• 생약학회지
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• 제40권2호
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• pp.128-136
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• 2009

This study was carried out to investigate the antidiabetic and antioxidative effect of Lycii fructus in the Streptozotocin(STZ)-induced diabetic rats. The effective fractions were prepared as a form of organic solvents of $CH_{3}(CH_{2})_{4}CH_{3}$ $CHCI_{3}$, EtOAc, BuOH and $H_{2}O$ fractions prepared from the EtOH extract of Lycii fructus and The diabetes were induced by an tail-intravenous injection of STZ with a dose of 45 mg/kg dissolved in citrate buffer. The various fractions of Lycii fructus were orally administrated once a day for 7 days. The contents of serum glucose, and triglyceride in the $CHCI_{3}$ fraction and hepatic lipid peroxidation in the EtOAc, BuOH and $H_{2}O$ fractions treated rats were significantly decreased when compared to those of the STZ-control group In addition, an activity of hepatic GST in the BuOH fraction treated rats was significantly increased compared to that of the STZ-control group. whereas, activities of hepatic catalase, GSH-Px in the BuOH fraction treated rats were significantly decreased compared to those of the STZ-control group. Meanwhile, The content of hepatic glycogen and avtivity of hepatic glucokinase in $CHCI_{3}$ fraction treated rats were significantly increased, but activity of glucose-6-pase was significantly decreased in the $CHCI_{3}$ fraction treated rats. In conclusion, these results indicated that the BuOH fraction of Lycii fructus was effective for the antioxidation, and also the $CHCI_{3}$ fraction of Lycii fructus was effective for the antidiabetes in the STZ-induced diabetic rats.

• 생약학회지
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• 제46권2호
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• pp.105-108
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• 2015

To establish the anti-diabetic(α-glucosidase inhibitory) activity of D. lotus leaf extract, isolate and identify the constituents responsible for the activity. The methanolic extract of leaves was partitioned between water, n-butanol and ethyl acetate. Bio-assay guided fractionation, based on inhibition of ;${\alpha}$-glucosidase, allowed isolation and identification of the active components. Liquid chromatography/mass spectrometry(LC/MS), ¹ H-NMR and ¹³ C-NMR spectra analyses demonstrated that the active compound was myricetin-3-O-;${\alpha}$-L-rhamnoside(1). Compound 1 demonstrated a strong inhibition on the α-glucosidase, in vitro and ;${\alpha}$-glucosidase inhibitory value was calculated as 98.08%, when that of a reference drug, acarbose was estimated as 83.03%. The present study indicates compound 1 could be considered as an ;${\alpha}$-glucosidase inhibitor and developed as an important antidiabetes agent for type II diabetes therapy.

• 한국식품영양학회지
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• 제25권1호
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• pp.123-131
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• 2012

The objective of the present study was to evaluate the potential antidiabetic and antioxidant effect of the ethanol extract from Chrysanthemum cornarium L. var. spatiosum(CSE) against alloxan-induced oxidative stress in pancreatic ${\beta}$-cells, HIT-T15. In this study, the antidiabetic effect of CSE was examined using the 3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazoliu bromide(MTT) cell proliferation assay, lactate dehydrogenase(LDH) release assay, $NAD^+$/NADH ratio and insulin secretion. To further investigate whether CSE is involved in the antioxidant activity of alloxan-damaged HIT-T15 cells, its antioxidant effect against alloxan-induced oxidative stress was measured in HIT-T15 cells by determining the levels of antioxidant enzymes including superoxide dismutase(SOD), glutathione S-transferase(GST), glutathione reductase(GR) and glutathione peroxidase(GPx). The results of this analysis showed that alloxan significantly decreased cell viability, increased LDH leakage, and lowered $NAD^+$/NADH ratio and insulin secretion in HIT-T15 cells. However, CSE significantly increased the viability of alloxan-treated cells and lowered LDH leakage. The intracellular NAD+/NADH ratio and insulin secretion were also significantly increased by 1.7-fold and 1.3-fold, respectively, after treatment with 100 ${\mu}g/m{\ell}$ CSE. The HIT-T15 cells treated with alloxan showed significant decreases in the activities of antioxidant enzymes, while CSE significantly elevated the levels of antioxidant enzymes. These findings suggest that CSE could have a protective effect against cytotoxicity and dysfunction of pancreatic cells in the presence of alloxan-induced oxidative stress.

