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[Enhancement of nociceptive reactions by naloxone in mice and rats (author's transl)].

作者信息

Jacob J J, Tremblay E C, Colombel M C

出版信息

Psychopharmacologia. 1974 Jul 11;37(3):217-23. doi: 10.1007/BF00421535.

DOI:10.1007/BF00421535
PMID:4848652
Abstract
摘要

相似文献

1
[Enhancement of nociceptive reactions by naloxone in mice and rats (author's transl)].纳洛酮对小鼠和大鼠伤害性反应的增强作用（作者译）
Psychopharmacologia. 1974 Jul 11;37(3):217-23. doi: 10.1007/BF00421535.
2
[The dependence of the effects of naloxone on the type of nociceptive stimulus].[纳洛酮作用对伤害性刺激类型的依赖性]
Eksp Klin Farmakol. 1994 Jan-Feb;57(1):15-7.
3
Intracerebroventricular naloxone produces a dose-dependent, monotonic increase in nociceptive threshold in the rat.脑室内注射纳洛酮会使大鼠的痛阈产生剂量依赖性的单调增加。
Brain Res. 1990 May 7;515(1-2):323-5. doi: 10.1016/0006-8993(90)90616-j.
4
Buprenorphine in combination with naloxone at a ratio of 15:1 does not enhance antinociception from buprenorphine in healthy cats.丁丙诺啡与纳洛酮以 15:1 的比例联合使用不会增强健康猫体内丁丙诺啡的镇痛作用。
Vet J. 2012 Jun;192(3):523-4. doi: 10.1016/j.tvjl.2011.09.008. Epub 2011 Oct 24.
5
Naloxone prolongs cutaneous nociceptive block by lidocaine in rats.纳洛酮可延长利多卡因对大鼠皮肤伤害性阻滞的作用时间。
Fundam Clin Pharmacol. 2017 Dec;31(6):636-642. doi: 10.1111/fcp.12302. Epub 2017 Jul 24.
6
Lumbar intrathecal administration of naloxone antagonizes analgesia produced by electrical stimulation of the hypothalamic arcuate nucleus in pentobarbital-anesthetized rats.在戊巴比妥麻醉的大鼠中，腰椎鞘内注射纳洛酮可拮抗下丘脑弓状核电刺激所产生的镇痛作用。
Neuropharmacology. 1990 Dec;29(12):1123-9. doi: 10.1016/0028-3908(90)90036-q.
7
Continuous intravenous infusion of naloxone does not change behavioral, cardiovascular, or inflammatory responses to subcutaneous formalin in the rat.
Pain. 1997 Jan;69(1-2):171-7. doi: 10.1016/s0304-3959(96)03265-4.
8
[Neurophysiological and neuropharmacological studies on (possible) mechanisms of peripheral stimulation analgesia (author's transl)].关于外周刺激镇痛（可能的）机制的神经生理学和神经药理学研究（作者译）
Wien Klin Wochenschr Suppl. 1980;113:1-21.
9
Effect of transient naloxone antagonism on tolerance development in rats receiving continuous spinal morphine infusion.短暂纳洛酮拮抗作用对持续脊髓内注入吗啡的大鼠耐受性形成的影响。
Pain. 1997 Apr;70(2-3):125-32. doi: 10.1016/s0304-3959(96)03283-6.
10
[Analgetic and antipyretic activity of SL-573 (author's transl)].SL-573的镇痛和解热活性（作者译）
Nihon Yakurigaku Zasshi. 1978 Sep;74(6):735-47. doi: 10.1254/fpj.74.735.

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Egg White Hydrolysate as a functional food ingredient to prevent cognitive dysfunction in rats following long-term exposure to aluminum.蛋清水解物作为一种功能性食品成分，可预防长期暴露于铝后大鼠的认知功能障碍。
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Aluminum Exposure at Human Dietary Levels for 60 Days Reaches a Threshold Sufficient to Promote Memory Impairment in Rats.

