Sleep and Performance Research Center, Department of Veterinary and Comparative Anatomy, Pharmacology and Physiology, College of Veterinary Medicine, Washington State University, Pullman, Washington 99164-6520, USA.
J Neurosci. 2010 Mar 17;30(11):4151-9. doi: 10.1523/JNEUROSCI.6047-09.2010.
Growth hormone-releasing hormone (GHRH) promotes non-rapid eye movement sleep (NREMS), in part via a well characterized hypothalamic sleep-promoting site. However, GHRH may also act in the cortex to influence sleep. Application of GHRH to the surface of the cortex changes electroencephalographic (EEG) delta power. GHRH and the GHRH receptor (GHRHR) mRNAs are detectable in the rat cortex, and the expression of cortical GHRHR is activity dependent. Here, we microinjected a GHRH antagonist or GHRHR small interfering RNA (siGHRHR) onto the somatosensory cortex surface in rats. The unilateral application of the GHRH antagonist ipsilaterally decreased EEG delta wave power during NREMS, but not wakefulness, during the initial 40 min after injection. Similarly, the injection of siGHRHR reduced cortical expression of GHRHR and suppressed NREMS EEG delta wave power during 20-24 h after injection. Using the fura-2 calcium imaging technique, cultured cortical cells responded to GHRH by increasing intracellular calcium. Approximately 18% of the GHRH-responsive cells were GABAergic as illustrated by glutamic acid decarboxylase-67 (GAD67) immunostaining. Double labeling for GAD67 and GHRHR in vitro and in vivo indicated that only a minority of cortical GHRHR-containing cells were GABAergic. Our data suggest that endogenous cortical GHRH activates local cortical cells to affect EEG delta wave power state-specifically. Results are also consistent with the hypothesis that GHRH contributes to local network state regulation.
生长激素释放激素 (GHRH) 促进非快速眼动睡眠 (NREMS),部分是通过一个特征明确的下丘脑促进睡眠的部位。然而,GHRH 也可能在大脑皮层中发挥作用,影响睡眠。将 GHRH 应用于皮层表面会改变脑电图 (EEG) 的 δ 波功率。在大鼠皮层中可检测到 GHRH 和 GHRH 受体 (GHRHR) 的 mRNA,并且皮层 GHRHR 的表达是依赖于活性的。在这里,我们在大鼠体感皮层表面微注射了 GHRH 拮抗剂或 GHRHR 小干扰 RNA (siGHRHR)。GHRH 拮抗剂的单侧应用在注射后 40 分钟内,会使 NREMS 期间的 EEG δ 波功率降低,但不会使觉醒状态的 EEG δ 波功率降低。同样,注射 siGHRHR 会降低皮质 GHRHR 的表达,并在注射后 20-24 小时内抑制 NREMS 的 EEG δ 波功率。使用 fura-2 钙成像技术,培养的皮质细胞通过增加细胞内钙对 GHRH 产生反应。大约 18%的 GHRH 反应性细胞为 GABA 能性,如谷氨酸脱羧酶-67 (GAD67) 免疫染色所示。体外和体内的 GAD67 和 GHRHR 的双标记表明,只有少数含有皮质 GHRHR 的细胞为 GABA 能性。我们的数据表明,内源性皮质 GHRH 激活局部皮质细胞,以特异性地影响 EEG δ 波功率状态。结果也与 GHRH 有助于局部网络状态调节的假设一致。