• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.201.3-201.3
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• 2003

The ethanol extract from the fruit of Terminalia chebula (Combretaceae) and the hook of Uncaria sinensis (Rubiaceae) exhibited significant inhibitory activity on oxidative stress and the age-dependent shortening of the telomeric DNA length. In the peroxidation model using t-BuOOH, human epidermal keratinocytes-neonatal foreskin (HEK-N/F) cells were treated with the T. chebula and U. sinensis extracts. The results showed a notable enhancing effect on the cell viability of 60.5 ${\pm}$ 3.8 and 65.0 ${\pm}$ 3.0%, respectively, by 50 $\mu\textrm{g}$/ml of the extracts. (omitted)

• ALGAE
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• 제32권4호
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• pp.379-388
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• 2017

In the present study, we enhanced the phenolic content of 70% ethanol extracts of Spirogyra sp. (SPE, $260.47{\pm}5.21$ gallic acid equivalent $[GAE]mg\;g^{-1}$), 2.97 times to $774.24{\pm}2.61GAE\;mg\;g^{-1}$ in the ethyl acetate fraction of SPE (SPEE). SPEE was evaluated for its antiradical activity in online high-performance liquid chromatography-ABTS analysis, and the peaks with the highest antiradical activities were identified as gallic acid derivatives containing gallic acid, methyl gallate, and ethyl gallate. Isolation of ethyl gallate from Spirogyra sp. was performed for the first time in this study. In ultraviolet B (UVB)-irradiated keratinocytes (HaCaT cells), SPEE improved cell viability by 8.22%, and 23.33% and reduced accumulation of cells in the sub-$G_1$ phase by 20.53%, and 32.11% at the concentrations of 50 and $100{\mu}g\;mL^{-1}$, respectively. Furthermore, SPEE (50 and $100{\mu}g\;mL^{-1}$) reduced reactive oxygen species generation in UVB-irradiated zebrafish by 66.67% and 77.78%. This study suggests a protective activity of gallic acid and its derivatives from Spirogyra sp. against UVB-induced stress responses in both in vitro and in vivo models, suggesting a potential use of SPEE in photoprotection.

• Food Science and Biotechnology
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• 제18권5호
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• pp.1193-1198
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• 2009

Ethylacetate and butanol fractions of leaf extracts (OLE) showed the higher contents of total phenolic compounds than hexane and water fractions. Oleuropein contents were $4.21{\pm}0.57,\;3.92{\pm}0.43,\;0.32{\pm}0.03,\;5.76{\pm}0.32$, and $32.47{\pm}0.25mg$/100g for ethanol extract, and hexane, chloroform, ethyl acetate, and butanol fraction, respectively. Treatment of ultraviolet-B (UVB) irradiated cells with 3 OLEs prepared by using ethylacetate and butanol at concentrations 0.001, 0.005, and 0.01% respectively showed significant recovery of cell viabilities. Treatment of dexametason 1 mM reduced tumor necrotic factor (TNF)-${\alpha}$ secretion by about 40%. UVB irradiated immortalized human keratinocytes (HaCaT) cells were treated with 3 different OLEs at the same concentrations. Ethylacetate fraction showed the strongest inhibition activity with respect of reduction of the elevated (TNF)-${\alpha}$. Cytotoxicity of OLEs on the B16-F1 cells was evaluated through thiazolyl blue tetrazolium bromide (MTT) assay. Ethylacetate fraction has no cytotoxicity in the range of 0.005-0.01%. A slight cytotoxicity was observed at the concentration of 0.1% butanol fraction of OLE that caused 10% decrease in cell viability.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2018년도 춘계학술발표회
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• pp.68-68
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• 2018

In this study, we investigated whether S. baicalensis rhizome ethanol extract (SBRE) has antioxidant capacities against oxidative stress induced cellular damage in the HaCaT keratinocytes. Our results revealed that treatment with SBRE prior to hydrogen peroxide ($H_2O_2$) exposure significantly increased the HaCaT cell viability. SBRE also effectively attenuated $H_2O_2$ induced comet tail formation, and inhibited the $H_2O_2$ induced phosphorylation levels of the histone ${\gamma}H2AX$, as well as the number of apoptotic bodies and Annexin V positive cells. In addition, SBRE exhibited scavenging activity against intracellular ROS generation and restored the mitochondria membrane potential loss induced by $H_2O_2$. Moreover, $H_2O_2$ enhanced the cleavage of caspase-3 and degradation of poly (ADP-ribose)-polymerase as well as DNA fragmentation; however, these events were almost totally reversed by pretreatment with SBRE. Furthermore, SBRE increased the levels of HO-1 associated with the induction of Nrf2. Therefore, we believed that SBRE may potentially serve as an agent for the treatment and prevention of neurodegenerative diseases caused by oxidative stress.

