A lack of supersensitivity to opioid receptor agonists following chronic spinal opioid receptor antagonist administration in the rat
1. 1. Male Sprague-Dawley rats were chronically tested with intrathecal (i.t.) receptor selective opioid antagonists to determine if antinociceptive supersensitivity developed to selective i.t. opioid receptor agonists. 2. 2. A subcutaneously implanted osmotic minipump was used to deliver the μ-opio...
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Veröffentlicht in: | General pharmacology 1995, Vol.26 (1), p.161-168 |
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1. Male Sprague-Dawley rats were chronically tested with intrathecal (i.t.) receptor selective opioid antagonists to determine if antinociceptive supersensitivity developed to selective i.t. opioid receptor agonists.
2.
2. A subcutaneously implanted osmotic minipump was used to deliver the μ-opioid receptor antagonist CTOP (0.3 nmol) or the b-opioid receptor antagonist naltrindole (5.5 nmol) for 7 days.
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3. Following a 24 hr washout period, rats received a single i.t. dose (ED
50) of either DAMPGO (for CTOP-treated animals) or DPDPE (for naltrindole-treated animals) and the antinociceptive effects of the agents were tested on the tail-flick test.
4.
4. Our findings revealed that chronic spinal treatment with selective opioid receptor antagonists did not induce an antinociceptive supersensitivity to selective opioid receptor agonists.
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5. Perhaps this lack of supersensitivity is reflective of difficulties inherent to opioid receptor antagonists that do not possess negative intrinsic activity
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ISSN: | 0306-3623 1879-0011 |
DOI: | 10.1016/0306-3623(94)00154-F |