Prostaglandin E2 mediates cellular effects of interleukin-1β on parvocellular neurones in the paraventricular nucleus of the hypothalamus

被引:36
|
作者
Ferri, CC [1 ]
Ferguson, AV [1 ]
机构
[1] Queens Univ, Dept Physiol, Kingston, ON K7L 3N6, Canada
关键词
interleukin-1; prostaglandin; GABA; paraventricular nucleus; patch clamp;
D O I
10.1111/j.1365-2826.2005.01336.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Interleukin-1 beta (IL-1 beta) 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-1 beta 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-1 beta 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 mu M PGE(2), 64% of parvocellular neurones tested exhibited a clear depolarisation, which was abolished in the presence of tetrodotoxin (TTX). Furthermore, neurones responsive to both IL-1 beta and PGE(2) 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-1 beta and 1 mu M PGE(2), and these effects were maintained in TTX. Furthermore, direct hyperpolarising effects of IL-1 beta were blocked in the presence of NS-398. Together, these data suggest that PGE(2), synthesised in response to IL-1 beta-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-1 beta exerts its neuroimmune-related actions in the PVN.
引用
收藏
页码:498 / 508
页数:11
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