Boscan Pedro, Dutschmann Mathias, Herbert Horst, Paton Julian F R
Department of Physiology, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, United Kingdom.
J Neurosci. 2005 Feb 9;25(6):1412-20. doi: 10.1523/JNEUROSCI.4075-04.2005.
We wanted to ascertain whether the lateral parabrachial nucleus was involved in mediating the heart-rate response evoked during stimulation of somatic nociceptors. Reversible inactivation of the lateral parabrachial nucleus, using a GABA(A) agonist, reduced the reflex tachycardia evoked during noxious (mechanical) stimulation of the forelimb by approximately 50%. The same effect was observed after blockade of neurokinin 1 receptors within the lateral parabrachial nucleus, indicating a possible involvement for substance P as a neurotransmitter. Immunocytochemistry revealed a strong expression of substance P-immunoreactive fibers and boutons in all lateral subnuclei, but they were particularly dense in the lateral crescent subnucleus. Histological verification showed that the most effective injection sites for attenuating the noxious-evoked tachycardia were all placed in or near to the lateral crescent nucleus of the lateral parabrachial complex. Many single units recorded from this region were activated by high-intensity brachial nerve stimulation. The brachial nerve evoked firing responses of some of these neurons was reversibly reduced after local delivery of a neurokinin 1 receptor antagonist. However, only a minority of these neurons followed a paired-pulse stimulation protocol applied to the spinal cord, suggesting a predominance of indirect projections from the spinal cord to the parabrachial nucleus. We conclude that the cardiac component of the response to somatic nociception involves indirect spinal pathways that most likely excite neurons located in the lateral crescent nucleus of the parabrachial complex via activation of neurokinin 1 receptors.
我们想要确定外侧臂旁核是否参与介导躯体伤害性感受器刺激期间诱发的心率反应。使用GABA(A)激动剂对外侧臂旁核进行可逆性失活,可使前肢受到伤害性(机械性)刺激时诱发的反射性心动过速降低约50%。在外侧臂旁核内阻断神经激肽1受体后也观察到了相同的效果,这表明P物质作为一种神经递质可能参与其中。免疫细胞化学显示,P物质免疫反应性纤维和终扣在所有外侧亚核中均有强烈表达,但在外侧新月形亚核中尤为密集。组织学验证表明,减弱伤害性诱发心动过速最有效的注射部位均位于外侧臂旁复合体的外侧新月形核内或其附近。从该区域记录的许多单个神经元在高强度臂丛神经刺激下被激活。在局部给予神经激肽1受体拮抗剂后,这些神经元中一些由臂丛神经诱发的放电反应可逆性降低。然而,这些神经元中只有少数遵循应用于脊髓的双脉冲刺激方案,这表明从脊髓到臂旁核的间接投射占主导地位。我们得出结论,对躯体伤害感受反应的心脏成分涉及间接的脊髓通路,该通路很可能通过激活神经激肽1受体来兴奋位于臂旁复合体外侧新月形核内的神经元。