• 한국식품영양과학회지
• /
• 제46권4호
• /
• pp.401-408
• /
• 2017

본 연구는 배암차즈기 에탄올 추출물(SPE)을 유효성분으로 함유하는 지방 생성 및 축적 저해 효능을 조사하였다. 배암 차즈기 에탄올 추출물은 마우스 배아 섬유아세포(mouse embryo fibroblast) 유래 지방세포인 3T3-L1에서 지방세포 분화를 억제하는 효능을 보유하고 있었으며, 지방세포 내 중성지방의 농도를 감소시키는 효능을 보유하고 있었다. 또한, $PPAR{\gamma}$, $C/EBP{\alpha}$, SREBP-1c, pACC, pAMPK, CPT-1, 지방산 합성효소(FAS, fatty acid synthase) 발현 억제, 호르몬자극지방분해효소(HSL, hormone sensitivity lipase) 활성화 등 지방합성 관련인자들의 발현을 조절하는 효능을 보유하고 있는 것으로 확인되었다. 이상의 결과로 SPE가 지방세포 분화 및 지방대사에 관련된 인자들의 발현을 조절함으로써 지방 생성 및 지방 축적을 저해하는 효능을 보유하기 때문에 배암차즈기를 활용한 비만 개선을 위한 소재로서의 활용이 가능할 것으로 보인다.

• 한국산림과학회지
• /
• 제104권1호
• /
• pp.67-75
• /
• 2015

본 연구는 4년근 산양삼을 4년 숙성된 감식초에 22주간 혼입숙성하여 만든 산양삼감식초(가칭: 산삼초)를 활용하여 식이제한을 하였을 때 나타나는 비만관련 요소들을 분석하였다. 웅성 흰쥐 63마리를 대상으로 고지방식을 공급하면서 식후 2회, 6주간 산삼초를 경구투여하였다. 집단은 대조군, 제한식이군, 웨이트사이클링군으로 구분하였으며, 이를 다시 대조군, 산삼초 2.5배 희석 섭취군, 산삼초 5.0배 희석 섭취군으로 각각 구분하였다. 각 집단은 7마리씩으로 하였다. 6주간의 사육이 종료된 후, 복강내 지방(복막후지방, 장간막지방, 부고환지방)과 대사관련 단백질(AMPK, PPAR-${\alpha}$, CPT-1)의 발현을 분석하였다. 결과를 볼 때, 모든 집단에서 산삼초 섭취에 의한 지방저장량의 유의한 감소 또는 감소 경향이 나타났으며, 지방저장량의 총합계 역시 산삼초 섭취에 의해 증가가 억제되었다. 이와는 반대로 대사관련 단백질 발현은 모든 항목에서 산삼초 섭취에 의해 유의한 증가 혹은 증가 경향이 나타났다. 이 결과는 산삼초 섭취에 의한 에너지 대사의 효과적인 상승이 고지방식이 또는 식이제한을 하였을 경우에도 체내 지방 저장량의 증가를 억제하였다는 것이다. 즉, 비만의 가장 큰 문제점인 웨이트사이클링의 억제를 위한 좋은 기능성을 보유하고 있다고 판단된다. 이를 통하여 임업산물인 산양삼과 감식초의 융합소재인 산삼초를 비만억제 식품으로 활용할 수 있을 것으로 기대된다.

