• 한국식생활문화학회지
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• 제37권6호
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• pp.503-509
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• 2022

Methylglyoxal is a highly reactive precursor which forms advanced glycation end products (AGEs). AGEs and methylglyoxal are known to induce various diseases such as diabetes, vascular disorders, Diabetes Mellitus (DM), and neuronal disorders. Juglans regia L is an important food commonly used worldwide, having nutritious components, including phenolic compounds. Since ancient times, Juglans regia L have been differently applied by various countries for health and in diverse diseases, including arthritis, asthma, skin disorders, cancer, and diabetes mellitus. However, the effect of diabetes-induced renal damage against AGEs remains unclear. This study evaluates the anti-glycation and renal protective effects of ethanol extract of Juglans regia L against methylglyoxal-induced renal tubular epithelial cell death. Exposure to methylglyoxal resulted in reduced cell viability in NRK-52E cells, but co-treatment with Juglans regia L extracts significantly increased the cell viability. In addition, we examined the anti-glycation effect of Juglans regia L extracts. Compared to the positive control aminoguanidine and Alagebrium, treatment with Juglans regia L extracts significantly inhibited the formation of AGEs, collagen cross-linking, and breaking collagen cross-linking. Taken together, our results indicate that Juglans regia L is a potential therapeutic agent for regulating diabetic complications by exerting anti-glycation and renal protective activities.

• 한국식품영양과학회지
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• 제43권11호
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• pp.1658-1664
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• 2014

본 연구에서는 고지방식이와 streptozotocin으로 유도된 제2형 당뇨 마우스에서 새싹추출물의 항당뇨 효과를 살펴보았다. 제2형 당뇨 유도 후 4주 동안의 체중 변화를 관찰한 결과 새싹추출물군과 메트포민군에서 유의한 체중 감소 변화가 나타났으며, 식이섭취량에 따른 변화는 모든 실험군 간의 차이가 없었다. 공복혈당은 고지방식이군의 경우 실험종료일까지 지속적으로 상승하였고, 이와 대조적으로 새싹추출물과 메트포민군의 경우 실험 2주째부터 감소하여 실험 종료 4주째에서는 고지방식이군보다 유의적으로 감소하였다. 경구 내당능 검사는 포도당 섭취 후 60분, 90분, 120분에서 새싹추출물과 메트포민군이 고지방식이군보다 유의적으로 감소하였으며, 인슐린 내성 검사는 120분에서 새싹추출물과 메트포민군이 고지방식이군보다 유의성 있게 감소하였다. 혈중 지질 농도 변화에서 총콜레스테롤, 중성지방 그리고 LDL 콜레스테롤 농도는 고지방식이군에 비해 새싹추출물과 메트포민군에서 유의적으로 감소하였고, HDL 콜레스테롤 농도는 고지방식이군에 비해 새싹추출물과 메트포민군에서 증가하였다. 간독성의 지표인 glutamate oxaloacetate transaminase와 glutamate pyruvate transaminase 효소 활성도는 메트포민투여군과 고지방식이군을 제외한 실험군들 간에 유의성이 나타나지 않았다. 혈중 인슐린과 렙틴 농도는 고지방식이군에 비해 새싹추출물과 메트포민군에서 유의적으로 감소하였다. 이상의 결과를 바탕으로 새싹추출물은 제2형 당뇨 마우스에서 체중을 감소시키고 혈중지질 대사 이상을 조절하면서 인슐린 저항성을 감소시켜 혈당을 개선하므로 항당뇨 효과가 있는 우수한 식품 소재로서의 개발 가능성을 시사하고 있다.

• 대한본초학회지
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• 제26권2호
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• pp.1-10
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• 2011

