Department of Anesthesiology and Perioperative Medicine, Center for Neuroscience and Pain Research, Houston, Texas 77030-4009, USA.
J Neurochem. 2013 Aug;126(3):338-48. doi: 10.1111/jnc.12290. Epub 2013 May 20.
Barrington's nucleus (BN), commonly known as the pontine micturition center, controls micturition and other visceral functions through projections to the spinal cord. In this study, we developed a rat brain slice preparation to determine the intrinsic and synaptic mechanisms regulating pre-sympathetic output (PSO) and pre-parasympathetic output (PPO) neurons in the BN using patch-clamp recordings. The PSO and PPO neurons were retrogradely labeled by injecting fluorescent tracers into the intermediolateral region of the spinal cord at T13-L1 and S1-S2 levels, respectively. There were significantly more PPO than PSO neurons within the BN. The basal activity and membrane potential were significantly lower in PPO than in PSO neurons, and A-type K(+) currents were significantly larger in PPO than in PSO neurons. Blocking A-type K(+) channels increased the excitability more in PPO than in PSO neurons. Stimulting μ-opioid receptors inhibited firing in both PPO and PSO neurons. The glutamatergic EPSC frequency was much lower, whereas the glycinergic IPSC frequency was much higher, in PPO than in PSO neurons. Although blocking GABAA receptors increased the excitability of both PSO and PPO neurons, blocking glycine receptors increased the firing activity of PPO neurons only. Furthermore, blocking ionotropic glutamate receptors decreased the excitability of PSO neurons but paradoxically increased the firing activity of PPO neurons by reducing glycinergic input. Our findings indicate that the membrane and synaptic properties of PSO and PPO neurons in the BN are distinctly different. This information improves our understanding of the neural circuitry and central mechanisms regulating the bladder and other visceral organs.
巴灵顿核(BN),通常称为桥脑排尿中枢,通过投射到脊髓来控制排尿和其他内脏功能。在这项研究中,我们开发了一种大鼠脑切片制备方法,使用膜片钳记录来确定调节 BN 中交感前输出(PSO)和副交感前输出(PPO)神经元的内在和突触机制。通过将荧光示踪剂分别注入 T13-L1 和 S1-S2 水平的脊髓中间外侧区域,将 PSO 和 PPO 神经元逆行标记。BN 内 PPO 神经元明显多于 PSO 神经元。PPO 神经元的基础活性和膜电位明显低于 PSO 神经元,并且 A 型 K(+)电流明显大于 PSO 神经元。阻断 A 型 K(+)通道会使 PPO 神经元的兴奋性增加得更多。刺激 μ-阿片受体抑制 PPO 和 PSO 神经元的放电。PPO 神经元的谷氨酸能 EPSC 频率明显较低,而甘氨酸能 IPSC 频率明显较高。尽管阻断 GABAA 受体增加了 PSO 和 PPO 神经元的兴奋性,但阻断甘氨酸受体仅增加了 PPO 神经元的放电活动。此外,阻断离子型谷氨酸受体降低了 PSO 神经元的兴奋性,但通过减少甘氨酸能输入,反而增加了 PPO 神经元的放电活动。我们的发现表明 BN 中的 PSO 和 PPO 神经元的膜和突触特性明显不同。这些信息提高了我们对调节膀胱和其他内脏器官的神经回路和中枢机制的理解。