• 한국약용작물학회지
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• 제26권5호
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• pp.382-390
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• 2018

Background: The plant Aster koraiensis has long been used as an ingredient in folk medicine. It has been reported that Aster koraiensis extract (AKE) prevents the progression of diabetes-induced retinopathy and nephropathy. However, although these beneficial effects of AKE on diabetes complications have been identified, the antidiabetic effects of AKE have not yet been completely investigated and quantified. In the present study, the glucose-lowering and antioxidant effects of aqueous and ethanolic AKEs were evaluated. Methods and Results: The glucose-lowering effects of aqueous and ethanolic (30%-, 50%-, and 80%-ethanol) AKEs were investigated via ${\alpha}$-glucosidase inhibitory assays. The mode of inhibition by AKEs on ${\alpha}$-glucosidase was identified through kinetic analysis. The total antioxidant capacity of each of the 4 AKEs was evaluated by assessing their conversion rate of $Cu^{2+}$ to $Cu^+$. The content of chlorogenic acid and 3,5-di-O-caffeoylquinic acid, the bioactive compounds in AKE, in each extract were analyzed by high performance liquid chromatography (HPLC). The AKEs showed potent ${\alpha}$-glucosidase inhibitory activity with mixed inhibition mode, and significant antioxidant capacity. Conclusions: These results of this study suggested that the AKEs tested had ${\alpha}$-glucosidase inhibitory and antioxidant effects. Among the extracts, the 80% ethanol extract showed the most significant ${\alpha}$-glucosidase inhibitory activity, with a half maximal inhibitory concentration ($IC_{50}$ value) of $1.65{\pm}0.36mg/m{\ell}$ and a half maximal effective concentration ($EC_{50}$ value) for its antioxidant activity of $0.42{\pm}0.10mg/m{\ell}$. It can therefore be used as a source of therapeutic agents to treat diabetes patients.

• 한국자원식물학회지
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• 제25권2호
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• pp.184-192
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• 2012

본 연구는 췌장베타세포인 HIT-T15 세포를 이용하여 매실주정추출물(PME)의 alloxan에 의한 산화스트레스로부터의 세포보호, 인슐린 분비능 및 항산화 효소 활성을 평가하였다. PME는 alloxan에 의해 유발된 산화스트레스로부터 세포를 보호하여 세포생존율을 증가시켰다. PME는 세포막 손상지표인 LDH 방출을 억제하였고 $NAD^+$/NADH ratio를 유의적으로 증가시켜 세포사멸이 억제되어짐을 확인하였다. 또한 alloxan 단독처리군에 비해 250 ${\mu}g$/ml PME 처리군에서 인슐린 분비량이 유의성 있게 증가하였다. Alloxan과 PME를 동시에 처리하여 HIT-T15세포의 항산화효소 활성을 측정했을 때 산화스트레스에 의해 감소되었던 항산화효소 활성이 PME에 의해 보호되는 효과를 확인하였다. 이상의 연구결과로부터 PME는 세포괴사 및 DNA fragmentation을 억제하고 세포내 항산화효소 활성을 증가시켜 alloxan에 의해 유발된 산화스트레스로부터 췌장베타세포를 보호하고 이에 따른 인슐린 분비능 조절 효과가 있는 것으로 생각된다.

• 분석과학
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• 제32권2호
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• pp.35-47
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• 2019

In this study, high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was employed to detect 26 antidiabetic compounds in adulterated dietary supplements using a simple, selective method. The work presented herein may help prevent incidents related to food adulteration and restrict the illegal food market. The best separation was obtained on a Shiseido Capcell Pak(R) C18 MG-II ($2.0mm{\times}100mm$, $3{\mu}m$), which improved the peak shape and MS detection sensitivity of the target compounds. A gradient elution system composed of 0.1 % (v/v) formic acid in distilled water and methanol at a flow rate of 0.3 mL/min for 18 min was utilized. A triple quadrupole mass spectrometer with an electrospray ionization source operated in the positive or negative mode was employed as the detector. The developed method was validated as follows: specificity was confirmed in the multiple reaction monitoring mode using the precursor and product ion pairs. For solid samples, LOD ranged from 0.16 to 20.00 ng/mL and LOQ ranged from 0.50 to 60.00 ng/mL, and for liquid samples, LOD ranged from 0.16 to 20.00 ng/mL and LOQ ranged from 0.50 to 60.00 ng/mL. Satisfactory linearity was obtained from calibration curves, with $R^2$ > 0.99. Both intra and inter-day precision were less than 13.19 %. Accuracies ranged from 80.69 to 118.81 % (intra/inter-day), with a stability of less than 14.88 %. Mean recovery was found to be 80.6-119.0 % and less than 13.4 % RSD. Using the validated method, glibenclamide and pioglitazone were simultaneously determined in one capsule at concentrations of 1.52 and 0.53 mg (per capsule), respectively.

