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[Permeation of active morphine-like substances at their sites of antinociceptive action in the brain as a function of their lipid-solubility following intravenous and intraventricular application].

作者信息

von Cube B, Teschemacher H, Herz A, Hess R

出版信息

Naunyn Schmiedebergs Arch Pharmakol. 1970;265(5):455-73.

PMID:4190489
Abstract
摘要

相似文献

1
[Permeation of active morphine-like substances at their sites of antinociceptive action in the brain as a function of their lipid-solubility following intravenous and intraventricular application].[静脉内和脑室内给药后，活性吗啡样物质在脑内抗伤害感受作用部位的渗透与其脂溶性的关系]
Naunyn Schmiedebergs Arch Pharmakol. 1970;265(5):455-73.
2
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3
Localization of narcotic analgesics in synaptic membranes of rat brain.麻醉性镇痛药在大鼠脑突触膜中的定位。
Res Commun Chem Pathol Pharmacol. 1974 Sep;9(1):55-77.
4
Differences in the autoradiographic localization of labelled morphine-like analgesics in the mouse.小鼠体内标记的吗啡样镇痛药放射自显影定位的差异。
Acta Physiol Scand. 1973 Jun;88(2):175-82. doi: 10.1111/j.1748-1716.1973.tb05444.x.
5
[A comparison of the analgetic action of intravenously and intraventricularly injected morphine-like substances, taking into account their fat solubility].[考虑到吗啡样物质的脂溶性，对静脉注射和脑室内注射吗啡样物质的镇痛作用进行比较]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1969;263(1):199-200.
6
Blood-brain barrier: penetration of morphine, codeine, heroin, and methadone after carotid injection.血脑屏障：颈动脉注射后吗啡、可待因、海洛因和美沙酮的穿透情况
Science. 1972 Dec 1;178(4064):984-6. doi: 10.1126/science.178.4064.984.
7
Differential pharmacokinetic and metabolic profiles of the stereoisomers of 3-hydroxy-N-methyl morphinan.3-羟基-N-甲基吗啡喃立体异构体的差异药代动力学和代谢特征
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8
Stereospecific uptake of narcotic analgesics by a subcellular fraction of the guinea-pig ileum. A preliminary communication.豚鼠回肠亚细胞组分对麻醉性镇痛药的立体特异性摄取。初步报告。
Ups J Med Sci. 1973 Jul;78(3):150-2. doi: 10.3109/03009737309178620.
9
Biochemistry of addiction.成瘾的生物化学
Annu Rev Biochem. 1970;39:821-40. doi: 10.1146/annurev.bi.39.070170.004133.
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Comparison of the antinociceptive response to morphine and morphine-like compounds in male and female Sprague-Dawley rats.雄性和雌性斯普拉格-道利大鼠对吗啡及吗啡样化合物的抗伤害感受反应比较。
J Pharmacol Exp Ther. 2006 Mar;316(3):1195-201. doi: 10.1124/jpet.105.094276. Epub 2005 Nov 16.

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3
[Not Available].
[无可用内容]。
Schmerz. 1989 Sep;3(3):155-65. doi: 10.1007/BF02527398.
4
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Transdermal fentanyl: an updated review of its pharmacological properties and therapeutic efficacy in chronic cancer pain control.透皮芬太尼：其药理特性及在慢性癌痛控制中的治疗效果的最新综述
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[Peridural analgesia with high doses of fentanyl: failure of the method for early postoperative kinesitherapy in knee surgery].[高剂量芬太尼硬膜外镇痛：膝关节手术早期术后运动疗法的方法失败]
Can Anaesth Soc J. 1982 Nov;29(6):587-92. doi: 10.1007/BF03007746.
7
Antinociceptive action of bradykinin and related kinins of larger molecular weights by the intraventricular route.通过脑室内途径研究缓激肽及相关较大分子量激肽的抗伤害感受作用。
Br J Pharmacol. 1973 Mar;47(3):517-28. doi: 10.1111/j.1476-5381.1973.tb08183.x.
8
Development of tolerance to the antinociceptive effect of morphine after intraventricular injection.脑室内注射后对吗啡抗伤害感受作用耐受性的发展。
Experientia. 1973 May 1;29(1):64-5. doi: 10.1007/BF01913254.
9
Pharmacokinetics of fentanyl in man and the rabbit.芬太尼在人和兔子体内的药代动力学。
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10
Anti-nociceptive effect of morphine, opioid analgesics and haloperidol injected into the caudate nucleus of the rat.
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