Winer Jeffery A, Chernock Michelle L, Larue David T, Cheung Steven W
Division of Neurobiology, Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, CA 94720-3200, USA.
Hear Res. 2002 Jun;168(1-2):181-95. doi: 10.1016/s0378-5955(02)00489-6.
Projections from the posterior thalamus and medial geniculate body were labeled retrogradely with wheat germ agglutinin conjugated to horseradish peroxidase injected into the rat, cat, and squirrel monkey inferior colliculus. Neurons were found ipsilaterally in the (1) medial division of the medial geniculate body, (2) central gray, (3) posterior limitans nucleus, and the (4) reticular part of the substantia nigra. Bilateral projections involved the (5) peripeduncular/suprapeduncular nucleus, (6) subparafascicular and posterior intralaminar nuclei, (7) nucleus of the brachium of the inferior colliculus, (8) lateral tegmental/lateral mesencephalic areas, and (9) deep layers of the superior colliculus. The medial geniculate projection was concentrated in the caudal one-third of the thalamus; in contrast, the labeling in the subparafascicular nucleus, substantia nigra, and central gray continued much further rostrally. Robust anterograde labeling corresponded to known patterns of tectothalamic projection. Biotinylated dextran amine deposits in the rat inferior colliculus revealed that (1) many thalamotectal cells were elongated multipolar neurons with long, sparsely branched dendrites, resembling neurons in the posterior intralaminar system, and that other labeled cells were more typical of thalamic relay neurons; (2) some cells have reciprocal projections. Similar results were seen in the cat and squirrel monkey. The widespread origins of descending thalamic influences on the inferior colliculus may represent a phylogenetically ancient feedback system onto the acoustic tectum, one that predates the corticocollicular system and modulates nonauditory centers and brainstem autonomic nuclei. Besides their role in normal hearing such pathways may influence behaviors ranging from the startle reflex to the genesis of sound-induced seizures.
将与辣根过氧化物酶结合的小麦胚芽凝集素注入大鼠、猫和松鼠猴的下丘,对丘脑后部和内侧膝状体的投射进行逆行标记。在同侧发现神经元位于:(1)内侧膝状体的内侧部;(2)中央灰质;(3)后界核;以及(4)黑质的网状部。双侧投射涉及:(5)脚周/脚上部核;(6)束旁下核和后内侧核;(7)下丘臂核;(8)外侧被盖/外侧中脑区;以及(9)上丘深层。内侧膝状体的投射集中在丘脑尾侧的三分之一处;相比之下,束旁下核、黑质和中央灰质中的标记向前延伸得更远。强大的顺行标记与已知的顶盖丘脑投射模式相对应。将生物素化葡聚糖胺注入大鼠下丘显示:(1)许多丘脑顶盖细胞是细长的多极神经元,具有长而稀疏分支的树突,类似于后内侧系统中的神经元,而其他标记细胞更具丘脑中继神经元的典型特征;(2)一些细胞有相互投射。在猫和松鼠猴中也观察到了类似结果。丘脑对下丘的下行影响的广泛起源可能代表了一种在系统发育上古老的对听觉顶盖的反馈系统,该系统早于皮质-皮质下系统,并调节非听觉中枢和脑干自主神经核。除了在正常听力中的作用外,这些通路可能会影响从惊吓反射到声音诱发癫痫发作的发生等一系列行为。