Blockade and reversal of spinal morphine tolerance by peptide and non-peptide calcitonin gene-related peptide receptor antagonists
Article first published online: 29 JAN 2009
2000 British Pharmacological Society
British Journal of Pharmacology
Volume 131, Issue 5, pages 875–884, November 2000
How to Cite
Powell, K. J., Ma, W., Sutak, M., Doods, H., Quirion, R. and Jhamandas, K. (2000), Blockade and reversal of spinal morphine tolerance by peptide and non-peptide calcitonin gene-related peptide receptor antagonists. British Journal of Pharmacology, 131: 875–884. doi: 10.1038/sj.bjp.0703655
- Issue published online: 29 JAN 2009
- Article first published online: 29 JAN 2009
- (Received July 15, 2000, Revised August 9, 2000, Accepted August 10, 2000)
- Morphine tolerance;
- calcitonin gene-related peptide;
- spinal cord;
This study examined the effects of the peptide CGRP receptor antagonist CGRP8-37 and the newly-developed non-peptide CGRP receptor antagonist BIBN4096BS for their potential to both inhibit the development and reverse tolerance to the antinociceptive action of morphine.
Repeated administration of intrathecal morphine (15 μg), once daily, produced a progressive decline of antinociceptive effect and an increase in the ED50 value in the tailflick and paw pressure tests. Co-administration of CGRP8-37 (4 μg) or BIBN4096BS (0.05, 0.1 μg) with morphine (15 μg) prevented the decline of antinociceptive effect and increase in ED50 value in the tailflick test. Intrathecal administration of the CGRP receptor antagonists did not alter the baseline responses in either tests. Acute CGRP8-37 also did not potentiate the acute actions of spinal morphine.
In animals rendered tolerant to intrathecal morphine, subsequent administration of CGRP8-37 (4 μg) with morphine (15 μg) partially restored the antinociceptive effect and ED50 value of acute morphine, reflecting the reversal of tolerance.
Animals tolerant to intrathecal morphine expressed increased CGRP and substance P-like immunostaining in the dorsal horn of the spinal cord. The increase in CGRP, but not substance P-like immunostaining, was blocked by a co-treatment with CGRP8-37 (4 μg). In animals already tolerant to morphine, the increase in CGRP but not substance P-like immunostaining was partially reversed by CGRP8-37 (4 μg).
These data suggest that activation of spinal CGRP receptors contributes to both the development and expression of spinal opioid tolerance. CGRP receptor antagonists may represent a useful therapeutic approach for preventing as well as reversing opioid tolerance.
British Journal of Pharmacology (2000) 131, 875–884; doi:10.1038/sj.bjp.0703655