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Biochemistry of addiction.

作者信息

Dole V P

出版信息

Annu Rev Biochem. 1970;39:821-40. doi: 10.1146/annurev.bi.39.070170.004133.

DOI:10.1146/annurev.bi.39.070170.004133
PMID:4320263
Abstract
摘要

相似文献

1
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.
2
[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.
3
Comparison of in vivo and in vitro parameters of opiate receptor binding in naive and tolerant dependent rodents.
Life Sci. 1975 Jun 15;16(12):1823-8. doi: 10.1016/0024-3205(75)90284-2.
4
Narcotic receptor sites in morphine-dependent rats.吗啡依赖大鼠体内的阿片受体位点
Nature. 1974 Mar 1;248(5443):61-3. doi: 10.1038/248061a0.
5
Possible actions of opiates upon synapses.阿片类药物对突触的可能作用。
Prog Neurobiol. 1976;3(2):81-102. doi: 10.1016/0301-0082(76)90010-1.
6
Opiate receptor mechanisms.阿片受体机制
Neurosci Res Program Bull. 1975 Feb;13(1):1-166.
7
Biochemistry of drug dependence.
Annu Rev Biochem. 1974;43(0):15-33. doi: 10.1146/annurev.bi.43.070174.000311.
8
Autoradiograhic localization of the opiate receptor in rat brain.
Life Sci. 1975 Jun 15;16(12):1849-53. doi: 10.1016/0024-3205(75)90289-1.
9
Biochemical basis for narcotic tolerance and physical dependence.麻醉耐受性和身体依赖性的生化基础。
Keio J Med. 1974 Mar;23(1):29-46. doi: 10.2302/kjm.23.29.
10
Opioids block long-term potentiation of inhibitory synapses.阿片类药物会阻断抑制性突触的长期增强。
Nature. 2007 Apr 26;446(7139):1086-90. doi: 10.1038/nature05726.

引用本文的文献

1
Opioid receptors: some perspectives from early studies of their role in normal physiology, stress responsivity, and in specific addictive diseases.阿片受体：关于其在正常生理学、应激反应性及特定成瘾性疾病中的作用的早期研究的一些观点。
Neurochem Res. 1996 Nov;21(11):1469-88. doi: 10.1007/BF02532387.
2
Decreased morphine intake by opiate addicted rats administered zimelidine, a 5-HT uptake inhibitor.给予5-羟色胺摄取抑制剂齐美利定的阿片类成瘾大鼠吗啡摄入量减少。
Psychopharmacology (Berl). 1984;82(1-2):30-5. doi: 10.1007/BF00426376.
3
The effects of acute and chronic administration of morphine on the turnover of brain and adrenal catecholamines in rats.
吗啡急性和慢性给药对大鼠脑和肾上腺儿茶酚胺代谢的影响。
Psychopharmacology (Berl). 1980;68(1):43-9. doi: 10.1007/BF00426648.
4
Stereospecific and nonspecific interactions of the morphine congener levorphanol in subcellular fractions of mouse brain.吗啡同系物左啡诺在小鼠脑亚细胞组分中的立体特异性和非特异性相互作用。
Proc Natl Acad Sci U S A. 1971 Aug;68(8):1742-7. doi: 10.1073/pnas.68.8.1742.
5
Potentiation of a non-narcotic analgesic, dipyrone, by cholinomimetic drugs.拟胆碱药对非麻醉性镇痛药安乃近的增效作用。
Psychopharmacologia. 1972;23(2):180-6. doi: 10.1007/BF00401193.
6
Morphine tolerance in a human neuroblastoma line: changes in choline acetylase and cholinesterase activities.人神经母细胞瘤系中的吗啡耐受性：胆碱乙酰化酶和胆碱酯酶活性的变化
Experientia. 1974 Feb 15;30(2):137-8. doi: 10.1007/BF01927692.
7
Prolongation of morphine anaesthesia in a patient with Gilbert's disease: report of a case.
Can Anaesth Soc J. 1973 Sep;20(5):709-12. doi: 10.1007/BF03026269.
8
Stereospecific binding of the potent narcotic analgesic (3H) Etorphine to rat-brain homogenate.强效麻醉性镇痛药（3H）埃托啡与大鼠脑匀浆的立体特异性结合。
Proc Natl Acad Sci U S A. 1973 Jul;70(7):1947-9. doi: 10.1073/pnas.70.7.1947.
9
Cellular biochemistry of narcotic analgesic drugs in the central nervous system of the rat.
Psychiatr Q. 1972;46(3):384-92. doi: 10.1007/BF01573011.
10
Psychopharmacological evidence for increase in receptor sensitivity following chronic morphine treatment.慢性吗啡治疗后受体敏感性增加的精神药理学证据。
Psychopharmacologia. 1974;38(4):287-302. doi: 10.1007/BF00429127.