• 제목/요약/키워드: Anti-oxidant Effect

검색결과 645건 처리시간 0.027초

Effect of Maillard Reaction Products on Inhibition of Burdock Polyphenol Oxidase and Their Antioxidant Activities

  • Kim, GyeYeong;Choi, Heesun;Park, Inshik
    • 한국식품영양학회지
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    • 제30권5호
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    • pp.853-859
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    • 2017
  • This study was conducted in an effort to investigate the effect of Maillard reaction products (MRPs) on enzymatic browning of burdock and their anti-oxidant activity. The MRPs were prepared by heating glucose and amino acids at $90^{\circ}C$, which served to produce a strong inhibitory effect on burdock polyphenol oxidase. As the reaction time of the solution containing glucose and amino acid increased at $90^{\circ}C$, the production of MRPs increased and intensity of the brown color deepened. When MRPs were prepared by heating at $90^{\circ}C$ for five hours, the absorbance of MRPs from glucose and lysine was 6.44, while those of glucose and glycine was 1.95. The MRPs synthesized from the glucose and lysine also reduced the pH of MRPs from 5.60 to 4.51, but those from glucose and glycine decreased slightly from 5.57 to 5.33. The Michealis-Menten constant value ($K_m$) of burdock PPO with pyrocatechol as a substrate was 16.0 mM, and MRPs were a non-competitive inhibitor against burdock PPO. The anti-oxidant activity of MRPs was measured by evaluating its radical scavenging activities of DPPH radicals, ABTS radicals and reducing power. The color intensity of MRPs produced by lysine and glucose were deeper than that produced by glucose and glycine. It was also found that MRPs produced from glucose and lysine exhibited stronger anti-oxidant properties than those produced by glucose and glycine.

목과(木瓜)추출물이 급성 간손상 흰쥐에 미치는 효과 (The Effect of Chaenomelis Fructus Extract on Acute Hepatic Injury in Rats)

  • 이진아;신미래;이지혜;노성수
    • 대한한방내과학회지
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    • 제42권1호
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    • pp.1-10
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    • 2021
  • Objective: This study was conducted to investigate the effect of Chaenomelis Fructus (CF) water extract on thioacetamide (TAA)-treated rats. Methods: Rats were divided into five groups: one normal group (n=8) and four with TAA-induced hepatic injury. These treatment groups were administered distilled water (n=8); silymarin 100 mg/kg (n=8); CF 100 mg/kg (n=8); and CF 200 mg/kg (n=8). In the TAA groups, the acute liver injury was induced via IP injection (200 mg/kg), and the silymarin and CF extract were then orally administered for three days. Subsequently, serum levels of GOT, GPT, and ammonia were confirmed as well as protein expressions using liver tissue. Results: In the liver injury-induced rats, CF administration reduced tissue damage and serum levels of GOT, GPT, and ammonia. In addition, CF increased the anti-oxidant proteins Nrf2, Keap1, HO-1, and catalase and significantly regulated matrix metalloproteinases (MMP-2 and MMP-9) and their tissue inhibitors (TIMP-1 and TIMP-2). Conclusions: In this animal model of liver injury induced by TAA, CF extract is determined to have a hepatoprotective effect by increasing anti-oxidant proteins that relieve damage and by regulating the expression of matrix metalloproteinases.

보리싹 추출물의 항산화 및 항염증 활성 (Anti-oxidant and Anti-inflammatory Activities of Barley Sprout Extract)

  • 은청수;황은영;이승욱;양선아;유미희
    • 생명과학회지
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    • 제26권5호
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    • pp.537-544
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    • 2016
  • 본 연구에서는 보리싹을 이용하여 항산화 활성 및 RAW 264.7 세포에서의 항염증 활성에 미치는 영향을 확인하였다. 보리싹 에탄올 추출물의 DPPH라디칼 소거활성은 1,000 μg/ml 농도에서 92.82±0.62%로 나타났으며, RC50 값은 442.34±5.54 μg/ml이었다. 보리싹 추출물의 총 폴리페놀과 플라보노이드 함량은 각각 17.55 μg/ml, 13.98 μg/ml로 나타났다. 또한 LPS로 염증을 유도한 RAW 264.7 세포에서 TNF-α와 PGE2 생성량은 LPS처리에 따라 증가하였으며, 보리싹 추출물 250, 500 μg/ml의 농도에서 유의적인 감소를 보였다. LPS에 의해 증가된 iNOS, COX-2 단백질 발현에 대해 보리싹 추출물 250 μg/ml의 농도에서 현저히 감소됨을 확인하였다. 이러한 결과들을 통해 보리싹은 항산화 및 항염증 효과를 가진 천연물 소재로 활용 가능할 것으로 생각된다.

