• 제목/요약/키워드: Ethyl radicals

검색결과 84건 처리시간 0.032초

Protective effect of Cirsium japonicum var. maackii against oxidative stress in C6 glial cells

  • Lee, Ah Young;Kim, Min Jeong;Lee, Sanghyun;Shim, Jae Suk;Cho, Eun Ju
    • 농업과학연구
    • /
    • 제45권3호
    • /
    • pp.509-519
    • /
    • 2018
  • This study was investigated the anti-oxidant property and neuro-protective effect of Cirsium japonicum var. maackii (CJM) against oxidative stress in hydrogen peroxide ($H_2O_2$)-induced C6 glial cells. We measured the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, hydroxyl radical (${\cdot}OH$), and superoxide ($O_2{^-}$) radical scavenging activities of an ethanol extract and four fractions [n-Butanol, ethyl acetate (EtOAc), $CHCl_3$, and n-Hexane] from CJM. The results of this study show that the extract and all fractions from CJM had a dose-dependent DPPH radical scavenging activity. In particular, the EtOAc fraction exhibited the strongest scavenging effect with 88.23% at a concentration of $500{\mu}g/mL$. In addition, the EtOAc fraction from CJM also effectively scavenged ${\cdot}OH$ radicals and $O_2{^-}$ radicals, compared to other extract and fractions. In C6 glial cells, $H_2O_2$ markedly decreased the cell viability as well as increased lactate dehydrogenase (LDH) release and reactive oxygen species (ROS) production. However, the EtOAc fraction of CJM attenuated the cellular damage from the oxidative stress by elevating the cell viability and inhibiting the LDH release and ROS over-production compared with the $H_2O_2$-treated control group. Our findings indicate that the EtOAc fraction from CJM has antioxidant effect and neuro-protective effect against oxidative stress, suggesting that it can be used as a natural antioxidant and therapeutic agent for the prevention of neurodegenerative disorders.

Inhibitory Activity of Flavonoids from Prunus davidiana and Other Flavonoids on Total ROS and Hydroxyl Radical Generation

  • Jung, Hyun-Ah;Jung, Mee-Jung;Kim, Ji-Young;Chung, Hae-Young;Choi, Jae-Sue
    • Archives of Pharmacal Research
    • /
    • 제26권10호
    • /
    • pp.809-815
    • /
    • 2003
  • Since reactive oxygen species (ROS) and hydroxyl radicals ($^-OH$) play an important role in the pathogenesis of many human degenerative diseases, much attention has focused on the development of safe and effective antioxidants. Preliminary experiments have revealed that the methanol (MeOH) extract of the stem of Prunus davidiana exerts inhibitory/scavenging activities on 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radicals, total ROS and peroxynitrites ($ONOO^-$). In the present study, the antioxidant activities of this MeOH extract and the organic solvent-soluble fractions, dichloromethane (CH$_2$Cl$_2$), ethyl acetate (EtOAc), and n-butanol (n-BuOH), and the water layer of P. davidiana stem were evaluated for the potential to inhibit $^-OH$ and total ROS generation in kidney homogenates using 2',7'-dichlorodihydrofluorescein diacetate (DCHF-DA), and for the potential to scavenge authentic $ONOO^-$. We also evaluated the inhibitory activity of seven flavonoids isolated from P. davidiana stem, kaempferol, kaempferol 7-Ο-$\beta$-D-glucoside, (+)-catechin, dihydrokaempferol, hesperetin 5-Ο-$\beta$-D-glucoside, naringenin and its 7-Ο-$\beta$-D-glucoside, on the total ROS, $^-OH$ and $ONOO^-$ systems. For the further elucidation of the structure-inhibitory activity relationship of flavonoids on total ROS and 'OH generation, we measured the antioxidant activity of sixteen flavonoids available, including three active flavonoids isolated from P. davidiana, on the total ROS and 'OH systems. We found that the inhibitory activity on total ROS generation increases in strength with more numerous hydroxyl groups on their structures. Also, the presence of an ortho-hydroxyl group, whether on the Aring or S-ring, and a 3-hydroxyl group on the C-ring increased the inhibitory activity on both total ROS and $^-OH$ generation.

