Abstract | AIMS: MAIN METHODS: Two intrathecal (i.t.) catheters were implanted in male Wistar rats for drug delivery. One was linked to a mini-osmotic pump for morphine or saline infusion. On the seventh day, 50μg of melatonin or vehicle was injected through the other catheter instantly after discontinuation of morphine or saline infusion; 3h later, 15μg of morphine or saline was injected. The antinociceptive response was then measured using the tail-flick test every 30min for 120min. KEY FINDINGS: The results showed that chronic morphine infusion elicited antinociceptive tolerance and upregulated heat shock protein 27 (HSP27) expression in the dorsal horn of the rat spinal cord. Melatonin pretreatment partially restored morphine's antinociceptive effect in morphine-tolerant rats and reversed morphine-induced HSP27 upregulation. In addition, chronic morphine infusion induced microglial cell activation and was reversed by melatonin treatment. SIGNIFICANCE:
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Authors | Sheng-Hsiung Lin, Ya-Ni Huang, Jen-Hsin Kao, Lu-Tai Tien, Ru-Yin Tsai, Chih-Shung Wong |
Journal | Life sciences
(Life Sci)
Vol. 152
Pg. 38-43
(May 01 2016)
ISSN: 1879-0631 [Electronic] Netherlands |
PMID | 27012766
(Publication Type: Journal Article)
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Copyright | Copyright © 2016 Elsevier Inc. All rights reserved. |
Chemical References |
- Analgesics, Opioid
- HSP27 Heat-Shock Proteins
- Hspb1 protein, rat
- Morphine
- Melatonin
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Topics |
- Analgesics, Opioid
(pharmacology)
- Animals
- Drug Tolerance
- Gene Expression Regulation
(drug effects)
- HSP27 Heat-Shock Proteins
(agonists, biosynthesis)
- Injections, Spinal
- Macrophage Activation
(drug effects)
- Male
- Melatonin
(pharmacology)
- Microglia
(drug effects)
- Morphine
(pharmacology)
- Pain Measurement
(drug effects)
- Rats
- Rats, Wistar
- Up-Regulation
(drug effects)
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