and 120 min after injections by measuring the time that it took each vat to remove its tail from a 52C water bath. Pirenperone, at 0.08,0.16. and 0.24 mg/kg (SC) attenuated morphine-induced antinociception. In contrast, only the high ID mg/kg (SC) dose of ketanserin attenuated the effect of morphine. Because pirenperone easily enters the central nervous system whereas ketanserin does not, these results indicate the involvement of central S, receptors in morphine-induced antinociception. The 10mg/kg, dose or ketanserin. however, did not attenuate the antinociception produced by 100rmg/kg f ketamine. Thus, the antianalgesic effect of s ± receptor blockers may be specific to opioid-mediated analgesia
Is there an intrinsic antinociceptive effect to explain the analgesic benefits afforded by the α2-ad...
The effects of cholecystokinin octapeptide sulphated (CCK) and the potent CCK antagonist MK-329 (L-3...
Neuropathic pain which is a chronic pain state can be produced by injury of peripheral nerves or tis...
It is generally accepted that the neurotransmitter, serotonin mediates morphine-produced analgesia, ...
Opioid analgesics devoid of central side effects are unmet medical need in the treatment of acute pa...
It is well known that there are three types of opioid receptors, mu- (MOR), delta- (DOR), and kappa-...
Opioid analgesics devoid of central side effects are unmet medical need in the treatment of acute pa...
The potential of ketamine, an N-methyl D-aspartate (NMDA) receptor antagonist, in preventing central...
Pain not responsive to morphine is often problematic. Animal and clinical studies have suggested tha...
It has previously been reported that the noncompetitive NMDA receptor antagonists ketamine and dextr...
The roles of central catecholamines.and 5-hydroxytryptamine in morphine analgesia were investigated....
OBJECTIVE: In pain management, alternative medications are necessary due to the development of toler...
The mechanisms of involvement of the opioidergic system in the antinociceptive effect of antidepress...
We studied the effects of the inhibition of prostaglandin biosynthesis and opioid antagonism in the ...
Kappa opioid receptor (KOR) agonists have been promising therapeutic candidates, owing to their pote...
Is there an intrinsic antinociceptive effect to explain the analgesic benefits afforded by the α2-ad...
The effects of cholecystokinin octapeptide sulphated (CCK) and the potent CCK antagonist MK-329 (L-3...
Neuropathic pain which is a chronic pain state can be produced by injury of peripheral nerves or tis...
It is generally accepted that the neurotransmitter, serotonin mediates morphine-produced analgesia, ...
Opioid analgesics devoid of central side effects are unmet medical need in the treatment of acute pa...
It is well known that there are three types of opioid receptors, mu- (MOR), delta- (DOR), and kappa-...
Opioid analgesics devoid of central side effects are unmet medical need in the treatment of acute pa...
The potential of ketamine, an N-methyl D-aspartate (NMDA) receptor antagonist, in preventing central...
Pain not responsive to morphine is often problematic. Animal and clinical studies have suggested tha...
It has previously been reported that the noncompetitive NMDA receptor antagonists ketamine and dextr...
The roles of central catecholamines.and 5-hydroxytryptamine in morphine analgesia were investigated....
OBJECTIVE: In pain management, alternative medications are necessary due to the development of toler...
The mechanisms of involvement of the opioidergic system in the antinociceptive effect of antidepress...
We studied the effects of the inhibition of prostaglandin biosynthesis and opioid antagonism in the ...
Kappa opioid receptor (KOR) agonists have been promising therapeutic candidates, owing to their pote...
Is there an intrinsic antinociceptive effect to explain the analgesic benefits afforded by the α2-ad...
The effects of cholecystokinin octapeptide sulphated (CCK) and the potent CCK antagonist MK-329 (L-3...
Neuropathic pain which is a chronic pain state can be produced by injury of peripheral nerves or tis...