Li Guo-cai, Jiao Yong-gang, Wu Zhong-hai, Fang Fang, Cheng Jing
Department of Physiology, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2010 Feb;30(2):245-8.
To investigate the effects of doxapram on the respiratory rhythmical discharge activity (RRDA) in the brainstem slices of neonatal rats.
Thirty neonatal SD rats (of either sex, 0-3 days old) were randomly divided into 6 equal groups (groups I-VI), and the brainstem slices which contained the medial region of the nucleus retrofacialis (mNRF) were prepared. All the slices were perfused with modified Kreb's solution (MKS), and in group I (control group), the slices were perfused with MKS only; in groups II to IV, the slices were perfused with doxapram in MKS continuously at the concentrations of 2, 5, and 10 micromol/L, respectively; in groups V and VI, the slices were perfused with 20 micromol/L propofol and 20 micromol/L propofol plus 5 micromol/L doxapram, respectively. The RRDA in the hypoglossal nerve was recorded by suction electrode. The discharge time course of the inspiratory (TI), expiratory (TE), respiratory cycle (RC) and integral amplitude of the inspiratory discharge (IA) were recorded at 1, 3, 5, 10, 15, and 30 min after the application of the drugs.
The hypoglossal nerve in groups I, II and VI showed no significant changes of RRDA in the entire course of the experiment (P>0.05). In groups III and IV, the TI, IA increased and TE decreased significantly 5 min after doxapram application (P<0.05), and the RC was shortened only at 10 min. In group V, the TI and IA decreased and the RC and TE increased significantly after the drug application (P<0.05).
Doxapram (>5 micromol/L ) can directly stimulate the RRDA and prevent propofol-induced inhibitory effects in the brainstem slice of neonatal rats, and the effects are mediated by its actions upon the inspiratory neurons in the mNRF.
研究多沙普仑对新生大鼠脑干切片呼吸节律性放电活动(RRDA)的影响。
将30只新生SD大鼠(0 - 3日龄,雌雄不限)随机分为6组(Ⅰ - Ⅵ组),制备含面神经后核内侧区域(mNRF)的脑干切片。所有切片均用改良Krebs液(MKS)灌注,Ⅰ组(对照组)仅用MKS灌注;Ⅱ至Ⅳ组分别用浓度为2、5和10 μmol/L的多沙普仑在MKS中持续灌注;Ⅴ组和Ⅵ组分别用20 μmol/L丙泊酚和20 μmol/L丙泊酚加5 μmol/L多沙普仑灌注。用吸引电极记录舌下神经的RRDA。在给药后1、3、5、10、15和30分钟记录吸气时间(TI)、呼气时间(TE)、呼吸周期(RC)和吸气放电积分幅度(IA)的放电时间进程。
Ⅰ、Ⅱ和Ⅵ组舌下神经在实验全过程中RRDA无明显变化(P>0.05)。Ⅲ组和Ⅳ组在应用多沙普仑5分钟后TI、IA显著增加,TE显著降低(P<0.05),仅在10分钟时RC缩短。Ⅴ组给药后TI和IA降低,RC和TE显著增加(P<0.05)。
多沙普仑(>5 μmol/L)可直接刺激新生大鼠脑干切片中的RRDA并预防丙泊酚诱导的抑制作用,其作用是通过作用于mNRF中的吸气神经元介导的。