The effects of alfentanil pretreatment on vascular pain and cardiovascular response associated with intravenous / 대한마취과학회지

BACKGROUND: The intravenous injection of rocuronium bromide is often painful, and different methods have been used to minimize the incidence and severity of this pain. This study determined the effective dose of alfentanil to minimize the injection pain of rocuronium and the cardiovascular response after endotracheal intubation. METHODS: Eighty ASA physical status 1 and 2 adult patients were divided into four groups. Sixty seconds before administering rocuronium 0.6 mg/kg, the groups were given 10 ml of intravenous normal saline or alfentanil 10, 15, and 20microgram/kg. Pain was assessed after rocuronium injection. The mean arterial pressure and heart rate were measured before induction and before and after intubation. RESULTS: Both 15 and 20microgram/kg alfentanil minimized the rocuronium injection pain, although 20microgram/kg alfentanil caused an undesirable decrease in the mean arterial pressure. CONCLUSIONS: A 15microgram/kg bolus of alfentanil may be useful for minimizing the rocuronium injection pain and blunting the cardiovascular response after endotracheal intubation.

Potentiation of Morphine's Antinociception by Group II and Group III Metabotropic Glutamate Receptors Agonists on a Rat Incisional Pain / 대한통증학회지

BACKGROUND: The aim of this study was to clarify the role of spinal groups II and III metabotropic glutamate receptors (mGluRs) with respect to postoperative pain at the spinal level. In addition, the nature of the pharmacological interaction between groups II and III mGluRs agonists and morphine was determined. METHODS: Catheters were inserted into the intrathecal space of male SD rats. To induce postoperative pain, an incision was made in the plantar surface of the hind paw. A pharmacological characteristic for the interaction between groups II and III mGluRs agonists and morphine was evaluated using a fixed-dose analysis. RESULTS: None of intrathecal group II and III mGluRs agonists modified the withdrawal threshold of the incisional pain. The administration of intrathecal morphine resulted in an increase of a dose dependent withdrawal threshold. A fixed-dose analysis revealed that the group III mGluRs agonist, ACPT-III, increased the antinociceptive action of morphine, while the group II mGluRs agonist, APDC, had no effect the antinociception of morphine. CONCLUSIONS: These results suggest that group II and III mGluRs may not play a direct modulatory role in the processing of postoperative pain at the spinal level. However, agonizing group III mGluRs may indirectly contributable to the potentiation of morphines antinociception in the spinal cord. Thus, the combination of morphine and a group III mGluRs agonist may be useful in the management of spinal postoperative pain.