• 대한화장품학회지
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• 제44권2호
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• pp.103-110
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• 2018

본 연구에서는 신규 기능성 화장품 소재 개발을 위해 어리연꽃으로부터 분리한 sweroside를 이용하여 섬유아세포 내에서의 항노화 효과를 확인하였다. CCD-986sk 세포를 이용하여 sweroside의 항노화 효과를 측정한 결과, UVB에 의해 증가된 ROS의 발현을 억제하였으며, pro-collagen의 발현을 증가시키며 MMP-1의 발현을 억제하는 것으로 확인되었다. 이 결과를 종합해보면, sweroside는 화장품 분야에서 신규 항노화 기능성 소재로서의 활용 가능성이 있는 것으로 판단된다.

• The Korean Journal of Physiology and Pharmacology
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• 제27권6호
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• pp.533-540
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• 2023

Sweroside is a natural monoterpene derived from Swertia pseudochinensis Hara. Recently, studies have shown that sweroside exhibits a variety of biological activities, such as anti-inflammatory, antioxidant, and hypoglycemic effects. However, its role and mechanisms in high glucose (HG)-induced renal injury remain unclear. Herein, we established a renal injury model in vitro by inducing human renal tubular epithelial cell (HK-2 cells) injury by HG. Then, the effects of sweroside on HK-2 cell activity, inflammation, reactive oxygen species (ROS) production, and epithelial mesenchymal transition (EMT) were observed. As a result, sweroside treatment ameliorated the viability, inhibited the secretion of inflammatory cytokines (TNF-α, IL-1β, and VCAM-1), reduced the generation of ROS, and inhibited EMT in HK-2 cells. Moreover, the protein expression of SIRT1 was increased and the acetylation of p65 NF-kB was decreased in HK-2 cells with sweroside treatment. More importantly, EX527, an inhibitor of SIRT1, that inactivated SIRT1, abolished the improvement effects of sweroside on HK-2 cells. Our findings suggested that sweroside may mitigate HG-caused injury in HK-2 cells by promoting SIRT1-mediated deacetylation of p65 NF-kB.

• 생약학회지
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• 제40권4호
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• pp.334-338
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• 2009

Six iridoids were isolated from the 70% ethanol extract of Lonicera Caulis (Caprifoliaceae) and their structures were identified as epialyxialactone (1), secologanin dimethyl acetal (2), sweroside (3), loganin (4), loganic acid (5) and demethylsecologanol (6). The chemical structures of these compounds were identified on the basis of spectroscopic methods and comparison with literature values. This is the first report of the iridolactone, epialyxialactone (1), from the Caprifoliaceae plants and loganic acid (5) and demethylsecologanol (6) from Lonicera Caulis.

• 생약학회지
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• 제53권2호
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• pp.57-63
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• 2022

Five secoiridoids (1-3, 5, 10), a iridoid (4) three flavonol glycosides (7-9) and a coumarin (6), were isolated from the flowers of Hydrangea paniculata. Their chemical structures were elucidated as kingiside (1), morroniside (2), sweroside (3), loganin (4), vogeloside (5), umbelliferone (6), quercetin-3-O-sambubioside (7), quercetin-3-O-neohesperidoside (8), kaempferol 3-O-sambubioside (9) and secologanin dimethyl acetal (10), respectively, by spectroscopic analysis. All isolated compounds 1-10 were assessed for their ability to induce C2C12 myotube hypertrophy. Among them, loganin (4) and kaempferol 3-O-sambubioside (9) increase the diameter of C2C12 myotubes. All isolated compounds 1-10 were firstly reported from the flowers of Hydrangea paniculata, and the skeletal muscle hypertrophic activity of 4 and 9 was also reported for the first time.

