Laursen H, Klysner R, Geisler A
Acta Physiol Scand. 1977 Jul;100(3):282-7. doi: 10.1111/j.1748-1716.1977.tb05951.x.
Altered catecholamine receptor sites within the striatum have been proposed to be an important pathogenetic factor in hepatic and porto-systemic encephalopathy and coma. The unstimulated, fluoride-, norepinephrine- and dopamine-stimulated adenylate cyclase activity were measured in the corpus striatum of rats with a four weeks old end-to-side porto-caval anastomosis. There was no difference in unstimulated, fluoride- or hormone-stimulated adenylate cyclase activity between porto-caval shunted and sham-operated rats. The in vitro dose-response curves of norepinephrine and dopamine were similar in both groups of animals. Half-maximum and maximum stimulation were achieved in shunted and sham-operated rats by identical concentrations of norepinephrine and dopamine, respectively. The results indicate that neither changes in unstimulated adenylate cyclase activity nor changes in the response of adenylate cyclase activity to fluoride, norepinephrine and dopamine had developed in the rats at the stage studied.
纹状体内儿茶酚胺受体位点的改变被认为是肝性和门体性脑病及昏迷的一个重要致病因素。在进行了四周端侧门腔静脉吻合术的大鼠纹状体内,测量了未受刺激、氟化物、去甲肾上腺素和多巴胺刺激后的腺苷酸环化酶活性。门腔分流大鼠和假手术大鼠在未受刺激、氟化物或激素刺激后的腺苷酸环化酶活性方面没有差异。两组动物中去甲肾上腺素和多巴胺的体外剂量反应曲线相似。在分流大鼠和假手术大鼠中,分别通过相同浓度的去甲肾上腺素和多巴胺达到最大刺激的半数和最大值。结果表明,在所研究阶段的大鼠中,未受刺激的腺苷酸环化酶活性变化以及腺苷酸环化酶活性对氟化物、去甲肾上腺素和多巴胺的反应变化均未出现。