Szabo B, Urban R, Starke K
Pharmakologisches Institut, Albert-Ludwigs-Universität, Freiburg, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1993 Dec;348(6):593-600. doi: 10.1007/BF00167235.
Cardiovascular and sympathetic nervous system effects of the mixed alpha 2-adrenoceptor and imidazoline receptor agonist rilmenidine were studied in conscious rabbits chronically instrumented for the recording of the firing rate of renal sympathetic fibers. Separate experiments were carried out on pithed rabbits with electrically stimulated (2 Hz) sympathetic outflow. Drugs were administered intravenously in a cumulative manner. In conscious rabbits, rilmenidine 0.1, 0.3 and 1.0 mg kg-1 dose-dependently lowered blood pressure, renal sympathetic nerve activity, heart rate and the plasma concentration of noradrenaline and adrenaline. The effect on blood pressure and plasma catecholamines was maximal after 0.3 mg kg-1 whereas heart rate and renal sympathetic nerve activity decreased further after rilmenidine 1.0 mg kg-1. Yohimbine 0.1 and 0.5 mg kg-1, when injected subsequently, attenuated and at the higher dose abolished all effects of rilmenidine. The effects of rilmenidine were also antagonized by the alpha 2-adrenoceptor antagonist 2-(2,3-dihydro-2-methoxy-1,4-benzodioxin-2-yl)-4,5-dihydro-1H-imid azole HCl (RX821002; 0.1 and 0.5 mg kg-1). Yohimbine 0.1 and 0.5 mg kg-1 did not attenuate or attenuated only slightly the decrease of heart rate and renal sympathetic nerve activity produced by infusion of vasopressin. In pithed rabbits with electrically-stimulated sympathetic outflow, yohimbine 0.1 submaximally and yohimbine 0.5 mg kg-1 maximally increased the plasma noradrenaline concentration. The experiments show by direct measurement of sympathetic nerve firing and plasma catecholamines that rilmenidine causes sympathoinhibition in conscious rabbits, presumably through central sites of action.(ABSTRACT TRUNCATED AT 250 WORDS)
在长期植入仪器以记录肾交感神经纤维放电频率的清醒家兔中,研究了混合α₂肾上腺素能受体和咪唑啉受体激动剂利美尼定对心血管和交感神经系统的作用。对脊髓横断的家兔进行单独实验,用电刺激(2Hz)交感神经传出纤维。药物以累积方式静脉给药。在清醒家兔中,0.1、0.3和1.0mg/kg的利美尼定剂量依赖性地降低血压、肾交感神经活动、心率以及去甲肾上腺素和肾上腺素的血浆浓度。0.3mg/kg后对血压和血浆儿茶酚胺的作用最大,但1.0mg/kg的利美尼定使心率和肾交感神经活动进一步降低。随后注射0.1和0.5mg/kg的育亨宾可减弱并在较高剂量时消除利美尼定的所有作用。α₂肾上腺素能受体拮抗剂2-(2,3-二氢-2-甲氧基-1,4-苯并二恶英-2-基)-4,5-二氢-1H-咪唑盐酸盐(RX821002;0.1和0.5mg/kg)也可拮抗利美尼定的作用。0.1和0.5mg/kg的育亨宾对血管加压素输注引起的心率和肾交感神经活动降低仅轻微减弱或未减弱。在脊髓横断且交感神经传出纤维电刺激的家兔中,0.1mg/kg的育亨宾次最大程度地增加,0.5mg/kg的育亨宾最大程度地增加血浆去甲肾上腺素浓度。这些实验通过直接测量交感神经放电和血浆儿茶酚胺表明,利美尼定在清醒家兔中引起交感神经抑制,可能是通过中枢作用部位。(摘要截断于250字)