Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/123786
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Toll-like receptor-4 antagonist (+)-naloxone confers sexually dimorphic protection from inflammation-induced fetal programming in mice
Author: Chin, P.Y.
Dorian, C.
Sharkey, D.J.
Hutchinson, M.R.
Rice, K.C.
Moldenhauer, L.M.
Robertson, S.A.
Citation: Endocrinology, 2019; 160(11):2646-2662
Publisher: Oxford University Press
Issue Date: 2019
ISSN: 0013-7227
1945-7170
Statement of
Responsibility: 
Peck Yin Chin, Camilla Dorian, David J. Sharkey, Mark R. Hutchinson, Kenner C. Rice, Lachlan M. Moldenhauer, and Sarah A. Robertson
Abstract: Inflammation elicited by infection or non-infectious insults during gestation induces pro-inflammatory cytokines that can shift the trajectory of development to alter offspring phenotype, promote adiposity and increase susceptibility to metabolic disease in later life. Here we utilize mice to investigate the utility of a small molecule TLR4 antagonist (+)-naloxone, the non-opioid isomer of the opioid receptor antagonist (-)-naloxone, for mitigating altered fetal metabolic programming induced by a modest systemic inflammatory challenge in late gestation. In adult progeny exposed to LPS challenge in utero, male but not female offspring exhibited elevated adipose tissue, reduced muscle mass and elevated plasma leptin at 20 weeks of age. Effects were largely reversed by co-administration of (+)-naloxone following LPS. When given alone without LPS, (+)-naloxone elicited accelerated post-weaning growth and elevated muscle and fat mass in adult male but not female offspring. LPS induced expression of inflammatory cytokines Il1a, Il1b, Il6, Tnf and Il10 in fetal brain, placental and uterine tissues, and (+)-naloxone suppressed LPS-induced cytokine expression. Fetal sex-specific regulation of cytokine expression was evident, with higher Il1a, Il1b, Il6 and Il10 induced by LPS in tissues associated with male fetuses, and greater suppression by (+)-naloxone of Il6 in females. These data demonstrate that modulating TLR4 signaling with (+)-naloxone provides protection from inflammatory diversion of fetal developmental programming in utero, associated with attenuation of gestational tissue cytokine expression in a fetal sex-specific manner. The results suggest that pharmacologic interventions targeting TLR4 warrant evaluation for attenuating developmental programming effects of fetal exposure to maternal inflammatory mediators.
Keywords: Animals
Mice, Inbred C57BL
Prenatal Exposure Delayed Effects
Naloxone
Lipopolysaccharides
Cytokines
Fetal Development
Pregnancy
Sex Characteristics
Female
Male
Toll-Like Receptor 4
Adipokines
Rights: © 2019 Endocrine Society
DOI: 10.1210/en.2019-00493
Grant ID: http://purl.org/au-research/grants/nhmrc/1026178
http://purl.org/au-research/grants/nhmrc/465423
http://purl.org/au-research/grants/arc/DP110100297
Appears in Collections:Aurora harvest 8
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.