Guo Zhi-Ling, Longhurst John C, Tjen-A-Looi Stephanie C, Fu Liang-Wu
Department of Medicine and Susan-Samueli Center for Integrative Medicine, School of Medicine, University of California at Irvine, Irvine, California
Department of Medicine and Susan-Samueli Center for Integrative Medicine, School of Medicine, University of California at Irvine, Irvine, California.
Am J Physiol Regul Integr Comp Physiol. 2016 Aug 1;311(2):R410-25. doi: 10.1152/ajpregu.00127.2016. Epub 2016 May 25.
The external lateral parabrachial nucleus (elPBN) within the pons and rostral ventrolateral medulla (rVLM) contributes to central processing of excitatory cardiovascular reflexes during stimulation of cardiac sympathetic afferent nerves (CSAN). However, the importance of elPBN cardiovascular neurons in regulation of rVLM activity during CSAN activation remains unclear. We hypothesized that CSAN stimulation excites the elPBN cardiovascular neurons and, in turn, increases rVLM activity through elPBN-rVLM projections. Compared with controls, in rats subjected to microinjection of retrograde tracer into the rVLM, the numbers of elPBN neurons double-labeled with c-Fos (an immediate early gene) and the tracer were increased after CSAN stimulation (P < 0.05). The majority of these elPBN neurons contain vesicular glutamate transporter 3. In cats, epicardial bradykinin and electrical stimulation of CSAN increased the activity of elPBN cardiovascular neurons, which was attenuated (n = 6, P < 0.05) after blockade of glutamate receptors with iontophoresis of kynurenic acid (Kyn, 25 mM). In separate cats, microinjection of Kyn (1.25 nmol/50 nl) into the elPBN reduced rVLM activity evoked by both bradykinin and electrical stimulation (n = 5, P < 0.05). Excitation of the elPBN with microinjection of dl-homocysteic acid (2 nmol/50 nl) significantly increased basal and CSAN-evoked rVLM activity. However, the enhanced rVLM activity induced by dl-homocysteic acid injected into the elPBN was reversed following iontophoresis of Kyn into the rVLM (n = 7, P < 0.05). These data suggest that cardiac sympathetic afferent stimulation activates cardiovascular neurons in the elPBN and rVLM sequentially through a monosynaptic (glutamatergic) excitatory elPBN-rVLM pathway.
脑桥内的外侧臂旁核(elPBN)和延髓头端腹外侧区(rVLM)在心脏交感传入神经(CSAN)受到刺激时,参与兴奋性心血管反射的中枢处理过程。然而,在CSAN激活期间,elPBN心血管神经元在调节rVLM活动中的重要性仍不清楚。我们推测,CSAN刺激会兴奋elPBN心血管神经元,进而通过elPBN-rVLM投射增加rVLM活动。与对照组相比,在向rVLM微量注射逆行示踪剂的大鼠中,CSAN刺激后,与即刻早期基因c-Fos和示踪剂双标的elPBN神经元数量增加(P < 0.05)。这些elPBN神经元中的大多数含有囊泡谷氨酸转运体3。在猫中,心外膜缓激肽和CSAN的电刺激增加了elPBN心血管神经元的活动,在用离子透入法施加犬尿氨酸(Kyn,25 mM)阻断谷氨酸受体后,该活动减弱(n = 6,P < 0.05)。在另一些猫中,向elPBN微量注射Kyn(1.25 nmol/50 nl)可降低缓激肽和电刺激诱发的rVLM活动(n = 5,P < 0.05)。通过微量注射dl-高半胱氨酸(2 nmol/50 nl)兴奋elPBN可显著增加基础状态和CSAN诱发的rVLM活动。然而,向rVLM离子透入Kyn后,向elPBN注射dl-高半胱氨酸所诱导的增强的rVLM活动被逆转(n = 7,P < 0.05)。这些数据表明,心脏交感传入刺激通过单突触(谷氨酸能)兴奋性elPBN-rVLM通路依次激活elPBN和rVLM中的心血管神经元。