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氟烷对筒箭毒碱诱导的组胺释放的抑制作用。

Inhibition of d-tubocurarine-induced histamine release by halothane.

作者信息

Kettlekamp N S, Austin D R, Downes H, Cheek D B, Hirshman C A

出版信息

Anesthesiology. 1987 May;66(5):666-9. doi: 10.1097/00000542-198705000-00012.

DOI:10.1097/00000542-198705000-00012
PMID:2437835
Abstract

To determine whether anesthetics modify mediator release, the authors measured the amount of histamine released by d-tubocurarine (dTC) in human foreskin preparations in the presence of high (2.0%) and low (0.5%) halothane concentrations and nitrous oxide (10%). Freshly excised human foreskins were divided into four matched pieces. Two matched pieces were aerated with oxygen, and the other two with an oxygen-anesthetic gas mixture. One chamber of each served as a control, while the other was stimulated with 3 X 10(-5) M d-tubocurarine for 30 min. Supernatant histamine concentrations were measured by automated fluorometry. Percent histamine release was determined by dividing the experimentally released histamine concentration by the total histamine released after the tissue was sonicated and boiled. Neither halothane nor N2O alone altered spontaneous histamine release. Histamine release by d-tubocurarine was significantly reduced by 2% halothane compared to d-tubocurarine alone (2.8% +/- 0.9 vs. 13.9% +/- 3.7, mean + SEM) (P less than 0.05) in the in vitro preparation. Histamine release was reduced in the preparations pretreated with 0.5% halothane group, but this was not statistically significant (P greater than 0.05) when compared to d-tubocurarine alone. N2O (10%) did not reduce d-tubocurarine-induced histamine release. The authors conclude that halothane, in clinically used concentrations, significantly impairs histamine release from human neonatal foreskin preparations.

摘要

为了确定麻醉剂是否会改变介质释放,作者在高浓度(2.0%)和低浓度(0.5%)氟烷以及一氧化二氮(10%)存在的情况下,测量了人包皮制剂中筒箭毒碱(dTC)释放的组胺量。将新鲜切除的人包皮分成四等份。两份用氧气通气,另外两份用氧气 - 麻醉气体混合物通气。每组中的一个腔室作为对照,另一个用3×10⁻⁵ M筒箭毒碱刺激30分钟。通过自动荧光法测量上清液中的组胺浓度。组胺释放百分比通过将实验释放的组胺浓度除以组织超声处理和煮沸后释放的总组胺浓度来确定。单独使用氟烷或一氧化二氮都不会改变组胺的自发释放。在体外制剂中,与单独使用筒箭毒碱相比,2%氟烷可使筒箭毒碱诱导的组胺释放显著降低(2.8%±0.9对13.9%±3.7,平均值±标准误)(P<0.05)。0.5%氟烷预处理组的组胺释放有所降低,但与单独使用筒箭毒碱相比,差异无统计学意义(P>0.05)。一氧化二氮(10%)不会降低筒箭毒碱诱导的组胺释放。作者得出结论,临床使用浓度的氟烷会显著损害人新生儿包皮制剂中组胺的释放。

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引用本文的文献

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Changes in the plasma histamine concentration after the administration of vecuronium bromide.注射溴化维库溴铵后血浆组胺浓度的变化。
J Anesth. 1991 Jan;5(1):24-9. doi: 10.1007/s0054010050024.
2
Potentiation of vancomycin-induced histamine release by muscle relaxants and morphine in rats.肌肉松弛剂和吗啡对大鼠万古霉素诱导组胺释放的增强作用。
Antimicrob Agents Chemother. 1999 Dec;43(12):2881-4. doi: 10.1128/AAC.43.12.2881.
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Anaphylaxis due to suxamethonium--manifested at induction of anaesthesia by bradycardia and cardiac arrest.
琥珀胆碱所致过敏反应——在麻醉诱导时表现为心动过缓和心脏骤停。
Ir J Med Sci. 1999 Apr-Jun;168(2):99-101. doi: 10.1007/BF02946473.
4
Large doses of vecuronium and plasma histamine concentrations.大剂量维库溴铵与血浆组胺浓度
Can J Anaesth. 1988 Jul;35(4):350-3. doi: 10.1007/BF03010854.