Objective ： Lonicera japonica contains anti complementary polysaccharides and polyphenolic compound. Among these polyphenolic substances, chlorogenic acid is the major active component of this plant. However, the immunological mechanisms for these activities, have not been elucidated, nor the active components. To clarify immunomodulatory effects of those we examined the relationship between the activity of CD8+ T cell-mediated lysis and the frequency of cytokine profiles in spleen, thymus (especially IFN-${\gamma}$, IL-4, GM-CSF etc.) expressing CD8+ T cells activated by IL-2. Methods : To study immunomodulatory effects ethyl acetate fraction from Lonicera japonica, chlorogenic acid on cytokine gene expression from spleen, thymus cells, RT-PCR was performed after quantitative normalization for each gene by a densitometry using ${\beta}$-actin gene expression. A modified standard $^{51}Cr$-release assay was used to measure cytotoxic activities of cytotoxic T cells. Spleen, thymus cells from NOD mice were stained with CD3, CD4, CD44, CD69 in staining buffer and analyzed by two color flow cytometry. Results : We showed that ethyl acetate fraction from Lonicera japonica in combination with IL-2 resulted in a significant enhancement of PCR products for IFN-${\gamma}$, IL-4, IL-10, GM-CSF, IL-6 and cytotoxtic CD8+ T cell proportion in spleen and thymus T cells in NOD mice. This suggests that IFN-${\gamma}$, IL-6 like IL-4 may be acting as a regulatory rather than proinflammatory cytokine. Conclusions : In conclusion, based on the results of the present study which showed that ethyl acetate fraction from Lonicera japonica and chlorogenic acid upregulating cytokine gene expression in spleen and thymus, we are tempted to speculate that some of the therapeutic efficacies such as anti-diabetic activity of Lonicera japonica are due to the immunomodulatory its ethylacetate fraction and chlorogenic acid.

• Biomolecules & Therapeutics
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• 제29권6호
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• pp.650-657
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• 2021

Metformin is an anti-diabetic drug and has anticancer effects on various cancers. Several studies have suggested that metformin reduces cell proliferation and stimulates cell-cycle arrest and apoptosis. However, the definitive molecular mechanism of metformin in the pathophysiological signaling in endometrial tumorigenesis and metastasis is not clearly understood. In this study, we examined the effects of metformin on the cell viability and apoptosis of human cervical HeLa and endometrial HEC-1-A and KLE cancer cells. Metformin suppressed cell growth in a dose-dependent manner and dramatically evoked apoptosis in HeLa cervical cancer cells, while apoptotic cell death and growth inhibition were not observed in endometrial (HEC-1-A, KLE) cell lines. Accordingly, the p27 and p21 promoter activities were enhanced while Bcl-2 and IL-6 activities were significantly reduced by metformin treatment. Metformin diminished the phosphorylation of mTOR, p70S6K and 4E-BP1 by accelerating adenosine monophosphate-activated kinase (AMPK) in HeLa cancer cells, but it did not affect other cell lines. To determine why the anti-proliferative effects are observed only in HeLa cells, we examined the expression level of liver kinase B1 (LKB1) since metformin and LKB1 share the same signalling system, and we found that the LKB1 gene is not expressed only in HeLa cancer cells. Consistently, the overexpression of LKB1 in HeLa cancer cells prevented metformin-triggered apoptosis while LKB1 knockdown significantly increased apoptosis in HEC-1-A and KLE cancer cells. Taken together, these findings indicate an underlying biological/physiological molecular function specifically for metformin-triggered apoptosis dependent on the presence of the LKB1 gene in tumorigenesis.

• 생명과학회지
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• 제27권9호
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• pp.1052-1058
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• 2017

우뭇가사리(Gelidium amansi)는 홍조류로서 우뭇가사리과(Gelidiaceae)에 속한다. 현재까지 우뭇가사리의 항산화 및 항비만 효과 등의 기능들이 연구되었으나 식후 혈당 수치에 미치는 영향에 관한 연구는 부족한 실정이다. 이에 본 연구에서는 Gelidium amansii extract (GAE)가 탄수화물 가수분해 효소(${\alpha}-glucosidase$, ${\alpha}-amylase$)에 미치는 억제 효과 및 streptozotocin (STZ)으로 유도된 당뇨병 마우스의 식후고혈당에 미치는 완화효과를 조사하였다. 정상군과 STZ으로 유도된 당뇨병 마우스에 수용성 전분(2 g/kg body weight)을 경구투여한 후 GAE (300 mg/kg body weight) 또는 acarbose (100 mg/kg body weight)를 단독 또는 함께 투여하였다. 혈당은 꼬리채혈을 통해 0, 30, 60, 120분 간격으로 측정하였다. ${\alpha}-glucosidase$와 ${\alpha}-amylase$에 대한 GAE의 $IC_{50}$ 값은 각각 $0.099{\pm}0.009mg/ml$와 $0.178{\pm}0.038mg/ml$의 결과값을 나타내어, 양성대조군인 acarbose보다 더 효과적이었다. STZ으로 유발된 당뇨병 마우스의 식후 혈당 수치는 대조군에 비해 GAE 투여 시 유의적으로 더 낮았다(p<0.05). 또한 GAE 투여는 당뇨병 마우스에서 포도당 반응에 대한 곡선하면적 감소와 관련이 있었다(p<0.05). 이러한 결과는 GAE가 ${\alpha}-glucosidase$, ${\alpha}-amylas$와 같은 탄수화물 가수분해 효소를 억제함으로써 식후 고혈당을 완화시키는 유용한 천연기능성 식품이 될 것으로 사료된다.

