Siwicki K K, Beltz B S, Kravitz E A
J Neurosci. 1987 Feb;7(2):522-32. doi: 10.1523/JNEUROSCI.07-02-00522.1987.
In order to explore the functions of the peptide proctolin in the lobster nervous system, 3 classes of neurons showing proctolin-like immunocytochemical staining were selected for study. These neurons were identified on the basis of physiological and/or morphological criteria, isolated by dissections, and analyzed with biochemical methods to determine whether they contained authentic proctolin and which classical neurotransmitters coexisted with the peptide. Pairs of large proctolin-immunoreactive neurons in fifth thoracic and first abdominal ganglia were identified as serotonin-immunoreactive neurons (Beltz and Kravitz, 1983, 1987) by staining serial sections of the ganglia alternately with the 2 antisera. Physiologically identified cells, dissected from the ganglia and analyzed with high-performance liquid chromatography (HPLC), contained approximately 20 microM proctolin and 0.5 mM serotonin. A large proctolin-immunoreactive neuron in the circumesophageal ganglion was identified as the lobster homolog of a dopaminergic neurosecretory cell found in other crustaceans (Cooke and Goldstone, 1970). The large lobster cell stained with antityrosine hydroxylase antiserum, and synthesized 3H-dopamine from 3H-tyrosine. Dissected cell bodies, analyzed by HPLC, contained approximately 25 microM proctolin. Proctolin-immunoreactive sensory neurons were identified as large stained fibers that terminated in sensory dendrites of the oval organ mechanoreceptor in the scaphognathite (Pasztor, 1979; Pasztor and Bush, 1982). The largest sensory fiber was isolated for biochemical studies. It synthesized 3H-acetylcholine from 3H-choline and, by HPLC analysis, was found to contain approximately 3 microM proctolin. Thus, proctolin coexists with different conventional transmitters in several classes of identified lobster neurons. Investigations of the actions of proctolin in these different contexts should contribute to a more complete understanding of the diverse functions of neuropeptides and their roles as cotransmitters.
为了探究肽类促肠肌肽在龙虾神经系统中的功能,选择了3类呈现促肠肌肽样免疫细胞化学染色的神经元进行研究。这些神经元是根据生理和/或形态学标准鉴定出来的,通过解剖分离,并采用生化方法进行分析,以确定它们是否含有真正的促肠肌肽以及与该肽共存的经典神经递质。通过用两种抗血清交替对胸神经节和第一腹神经节的连续切片进行染色,将第五胸神经节和第一腹神经节中一对大的促肠肌肽免疫反应性神经元鉴定为5-羟色胺免疫反应性神经元(贝尔茨和克拉维茨,1983年,1987年)。从神经节中解剖出并通过高效液相色谱法(HPLC)分析的生理鉴定细胞,含有约20微摩尔的促肠肌肽和0.5毫摩尔的5-羟色胺。食管周围神经节中一个大的促肠肌肽免疫反应性神经元被鉴定为在其他甲壳类动物中发现的多巴胺能神经分泌细胞的龙虾同源物(库克和戈德斯通,1970年)。这个大的龙虾细胞用抗酪氨酸羟化酶抗血清染色,并从3H-酪氨酸合成3H-多巴胺。通过HPLC分析解剖得到的细胞体,发现其含有约25微摩尔的促肠肌肽。促肠肌肽免疫反应性感觉神经元被鉴定为终止于颚舟片椭圆形器官机械感受器感觉树突中的大的染色纤维(帕斯托尔,1979年;帕斯托尔和布什,1982年)。分离出最大的感觉纤维用于生化研究。它从3H-胆碱合成3H-乙酰胆碱,并且通过HPLC分析发现其含有约3微摩尔的促肠肌肽。因此,促肠肌肽在几类已鉴定的龙虾神经元中与不同的传统递质共存。对促肠肌肽在这些不同情况下作用的研究应有助于更全面地理解神经肽的多种功能及其作为共递质的作用。