Kiriakov A, Khlebarova M, Staneva-Stoicheva D, Panova I
Eksp Med Morfol. 1973;12(3):135-41.
The authors examined the changes in arterial blood pressure and the content of noradrenaline in the myocardium, brain and aorta of rats with hypertention caused by nephrectomy, desoxycorticosterone and NaCl after a chronic six-month treatment with antihypertensive drugs. The most significant decrease of noradrenaline in the three of the examined organs was found in rats, receiving disulfiram (100 mg/kg per os). Clonidine (10 mkg/kg per os) had the strongest hypotensive effect and lowered the level of noradrenaline in the heart while it was raised in the aorta. Reserpine (10 mkg/kg subcutaneously) induced distinct reduction of NA-content in the brain, but in the other two organs--an increase. Insignificant hypotensive effect was observed in animals, receiving guanethidine (0,5 mg/kg per os), which did not affect significantly noradrenaline content in the examined organs. The increase of NA-level was found in the three of the organs of the animals, treated with alpha-methyl-DOPA (25 mg/kg per os). Furoseamide (1 mg/kg subcutaneously) induced a statisticaly significant increase of NA in the aorta and was inefficientupon the noradrenaline in the myocardium and brain.
作者研究了肾切除、脱氧皮质酮和氯化钠诱导高血压大鼠经六个月慢性抗高血压药物治疗后,其动脉血压以及心肌、脑和主动脉中去甲肾上腺素含量的变化。在所研究的三个器官中,去甲肾上腺素含量下降最为显著的是接受双硫仑(100毫克/千克口服)的大鼠。可乐定(10微克/千克口服)具有最强的降压作用,降低了心脏中的去甲肾上腺素水平,而主动脉中的去甲肾上腺素水平升高。利血平(10微克/千克皮下注射)使脑中的去甲肾上腺素含量明显降低,但在其他两个器官中却使其增加。接受胍乙啶(0.5毫克/千克口服)的动物观察到降压作用不显著,且对所研究器官中的去甲肾上腺素含量没有显著影响。用α-甲基多巴(25毫克/千克口服)治疗的动物,其三个器官中的去甲肾上腺素水平均升高。速尿(1毫克/千克皮下注射)使主动脉中的去甲肾上腺素含量有统计学意义的增加,而对心肌和脑中的去甲肾上腺素则无作用。