Duan X, Li Y, Zhou C, Huang L, Dong Z
Department of Anaesthesiology, The Second Hospital of Hebei Medical University, Shijiazhaung, China.
Acta Anaesthesiol Scand. 2014 Oct;58(9):1121-6. doi: 10.1111/aas.12356. Epub 2014 Jul 18.
Ketamine and dexmedetomidine are increasingly used in combination in pediatric patients. This study examined the hypothesis that dexmedetomidine attenuated ketamine-induced neurotoxicity.
Neonatal rats were randomly divided into four groups (n=10, male 5, female 5). Group S+S received an equal volume of normal saline intraperitoneally and subcutaneously at an interval of 5 min. Group K+S received an intraperitoneal injection of 75 mg/kg ketamine followed by subcutaneous injection of normal saline 5 min later. Group S+D were given subcutaneously 25 μg/kg dexmedetomidine 5 min after injection of normal saline. Group K+D received a subcutaneous injection of 25 μg/kg dexmedetomidine 5 min after ketamine injection. The above drugs were given once daily for 3 days. Neuronal apoptosis in the CA1 region and the dentate gyrus of rats was examined by transferase dUTP nick end labeling (TUNEL) assays. Learning and memory abilities of 2-month old rats were examined by Morris water maze test. The results were analyzed by analysis of variance.
The percentage of TUNEL-positive cells in group K+S (CA1, 49.0±9.46 and dentate gyrus, 49.4±5.41) was markedly higher than that in group K+D (CA1, 37.2±5.54 and dentate gyrus, 35.2±5.06) (F=5.49, P<0.05 and F=13.51, P<0.001, respectively). Group K+S took significantly longer time and swimming distance to find the hidden platform on the fourth and fifth training days than group K+D (P<0.05). Moreover, group K+D spent considerably more time in the target quadrant than group K+S (P<0.05). Dexmedetomidine alone caused a small but statistically insignificant increase in neuronal apoptosis of the CA1 region and the dentate gyrus of neonatal rats compared with normal saline.
In conclusion, ketamine caused neuroapoptosis and impaired brain functions in the developing rat brain which can be effectively attenuated by dexmedetomidine. Dexmedetomidine alone was not neurotoxic to the developing brain.
氯胺酮和右美托咪定越来越多地联合用于儿科患者。本研究检验了右美托咪定可减轻氯胺酮诱导的神经毒性这一假设。
将新生大鼠随机分为四组(n = 10,雄性5只,雌性5只)。S + S组每隔5分钟腹腔内和皮下注射等体积的生理盐水。K + S组腹腔注射75 mg/kg氯胺酮,5分钟后皮下注射生理盐水。S + D组在注射生理盐水5分钟后皮下注射25 μg/kg右美托咪定。K + D组在注射氯胺酮5分钟后皮下注射25 μg/kg右美托咪定。上述药物每天给药1次,共3天。通过末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)法检测大鼠海马CA1区和齿状回的神经元凋亡。通过Morris水迷宫试验检测2月龄大鼠的学习和记忆能力。结果采用方差分析。
K + S组(CA1区,49.0±9.46;齿状回,49.4±5.41)TUNEL阳性细胞百分比显著高于K + D组(CA1区,37.2±5.54;齿状回,35.2±5.06)(F分别为5.49,P < 0.05;F为13.51,P < 0.001)。在第4和第5个训练日,K + S组找到隐藏平台的时间和游泳距离显著长于K + D组(P < 0.05)。此外,K + D组在目标象限的停留时间显著长于K + S组(P < 0.05)。与生理盐水相比,单独使用右美托咪定使新生大鼠CA1区和齿状回的神经元凋亡有少量增加,但无统计学意义。
总之,氯胺酮可导致发育中大鼠脑内神经细胞凋亡并损害脑功能,而右美托咪定可有效减轻这种损害。单独使用右美托咪定对发育中的脑无神经毒性。