Landfield P W, Thibault O, Mazzanti M L, Porter N M, Kerr D S
Department of Pharmacology, University of Kentucky, College of Medicine, Lexington 40536-0084.
J Neurobiol. 1992 Nov;23(9):1247-60. doi: 10.1002/neu.480230914.
This paper reviews evidence that brain aging and Alzheimer's disease (AD) are somehow closely related and that the hippocampus (CA1) is highly vulnerable to cell loss under both conditions. In addition, two current lines of evidence on the mechanisms of hippocampal cell loss with aging are considered, including studies of neuronal calcium dysregulation and studies of cumulative glucocorticoid (GC) neurotoxicity. Moreover, recent electrophysiological studies have shown that excess glucocorticoid activation of hippocampal neurons increases the influx of calcium through voltage-activated calcium channels. Second messenger systems may mediate the steroid modulation of calcium channels. Therefore, it is hypothesized that excess glucocorticoid activation and neuronal calcium dysregulation may be two phases of a single process that increases the susceptibility of neurons to neurodegeneration during aging and Alzheimer's disease.
本文综述了相关证据,表明大脑衰老与阿尔茨海默病(AD)在某种程度上密切相关,且在这两种情况下海马体(CA1)极易发生细胞丢失。此外,还探讨了目前关于衰老导致海马体细胞丢失机制的两条研究线索,包括神经元钙调节异常的研究和累积糖皮质激素(GC)神经毒性的研究。此外,最近的电生理研究表明,海马神经元的糖皮质激素过度激活会增加通过电压激活钙通道的钙内流。第二信使系统可能介导类固醇对钙通道的调节。因此,据推测,糖皮质激素过度激活和神经元钙调节异常可能是一个单一过程的两个阶段,该过程会增加衰老和阿尔茨海默病期间神经元对神经退行性变的易感性。