화가 많이 일어난 것을 확인하였으나, 기능성 들깻잎 추출물을 투여한 그룹의 MDA의 생성량은 $669.2{\pm}145.0$, $595.1{\pm}142.6$, $415.9{\pm}133.8{\mu}M/g$ protein 로 농도에 따라 감소하는 경향을 확인하였다. 랫드의 간 조직에서, 독성을 유발하는 t-BHP를 복강 투여 후 기능성 들깻잎 추출물을 경구 투여하였을 때 지질과산화의 지표인 MDA의 감소와 항산화의 지표인 GSH 함량이 증가하였다. 조직병리학적 확인을 위하여 간 조직을 H&E 염색 후 광학현미경으로 관찰하였을 때, t-BHP만 처리한 음성 대조군의 경우 간 세포의 괴사와 조직의 변형을 확인할 수 있었지만 기능성 들깻잎 추출물을 처리하였을 경우 모두 정상 상태의 조직을 관찰할 수 있었다. 위의 결과들을 종합하였을 때, t-BHP가 간에서 산화스트레스를 유발하여 간 손상을 야기시키고, 간 조직의 인지질 막 손상을 줄 수 있으며, 기능성 들깻잎 추출물은 간 손상에 대한 보호 효과가 있음을 확인하였다.