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川芎嗪增强氯胺酮对小鼠的催眠和镇痛作用。

Ligustrazine Enhances the Hypnotic and Analgesic Effect of Ketamine in Mice.

作者信息

Liu Chuiliang, Li Zhipeng, Huang Zeqi, Zhang Kun, Hu Chuwen, Zuo Zhiyi, Li Yujuan

机构信息

Department of Anesthesiology, ChanCheng Center Hospital.

Department of Anesthesiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University.

出版信息

Biol Pharm Bull. 2018 May 1;41(5):690-696. doi: 10.1248/bpb.b17-00869. Epub 2018 Feb 21.

DOI:10.1248/bpb.b17-00869
PMID:29467345
Abstract

The purpose of this study was to determine the effects of different concentrations of ligustrazine, an extract from Chinese herb, on ketamine requirement for hypnosis and analgesia in mice. In the hypnotic response study, mice were randomly allocated to receive saline or ligustrazine at 10, 20, 40, 80 or 160 mg·kg by intraperitoneal injection. Ketamine was administrated 15 min after ligustrazine injection. The hypnotic response was determined by assessing loss of the righting reflex (LORR) after ketamine injection. The dose of ketamine was determined by modified Dixon's up-and-down method in each group. In the analgesia study, different doses of ligustrazine were administrated 15 min before 50 mg·kg ketamine injection. The analgesia effects (pain threshold) were determined by heat radiation-induced tail-flick latency and evaluated before ligustrazine administration or 5, 15, 30 and 60 min after ketamine administration. The ED [95% confidence interval (CI)] for hypnosis induced by ketamine was 54.1 (44.8, 65.3) mg·kg. Ligustrazine dose-dependently decreased the ED for ketamine to induce hypnosis, which was [31.6 (26.2, 38.1)] mg·kg with the addition of 80 mg·kg ligustrazine and [27.7 (22.6, 33.7)] mg·kg with the addition of 160 mg·kg ligustrazine, respectively (p<0.05). Ligustrazine at 160 mg·kg also increased pain threshold in the presence of ketamine. Ligustrazine enhanced the hypnotic effect of ketamine in a dose-dependent manner. Ligustrazine at a large dose also increased the analgesic effect of ketamine.

摘要

本研究旨在确定不同浓度的川芎嗪(一种中草药提取物)对小鼠催眠和镇痛所需氯胺酮剂量的影响。在催眠反应研究中,将小鼠随机分为几组,分别腹腔注射生理盐水或10、20、40、80或160mg·kg的川芎嗪。注射川芎嗪15分钟后给予氯胺酮。通过评估注射氯胺酮后翻正反射消失(LORR)来确定催眠反应。每组中氯胺酮的剂量通过改良的Dixon上下法确定。在镇痛研究中,在注射50mg·kg氯胺酮前15分钟给予不同剂量的川芎嗪。通过热辐射诱导的甩尾潜伏期来确定镇痛效果(痛阈),并在给予川芎嗪前或注射氯胺酮后5、15、30和60分钟进行评估。氯胺酮诱导催眠的ED[95%置信区间(CI)]为54.1(44.8,65.3)mg·kg。川芎嗪剂量依赖性地降低了氯胺酮诱导催眠的ED,分别添加80mg·kg川芎嗪时为[31.6(26.2,,38.1)]mg·kg,添加160mg·kg川芎嗪时为[27.7(22.6,33.7)]mg·kg(p<0.05)。160mg·kg的川芎嗪在存在氯胺酮的情况下也提高了痛阈。川芎嗪以剂量依赖性方式增强了氯胺酮的催眠效果。大剂量的川芎嗪还增强了氯胺酮的镇痛效果。

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