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本文引用的文献

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Phenylpiperazine derivatives with selectivity for dopamine D3 receptors modulate cocaine self-administration in rats.苯哌嗪衍生物对多巴胺 D3 受体具有选择性,可调节大鼠可卡因的自我给药。
Neuropharmacology. 2012 Dec;63(8):1346-59. doi: 10.1016/j.neuropharm.2012.08.011. Epub 2012 Aug 31.
2
Synthesis and pharmacological evaluation of fluorine-containing D₃ dopamine receptor ligands.含氟 D₃ 多巴胺受体配体的合成与药理学评价。
J Med Chem. 2011 Mar 24;54(6):1555-64. doi: 10.1021/jm101323b. Epub 2011 Feb 24.
3
Yawning and locomotor behavior induced by dopamine receptor agonists in mice and rats.多巴胺受体激动剂在小鼠和大鼠中诱发的打哈欠及运动行为。
Behav Pharmacol. 2010 May;21(3):171-81. doi: 10.1097/FBP.0b013e32833a5c68.
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Dopamine receptor expression and distribution dynamically change in the rat nucleus accumbens after withdrawal from cocaine self-administration.可卡因自我给药戒断后大鼠伏隔核多巴胺受体表达和分布的动态变化。
Neuroscience. 2010 Aug 11;169(1):182-94. doi: 10.1016/j.neuroscience.2010.04.056. Epub 2010 May 7.
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Current perspectives on selective dopamine D(3) receptor antagonists as pharmacotherapeutics for addictions and related disorders.当前对选择性多巴胺 D(3)受体拮抗剂作为成瘾和相关障碍的药物治疗的看法。
Ann N Y Acad Sci. 2010 Feb;1187:4-34. doi: 10.1111/j.1749-6632.2009.05149.x.
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[3H]4-(dimethylamino)-N-(4-(4-(2-methoxyphenyl)piperazin-1-yl) butyl)benzamide: a selective radioligand for dopamine D(3) receptors. II. Quantitative analysis of dopamine D(3) and D(2) receptor density ratio in the caudate-putamen.[3H]4-(二甲基氨基)-N-(4-(4-(2-甲氧基苯基)哌嗪-1-基)丁基)苯甲酰胺:多巴胺 D(3)受体的选择性放射性配体。Ⅱ.纹状体中多巴胺 D(3)和 D(2)受体密度比值的定量分析。
Synapse. 2010 Jun;64(6):449-59. doi: 10.1002/syn.20748.
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8
Ventral striatal neurons encode the value of the chosen action in rats deciding between differently delayed or sized rewards.在大鼠决定选择不同延迟或大小的奖励时,腹侧纹状体神经元对所选行动的价值进行编码。
J Neurosci. 2009 Oct 21;29(42):13365-76. doi: 10.1523/JNEUROSCI.2572-09.2009.
9
Neurocircuitry of addiction.成瘾的神经回路。
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10
Cocaine-induced Fos expression is detectable in the frontal cortex and striatum of rats under isoflurane but not alpha-chloralose anesthesia: implications for FMRI.在异氟烷麻醉而非氯醛糖麻醉下,可在大鼠额叶皮质和纹状体中检测到可卡因诱导的Fos表达:对功能磁共振成像的启示。
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对多巴胺 D3 偏好的苯哌嗪类药物与可卡因联合使用和不联合使用时 Fos 表达的影响。

Fos expression in response to dopamine D3-preferring phenylpiperazine drugs given with and without cocaine.

机构信息

Department of Psychology, Arizona State University, Tempe, Arizona, 85287; School of Life Sciences, Arizona State University, Tempe, Arizona, 85287.

出版信息

Synapse. 2013 Dec;67(12):847-55. doi: 10.1002/syn.21691. Epub 2013 Jul 17.

DOI:10.1002/syn.21691
PMID:23766142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4041163/
Abstract

WC 44 and WC 10 are phenylpiperazines with low (23 fold) to moderate (42 fold) selectivity for dopamine D3 receptors (D3Rs) over D2Rs, respectively. WC 44 is a full D3R agonist in the forskolin-stimulated adenylyl cyclase (AC) assay, whereas WC 10 has little efficacy. In contrast to their opposite effects in the AC assay, these drugs often produce similar behavioral effects, suggesting that the AC assay does not predict the efficacy of these drugs in vivo. Here, we examined whether Fos protein expression induced by these drugs would be more consistent with their behavioral effects in vivo. Rats received either vehicle, WC 10 (5.6 mg/kg, i.p.), WC 44 (10.0 mg/kg, i.p), cocaine (10.0 mg/kg, i.p.), or cocaine with WC 10 (5.6 mg/kg, i.p.) or with WC 44 (10.0 mg/kg, i.p). Locomotion was monitored for 90 min and the brains were harvested for immunohistochemistry. Both WC 10 and WC 44 decreased spontaneous and cocaine-induced locomotion. Both compounds also increased Fos expression relative to saline in the dorsal striatum and nucleus accumbens core and shell, and relative to cocaine alone in the nucleus accumbens shell. The findings suggest that even though these compounds have different efficacy in the AC bioassy, they produce similar brain activation and attenuation of cocaine hyperlocomotion. Together with our previous research demonstrating that these compounds down-shift the cocaine self-administration dose-effect function, the findings support the idea that D3R-selective compounds may be useful for cocaine dependence medications development.

摘要

WC 44 和 WC 10 是苯哌嗪类化合物,对多巴胺 D3 受体 (D3R) 的选择性分别为低 (23 倍) 和中度 (42 倍),而对 D2R 的选择性较低。在福斯高林刺激的腺苷酸环化酶 (AC) 测定中,WC 44 是一种完全的 D3R 激动剂,而 WC 10 则几乎没有疗效。与它们在 AC 测定中的相反作用相反,这些药物通常会产生类似的行为效应,这表明 AC 测定不能预测这些药物在体内的疗效。在这里,我们研究了这些药物诱导的 Fos 蛋白表达是否会与它们在体内的行为效应更一致。大鼠接受了载体、WC 10(5.6mg/kg,ip)、WC 44(10.0mg/kg,ip)、可卡因(10.0mg/kg,ip)或可卡因与 WC 10(5.6mg/kg,ip)或与 WC 44(10.0mg/kg,ip)。监测了 90 分钟的运动,然后收获大脑进行免疫组织化学分析。WC 10 和 WC 44 都减少了自发和可卡因诱导的运动。这两种化合物还增加了背侧纹状体和伏隔核核心和壳中与盐水相比的 Fos 表达,与单独的可卡因相比,在伏隔核壳中增加了 Fos 表达。这些发现表明,尽管这些化合物在 AC 生物测定中具有不同的疗效,但它们会产生类似的大脑激活和减弱可卡因过度运动。结合我们之前的研究表明,这些化合物会降低可卡因自我给药剂量效应函数,这些发现支持了这样一种观点,即 D3R 选择性化合物可能对可卡因依赖药物的开发有用。