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有证据支持在体内犬肝脏中,肝交感神经刺激时,突触前α-肾上腺素能受体在调节内源性去甲肾上腺素释放中发挥作用。

Evidence supporting the existence of presynaptic alpha-adrenoceptors in the regulation of endogenous noradrenaline release upon hepatic sympathetic nerve stimulation in the dog liver in vivo.

作者信息

Yamaguchi N

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1982 Dec;321(3):177-84. doi: 10.1007/BF00505482.

Abstract

The existence and functional significance of presynaptic alpha-adrenoceptors within the liver was investigated in anesthetized dogs. The stimulation-evoked endogenous catecholamine overflow was determined in hepatic venous blood upon hepatic nerve stimulation (12 V, 1-8 Hz, 1 min). Under resting conditions, average plasma catecholamine levels in hepatic venous and aortic blood were 0.064 ng/ml and 0.334 ng/ml, respectively. A frequency-dependent increase (P less than 0.001) was found in the hepatic venous catecholamine overflow, while aortic catecholamine levels did not change significantly at any stimulation frequency tested. The increases in catecholamine overflow were associated with decreases in hepatic arterial vascular conductance (35-66%, P less than 0.001) at all frequencies tested. Yohimbine (0.3 mg/kg, i.v.) potentiated the catecholamine overflow by 110-140% (P less than 0.05) upon stimulation at low frequencies (1-4 Hz). Clonidine (20 micrograms/kg, i.v.) inhibited the catecholamine overflow by 55-76% (P less than 0.05) at frequencies of 1 and 2 Hz, and reduced the hepatic arterial response by 46% (P less than 0.01) at 1 Hz. The pretreatment with yohimbine (0.1 mg/kg, i.v.) abolished the inhibitory effects of clonidine both on the catecholamine overflow and the hepatic arterial responses. The results support the existence of a negative feedback mechanism mediated by presynaptic alpha-adrenoceptors in the local regulation of noradrenaline release from hepatic sympathetic fibers. A functional significance of this process was suggested by an improved correlation found in the presence of clonidine between the catecholamine overflow and the hepatic arterial vascular conductance.

摘要

在麻醉犬中研究了肝脏内突触前α-肾上腺素能受体的存在及其功能意义。通过刺激肝神经(12伏,1 - 8赫兹,1分钟)来测定肝静脉血中刺激诱发的内源性儿茶酚胺溢出。在静息状态下,肝静脉血和主动脉血中的平均血浆儿茶酚胺水平分别为0.064纳克/毫升和0.334纳克/毫升。发现肝静脉儿茶酚胺溢出呈频率依赖性增加(P < 0.001),而在任何测试的刺激频率下主动脉儿茶酚胺水平均无显著变化。在所有测试频率下,儿茶酚胺溢出的增加与肝动脉血管传导性降低(35 - 66%,P < 0.001)相关。育亨宾(0.3毫克/千克,静脉注射)在低频(1 - 4赫兹)刺激时使儿茶酚胺溢出增强110 - 140%(P < 0.05)。可乐定(20微克/千克,静脉注射)在1和2赫兹频率时使儿茶酚胺溢出抑制55 - 76%(P < 0.05),并在1赫兹时使肝动脉反应降低46%(P < 0.01)。用育亨宾(0.1毫克/千克,静脉注射)预处理可消除可乐定对儿茶酚胺溢出和肝动脉反应的抑制作用。这些结果支持在肝脏交感神经纤维去甲肾上腺素释放的局部调节中存在由突触前α-肾上腺素能受体介导的负反馈机制。可乐定存在时儿茶酚胺溢出与肝动脉血管传导性之间发现的更好相关性提示了这一过程的功能意义。

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