Alonso G, Siaud P, Assenmacher I
Laboratoire de Neurobiologie Endocrinologique, UA 1197 CNRS, Université de Montpellier II, France.
Neuroscience. 1988 Feb;24(2):553-65. doi: 10.1016/0306-4522(88)90349-1.
The neurons of the rat hypothalamus which secrete corticotropin-releasing factor were studied by using a pre-embedding immunocytochemical staining technique that improves both the penetration of immunoreagents within the tissue and the preservation of the ultrastructural morphology of labeled structures. Comparison was made between the subcellular location of corticotropin-releasing factor-41 in perikarya of the paraventricular nucleus and axons of the median eminence, both in intact and adrenalectomized animals either untreated or 24 h after the intracerebral injection of colchicine. Morphometric analysis of the numerical density and of the diameter of corticotropin-releasing factor immunoreactive neurosecretory granules in axons of the median eminence of rats not treated with colchicine, indicated that the main modifications induced by adrenalectomy concerned (1) the differential repartition of labeled granules within the preterminal and terminal axonal portions of the median eminence, and (2) the enlargement of the diameter of labeled granules contained in these axons (from 98 nm to 165 nm). In the hypothalamus of intact and adrenalectomized rats, colchicine treatment increased the number of corticotropin-releasing factor-immunoreactive granules in the neuronal perikarya and reduced their number in the axons, but both these variations were much more marked in adrenalectomized rats. Although the corticotropin-releasing factor immunoreactive granules that accumulated in the perikarya after colchicine treatment were slightly smaller than those in the corresponding axons, the diameter of perikaryal-labeled granules was larger in adrenalectomized than in intact animals (129 nm vs 93 nm). These findings fit the idea that adrenalectomy markedly stimulates both the synthesis and axonal excretion of secretory granules in the hypothalamic neurons secreting corticotropin-releasing factor. They also indicate that suppression of circulating corticosteroids induces qualitative modifications in these neurons leading to the visualization of larger neurosecretory granules, which may reflect differential synthesis and granular packing of synergistic peptides other than corticotropin-releasing factor and/or changes in the process of intragranular maturation of hormonal material.
采用一种包埋前免疫细胞化学染色技术对大鼠下丘脑分泌促肾上腺皮质激素释放因子的神经元进行了研究,该技术既能提高免疫试剂在组织内的穿透力,又能保存标记结构的超微结构形态。对完整动物以及肾上腺切除动物(未处理或脑室内注射秋水仙碱24小时后)室旁核的核周体和正中隆起轴突中促肾上腺皮质激素释放因子-41的亚细胞定位进行了比较。对未用秋水仙碱处理的大鼠正中隆起轴突中促肾上腺皮质激素释放因子免疫反应性神经分泌颗粒的数量密度和直径进行形态计量分析,结果表明,肾上腺切除引起的主要变化涉及:(1)标记颗粒在正中隆起终末前和终末轴突部分的差异分布;(2)这些轴突中所含标记颗粒直径增大(从98纳米增至165纳米)。在完整和肾上腺切除大鼠的下丘脑中,秋水仙碱处理增加了神经元核周体中促肾上腺皮质激素释放因子免疫反应性颗粒的数量,减少了轴突中的颗粒数量,但这两种变化在肾上腺切除大鼠中更为明显。尽管秋水仙碱处理后在核周体中积累的促肾上腺皮质激素释放因子免疫反应性颗粒比相应轴突中的略小,但肾上腺切除大鼠核周体标记颗粒的直径大于完整动物(分别为129纳米和93纳米)。这些发现符合以下观点:肾上腺切除显著刺激了分泌促肾上腺皮质激素释放因子的下丘脑神经元中分泌颗粒的合成和轴突排泄。它们还表明,循环皮质类固醇的抑制会导致这些神经元发生质性改变,从而使更大的神经分泌颗粒可视化,这可能反映了除促肾上腺皮质激素释放因子之外的协同肽的差异合成和颗粒包装,和/或激素物质颗粒内成熟过程的变化。