Jiao Yong-Gang, Wu Zhong-Hai
Department of Physiology, Southern Medical University, Guangzhou, China.
Sheng Li Xue Bao. 2008 Dec 25;60(6):704-8.
To explore the role of D(1)-dopamine receptor in the modulation of basic respiratory rhythm, neonatal (0-3 d) Sprague-Dawley rats of either sex were used. The medulla oblongata slice was prepared and the surgical procedure was performed in the modified Kreb's solution (MKS) with continuous ventilating 95% O2 and 5% CO2 and ended in 3 min. A 600-700 mum single transverse slice containing the hypoglossal nerve roots and some parts of the ventral respiratory group was cut. The preparation was quickly transferred to a recording chamber and continuously perfused with oxygen-saturated MKS at a rate of 4-6 mL/min at 27-29 degrees C. Ten medulla oblongata slice preparations were randomly divided into two groups. In group I, the preparations were perfused with perfusion solution containing D(1)-dopamine receptor specific agonist cis-(+/-)-1-(Aminomethyl)-3,4-dihydro-3-phenyl-1H-2-Benzopyran-5,6-Diolhy-drochlo-ride (A68930, 5 mumol/L) for 10 min first; after washing out, the preparations were then perfused with perfusion solution containing D(1)-dopamine receptor specific antagonist R(+)-7-Chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride (SCH-23390, 2 mumol/L) for 10 min. In group II, after perfusion with A68930 for 10 min, the preparations were perfused with additional A68930 + SCH-23390 for 10 min. Respiratory rhythmical discharge activity (RRDA) of the rootlets of hypoglossal nerve was recorded by suction electrodes. The results showed that A68930 shortened the respiratory cycle (RC) and expiratory time (TE) with an increase in the integral amplitude (IA). However, SCH-23390 significantly prolonged RC and TE, and decreased IA with a decrease in inspiratory time (TI). Moreover, the effect of A68930 on the respiratory rhythm was partially reversed by additional application of A68930 + SCH-23390. These results indicate that D(1)-dopamine receptor is possibly involved in the modulation of the RRDA in the isolated neonatal rat brainstem slice.
为探究D(1)-多巴胺受体在调节基本呼吸节律中的作用,选用新生(0 - 3日龄)的Sprague-Dawley大鼠,雌雄不限。制备延髓切片,手术操作在改良的克雷布斯溶液(MKS)中进行,持续通入95% O2和5% CO2,3分钟结束。切取一片包含舌下神经根和腹侧呼吸组部分区域的600 - 700μm单横切片。制备物迅速转移至记录室,在27 - 29℃下以4 - 6 mL/分钟的速率持续用饱和氧的MKS灌注。将十片延髓切片制备物随机分为两组。在第一组中,制备物首先用含有D(1)-多巴胺受体特异性激动剂顺式-(+/-)-1-(氨甲基)-3,4-二氢-3-苯基-1H-2-苯并吡喃-5,6-二醇盐酸盐(A68930,5μmol/L)的灌注液灌注10分钟;洗脱后,制备物再用含有D(1)-多巴胺受体特异性拮抗剂R(+)-7-氯-8-羟基-3-甲基-1-苯基-2,3,4,5-四氢-1H-3-苯并氮杂卓盐酸盐(SCH-23390,2μmol/L)的灌注液灌注10分钟。在第二组中,用A68930灌注10分钟后,制备物再用A68930 + SCH-23390灌注10分钟。用吸引电极记录舌下神经根的呼吸节律性放电活动(RRDA)。结果显示,A68930缩短了呼吸周期(RC)和呼气时间(TE),积分幅度(IA)增加。然而,SCH-23390显著延长了RC和TE,降低了IA,吸气时间(TI)减少。此外,额外应用A68930 + SCH-23390部分逆转了A68930对呼吸节律的影响。这些结果表明,D(1)-多巴胺受体可能参与了离体新生大鼠脑干切片中RRDA的调节。