• Journal of Ginseng Research
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• 제45권1호
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• pp.48-57
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• 2021

Background: Ginsenoside Rh2 is well known for many pharmacological activities, such as anticancer, antidiabetes, antiinflammatory, and antiobesity properties. Glycosyltransferases (GTs) are ubiquitous enzymes present in nature and are widely used for the synthesis of oligosaccharides, polysaccharides, glycoconjugates, and novel derivatives. We aimed to synthesize new ginsenosides from Rh2 using the recombinant GT enzyme and investigate its cytotoxicity with diverse cell lines. Methods: We have used a GT gene with 1,224-bp gene sequence cloned from Lactobacillus rhamnosus (LRGT) and then expressed in Escherichia coli BL21 (DE3). The recombinant GT protein was purified and demonstrated to transform Rh2 into two novel ginsenosides, and they were characterized by nuclear magnetic resonance (NMR) techniques and evaluated by 3-(4, 5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide assay. Results: Two novel ginsenosides with an additional glucopyranosyl (6→1) and two additional glucopyranosyl (6→1) linked with the C-3 position of the substrate Rh2 were synthesized, respectively. Cell viability assay in the lung cancer (A549) cell line showed that glucosyl ginsenoside Rh2 inhibited cell viability more potently than ginsenoside Rg3 and Rh2 at a concentration of 10 μM. Furthermore, glucosyl ginsenoside Rh2 did not exhibit any cytotoxic effect in murine macrophage cells (RAW264.7), mouse embryo fibroblasts cells (3T3-L1), and skin cells (B16BL6) at a concentration of 10 μM compared with ginsenoside Rh2 and Rg3. Conclusion: This is the first report on the synthesis of two novel ginsenosides, namely, glucosyl ginsenoside Rh2 and diglucosyl ginsenoside Rh2 from Rh2 by using recombinant GT isolated from L. rhamnosus. Moreover, diglucosyl ginsenoside Rh2 might be a new candidate for treatment of inflammation, obesity, and skin whiting, and especially for anticancer.

• 생명과학회지
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• 제22권7호
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• pp.920-927
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• 2012

생리활성을 갖는 새로운 기능성 물질을 개발할 목적으로 9종의 오디(Morus alba L.)를 이용하여 물과 60% 에탄올 추출물을 제조하고 이들의 angiotensin converting enzyme 활성억제효과, xanthine oxidase 활성억제효과, ${\alpha}$-amylase 활성억제효과 및 ${\alpha}$-glucosidase 활성억제효과를 탐색하여 본 결과, 페놀함량이 청일뽕과 강원3호 품종의 오디에서 물추출물에서 청일뽕과 강원3호 두품종이, 에탄올 추출물에서 대엽조생, 청일뽕, 강원3호, 희학 및 카타네오 등 5 품종이 2 mg/g 이상의 phenolic compound 함량을 나타내었으며, angiotensin converting enzyme 활성억제효과는 물 추출물에서 백운3호가 $90.9{\pm}4.5%$, 에탄올 추출물에서는 희학 품종이 $81.8{\pm}4.5%$의 활성억제효과를 나타내었다. 또한 xanthine oxidase 활성억제효과는 물 추출물에서 국상20호가 약 10% 정도, 에탄올 추출물에서는 카타네오가 $21.4{\pm}2.3%$의 활성억제효과를 나타내었다. 당분해활성에 관여하는 ${\alpha}$-amylase와 ${\alpha}$-glucosidase 활성억제효과를 측정해 본 결과 물추출물에서만 대엽조생, 수원뽕, 청일뽕, 강원3호, 희학 및 국상20호 등 6품종이 100%의 ${\alpha}$-amylase 저해효과가 관찰되었으며, 백운3호, 대엽조생, 청일뽕 및 희학은 물추출물에서, 대축면, 강원3호 및 국상20호는 에탄올 추출물에서 20% 이상의 ${\alpha}$-glucosidase 저해효과가 확인되었다. 이상의 결과, 높은 생리활성기능을 나타내는 여러 종의 오디의 물과 에탄올 추출물들은 항고혈압 및 항당뇨 효과가 있는 기능성 식품소재로 활용할 수 있을 것으로 판단되었다.

