Battaglia G, Monn J A, Schoepp D D
Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Neurosci Lett. 1997 Jul 4;229(3):161-4. doi: 10.1016/s0304-3940(97)00442-4.
In vivo microdialysis in freely moving rats was used to investigate the presynaptic mechanisms by which LY354740, a novel, potent, selective, and systemically active agonist for group II metabotropic glutamate receptors (mGluRs), alters glutamate neuronal transmission. Basal levels of glutamate and aspartate in striatal dialysates of LY354740 (10 mg/kg i.p.)-treated animals were not significantly different from the saline-treated control animals. In the saline treated controls, veratridine (100 microM) induced a 6-fold increase in glutamate and 9-fold increase in aspartate. However, following LY354740 administration the veratridine-evoked release of glutamate and aspartate was completely prevented. These data demonstrate that LY354740 blocks the evoked release of endogenous excitatory amino acids, and indicate a role for group II mGluRs in presynaptic modulation of glutamate neuronal transmission in vivo. Ireland Ltd.
在自由活动的大鼠体内进行微透析,以研究LY354740(一种新型、强效、选择性且具有全身活性的II型代谢型谷氨酸受体(mGluRs)激动剂)改变谷氨酸能神经元传递的突触前机制。腹腔注射LY354740(10 mg/kg)处理的动物纹状体透析液中谷氨酸和天冬氨酸的基础水平与生理盐水处理的对照动物无显著差异。在生理盐水处理的对照中,藜芦碱(100 microM)使谷氨酸增加6倍,天冬氨酸增加9倍。然而,给予LY354740后,藜芦碱诱发的谷氨酸和天冬氨酸释放被完全阻断。这些数据表明LY354740可阻断内源性兴奋性氨基酸的诱发释放,并提示II型mGluRs在体内谷氨酸能神经元传递的突触前调节中起作用。爱尔兰有限公司