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去甲丙咪嗪对家兔主动脉条外膜层及中膜 - 内膜层放射性标记的溴苄铵和苄乙胍摄取与流出的影响。

Influence of desipramine on the uptake and efflux of radiolabelled bretylium and bethanidine in the adventitial and media-intimal layers of rabbit aortic strips.

作者信息

Batmanglidj Eckhardt S, Maxwell R A, Copp F C

出版信息

Blood Vessels. 1977;14(5):303-17. doi: 10.1159/000158137.

DOI:10.1159/000158137
PMID:871533
Abstract

The desipramine-sensitive uptake (neuronal uptake) of 14C-bretylium and 14C-bethanidine into the rabbit aortic adventitial layer from 3 X 10(-6) M solutions increased with time during a 20 min incubation. For both compounds a neuronal uptake of 50 pmol/50 mg wet weight adventitia was associated with 10% block of the contractile response to field stimulation at 16 Hz and 150 pmol/50 mg with 60% block. The concentration of blocking agents inside the neuron at 50% blockade was calculated to be 260 X 10(-6) M, an 87-fold increase over the medium. The bretylium in the neuron decreased by 50% during 20 min washout, and bethanidine by 29%. Desipramine when added to the bath 20 min following the addition of the blocking agents led to a loss of bretylium but not of bethanidine from the adventitia. Desipramine had little or no effect on the uptake, washout or disposition of either blocking agent in the media-intimal layers. The data indicate that bretylium has a greater propensity than bethanidine to be lost from the neurons; however, it appears to be recycled back through the membrane via the amine pump more readily than bethanidine. The fact that conservative calculations indicate that the neuronal membrane slowly established a concentration of the blocking agents within the neuron that is known to produce rapid local anesthesia when topically applied to adrenergic nerve trunks and which approaches a concentration needed to inhibit sensory endings suggests that local anesthesia may play a role in the mechanism of neuron blockade.

摘要

在3×10⁻⁶M溶液中,¹⁴C - 溴苄铵和¹⁴C - 苄乙胍对兔主动脉外膜层的去甲丙咪嗪敏感摄取(神经元摄取)在20分钟孵育期间随时间增加。对于这两种化合物,每50mg湿重外膜摄取50pmol神经元摄取量与16Hz场刺激收缩反应的10%阻断相关,每50mg摄取150pmol时与60%阻断相关。计算得出在50%阻断时神经元内阻断剂的浓度为260×10⁻⁶M,比培养基中增加了87倍。在20分钟洗脱过程中,神经元内的溴苄铵减少了50%,苄乙胍减少了29%。在加入阻断剂20分钟后将去甲丙咪嗪加入浴液中,导致外膜中溴苄铵流失,但苄乙胍没有流失。去甲丙咪嗪对培养基 - 内膜层中任何一种阻断剂的摄取、洗脱或分布几乎没有影响。数据表明,溴苄铵比苄乙胍更容易从神经元中流失;然而,它似乎比苄乙胍更容易通过胺泵通过膜再循环回来。保守计算表明神经元膜在神经元内缓慢建立了阻断剂浓度,已知该浓度在局部应用于肾上腺素能神经干时会产生快速局部麻醉,并且接近抑制感觉末梢所需的浓度,这一事实表明局部麻醉可能在神经元阻断机制中起作用。

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