Bering R, Johansen F F
Institute of Neuropathology, University of Copenhagen, Denmark.
Regul Pept. 1993 Nov 19;49(1):41-8. doi: 10.1016/0167-0115(93)90382-i.
The influence of transient cerebral ischemia on the expression of somatostatin (SS) mRNA and peptide in hippocampal neurons was studied in the rat. Animals survived 10 min of 4-vessel occlusion ischemia during systemic hypotension for 1 h, 1 day, 2 days, 4 days, and 16 days, respectively. SS mRNA and peptide were detected with nonradioactive probes in brain sections by means of in situ hybridisation and immunocytochemistry. Then SS mRNA and peptide positive neurons in hippocampus were counted. The neuronal expression of the two markers correlated well in control and ischemic sections. In the dentate hilus, SS mRNA and peptide were lost permanently from day 2 after ischemia, in parallel with ischemic cell death and loss of the neurons. In CA1, where all interneurons containing SS survive an ischemic insult, we found a transient decrease of SS mRNA and peptide at 2-4 days after ischemia. The SS mRNA was most reduced. We conclude that ischemia transiently reduces levels of SS mRNA and peptide in surviving hippocampal interneurons. This process is brief and delayed in mild ischemia, and not expressed in vulnerable hilar neurons.
研究了短暂性脑缺血对大鼠海马神经元中生长抑素(SS)mRNA和肽表达的影响。动物分别在系统性低血压期间经历4血管闭塞缺血10分钟,存活1小时、1天、2天、4天和16天。通过原位杂交和免疫细胞化学方法,用非放射性探针在脑切片中检测SS mRNA和肽。然后对海马中SS mRNA和肽阳性神经元进行计数。在对照和缺血切片中,这两种标志物的神经元表达具有良好的相关性。在齿状回门区,缺血后第2天起,SS mRNA和肽永久性丢失,同时伴有缺血性细胞死亡和神经元丧失。在CA1区,所有含SS的中间神经元在缺血性损伤中存活,我们发现在缺血后2 - 4天,SS mRNA和肽短暂减少。其中SS mRNA减少最为明显。我们得出结论,缺血会短暂降低存活海马中间神经元中SS mRNA和肽的水平。这个过程在轻度缺血中短暂且延迟,而在易损的门区神经元中未表现出来。