• 한국식품과학회지
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• 제48권6호
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• pp.531-535
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• 2016

천속단과 한속단은 명칭이 유사하여 '속단'으로 통칭하여 판매되고 있으나, 종과 속이 서로 다른 약재일 뿐만 아니라 함유 성분이 다르므로 주의가 필요하다. 천속단은 골격강화, 골절치료 작용이 있는 한약재로 식품원료로는 사용할 수 없으나, 한속단의 뿌리와 잎은 식품원료로 사용이 가능하다. 본 연구에서는 식품 중 천속단 혼입여부 판별을 위하여 LC-MS/MS를 이용한 동시분석법을 개발하였으며, 선택성, 직선성, 검출한계, 정량한계, 정확성, 정밀성을 검토하였다. 국내 유통중인 식품 중 어린이 키성장을 표방하는 제품 17건을 구매하여 천속단 혼입여부에 대한 실태조사를 하였다. 분석결과 17건의 시료 중 5건의 시료에서 천속단이 검출되었으며, 천속단 지표성분의 함량은 loganin $0.19-14.45{\mu}g/mL$, sweroside $0.13-4.61{\mu}g/mL$, akebia saponin D $0.59-19.29{\mu}g/mL$이었다. 본 연구에서 개발된 동시분석법은 식품 중 불법 혼입된 천속단을 간단하면서도 신속하게 판별하는데 도움이 될 것으로 사료된다.

• 대한화장품학회지
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• 제45권3호
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• pp.307-317
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• 2019

본 연구에서는 국내 자생식물로부터 지속가능한 천연 항노화 화장품 신소재 개발을 위해 수생식물인 어리연꽃의 친환경 아쿠아포닉스 시스템 적용 가능성 및 항노화 효능을 검증하였다. 어리연꽃은 아쿠아포닉스 시스템내에서 부엽형태의 담액식 방식에서 성장 가능하고, 근경번식을 통해 증식됨이 확인되었다. 또한, 어리연꽃의 재배에 질산염, 칼륨 및 수온이 크게 영향을 미치며, 최적 조건은 각각 $80{\mu}g/mL$, $63.5{\mu}g/mL$ 및 $25^{\circ}C$로 확인되었다. 특히 주성분 2종(3,7-di-O-methylquercetin-4'-O-${\beta}$-glucoside 및 sweroside)이 약 $5{\mu}g/mL$ 이상 함께 존재 시 시너지 유효성이 있었다. 어리연꽃 추출물은 환경 유해물질 $benzo[{\alpha}]pyrene$, ammonium nitrate, formaldehyde에 의해 손상된 피부 세포의 회복에 유의미한 효과가 있으며, 염증성 조절 인자인 $PGE_2$, $TNF-{\alpha}$ 및 COX-2를 억제하고, 콜라겐 분해 효소인 MMP-1의 생성을 억제함으로써 항염 및 항노화 효과가 있음이 확인되었다. 따라서 아쿠아포닉스 기술 기반 어리연꽃 추출물의 원료 표준화는 화장품 분야에서 신규 항노화 기능성 소재로서의 활용 가능성이 있을 것으로 사료된다.

• 대한본초학회지
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• 제27권6호
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• pp.15-21
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• 2012

Objective : Lonicera japonica THUNB. a traditional herbal medicine, has been commonly used anti-inflammatory disease. It has been very complicated with respect to its sources on the market. The significant selection of medicine depends on its origin. However, it is difficult to discrimination criteria for confirming L. japonica authenticity using the senses. This study was performed to determine the discriminant analysis of L. japonica and L. confusa. Methods : The identification of L. japonica and L. confusa were performed by the classification and identification committee of the national center for standardization of herbal medicines. And we examined its differences using HPLC and genetic marker analysis. Results : The analytical pattern of High Performance Liquid Chromatography was determined from the corresponding peak curves ((E)-aldosecologanin, chlorogenic acid, luteolin 7-O-glucoside, sweroside). For L. japonica, additional unknown peaks were detected at 13.8 min, 20.6 min, and 36.9 min. And, we developed genetic marker using the the tRNA-Leu gene, trnL-trnF intergenic spacer and tRNA-Phe region of chloroplast DNA. By the method, 164 bp PCR product amplified from L. confusa was distinguished into L. japonica and L. confusa efficiently. Conclusion : Base on these results, two techniques provide effective approaches to distinguish L. japonica from L. confusa.

