The islands of Calleja (IC) in the rate are composed of seven small groups of granule cells in the polymorph layer of the olfactory tubercle and one large group, the insula magna, which lies along the border between septum, nucleus accumbens and nucleus of the diagonal band. The cytoarchitecture and neuronal morphology of the IC and surrounding cells, studied using Nissl-stained and Golgi-Kopsch material, are described. In addition, the afferent and efferent connections of the IC were analyzed using fluorescence histochemistry, the autoradiographic tracing method, and the anterograde and retrograde horseradish peroxidase methods. Topographically organized projections to the IC from the dopamine-containing cells of the substantia nigra-ventral tegmental area are demonstrated by the glyoxylic acid fluorescence histochemical method and the autoradiographic tracing technique. Anterograde and retrograde horseradish peroxidase studies provide evidence for reciprocal, topographically organized interconnections between the IC and the septum, nucleus accumbens, amygdala and piriform cortex. These observations indicate that the IC constitute a unique population of granule cells, located in the olfactory tubercle, innervated by dopamine neurons of the mesencephalon and interconnected with olfactory and non-olfactory components of the basal forebrain.
Golgi methods were used to examine the hippocampus of laboratory mice that received alcohol-containing or control diets for 4 months followed by a 2-month alcohol-free period. Long-term alcohol consumption resulted in a significant loss of dendritic spines on hippocampal pyramidal cells and dentate granule cells. This study provides evidence that long-term alcohol consumption, in the absence of malnutrition, produces morphological damage to the central nervous system.
The organization of the rat motor trigeminal nucleus (MTN) and the morphology of noradrenergic afferents terminating in this cranial motor nucleus were analyzed with light and transmission electron microscopy. Two morphologically distinct types of neurons are present in the MTN. Large multipolar neurons are the most prevalent cell type and are distributed uniformly throughout the nucleus. The morphology of these cells is identical to that of motor neurons described previously in both the brainstem and spinal cord. The neurons are characterized ultrastructurally by a light, organelle-rich cytoplasmic matrix containing numerous cisternal arrays of rough endoplasmic reticulum (RER) and a centrally placed spherical nucleus containing a single prominent nucleolus. Approximately 80% of the surface of these cells is contacted by axon terminals. The second major class of neuron consists of small spherical and fusiform cells that are located predominantly at the peripheral borders of the MTN. These cells are significantly smaller than motor neurons and exhibit only scattered axosomatic contacts. This small cell population appears to be composed of two distinct subclasses of neurons that probably represent interneurons and gamma motor neurons. The MTN neuropil contains four morphologically distinct classes of axon terminals that are characterized by either spherical or pleomorphic vesicles within cytoplasm that is lucent or dense. Quantitative morphometric analysis demonstrated differential distribution of each of the four terminal types upon motor neuron somata and dendrites. Intracerebral injection of 5-hydroxydopamine into the brainstem tegmentum immediately adjacent to the MTN labeled axon terminals containing spherical vesicles and a lucent axoplasmic matrix. Intracerebral injection of the neurotoxin 6-hydroxydopamine resulted in degeneration of the same terminal population and thus confirmed that noradrenaline-containing axons innervating the MTN exhibit a distinctive terminal morphology. The number of synaptic complexes exhibited by noradrenergic terminals did not differ significantly from other terminal populations in the MTN.
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