• 한국식품과학회지
• /
• 제46권4호
• /
• pp.477-482
• /
• 2014

본 연구에서는 흰쥐에게 고지방-고콜레스테롤 식이를 6주간 급여하여 고지혈증을 유발한 후, 현미, 발아현미, 보리, 맥아, 대두, 흑두 등이 혼합된 식물성 식이조성물을 각각 다른 비율로 6주간 급여하면서 체중감량, 배변량, 체지방 및 혈청지질농도에 미치는 영향을 조사하였다. 실험기간 동안 일당증체량은 식물성 식이조성물군이 HFCD 대조군과 비교할 때 유의적으로 낮았으며, 배변량은 증가하고 장 통과시간은 HFCD 대조군에 비하여 감소하였다. 내장지방 중 신장주변지방패드(RFP)와 정소상체지방패드(EPF)는 일반식이 대조군에 비하여 고지방-고콜레스테롤 식이를 급여한 HFCD 대조군에서 증가하였으며, 식물성 식이조성물군에서는 HFCD대조군에 비하여 통계적으로 유의하게 감소하였다. 고지방-고콜레스테롤 첨가로 인하여 HFCD 대조군에서 간 무게가 증가하였고, 반면, 식물성 식이조성물군은 HFCD 대조군에 비하여 간조직의 무게가 유의하게 감소하는 경향을 보였다. 또한 고지방-고콜레스테롤 식이에 의해 증가된 혈청 지질 중 TC, TG, LDL-콜레스테롤 농도가 식물성 식이조성물군에서 유의하게 감소하였으며, 동맥경화지수 역시 감소하였다. 이상에서 고지방-고콜레스테롤 식이를 급여한 흰쥐에게 발아현미, 흑두, 검정깨, 다시마, 녹차 등의 식이조성물 첨가식이를 급여했을 때 체중감소, 배변량 증가, 체지방함량 저하, 혈청 중 TC, TG 감소의 유의한 감소작용이 있는 것으로 나타나서, 앞으로 이들 혼합조성물의 적절한 처방으로 다이어트와 고지혈증 개선을 위한 소재로 이용될 수 있을 것으로 사료된다. 또한, 본 연구는 고지혈증 개선 효능이 있는 생식제품 개발시 원료의 레시피 선정에 있어서 기초자료로 활용 가능한 것으로 판단된다.

• 한방재활의학과학회지
• /
• 제31권2호
• /
• pp.1-14
• /
• 2021

Objectives We evaluated the improving effects of Taeksa-tang (TST) using 3T3-L1 cells and C57BL/6 mice were fed on a high-fat diet. Methods The anti-radical activities of TST were studied using 2,2-diphenyl-1-picrylhydrazyl and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid). The content of total polyphenol was measured using Folin-Ciocalteu reagent, whereas aluminum chloride colorimetric method was used for the content of total flavonoid. Moreover, the factors related to lipid profile and the protein expressions such as 𝛽-oxidation and anti-oxidant enzyme were analyzed using serum and western blotting of 3T3-L1 cells. Additionally, we examined lipolysis through glycerol appearance in mouse adipose tissue. Results TST treatment showed strong free radical scavenging activities with half maximal inhibitory concentration and the presence of a amount of total polyphenol and total flavonoid. TST treatment significantly increased factors related to 𝛽-oxidation such as carnitine palmitoyl transferase-1 and uncoupling protein 2 via the phosphorlyation of liver kinase B1 (LKB1) and AMP-activated protein kinase (AMPK). Moreover, the protein expressions of anti-oxidant enzyme and lipolysis were significantly elevated by TST administration. In addition, TST supplementation lowered serum malondialdehyde, triglyceride, and total cholesterol levels compared with the control group. Taken together, these data suggest that TST treatment regulated lipid parameters via the increase of 𝛽-oxidation by LKB1-AMPK signaling pathway. Conclusions TST may have a potential remedy in the prevention and treatment of obesity. Therefore, this study may provide the scientific basis for TST use.

