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腺苷A2受体拮抗剂促进诱发突触后电位的长期增强(去增强)的逆转,但抑制海马CA1神经元群体峰电位的长期增强的逆转。

Adenosine A2 receptor antagonist facilitates the reversal of long-term potentiation (depotentiation) of evoked postsynaptic potentials but inhibits that of population spikes in hippocampal CA1 neurons.

作者信息

Fujii S, Wakizaka A, Sekino Y, Kuroda Y, Ito K, Miyakawa H, Kato H

机构信息

Department of Biochemistry and Molecular Biology, Kyorin University School of Medicine, Tokyo, Japan.

出版信息

Neurosci Lett. 1992 Dec 14;148(1-2):148-50. doi: 10.1016/0304-3940(92)90826-s.

Abstract

The effects of the adenosine A2 receptor antagonist CP-66713 on the reversal of long-term potentiation (LTP) were studied in CA1 neurons of guinea pig hippocampal slices. Reduction of LTP (depotentiation, DP) was effected by delivering a train of low-frequency afferent stimuli (depotentiation stimulation, DPS) which was given 20 min after tetanus (100 Hz, 100 pulses). DPS (1 Hz, 1000 pulses) was applied during perfusion of CP-66713 (10 microM). In the presence of CP-66713, DPS reduced the potentiated component of the slope of the field EPSP (S-EPSP) and the amplitude of the population spike (A-PS) by 101.7% and 19.1% of the potentiated amount, respectively (mean, n = 8). The reduction of LTP of the S-EPSP was significantly larger than the control (68.5% (mean, n = 6)) while that of the A-PS was significantly smaller than the control (80.1% (mean, n = 6)). Based on these results, we conclude that the inhibition of DP in the EPSP, the facilitation of DP in the PS, and the consequent attenuation in the EPSP-PS relationship follow from activation of adenosine A2 receptors.

摘要

在豚鼠海马脑片的CA1神经元中研究了腺苷A2受体拮抗剂CP-66713对长时程增强(LTP)反转的影响。通过在强直刺激(100Hz,100个脉冲)后20分钟给予一串低频传入刺激(去增强刺激,DPS)来实现LTP的降低(去增强,DP)。在灌注CP-66713(10μM)期间施加DPS(1Hz,1000个脉冲)。在CP-66713存在的情况下,DPS分别将场兴奋性突触后电位(S-EPSP)斜率的增强成分和群体峰电位(A-PS)的幅度降低了增强量的101.7%和19.1%(平均值,n = 8)。S-EPSP的LTP降低显著大于对照组(68.5%(平均值,n = 6)),而A-PS的降低显著小于对照组(80.1%(平均值,n = 6))。基于这些结果,我们得出结论,腺苷A2受体的激活导致EPSP中DP的抑制、PS中DP的促进以及EPSP-PS关系的相应减弱。

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