Witkin J W
Department of Anatomy and Cell Biology, Columbia University College, New York, NY 10032.
Neuroscience. 1987 Sep;22(3):1003-13. doi: 10.1016/0306-4522(87)92976-9.
This study was undertaken to examine some aspects of the anatomical substrate for reproductive senescence. Immunocytochemically identified luteinizing hormone-releasing hormone neurons and their processes in the male rat brain preoptic area were compared in young adult (2-4 months), middle-aged (12-14 months) and old (20-23 months) animals. At the light microscopic level there were no age-dependent differences in total numbers or sizes of LHRH neurons nor in their distribution in the brain. Examination of these neurons at the electron microscopic level did reveal significant differences in certain organelles and in the degree and kind of synaptic input. Random sections of middle-aged luteinizing hormone-releasing hormone neurons more frequently passed through the nucleolus and the incidence of nematosomes was higher than in luteinizing hormone-releasing hormone neurons from the young and old animals. Quantitative measures of synaptic input to luteinizing hormone-releasing hormone soma and dendrites as well as to unidentified neurons in the same thin section were made. These are reported as percent of membrane that showed synaptic structure. Dendrites of both luteinizing hormone-releasing hormone and nonidentified neurons were more densely innervated than perikarya. The density of synaptic input to luteinizing hormone-releasing hormone neurons was significantly greater than that to nonidentified neurons in young and middle-aged animals, but was equal to that of nonidentified neurons by old age. Age-related changes were noted in synaptic organization with the most significant change being an increased input to luteinizing hormone-releasing hormone perikarya. Indeed, synaptic input to luteinizing hormone-releasing hormone perikaryal membrane was increased three-fold by middle age and ten-fold by old age. Density of synaptic input to luteinizing hormone-releasing hormone dendritic membrane did not change with age. There were no aging changes in percentage of membrane with synaptic structure in nonidentified elements. Synapses were also classified on the basis of their synaptic vesicle content. There were proportionately more synaptic boutons containing round clear than pleomorphic vesicles in the young sample. The proportion of synapses with pleomorphic vesicles increased with age onto both luteinizing hormone-releasing hormone perikarya and their dendrites. The proportion of boutons containing some electron dense-core vesicles along with clear vesicles decreased with age onto both luteinizing hormone-releasing hormone and nonidentified neurons and their processes.
本研究旨在探讨生殖衰老的解剖学基础的某些方面。对年轻成年(2 - 4个月)、中年(12 - 14个月)和老年(20 - 23个月)雄性大鼠脑视前区中免疫细胞化学鉴定的促黄体生成激素释放激素(LHRH)神经元及其突起进行了比较。在光学显微镜水平,LHRH神经元的总数、大小及其在脑中的分布均无年龄依赖性差异。在电子显微镜水平对这些神经元的检查确实揭示了某些细胞器以及突触输入的程度和种类存在显著差异。中年促黄体生成激素释放激素神经元的随机切片更频繁地穿过核仁,并且线虫小体的发生率高于年轻和老年动物的促黄体生成激素释放激素神经元。对促黄体生成激素释放激素胞体和树突以及同一薄切片中未识别神经元的突触输入进行了定量测量。这些以显示突触结构的膜的百分比来报告。促黄体生成激素释放激素和未识别神经元的树突比胞体接受的神经支配更密集。在年轻和中年动物中,促黄体生成激素释放激素神经元的突触输入密度显著大于未识别神经元,但在老年时与未识别神经元的突触输入密度相等。在突触组织中观察到与年龄相关的变化,最显著的变化是促黄体生成激素释放激素胞体的输入增加。实际上,到中年时,促黄体生成激素释放激素胞体膜的突触输入增加了三倍,到老年时增加了十倍。促黄体生成激素释放激素树突膜的突触输入密度不随年龄变化。未识别成分中具有突触结构的膜的百分比没有衰老变化。突触也根据其突触小泡内容物进行分类。在年轻样本中,含有圆形清亮突触小泡的突触终扣比例相对较高。随着年龄增长,在促黄体生成激素释放激素胞体及其树突上,具有多形性突触小泡的突触比例增加。在促黄体生成激素释放激素和未识别神经元及其突起上,含有一些电子致密核心小泡以及清亮小泡的终扣比例随着年龄增长而降低。