McLennan H, Lodge D
Brain Res. 1979 Jun 15;169(1):83-90. doi: 10.1016/0006-8993(79)90375-5.
DL-alpha-Aminoadipate (DLalphaAA) and L-glutamic acid diethylester (GDEE) were compared as antagonists of the excitatory effects of a number of amino acids on interneurones, and also of acetylcholine on Renshaw cells of the cat spinal cord. The excitants could be ranked in order of their sensitivity of the two antagonists. Ibotenate and the optical isomers of N-methylaspartate were the most readily antagonised by DLalphaAA and the least by GDEE; L-glutamate and quisqualate were most affected by GDEE and least by DLalphaAA; the actions of L-cysteate, L-aspartate and D- and L-homocysteate were reduced to some extent by both; and kainate was relatively insensitive to both antagonists. Acetylcholine excitations of Renshaw cells were often reduced by GDEE and occasionally by DLalphaAA. The results indicate the existence on spinal neurones of at least two populations of amino acid receptors which have differing sensitivities to the antagonists, and which do not precisely conform to the "glutamate-perferring" and "aspartate-preferring" categories which have been proposed on other grounds.
将DL-α-氨基己二酸(DLαAA)和L-谷氨酸二乙酯(GDEE)作为多种氨基酸对中间神经元兴奋作用的拮抗剂,以及乙酰胆碱对猫脊髓闰绍细胞兴奋作用的拮抗剂进行了比较。这些兴奋剂可根据它们对这两种拮抗剂的敏感性进行排序。鹅膏蕈氨酸和N-甲基天冬氨酸的旋光异构体最容易被DLαAA拮抗,而被GDEE拮抗的程度最小;L-谷氨酸和quisqualate受GDEE影响最大,受DLαAA影响最小;L-半胱氨酸、L-天冬氨酸以及D-和L-高半胱氨酸的作用在一定程度上均被二者降低;而红藻氨酸对这两种拮抗剂相对不敏感。闰绍细胞的乙酰胆碱兴奋作用常被GDEE降低,偶尔也会被DLαAA降低。结果表明,脊髓神经元上至少存在两类氨基酸受体,它们对拮抗剂的敏感性不同,且并不完全符合基于其他理由提出的“偏爱谷氨酸”和“偏爱天冬氨酸”类别。