Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, NEO, Stockholm, Sweden.
Gut. 2019 Jul;68(7):1210-1223. doi: 10.1136/gutjnl-2018-316279. Epub 2018 Sep 18.
To determine if human colonic neuromuscular functions decline with increasing age.
Looking for non-specific changes in neuromuscular function, a standard burst of electrical field stimulation (EFS) was used to evoke neuronally mediated (cholinergic/nitrergic) contractions/relaxations in muscle strips of human ascending and descending colon, aged 35-91 years (macroscopically normal tissue; 239 patients undergoing cancer resection). Then, to understand mechanisms of change, numbers and phenotype of myenteric neurons (30 306 neurons stained with different markers), densities of intramuscular nerve fibres (51 patients in total) and pathways involved in functional changes were systematically investigated (by immunohistochemistry and use of pharmacological tools) in elderly (≥70 years) and adult (35-60 years) groups.
With increasing age, EFS was more likely to evoke muscle relaxation in ascending colon instead of contraction (linear regression: n=109, slope 0.49%±0.21%/year, 95% CI), generally uninfluenced by comorbidity or use of medications. Similar changes were absent in descending colon. In the elderly, overall numbers of myenteric and neuronal nitric oxide synthase-immunoreactive neurons and intramuscular nerve densities were unchanged in ascending and descending colon, compared with adults. In elderly ascending, not descending, colon numbers of cell bodies exhibiting choline acetyltransferase immunoreactivity increased compared with adults (5.0±0.6 vs 2.4±0.3 neurons/mm myenteric plexus, p=0.04). Cholinergically mediated contractions were smaller in elderly ascending colon compared with adults (2.1±0.4 and 4.1±1.1 g-tension/g-tissue during EFS; n=25/14; p=0.04); there were no changes in nitrergic function or in ability of the muscle to contract/relax. Similar changes were absent in descending colon.
In ascending not descending colon, ageing impairs cholinergic function.
确定人类结肠的神经肌肉功能是否随年龄增长而下降。
寻找神经肌肉功能的非特异性变化,使用标准的电刺激脉冲(EFS)来诱发人升结肠和降结肠的神经元介导的(胆碱能/硝能)收缩/松弛。然后,为了了解变化的机制,我们系统地研究了老年(≥70 岁)和成年(35-60 岁)组中肌间神经元的数量和表型(用不同标志物染色的 30306 个神经元)、肌内神经纤维密度(总共 51 个患者)以及参与功能变化的途径(通过免疫组织化学和药理学工具)。
随着年龄的增长,EFS 更有可能在升结肠中引起肌肉松弛而不是收缩(线性回归:n=109,斜率 0.49%±0.21%/年,95%置信区间),通常不受合并症或药物使用的影响。降结肠则没有类似的变化。在老年人中,与成年人相比,升结肠和降结肠的肌间神经元和神经元一氧化氮合酶免疫反应性神经元的总数以及肌内神经密度没有变化。与成年人相比,老年人升结肠中胆碱乙酰转移酶免疫反应性的细胞体数量增加(5.0±0.6 对 2.4±0.3 个神经元/mm 肌间神经丛,p=0.04)。与成年人相比,老年人升结肠中的胆碱能介导的收缩较小(EFS 期间 2.1±0.4 和 4.1±1.1 g 张力/g 组织;n=25/14;p=0.04);硝能功能或肌肉收缩/松弛的能力没有变化。降结肠中没有类似的变化。
在升结肠而非降结肠中,衰老会损害胆碱能功能。