• 치위생과학회지
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• 제23권4호
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• pp.369-377
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• 2023

Background: In this study, we investigated the potential use of keratin for oral tissue regeneration. Keratin is well-known for its effectiveness in skin regeneration by promoting keratinization and enhancing the elasticity and activity of fibroblasts. Because of its structural stability, high storability, biocompatibility, and safety in humans, existing research has predominantly focused on its role in skin wound healing. Herein, we propose using keratin proteins as biocompatible materials for dental applications. Methods: To assess the suitability of alpha-keratin protein as a substrate for cell culture, keratin was extracted from human hair via PEGylation. Viabilities of primary human gingival fibroblasts (HGFs) and human oral keratinocytes (HOKs) were assessed. Fluorescence immunostaining and migration assays were conducted using a fluorescence microscope and confocal laser scanning microscope. Wound healing and migration assays were performed using automated software to analyze the experimental readout and gap closure rate. Results: We confirmed the extraction of alpha-keratin and formation of the PEG-g-keratin complex. Treatment of HGFs with keratin protein at a concentration of 5 mg/ml promoted proliferation and maintained cell viability in the test group compared to the control group. HOKs treated with 5 mg/ml keratin exhibited a slight decrease in cell proliferation and activity after 48 hours compared to the untreated group, followed by an increase after 72 hours. Wound healing and migration assays revealed rapid closure of the area covered by HOKs over time following keratin treatment. Additionally, HOKs exhibited changes in cell morphology and increased the expression of the mesenchymal marker vimentin. Conclusion: Our study demonstrated the potential of hair keratin for soft tissue regeneration, with potential future applications in clinical settings for wound healing.

• 대한의용생체공학회:의공학회지
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• 제44권6호
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• pp.443-449
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• 2023

The purpose of this study was to observe cell death in human keratinocytes stimulated against the infectious cytokines TNF-α and IFN-γ, and to observe the expression of Phospho-NF-κB due to phosphorylation of IkB to confirm the mechanism of inhibiting the expression of inflammatory cytokines. As a result of cell viability analysis, differences in PEMF stimulation time were observed little by little after 1 hour, 3 hours, 6 hours, 12 hours, 24 hours, and 48 hours, but there was no statistical significance according to PEMF stimulation time for each time (p>0.05). No significant difference was observed in the total amount of NF-κB present in the cytoplasm and nucleus, but a significant decrease in the expression of phosphorylated NF-κB was observed in the group exposed to PEMF stimulation for 24 hours (^*p<0.05). The expression of IL-1β was observed in all inflammation-induced groups, and the concentration of IL-1β compared to α-Tubulin expression was reduced by about 54% in the PEMF-stimulated group for 24 hours compared to the control group (^***p<0.001). As a result of the study, it is shown that PEMF stimulation does not negatively affect HaCaT cells from 0 to 48 hours and can inhibit the expression of inflammatory cytokines by inhibiting the pathway of NF-κB.

• 생명과학회지
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• 제27권3호
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• pp.310-317
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• 2017

본 연구진은 HaCaT-ARE-luciferase 세포를 이용하여 400 여개의 약용식물 에탄올 추출물 중 NRF2/ARE 유도효과가 있는 신규 추출물을 검색하였고 이를 통하여 종대황(Rheum undulatum)과 선복화(Inula japonica)의 주정 추출물이 HaCaT-ARE-luciferase 세포에서 ARE 활성을 강하게 유도하는 것을 관찰하였다. 종대황과 선복화 에탄올 추출물은 HaCaT 세포에서 생존(viability)을 증가시켰고 NRF2/ARE에 의존적인 phase II cytoprotective 효소인 heme oxygenase-1 (HO-1)와 NADPH:quinone oxidoreductase-1 (NQO1)의 전사 및 단백질 발현을 강하게 유도하였다. 또한 종대황과 선복화 추출물은 HaCaT 세포에서 TPA로 유도한 세포 내 활성 산소 및 이를 통하여 생성되는 스트레스 마커인 8-hydroxydeoxyguanosine (8-OH-dG)과 4-hydroxynonenal (4HNE)의 발생을 강하게 억제하였다. 본 연구는 종대황과 선복화의 에탄올 추출물이 인간 피부 세포주인 HaCaT 세포에서 NRF2/ARE에 의존적인 유전자 발현의 유도를 통하여 강력한 항산화 효과를 발휘한다는 것을 증명한다.

