Beneyto M, Winer J A, Larue D T, Prieto J J
Department of Histology, Institute of Neuroscience, University Miguel Hernández, San Juan, Spain.
J Comp Neurol. 1998 Nov 23;401(3):329-51.
We studied the cytoarchitecture, neurochemical organization, and connections of the sagulum. The goal was to clarify its role in midbrain, lateral tegmental, and thalamic auditory processing. On cytoarchitectonic grounds, ventrolateral (parvocellular) and dorsomedial (magnocellular) subdivisions were recognized. The patterns of immunostaining for gamma-aminobutyric acid (GABA) and glycine were distinct. Approximately 5-10% of the neurons were GABAergic, and more than one type was identified; GABAergic axon terminals were abundant in number and varied in form. Glycinergic neurons were much rarer, < 1% of the population, and glycinergic axon terminals were correspondingly sparse. Wheat germ agglutinin conjugated to horseradish peroxidase was used for purposes of connectional mapping, and biotinylated dextran amines revealed the structure of corticosagular axons. All nine cortical areas injected project to the ipsilateral sagulum. Five (areas AI, AII, SF, EPD, and Te) had heavier projections than the others. Areas AI and AII projected throughout the rostrocaudal sagulum. Labeling from AI was moderate in density and concentrated in the central sagulum, whereas the input from AII was heavier and ended more laterally. Suprasylvian fringe input was light, especially caudally, and was chiefly in the central sagulum. The projection from the dorsal region of the posterior ectosylvian gyrus was comparatively stronger and was in the dorsolateral sagulum. Finally, the temporal cortex sent axons to the most lateral sagulum, spanning the dorsoventral extent, whereas insular cortex axons ended diffusely in the dorsolateral sagulum. Corticofugal axons ranged from fine boutons en passant to larger globular terminals. The sagulum may represent the earliest significant opportunity in the ascending auditory pathway for corticofugal modulation. The most extensive input arises from the polymodal association areas. The sagulum then projects divergently to the dorsal cortex of the inferior colliculus and the dorsal division of the medial geniculate body. The projection from the dorsal division of the auditory thalamus to nonprimary auditory cortex completes this circuit between the forebrain and the midbrain and represents a nexus in the ascending and descending auditory systems. Such circuits could play a critical role in auditory-motor adjustments to sound.
我们研究了矢状区的细胞结构、神经化学组织和连接。目的是阐明其在中脑、外侧被盖和丘脑听觉处理中的作用。基于细胞构筑学,识别出腹外侧(小细胞)和背内侧(大细胞)亚区。γ-氨基丁酸(GABA)和甘氨酸的免疫染色模式不同。约5%-10%的神经元是GABA能的,且鉴定出不止一种类型;GABA能轴突终末数量丰富且形态各异。甘氨酸能神经元则罕见得多,占总数不到1%,且甘氨酸能轴突终末相应稀少。与辣根过氧化物酶结合的小麦胚凝集素用于连接图谱绘制,生物素化葡聚糖胺揭示了皮质-矢状区轴突的结构。所有九个注入的皮质区域都投射到同侧矢状区。五个区域(AI、AII、SF、EPD和Te)的投射比其他区域更密集。AI和AII区域投射到矢状区的整个前后范围。来自AI的标记密度适中,集中在矢状区中部,而来自AII的输入更密集,且在更外侧终止。上薛氏回边缘的输入较稀疏,尤其是在尾部,主要位于矢状区中部。后外侧薛氏回背侧区域的投射相对较强,位于矢状区背外侧。最后,颞叶皮质将轴突发送到矢状区最外侧,跨越背腹范围,而岛叶皮质轴突则分散地终止于矢状区背外侧。皮质传出轴突范围从纤细的旁支终扣到较大的球状终末。矢状区可能代表了听觉传导通路中皮质传出调制的最早重要机会。最广泛的输入来自多模式联合区。然后,矢状区发散地投射到下丘的背侧皮质和内侧膝状体的背侧部分。听觉丘脑背侧部分向非初级听觉皮质的投射完成了前脑和中脑之间的这一回路,并代表了听觉系统升、降支中的一个连接点。这样的回路可能在对声音的听觉-运动调整中起关键作用。