Bond A, Monn J A, Lodge D
Lilly Research Centre, Surrey, UK.
Neuroreport. 1997 Apr 14;8(6):1463-6. doi: 10.1097/00001756-199704140-00027.
Non-specific metabotropic glutamate receptor (mGluR) agonists have previously been shown to potentiate responses of spinal neurones to ionotropic glutamate receptor agonists. In this study we show that LY354740, which is a highly selective Group 2 mGluR agonist with nanomolar potency in vitro, also mimics the above effects following local ejection on spinal neurones in vivo, an action which is blocked by a Group 2 antagonist. Despite its polar nature, LY354740 is also active given either by the i.v. or the oral route (2.5-20 mg/kg) and thus will be a useful agent for investigating the role of Group 2 mGluRs both physiologically and clinically.
非特异性代谢型谷氨酸受体(mGluR)激动剂此前已被证明可增强脊髓神经元对离子型谷氨酸受体激动剂的反应。在本研究中,我们表明LY354740,一种在体外具有纳摩尔效力的高度选择性2组mGluR激动剂,在体内对脊髓神经元进行局部喷射后也能模拟上述效应,该作用可被2组拮抗剂阻断。尽管LY354740具有极性,但通过静脉注射或口服途径(2.5 - 20 mg/kg)给药时也具有活性,因此它将成为一种用于在生理和临床方面研究2组mGluR作用的有用药物。