Doyle Mark W, Bailey Timothy W, Jin Young-Ho, Andresen Michael C
Department of Physiology and Pharmacology, Oregon Health and Science University, Portland, Oregon 97201-3098, USA.
J Neurosci. 2002 Sep 15;22(18):8222-9. doi: 10.1523/JNEUROSCI.22-18-08222.2002.
Although the central terminals of cranial visceral afferents express vanilloid receptor 1 (VR1), little is known about their functional properties at this first synapse within the nucleus tractus solitarius (NTS). Here, we examined whether VR1 modulates afferent synaptic transmission. In horizontal brainstem slices, solitary tract (ST) activation evoked EPSCs. Monosynaptic EPSCs had low synaptic jitter (SD of latency to successive shocks) averaging 84.03 +/- 3.74 microsec (n = 72) and were completely blocked by the non-NMDA antagonist 2,3-dihydroxy-6-nitro-7-sulfonyl-benzo[f]quinoxaline (NBQX). Sustained exposure to the VR1 agonist capsaicin (CAP; 100 nm) blocked ST EPSCs (CAP-sensitive) in some neurons but not others (CAP-resistant). CAP-sensitive EPSCs had longer latencies than CAP-resistant EPSCs (4.65 +/- 0.27 msec, n = 48 vs 3.53 +/- 0.28 msec, n = 24, respectively; p = 0.011), but they had similar jitter. CAP evoked two transient responses in CAP-sensitive neurons: a rapidly developing inward current (I(cap)) (108.1 +/- 22.9 pA; n = 21) and an increase in spontaneous synaptic activity. After 3-5 min in CAP, I(cap) subsided and ST EPSCs disappeared. NBQX completely blocked I(cap). The VR1 antagonist capsazepine (10-20 microm) attenuated CAP responses. Anatomically, second-order NTS neurons were identified by 4-(4-dihexadecylamino)styryl)-N-methylpyridinium iodide transported from the cervical aortic depressor nerve (ADN) to stain central terminals. Neurons with fluorescent ADN contacts had CAP-sensitive EPSCs (n = 5) with latencies and jitter similar to those of unlabeled monosynaptic neurons. Thus, consistent with presynaptic VR1 localization, CAP selectively activates a subset of ST axons to release glutamate that acts on non-NMDA receptors. Because the CAP sensitivity of cranial afferents is exclusively associated with unmyelinated axons, VR1 identifies C-fiber afferent pathways within the brainstem.
虽然颅内脏传入神经的中枢终末表达香草酸受体1(VR1),但对于它们在孤束核(NTS)内这第一个突触处的功能特性却知之甚少。在此,我们研究了VR1是否调节传入突触传递。在水平脑干切片中,孤束(ST)激活可诱发兴奋性突触后电流(EPSCs)。单突触EPSCs具有低突触抖动(连续刺激潜伏期的标准差),平均为84.03±3.74微秒(n = 72),并被非NMDA拮抗剂2,3 - 二羟基 - 6 - 硝基 - 7 - 磺酰基 - 苯并[f]喹喔啉(NBQX)完全阻断。持续暴露于VR1激动剂辣椒素(CAP;100 nM)可阻断某些神经元中的ST EPSCs(CAP敏感型),但对其他神经元(CAP抵抗型)则无影响。CAP敏感型EPSCs的潜伏期比CAP抵抗型EPSCs更长(分别为4.65±0.27毫秒,n = 48 与3.53±0.28毫秒,n = 24;p = 0.011),但它们具有相似的抖动。CAP在CAP敏感型神经元中诱发两种瞬态反应:一种快速发展的内向电流(I(cap))(108.1±22.9 pA;n = 21)和自发突触活动的增加。在CAP作用3 - 5分钟后