1. Hypothalamic cerebrospinal fluid‐contacting neurons project to the rostral agranular insular cortex: An immunofluorescence and ultrastructural analysis in the rat.
- Author
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Martínez‐Lorenzana, Guadalupe, Gamal‐Eltrabily, Mohammed, Palma‐Tirado, Lourdes, González‐Hernández, Abimael, and Condés‐Lara, Miguel
- Abstract
Cerebrospinal fluid‐contacting neurons (CSF‐cNS) are considered mechanoreceptors and chemoreceptors involved in detecting changes in CSF circulation. However, considering that recent data suggest that this type of cell could exert an active response when an external stimulus is sensed, identification of CSF‐cNS may be relevant. In this regard, some data suggest that a neuronal connection exists between the ventral region of the hypothalamic paraventricular nucleus (PVN) and rostral agranular insular cortex (RAIC); indeed, a potential CSF‐cNS is hypothesized. However, a detailed analysis of this connection has not been conducted. Thus, using neuronal tracers (Fluoro‐Gold® (FG) and cholera toxin (ChT)) coupled with transmission electron microscopy and immunofluorescence assays against Fluoro‐Gold®, oxytocin (OXT), vasopressin (AVP) and oxytocin receptors (OTR), we describe an oxytocinergic or vasopressinergic CSF‐cNS between the PVN and RAIC. Our results showed that CSF‐cNS along the PVN labelled with oxytocin and/or AVP were present in dendritic projections near the third ventricle. This CSF‐cNS in the PVN seems to project to the RAIC. Inside the RAIC, ultrastructural analysis showed that axons immunopositive for oxytocin from the PVN sustained synaptic connections with neurons that expressed OTR. These findings show that the CSF‐cNS from the PVN sends projections to the RAIC. To the best of our knowledge, the relevance of CSF‐cNS has not been elucidated; however, we hypothesized that the activation of cells could concomitantly release neuropeptides (i.e., oxytocin and AVP) in the CSF and RAIC. Thus, further analysis of the impact of neuropeptides released into the third ventricle and RAIC is warranted. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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