접골산(接骨散)이 골절치유에 미치는 영향 (Effects of Jeopgolsan (JGS) Extract on Fracture Healing)

  • 이한길;오민석
    • 한방재활의학과학회지
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    • 제28권1호
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    • pp.1-17
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    • 2018
  • Objectives The purpose of this study was to evaluate the effect of Jeopgolsan (JGS) extract on anti-oxidant, anti-inflammatory activities in RAW 264.7 cells and on factors related with fracture healing in skull fractured rat. Methods Experimental animals were divided into four groups: normal group without any treatment (Normal), contral group were treated orally with distilled water (Control), Experimental group were treated orally with JGS at a concentration of 200 mg/kg/day (JGS 200) and Experimental group were treated orally with JGS at a concentration of 200 mg/kg/day (JGS 400). Rats in each group except the normal group were induced fractures in the skull. The 1,1-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid (ABTS) radical scavenging activity were measured to evaluate antioxidant activity. The production of nitric oxide (NO), $interleukin-1{\beta}$ ($IL-1{\beta}$), interleukin-6 (IL-6) and tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) in the RAW 264.7 cells were measured to evaluate anti-inflammatory activity. The production of osteocalcin calcitonin, carboxy-terminal telepeptides of type II collagen (CTX II), transforming growth $factor-{\beta}$ ($TGF-{\beta}$), bone morphogenetic protein-2 (BMP-2), Insulin and alkaline phosphatase (ALP) in serum of rats were measured to evaluate the effects of fracture healing at 0, 2, 4, and 6th week. X-rays were taken every 3 week from 0 to 6th week to evaluate fracture healing effect. Results 1. No cytotoxicity was observed. 2. DPPH and ABTS radical scavenging activity were increased in a concentration dependent manner, indicating anti-oxidant effect. 3. NO, $IL-1{\beta}$, IL-6, and $TNF-{\alpha}$ were not significantly changed, indicating no anti-inflammatory effect. 4. Osteocalcin, Calcitonin, $TGF-{\beta}$ and ALP were significantly increased in the experimental groups. 5. CTX II, insulin were significantly decreased in the expermental groups. 6. Radiologic examination showed that union of fracture was promoted. Conclusions From above results, JGS showed significant results in factors related with fracture healing and radiologic examination. Threfore, JGS is expected to be effective in the treatment of fracture.

Saccharomycopsis fibuligera로 발효된 블랙커런트추출물의 항산화 및 항염증 효과 (Antioxidant and Anti-inflammatory Effects of Fermented Blackcurrant Fruit Extracts with Saccharomycopsis fibuligera)

  • 장준환;이형규;배준태;이재섭;황방연
    • 대한화장품학회지
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    • 제46권4호
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    • pp.403-413
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    • 2020
  • 유용한 미생물을 탐색하던 중, 제주도의 전통발효식품에서 화장품소재로 활용이 가능한 Saccharomycopsis fibuligera을 분리하였다. 본 연구에서는 안토시아닌 배당체를 많이 함유한 블랙커런트추출물(blackcurrant fruit extract, BE)을 S. fibuligera로 발효시켰다. 블랙커런트추출물(BE)과 발효된 블랙커런트추출물(fermented blackcurrant fruit extract, FBE)의 성분 분석을 위해 HPLC분석을 실시하였다. 그 결과, delphinidin과 cyanidin의 생물전환을 확인할 수 있었다. 블랙커런트추출물(BE)과 발효된 블랙커런트추출물(FBE)의 항산화 효능을 검증하기 위해 DPPH 및 ABTS 라디칼소거활성을 수행하였다. 또한 항염증 효능을 확인하기 위해 LPS(lipopolysaccharide)로 염증반응을 유도시킨 RAW 264.7 대식세포에서의 Nitric Oxide (NO)생성 저해력과 western blot분석을 통한 염증관련 단백질 iNOS와 COX-2의 발현 저해를 확인하였다. 그 결과, 발효된 블랙커런트추출물(FBE)은 항산화 및 항염증 효과를 가지고 있어 화장품을 위한 효과적인 원료로 사용 가능할 것으로 사료된다.