• 생명과학회지
• /
• 제29권9호
• /
• pp.964-971
• /
• 2019

간의 지질 축적과 인슐린 저항성은 비알콜성 지방간 환자에게서 증가한다. Piperine은 후추(Piper nigrum)와 필발(인도산 후추, P. longum)의 주요 성분으로 항암, 항비만, 항 당뇨병, 항염증 및 항산화 등의 생리활성이 보고되었다. 그러나 piperine의 인간 간세포 HepG2 세포에서 지질 축적과 인슐린 저항성의 억제제로서의 연구는 보고된 바가 없다. 본 연구의 목적은 지질 축적 및 인슐린 저항성에 대한 piperine의 효과를 palmitate처리된 HepG2 세포에서 잠재적인 분자 기전을 밝히는 것이다. 그 결과 piperine처리군은 지질 함량을 감소시켰고, 지방 형성 표적 유전자인 SREBP-1c와 FAS의 발현을 억제함으로써 palmitate처리된 세포내 지질 축적을 감소시켰다. 게다가 piperine처리군은 지방산 산화에 관련된 CPT-1과 인산화된 ACC 및 인산화된 IRS-1 (Tyr632)와 Akt의 레벨을 증가시켰다. 또한, piperine처리군은 인산화된 IRS-1 (Ser307)의 레벨을 감소시켰다. 결론적으로 palmitate처리된 HepG2 세포에서 piperine은 SREBP-1와 FAS발현의 감소 및 CPT-1과 ACC 인산화의 증가 및 인산화된 IRS-1(Try632)와 Akt 신호전달 경로를 조절함으로써 지질 축적 및 인슐린 저항성을 개선함을 확인하였다. 따라서 piperine의 지질 축적 및 인슐린 저항성을 예방하는 약물로써 가능성이 제시되었다.

• Journal of Applied Biological Chemistry
• /
• 제62권3호
• /
• pp.229-237
• /
• 2019

More effective treatments are needed for non-alcoholic fatty liver disease (NAFLD). We hypothesized that water extracts of blackberry fruits (BF) and leaves (BL) and their combinations (BFL) reduce fat deposition in HepG2 cells and modulate shor-tchain fatty acids (SCFA) and fecal bacteria in vitro. HepG2 cells were treated with BF, BL, BFL1:2, and BFL1:3 for 1 h, and 0.5 mM palmitate was added to the cells. Moreover, low ($30{\mu}g/mL$) and high doses ($90{\mu}g/mL$) of BL and BF were applied to fecal bacteria in vitro, and SCFA was measured by GC. BL, BF, BFL1:2, and BFL1:3 reduced triglyceride deposition in the cells in a dose-dependent manner, and BFL1:2 and BFL1:3 had a stronger effect than BF. The content of malondialdehyde, an index of oxidative stress, was also reduced in BL, BF, and BFL1:2 with increasing superoxide dismutase and glutathione peroxidase activities. The mRNA expression of acetyl CoA carboxylase, fatty acid synthase, and sterol regulatory element-binding protein-1c was reduced in BL, BF, BFL1:2, and BFL1:3 compared to the control, and BFL1:2 had the strongest effect. By contrast, the carnitine palmitolytransferase-1expression, a regulator of fatty acid oxidation, increased mostly in BFL1:2 and BFL1:3. Tumor necrosis factor-${\alpha}$ and interleukin-$1{\beta}$ expression was reduced in BL compared to that in BF and BFL1:2 in HepG2 cells. Interestingly, BL increased propionate production, and BF increased butyrate and propionate production and increased total SCFA content in fecal incubation. BF increased the contents of Bifidobacteriales and Lactobacillales and decreased those of Clostridiales, whereas BL elevated the contents of Bacteroidales and decreased those of Enterobacteriales. In conclusion, BFL1:2 and BFL1:3 may be potential therapeutic candidates for NAFLD.