• 한국자원식물학회지
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• 제29권1호
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• pp.11-19
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• 2016

본 연구에서는 익모초 추출물의 항산화 효과 및 자외선으로 유도된 각질형성세포 손상에 대한 보호효과를 확인하고자 익모초 열수 추출물의 생체 내 산화적 스트레스와 관련되어 있는 DPPH radical, hydroxyl radical, hydrogen peroxide, superoxide radical, lipid peroxidation에 대한 익모초 열수추출물의 소거효과 및 환원력 평가 시험을 진행하였으며, 사람 각질형성세포주인 HaCaT 세포주에서 UVB로 유도된 apoptosis에 대한 익모초의 억제 정도를 확인하였다. 그결과, 익모초 열수추출물에서 농도 의존적으로 항산화 효과가 증가함을 확인할 수 있었으며, UVB로 유도된 apoptosis에 발현 또한 억제됨을 확인할 수 있었다. 현재 국내외적으로 천연물에 대한 항산화 활성에 대한 연구가 활발히 진행되고 있는데, 이를 바탕으로 하는 피부 보호 효과에 대한 연구는 항노화 측면에서 그 효용가치가 높다고 여겨진다. 따라서 본 실험 연구의 결과를 토대로 항산화 효과가 우수한 식물종에 대해 단일 물질에 대한 분리 작업과 함께 항노화 실험 뿐만 아니라 항염증이나 항암 등의 실험이 더깊이 있게 진행된다면 새로운 천연물 유래 생리 활성 물질로서 효과적이면서도 안전한 화장품 소재로의 활용 또한 가능할 것으로 기대된다.

• 대한화장품학회지
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• 제41권1호
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• pp.9-20
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• 2015

자외선은 피부 광노화의 주요 요인이며, 효과적인 자외선 차단제가 피부의 건강과 아름다움을 위해 필요하다. 본 연구는 세포 실험을 통하여 자외선에 의해 유도된 세포 사멸, 산화적 스트레스, matrix metalloproteinase 1 발현에 미치는 죽여추출물의 영향을 알아보고자 수행하였다. HaCaT 인간 각질세포를 여러 농도의 죽여추출물 유무 조건에서 자외선을 조사하고 세포의 생존율과 생화학적 과정들의 변화를 분석하였다. 죽여추출물은 자외선을 조사한 세포의 생존율을 증진시켰고, procaspase 3가 활성화 형태로 절단되고, Bax/Bcl-2 비율이 증가하는 세포 자살 과정을 완화시켰다. 죽여추출물은 자외선에 노출된 세포에서 활성산소의 발생과 지질 과산화도 감소시켰다. 또한 죽여추출물은 자외선에 의해 자극된 matrix metalloproteinase 1의 발현과 c-Jun N-terminal kinase의 인산화를 억제하였다. 본 연구는 죽여추출물이 자외선에 의한 세포 사멸, 산화적 스트레스, 그리고 matrix metalloproteinase 1 발현을 억제함을 보여 주었으며, 이 추출물이 피부 광노화의 일부 현상을 억제하는 화장품 원료로 유용함을 시사하였다.

• Journal of Applied Biological Chemistry
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• 제65권4호
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• pp.405-412
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• 2022

Echinodorus cordifolius (L.)은 택사과(Alismataceae)에 속하는 수생 식물이다. Echinodorus cordifolius (L.)의 피부 항노화 활성에 대한 연구는 아직까지 보고되지 않았다. 따라서 본 연구의 목적은 Echinodorus cordifolius (L.)로부터 70% 에탄올 추출물 (ECEE)을 제조하고 항산화 및 hyaluronidase 억제 활성을 통해 피부 항노화 기능성 소재로서의 가능성을 확인하였다. ECEE는 EC₅₀과 IC₅₀ 값이 각각 31.4, 300, 450 ㎍/mL로 우수한 DPPH, hydrogen peroxide 소거 활성 및 hyaluronidase 억제 활성을 가지는 것으로 나타났다. ECEE는 불멸화된 인간 각질세포인 HaCaT 세포에서 1 mM H₂O₂로 유도된 산화적 스트레스에 대해 농도 의존적으로 세포 보호 효과 증가 및 세포 내 활성산소종을 생성을 억제하는 것으로 나타났다. 또한 ECEE는 hyaluronic acid (HA) 합성 효소인 hyaluronan synthase 2 발현 수준을 상향 조절하고 HA 분해 효소인 hyaluronidase 2(HYAL2)의 발현 수준을 하향 조절하여 HaCaT 세포에서 HA 생성량을 증가시켰다. 따라서 이러한 결과를 종합하면 ECEE는 항산화, hyaluronidase 억제 및 HA 생성 촉진의 우수한 잠재력을 가진다는 것을 확인하였고 이를 통해 피부 노화를 방지하기 위한 천연 기능성 화장품 소재로서의 충분한 활용 가치가 있다고 판단된다.