Soltis E E, Soltis T D, Katovich M J, Field F P
Artery. 1986;13(6):325-39.
The in vitro responsiveness of rat aortic and femoral arterial smooth muscle from normotensive and deoxycorticosterone acetate (DOCA)/NaCl-induced hypertensive rats to potassium chloride (KCl) and isoproterenol (ISO) in the presence and absence of the alpha-adrenergic blocker phentolamine was investigated. Femoral but not aortic smooth muscle from the DOCA/NaCl rat exhibited an enhanced sensitivity to KCl stimulation when compared to controls. Phentolamine had no effect on femoral smooth muscle from control or DOCA/NaCl rats. However, a significant decrease in the sensitivity of aortic smooth muscle responsiveness to KCl in the presence of phentolamine was observed in both the control and hypertensive groups. Isoproterenol-induced relaxation of both aortic and femoral smooth muscle was significantly attenuated in the DOCA/NaCl rat when compared to controls. Incubation with phentolamine resulted in a significant increase in the relaxation response to ISO in aortic and femoral smooth muscle from controls. This increased responsiveness, however, was not observed in DOCA/NaCl rats. The contractile response to high doses of ISO was attenuated with phentolamine in all groups. A significant increase in the sensitivity to norepinephrine (NE) was observed in both aortic and femoral smooth muscle from the DOCA/NaCl rat when compared to controls. Whereas aortic and femoral smooth muscle from the DOCA/NaCl rat which had been exposed to phentolamine previously in the experiment exhibited a significant decrease in the sensitivity to NE following a one hour washout of the phentolamine, no long-lasting effect of phentolamine was apparent in vessels from controls. The results of this study confirm previous studies that the vascular smooth muscle responsiveness to NE is increased and ISO-induced relaxation is decreased in the DOCA/NaCl rat and demonstrate that these altered adrenergic responses are similarly manifested in the femoral smooth muscle.(ABSTRACT TRUNCATED AT 400 WORDS)
研究了正常血压大鼠以及醋酸脱氧皮质酮(DOCA)/氯化钠诱导的高血压大鼠的主动脉和股动脉平滑肌在体外对氯化钾(KCl)和异丙肾上腺素(ISO)的反应性,实验分别在存在和不存在α-肾上腺素能阻滞剂酚妥拉明的情况下进行。与对照组相比,DOCA/氯化钠大鼠的股动脉平滑肌而非主动脉平滑肌对KCl刺激的敏感性增强。酚妥拉明对对照组或DOCA/氯化钠大鼠的股动脉平滑肌均无影响。然而,在对照组和高血压组中均观察到,在酚妥拉明存在的情况下,主动脉平滑肌对KCl反应性的敏感性显著降低。与对照组相比,DOCA/氯化钠大鼠中,ISO诱导的主动脉和股动脉平滑肌舒张均显著减弱。用酚妥拉明孵育导致对照组主动脉和股动脉平滑肌对ISO的舒张反应显著增加。然而,在DOCA/氯化钠大鼠中未观察到这种反应性增加。在所有组中,酚妥拉明均可减弱对高剂量ISO的收缩反应。与对照组相比,DOCA/氯化钠大鼠的主动脉和股动脉平滑肌对去甲肾上腺素(NE)的敏感性均显著增加。在实验中预先暴露于酚妥拉明的DOCA/氯化钠大鼠的主动脉和股动脉平滑肌,在洗脱酚妥拉明1小时后,对NE的敏感性显著降低,而在对照组血管中未观察到酚妥拉明的长期效应。本研究结果证实了先前的研究,即DOCA/氯化钠大鼠的血管平滑肌对NE的反应性增加,而ISO诱导的舒张减弱,并表明这些改变的肾上腺素能反应在股动脉平滑肌中也有类似表现。(摘要截短至400字)