Chen S, He R R
Department of Physiology, Hebei Medical University, Shijiazhuang 050017.
Sheng Li Xue Bao. 1998 Dec;50(6):629-35.
To observe the effect of intracarotid administration of adenosine on neurons in the rostral ventrolateral medulla (RVLM) region, 72 spontaneous active units were extracellularly recorded from 28 Sprague-Dawley rats with sino-aortic denervation. The results obtained are as follows: (1) intracarotid administration of Ado (25 micrograms/kg) reduced the discharge rate from (23.5 +/- 3.0) to (16.5 +/- 2.6) spikes/s (P < 0.001) in 31 out of 36 RVLM neurons, while the blood pressure and heart rate had no significant change (P > 0.05); (2) 8-phenyltheophylline (8-PT, 15 micrograms/kg), a nonselective adenosine receptor antagonist, and 8-cyclopentyl-1,3-dipropylxanthine (DPCPX, 50 micrograms/kg), a selective A1 adenosine receptor antagonist, completely blocked the inhibitory effects of Ado in 24 units; and (3) in 12 units, glibenclamide (500 micrograms/kg), a blocker of ATP-sensitive potassium channel, abolished the effect of Ado. These results indicate that Ado can induce an inhibition of spontaneous electrical activity of RVLM neurons, an effect which is mediated by adenosine A1-receptor with the involvement of ATP-sensitive potassium channels.
为观察颈内动脉注射腺苷对延髓头端腹外侧区(RVLM)神经元的影响,从28只去窦弓神经的Sprague-Dawley大鼠中细胞外记录了72个自发放电单位。结果如下:(1)36个RVLM神经元中有31个,颈内动脉注射Ado(25微克/千克)后放电频率从(23.5±3.0)降至(16.5±2.6)次/秒(P<0.001),而血压和心率无显著变化(P>0.05);(2)非选择性腺苷受体拮抗剂8-苯基茶碱(8-PT,15微克/千克)和选择性A1腺苷受体拮抗剂8-环戊基-1,3-二丙基黄嘌呤(DPCPX,50微克/千克)完全阻断了24个单位中Ado的抑制作用;(3)在12个单位中,ATP敏感性钾通道阻滞剂格列本脲(500微克/千克)消除了Ado的作用。这些结果表明,Ado可诱导RVLM神经元自发放电活动的抑制,该作用由腺苷A1受体介导,并涉及ATP敏感性钾通道。