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尼莫地平降低犬异氟烷的最低肺泡浓度。

Nimodipine decreases the minimum alveolar concentration of isoflurane in dogs.

作者信息

Schwartz A E, Maneksha F R, Backus W W, Kanchuger M S, Young W L

机构信息

Department of Anesthesiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032.

出版信息

Can J Anaesth. 1991 Mar;38(2):239-42. doi: 10.1007/BF03008154.

DOI:10.1007/BF03008154
PMID:2021997
Abstract

Nimodipine is a calcium antagonist that binds with high affinity to neuronal membranes. It is a potent cerebrovasodilator and has been demonstrated also to affect neurotransmitter synthesis and release. Because patients undergoing surgery for intracranial aneurysms are frequently receiving nimodipine, the authors determined the MAC of isoflurane in six dogs before and during three infusion doses of nimodipine (0.5, 1.0 and 2.0 micrograms.kg-1.min-1). MAC was also determined in five dogs before and during infusion of the drug vehicle (10 microliters.kg-1.min-1). Nimodipine produced a reduction in MAC from 1.47 +/- 0.33% to 1.19 +/- 0.18, 1.15 +/- 0.18 and 1.15 +/- 0.09% during infusions of nimodipine 0.5, 1.0 and 2.0 micrograms.kg-1.min-1, respectively (P less than 0.05). Infusion of drug vehicle alone produced no change in MAC (1.39 +/- 0.15%). This reduction in anaesthetic requirement by nimodipine may be due to its effect on neurotransmission. Adjustments in anaesthetic dosage may be necessary in patients receiving nimodipine.

摘要

尼莫地平是一种钙拮抗剂,它能与神经元膜高亲和力结合。它是一种强效脑血管扩张剂,并且已被证明还能影响神经递质的合成与释放。由于接受颅内动脉瘤手术的患者经常使用尼莫地平,作者测定了6只狗在输注三种剂量尼莫地平(0.5、1.0和2.0微克·千克⁻¹·分钟⁻¹)之前和期间异氟烷的最低肺泡有效浓度(MAC)。还测定了5只狗在输注药物载体(10微升·千克⁻¹·分钟⁻¹)之前和期间的MAC。在输注尼莫地平0.5、1.0和2.0微克·千克⁻¹·分钟⁻¹期间,尼莫地平分别使MAC从1.47±0.33%降至1.19±0.18%、1.15±0.18%和1.15±0.09%(P<0.05)。单独输注药物载体对MAC无影响(1.39±0.15%)。尼莫地平降低麻醉需求可能是由于其对神经传递的作用。接受尼莫地平治疗的患者可能需要调整麻醉剂量。

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本文引用的文献

1
Behavioral effects of nimodipine in animals.尼莫地平对动物的行为影响。
Arzneimittelforschung. 1982;32(4):347-60.
2
Cerebrovascular effects of the calcium antagonistic dihydropyridine derivative nimodipine in animal experiments.钙拮抗二氢吡啶衍生物尼莫地平在动物实验中的脑血管效应
Arzneimittelforschung. 1982;32(4):331-8.
3
Verapamil decreases MAC for halothane in dogs.维拉帕米可降低犬类氟烷的最低肺泡有效浓度。
Anesthesiology. 1983 Oct;59(4):327-9. doi: 10.1097/00000542-198310000-00010.
4
The calcium antagonist nimodipine increases beta-endorphin release from rat hypophysis through an action on adrenal glands. An "in vivo" and "in vitro" study.钙拮抗剂尼莫地平通过作用于肾上腺增加大鼠垂体β-内啡肽的释放。一项“体内”和“体外”研究。
Pharmacol Res Commun. 1984 Oct;16(10):959-68. doi: 10.1016/s0031-6989(84)80060-0.
5
Nimodipine improves outcome when given after complete cerebral ischemia in primates.
Anesthesiology. 1985 Apr;62(4):406-14. doi: 10.1097/00000542-198504000-00007.
6
Dopamine release is enhanced while acetylcholine release is inhibited by nimodipine (Bay e 9736).尼莫地平(Bay e 9736)可增强多巴胺释放,同时抑制乙酰胆碱释放。
Acta Physiol Scand. 1986 Jan;126(1):115-9. doi: 10.1111/j.1748-1716.1986.tb07794.x.
7
Nimodipine treatment in poor-grade aneurysm patients. Results of a multicenter double-blind placebo-controlled trial.尼莫地平治疗低级别动脉瘤患者。一项多中心双盲安慰剂对照试验的结果。
J Neurosurg. 1988 Apr;68(4):505-17. doi: 10.3171/jns.1988.68.4.0505.
8
Prevention by nimodipine, a calcium entry blocker, of the effect of alpha 2-adrenoceptor blocking agents on noradrenaline release: differential effects of nimodipine, on [3H]noradrenaline and [14C]acetylcholine release measured concomitantly from the guinea-pig ileum.钙通道阻滞剂尼莫地平对α2-肾上腺素能受体阻断剂去甲肾上腺素释放作用的预防:尼莫地平对豚鼠回肠中同时测定的[3H]去甲肾上腺素和[14C]乙酰胆碱释放的不同影响。
Arch Int Pharmacodyn Ther. 1986 Dec;284(2):212-24.
9
Augmentation by calcium channel antagonists of general anaesthetic potency in mice.钙通道拮抗剂增强小鼠全身麻醉效能的作用
Br J Pharmacol. 1986 Aug;88(4):909-14. doi: 10.1111/j.1476-5381.1986.tb16265.x.
10
Pharmacological basis for the use of nimodipine in central nervous system disorders.尼莫地平用于中枢神经系统疾病的药理学基础。
FASEB J. 1989 May;3(7):1799-806.