Hansen T R, Greenberg J, Mosnaim A D
Eur J Pharmacol. 1980 May 2;63(2-3):95-101. doi: 10.1016/0014-2999(80)90433-1.
Phenylethylamine (PEA) has been implicated in a number of central and peripheral nervous system disorders. Its possible mechanisms of action include stimulation via catecholamine release and direct stimulation by PEA. We have examined the effects of PEA on isolated vascular smooth muscle (VSM) to further explore the mechanism by which PEA produces contraction in this tissue. Helical strips of rat aorta were suspended in a muscle bath. Smooth muscle contractions were recorded via force transducer. PEA elicited a concentration dependent contraction from these strips with a threshold near 10(-6) M and a maximum response at 5 X 10(-3) M. Pretreatment of rats with reserpine dramatically reduced the norepinephrine (NE) content of kidney, heart and spleen of these animals but did not prevent the action of PEA on VSM. The presence of phentolamine (10(-4) M) completely blocked the strip response to PEA. The presence of propranolol (10(-7) or 10(-4) M) altered but did not block the VSM response to PEA. These results argue that the effects of PEA upon the aortic strip preparation involve a direct action of this amine upon VSM.
苯乙胺(PEA)与多种中枢和外周神经系统疾病有关。其可能的作用机制包括通过儿茶酚胺释放产生刺激以及PEA的直接刺激。我们研究了PEA对离体血管平滑肌(VSM)的影响,以进一步探讨PEA在该组织中产生收缩的机制。将大鼠主动脉螺旋条悬挂在肌肉浴中。通过力传感器记录平滑肌收缩。PEA从这些条带引发浓度依赖性收缩,阈值接近10^(-6) M,在5×10^(-3) M时达到最大反应。用利血平预处理大鼠可显著降低这些动物肾脏、心脏和脾脏中的去甲肾上腺素(NE)含量,但不能阻止PEA对VSM的作用。酚妥拉明(10^(-4) M)的存在完全阻断了条带对PEA的反应。普萘洛尔(10^(-7)或10^(-4) M)的存在改变但未阻断VSM对PEA的反应。这些结果表明,PEA对主动脉条制剂的作用涉及该胺对VSM的直接作用。