Fuller R W, Felten S Y, Perry K W, Snoddy H D, Felten D L
J Pharmacol Exp Ther. 1981 Jul;218(1):282-8.
Norepinephrine concentration was higher in guinea-pig liver than in rat or mouse liver and evidence was obtained that the norepinephrine was present within nerves. In guinea pigs, norepinephrine in liver was depleted by reserpine, 6-hydroxydopamine and metaraminol. The depletion by 6-hydroxydopamine and metaraminol was antagonized by prior treatment with desipramine, an inhibitor of uptake into norepinephrine neurons. Guinea-pig liver concentrated metaraminol to a greater extent than did rat liver; the concentration of metaraminol was lowered by desipramine pretreatment and, within three tissues of the guinea pig (heart greater than liver greater than muscle), paralleled the concentration of endogenous norepinephrine. These findings constitute pharmacological evidence for noradrenergic innervation of guinea-pig liver to a greater extent than in other species. Histofluorescence studies confirmed the existence of norepinephrine-containing nerve terminals in guinea-pig liver. Norepinephrine-containing varicosities were seen adjacent to the hepatic artery, portal vein and bile duct in the portal spaces and adjacent to sinusoid capillaries and hepatocytes in the liver parenchyma. These findings strengthen the evidence for sympathetic innervation of liver and suggest the guinea pig as a useful species in exploring physiological roles of noradrenergic innervation of liver.
豚鼠肝脏中的去甲肾上腺素浓度高于大鼠或小鼠肝脏,并且有证据表明去甲肾上腺素存在于神经内。在豚鼠中,肝脏中的去甲肾上腺素会被利血平、6-羟基多巴胺和间羟胺耗尽。6-羟基多巴胺和间羟胺造成的耗尽会被事先用去甲丙咪嗪(一种去甲肾上腺素神经元摄取抑制剂)处理所拮抗。豚鼠肝脏比大鼠肝脏更能大量摄取间羟胺;去甲丙咪嗪预处理会降低间羟胺的摄取量,并且在豚鼠的三种组织(心脏>肝脏>肌肉)中,间羟胺的摄取量与内源性去甲肾上腺素的浓度平行。这些发现构成了豚鼠肝脏比其他物种有更广泛的去甲肾上腺素能神经支配的药理学证据。组织荧光研究证实了豚鼠肝脏中存在含去甲肾上腺素的神经末梢。在门管区,可见含去甲肾上腺素的曲张体毗邻肝动脉、门静脉和胆管,在肝实质中毗邻肝血窦毛细血管和肝细胞。这些发现强化了肝脏受交感神经支配的证据,并表明豚鼠是探索肝脏去甲肾上腺素能神经支配生理作用的有用物种。