Jhamandas Jack H, Mactavish David
Division of Neurology, Department of Medicine, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.
J Comp Neurol. 2002 Jun 3;447(3):300-7. doi: 10.1002/cne.10246.
Neuropeptide FF (NPFF) is a morphine modulatory peptide that plays an important role in a wide variety of physiological functions, including those related to nociception and central autonomic regulation. NPFF fibers and cells have been shown to be discretely localized in key autonomic centers within the brain, including the brainstem nucleus of the solitary tract (NTS). Central applications of NPFF evoke a number of important biological effects through activation of central neuronal circuits whose identities remain unknown at present. NPFF administered in this manner may also be capable of up- or down-regulating its own gene expression. In this study, we investigated the effects of intracerebroventricular (i.c.v.) administration of NPFF on the activation and the gene expression of NPFF in NTS neurons. Conscious rats received saline or NPFF (8 or 10 microg i.c.v.), with concomitant monitoring of arterial blood pressure. Brains were prepared for Fos immunohistochemistry to identify neuronal activation and NPFF in situ hybridization to determine cells expressing NPFF mRNA in the NTS. At a dose of 8 microg, i.c.v., NPFF did not evoke alterations in blood pressure, but, at 10 microg, there was an increase in arterial blood pressure of 30-40 mmHg. Image analysis showed a dose-dependent increase in number of NPFF neurons that were activated in rats receiving i.c.v. NPFF compared with saline controls. NPFF gene expression in the NTS showed a similar dose-dependent increase following i.c.v. administration of either 8 or 10 microg of NPFF. Significantly greater numbers of activated neurons expressing the NPFF gene (double labeled) were observed in the NTS at the level of the area postrema in animals receiving i.c.v. NPFF compared with saline controls. These data indicate that centrally administered NPFF is capable of up-regulating its own gene expression in the NTS and that this effect appears in part to be independent of elevations in arterial blood pressure that this peptide can evoke when administered i.c.v. at the higher dose. The up-regulation of NPFF may play a homeostatic role in response to specific cardiovascular challenges, such as hypotension.
神经肽FF(NPFF)是一种吗啡调节肽,在多种生理功能中发挥重要作用,包括与痛觉感受和中枢自主神经调节相关的功能。NPFF纤维和细胞已被证明离散地定位于脑内的关键自主神经中枢,包括孤束核(NTS)。NPFF的中枢应用通过激活目前身份尚不清楚的中枢神经回路引发许多重要的生物学效应。以这种方式给予的NPFF也可能能够上调或下调其自身的基因表达。在本研究中,我们研究了脑室内(i.c.v.)给予NPFF对NTS神经元中NPFF激活和基因表达的影响。清醒大鼠接受生理盐水或NPFF(8或10微克i.c.v.),同时监测动脉血压。制备大脑用于Fos免疫组织化学以鉴定神经元激活,并进行NPFF原位杂交以确定NTS中表达NPFF mRNA的细胞。在8微克i.c.v.的剂量下,NPFF未引起血压变化,但在10微克时,动脉血压升高30 - 40 mmHg。图像分析显示,与生理盐水对照组相比,接受i.c.v. NPFF的大鼠中被激活的NPFF神经元数量呈剂量依赖性增加。在给予8或10微克NPFF i.c.v.后,NTS中的NPFF基因表达呈现相似的剂量依赖性增加。与生理盐水对照组相比,在接受i.c.v. NPFF的动物中,在最后区水平的NTS中观察到表达NPFF基因的激活神经元(双标记)数量明显更多。这些数据表明,中枢给予的NPFF能够上调其在NTS中的自身基因表达,并且这种效应似乎部分独立于该肽在较高剂量i.c.v.给药时可引起的动脉血压升高。NPFF的上调可能在应对特定的心血管挑战(如低血压)时发挥稳态作用。