• 한국식품영양과학회지
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• 제37권5호
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• pp.542-547
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• 2008

본 연구에서는 제2형 당뇨병를 가진 GK 흰쥐(Goto-Kakizaki) 간에서 추출한 cytosol과 심장에서 추출한 mitochondria를 이용한 모델계에서 당대사 관련 효소인 glucokinase glucokinase(GCK), pyruvate dehydrogenase(PDH), acetyl-CoA carboxylase(ACC) 및 glucosidase 활성에 대한 한약재의 물 추출물의 항당뇨 효과를 연구하였다. 그리고 역시 그들의 물 추출물의 free radical 소거활성을 DPPH 방법으로 알아보았다. Free radical 소거활성은 산수유(CF), 목단피(MDB), 천화분(CHB) 그리고 산약(SY)의 물 추출물이 강했고 반면에 백목령(BBR), 숙지황(SGH)과 택사(TS)는 낮은 소거작용을 나타내었다. 간 cytosol의 GCK 활성은 산수유(CF)와 천화분(CHB)에서 다른 추출물보다 더 강했다. 심장미토콘드리아의 PDH 활성은 택사(TS)를 제외하고 모든 추출물에서 대조군과 비교하여 높았다. 간 cytosol의 ACC 활성은 대조군보다 산수유(CF), 천화분(CHB), 숙지황(SGH), 택사(TS) 그리고 산약(SY) 추출물에서 높았다. 산수유(CF), 백복령(BBR) 및 목단피(MDB) 추출물은 ${\alpha}$-glucosidase 활성 감소를 유도했다. 따라서 모든 추출물은 혈당 상승을 억제할 수 있는 항당뇨 기능성식품이나 약품 개발을 위한 기능성 천연 소재로 이용될 수 있을 가능성을 제시하였다.

• 한국식품저장유통학회지
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• 제24권6호
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• pp.879-884
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• 2017

몽골산 I. bungei를 80% 메탄올로 침지 추출하여 얻어진 추출물에 대해 n-hexane, EtOAc 및 n-BuOH의 유기용매를 활용하여 순차 분획을 실시하였고, 얻어진 결과물에 대하여 총 페놀함량, DPPH, $ABTS^+$ 라디칼 소거능 및 ${\alpha}$-glucosidase 저해활성을 평가하였다. DPPH 라디칼 소거활성은 페놀성 화합물의 함량이 높은 EtOAc 가용 분획물에서 $IC_{50}$ 값이 $148.7{\pm}1.6{\mu}g/mL$으로 우수한 DPPH 라디칼 소거 활성을 확인하였고, $ABTS^+$ 라디칼 소거활성 역시 I. bungei의 EtOAc 가용 분획물에서 $IC_{50}$ 값이 $27.8{\pm}0.9{\mu}g/mL$의 매우 우수한 라디칼 소거활성을 확인하였고, 다량 존재하는 페놀성 화합물과 라디칼 소거활성의 관련성을 나타내었다. 또한 ${\alpha}$-glucosidase 저해활성을 평가한 결과 EtOAc 가용 분획물에서 $IC_{50}$값은 $4.6{\pm}0.1{\mu}g/mL$의 강력한 저해활성을 나타내었으며, 이는 양성 대조군인 acarbose의 $IC_{50}$ 값인 $473.2{\pm}5.5{\mu}g/mL$과 비교했을 때 매우 우수한 활성을 나타내었으며, 다양한 화합물이 함유된 상태의 추출물 시료를 단일물질로 정제할 경우 더욱 우수한 활성의 화합물이 존재할 가능성을 기대하게 한다. 향후 이들 추출물의 활성물질 동정을 통한 활성 기작에 대한 연구가 필요하며, 본 연구결과로 보다 우수한 라디칼 소거활성 및 ${\alpha}$-glucosidase 저해활성을 가지는 새로운 천연 기능성 소재 발굴을 위한 기초자료로 활용 가능할 것으로 사료된다.

