Different roles of the spinal protein kinase C alpha and gamma in morphine dependence and naloxone-precipitated withdrawal.
- Author:
Jun-Li CAO
1
;
Hai-Lei DING
;
Jian-Hua HE
;
Li-Cai ZHANG
;
Jun-Ke WANG
;
Yin-Ming ZENG
Author Information
1. Department of Anesthesiology, Affiliated Hospital of First Clinical College, China Medical University, Shenyang 110001, China. caojl0310@163.com
- Publication Type:Journal Article
- MeSH:
Animals;
Male;
Morphine Dependence;
physiopathology;
Naloxone;
pharmacology;
Protein Kinase C;
metabolism;
physiology;
Protein Kinase C-alpha;
metabolism;
physiology;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Spinal Cord;
metabolism;
physiopathology;
Substance Withdrawal Syndrome;
enzymology;
physiopathology
- From:
Acta Physiologica Sinica
2005;57(2):161-168
- CountryChina
- Language:Chinese
-
Abstract:
Our previous studies showed that spinal neurons sensitization was involved in morphine withdrawal response. This study was to investigate the roles of spinal protein kinase C (PKC) alpha, gamma in morphine dependence and naloxone-precipitated withdrawal response. To set up morphine dependence model, rats were subcutaneously injected with morphine (twice a day, for 5 d). The dose of morphine was 10 mg/kg in the first day and was increased by 10 mg/kg each day. On day 6, 4 h after the injection of morphine (50 mg/kg), morphine withdrawal syndrome was precipitated by an injection of naloxone (4 mg/kg, i.p.). Chelerythrine chloride (CHE), a PKC inhibitor, was intrathecally injected 30 min before the administration of naloxone. The scores of morphine withdrawal symptom and morphine withdrawal-induced allodynia were observed. One hour after naloxone-precipitated withdrawal, Fos protein expression was assessed by immunohistochemical analysis and Western blot was used to detect the expression of cytosol and membrane fraction of PKC alpha and gamma in the rat spinal cord. The results showed that intrathecal administration of CHE decreased the scores of morphine withdrawal, attenuated morphine withdrawal-induced allodynia and also inhibited the increase of Fos protein expression in the spinal cord of morphine withdrawal rats. The expression of cytosol and membrane fraction of PKC alpha was significantly increased in the spinal cord of rats with morphine dependence. Naloxone-precipitated withdrawal induced PKC alpha translocation from cytosol to membrane fraction, which was prevented by intrathecal administration of CHE. During morphine dependence, but not naloxone-precipitated withdrawal, PKC gamma in the spinal cord translocated from cytosol to membrane fraction, and intrathecal administration of CHE did not change the expression of PKC gamma in the spinal cord of naloxone-precipitated withdrawal rats. It is suggested that up-regulation and translocation of PKC in the spinal cord contribute to morphine dependence and naloxone-precipitated withdrawal in rats and that PKC alpha and gamma play different roles in the above-mentioned effect.
