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21-氨基类固醇U74006F对缺血后脑灌注不足的减轻作用。

Attenuation of postischemic cerebral hypoperfusion by the 21-aminosteroid U74006F.

作者信息

Hall E D, Yonkers P A

机构信息

Central Nervous System Diseases Research Unit, Upjohn Company, Kalamazoo, Michigan 49001.

出版信息

Stroke. 1988 Mar;19(3):340-4. doi: 10.1161/01.str.19.3.340.

Abstract

The ability of the nonglucocorticoid 21-aminosteroid U74006F, a potent inhibitor of iron-dependent lipid peroxidation, to antagonize progressive brain hypoperfusion after a 5-minute episode of global brain ischemia was examined in alpha-chloralose-anesthetized cats. Immediately after a 5-minute episode of near-total tourniquet-induced brain ischemia, cortical blood flow returned to normal or above normal. Thereafter, cortical blood flow fell progressively to a level 71.7% below normal by 3 hours after ischemia. In contrast, in cats that received 1 mg/kg i.v. U74006F 15 minutes after the ischemic episode, cortical blood flow remained significantly greater than that seen in vehicle-treated cats. At 3 hours, cortical blood flow had declined by only 45.7% (p less than 0.04 compared with vehicle). In addition, U74006F treatment significantly improved postischemic maintenance of blood pressure and recovery of somatosensory evoked potentials and reduced postischemic arterial blood acidosis. U74006F had no effect on cortical blood flow, somatosensory evoked potentials, or blood pressure in nonischemic cats. Our results suggest that U74006F may be useful in the early treatment of global cerebral ischemia.

摘要

在α-氯醛糖麻醉的猫身上,研究了非糖皮质激素21-氨基类固醇U74006F(一种铁依赖性脂质过氧化的有效抑制剂)拮抗5分钟全脑缺血发作后进行性脑灌注不足的能力。在近全脑缺血发作5分钟后,皮质血流量立即恢复到正常或高于正常水平。此后,缺血3小时后皮质血流量逐渐下降至低于正常水平71.7%。相比之下,在缺血发作15分钟后静脉注射1mg/kg U74006F的猫中,皮质血流量仍显著高于接受载体治疗的猫。在3小时时,皮质血流量仅下降了45.7%(与载体相比,p<0.04)。此外,U74006F治疗显著改善了缺血后血压的维持以及体感诱发电位的恢复,并减轻了缺血后动脉血酸中毒。U74006F对非缺血猫的皮质血流量、体感诱发电位或血压没有影响。我们的结果表明,U74006F可能对全脑缺血的早期治疗有用。

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