• 생명과학회지
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• 제28권1호
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• pp.26-36
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• 2018

명월초, 여주 및 울금의 물 및 70% 에탄올 추출물에서 항산화 및 ${\alpha}$-glucosidase 저해활성을 측정하였으며, 돼지감자 농축액에 이들 식물류의 에탄올 추출물을 첨가한 5종의 돼지감자 복합물(JA1~5)에서 항산화 및 항당뇨 활성을 비교하였다. 명월초, 여주 및 울금의 에탄올 추출물은 물 추출물에 비해 총 페놀 및 플라보노이드 함량이 많았다. DPPH, ABTS 라디칼 소거활성 및 FRAP법에 의한 환원력은 총 페놀 및 플라보노이드 함량에 의존적이었으며, 특히 명월초와 울금의 에탄올 추출물은 항산화 활성이 비슷한 수준이었다. ${\alpha}$-Glucosidase 저해활성은 에탄올 추출물의 $2,000{\mu}g/ml$ 농도에서 50% 이상이었다. 5종의 복합물은 돼지감자 농축액에 비해 총 페놀 및 플라보노이드 함량이 많았다. 또한 항산화 활성 및 ${\alpha}$-glucosidase 저해활성도 복합물에서 모두 증가되었으며, 특히 JA1의 활성이 유의적으로 높았다. 돼지감자 복합물은 인체 정상 간세포주인 Chang세포에 대해 세포독성이 없었으며, Chang세포에서 AMPK 활성화 및 근육세포인 C2C12세포에서 세포 내 당 유입을 유의적으로 증가시켰다. 이로써 명월초, 여주 및 울금의 추출물이 혼합된 돼지감자 복합물은 항산화 및 항당뇨 활성 증대에 효과적인 것으로 판단된다.

• 동아시아식생활학회지
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• 제18권6호
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• pp.939-948
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• 2008

삼나물 에탄올 추출물이 streptozotocin으로 유발한 쥐의 당뇨증상과 산화적 스트레스에 미치는 영향을 조사하였다. 실험군은 정상군(NC), 당뇨군(DM), 당뇨유발 후 식이에 삼나물 에탄올 추출물을 0.3%를 첨가한 식이군(SA), 당뇨유발 후 식이에 삼나물 에탄올 추출물을 0.6% 첨가한 식이군(SB)으로 구분하여 5주간 사육하였다. SA군과 SB군은 NC군에는 미치지 못하였으나, 당뇨로 인해 초래되는 병리적 증상인 체중 감소, 식이섭취량 및 음용수 섭취량의 증가, 식이효율저하, 간장 및 신장 무게의 증가 현상을 개선하는 효과가 있었다. 실험식이로 5주간 사육한 당뇨쥐의 혈당은 DM군에 비하여 $17.9{\sim}27.2%$를 감소시켰으며 fructosamine의 함량은 $25.6{\sim}32.6%$를 감소시켰다. 또한, 당뇨로 인하여 증가된 alanine aminotransferase(ALT)와 aspartate aminotransferase(AST) 활성을 각각 25.6 및 30.3% 감소시켰다. SA 및 SB군은 DM군에 비하여 혈청 중성지질은 $42.37{\sim}55.51%$ 감소, total cholesterol 함량은 $26.85{\sim}30.44%$ 감소, HDL-cholesterol 함량은 $13.01{\sim}17.35%$ 증가, LDL-cholesterol 함량은 $37.29{\sim}39.11%$가 감소하였다. SA 및 SB군의 xanthine oxidoreductase의 total type, O type 및 O/T(%)은 DM군에 비하여 유의적으로 감소하였으며 간 조직 glutathione함량은 유의적으로 증가 lipid peroxide 함량은 유의적으로 감소시켰다. Superoxide dismutase와 glutathione S-transferase 활성도 DM군에 비하여 각각 $56.84{\sim}94.90%$ 및 $57.14{\sim}68.92%$를 증가시켰다. 이상의 실험 결과 삼나물 에탄을 추출물은 STZ로 유도한 당뇨쥐의 고혈당을 완화시킴과 동시에 ROS 생성계를 억제하고 ROS 소거계를 활성화시킴으로써 당뇨를 경감시키는 효과가 있는 것으로 사료된다.