코코아 폴리페놀 성분의 in vitro 항산화 활성 (In vitro Antioxidant Activities of Cocoa Phenolics)

  • 정창호;최귀남;곽지현;김지혜;최성길;심기환;허호진
    • 한국식품저장유통학회지
    • /
    • 제17권1호
    • /
    • pp.100-106
    • /
    • 2010
  • 본 연구에서는 국내에서 시판되는 코코아 분말로부터 polyphenol 분획물의 다양한 in vitro 항산화활성을 조사하였다. 코코아 80% 메탄올 추출물로부터 분리한 0.01N 염산, 에틸아세테이트 및 산성 메탄올 분획물의 총 페놀화합물 함량은 각각 19.25, 202.24 및 295.83 mg/g이었다. 코코아 용매분획물의 DPPH 라디칼 소거활성을 농도의존적인 경향을 보였으며, ABTS 라디칼 소거활성은 산성 메탄올 분획물에서 가장 높은 활성을 보였다. 0.01 N 염산, 에틸아세테이트 및 산성메탄올 분획물의 농도 1,000 ${\mu}g/mL$에서 환원력은 각각 0.44, 3.15 및 3.87이었다. $\beta$-carotene 표백저해 및 자동산화억제에 대한 코코아 용매분획물의 활성은 산성 메탄올, 에틸아세테이트 및 0.01 N 염산 분획물 순이었으며, 에틸아세테이트와 산성 메탄올 분획물의 농도 1,000 ${\mu}g/mL$에서 $\beta$-carotene 표백저해활성은 각각 58.97과 60.18%로 유사한 활성을 보였다. 따라서 이 실험의 결과로 볼 때, 코코아 함유 제품은 내재 polyphenol 성분으로부터 기인되는 우수한 항산화 활성으로 인해 노화관련 질병을 예방/억제할 수 있는 매우 유용한 식품 소재로서 그 활용가능성이 우수할 것으로 판단된다.

꾸지뽕나무 추출물의 생리 활성(제1보) (Physiological Activities of Cudrania tricuspidata Extracts (Part I))

  • 최학주;김청택;도민연;랑문정
    • 한국산학기술학회논문지
    • /
    • 제14권8호
    • /
    • pp.3907-3915
    • /
    • 2013
  • 꾸지뽕나무는 한국과 중국에서 전통 한방약재로 오랫동안 사용되어 왔다. 본 논문은 꾸지뽕나무의 잎,줄기, 뿌리부분의 에탄올 추출물의 물, 에탄올, 에칠아세테이트 용해성 분획물에 대한 생리활성에 관한 실험결과이다. 이들 분획물들의 다양한 세포들의 성장에 대한 영향을 검토한 결과, 잎, 줄기, 뿌리의 에칠아세테이트 분획물이 macrophage(RAW 264.7 cell), melanoma cell(B16-F10 cell), fibroblast cell(CCD-986sk cell), lung carcinoma cell(A549 cell) 들의 성장을 현저하게 억제시키는 세포독성을 나타내었다. 자유라디칼 DPPH (di(phenyl)- (2,4,6-trinitrophenyl) iminoazanium)를 소거할 수 있는 분획물의 농도를 비교한 결과, 잎과 뿌리의 물분획물 그리고 뿌리의 에탄올분획물이 다른 분획물들에 비해 라디칼을 소거하는 항산화효과가 더 우수한 것으로 나타났다.

실내 방향제 사용에 의한 유해 가스상 오염물질 배출 산정 및 노출 평가 (Emission Estimation and Exposure to Hazardous Gaseous Pollutants Associated with Use of Air Fresheners Indoors)

  • 조완근;신승호;권기동;이종효
    • Environmental Analysis Health and Toxicology
    • /
    • 제24권2호
    • /
    • pp.137-148
    • /
    • 2009
  • This study quantitatively investigated the emissions of indoor air pollutants associated with the utilization of air fresheners indoors, and evaluated individual exposure to five specified indoor air pollutants, which were chosen on the basis of selection criteria. An electrically-polished stainless steel chamber (50L) was employed to achieve this purpose. Test air fresheners were selected through three steps: first, on the basis of market sales; second, on the basis on a preliminary head-space study; and lastly, on the basis of emissions of toxic compounds (benzene, ethyl benzene, limonene, toluene, and xylene). The empirical mathematical model fitted well with the time-series concentrations in the environmental chamber (in most cases, determination coefficient, $R^2{\gtrsim}$0.9), thereby suggesting that the empirical model was suitable for testing emissions. The concentration equilibrium appeared 180 min after the introduction of sample air fresheners into the chamber. Both the chamber concentrations of emission rates or factors varied greatly according to air freshener type. It is noteworthy that although benzene, ethyl benzene, toluene, and xylene were emitted from all test air fresheners, their exposure levels were not significant enough to result in any significant health risk. However, certain type of air fresheners were observed to emit significant amount of limonene, which is potentially reactive with ozone to generate secondary pollutants with oxidants such as ozone, hydroxyl radicals, and nitrogen oxides. The exposure levels to limonene associated with the utilization of three air fresheners were estimated to be 13 to 175 times higher than that of other air fresheners. This information can help consumers to select low-pollutant-emitting air fresheners.