• 생약학회지
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• 제43권2호
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• pp.137-146
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• 2012

Dipsaci Radix (Dipsacaceae) has been used as a tonic, an analgesic, anti-inflammatory and anti-complement agents in traditional herbal medicine for the therapy of low back pain, knee pain, rheumatic arthritis, traumatic hematoma, and bone fractures. A high-performance liquid chromatography-electrospray ionization-mass spectrometric method (HPLC-ESI-MS) was developed for the simultaneous quantitation method of the five compounds from the herbal drug: asperosaponin VI and asperosaponin XII (terpene glycosides), sweroside, loganin and dipsacus A(iridoid glycosides). HPLC separation of the analytes was achieved on a C18 column ($150{\times}2.0$ mm i.d., 5 ${\mu}m$) using the aqueous methanol containing 5 mM ammonium acetate with gradient flow of the mobile phase. Detection of the analytes was performed by positive ion electrospray ionization, and selected ion monitoring was used for data acquisition using m/z corresponding molecular adduct ion, $[M+NH_4]^+$ and $[M+H]^+$. Calibration graphs showed good linearity ($r^2$=0.9997) over the wide range of the analytes; intra- and inter-day precisions (RSD, %) were within 9.1% and the accuracy between 94.0-111.0%. Recoveries of the analytes through the assay procedure were in the range of 93.7-110.8%. Analytical results of the herbal drugs of Dipsaci Radix (17 samples) show wide distribution of the five marker compounds and clear difference of the species from Phlomidis Radix (4 samples). The developed method would provide a practical guide for the quality control of the herbal drug.

• 약학회지
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• 제54권3호
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• pp.157-163
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• 2010

A high-performance liquid chromatography (HPLC) with DAD detector and electrospray ionization mass spectrometry (ESI-MS) was established for the simultaneous determination of coniferin (1), loganic acid (2), demethylsecologanol (3), sweroside (4) and loganin (5) from caulis Lonicera joponica. The optimal chromatographic conditions were obtained on an ODS column ($5{\mu}m$, $4.6{\times}150mm$) with the column temperature $35^{\circ}C$. The mobile phase was composed of (A) water with 0.1% formic acid and (B) methanol with 0.1% formic acid using a gradient elution, the flow rate was 0.3 ml/min. Detection wavelength was set at 254 nm. All calibration curves showed good linear regression ($r^2$>0.998) within test ranges. The developed method provided satisfactory precision and accuracy with overall intra-day and interday variations of 0.16~3.28% and 0.14~1.99%, respectively, and the overall recoveries of 99.39~105.89% for the five compounds analyzed. The verified method was successfully applied to quantitative determination of the two types (phenolic compounds and iridoids) of bioactive compounds in 24 commercial caulis L. japonica samples from different markets in Korea and China. The analytical results demonstrated that the contents of the five analytes vary significantly with sources.

• 약학회지
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• 제52권6호
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• pp.446-451
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• 2008

A high-performance liquid chromatography (HPLC) with diode array detector (DAD) and electrospray ionization mass spectrometry (ESI-MS) was established for the simultaneous determination of chlorogenic acid (1), sweroside (2), luteolin-7-O-glucoside (3), (E)-aldosecologanin (4) and 3,5-dicaffeoylquinic acid (5) from Lonicera joponica flower buds. The optimal chromatographic conditions were obtained on an ODS column (5 ${\mu}m$, 4.6${\times}$150 mm) with the column temperature $25^{\circ}C$. The mobile phase was composed of (A) water with 0.1% formic acid and (B) acetonitrile with 0.1% formic acid using a gradient elution, the flow rate was 0.3 ml/min. Detection wavelength was set at 250 nm. All calibration curves showed good linear regression ($r^2$>0.994) within test ranges. The developed method provided satisfactory precision and accuracy with overall intra-day and inter-day variations of 0.05${\sim}$1.95% and 0.15${\sim}$2.26%, respectively, and the overall recoveries of 97.71${\sim}$103.65% for the five compounds analyzed. The verified method was successfully applied to quantitative determination of the three types (phenolic compounds, iridoids and flavonoids) of bioactive compounds in 21 commercial L. japonica flower buds samples from different markets in Korea and China. The analytical results demonstrated that the contents of the five analytes vary significantly with sources.