Srinivasan M, Yamamoto Y, Brodin E, Persson H
Nobel Institute for Neurophysiology, Karolinska Institutet, Stockholm, Sweden.
Brain Res Mol Brain Res. 1991 Feb;9(3):233-8. doi: 10.1016/0169-328x(91)90006-j.
Acute intravenous administration of the selective D1 receptor blocker SCH-23390 resulted in an enhanced respiratory motor output as evidenced by the phrenic nerve activity, whereas local perfusion into the region of nucleus tractus solitarii had no effect. The increase in phrenic nerve activity was accompanied by a concomitant increase in the release of substance P in the region of nucleus tractus solitarii as measured by in vivo microdialysis technique. Chronic administration of SCH-23390 via subcutaneously implanted Alzet mini osmotic pumps, significantly decreased the level of preprotachykinin-A mRNA in the region of respiratory relay neurons in nucleus tractus solitarii but was without effect in the ventral medullary surface structure, wherein the central chemoreceptors are thought to be located. A smaller, but significant decrease was also seen in the striatum. The results suggest that chronic treatment with SCH-23390 leads to a disinhibition of an inhibitory dopaminergic input to the neurons in nucleus tractus solitarii from a suprapontine level, which may account for a subsequent inhibition of tachykinin-containing neurons in the nucleus tractus solitarii, the relay station for respiratory reflexes.
选择性D1受体阻滞剂SCH-23390的急性静脉给药导致呼吸运动输出增强,这由膈神经活动证明,而向孤束核区域局部灌注则无作用。膈神经活动的增加伴随着通过体内微透析技术测量的孤束核区域内P物质释放的相应增加。通过皮下植入的Alzet微型渗透泵慢性给予SCH-23390,显著降低了孤束核呼吸中继神经元区域中前速激肽原A mRNA的水平,但对腹侧延髓表面结构无影响,中央化学感受器被认为位于该结构中。纹状体中也出现了较小但显著的下降。结果表明,用SCH-23390进行慢性治疗导致来自脑桥上水平对孤束核中神经元的抑制性多巴胺能输入的去抑制,这可能解释了随后对孤束核中含速激肽神经元的抑制,孤束核是呼吸反射的中继站。