首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Thalamocortical and corticocortical excitatory postsynaptic potentials mediated by excitatory amino acid receptors in the cat motor cortex in vivo.
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Thalamocortical and corticocortical excitatory postsynaptic potentials mediated by excitatory amino acid receptors in the cat motor cortex in vivo.

机译:在猫的运动皮层中,由兴奋性氨基酸受体介导的丘脑皮质和皮层皮质兴奋性突触后电位。

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Intracellular recordings were made from neurons in the motor cortex of an anaesthetized cat, together with iontophoretic application of excitatory amino acid receptor agonists and antagonists, in order to evaluate the role of such receptors in excitatory postsynaptic potentials evoked from stimulation of afferent and recurrent pathways in vivo. Excitatory postsynaptic potentials which were evoked by stimulation of the ventrolateral thalamus were found to be largely insensitive to antagonism by N-methyl-D-aspartate receptor antagonists, although they were susceptible to blockade by the non-N-methyl-D-aspartate receptor antagonist, 6-cyano-7-nitroquinoxaline-2,3-dione. Increasing the ventrolateral thalamus stimulation frequency from 0.5 or 1 to 5 Hz caused an increase of evoked excitatory postsynaptic potential amplitudes and number of action potentials. These augmented excitatory postsynaptic potentials remained insensitive to application of N-methyl-D-aspartate antagonists. In contrast, recurrent excitatory postsynaptic potentials evoked by stimulation of the pyramidal tract were found to be sensitive to N-methyl-D-aspartate receptor antagonists and/or non-N-methyl-D-aspartate receptor antagonists in some neurons. These results demonstrate the involvement of both N-methyl-D-aspartate- and non-N-methyl-D-aspartate receptors in synaptic responses of cat motor cortex neurons in vivo, and that the synaptic pharmacology of the thalamic input may differ from that of the local recurrent pathways.
机译:麻醉猫的运动皮层神经元进行细胞内记录,并通过离子电渗法应用兴奋性氨基酸受体激动剂和拮抗剂,以评估此类受体在刺激大鼠突触和递归途径中引起的兴奋性突触后电位中的作用。体内。发现通过刺激腹侧丘脑引起的兴奋性突触后电位对N-甲基-D-天冬氨酸受体拮抗剂的拮抗作用基本上不敏感,尽管它们很容易受到非N-甲基-D-天冬氨酸受体拮抗剂的阻滞。 ,6-氰基-7-硝基喹喔啉-2,3-二酮。将腹外侧丘脑刺激频率从0.5或1 Hz增加到5 Hz会引起诱发的兴奋性突触后突触电位振幅和动作电位数目的增加。这些增加的兴奋性突触后电位对N-甲基-D-天冬氨酸拮抗剂的应用仍然不敏感。相反,发现在某些神经元中,通过刺激锥体束引起的复发性兴奋性突触后电位对N-甲基-D-天冬氨酸受体拮抗剂和/或非N-甲基-D-天冬氨酸受体拮抗剂敏感。这些结果表明,N-甲基-D-天门冬氨酸和非N-甲基-D-天冬氨酸受体都参与了猫运动皮层神经元在体内的突触反应,并且丘脑输入的突触药理作用可能与局部复发途径。

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