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短暂性缺血对大鼠海马脑片突触传递长时程增强的影响。

Effect of transient ischemia on long-term potentiation of synaptic transmission in rat hippocampal slices.

作者信息

Gasparova Zdenka, Jariabka Pavol, Stolc Svorad

机构信息

Institute of Experimental Pharmacology, Slovak Academy of Sciences, Bratislava, Slovakia.

出版信息

Neuro Endocrinol Lett. 2008 Oct;29(5):702-5.

Abstract

OBJECTIVES

Long-term potentiation (LTP) of neuronal activity in the hippocampus is thought to be a substrate for learning and memory. The influence of ischemia (IS) (hypoxia/hypoglycemia) on induction of LTP of synaptic transmission (ST) by high frequency stimulation (HFS) was investigated in rat hippocampal slices.

METHODS

Neurons were stimulated via Schäffer collaterals and field excitatory postsynaptic potentials (fEPSP) were recorded extracellularly from the CA1 region. LTP was induced by one single train (100 Hz, 1s).

RESULTS

In controls LTP of ST after HFS was 179.70+/-12.53%. Short IS of 2.5-4.5 min elicited a transient failure of ST, with return to former value followed by further increase of fEPSP amplitude to 142.28+/-16.24%, compared to amplitude before IS. HFS was elicited 40 min after exposure to IS and LTP was measured over further 40-60 min. LTP in slices exposed to 2.5-4.5-min IS was 139.94+/-14.01%. IS of 6-7.5 min elicited a prolonged failure of ST, with almost full recovery (96.69+/-14.42%). LTP was not activated 40 min after 6-7.5-min IS and the amplitude of fEPSP was even reduced to 80.14+/-19.19% compared to the former mean value of fEPSP 10 min before HFS.

CONCLUSION

The results revealed that prolonged 6-7.5-min IS influenced induction of LTP of ST in the hippocampus and thus it could have deleterious effects on learning and memory. These findings may have clinical implications in stroke, brain ischemia, sleep apnoe and call for studying the effect of neuroprotectants on the induction of LTP in hippocampus exposed to oxidative stress.

摘要

目的

海马体中神经元活动的长时程增强(LTP)被认为是学习和记忆的基础。本研究在大鼠海马体切片中,探究了缺血(IS)(缺氧/低血糖)对高频刺激(HFS)诱导突触传递(ST)的LTP的影响。

方法

通过施affer侧支刺激神经元,并在细胞外记录CA1区的场兴奋性突触后电位(fEPSP)。LTP由单次刺激序列(100Hz,1s)诱导产生。

结果

在对照组中,HFS后ST的LTP为179.70±12.53%。2.5 - 4.5分钟的短暂IS引发了ST的短暂性阻断,随后恢复到先前值,接着fEPSP幅度进一步增加至142.28±16.24%(与IS前的幅度相比)。在暴露于IS后40分钟施加HFS,并在接下来的40 - 60分钟内测量LTP。暴露于2.5 - 4.5分钟IS的切片中的LTP为139.94±14.01%。6 - 7.5分钟的IS引发了ST的长时间阻断,几乎完全恢复(96.69±14.42%)。在6 - 7.5分钟IS后40分钟,LTP未被激活,并且与HFS前10分钟fEPSP的先前平均值相比,fEPSP幅度甚至降低至80.14±19.19%。

结论

结果表明,6 - 7.5分钟的长时间IS影响了海马体中ST的LTP诱导,因此可能对学习和记忆产生有害影响。这些发现可能对中风、脑缺血、睡眠呼吸暂停具有临床意义,并呼吁研究神经保护剂对暴露于氧化应激的海马体中LTP诱导的影响。

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