흑양파로부터 항산화 활성 물질인 3,4-Dihydroxybenzoic acid의 분리 및 동정 (Isolation and Identification of Antioxidative Compounds 3,4-Dihydroxybenzoic acid from Black Onion)

  • 양아여;조정용;박양균
    • 한국식품저장유통학회지
    • /
    • 제19권2호
    • /
    • pp.229-234
    • /
    • 2012
  • 양파의 매운 맛과 냄새를 감소시켜 섭취가 용이하도록 제조된 흑양파가 항산화 활성이 있다고 보고되어있어서 흑양파로부터 항산화 활성물질을 구명하고자 하였다. 흑양파 MeOH 추출물을 용매분획하여 얻어진 분획물들 중 EtOAc층이 높은 DPPH와 $ABTS^+$ radical scavenging 활성이 있었다. 그래서 EtOAc층을 silica gel과 Sephadex LH-20 등의 column chromatography를 이용하여 2종의 항산화 활성물질을 분리하였다. 단리한 이들 화합물을 대상으로 ESI-MS 및 NMR 분석을 통하여 3,4-dihydroxybenzoic acid (1)와 quercetin (2)로 각각 동정하였다. 이 화합물들은 $ABTS^+$ 및 DPPH radical scavenging 활성이 있었으며, 화합물 2는 화합물 1에 비해 더 높은 radical scavenging 활성이 있었다.

금불초 추출물의 항산화 효과 및 산화 스트레스에 대한 신경세포 보호작용 (Antioxidant Properties and Protective Effects of Inula britannica var. chinensis Regel on Oxidative Stress-induced Neuronal Cell Damage)

  • 이나현;홍정일;김진영;장매희
    • 한국식품과학회지
    • /
    • 제41권1호
    • /
    • pp.87-92
    • /
    • 2009
  • 본 연구에서는 금불초(Inula britannica) 추출물의 항산화 효과와 ${H_2}{O_2}$로부터 유도된 SH-SY5Y 신경모세포종의 세포독성에 대한 보호능을 측정하였다. 금불초 지상부위의 70% 메탄올 추출물에 대하여 용매별로 분획을 실시하였고 핵산(Fr.H), 에틸아세테이트(Fr.EA) 및 물(Fr.W) 분획에 대하여 활성을 조사하였다. 분획 중 Fr.W의 폴리페놀/플라보노이드 함량이 가장 높았으며 Fr.W의 총 폴리페놀 함량은 $318.1{\pm}20.6{\mu}g$/mg solid로, Fr.EA 및 Fr.H와 비교하여 각각 약 2.5배, 23.1배 수준이었다. DPPH radical, ABTS radical 및 nitric oxide 소거능 등의 항산화 활성에서도 Fr.W가 가장 높은 활성을 나타내었고 Fr.H는 거의 활성을 나타내지 않았다. Fr.W는 ${H_2}{O_2}$에 의해 유도된 세포사멸에 대하여 62.5 ${\mu}g$/mL 농도에서 현저하게 세포독성을 감소시켰으며 250 ${\mu}g$/mL에서는 77.0%의 세포사멸 억제능을 보였다. Fr.EA는 보호 효과를 나타 내지 않았으며 Fr.H는 오히려 ${H_2}{O_2}$로 인한 세포 독성을 증가시키는 것으로 나타났다. 세포 내 ROS에 대한 영향으로 Fr.W 250 ${\mu}g$/mL 처리시 39.2% 세포내 ROS를 감소시켰으며 Fr.EA는 25 ${\mu}g$/mL에서 26.8%의 세포내 ROS를 소거하였다. 이러한 금불초 Fr.W의 항산화 활성은 ROS에 의해 야기되는 뇌세포 독성에 대한 보호 작용에 공헌할 수 있을 것으로 예상된다.