• Nutrition Research and Practice
• /
• 제16권1호
• /
• pp.14-32
• /
• 2022

BACKGROUND/OBJECTIVES: Peroxisome proliferator-activated receptor-gamma co-activator-1α (PGC-1α) has a central role in regulating muscle differentiation and mitochondrial metabolism. PGC-1α stimulates muscle growth and muscle fiber remodeling, concomitantly regulating lactate and lipid metabolism and promoting oxidative metabolism. Gynostemma pentaphyllum (Thumb.) has been widely employed as a traditional herbal medicine and possesses antioxidant, anti-obesity, anti-inflammatory, hypolipemic, hypoglycemic, and anticancer properties. We investigated whether G. pentaphyllum extract (GPE) and its active compound, gypenoside L (GL), affect muscle differentiation and mitochondrial metabolism via activation of the PGC-1α pathway in murine C2C12 myoblast cells. MATERIALS/METHODS: C2C12 cells were treated with GPE and GL, and quantitative reverse transcription polymerase chain reaction and western blot were used to analyze the mRNA and protein expression levels. Myh1 was determined using immunocytochemistry. Mitochondrial reactive oxygen species generation was measured using the 2'7'-dichlorofluorescein diacetate assay. RESULTS: GPE and GL promoted the differentiation of myoblasts into myotubes and elevated mRNA and protein expression levels of Myh1 (type IIx). GPE and GL also significantly increased the mRNA expression levels of the PGC-1α gene (Ppargc1a), lactate metabolism-regulatory genes (Esrra and Mct1), adipocyte-browning gene fibronectin type III domain-containing 5 gene (Fndc5), glycogen synthase gene (Gys), and lipid metabolism gene carnitine palmitoyltransferase 1b gene (Cpt1b). Moreover, GPE and GL induced the phosphorylation of AMP-activated protein kinase, p38, sirtuin1, and deacetylated PGC-1α. We also observed that treatment with GPE and GL significantly stimulated the expression of genes associated with the anti-oxidative stress response, such as Ucp2, Ucp3, Nrf2, and Sod2. CONCLUSIONS: The results indicated that GPE and GL enhance exercise performance by promoting myotube differentiation and mitochondrial metabolism through the upregulation of PGC-1α in C2C12 skeletal muscle.

• 한방재활의학과학회지
• /
• 제32권2호
• /
• pp.19-36
• /
• 2022

Objectives This study is to investigate the effects and mechanisms of Imyo-san (IMS) on the obese mice model induced by high-fat diet. Methods Antioxidative capacity was measured by in vitro method. C57BL/6 mice were randomly assigned into 5 groups (n=7). Normal group was fed general diet (Normal). The other 4 groups were fed high fat diet (HFD) with water (Control), with Garcinia gummi-gutta (GG, Garcinia gummi-gutta 200 mg/kg), with low-dose IMS (IMSL, Imyo-san 0.54 g/kg) and with high-dose IMS (IMSH, Imyo-san 1.08 g/kg). Results IMS showed high radical scavenging activity. After 6 week experiment, body weight, food intake, food efficiency ratio (FER), epididymal fat and liver weight, triglyceride (TG), total cholesterol (TC), high density lipoprotein (HDL) cholesterol, low density lipoprotein (LDL) cholesterol, very low density lipoprotein (VLDL) cholesterol, sterol regulatory element-binding protein-1 (SREBP-1), phospho-acetyl-CoA carboxylase (p-ACC), fatty acid synthase (FAS), stearoyl-CoA desaturase-1 (SCD-1), SREBP-2, 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), phospho-liver kinase B1 (p-LKB1), phospho-AMP-activated protein kinase (p-AMPK), peroxisome proliferator-activated receptor 𝛼 (PPAR𝛼), peroxisome proliferator-activated receptor 𝛾 coactivator-1𝛼 (PGC-1𝛼), uncoupling protein-2 (UCP-2), carnitine palmitoyltransferase 1A (CPT-1A), and histology of liver and epididymal fat were measured and analysed. Body weight gain, FER, liver and epididymal fat weight of IMS groups were significantly decreased. There were significant improvements in blood lipids with less TG, TC, LDL-cholesterol, VLDL-cholesterol and more HDL-cholesterol. Proteins associated with lipid synthesis (SREBP-1, p-ACC, FAS, SCD-1) and cholesterol (SREBP-2, HMGCR) was improved. Factors regulating lipid synthesis and lipid catabolism (p-LKBI, p-AMPK, PPARα, PGC-1α, UCP-2, CPT-1A) were increased. In histological examinations, IMS group had smaller fat droplets than control group. All results increased depending on concentration. Conclusions It can be suggested that IMS has anti-obesity effects with improving lipid metabolism.

