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关于谷氨酸拮抗剂对缺血性CA-1损伤影响的扩展性研究。

Extended studies on the effect of glutamate antagonists on ischemic CA-1 damage.

作者信息

Diemer N H, Balchen T, Bruhn T, Christensen T, Vanicky I, Nielsen M, Johansen F F

机构信息

Institute of Neuropathology, University of Copenhagen, Denmark.

出版信息

Acta Neurochir Suppl. 1996;66:73-5. doi: 10.1007/978-3-7091-9465-2_13.

Abstract

Glutamate receptors are numerous on the ischemia vulnerable CA-1 pyramidal cells. Postischemic use of the AMPA antagonist NBQX has shown up to 80% protection against cell death. Three aspects of this were studied: In the first study, male Wistar rats were given NBQX (30 mg/kg x 3) either 20 hours or immediately (0 h) before 12 min of 4-vessel occlusion with hypotension. After six days of reperfusion comparison with an untreated group showed almost full protection in the 0 h group (4% cell loss, p < 0.001) but only slight protection in the 20 h group (62% cell loss, p < 0.05). After 12 min of ischemia in the present model, eosinophilic CA-1 cells are seen from day 2 on. Since there could be a late, deleterious calcium influx via NMDA receptors, one group of ischemic rats was given MK-801 (5 mg/kg i.p.) 24 hours after ischemia. However, quantitation 6 days later of remaining CA-1 cells showed no protection. In the third study referred here, two groups of ischemic rats were given NBQX (30 mg/kg x 3) immediately after ischemia. The groups survive for six and 21 days, respectively. Counting of CA-1 pyramidal cells showed an equal, significant protection in both groups (approx 20% cell loss).

摘要

谷氨酸受体在易受缺血损伤的CA-1锥体细胞上大量存在。缺血后使用AMPA拮抗剂NBQX已显示出对细胞死亡有高达80%的保护作用。对此进行了三个方面的研究:在第一项研究中,雄性Wistar大鼠在4血管闭塞伴低血压12分钟前20小时或立即(0小时)给予NBQX(30mg/kg×3)。再灌注6天后,与未治疗组相比,0小时组显示出几乎完全的保护作用(细胞损失4%,p<0.001),而20小时组只有轻微的保护作用(细胞损失62%,p<0.05)。在本模型中缺血12分钟后,从第2天开始可见嗜酸性CA-1细胞。由于可能存在通过NMDA受体的晚期有害钙内流,一组缺血大鼠在缺血24小时后给予MK-801(5mg/kg腹腔注射)。然而,6天后对剩余CA-1细胞的定量分析显示没有保护作用。在这里提到的第三项研究中,两组缺血大鼠在缺血后立即给予NBQX(30mg/kg×3)。两组分别存活6天和21天。对CA-1锥体细胞的计数显示两组都有同等程度的显著保护作用(细胞损失约20%)。

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