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两种具有不同定位、功能和药理学特性的中枢性AMPA优先型受体的特性研究。

Characterization of two central AMPA-preferring receptors having distinct location, function and pharmacology.

作者信息

Pittaluga A, Thellung S, Maura G, Raiteri M

机构信息

Istituto di Farmacologia e Farmacognosia, Università di Genova, Italy.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1994 Jun;349(6):555-8. doi: 10.1007/BF01258458.

Abstract

The existence of a pharmacological heterogeneity among the glutamate receptors sensitive to (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) has been investigated in the adult rat central nervous system (CNS). AMPA stimulated [3H]noradrenaline ([3H]NA) release from hippocampal synaptosomes (pD2 = 4.58) and the production of cGMP in cerebellar slices (pD2 = 7.75). The AMPA effects in the two systems were tested against several glutamate receptor antagonists including 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), 6,7-dinitro-quinoxaline-2,3-dione (DNQX), L-glutamate diethylester (GDEE), gamma-D-glutamyl-glycine (GDGG) and gamma-D-glutamyl-aminomethylsulphonate (GAMS). In both systems the AMPA effect was equally sensitive to CNQX or DNQX. However, while the AMPA-evoked increase of [3H]NA release from presynaptic terminals was not affected by GAMS, GDGG or GDEE, the postsynaptic cGMP response was prevented by GDGG and GDEE. It is concluded that rat hippocampus and cerebellum possess, respectively, presynaptic and postsynaptic AMPA-sensitive receptors involved in different functions and endowed with diverse pharmacological properties.

摘要

在成年大鼠中枢神经系统(CNS)中,已对(RS)-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)敏感的谷氨酸受体之间的药理学异质性进行了研究。AMPA刺激海马突触体释放[3H]去甲肾上腺素([3H]NA)(pD2 = 4.58),并刺激小脑切片中cGMP的生成(pD2 = 7.75)。在这两个系统中,针对几种谷氨酸受体拮抗剂测试了AMPA的作用,这些拮抗剂包括6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)、6,7-二硝基喹喔啉-2,3-二酮(DNQX)、L-谷氨酸二乙酯(GDEE)、γ-D-谷氨酰甘氨酸(GDGG)和γ-D-谷氨酰氨基甲基磺酸盐(GAMS)。在这两个系统中,AMPA的作用对CNQX或DNQX同样敏感。然而,虽然AMPA诱发的突触前终末[3H]NA释放增加不受GAMS、GDGG或GDEE的影响,但突触后cGMP反应却被GDGG和GDEE所阻断。结论是,大鼠海马体和小脑分别具有参与不同功能且具有不同药理学特性的突触前和突触后AMPA敏感受体。

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