Roberts D, Gelperin D, Wiley J W
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.
Am J Physiol. 1994 Oct;267(4 Pt 1):G515-22. doi: 10.1152/ajpgi.1994.267.4.G515.
The effect of aging was examined on cholinergically mediated contractions and acetylcholine (ACh) release in isolated colonic segments from Fischer (F344 x BN) F1 rats, 4-8 mo (postpubertal) and 22-28 mo (senescent) of age. This species demonstrates age-dependent slowing of colonic transit. Muscle tension response to electrical stimulation of cholinergic neural pathways and application of ACh was significantly decreased in preparations from senescent compared with postpubertal animals. We focused on the hypothesis that aging was associated with reduced ACh release that resulted from decreased calcium influx through membrane calcium channels. Aging did not affect either the synthesis of [3H]ACh from [3H]choline or the percentage of 3H released in the form of [3H]ACh. However, elevated KCl-evoked release of [3H]ACh was significantly reduced in tissue from senescent compared with postpubertal animals. Treatment with the calcium ionophore ionomycin increased [3H]ACh release in tissue from senescent animals to near postpubertal levels. However, increasing extracellular calcium concentration ([Ca2+]o) from 1.2 to 5 mM did not increase the amount of transmitter release in tissue from senescent animals to the levels observed with 1.2 mM [Ca2+]o in postpubertal tissue. The neuronal calcium channel antagonist omega-conotoxin GVIA inhibited acetylcholine release in a concentration-dependent manner with half-maximal inhibitory values of 1.8 and 8.2 nM for senescent and postpubertal preparations, respectively. In summary, age-dependent reduction in ACh release was observed in the rat colon myenteric plexus that may, in part, be associated with decreased calcium influx via membrane calcium channels.
研究了衰老对4至8个月大(青春期后)和22至28个月大(衰老期)的Fischer(F344×BN)F1大鼠离体结肠段胆碱能介导的收缩和乙酰胆碱(ACh)释放的影响。该物种表现出结肠转运随年龄增长而减慢。与青春期后动物相比,衰老动物制备物中对胆碱能神经通路电刺激和应用ACh的肌肉张力反应显著降低。我们关注的假设是,衰老与ACh释放减少有关,这是由于通过膜钙通道的钙内流减少所致。衰老既不影响[³H]胆碱合成[³H]ACh,也不影响以[³H]ACh形式释放的³H百分比。然而,与青春期后动物相比,衰老动物组织中氯化钾诱发的[³H]ACh释放显著减少。用钙离子载体离子霉素处理可使衰老动物组织中的[³H]ACh释放增加至接近青春期后水平。然而,将细胞外钙浓度([Ca²⁺]o)从1.2 mM增加到5 mM,并未使衰老动物组织中的递质释放量增加到青春期后组织中1.2 mM [Ca²⁺]o时观察到的水平。神经元钙通道拮抗剂ω-芋螺毒素GVIA以浓度依赖性方式抑制乙酰胆碱释放,衰老和青春期后制备物的半数最大抑制值分别为1.8 nM和8.2 nM。总之,在大鼠结肠肌间神经丛中观察到ACh释放随年龄增长而减少,这可能部分与通过膜钙通道的钙内流减少有关。