{"title":"Dopaminergic Central Neurons and Peripheral Sensory Systems in Pteropod and Nudibranch Molluscs","authors":"Tigran P. Norekian, Leonid L. Moroz","doi":"10.1002/cne.70054","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>In Euthyneuran molluscs, the distribution and plethora of dopamine (DA) functions are likely coupled to the feeding ecology with a broad spectrum of modifications both in the central and peripheral neural systems. However, studies of benthic grazers currently dominate the analysis of DA-mediated signaling, whereas adaptations to pelagic lifestyles and other feeding strategies are unknown. Here, we characterize the distribution of central and peripheral neurons in representatives of distinct ecological groups: the pelagic predatory pteropod <i>Clione limacina</i> (Pteropoda, Gymnosomata) and its prey — <i>Limacina helicina</i> (Pteropoda, Thecosomata), as well as the plankton eater <i>Melibe leonina</i> (Nudipleura, Nudibranchia). By using tyrosine hydroxylase immunoreactivity as a reporter, we mapped their dopaminergic systems. Across all studied species, despite their differences in ecology, small numbers of dopaminergic neurons in the central ganglia contrast to an incredible density of these neurons in the peripheral nervous system, primarily representing sensory-like cells, which are predominantly concentrated in the chemotactic areas and project afferent axons to the central nervous system. Combined with tubulin immunoreactivity, this study illuminates the complexity of sensory signaling and peripheral neural systems in Euthyneuran molluscs with lineage-specific adaptations across different taxonomical and ecological groups.</p>\n </div>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"533 5","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70054","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
In Euthyneuran molluscs, the distribution and plethora of dopamine (DA) functions are likely coupled to the feeding ecology with a broad spectrum of modifications both in the central and peripheral neural systems. However, studies of benthic grazers currently dominate the analysis of DA-mediated signaling, whereas adaptations to pelagic lifestyles and other feeding strategies are unknown. Here, we characterize the distribution of central and peripheral neurons in representatives of distinct ecological groups: the pelagic predatory pteropod Clione limacina (Pteropoda, Gymnosomata) and its prey — Limacina helicina (Pteropoda, Thecosomata), as well as the plankton eater Melibe leonina (Nudipleura, Nudibranchia). By using tyrosine hydroxylase immunoreactivity as a reporter, we mapped their dopaminergic systems. Across all studied species, despite their differences in ecology, small numbers of dopaminergic neurons in the central ganglia contrast to an incredible density of these neurons in the peripheral nervous system, primarily representing sensory-like cells, which are predominantly concentrated in the chemotactic areas and project afferent axons to the central nervous system. Combined with tubulin immunoreactivity, this study illuminates the complexity of sensory signaling and peripheral neural systems in Euthyneuran molluscs with lineage-specific adaptations across different taxonomical and ecological groups.
期刊介绍:
Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states.
Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se.
JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.