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Splenic autonomic denervation increases inflammatory status but does not aggravate atherosclerotic lesion development.

Authors :
Kooijman S
Meurs I
van Beek L
Khedoe PP
Giezekamp A
Pike-Overzet K
Cailotto C
van der Vliet J
van Harmelen V
Boeckxstaens G
Berbée JF
Rensen PC
Source :
American journal of physiology. Heart and circulatory physiology [Am J Physiol Heart Circ Physiol] 2015 Aug 15; Vol. 309 (4), pp. H646-54. Date of Electronic Publication: 2015 Jun 19.
Publication Year :
2015

Abstract

Unlabelled: The brain plays a prominent role in the regulation of inflammation. Immune cells are under control of the so-called cholinergic anti-inflammatory reflex, mainly acting via autonomic innervation of the spleen. Activation of this reflex inhibits the secretion of proinflammatory cytokines and may reduce the development of atherosclerosis. Therefore, the aim of this study was to evaluate the effects of selective parasympathetic (Px) and sympathetic (Sx) denervation of the spleen on inflammatory status and atherosclerotic lesion development. Female APOE*3-Leiden.CETP mice, a well-established model for human-like lipid metabolism and atherosclerosis, were fed a cholesterol-containing Western-type diet for 4 wk after which they were subdivided into three groups receiving either splenic Px, splenic Sx, or sham surgery. The mice were subsequently challenged with the same diet for an additional 15 wk. Selective Px increased leukocyte counts (i.e., dendritic cells, B cells, and T cells) in the spleen and increased gene expression of proinflammatory cytokines in the liver and peritoneal leukocytes compared with Sx and sham surgery. Both Px and Sx increased circulating proinflammatory cytokines IL-1β and IL-6. However, the increased proinflammatory status in denervated mice did not affect atherosclerotic lesion size or lesion composition.<br />Conclusion: Predominantly selective Px of the spleen enhances the inflammatory status, which, however, does not aggravate diet-induced atherosclerotic lesion development.<br /> (Copyright © 2015 the American Physiological Society.)

Details

Language :
English
ISSN :
1522-1539
Volume :
309
Issue :
4
Database :
MEDLINE
Journal :
American journal of physiology. Heart and circulatory physiology
Publication Type :
Academic Journal
Accession number :
26092978
Full Text :
https://doi.org/10.1152/ajpheart.00787.2014