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阿片受体-1(MOR-1)第1至4外显子对吗啡和海洛因镇痛及成瘾性的作用。

The contribution of MOR-1 exons 1-4 to morphine and heroin analgesia and dependence.

作者信息

Klein Gad, Rossi Grace C, Waxman Amanda R, Arout Carolne, Juni Aaron, Inturrisi Charles E, Kest Benjamin

机构信息

Neuropsychology Doctoral Subprogram, Queens College, City University of New York, Flushing, NY 11367, United States.

出版信息

Neurosci Lett. 2009 Jul 3;457(3):115-9. doi: 10.1016/j.neulet.2009.04.012. Epub 2009 Apr 9.

Abstract

Although morphine and heroin analgesia is mediated by mu-opioid receptors encoded by the MOR-1 gene, distinct isoforms are involved. Both opioids also induce dependence by acting at mu-opioid receptors, but which variants are utilized is not known. Here, we assayed morphine and heroin analgesia and dependence in mice treated with antisense oligodeoxynucleotides (AO) targeting MOR-1 exons 1-4. Whereas AOs targeting exons 1 and 4 blocked morphine analgesia, those targeting exons 2 and 3 blocked heroin analgesia. Neither morphine nor heroin analgesia was compromised 5 days after the last AO injection. In morphine and heroin dependent mice, only exon 1 AO significantly reduced jumping incidence during naloxone (50mg/kg) precipitated withdrawal. Neither analgesia nor withdrawal jumping was attenuated in controls pretreated with saline or a mismatch oligodeoxynucleotide control sequence. While these data confirm previous reports that morphine and heroin analgesia are not mediated by a single mu-opioid receptor, both opiates nonetheless apparently induce dependence via a mu-opioid receptor isoform containing exon 1. For heroin, the possibility that analgesia and dependence are mediated by distinct mu-opioid receptor isoforms offers the prospect of developing potent opiate analgesics possessing reduced dependence liability.

摘要

尽管吗啡和海洛因的镇痛作用是由MOR-1基因编码的μ-阿片受体介导的,但涉及不同的亚型。两种阿片类药物也通过作用于μ-阿片受体诱导成瘾,但具体利用了哪些变体尚不清楚。在此,我们检测了用靶向MOR-1基因第1至4外显子的反义寡脱氧核苷酸(AO)处理的小鼠对吗啡和海洛因的镇痛及成瘾情况。靶向第1和4外显子的AO阻断了吗啡的镇痛作用,而靶向第2和3外显子的AO则阻断了海洛因的镇痛作用。在最后一次注射AO后5天,吗啡和海洛因的镇痛作用均未受到影响。在吗啡和海洛因成瘾的小鼠中,只有靶向第1外显子的AO显著降低了纳洛酮(50mg/kg)诱发戒断期间的跳跃发生率。用生理盐水或错配寡脱氧核苷酸对照序列预处理的对照组中,镇痛和戒断跳跃均未减弱。虽然这些数据证实了之前的报道,即吗啡和海洛因的镇痛作用不是由单一的μ-阿片受体介导的,但两种阿片类药物显然都是通过含有第1外显子的μ-阿片受体亚型诱导成瘾的。对于海洛因来说,镇痛和成瘾由不同的μ-阿片受体亚型介导的可能性为开发依赖性较低的强效阿片类镇痛药提供了前景。

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