C. W. Gruber: Center for Physiology and Pharmacology, Medical University of Vienna, Schwarzspanierstraße 17, A-1090 Vienna, Austria.
Exp Physiol. 2014 Jan;99(1):55-61. doi: 10.1113/expphysiol.2013.072561. Epub 2013 Aug 16.
Neuropeptides and regulatory peptide hormones control many developmental, physiological and behavioural processes in animals, including humans. The nonapeptides oxytocin and arginine vasopressin are produced and released by the pituitary gland and have actions on many organs and tissues. Receptive cells possess particular receptors to which the peptides bind as ligands, leading to activation of G-protein-coupled receptors, hence cellular responses. In humans and other mammalian species, oxytocin and vasopressin mediate a range of peripheral and central physiological functions that are important for osmoregulation, reproduction, complex social behaviours, memory and learning. The origin of the oxytocin/vasopressin signalling system is thought to date back more than 600 million years. All vertebrate oxytocin- and vasopressin-like peptides have presumably evolved from the ancestral nonapeptide vasotocin by gene duplication and today are present in vertebrates, including mammals, birds, reptiles, amphibians and fish. Oxytocin- and vasopressin-like peptides have been identified in several invertebrate species, including molluscs, annelids, nematodes and arthropods. Members of this peptide family share high sequence similarity, and it is possible that they are functionally related across the entire animal kingdom. However, it is evident that not all animals express oxytocin/vasopressin neuropeptides and that there is little information available about the biology and physiology of this signalling system of invertebrates and, in particular, of insects, which represent more than half of all known living organisms. This report describes the discovery of novel oxytocin- and vasopressin-like peptides in arthropods and summarizes the status quo of the functional relevance of this neuropeptide signalling system in invertebrates, which will have beneficial implications for the design of selective and potent ligands to human oxytocin and vasopressin receptors.
神经肽和调节肽激素控制着动物(包括人类)的许多发育、生理和行为过程。神经垂体分泌的神经肽催产素和精氨酸加压素作用于许多器官和组织。受体细胞具有特定的受体,这些肽作为配体与受体结合,从而激活 G 蛋白偶联受体,进而引发细胞反应。在人类和其他哺乳动物中,催产素和加压素介导了一系列外周和中枢生理功能,这些功能对于渗透压调节、生殖、复杂的社会行为、记忆和学习都很重要。催产素/加压素信号系统的起源可以追溯到 6 亿多年前。所有脊椎动物的催产素和加压素样肽可能都是由祖先的九肽加压素通过基因复制进化而来的,如今存在于包括哺乳动物、鸟类、爬行动物、两栖动物和鱼类在内的脊椎动物中。在一些无脊椎动物物种中,如软体动物、环节动物、线虫和节肢动物,也发现了催产素和加压素样肽。这个肽家族的成员具有高度的序列相似性,它们在整个动物界可能具有功能相关性。然而,并非所有动物都表达催产素/加压素神经肽,而且关于无脊椎动物,特别是昆虫的这种信号系统的生物学和生理学的信息很少。昆虫占所有已知生物的一半以上。本报告描述了在节肢动物中发现的新型催产素和加压素样肽,并总结了这种神经肽信号系统在无脊椎动物中的功能相关性的现状,这将对设计选择性和有效的人类催产素和加压素受体配体具有有益的意义。