Prostaglandin E2 Mediates Cellular Effects of Interleukin-1beta on Parvocellular Neurones in the Paraventricular Nucleus of the Hypothalamus
- 1 August 2005
- journal article
- research article
- Published by Wiley in Journal of Neuroendocrinology
- Vol. 17 (8) , 498-508
- https://doi.org/10.1111/j.1365-2826.2005.01336.x
Abstract
Interleukin-1beta (IL-1beta) is involved in hypothalamic regulation of corticotrophin-releasing hormone secretion, autonomic activation and consequent downstream modulation of the neuroimmune response. Previously, we have shown that IL-1beta depolarises parvocellular neurones in the paraventricular nucleus (PVN) of the hypothalamus, and these effects are dependent on attenuation of gamma-amino butyric acid (GABA)-ergic input. In the present study, using whole-cell patch clamp recordings of rat neurones in a slice preparation of the PVN, we show that the effects of IL-1beta are abolished in the presence of a cyclooxygenase (COX)-2 inhibitor, NS-398, indicating a dependence on prostaglandin (PG) synthesis and activation. In response to 1 microM PGE2, 64% of parvocellular neurones tested exhibited a clear depolarisation, which was abolished in the presence of tetrodotoxin (TTX). Furthermore, neurones responsive to both IL-1beta and PGE2 exhibited a decrease in the frequency of inhibitory post-synaptic potentials, suggesting that effects of these modulators are mediated via a decrease in GABA-ergic input to these neurones. A proportion (44% and 40%, respectively) of putative GABA-ergic neurones in the halo region surrounding the PVN demonstrated hyperpolarising responses to 1 nM IL-1beta and 1 microM PGE2, and these effects were maintained in TTX. Furthermore, direct hyperpolarising effects of IL-1beta were blocked in the presence of NS-398. Together, these data suggest that PGE2, synthesised in response to IL-1beta-activation of COX-2 expressing cells, directly hyperpolarises putative GABA-ergic neurones in the halo zone surrounding and projecting to the PVN, resulting in a decrease in GABA-ergic input to parvocellular neurones and consequent depolarisation. These data further elucidate the cellular mechanisms by which IL-1beta exerts its neuroimmune-related actions in the PVN.Keywords
This publication has 44 references indexed in Scilit:
- Rat brain vascular distribution of interleukin‐1 type‐1 receptor immunoreactivity: Relationship to patterns of inducible cyclooxygenase expression by peripheral inflammatory stimuliJournal of Comparative Neurology, 2004
- Corticotropin releasing hormone receptors: two decades laterPeptides, 2004
- Induction of microsomal prostaglandin E synthase in the rat brain endothelium and parenchyma in adjuvant‐induced arthritisJournal of Comparative Neurology, 2002
- Electrophysiological and morphological properties of pre‐autonomic neurones in the rat hypothalamic paraventricular nucleusThe Journal of Physiology, 2001
- CYCLOOXYGENASES 1 AND 2Annual Review of Pharmacology and Toxicology, 1998
- C-fos mRNA pattern and corticotropin-releasing factor neuronal activity throughout the brain of rats injected centrally with a prostaglandin of E2 typeJournal of Neuroimmunology, 1996
- Lesions of the Afferent Catecholaminergic Pathways Inhibit the Temporal Activation of the CRH and POMC Gene Expression and ACTH Release Induced by Human Interleukin-1 ? in the Male RatNeuroendocrinology, 1995
- Effects of Intravenous Administration of Interleukin-1-Beta on the Release of Prostaglandin E2, Corticotropin-Releasing Factor, and Arginine Vasopressin in Several Hypothalamic Areas of Freely Moving Rats: Estimation by Push-Pull PerfusionNeuroendocrinology, 1994
- Hypothalamic Integration: Organization of the Paraventricular and Supraoptic NucleiAnnual Review of Neuroscience, 1983
- Organization of Ovine Corticotropin-Releasing Factor Immunoreactive Cells and Fibers in the Rat Brain: An Immunohistochemical StudyNeuroendocrinology, 1983