Cross R J, Brooks W H, Roszman T L, Markesbery W R
Neurobiol Aging. 1984 Summer;5(2):89-92. doi: 10.1016/0197-4580(84)90036-8.
Numerous reports indicate that both central nervous system (CNS) and immune system functions decline with age. We have previously shown that the CNS can modulate both mitogen-induced spleen cell proliferation and NK activity in young Fischer 344 rats. In the present study we have determined the effects of AHT lesions on the lymphocyte reactivity of aged Fischer 344 rats. These data show that lesions in the AHT of aged rats cannot modulate splenic mitogen responsiveness, however, NK activity is impaired. This differential effect may be due to multiple factors including enhanced splenic suppressor cell activity, the inability of the brain to send modulatory signals following lesioning, or the failure of the immune system to receive a neural signal and react to it.
大量报告表明,中枢神经系统(CNS)和免疫系统的功能都会随着年龄的增长而衰退。我们之前已经表明,中枢神经系统可以调节幼年Fischer 344大鼠有丝分裂原诱导的脾细胞增殖和自然杀伤(NK)活性。在本研究中,我们确定了下丘脑前部(AHT)损伤对老年Fischer 344大鼠淋巴细胞反应性的影响。这些数据表明,老年大鼠下丘脑前部的损伤无法调节脾有丝分裂原反应性,然而,自然杀伤活性受损。这种差异效应可能是由于多种因素造成的,包括脾抑制细胞活性增强、损伤后大脑无法发送调节信号,或者免疫系统无法接收神经信号并对其做出反应。