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花生四烯酸导致神经胶质肿胀的机制。

Mechanisms of glial swelling by arachidonic acid.

作者信息

Staub F, Winkler A, Peters J, Kempski O, Baethmann A

机构信息

Institute for Surgical Research, Ludwig-Maximilians-University, München, Federal Republic of Germany.

出版信息

Acta Neurochir Suppl (Wien). 1994;60:20-3. doi: 10.1007/978-3-7091-9334-1_5.

Abstract

The effect of arachidonic acid (AA, 20:4) was analyzed in vitro by employment of C6 glioma cells and astrocytes from primary culture. The cells were suspended in an incubation chamber under continuous control of pH, pO2, and temperature. Cell swelling was quantified by flow cytometry. After a control period, the suspension was added with AA at concentrations of 0.01 to 1.0 mM. Administration of AA induced an immediate, dose dependent swelling in C6 glioma cells or astrocytes. AA-concentrations of 0.01 mM led to an increase of the glial cell volume to 103.0 +/- 1.0% of control, 0.1 mM to 110.0 +/- 1.5%, and 1.0 mM to 118.8 +/- 1.5% within 10 min. The swelling response to linoleic acid (18:2) was only about half of what was found when AA was administered at a concentration of 0.1 mM, whereas stearic acid (18:0) did not induce any cell volume changes. Inhibition of the cyclo- and lipoxygenase pathway by BW 755C did not prevent glial swelling from AA, whereas it was reduced by SOD, or almost completely abolished by the aminosteroid U-74389F, an antagonist of lipid peroxidation. Replacement of Na(+)- and Cl- -ions in the suspension medium by choline chloride was also associated with complete abolishment of cell swelling from AA. The results demonstrate an impressive efficacy of arachidonic acid to induce glial swelling which might be attributable to activation of lipid peroxidation by the fatty acid, leading to an increased Na(+)-permeability and subsequent influx of water into the cells.

摘要

通过使用C6胶质瘤细胞和原代培养的星形胶质细胞,在体外分析了花生四烯酸(AA,20:4)的作用。细胞悬浮于孵育室中,pH、pO2和温度处于持续控制之下。通过流式细胞术对细胞肿胀进行定量分析。在一段对照期后,向悬浮液中加入浓度为0.01至1.0 mM的AA。给予AA可立即在C6胶质瘤细胞或星形胶质细胞中引起剂量依赖性肿胀。0.01 mM的AA浓度在10分钟内可使神经胶质细胞体积增加至对照的103.0±1.0%,0.1 mM时增加至110.0±1.5%,1.0 mM时增加至118.8±1.5%。对亚油酸(18:2)的肿胀反应仅约为给予0.1 mM AA时所观察到反应的一半,而硬脂酸(18:0)未引起任何细胞体积变化。BW 755C对环氧化酶和脂氧化酶途径的抑制并不能阻止AA引起的神经胶质肿胀,而超氧化物歧化酶(SOD)可使其减轻,脂质过氧化拮抗剂氨基类固醇U-74389F几乎可将其完全消除。用氯化胆碱替代悬浮培养基中的Na+和Cl-离子也可使AA引起的细胞肿胀完全消除。结果表明花生四烯酸诱导神经胶质肿胀的效力令人印象深刻,这可能归因于该脂肪酸激活脂质过氧化,导致Na+通透性增加,随后水流入细胞。

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