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腹腔内注射戊巴比妥钠有可能引起成年大鼠(Rattus norvegicus)产生疼痛。

Intraperitoneal injection of sodium pentobarbital has the potential to elicit pain in adult rats (Rattus norvegicus).

机构信息

Veterinary Clinical and Diagnostic Sciences, Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.

Department of Clinical Sciences, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, QC, Canada.

出版信息

PLoS One. 2020 Sep 3;15(9):e0238123. doi: 10.1371/journal.pone.0238123. eCollection 2020.

Abstract

An effective and pain-free killing method is required to achieve the goal of euthanasia, a "good death". Overdose of sodium pentobarbital (PB) by intraperitoneal (IP) injection is a widely accepted technique in laboratory rats, but questions remain regarding pain associated with administration. As PB rapidly causes sedation and loss of consciousness, most studies have relied on indirect evidence of pain. The objective of this study was to assess pain associated with IP PB using an appropriate vehicle control. Adult male and female Sprague Dawley (SD) and female Wistar rats (N = 84) were block randomised by sex and strain to receive one of three treatments: 1) 800 mg/kg PB (pH 11), 2) saline or 3) vehicle controls (pH 11 or 12.5). Behavior (Rat Grimace Scale (RGS), writhing, back arching) was evaluated at baseline, before loss of righting reflex (LORR, PB group), and at 80s, 151s and 10 min post-injection (PI; saline and vehicle control groups). In the PB group, mean time to LORR was 78 ± 7.9 seconds. In the vehicle control groups, RGS scores were increased at 151s PI (SD: p = 0.0002, 95%CI 0.73 to 0.20) from baseline, as was relative frequency of writhing (SD: p < 0.0001; Wistar; p = 0.0004). RGS scores remained elevated 10 mins PI (SD: p = 0.0005, 95%CI 0.71 to 0.18; Wistar: p = 0.0234, 95%CI 0.91 to 0.07) but the relative frequency of writhing did not (p > 0.999). The RGS scores and the relative frequency of writhing remained low in the PB and saline groups (p > 0.05). These results show that, vehicle controls for IP PB result in signs associated with pain, pain may not be experienced following IP PB when LORR occurs quickly, and that the effects of PB limit behavioral pain assessments.

摘要

需要一种有效且无痛的致死方法来实现安乐死这一“善终”的目标。通过腹腔内(IP)注射给予戊巴比妥钠(PB)过量是实验室大鼠中广泛接受的技术,但给药相关疼痛问题仍存在争议。由于 PB 会迅速引起镇静和意识丧失,因此大多数研究依赖于疼痛的间接证据。本研究的目的是使用适当的载体对照物来评估与 IP PB 相关的疼痛。成年雄性和雌性 Sprague Dawley(SD)和雌性 Wistar 大鼠(N = 84)按性别和品系分为块随机分组,接受以下三种处理之一:1)800 mg/kg PB(pH 11),2)生理盐水或 3)载体对照物(pH 11 或 12.5)。行为(大鼠面部表情评分量表(RGS)、扭动、背部拱起)在基线、失去翻正反射(LORR,PB 组)之前以及注射后 80 秒、151 秒和 10 分钟(生理盐水和载体对照组)进行评估。在 PB 组中,平均 LORR 时间为 78 ± 7.9 秒。在载体对照组中,在 151 秒 PI 时 RGS 评分升高(SD:p = 0.0002,95%CI 0.73 至 0.20),扭动的相对频率也增加(SD:p < 0.0001;Wistar;p = 0.0004)。RGS 评分在 10 分钟 PI 时仍升高(SD:p = 0.0005,95%CI 0.71 至 0.18;Wistar:p = 0.0234,95%CI 0.91 至 0.07),但扭动的相对频率没有增加(p > 0.999)。在 PB 和生理盐水组中,RGS 评分和扭动的相对频率均较低(p > 0.05)。这些结果表明,IP PB 的载体对照会导致与疼痛相关的迹象,当 LORR 迅速发生时,IP PB 后可能不会感到疼痛,并且 PB 的作用限制了行为疼痛评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da9d/7470368/a099b2e2aeb2/pone.0238123.g001.jpg

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