Muszak J, Krzymowski T, Gilun P, Stefanczyk-Krzymowska S
Department of Local Physiological Regulations, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland.
J Physiol Pharmacol. 2014 Oct;65(5):641-8.
The objective of the current study was to check whether countercurrent transfer of dopamine occurs in the cavernous sinus of the rabbit and whether the rabbit can be used as an animal model to study cavernous sinus function. After exsanguination of the animal, oxygenated and warmed (37°C) Hanseneleit-Krebs buffer with autologous or homologous blood (in a 3:1 or 1:1 ratio) was pumped through both common carotid arteries into the head (60 ml/min; 80-100 mm Hg) and radiolabeled dopamine (3(H)-DA, 10 μCi) was infused into the cavernous sinus through the angular oculi vein. Cerebral blood from the basilar artery was collected from the cannulated vertebral artery during 3(H)-DA infusion and for 10 minutes after completion of infusion. Selected brain tissue samples were collected after completion of the head perfusion. It was demonstrated that dopamine can penetrate from the rabbit's cavernous sinus to the internal carotid artery supplying the brain. Dopamine permeation was greater when the rabbit head was perfused with buffer and blood in a 3:1 ratio than with 1:1 (P<0.01). When the head was perfused with buffer and blood in a 3:1 ratio, significant radioactivity was found in samples collected from the brain basilar artery during and after 3(H)-DA infusion (P<0.001). The radioactivity was identified as 34.13 ± 2.7% unmetabolized 3(H)-DA and 65.9 ± 2.7% its metabolites. Significant radioactivity was also found in some brain tissue samples in both groups (P<0.05). The concentration of free radiolabeled dopamine particles in the dialysate of blood plasma and plasma diluted with buffer did not differ significantly. Because the structures of the cavernous sinus and cavernous fragment of the internal carotid artery of the rabbit are similar to those in humans, it suggests that rabbits can serve as a model for experimental physiological studies of cavernous sinus function and retrograde dopamine transfer in the cavernous sinus should be considered as an important link in the genesis of Attention Deficit Hyperactivity Disorder (ADHD) and Parkinson's disease.
本研究的目的是检查多巴胺在兔海绵窦中是否发生逆流转移,以及兔是否可作为研究海绵窦功能的动物模型。动物放血后,将充氧并加温至37°C的汉森莱伊特 - 克雷布斯缓冲液与自体或同源血液(比例为3:1或1:1)通过双侧颈总动脉泵入头部(60毫升/分钟;80 - 100毫米汞柱),并将放射性标记的多巴胺(3(H)-DA,10微居里)通过眼内角静脉注入海绵窦。在注入3(H)-DA期间以及注入完成后10分钟,从插管的椎动脉收集来自基底动脉的脑血。头部灌注完成后收集选定的脑组织样本。结果表明,多巴胺可从兔的海绵窦渗透至供应脑部的颈内动脉。当兔头部用3:1比例的缓冲液和血液灌注时,多巴胺的渗透比1:1比例时更大(P<0.01)。当头部用3:1比例的缓冲液和血液灌注时,在注入3(H)-DA期间及之后从脑基底动脉收集的样本中发现显著的放射性(P<0.001)。该放射性被鉴定为34.13±2.7%未代谢的3(H)-DA及其65.9±2.7%的代谢产物。两组的一些脑组织样本中也发现了显著的放射性(P<0.05)。血浆透析液和用缓冲液稀释的血浆中游离放射性标记多巴胺颗粒的浓度无显著差异。由于兔海绵窦和颈内动脉海绵窦段的结构与人类相似,这表明兔可作为海绵窦功能实验生理学研究的模型,并且海绵窦中多巴胺的逆行转移应被视为注意力缺陷多动障碍(ADHD)和帕金森病发病机制中的一个重要环节。