Abstract | BACKGROUND: METHODS: Anesthetized Sprague Dawley rats were divided into five groups. Group NS received 2 ml·kg-1·min-1 normal saline, group LE received 2 ml·kg-1·min-1 30% lipid emulsion and group BW received 0.1, 1.0, or 5.0 mg/kg BW373U86, a delta-opioid-receptor agonist, for 5 min. Then 0.5% bupivacaine was infused intravenously at a rate of 3.0 mg·kg-1·min-1 until asystole. The time of arrhythmia, 50% mean arterial pressure-, 50% heart rate-reduction and asystole were recorded, and the dose of bupivacaine at each time point was calculated. RESULTS: All three different doses of BW373U86 did not affect the arrhythmia, 50% mean arterial pressure-reduction, 50% heart rate-reduction and asystole dose of bupivacaine compared with group NS. 30% LE significantly increased the bupivacaine threshold of 50% mean arterial pressure-reduction (17.9 [15.4-20.7] versus 7.2 [5.9-8.7], p = 0.018), 50% heart rate-reduction (18.7 ± 4.2 versus 8.8 ± 1.7, p < 0.001) and asystole (26.5 [21.0-29.1] versus 11.3 [10.7-13.4], p = 0.008) compared with group NS. There was no difference between group LE and group NS in the arrhythmia dose of bupivacaine (9.9 [8.9-11.7] versus 5.6 [4.5-7.0], p = 0.060). CONCLUSIONS:
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Authors | Chenran Wang, Shen Sun, Jing Jiao, Xinhua Yu, Shaoqiang Huang |
Journal | BMC anesthesiology
(BMC Anesthesiol)
Vol. 22
Issue 1
Pg. 19
(01 12 2022)
ISSN: 1471-2253 [Electronic] England |
PMID | 35021986
(Publication Type: Journal Article)
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Copyright | © 2022. The Author(s). |
Chemical References |
- Anesthetics, Local
- Benzamides
- Piperazines
- Receptors, Opioid
- BW 373U86
- Bupivacaine
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Topics |
- Anesthetics, Local
(adverse effects)
- Animals
- Benzamides
(pharmacology)
- Bupivacaine
(adverse effects)
- Cardiotoxicity
(prevention & control)
- Disease Models, Animal
- Dose-Response Relationship, Drug
- Piperazines
(pharmacology)
- Rats
- Rats, Sprague-Dawley
- Receptors, Opioid
(agonists)
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