Theodosis D T, Paut L, Tappaz M L
Neuroscience. 1986 Sep;19(1):207-22. doi: 10.1016/0306-4522(86)90016-3.
Antisera specific for gamma-aminobutyric acid (GABA) or its biosynthetic enzyme, glutamate decarboxylase, were used in pre- and postembedding immunocytochemical techniques at the light and electron microscopic levels, to visualize the GABAergic innervation of the hypothalamic supraoptic nucleus. Immunostaining for glutamate decarboxylase or gamma-aminobutyric acid were also combined with oxytocin and vasopressin immunolocalization, thereby permitting evaluation of the contribution of the innervation onto each type of neuron in this nucleus. Light microscopy of semithin plastic sections or vibratome slices stained for glutamate decarboxylase or gamma-aminobutyric acid, with peroxidase-antiperoxidase as immunolabel, revealed an extensive punctate labeling in the supraoptic nucleus and its immediate surroundings. Quantitative analysis of glutamate decarboxylase immunostaining in semithin sections indicated a comparable density of immunopositive punctae at the anterior and posterior levels of the nucleus (14-27 X 10(6) per mm3 tissue). Glutamate decarboxylase- or gamma-aminobutyric acid-immunoreactive cell bodies were never observed within the nucleus although they were detected in the hypothalamus immediately dorsolateral to the nucleus. Electron microscopy of vibratome slices treated with antiglutamate decarboxylase or antigamma-aminobutyric acid and peroxidase-antiperoxidase, or of ultrathin sections stained directly with antigamma-aminobutyric acid and immunoglobulin-coupled colloidal gold, showed that the immuno-reactive punctae represented, in the main, axonal terminals. They invariably contained small, rounded clear vesicles and, at times, one or two larger, dense cored vesicles; they all formed symmetrical synapses onto magnocellular cell bodies and dendrites. Oxytocin and vasopressin neurons were contacted in a similar fashion by glutamate decarboxylase- or gamma-aminobutyric acid-positive boutons in semithin sections of the nucleus stained simultaneously for glutamate decarboxylase and oxytocin and in ultrathin sections stained for glutamate decarboxylase or gamma-aminobutyric acid and oxytocin or vasopressin. Glutamate decarboxylase- or gamma-aminobutyric acid-positive terminals often formed synapses onto two postsynaptic elements in the same plane of section ("double" synapses), a synaptic configuration usually encountered in supraoptic nuclei of lactating animals. In such cases, the postsynaptic somata were oxytocinergic.(ABSTRACT TRUNCATED AT 400 WORDS)
针对γ-氨基丁酸(GABA)或其生物合成酶谷氨酸脱羧酶的抗血清,被用于光镜和电镜水平的包埋前和包埋后免疫细胞化学技术,以观察下丘脑视上核的GABA能神经支配。谷氨酸脱羧酶或γ-氨基丁酸的免疫染色也与催产素和血管加压素的免疫定位相结合,从而能够评估该核中神经支配对每种类型神经元的作用。对用谷氨酸脱羧酶或γ-氨基丁酸染色的半薄塑料切片或振动切片进行光镜观察,以过氧化物酶-抗过氧化物酶作为免疫标记,发现在视上核及其紧邻区域有广泛的点状标记。对半薄切片中谷氨酸脱羧酶免疫染色的定量分析表明,在核的前部和后部水平,免疫阳性小点的密度相当(每立方毫米组织14 - 27×10⁶个)。在核内从未观察到谷氨酸脱羧酶或γ-氨基丁酸免疫反应性细胞体,尽管在紧邻核背外侧的下丘脑区域检测到了它们。对用抗谷氨酸脱羧酶或抗γ-氨基丁酸和过氧化物酶-抗过氧化物酶处理的振动切片,或直接用抗γ-氨基丁酸和免疫球蛋白偶联胶体金染色的超薄切片进行电镜观察,结果显示免疫反应性小点主要代表轴突终末。它们总是含有小的、圆形清亮小泡,有时还含有一两个较大的、有致密核心的小泡;它们都在大细胞性细胞体和树突上形成对称突触。在同时用谷氨酸脱羧酶和催产素染色的核的半薄切片以及用谷氨酸脱羧酶或γ-氨基丁酸和催产素或血管加压素染色的超薄切片中,谷氨酸脱羧酶或γ-氨基丁酸阳性终末以类似方式与催产素和血管加压素神经元接触。谷氨酸脱羧酶或γ-氨基丁酸阳性终末常常在同一切片平面上与两个突触后成分形成突触(“双”突触),这种突触构型通常见于泌乳动物的视上核。在这种情况下,突触后胞体是催产素能的。(摘要截短于400字)