Whitening and Anti-oxidative Activities of Chemical Components Extracted from Branches of Sorbus alnifolia

  • Bo Shi Liu;Jung Eun Kim;Nam Ho Lee
    • 대한화학회지
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    • 제67권2호
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    • pp.137-144
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    • 2023
  • In this study were evaluated the whitening and anti-oxidative activities from the extracts of Sorbus alnifolia branches, and identified the chemical structures of the active ingredients. In the whitening tests using α-MSH stimulated B16F10 melanoma cells, the 70% ethanol extract and n-butanol (n-BuOH) fractions concentration-dependently inhibited cellular melanogenesis and intracellular tyrosinase activities without causing cell toxicity. The total polyphenol content of n-BuOH and ethyl acetate (EtOAc) fractions were measured to be respectively 241.1 ± 1.1 and 222.9 ± 2.4 (mg/g GAE), and the total flavonoid content of EtOAc fraction was 75.3 ± 2.0 (mg/g QE). Upon anti-oxidant studies with DPPH and ABTS+ radicals, potent radical scavenging activities were observed in the EtOAc and n-BuOH fractions. Moreover, in the study of cell protection efficacy using HaCaT keratinocytes damaged by H2O2, the EtOAc and n-BuOH fractions showed a very positive results on prevention of oxidative stress. Phytochemical studies for this extract resulted in the isolation of four compounds; 2-oxopomolic acid (1), euscaphic acid (2), epi-catechin (3), prunasin (4). These results suggested that the extract of S. alnifolia branches containing compounds 1-4 as natural ingredients could be used as whitening and anti-oxidant ingredients in cosmetic formulations.

아토피 피부염 외치치료제 처방 개발을 위한 실험적 연구 (An experimental study for the development of prescription on atopic dermatitis)

  • 김건우;박지원;심부용;김동희
    • 대한본초학회지
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    • 제29권4호
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    • pp.13-20
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    • 2014
  • Objectives : Atotang was composed of 10 kinds of traditional medicinal herb. This research was performed to examine biological effects of Atotang for the development of prescription on atopic dermatitis. Methods : Atotang was extracted with 80% EtOH. Free radical scavenging assay has tested for anti-oxidative activity as well as the contents of total polyphenol. We observed the production of ROS, nitric oxide(NO) and the inflammatory cytokines such as interleukin-1beta(IL-${\beta}$), IL-6, tumor necrosis factor-alpha(TNF-${\alpha}$), Prostaglandin E2($PGE_2$) in Raw 264.7 cells stimulated by LPS. We used Disc diffusion method to investigate antibacterial activity on Candida albicans, Staphylococcus aureus and Staphylococcus epidermis. Result : Content of total phenolic compound of Atotang was 36.3 mg/g ext. DPPH and ABTS scavenging activities were 77% and 46% at 200 ug/ml respectively, showing dose-dependent increase. The amounts of ROS and NO in RAW 264.7 cells were decreased by 30% and 19% at 200 ug/ml, respectively, showing dose-dependent decrease. The prodcution of IL-1beta, IL-6 and TNF-alpha in RAW 264.7 cells were decreased dose-dependently by 81%, 67%, and 20% at 200 ug/ml, respectively. Atotang was reduced LPS-stimulated production of $PGE_2$ by 33%. Atotang on C. albicans, S. aureus and S. epidermis was selected by a disc diffusion method and inhibition effect of the Atotang on the growth of S. epidermis was the greatest. Conclusion : The results indicated that Atotang showed biological activities showing anti-oxidant, anti-inflammatory and antibacterial effects. Based on these results, it is concluded that Atotang can be applied to the prescription on atopic dermatitis.

우산고로쇠의 향장효과 (The Effect of Cosmetic on Anti-Wrinkle of Acer mono Sap)

  • 손상현;이상원;신유수;김형돈;양승옥;김승유;김영옥
    • 한국약용작물학회지
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    • 제21권4호
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    • pp.262-267
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    • 2013
  • The purpose of this study was to research for anti-oxidation and anti-wrinkle effects of Acar mono Sap (AM). To cosmetic effect of AM, safety effect (MTT assay), anti-wrinkle effect (elastase, MMP-1 inhibition assay) and anti-oxidant effect (DPPH assay) were measured. When water extract of AM was used for cell viability, it was over 100% at 6% (6 ml/100 ml in phosphate buffer) concentration. AM showed 45.7% elastase inhibition and 23.7% MMP-1 inhibition at 50% (50 ml/100 ml in phosphate buffer) concentration so that it had good anti-wrinkle characteristic. And AM showed 68.9% antioxidation capacity at 50% concentration by using a DPPH assay. Consequently, AM can be used as natural materials or additives for human skin owing to their beneficial biologic functions, including the anti-wrinkle effect, for cosmetic compositions.

