Cited by 102Stress Responses and CortisolNeuroinflammation and Neurodegeneration MechanismsNeuropeptides and Animal Physiology

Neurons of the superior nucleus of the medial habenula and ependymal cells express IL-18 in rat CNS

Sugama, Shuei, Cho, Byung Pil, Baker, Harriet, Joh, Tong H, Lucero, Jacinta, Conti, Bruno·2002·Brain Research

Abstract

The habenular-interpeduncular pathway is involved in the modulation of several functions including neuroendocrine and stress responses. Interleukin-18 (IL-18) is a pro-inflammatory cytokine predominantly studied as a modulator of immune functions and also produced in the adrenal cortex following activation of the hypothalamic-pituitary-adrenal axis. In the central nervous system, IL-18 was demonstrated to induce sleep and to influence long-term potentiation and was proposed to mediate local inflammatory reactions. The present study investigated the localization of IL-18 and its expression following either acute or chronic restraint stress in the brain of adult male Wistar rats. Using immunocytochemistry and in situ hybridization we report the unprecedented localization of IL-18 in the neurons of the superior part of the medial habenula (MHbS), their projections to the interpenducular nucleus and its expression in the ependymal cells surrounding the third and the lateral ventricles. In addition, acute (2 h) or chronic (6 h/day for 3 weeks) restraint stress induced a strong elevation of IL-18 immunostaining in the MHbS but not in ependymal cells. The present data suggest that IL-18 may participate in the modulation of stress responses in the MHbS. They also suggest that ependymal cells may be the source of IL-18 previously reported in the cerebrospinal fluid (CSF). The role of IL-18 in the ependyma and the CSF remains to be elucidated.

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Crossref · 10.1016/s0006-8993(02)03363-2

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  • The MHb contains neurons that produce acetylcholine or substance P, and a small population that produces interleukin-18.

    “MHb is comprised of neurons that produce the neurotransmitters acetylcholine (ACh) or substance P (Cuello et al. 1978;Eckenrode et al. 1987), and a small population that produce the cytokine interleukin-18 (IL-18) (Sugama et al. 2002).”

    From Mechanisms of Nicotine Addiction (2021) · cites this paper as Sugama et al. 2002

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References 61 · Cited by 102

Authors
Sugama, S., Cho, B. P., Baker, H., Joh, T. H., Lucero, J., & Conti, B.
Affiliations
  • Scripps Research Institute (US)
  • Cornell University (US)
Corresponding author
Conti, Bruno
Venue
Brain Research
Publisher
Elsevier BV
Published
2002-12
Volume
958
Issue
1
Pages
1-9
ISSN
0006-8993 (ISSN-L)
OpenAlex
W2115119251
Cited by
102
References
61
Citations by year
2026: 3 · 2025: 4 · 2024: 7 · 2023: 1 · 2022: 5 · 2021: 1 · 2020: 5 · 2019: 2 · 2018: 2 · 2017: 5 · 2016: 7 · 2015: 5 · 2014: 5 · 2013: 7 · 2012: 11
FWCI
1.10
Type
journal article
Language
en
Open access
closed
Locations
  • Brain Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords
IL-18, medial habenula, ependymal cells, restraint stress, stress response, inflammatory cytokines, cerebrospinal fluid, hypothalamic-pituitary-adrenal axis, neuroinflammation, rat brain
MeSH terms
Animals, Cerebrospinal Fluid, Efferent Pathways, Ependyma, Immunohistochemistry, Male, Neurons, RNA, Messenger, Stress, Physiological, Neuroimmunomodulation, Rats, Wistar, Habenula, Interleukin-18, Third Ventricle, Lateral Ventricles, Rats

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