Helke C J, Kellar K J, Gillis R A
Eur J Pharmacol. 1978 Nov 1;52(1):47-55. doi: 10.1016/0014-2999(78)90020-1.
The purpose of our study was to determine whether a toxic arrhythmogenic dose of digitalis administered to an in vivo preparation would affect the neuronal uptake of norepinephrine, serotonin and dopamine in brain tissue and norepinephrine in cardiac tissue. This was investigated by intoxicating anesthetized cats with deslanoside, removing cardiac and brain tissue at the onset of ventricular fibrillation, and examining the ability of brain tissue to accumulate [3H]-NE, [3H]-T-HT and [3H]-DA and cardiac tissue to accumulate [3H]-NE. It was found that deslanoside inhibited uptake of [3H]-NE into the left ventricle and [3H]5-HT into the area postrema. These selective effects may reflect greater blood flow to these regions or different sensitivities of the transport mechanisms for these amines. This inhibition of uptake into both left ventricular tissue and area postrema may contribute to some of the cardiovascular and emetic effects seen with digitalis drugs.
我们研究的目的是确定给予体内制剂致心律失常毒性剂量的洋地黄是否会影响脑组织中去甲肾上腺素、5-羟色胺和多巴胺以及心脏组织中去甲肾上腺素的神经元摄取。通过用去乙酰毛花苷使麻醉猫中毒,在心室颤动开始时取出心脏和脑组织,并检测脑组织积累[3H]-去甲肾上腺素([3H]-NE)、[3H]-5-羟色胺([3H]-5-HT)和[3H]-多巴胺([3H]-DA)以及心脏组织积累[3H]-NE的能力来进行此项研究。结果发现,去乙酰毛花苷抑制[3H]-NE进入左心室以及[3H]-5-HT进入最后区。这些选择性作用可能反映了这些区域有更多的血流供应,或者这些胺类转运机制的敏感性不同。对左心室组织和最后区摄取的这种抑制作用可能是洋地黄类药物所产生的某些心血管和催吐作用的原因。