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6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)对体外培养海马体CA3区自发性和诱发性爆发的拮抗作用。

Antagonism of spontaneous and evoked bursts by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) in the CA3 region of the in vitro hippocampus.

作者信息

Neuman R S, Ben-Ari Y, Cherubini E

机构信息

INSERM U29, Hôpital de Port-Royal, Paris, France.

出版信息

Brain Res. 1988 Nov 22;474(1):201-3. doi: 10.1016/0006-8993(88)90686-5.

Abstract

Superfusion of hippocampal slices with 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) antagonized kainate-induced bursts and bursts of unknown origin in the CA3 region. CNQX also increased the latency of and eventually blocked evoked bursts which persist following kainate washout. In contrast, D-(-)-2-amino-7-phosphonoheptanoic acid did not alter burst latency or block bursts unless applied subsequent to CNQX. We conclude that the quisqualate type receptor has a prominent role in burst generation with a smaller contribution from N-methyl-D-aspartate receptors.

摘要

用6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)对海马切片进行灌流,可拮抗海人酸诱导的CA3区爆发性放电以及来源不明的爆发性放电。CNQX还延长了海人酸洗脱后持续存在的诱发爆发性放电的潜伏期,并最终将其阻断。相比之下,D-(-)-2-氨基-7-磷酸庚酸不会改变爆发性放电的潜伏期,也不会阻断爆发性放电,除非在CNQX之后应用。我们得出结论,quisqualate型受体在爆发性放电的产生中起主要作用,而N-甲基-D-天冬氨酸受体的作用较小。

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