Toescu Emil C, Verkhratsky Alexei, Landfield Philip W
Department of Physiology, Division of Medical Sciences, The University of Birmingham, Edgbaston B15 2TT, UK.
Trends Neurosci. 2004 Oct;27(10):614-20. doi: 10.1016/j.tins.2004.07.010.
Understanding the cellular mechanisms that characterize the functional changes of the aged brain is an ongoing and formidable challenge for the neuroscience community. Evidence now links changes in Ca(2+) influx and homeostasis with perturbations induced by the aging process in the function of the main intracellular organelles involved in Ca(2+) regulation: the endoplasmic reticulum and mitochondria. New perspectives are also offered by recent gene microarray studies, illustrating the multifactorial nature of the aging process.
对于神经科学界来说,了解表征衰老大脑功能变化的细胞机制是一项持续且艰巨的挑战。目前有证据表明,钙离子内流和内环境稳态的变化与衰老过程所引发的、参与钙离子调节的主要细胞内细胞器(内质网和线粒体)功能扰动有关。近期的基因微阵列研究也提供了新的视角,阐明了衰老过程的多因素性质。