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Chronic methadone treatment shows a better cost/benefit ratio than chronic morphine in mice.慢性美沙酮治疗在小鼠中显示出比慢性吗啡更好的成本效益比。
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2
Methadone Reverses Analgesic Tolerance Induced by Morphine Pretreatment.美沙酮可逆转吗啡预处理诱导的镇痛耐受性。
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Endocytosis of the mu opioid receptor reduces tolerance and a cellular hallmark of opiate withdrawal.μ阿片受体的内吞作用可降低耐受性以及阿片类药物戒断的细胞特征。
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Morphine-induced analgesic tolerance, locomotor sensitization and physical dependence do not require modification of mu opioid receptor, cdk5 and adenylate cyclase activity.吗啡诱导的镇痛耐受性、运动敏化和身体依赖性并不需要改变μ阿片受体、cdk5和腺苷酸环化酶的活性。
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Analgesic tolerance to high-efficacy agonists but not to morphine is diminished in phosphorylation-deficient S375A μ-opioid receptor knock-in mice.在磷酸化缺陷 S375A μ 阿片受体敲入小鼠中,高效激动剂的镇痛耐受降低,但吗啡的镇痛耐受没有降低。
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本文引用的文献

1
A novel knock-in mouse reveals mechanistically distinct forms of morphine tolerance.一种新型敲入小鼠揭示了吗啡耐受的机制上不同形式。
J Pharmacol Exp Ther. 2011 Aug;338(2):633-40. doi: 10.1124/jpet.111.179754. Epub 2011 May 11.
2
Recovery from mu-opioid receptor desensitization after chronic treatment with morphine and methadone.慢性吗啡和美沙酮治疗后μ-阿片受体脱敏的恢复。
J Neurosci. 2011 Mar 23;31(12):4434-43. doi: 10.1523/JNEUROSCI.4874-10.2011.
3
Heteromerization of the μ- and δ-opioid receptors produces ligand-biased antagonism and alters μ-receptor trafficking.μ-和 δ-阿片受体的异源二聚化产生配体偏向性拮抗作用,并改变 μ-受体的转运。
J Pharmacol Exp Ther. 2011 Jun;337(3):868-75. doi: 10.1124/jpet.111.179093. Epub 2011 Mar 21.
4
Heroin-dependent inmates' experiences with buprenorphine or methadone maintenance.海洛因依赖囚犯使用丁丙诺啡或美沙酮维持治疗的体验。
J Psychoactive Drugs. 2010 Sep;42(3):339-46. doi: 10.1080/02791072.2010.10400696.
5
Rapid delivery of internalized signaling receptors to the somatodendritic surface by sequence-specific local insertion.通过序列特异性局部插入,将内化的信号转导受体快速递送到胞体树突表面。
J Neurosci. 2010 Sep 1;30(35):11703-14. doi: 10.1523/JNEUROSCI.6282-09.2010.
6
The role of beta-arrestin2 in the severity of antinociceptive tolerance and physical dependence induced by different opioid pain therapeutics.β-arrestin2 在不同阿片类药物治疗引起的镇痛耐受和躯体依赖严重程度中的作用。
Neuropharmacology. 2011 Jan;60(1):58-65. doi: 10.1016/j.neuropharm.2010.08.003. Epub 2010 Aug 14.
7
Increased abundance of opioid receptor heteromers after chronic morphine administration.慢性吗啡给药后阿片受体异源二聚体丰度增加。
Sci Signal. 2010 Jul 20;3(131):ra54. doi: 10.1126/scisignal.2000807.
8
How to design an opioid drug that causes reduced tolerance and dependence.如何设计一种导致耐受性和依赖性降低的阿片类药物。
Ann Neurol. 2010 May;67(5):559-69. doi: 10.1002/ana.22002.
9
micro-Opioid receptor endocytosis prevents adaptations in ventral tegmental area GABA transmission induced during naloxone-precipitated morphine withdrawal.μ-阿片受体内化可防止纳洛酮诱发的吗啡戒断过程中腹侧被盖区 GABA 传递的适应。
J Neurosci. 2010 Mar 3;30(9):3276-86. doi: 10.1523/JNEUROSCI.4634-09.2010.
10
The pharmacological treatment of opioid addiction--a clinical perspective.阿片类药物成瘾的药理学治疗——临床视角。
Eur J Clin Pharmacol. 2010 Jun;66(6):537-45. doi: 10.1007/s00228-010-0793-6. Epub 2010 Feb 19.

慢性美沙酮治疗在小鼠中显示出比慢性吗啡更好的成本效益比。

Chronic methadone treatment shows a better cost/benefit ratio than chronic morphine in mice.

机构信息

Ernest Gallo Clinic and Research Center, Emeryville, CA 94608, USA.

出版信息

J Pharmacol Exp Ther. 2012 Feb;340(2):386-92. doi: 10.1124/jpet.111.187583. Epub 2011 Nov 7.

DOI:10.1124/jpet.111.187583
PMID:22062352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3263965/
Abstract

Chronic treatment of pain with opiate drugs can lead to analgesic tolerance and drug dependence. Although all opiate drugs can promote tolerance and dependence in practice, the severity of those unwanted side effects differs depending on the drug used. Although each opiate drug has its own unique set of pharmacological profiles, methadone is the only clinically used opioid drug that produces substantial receptor endocytosis at analgesic doses. Here, we examined whether moderate doses of methadone carry any benefits over chronic use of equianalgesic morphine, the prototypical opioid. Our data show that chronic administration of methadone produces significantly less analgesic tolerance than morphine. Furthermore, we found significantly reduced precipitated withdrawal symptoms after chronic methadone treatment than after chronic morphine treatment. Finally, using a novel animal model with a degrading μ-opioid receptor we showed that, although endocytosis seems to protect against tolerance development, endocytosis followed by receptor degradation produces a rapid onset of analgesic tolerance to methadone. Together, these data indicated that opioid drugs that promote receptor endocytosis and recycling, such as methadone, may be a better choice for chronic pain treatment than morphine and its derivatives that do not.

摘要

慢性使用阿片类药物治疗疼痛会导致镇痛耐受和药物依赖。虽然所有阿片类药物在实践中都会促进耐受和依赖,但这些不良副作用的严重程度因药物的不同而有所差异。虽然每种阿片类药物都有其独特的药理学特征,但美沙酮是唯一一种在临床中使用的能在镇痛剂量下产生大量受体内化的阿片类药物。在这里,我们研究了在慢性使用等效镇痛剂量的吗啡的情况下,中等剂量的美沙酮是否有任何益处。我们的数据表明,慢性给予美沙酮比吗啡产生的镇痛耐受要少得多。此外,我们发现慢性美沙酮治疗后的戒断症状明显少于慢性吗啡治疗后的戒断症状。最后,我们使用一种新型具有降解 μ-阿片受体的动物模型表明,虽然内化似乎可以防止耐受的发展,但内化后受体降解会导致美沙酮迅速出现镇痛耐受。总之,这些数据表明,促进受体内化和再循环的阿片类药物,如美沙酮,可能是慢性疼痛治疗的更好选择,而不是不促进受体内化和再循环的吗啡及其衍生物。