• 대한의생명과학회지
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• 제20권4호
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• pp.209-220
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• 2014

Vascular endothelial growth factor (VEGF) is a key factor involved in the induction of angiogenesis and has become an attractive target for anti-angiogenesis therapies. The purpose of this study was to elucidate the anti-angiogenic activity of Rubus coreanus Miquel water extract (RCME). Rubus coreanus Miquel has long been employed as a traditional medicine, and recent studies have demonstrated that it has measureable biological activities. Thus, we investigated for the first time the effect of RCME on angiogenesis and its underlying signaling pathways. The effects of RCME were tested on in vitro models of angiogenesis, namely, proliferation, migration, invasion and tube formation of human umbilical vein endothelial cells as well as an ex vivo model of vessel sprouting from the rat aorta in response to VEGF. We observed that VEGF-induced angiogenesis was strongly suppressed by RCME treatment compared to that of the control group. Moreover, we found that RCME inhibited VEGF-induced activation of matrix metalloproteinases and phosphorylation of extracellular signal-regulated kinase and p38, and also effectively inhibited phosphorylation of VEGF receptor 2. These results indicated that RCME inhibits angiogenesis by suppressing phosphorylation of the VEGF receptor and may be useful for the treatment of angiogenesis-dependent diseases such as cancer and diabetic retinopathy.

• Nutrition Research and Practice
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• 제10권3호
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• pp.282-287
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• 2016

BACKGROUND/OBJECTIVES: Jerusalem artichoke has inhibitory activity against ${\alpha}$-glucosidase and decreases fasting serum glucose levels, which may be related to its fructan content. The biological activity of fructan can be influenced by the degree of polymerization. Thus, in this study, the inhibitory effects of original and fermented purple Jerusalem artichoke (PJA) on ${\alpha}$-glucosidase were compared in vitro. Additionally, the anti-diabetes effect of Lactobacillus plantarum-fermented PJA (LJA) was studied in a non-insulin-dependent diabetes mellitus animal model (C57BIKsJ db/db). MATERIALS/METHODS: The water extract of PJA was fermented by L. plantarum, and two strains of Bacillus subtilis to compare their anti-${\alpha}$-glucosidase activities in vitro by ${\alpha}$-glucosidase assays. The anti-diabetes effect of LJA was studied in a non-insulin-dependent diabetes mellitus animal model (C57BIKsJ db/db) for seven weeks. During the experiment, food intake, body weight, and fasting blood glucose were measured every week. At the end of the treatment period, several diabetic parameters and the intestinal ${\alpha}$-glucosidase activity were measured. RESULTS: The LJA showed the highest ${\alpha}$-glucosidase inhibitory activity in vitro. In the in vivo study, it resulted in a significantly lower blood glucose concentration than the control. Serum insulin and HDL cholesterol levels were significantly higher and the concentrations of triglycerides, non-esterified fatty acids, and total cholesterol were significant lower in mice treated with LJA after seven weeks. In addition, the intestinal ${\alpha}$-glucosidase activity was partially inhibited. CONCLUSIONS: These results suggested that LJA regulates blood glucose and has potential use as a dietary supplement.

• The Korean Journal of Physiology and Pharmacology
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• 제22권5호
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• pp.525-538
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• 2018

Post-traumatic stress disorder (PTSD) is a trauma-induced psychiatric disorder characterized by impaired fear extermination, hyperarousal, and anxiety that may involve the release of monoamines in the fear circuit. The reported pharmacological properties of tetramethylpyrazine (TMP) include anti-cancer, anti-diabetic, anti-atherosclerotic, and neuropsychiatric activities. However, the anxiolytic-like effects of TMP and its mechanism of action in PTSD are unclear. This study measured several anxiety-related behavioral responses to examine the effects of TMP on symptoms of anxiety in rats after single prolonged stress (SPS) exposure by reversing the serotonin (5-HT) and hypothalamic-pituitary-adrenal (HPA) axis dysfunction. Rats were given TMP (10, 20, or 40 mg/kg, i.p.) for 14 days after SPS exposure. Administration of TMP significantly reduced grooming behavior, increased the time spent and number of visits to the open arm in the elevated plus maze test, and significantly increased the number of central zone crossings in the open field test. TMP administration significantly reduced the freezing response to contextual fear conditioning and significantly restored the neurochemical abnormalities and the SPS-induced decrease in 5-HT tissue levels in the prefrontal cortex and hippocampus. The increased 5-HT concentration during TMP treatment might be partially attribute to the tryptophan and 5-hydroxyindoleacetic acid mRNA level expression in the hippocampus of rats with PTSD. These findings support a role for reducing the altered serotonergic transmission in rats with PTSD. TMP simultaneously attenuated the HPA axis dysfunction. Therefore, TMP may be useful for developing an agent for treating psychiatric disorders, such those observed in patients with PTSD.