Veldhuis J D
Division of Endocrinology, Department of Internal Medicine, General Clinical Research Center, University of Virginia School of Medicine, 22908-0202, Charlottesville, VA, USA.
Exp Gerontol. 2000 Dec;35(9-10):1281-308. doi: 10.1016/s0531-5565(00)00123-6.
We recently identified consistent attenuation of LH and testosterone secretory pulse amplitude and associated disruption of their orderly patterns of release in healthy older men. These dynamic changes emerge despite young-adult concentrations of LH and total testosterone. Moreover, we could document disruption of synchrony between LH secretion and oscillations in FSH, prolactin, sleep-stage and NPT (nocturnal penile tumescence), thus pointing to loss of coordinate neurohormone outflow. Such data suggest that CNS-hypothalamically based regulatory defects may be important in aging, as inferred indirectly in the old male rat and mouse more than 15 years ago. How such alterations are related to specific hypothalamic neurotransmitter changes in aging will be critical to unravel.
我们最近发现,健康老年男性的促黄体生成素(LH)和睾酮分泌脉冲幅度持续降低,且其有序的释放模式受到破坏。尽管LH和总睾酮水平处于年轻成年人的浓度范围,但这些动态变化依然出现。此外,我们能够证明LH分泌与促卵泡生成素(FSH)、催乳素、睡眠阶段及夜间阴茎勃起(NPT)振荡之间的同步性受到破坏,从而表明神经激素协调输出丧失。这些数据表明,基于中枢神经系统下丘脑的调节缺陷在衰老过程中可能很重要,这在15年多以前的老年雄性大鼠和小鼠中已得到间接推断。弄清楚这些改变如何与衰老过程中下丘脑特定神经递质的变化相关,将至关重要。