Baldridge W H
Department of Physiology and Pharmacology, University of Queensland, Brisbane, Australia.
J Neurosci. 1996 Aug 15;16(16):5060-72. doi: 10.1523/JNEUROSCI.16-16-05060.1996.
Cholinergic regulation of the activity of rabbit retinal ganglion cells and displaced amacrine cells was investigated using optical recording of changes in intracellular free calcium ([Ca2+]i). Labeling of neurons in the mature retina was achieved by injecting calcium green-1 dextran (CaGD) into the isolated retina. Nicotine increased ganglion cell [Ca2+]i, affecting every loaded cell in some preparations; the pharmacology of nicotine was consistent with an action at neuronal nicotinic receptors, and specifically it was kappa-(neuronal-)bungarotoxin-sensitive but alpha-bungarotoxin-insensitive. Muscarine also raised [Ca2+]i, but it was less potent than nicotine, affecting only a subpopulation of ganglion cells, with an M1-like muscarinic receptor pharmacology. Neither the nicotine- nor muscarine-induced increases of ganglion cell [Ca2+]i were blocked by the glutamate receptor antagonists 6,7-dinitroquinoxaline-2,3-dione and aminophosphonopentanoic acid. Therefore, the effects of cholinergic agonists on ganglion cell [Ca2+]i were not attributable to an indirect effect mediated by glutamatergic bipolar cells. The effects of nicotine and muscarine were abolished in calcium-free solution, indicating that the responses depend on calcium influx. Displaced (Cb) cholinergic amacrine cells were also loaded with CaGD and were identified by selective labeling with the nuclear dye 4',6-diamidino-2-phenyl-indole. Cb amacrine cells did not respond to either nicotine or muscarine, but responded vigorously to the glutamate receptor agonist kainic acid. There is anatomical evidence indicating that cholinergic amacrine cells make synaptic contact with each other, but the present results do not support the hypothesis that communication between these cells is cholinergic.
利用光学记录细胞内游离钙([Ca2+]i)的变化,研究了胆碱能对兔视网膜神经节细胞和移位无长突细胞活性的调节作用。通过将钙绿-1葡聚糖(CaGD)注入离体视网膜,实现对成熟视网膜中神经元的标记。尼古丁增加了神经节细胞的[Ca2+]i,在某些标本中影响了每个被标记的细胞;尼古丁的药理学特性与作用于神经元烟碱受体一致,具体而言,它对κ-(神经元型)银环蛇毒素敏感,但对α-银环蛇毒素不敏感。毒蕈碱也升高了[Ca2+]i,但效力不如尼古丁,仅影响神经节细胞的一个亚群,具有M1样毒蕈碱受体药理学特性。谷氨酸受体拮抗剂6,7-二硝基喹喔啉-2,3-二酮和氨基膦酰戊酸均不能阻断尼古丁或毒蕈碱诱导的神经节细胞[Ca2+]i升高。因此,胆碱能激动剂对神经节细胞[Ca2+]i的作用并非归因于由谷氨酸能双极细胞介导的间接作用。尼古丁和毒蕈碱的作用在无钙溶液中消失,表明这些反应依赖于钙内流。移位的(Cb)胆碱能无长突细胞也用CaGD进行标记,并通过用核染料4',6-二脒基-2-苯基吲哚进行选择性标记来鉴定。Cb无长突细胞对尼古丁或毒蕈碱均无反应,但对谷氨酸受体激动剂 kainic 酸有强烈反应。有解剖学证据表明胆碱能无长突细胞彼此之间形成突触联系,但目前的结果不支持这些细胞之间的通讯是胆碱能的这一假设。