Substance P analogues potentiate the pressor response to microinjection of L-glutamate into laminas I and II of the cat dorsal horn

被引:4
作者
Beyaert, CA
Hill, JM
Kaufman, MP
机构
[1] UNIV CALIF DAVIS,DEPT INTERNAL MED,DIV CARDIOVASC MED,DAVIS,CA 95616
[2] UNIV CALIF DAVIS,DEPT HUMAN PHYSIOL,DAVIS,CA 95616
关键词
sympathetic nervous system; neuropeptide; excitatory amino acid; spinal cord;
D O I
10.1016/S0006-8993(97)00362-4
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Microinjection of a substance P analogue (1 mM; 7 or 10 nl) into laminae I and II of the L-7, dorsal horn of decerebrate cats significantly potentiated (P < 0.05) the increase in arterial pressure evoked by microinjection of L-glutamate (109 mM; 7 or 10 nl) into these spinal sites. Microinjection of the substance P analogues (i.e., GR73638 and [Sar(9),Met(O-2)(11)]-substance P) which were selective NK-1 receptor agonists, had no impact on the cardioacceleration evoked by microinjection of L-glutamate (P > 0.05). In addition, microinjection of these analogues had no effect on the modest and non-significant increase in phrenic nerve discharge evoked by L-glutamate. We conclude that stimulation of NK-1 receptors in the superficial laminae of the dorsal horn potentiates the presser responses to microinjection of L-glutamate.
引用
收藏
页码:175 / 179
页数:5
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