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[晶状体诱导脂质过氧化]

[Crystalline lens induction of lipid peroxidation].

作者信息

Babizhaev M A, Aĭtmagambetov M T, Deev A I, Vladimirov Iu A

出版信息

Biull Eksp Biol Med. 1987 Jan;103(1):38-40.

PMID:3801649
Abstract

The level of lipid peroxidation products (LPP) was determined in the aqueous humor from the anterior chamber of patients with cataract and donor eyes. The content of LPP in senile cataract aqueous humor was shown to be significantly increased. To determine the possible mechanism of LPP increase in aqueous humor, human lenses at different stages of cataract as well as transparent human and rabbit lenses were incubated for 3 hours in 3.0 ml medium containing liposomes (0.5 mg/ml) prepared from phospholipids from the egg yolk and 0.14 M NaCl + 0.01 M TRIS-HCl buffer, pH 7.4). Corrections were made for phospholipid autooxidation. The level of LPP accumulation in the medium was determined by MDA assay. The rate of LPP production increased significantly in transparent lenses and in early senile cataract, as compared to controls and advanced (mature) cataracts. EDTA (1 mM), superoxide dismutase (114 u/sample), catalase (900 u/sample), chelated iron (III): Fe3+-ADP addition to the incubation medium depressed the level of LPP accumulation. This suggests the participation of Fe2+, O2-., H2O2 in the mechanism of LPP production in the lens. The induction of lipid peroxidation in the lens can be significant for leukotriene and prostaglandin synthesis in the eye.

摘要

测定了白内障患者前房房水及供体眼房水中脂质过氧化产物(LPP)的水平。结果显示,老年性白内障房水中LPP的含量显著增加。为了确定房水中LPP增加的可能机制,将处于不同白内障阶段的人晶状体以及透明的人晶状体和兔晶状体在含有由蛋黄磷脂制备的脂质体(0.5mg/ml)以及0.14M NaCl + 0.01M Tris-HCl缓冲液(pH 7.4)的3.0ml培养基中孵育3小时。对磷脂的自动氧化进行了校正。通过丙二醛(MDA)测定法确定培养基中LPP的积累水平。与对照组和晚期(成熟)白内障相比,透明晶状体和早期老年性白内障中LPP的产生速率显著增加。向孵育培养基中添加乙二胺四乙酸(EDTA,1mM)、超氧化物歧化酶(114u/样品)、过氧化氢酶(900u/样品)、螯合铁(III):Fe3 + -ADP可降低LPP的积累水平。这表明Fe2 +、O2 - 、H2O2参与了晶状体中LPP产生的机制。晶状体中脂质过氧化的诱导对于眼内白三烯和前列腺素的合成可能具有重要意义。

相似文献

1
[Crystalline lens induction of lipid peroxidation].[晶状体诱导脂质过氧化]
Biull Eksp Biol Med. 1987 Jan;103(1):38-40.
2
Mitochondria induce oxidative stress, generation of reactive oxygen species and redox state unbalance of the eye lens leading to human cataract formation: disruption of redox lens organization by phospholipid hydroperoxides as a common basis for cataract disease.线粒体诱导氧化应激,产生活性氧和眼睛晶状体的氧化还原状态失衡,导致人类白内障形成:磷脂氢过氧化物破坏晶状体的氧化还原组织,作为白内障疾病的共同基础。
Cell Biochem Funct. 2011 Apr;29(3):183-206. doi: 10.1002/cbf.1737. Epub 2011 Mar 7.
3
[Accumulation of lipid peroxidation products in cataractous lenses].
Biull Eksp Biol Med. 1985 Sep;100(9):299-301.
4
[Antioxidative enzyme activity and metabolism of peroxide compounds in the crystalline lens during cataractogenesis].[白内障形成过程中晶状体的抗氧化酶活性及过氧化物代谢]
Biull Eksp Biol Med. 1987 Feb;103(2):143-6.
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Potentiation of intraocular absorption and drug metabolism of N-acetylcarnosine lubricant eye drops: drug interaction with sight threatening lipid peroxides in the treatment for age-related eye diseases.N-乙酰肌肽润滑滴眼液的眼内吸收及药物代谢增强作用:在年龄相关性眼病治疗中药物与威胁视力的脂质过氧化物的相互作用
Drug Metabol Drug Interact. 2009;24(2-4):275-323. doi: 10.1515/dmdi.2009.24.2-4.275.
6
Lipid peroxide and reactive oxygen species generating systems of the crystalline lens.晶状体的脂质过氧化物和活性氧生成系统。
Biochim Biophys Acta. 1994 Feb 22;1225(3):326-37. doi: 10.1016/0925-4439(94)90014-0.
7
[Accumulation of lipid peroxidation products in the human lens during cataract maturation].[白内障成熟过程中人类晶状体脂质过氧化产物的积累]
Vopr Med Khim. 1985 Nov-Dec;31(6):100-4.
8
Failure to withstand oxidative stress induced by phospholipid hydroperoxides as a possible cause of the lens opacities in systemic diseases and ageing.无法承受磷脂氢过氧化物诱导的氧化应激可能是全身疾病和衰老过程中晶状体混浊的一个原因。
Biochim Biophys Acta. 1996 Mar 1;1315(2):87-99. doi: 10.1016/0925-4439(95)00091-7.
9
[Peroxidation crystalline lens damage--a possible cause of the development of traumatic cataract].[过氧化晶状体损伤——外伤性白内障发生的一个可能原因]
Biull Eksp Biol Med. 1986 Apr;101(4):412-3.
10
[Cataract induction by products of lipid peroxidation].
Biofizika. 1987 Jan-Feb;32(1):121-4.