MEK inhibitors suppressed expression of NOS in spinal cord of morphine-induced dependent and withdrawal rats.

Hai-lin Liu; Xiang-cheng LI; Yan-ning Qiang

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MEK inhibitors suppressed expression of NOS in spinal cord of morphine-induced dependent and withdrawal rats.

Author: Hai-lin LIU ¹ ; Xiang-cheng LI ; Yan-ning QIANG
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1. Department of Anesthesiology, the 1st Hospital of Huai'an, Affiliated Hospital of Nanjing Medical University, Huai'an 223300, China.
Publication Type:Journal Article
MeSH: Animals; Behavior, Animal; drug effects; Butadienes; pharmacology; Enzyme Inhibitors; pharmacology; Extracellular Signal-Regulated MAP Kinases; metabolism; Male; Mitogen-Activated Protein Kinases; antagonists & inhibitors; Morphine; adverse effects; Morphine Dependence; metabolism; Nitric Oxide Synthase; metabolism; Nitriles; pharmacology; Rats; Rats, Sprague-Dawley; Spinal Cord; metabolism; Substance Withdrawal Syndrome; metabolism
From: Chinese Journal of Applied Physiology 2011;27(3):343-347
CountryChina
Language:Chinese
Abstract:
OBJECTIVETo explore the effects of intrathecal injection of mitogen-activated protein kinases inhibitors U0126 on the behavioral changes of morphine-induced dependent and withdrawal rats and the expression of nitric oxide synthase (NOS) in spinal cord.
METHODSAll the rats were divided into 4 groups: control group, dependent group, withdrawal group, U0126 group (5 microg). Global withdrawal score, Touch evoked agitation scores (TEA score), immunohistochemical and Western blot technique were undertaken to evaluate behavioral changes and expression of FOS, nNOS and iNOS in spinal cord respectively.
RESULTSThe results showed that intrathecal administration of U0126 significantly alleviated withdrawal symptom, withdrawal scores of U0126 group (22.5 +/- 4.09) were significantly lower than than those of withdrawal group (28.6 +/- 4.89) (P < 0.05). TEA scores of withdrawal group were 13.5 +/- 2.55, which were significantly higher than those of U0126 group (10.0 +/- 2.76, P < 0.05). Fos-like positive neurons in dorsal horn of withdrawal group were 380 +/- 71, which were higher than those of U0126 group(287 +/- 54, P < 0.05). Also nNOS and iNOS positive neurons in dorsal horn of U0126 group were 180 +/- 32, 10.8 +/- 2.8 respectively, which were significantly lower than that of withdrawal group (239 +/- 45, 16.8 +/- 5.1, P < 0.05). Compared with withdrawal group, levels of nNOS and iNOS protein in spinal cord of U0126 group were significantly lower.
CONCLUSIONMEK inhibitors could alleviate withdrawal symptom of morphine-induced dependent rats and could suppress expression of NOS in spinal cord, and extracellular signal-regulate kinase (ERK) might involve the expression of NOS in spinal cord.