• 한방비만학회지
• /
• 제22권2호
• /
• pp.93-101
• /
• 2022

Objectives: This study aimed to observe the anti-diabetic effect and underlying mechanisms of Galgunhwanggumhwangryun-tang (GHH; Gegen-Qinlian-decoction) in the C2C12 myotubes. Methods: GHH (1.0 mg/ml) or metformin (0.75 mM) or insulin (100 nM) were treated in C2C12 myotubes after 4 days differentiation. The glucose uptake was assessed by 2-[N-(7-160 nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-d-glucose uptake by C2C12 cells. The expression of adenosine monophosphate-activated protein kinase (AMPK) and phosphorylation AMPK (pAMPK) were measured by western blot. We also evaluated gene expression of glucose transporter type 4 (Slc2a4, formerly known as GLUT4), glucokinase (Gk), carnitine palmitoyltransferase IA (Cpt1a), nuclear respiratory factors 1 (Nrf1), mitochondrial transcription factor A (Tfam), and peroxisome proliferator-activated receptor γ coactivator 1α (Ppargc1a) by quantitative real-time polymerase chain reaction. Results: GHH promoted glucose uptake in C2C12 myotubes. The expression of AMPK protein, which plays an essential role in glucose metabolism, was increased by treatment with GHH. GHH treatment tended to increase gene expression of Slc2a4, Gk, and Nrf1 but was not statistically significant. However, GHH significantly improved Tfam and Ppargc1a gene expression in C2C12 myotubes. Conclusions: In summary, GHH treatment promoted glucose uptake in C2C12 myotubes. We suggest that these effects are associated with increased gene expression involved in mitochondrial biosynthesis and oxidative phosphorylation, such as Tfam and Ppargc1a, and increased expression of AMPK protein.

• Journal of Ginseng Research
• /
• 제47권2호
• /
• pp.302-310
• /
• 2023

Background: The most common type of dementia, Alzheimer's disease (AD), is marked by the formation of extracellular amyloid beta (Aβ) plaques. The impairments of axons and synapses appear in the process of Aβ plaques formation, and this damage could cause neurodegeneration. We previously reported that non-saponin fraction with rich polysaccharide (NFP) from Korean Red Ginseng (KRG) showed neuroprotective effects in AD. However, precise molecular mechanism of the therapeutic effects of NFP from KRG in AD still remains elusive. Methods: To investigate the therapeutic mechanisms of NFP from KRG on AD, we conducted proteomic analysis for frontal cortex from vehicle-treated wild-type, vehicle-treated 5XFAD mice, and NFP-treated 5XFAD mice by using nano-LC-ESI-MS/MS. Metabolic network analysis was additionally performed as the effects of NFP appeared to be associated with metabolism according to the proteome analysis. Results: Starting from 5,470 proteins, 2,636 proteins were selected for hierarchical clustering analysis, and finally 111 proteins were further selected for protein-protein interaction network analysis. A series of these analyses revealed that proteins associated with synapse and mitochondria might be linked to the therapeutic mechanism of NFP. Subsequent metabolic network analysis via genome-scale metabolic models that represent the three mouse groups showed that there were significant changes in metabolic fluxes of mitochondrial carnitine shuttle pathway and mitochondrial beta-oxidation of polyunsaturated fatty acids. Conclusion: Our results suggested that the therapeutic effects of NFP on AD were associated with synaptic- and mitochondrial-related pathways, and they provided targets for further rigorous studies on precise understanding of the molecular mechanism of NFP.