Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/92391
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Type: Journal article
Title: Glial TLR4 signaling does not contribute to opioid-induced depression of respiration
Author: Zwicker, J.
Zhang, Y.
Ren, J.
Hutchinson, M.
Rice, K.
Watkins, L.
Greer, J.
Funk, G.
Citation: Journal of Applied Physiology, 2014; 117(8):857-868
Publisher: American Physiological Society
Issue Date: 2014
ISSN: 8750-7587
1522-1601
Statement of
Responsibility: 
Jennifer D. Zwicker, Yong Zhang, Jun Ren, Mark R. Hutchinson, Kenner C. Rice, Linda R. Watkins, John J. Greer, Gregory D. Funk
Abstract: Opioids activate glia in the central nervous system in part by activating the toll-like receptor 4 (TLR4)/myeloid differentiation 2 (MD2) complex. TLR4/MD2-mediated activation of glia by opioids compromises their analgesic actions. Glial activation is also hypothesized as pivotal in opioid-mediated reward and tolerance and as a contributor to opioid-mediated respiratory depression. We tested the contribution of TLR4 to opioid-induced respiratory depression using rhythmically active medullary slices that contain the pre-Bötzinger Complex (preBötC, an important site of respiratory rhythm generation) and adult rats in vivo. Injection with DAMGO (μ-opioid receptor agonist; 50 μM) or bath application of DAMGO (500 nM) or fentanyl (1 μM) slowed frequency recorded from XII nerves to 40%, 40%, or 50% of control, respectively. This DAMGO-mediated frequency inhibition was unaffected by preapplication of lipopolysaccharides from Rhodobacter sphaeroides (a TLR4 antagonist, 2,000 ng/ml) or (+)naloxone (1-10 μM, a TLR4-antagonist). Bath application of (-)naloxone (500 nM; a TLR4 and μ-opioid antagonist), however, rapidly reversed the opioid-mediated frequency decrease. We also compared the opioid-induced respiratory depression in slices in vitro in the absence and presence of bath-applied minocycline (an inhibitor of microglial activation) and in slices prepared from mice injected (ip) 18 h earlier with minocycline or saline. Minocycline had no effect on respiratory depression in vitro. Finally, the respiratory depression evoked in anesthetized rats by tail vein infusion of fentanyl was unaffected by subsequent injection of (+)naloxone, but completely reversed by (-)naloxone. These data indicate that neither activation of microglia in preBötC nor TLR4/MD2-activation contribute to opioid-induced respiratory depression.
Keywords: opioid; pre-Bötzinger complex; rat; respiratory depression; toll-like receptor
Rights: Copyright status unknown
RMID: 0030016373
DOI: 10.1152/japplphysiol.00534.2014
Grant ID: http://purl.org/au-research/grants/arc/DP110100297
Appears in Collections:Physiology publications

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