Abstract

The medial septum (MS) is critically involved in theta rhythmogenesis and control of the hippocampal network, with which it is reciprocally connected. MS activity is influenced by brainstem structures, including the stress-sensitive, nucleus incertus (NI), the main source of the neuropeptide relaxin-3 (RLN3). In the current study, we conducted a comprehensive neurochemical and electrophysiological characterization of NI neurons innervating the MS in the rat, by employing classical and viral-based neural tract-tracing and electrophysiological approaches, and multiplex fluorescent in situ hybridization. We confirmed earlier reports that the MS is innervated by RLN3 NI neurons and documented putative glutamatergic (vGlut2 mRNA-expressing) neurons as a relevant NI neuronal population within the NI–MS tract. Moreover, we observed that NI neurons innervating MS can display a dual phenotype for GABAergic and glutamatergic neurotransmission, and that 40% of MS-projecting NI neurons express the corticotropin-releasing hormone-1 receptor. We demonstrated that an identified cholecystokinin (CCK)-positive NI neuronal population is part of the NI–MS tract, and that RLN3 and CCK NI neurons belong to a neuronal pool expressing the calcium-binding proteins, calbindin and calretinin. Finally, our electrophysiological studies revealed that MS is innervated by A-type potassium current-expressing, type I NI neurons, and that type I and II NI neurons differ markedly in their neurophysiological properties. Together these findings indicate that the MS is controlled by a discrete NI neuronal network with specific electrophysiological and neurochemical features; and these data are of particular importance for understanding neuronal mechanisms underlying the control of the septohippocampal system and related behaviors.

Highlights

  • The septohippocampal pathway, most extensively studied in rodents, consists of projections between the medial septum (MS) and hippocampus, and is critically involved in theta rhythmogenesis and the control of hippocampal network excitability to fine-tune it to different behavioral states (Müller and Remy, 2018)

  • In studies to determine the neuropeptide content of nucleus incertus (NI) neurons innervating MS, we performed an injection of the retrograde tracer, FluoroPink, into the MS of adult rats and subsequent immunofluorescent detection of RLN3 and CCK in the NI

  • Viral-based, retrograde neural tract-tracing combined with in situ hybridization revealed that the MS is innervated by RLN3/GABAergic, and putative glutamatergic NI neurons

Read more

Summary

Introduction

The septohippocampal pathway, most extensively studied in rodents, consists of projections between the medial septum (MS) and hippocampus, and is critically involved in theta rhythmogenesis and the control of hippocampal network excitability to fine-tune it to different behavioral states (Müller and Remy, 2018). MS neurons form a tightly interconnected network, in which three major cell types can be distinguished: (i) slow firing, theta-independent cholinergic neurons; (ii) cluster or slow-firing glutamatergic neurons, with activity correlated with running speed; and (iii) theta-modulated, fast and burst-firing GABAergic neurons (Sotty et al, 2003; Leão et al, 2015; Müller and Remy, 2018). Septal GABAergic and glutamatergic neurons innervate predominantly GABAergic neurons in the hippocampus, while the main targets of septal cholinergic projections are hippocampal pyramidal neurons (Sun et al, 2014). MS neurons are under modulatory influences from several brain areas, including ascending cholinergic projections from the dorsolateral tegmental nucleus, serotonergic projections from the raphe nuclei, adrenergic inputs from the locus coeruleus (Takeuchi et al, 2021) and a dense projection from the brainstem, nucleus incertus (NI), an enigmatic structure involved in the control of contextual memories, locomotor speed, arousal, and stress responses (Ma et al, 2013, 2017a; Szonyi et al, 2019; Lu et al, 2020)

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call