本文引用的文献

1
N-Allylnoroxy-morphone: a new potent narcotic antagonist.N-烯丙基去氧吗啡：一种新型强效麻醉拮抗剂。
Am J Med Sci. 1963 Jan;245:23-30.
2
The human pharmacology and abuse potential of N-allylnoroxymorphone (naloxone).N-烯丙基去甲羟吗啡酮（纳洛酮）的人体药理学及滥用可能性
J Pharmacol Exp Ther. 1967 Aug;157(2):420-6.
3
Kinetic parameters of narcotic agonists and antagonists, with particular reference to N-allylnoroxymorphone (naloxone).麻醉性激动剂和拮抗剂的动力学参数，尤其涉及N-烯丙基去甲羟吗啡酮（纳洛酮）。
人类饮食水平的铝暴露60天达到足以促进大鼠记忆障碍的阈值。
Neurotox Res. 2017 Jan;31(1):20-30. doi: 10.1007/s12640-016-9656-y. Epub 2016 Jul 29.
4
A critical analysis of the experimental evaluation of nociceptive reactions in animals.对动物伤害性反应的实验评估的批判性分析。
Pharm Res. 1986 Oct;3(5):263-70. doi: 10.1023/A:1016355200944.
5
Phytochemical characterization and antinociceptive effect of Lippia gracilis Schauer.香根草的植物化学特征及镇痛作用。
J Nat Med. 2012 Jul;66(3):428-34. doi: 10.1007/s11418-011-0601-3. Epub 2011 Oct 22.
6
[Oral administration of slow-release naloxone for prevention of constipation but not analgesia following oral morphine.].口服缓释纳洛酮预防口服吗啡后的便秘而非镇痛作用。
Schmerz. 1993 Dec;7(4):314-21. doi: 10.1007/BF02529868.
7
Nociceptive flexion reflex and pain rating responses during endogenous opiate blockade with naltrexone in healthy young adults.健康年轻成年人在使用纳曲酮进行内源性阿片类药物阻断期间的伤害性屈曲反射和疼痛评分反应。
Biol Psychol. 2007 Apr;75(1):95-100. doi: 10.1016/j.biopsycho.2006.12.005. Epub 2006 Dec 27.
8
The four-plates test-retest paradigm to discriminate anxiolytic effects.用于区分抗焦虑作用的四板重复测试范式。
Psychopharmacology (Berl). 2005 Jun;180(1):73-83. doi: 10.1007/s00213-004-2130-1. Epub 2005 Jan 26.
9
Effects of morphine and naloxone on behaviour in the hot plate test: an ethopharmacological study in the rat.吗啡和纳洛酮对热板试验中大鼠行为的影响：一项大鼠行为药理学研究
Psychopharmacology (Berl). 1994 Jan;113(3-4):500-10. doi: 10.1007/BF02245230.
10
Model of opiate dependence in the guinea-pig isolated ileum.豚鼠离体回肠阿片类药物依赖模型。
Br J Pharmacol. 1981 Aug;73(4):921-32. doi: 10.1111/j.1476-5381.1981.tb08747.x.
Br J Pharmacol Chemother. 1968 Jun;33(2):266-76. doi: 10.1111/j.1476-5381.1968.tb00988.x.
4
Profiles of activity in rodents of some narcotic and narcotic antagonists drugs.某些麻醉药和麻醉拮抗药在啮齿动物体内的活性概况。
Nature. 1969 Nov 8;224(5219):610-2. doi: 10.1038/224610a0.
5
Drug interaction in the field of analgesic drugs.镇痛药领域的药物相互作用。
Proc R Soc Med. 1965 Nov;58(11 Part 2):978-83. doi: 10.1177/003591576505811P207.
6
Effects of morphine, nalorphine, cyclazocine, and naloxone on the flexor reflex.吗啡、烯丙吗啡、环唑辛和纳洛酮对屈肌反射的影响。
Int J Neuropharmacol. 1967 Mar;6(2):89-98. doi: 10.1016/0028-3908(67)90057-3.
7
Failure of an opiate to protect mice against naloxone-precipitated withdrawal.阿片类药物未能保护小鼠免受纳洛酮诱发的戒断反应。
J Pharmacol Exp Ther. 1972 Aug;182(2):189-94.
8
Potential usefulness of single-dose acute physical dependence on and tolerance to morphine for the evaluation of narcotic antagonists.单剂量急性吗啡身体依赖性和耐受性在麻醉性拮抗剂评价中的潜在用途。
Adv Biochem Psychopharmacol. 1973;8(0):299-318.
9
Acute physical dependence in the waking dog after a single low dose of morphine.单次低剂量吗啡给药后清醒犬的急性身体依赖性。
Psychol Med. 1974 Aug;4(3):270-3. doi: 10.1017/s0033291700042951.
10
Opiate agonists and antagonists discriminated by receptor binding in brain.通过大脑中的受体结合来区分的阿片类激动剂和拮抗剂。
Science. 1973 Dec 28;182(4119):1359-61. doi: 10.1126/science.182.4119.1359.