Salt T E, Turner J P
Department of Visual Science, University College London, UK.
Neuropharmacology. 1996 Feb;35(2):239-41. doi: 10.1016/0028-3908(95)00184-0.
The metabotropic glutamate receptor (mGluR) agonists CCG-I and L-AP4, acting at Group II and Group III mGluRs respectively, can reduce GABAergic synaptic inhibition on single neurones in the rat thalamus in vivo via a presumed presynaptic mechanism. The actions of L-AP4 were antagonized by (+/-)-alpha-methyl-4-phosphonophenylglycine (MPPG), whereas CCG-I was significantly less affected. Thus MPPG may be a useful tool for detecting physiological roles for Group III mGluRs.
代谢型谷氨酸受体(mGluR)激动剂CCG-I和L-AP4,分别作用于II组和III组mGluR,可通过一种推测的突触前机制,在体内降低大鼠丘脑单个神经元上的GABA能突触抑制。L-AP4的作用被(±)-α-甲基-4-膦酰基苯甘氨酸(MPPG)拮抗,而CCG-I受影响明显较小。因此,MPPG可能是检测III组mGluR生理作用的有用工具。