Farah M B, Langer S Z
Br J Pharmacol. 1974 Dec;52(4):549-57. doi: 10.1111/j.1476-5381.1974.tb09723.x.
1 The effects of cocaine, phentolamine and phenoxybenzamine on neuronal uptake of [(3)H]-noradrenaline and on (3)H-transmitter and noradrenaline overflow elicited by nerve stimulation were determined in the perfused heart of the cat.2 During perfusion with cocaine 3.4 x 10(-7)M, there was a 2-fold increase in transmitter overflow while neuronal uptake of [(3)H]-noradrenaline was inhibited by 31.3 +/- 2.1%.3 After exposure to phenoxybenzamine 8.7 x 10(-7)M for 20 min and washing with drug-free solution for 165 min there was an 8-fold increase in transmitter overflow during nerve stimulation. Under these conditions neuronal uptake of [(3)H]-noradrenaline was inhibited by only 17.5 +/- 5.4%.4 There was no significant change in transmitter overflow or in neuronal uptake of [(3)H]-noradrenaline, 155 min after a 30 min exposure to phentolamine (3.2 x 10(-5)M).5 Perfusion with phentolamine (3.2 x 10(-5)M) before and during exposure to phenoxybenzamine (8.7 x 10(-7)M), prevented the increase in transmitter overflow observed after perfusion with phenoxybenzamine alone.6 Protection by phentolamine against the effects of phenoxybenzamine supports the view that the effects on transmitter release obtained after perfusion with phenoxybenzamine are due to the blockade of presynaptic alpha-adrenoceptors which regulate transmitter release through a negative feed-back mechanism.
1 在猫的灌注心脏中,测定了可卡因、酚妥拉明和酚苄明对神经元摄取[(3)H]-去甲肾上腺素以及对神经刺激引发的(3)H-递质和去甲肾上腺素溢出的影响。
2 在灌注3.4×10(-7)M可卡因期间,递质溢出增加了2倍,而神经元对[(3)H]-去甲肾上腺素的摄取被抑制了31.3±2.1%。
3 在暴露于8.7×10(-7)M酚苄明20分钟并用无药溶液冲洗165分钟后,神经刺激期间递质溢出增加了8倍。在这些条件下,神经元对[(3)H]-去甲肾上腺素的摄取仅被抑制了17.5±5.4%。
4 在暴露于3.2×10(-5)M酚妥拉明30分钟后155分钟,递质溢出或神经元对[(3)H]-去甲肾上腺素的摄取没有显著变化。
5 在暴露于酚苄明(8.7×10(-7)M)之前和期间灌注酚妥拉明(3.2×10(-5)M),可防止单独灌注酚苄明后观察到的递质溢出增加。
6 酚妥拉明对酚苄明作用的保护支持了这样一种观点,即灌注酚苄明后对递质释放的影响是由于阻断了通过负反馈机制调节递质释放的突触前α-肾上腺素能受体。