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重复给予吗啡、可卡因和乙醇对大鼠伏隔核和纹状体中μ和δ阿片受体密度的影响。

The effect of repeated administration of morphine, cocaine and ethanol on mu and delta opioid receptor density in the nucleus accumbens and striatum of the rat.

作者信息

Turchan J, Przewłocka B, Toth G, Lasoń W, Borsodi A, Przewłocki R

机构信息

Department of Molecular Neuropharmacology, Institute of Pharmacology, Kraków, Poland.

出版信息

Neuroscience. 1999;91(3):971-7. doi: 10.1016/s0306-4522(98)00637-x.

Abstract

The present study was carried out to evaluate the effect of morphine, cocaine and ethanol on the density of opioid receptors in the nucleus accumbens and striatum of rat brain. The animals were injected i.p. with morphine in a single dose 20 mg/kg, or twice daily for 10 days in increasing doses of 20-100 mg/kg. Cocaine was administered in a dose of 60 mg/kg/day following the "binge" paradigm, every hour for 3 h, one day (single treatment) or five days (chronic treatment). Ethanol was administered in drinking water at increasing concentrations of 1-6% v/v, for one month. As shown by receptor autoradiography, single morphine and cocaine administration did not influence the binding density of the selective ligand of delta2 receptors [3H]Ile5,6deltorphin b, but single administration of cocaine decreased binding density of a highly selective antagonist of delta receptors, [3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH. Repeated morphine administration decreased the receptor density after both ligands of the delta receptor in the nucleus accumbens after 3, 24 and 48 h, and in the striatum after 24 and 48 h. The density of [3H]Ile5,6deltorphin b binding remained unchanged in both structures following repeated cocaine administration. After repeated cocaine administration either no changes (3 h) or a decrease in the binding of [3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH in the nucleus accumbens and striatum were observed after 24 and 48 h. Ethanol did not influence the binding density of [3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH and [3H]Ile5,6deltorphin b in the nucleus accumbens and striatum at any time-point studied. In the nucleus accumbens and striatum, no changes were found in the binding density of [3H]Tyr-D-Ala-Gly-MePhe-Gly-ol following single or repeated morphine administration. At 3 h after single or repeated "binge" cocaine administration, the binding of [3H]Tyr-D-Ala-Gly-MePhe-Gly-ol was not changed in either structure, but after 24 h the density of mu opioid receptors was decreased in both structures. Ethanol given to rats in drinking water decreased the binding of [3H]Tyr-D-Ala-Gly-MePhe-Gly-ol at the time of exposure to ethanol, yet in the nucleus accumbens only. Ethanol withdrawal decreased the density of the mu receptor in both structures after 24, 48 and 96 h. The above data indicate that repeated administration of morphine evokes a long-lasting down-regulation of the density of delta1 and delta2 opioid receptors, whereas cocaine affects in a similar way only the delta1 subtype in the nucleus accumbens, and to a lesser extent in the striatum. A long-term intake of ethanol solution down-regulates mu opioid receptors in both structures, but has no effect on any type of delta receptors. Thus changes in the particular opioid receptor depend on the type of drug used. Furthermore, the most profound changes are observed after late withdrawal, which may play some role in maintaining the state of dependence.

摘要

本研究旨在评估吗啡、可卡因和乙醇对大鼠脑海马核和纹状体中阿片受体密度的影响。动物腹腔注射单次剂量20mg/kg的吗啡,或每日两次、连续10天注射剂量递增(20 - 100mg/kg)的吗啡。可卡因按照“暴饮暴食”模式,以60mg/kg/天的剂量给药,每小时给药一次,持续3小时,给药一天(单次治疗)或五天(慢性治疗)。乙醇以1 - 6% v/v浓度递增的方式添加到饮用水中,持续给药一个月。受体放射自显影结果显示,单次注射吗啡和可卡因不影响δ2受体选择性配体[3H]Ile5,6deltorphin b的结合密度,但单次注射可卡因会降低δ受体高选择性拮抗剂[3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH的结合密度。重复注射吗啡后,在3小时、24小时和48小时,海马核中δ受体的两种配体结合后的受体密度降低,在24小时和48小时纹状体中的受体密度也降低。重复注射可卡因后,[3H]Ile5,6deltorphin b在两种结构中的结合密度均保持不变。重复注射可卡因后,在24小时和48小时,海马核和纹状体中要么没有变化(3小时),要么[3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH的结合减少。在研究的任何时间点,乙醇均不影响海马核和纹状体中[3H]H-Tyr-Tic psi[CH2-NH]Phe-Phe-OH和[3H]Ile5,6deltorphin b的结合密度。在海马核和纹状体中,单次或重复注射吗啡后,[3H]Tyr-D-Ala-Gly-MePhe-Gly-ol的结合密度未发生变化。单次或重复“暴饮暴食”注射可卡因后3小时,两种结构中[3H]Tyr-D-Ala-Gly-MePhe-Gly-ol的结合均未改变,但24小时后两种结构中μ阿片受体的密度均降低。给大鼠饮用含乙醇的水,在接触乙醇时,仅海马核中[3H]Tyr-D-Ala-Gly-MePhe-Gly-ol的结合减少。乙醇戒断后24小时、48小时和96小时,两种结构中μ受体的密度均降低。上述数据表明,重复注射吗啡会引起δ1和δ2阿片受体密度的长期下调,而可卡因仅以类似方式影响海马核中的δ1亚型,对纹状体的影响较小。长期摄入乙醇溶液会下调两种结构中的μ阿片受体,但对任何类型的δ受体均无影响。因此,特定阿片受体的变化取决于所用药物的类型。此外,在后期戒断后观察到最显著的变化,这可能在维持依赖状态中起一定作用。

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