Duve H, Thorpe A
School of Biological Sciences, Queen Mary and Westfield College, University of London, UK.
Cell Tissue Res. 1994 May;276(2):367-79. doi: 10.1007/BF00306122.
The Leu-callatostatins are a series of four neuropeptides isolated from nervous tissues of the blowfly Calliphora vomitoria that show C-terminal sequence homology to the allatostatins of cockroaches. The allatostatins have an important role in the reproductive processes of insects as inhibitors of the synthesis and release of juvenile hormone from the corpus allatum. In this study, the distribution of the Leu-callatostatin-immunoreactive neurones and endocrine cells has been mapped in C. vomitoria and, in contrast to the cockroach allatostatins, it has been shown that there is no cytological basis to suggest that the dipteran peptides act as regulators of juvenile hormone. Although occurring in various neurones in the brain and thoracico-abdominal ganglion, there is no evidence of Leu-callatostatin-immunoreactive pathways linking the brain to the corpus allatum, or of immunoreactive terminals in this gland. Three different types of functions for the Leu-callatostatins are suggested by the occurrence of immunoreactive material in cells and by the pathways that have been identified. (1) A role in neurotransmission or neuromodulation appears evident from immunoreactive neurones in the medulla of the optic lobes, and from immunoreactive material in the central body and in descending interneurones in the suboesophageal ganglion that project to the neuropile of the thoracico-abdominal ganglion. (2) Leu-callatostatin neurones directly innervate muscles of the hindgut and the heart. Immunoreactive fibres from neurones of the abdominal ganglion pass by way of the median abdominal nerve to ramify extensively over several areas of the hindgut. Physiological experiments with synthetic peptides show that the Leu-callatostatins are potent inhibitors of peristaltic movements of the ileum. Leu-callatostatin 3 is active at 10(-16) to 10(-13) M. This form of regulatory control over gut motility appears to be highly specific since the patterns of contraction in other regions are unaffected by these peptides. (3) Evidence that the Leu-callatostatins act as neurohormones comes from the presence of varicosities in axons passing through the corpus cardiacum (but not the corpus allatum) and also from material in extraganglionic neurosecretory cells in the thorax. Fibres from these peripheral neurones are especially prominent over the large nerve bundles supplying the legs. There are also a considerable number of Leu-callatostatin-immunoreactive endocrine cells in a specific region of the midgut. The conclusion from this study is that although conservation of the structure of the allatostatin-type of peptides is evident through a long period of evolution it cannot be assumed that all of their functions have also been conserved.(ABSTRACT TRUNCATED AT 400 WORDS)
亮氨酸抑咽侧体素是从丽蝇(Calliphora vomitoria)神经组织中分离出的一系列四种神经肽,它们在C末端序列上与蟑螂的抑咽侧体素具有同源性。抑咽侧体素作为咽侧体合成和释放保幼激素的抑制剂,在昆虫的生殖过程中发挥着重要作用。在本研究中,已绘制出丽蝇中亮氨酸抑咽侧体素免疫反应性神经元和内分泌细胞的分布图,并且与蟑螂的抑咽侧体素不同,研究表明没有细胞学依据表明双翅目肽可作为保幼激素的调节因子。尽管亮氨酸抑咽侧体素存在于大脑和胸腹神经节的各种神经元中,但没有证据表明存在将大脑与咽侧体相连的亮氨酸抑咽侧体素免疫反应性通路,也没有证据表明该腺体中有免疫反应性终末。亮氨酸抑咽侧体素在细胞中的存在情况以及已确定的通路提示了其三种不同类型的功能。(1)视叶髓质中的免疫反应性神经元,以及中央体和投射到胸腹神经节神经纤维网的咽下神经节中下行中间神经元中的免疫反应性物质,表明亮氨酸抑咽侧体素在神经传递或神经调节中发挥作用。(2)亮氨酸抑咽侧体素神经元直接支配后肠和心脏的肌肉。来自腹神经节神经元的免疫反应性纤维通过腹正中神经,在后肠的几个区域广泛分支。用合成肽进行的生理学实验表明,亮氨酸抑咽侧体素是回肠蠕动运动的有效抑制剂。亮氨酸抑咽侧体素3在10^(-16)至10^(-13) M时具有活性。这种对肠道运动的调节控制形式似乎具有高度特异性,因为其他区域的收缩模式不受这些肽的影响。(3)亮氨酸抑咽侧体素作为神经激素发挥作用的证据来自于穿过心侧体(而非咽侧体)的轴突中存在膨体,以及胸部神经节外神经分泌细胞中的物质。来自这些外周神经元的纤维在供应腿部的大神经束上尤为突出。中肠的特定区域也有大量亮氨酸抑咽侧体素免疫反应性内分泌细胞。这项研究的结论是,尽管抑咽侧体素型肽的结构在长期进化过程中明显保守,但不能假定它们的所有功能也都保守。(摘要截短至400字)