Madeira M D, Sousa N, Lima-Andrade M T, Calheiros F, Cadete-Leite A, Paula-Barbosa M M
Department of Anatomy, Porto Medical School, Portugal.
J Comp Neurol. 1992 Aug 22;322(4):501-18. doi: 10.1002/cne.903220405.
Thyroid hormone deficiency has long been considered to affect profoundly such cognitive functions as learning and memory, which are known to depend on the structural integrity of the hippocampal formation. Since we previously found that the number of granule cells of the dentate gyrus is reduced in hypothyroid animals, we decided to extend our observations to the pyramidal cells of the hippocampus in order to gain further insight into the effects of hypothyroidism upon the other neuronal links of the hippocampal trisynaptic circuitry, inasmuch as CA1 neurons are known to be particularly vulnerable to aggressive agents. Groups of 6 male and 6 female rats aged 30 and 180 days were analysed separately after being treated as follows: (1) hypothyroid from day 0 until day 30 (30-day-old hypothyroid group); (2) respective 30-day-old control; (3) hypothyroid from day 0 until day 180 (180-day-old hypothyroid group); (4) hypothyroid until day 30 and thenceforth maintained euthyroid (recovery group); (5) hypothyroid since day 30 (adult hypothyroid group); and (6) respective 180-day-old control. The volume of the pyramidal cell layer of the CA1 and CA3 regions and the numerical density of the respective neurons were evaluated, thereby allowing us to estimate the total number of pyramidal cells in each hippocampal region. The areal density and the mean nuclear volume of CA1 and CA3 pyramidal cells were also estimated. In the CA3 region, we found that hypothyroidism, whatever its duration and time of onset, induces a reduction in the volume of the pyramidal cell layer and a parallel increase in the numerical density of its neurons, without interfering with the total number of pyramidal cells. Conversely, in the CA1 region, thyroid hormone deficiency started either neonatally or during maturity was found to lead to a decrease in the total number of pyramidal cells. Reductions ranging between 14.2 and 22.5% were found in 30 and 180-day-old hypothyroid groups. The reestablishment of a euthyroid state did not ameliorate the referred neuronal loss. The present results support the view that hypothyroidism induces small alterations in the structural organization of the hippocampal CA3 region, contrary to what happens in CA1 in which neuronal death occurs. Furthermore, the data presented herein demonstrate that the total number of CA1 pyramidal cells displays sexual dimorphism that is not affected by thyroid hormone manipulations.(ABSTRACT TRUNCATED AT 400 WORDS)
长期以来,甲状腺激素缺乏一直被认为会深刻影响学习和记忆等认知功能,而这些功能已知依赖于海马结构的结构完整性。由于我们之前发现甲状腺功能减退的动物齿状回颗粒细胞数量减少,我们决定将观察范围扩大到海马体的锥体细胞,以便进一步了解甲状腺功能减退对海马三突触回路其他神经元连接的影响,因为已知CA1神经元特别容易受到侵袭性因素的影响。将6只30日龄和6只180日龄的雄性和雌性大鼠分为不同组,分别进行如下处理后进行分析:(1)从第0天到第30天甲状腺功能减退(30日龄甲状腺功能减退组);(2)相应的30日龄对照组;(3)从第0天到第180天甲状腺功能减退(180日龄甲状腺功能减退组);(4)甲状腺功能减退至第30天,此后维持甲状腺功能正常(恢复组);(5)从第30天开始甲状腺功能减退(成年甲状腺功能减退组);(6)相应的180日龄对照组。评估CA1和CA3区域锥体细胞层的体积以及相应神经元的数值密度,从而使我们能够估计每个海马区域锥体细胞的总数。还估计了CA1和CA3锥体细胞的面密度和平均核体积。在CA3区域,我们发现无论甲状腺功能减退的持续时间和发病时间如何,都会导致锥体细胞层体积减小,其神经元的数值密度相应增加,而不影响锥体细胞的总数。相反,在CA1区域,无论是新生儿期还是成年期开始的甲状腺激素缺乏都被发现会导致锥体细胞总数减少。在30日龄和180日龄的甲状腺功能减退组中发现减少幅度在14.2%至22.5%之间。恢复甲状腺功能正常状态并不能改善上述神经元损失。目前的结果支持这样一种观点,即甲状腺功能减退会导致海马CA3区域的结构组织发生微小改变,这与CA1区域发生神经元死亡的情况相反。此外,本文提供的数据表明,CA1锥体细胞的总数表现出性别二态性,且不受甲状腺激素操作的影响。(摘要截取自400字)