Halberstadt A L, Balaban C D
Department of Otolaryngology, Eye and Ear Institute, Room 107, 203 Lothrop Street, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Neuroscience. 2007 Jun 15;147(1):207-23. doi: 10.1016/j.neuroscience.2007.03.049. Epub 2007 May 15.
It is well known that the dorsal raphe nucleus (DRN) sends serotonergic and nonserotonergic projections to target regions in the brain stem and forebrain, including the vestibular nuclei. Although retrograde tracing studies have reported consistently that there are differences in the relative innervation of different target regions by serotonergic and nonserotonergic DRN neurons, the relative termination patterns of these two projections have not been compared using anterograde tracing methods. The object of the present investigation was to trace anterogradely the individual serotonergic and nonserotonergic components of the projection from DRN to the vestibular nuclei in rats. To trace nonserotonergic DRN projections, animals were pretreated with the serotonergic neurotoxin 5,7-dihydroxytryptamine (5,7-DHT), and then, after 7 days, the anterograde tracer biotinylated dextran amine (BDA) was iontophoretically injected into the DRN. In animals treated with 5,7-DHT, nonserotonergic BDA-labeled fibers were found to descend exclusively within the ventricular plexus and to terminate predominantly within the periventricular aspect of the vestibular nuclei. Serotonergic DRN projections were traced by injecting 5,7-DHT directly into DRN, and amino-cupric-silver staining was used to visualize the resulting pattern of terminal degeneration. Eighteen hours after microinjection of 5,7-DHT into the DRN, fine-caliber degenerating serotonergic terminals were found within the region of the medial vestibular nucleus (MVN) that borders the fourth ventricle, and a mixture of fine- and heavier-caliber degenerating serotonergic terminals was located further laterally within the vestibular nuclear complex. These findings indicate that fine-caliber projections from serotonergic and nonserotonergic DRN neurons primarily innervate the periventricular regions of MVN, whereas heavier-caliber projections from serotonergic DRN neurons innervate terminal fields located in more lateral regions of the vestibular nuclei. Thus, serotonergic and nonserotonergic DRN axons target distinct but partially overlapping terminal fields within the vestibular nuclear complex, raising the possibility that these two DRN projection systems are organized in a manner that permits regionally-specialized regulation of processing within the vestibular nuclei.
众所周知,中缝背核(DRN)向脑干和前脑的靶区域发送5-羟色胺能和非5-羟色胺能投射,包括前庭核。尽管逆行追踪研究一致报道,5-羟色胺能和非5-羟色胺能DRN神经元对不同靶区域的相对支配存在差异,但尚未使用顺行追踪方法比较这两种投射的相对终末模式。本研究的目的是顺行追踪大鼠DRN到前庭核投射的单个5-羟色胺能和非5-羟色胺能成分。为了追踪非5-羟色胺能DRN投射,动物先用5-羟色胺能神经毒素5,7-二羟基色胺(5,7-DHT)预处理,然后在7天后,将顺行示踪剂生物素化葡聚糖胺(BDA)离子导入注射到DRN中。在用5,7-DHT处理的动物中,发现非5-羟色胺能BDA标记的纤维仅在脑室丛内下行,并主要终止于前庭核的室周区域。通过将5,7-DHT直接注射到DRN中来追踪5-羟色胺能DRN投射,并使用氨基铜银染色来观察终末变性的结果模式。将5,7-DHT微量注射到DRN中18小时后,在内侧前庭核(MVN)与第四脑室相邻的区域内发现了细口径的变性5-羟色胺能终末,而在更外侧的前庭核复合体内则有细口径和粗口径混合的变性5-羟色胺能终末。这些发现表明,5-羟色胺能和非5-羟色胺能DRN神经元的细口径投射主要支配MVN的室周区域,而5-羟色胺能DRN神经元的粗口径投射支配位于前庭核更外侧区域的终末场。因此,5-羟色胺能和非5-羟色胺能DRN轴突靶向前庭核复合体内不同但部分重叠的终末场,这增加了这两个DRN投射系统以允许在前庭核内进行区域特异性加工调节的方式组织的可能性。