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β-胡萝卜素可减轻过氧化物诱导的人胎盘血管收缩。

beta-Carotene attenuates peroxide-induced vasoconstriction in the human placenta.

作者信息

Cueto S M, Romney A D, Wang Y, Walsh S W

机构信息

Department of Obstetrics and Gynecology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0034, USA.

出版信息

J Soc Gynecol Investig. 1997 Mar-Apr;4(2):64-71.

PMID:9101463
Abstract

OBJECTIVE

Placental lipid peroxides and thromboxane are abnormally increased in preeclampsia. Peroxides stimulate thromboxane to increase placental vasoconstriction. Antioxidants, such as beta-carotene, control lipid peroxidation. Reduced levels of beta-carotene (0.25 mumol/L) have been found in preeclamptic women. We hypothesized that normal (0.5 mumol/L) or elevated (1.0 mumol/L) levels of beta-carotene would attenuate peroxide-induced vasoconstriction in the human placenta, whereas low levels would not.

METHODS

Isolated human placental cotyledons (n = 8) were sequentially perfused with control Krebs-Ringer-bicarbonate buffer, 200 mumol/L t-butyl hydroperoxide, and then with progressively increasing concentrations of beta-carotene (0.25, 0.5, and 1 mumol/L) plus t-butyl hydroperoxide. Fetal perfusion pressure was monitored continuously, and maternal and fetal effluent samples were collected for each treatment. Samples were analyzed for lipid peroxides and for thromboxane and prostacyclin by their stable metabolites thromboxane B2 (TXB2) and 6-keto-prostaglandin (PG)F1 alpha.

RESULTS

Compared with control, t-butyl hydroperoxide significantly increased perfusion pressure, vascular resistance, and the secretion rates of lipid peroxides, TXB2 and 6-keto-PGF1 alpha. Perfusion with normal (0.5 mumol/L) or increased (1 mumol/L) levels of beta-carotene significantly or completely inhibited t-butyl hydroperoxide-induced vasoconstriction and the increases in lipid peroxide and TXB2 secretion, but did not inhibit peroxide-induced increases in 6-keto-PGF1 alpha secretion. Reduced levels of beta-carotene (0.25 mumol/L) did not inhibit t-butyl hydroperoxide-induced vasoconstriction or the increases in lipid peroxide secretion.

CONCLUSIONS

beta-carotene at levels found in normal pregnant women (0.5 mumol/L) or at levels achieved with beta-carotene supplementation (1 mumol/L) inhibited peroxide-induced vasoconstriction and lipid peroxide and thromboxane secretion. Levels of beta-carotene found in preeclamptic women (0.25 mumol/L) did not inhibit peroxide-induced vasoconstriction or lipid peroxide secretion.

摘要

目的

子痫前期患者胎盘脂质过氧化物和血栓素异常增加。过氧化物刺激血栓素增加胎盘血管收缩。抗氧化剂如β-胡萝卜素可控制脂质过氧化。子痫前期女性体内β-胡萝卜素水平降低(0.25μmol/L)。我们假设正常(0.5μmol/L)或升高(1.0μmol/L)水平的β-胡萝卜素会减弱过氧化物诱导的人胎盘血管收缩,而低水平则不会。

方法

将分离的人胎盘小叶(n = 8)依次用对照的 Krebs-Ringer-碳酸氢盐缓冲液、200μmol/L叔丁基过氧化氢灌注,然后用浓度逐渐增加的β-胡萝卜素(0.25、0.5和1μmol/L)加叔丁基过氧化氢灌注。持续监测胎儿灌注压力,并收集每种处理的母体和胎儿流出液样本。分析样本中的脂质过氧化物以及通过其稳定代谢产物血栓素B2(TXB2)和6-酮-前列腺素(PG)F1α检测血栓素和前列环素。

结果

与对照相比,叔丁基过氧化氢显著增加灌注压力、血管阻力以及脂质过氧化物、TXB2和6-酮-PGF1α的分泌率。用正常(0.5μmol/L)或升高(1μmol/L)水平的β-胡萝卜素灌注可显著或完全抑制叔丁基过氧化氢诱导的血管收缩以及脂质过氧化物和TXB2分泌的增加,但不抑制过氧化物诱导的6-酮-PGF1α分泌增加。降低水平的β-胡萝卜素(0.25μmol/L)不抑制叔丁基过氧化氢诱导的血管收缩或脂质过氧化物分泌增加。

结论

正常孕妇体内水平(0.5μmol/L)或补充β-胡萝卜素后达到的水平(1μmol/L)的β-胡萝卜素可抑制过氧化物诱导的血管收缩以及脂质过氧化物和血栓素分泌。子痫前期女性体内的β-胡萝卜素水平(0.25μmol/L)不抑制过氧化物诱导的血管收缩或脂质过氧化物分泌。

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