Isolation and Antioxidative Activities of Caffeoylquinic Acid Derivatives and Flavonoid Glycosides from Leaves of Sweet Potato (Ipomoea batatas L.)

  • Kim, Hyoung-Ja;Jin, Chang-Bae;Lee, Yong-Sup
    • Biomolecules & Therapeutics
    • /
    • 제15권1호
    • /
    • pp.46-51
    • /
    • 2007
  • Bioassay-directed chromatographic fractionation of an ethyl acetate extract from leaves of sweet potato (Ipomoea batatas L.) afforded six quinic acid derivatives: 3,5-epi-dicaffeoylquinic acid (1), 3,5-dicaffeoylquinic acid (2), methyl 3,5-O-dicaffeoylquinate (3), methyl 3,4-dicaffeoylquinate (4), methyl 4,5-dicaffeoylquinic acid (5),4,5-dicaffeoylquinate (6), and two phenolic compounds: caffeic acid (7) and caffeic acid methyl ester (8) together with three flavonoids: quercetin 3-O-${\beta}$-D-glucopyranoside (9), quercetin 3-O-${\beta}$-D-glucopyranoside, isoquercitrin (10) and kaempferol 3-O-${\beta}$-D-glucopyranoside (11). The structures of these compounds were elucidated by the aid of spectroscopic methods. These compounds were assessed for antioxidant activities using three different cell-free bioassay systems. All isolates except 11 showed potent DPPH and superoxide anion radicals scavenging, and lipid peroxidation inhibitory activities. 3,5-epi-DCQA (1) and methyl quinates (3-5) along with flavonoide 9 were isolated for the first time from this plant.

Isolation, Identification and Determination of Antioxidant in Ginger (Zingiber officinale) Rhizome

  • Cho, Kang-Jin;Kim, Jin-Weon;Choi, In-Lok;Kim, Jung-Bong;Hwang, Young-Soo
    • Journal of Applied Biological Chemistry
    • /
    • 제44권1호
    • /
    • pp.12-15
    • /
    • 2001
  • The antioxidative compounds and antioxidant contents of ginger (Zingiber officinale) rhizomes were determined. Substances reextracted using ethyl acetate from crude methanol extract of fresh ginger rhizome were separated through thin layer chromatography. Ten phenolic antioxidative bands were visualized through color reactions using ferric chloride-potassium ferricyanide and 1,1-diphenyl-2-picrylbydrazyl (DPPH). The antioxidative compounds were purified through preparative TLC and high performance liquid chromatography (HPLC), among which, five antioxidants were identified as 4-, 6-, 8-. and 10-gingerols and 6-shogaol on the basis of their molecular weights determined through LC-MS. As shown in experiments using DPPH free radicals, 6-Gingerol and PT4-HP8 (unknown) were revealed to be more efficient than BHT (butylated hydroxy toluene). Contents of gingerols were determined through reverse phase HPLC. Total gingerol contents (sum of 6-,8-, and 10-gingerols) in rhizomes of different ginger varieties varied significantly. The HG55 (collected at Wanju district in Korea) and the HG52 (imported from Brazil) showed the highest gingerol contents.

  • PDF

In Vitro and Intracellular Antioxidant Activities of Brown Alga Eisenia bicyclis

  • Yoon, Na-Young;Lee, Sang-Hoon;Wijesekara, Isuru;Kim, Se-Kwon
    • Fisheries and Aquatic Sciences
    • /
    • 제14권3호
    • /
    • pp.179-185
    • /
    • 2011
  • The antioxidant activities of a methanolic extract of Eisenia bicyclis and its organic solvent fractions, including dichloromethane ($CH_2Cl_2$), ethyl acetate (EtOAc), n-butanol (n-BuOH), and water ($H_2O$) fractions, were investigated. Scavenging activities against DPPH, hydroxyl, superoxide anion, and peroxynitrite radicals were evaluated using electron spin resonance spectrometry; intracellular reactive oxygen species (ROS) were evaluated by a 2',7'-dichlorofluorescein diacetate assay using RAW264.7 mouse macrophages. The antioxidant activities of the individual fractions were: EtOAc>n-BuOH>$CH_2Cl_2$ >$H_2O$. The EtOAc fraction exhibited strong radical scavenging activity and a significantly reduced ROS level in RAW264.7 cells. Moreover, the phenolic contents of the extract and fractions followed the same order as their radical scavenging activities. Our results indicate that E. bicyclis is a valuable natural source of antioxidants that may be applicable to the functional food industry.