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丁丙诺啡/纳洛酮单独和联合地西泮对未耐受和耐受大鼠的呼吸影响。

Respiratory effects of buprenorphine/naloxone alone and in combination with diazepam in naive and tolerant rats.

机构信息

Inserm, U1144, Paris F-75006, France; Université Paris Descartes, UMR-S 1144, Paris F-75006, France; Université Paris Diderot, UMR-S 1144, Paris F-75013, France.

Inserm, U1144, Paris F-75006, France; Université Paris Descartes, UMR-S 1144, Paris F-75006, France; Université Paris Diderot, UMR-S 1144, Paris F-75013, France; IRCGN, département Toxicologie, Rosny sous-Bois, France.

出版信息

Toxicol Lett. 2014 Jul 15;228(2):75-84. doi: 10.1016/j.toxlet.2014.04.009. Epub 2014 Apr 21.

Abstract

Respiratory depression has been attributed to buprenorphine (BUP) misuse or combination with benzodiazepines. BUP/naloxone (NLX) has been marketed as maintenance treatment, aiming at preventing opiate addicts from self-injecting crushed pills. However, to date, BUP/NLX benefits in comparison to BUP alone remain debated. We investigated the plethysmography effects of BUP/NLX in comparison to BUP/solvent administered by intravenous route in naive and BUP-tolerant Sprague-Dawley rats, and in combination with diazepam (DZP) or its solvent. In naive rats, BUP/NLX in comparison to BUP significantly increased respiratory frequency (f, P<0.05) without altering minute volume (VE). In combination to DZP, BUP/NLX significantly increased expiratory time (P<0.01) and decreased f (P<0.01), tidal volume (VT, P<0.001), and VE (P<0.001) while BUP only decreased VT (P<0.5). In BUP-tolerant rats, no significant differences in respiratory effects were observed between BUP/NLX and BUP. In contrast, in combination to DZP, BUP/NLX did not significantly alter the plethysmography parameters, while BUP increased inspiratory time (P<0.001) and decreased f (P<0.01) and VE (P<0.001). In conclusion, differences in respiratory effects between BUP/NLX and BUP are only significant in combination with DZP, with increased depression in naive rats but reduced depression in BUP-tolerant rats. However, BUP/NLX benefits in humans remain to be determined.

摘要

呼吸抑制归因于丁丙诺啡(BUP)的滥用或与苯二氮䓬类药物联合使用。丁丙诺啡/纳洛酮(NLX)已被作为维持治疗药物上市,旨在防止阿片类药物成瘾者自行注射压碎的药丸。然而,迄今为止,BUP/NLX 与单独使用 BUP 相比的益处仍存在争议。我们通过静脉途径,在未接触过药物的 Sprague-Dawley 大鼠和 BUP 耐受大鼠中,研究了 BUP/NLX 与 BUP/溶剂的呼吸效应,并将其与地西泮(DZP)或其溶剂联合使用。在未接触过药物的大鼠中,与 BUP 相比,BUP/NLX 显著增加了呼吸频率(f,P<0.05),而分钟通气量(VE)没有变化。与 DZP 联合使用时,BUP/NLX 显著增加呼气时间(P<0.01)并降低 f(P<0.01)、潮气量(VT,P<0.001)和 VE(P<0.001),而 BUP 仅降低 VT(P<0.5)。在 BUP 耐受大鼠中,BUP/NLX 和 BUP 之间的呼吸效应没有显著差异。相反,与 DZP 联合使用时,BUP/NLX 对呼吸参数没有显著影响,而 BUP 增加了吸气时间(P<0.001)并降低了 f(P<0.01)和 VE(P<0.001)。总之,BUP/NLX 和 BUP 之间的呼吸效应差异仅在与 DZP 联合使用时才具有显著性,在未接触过药物的大鼠中增加了抑制作用,但在 BUP 耐受大鼠中减少了抑制作用。然而,BUP/NLX 在人类中的益处仍有待确定。

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