효소 처리에 의한 흑미 호분 추출물의 산화방지와 항염증 활성 증진 (Improvement of anti-oxidant and anti-inflammatory activities of aleurone layer extracts of black rice (Oryza sativa L.) by enzyme treatment)

  • 이미경;유수인;이민호
    • 한국식품과학회지
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    • 제50권5호
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    • pp.528-534
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    • 2018
  • 본 연구에서는 흑미 호분을 실험소재로 선택하여, 흑미 호분에 효소(lipase, lecitase, lipopan)를 처리함으로써 산화방지와 항염증활성을 증진하고자 하였다. 항산화 활성을 확인해보고자 DPPH 라디칼 제거능과 ABTS 라디칼 제거능을 실시하였다. 그 결과 효소 처리군이 무 처리군에 비해 산화방지 활성이 증가됨을 확인할 수 있었고, 특히 라이페이스를 처리한 후 추출한 시료에서 산화방지활성 증진이 가장 효과적이었다. 이것은 총 안토사이아노 사이드 함량 측정 결과와 일치한 것을 확인하였다. 이러한 산화방지 활성의 증가에서 라이페이스의 작용이 흑미 호분 겉면의 지방 분해를 도와 산화방지능과 관련된 유효성분들을 효과적으로 추출한 것으로 생각된다. 항염증 활성을 비교하기 위해서는 효소처리한 흑미 호분 추출물(OLAE)과 LPS를 함께 처리하여 RAW 264.7 세포가 생산하는 NO의 양과 염증성 사이토카인의 분비량을 측정해 보았다. 효소 처리를 한 경우, 라이페이스와 lecitase를 연이어 처리한 경우의 시료에서 NO의 생성이 억제되고, 염증성 사이토카인($TNF-{\alpha}$, IL-6)의 분비량이 감소됨을 확인하였다. 항염증 활성의 증진은 두 가지의 효소를 처리하는 과정 중에 일어나는 유효성분의 변화 또는 성분의 전환이 되었기 때문이라 여겨지며, 이를 확인하는 후속연구가 필요하다고 생각된다. 이상의 결과는 부산물로 버려지는 흑미 호분을 효소 처리 과정을 이용하여 만든 흑미 호분층 추출물(OLAE)로 활용하면 유용하고 안정하고 효과적인 산화방지 및 항염증 기능성 식품 소재 개발로 가능함을 제시할 수 있다.

전복내장추출물의 항산화 및 human dermal fibroblasts에 대한 항피부노화 효과 (Anti-oxidant and Anti-skin-aging Effects of Abalone Viscera Extracts in Human Dermal Fibroblasts)

  • 이정뢰;동도;고두옥;정동옥;정원철;김지은;강성국
    • 한국식품저장유통학회지
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    • 제19권4호
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    • pp.463-469
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    • 2012
  • 전복가공부산물인 내장의 이용가치를 향상시키고자 열수추출, 에탄올추출 등의 방법으로 유효성분을 추출하고 항산화 및 항피부노화 활성을 측정하였다. DPPH 라디칼소거능 분석결과 Tris-HCl 추출물은 $58.60{\pm}0.88%$으로 높은 라디칼소거능을 보였으며, 다음으로 에탄올추출물은 $55.40{\pm}0.62%$의 라디칼소거능을 보였다. Anti-elastase활성을 분석한 결과 에탄올추출물이 다른 시험구에 비하여 현저하게 높은 활성을 보였다. 전복내장추출물의 세포독성을 확인하기 위하여 human dermal fibroblast 세포에 대하여 MTT 시험결과 세포독성은 전혀 나타나지 않았다. 에탄올 추출물의 농도를 달리하여 human dermal fibroblast 세포에 대해pro-collagen type I 생합성능시험결과 10.0 ${\mu}g/mL$에서 $705.30{\pm}3.06$ ng/mL로 retinoic acid $453.60{\pm}2.82$ ng/mL보다 우수한 결과를 보였다. MMP-1 활성은 10 ${\mu}g/mL$에서 $45.30{\pm}0.80$ ng/mL를 보여 control의 $62.37{\pm}0.56$ ng/mL 보다 감소정도가 낮았다. 본 연구는 전복내장추출물의 항산화와 항노화활성에 관하여 최초로 시도되었으며 향후 전복내장을 이용한 다양한 연구의 기초자료로서 중요한 의미가 있다.