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Minocycline prevents the impairment of hippocampal long-term potentiation in the septic mouse

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/71139

Title: Minocycline prevents the impairment of hippocampal long-term potentiation in the septic mouse
Other Titles: MINO prevents LTP impairment during sepsis
Authors: Hoshino, Koji Browse this author
Hayakawa, Mineji Browse this author →KAKEN DB
Morimoto, Yuji Browse this author →KAKEN DB
Keywords: Interleukin-1 beta
microglia
neuroinflammation
sepsis-associated encephalopathy
synaptic plasticity
Issue Date: Aug-2017
Publisher: Lippincott Williams & Wilkins
Journal Title: Shock
Volume: 48
Issue: 2
Start Page: 209
End Page: 214
Publisher DOI: 10.1097/SHK.0000000000000847
PMID: 28187038
Abstract: Sepsis-associated encephalopathy is a major complication during sepsis, and an effective treatment remains unknown. Although minocycline (MINO) has neuroprotective effects and is an attractive candidate for treating sepsis-associated encephalopathy, the effect of MINO on synaptic plasticity during sepsis is still unclear. In the present study, we investigated the effects of MINO on long-term potentiation (LTP) in the hippocampus in a cecal ligation and puncture (CLP) mouse model. We divided mice into four groups; sham + vehicle, sham + MINO (60 mg/kg, i.p. for 3 consecutive days before slice preparation), CLP + vehicle, and CLP + MINO. We tested LTP in the CA1 region of the hippocampus, using slices taken 24 h after surgery. Because MINO is also anti-inflammatory, LTP was analyzed following 30 min of IL-1 receptor antagonist (IL-1ra) perfusion. The endotoxin level in the blood was increased at 24 h after CLP operations regardless of MINO administrations, and LTP in the CLP + vehicle group mice was severely impaired (P < 0.05). High doses of MINO prevented the LTP impairment during sepsis in the CLP + MINO group. Interleukin (IL)-1ra administration ameliorated LTP impairment only in the CLP + vehicle group (P < 0.05); it had no additional effects on LTP in the CLP + MINO group. In conclusion, we have provided the first evidence that MINO prevents impaired LTP related to sepsis-induced encephalopathy in the mouse hippocampus, and that mechanisms associated with IL-1 receptor activity may be involved.
Rights: This is a non-final version of an article published in final form in Hoshino Koji, Hayakawa Mineji, Morimoto Yuji, Minocycline Prevents the Impairment of Hippocampal Long-Term Potentiation in the Septic Mouse, Shock: 2017, Volume 48, Issue 2, pp.209–214.
Relation: http://www.shockjournal.com
Type: article (author version)
URI: http://hdl.handle.net/2115/71139
Appears in Collections:北海道大学病院 (Hokkaido University Hospital) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 干野 晃嗣

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