Hoffmann P, Carlsson S, Skarphedinsson J O, Thorén P
Department of Physiology, University of Göteborg, Sweden.
Acta Physiol Scand. 1990 Jun;139(2):305-10. doi: 10.1111/j.1748-1716.1990.tb08928.x.
In a previous study prolonged low-frequency muscle stimulation in the hind leg of the spontaneously hypertensive rat (SHR) was shown to induce a reduction in blood pressure (about 15 mmHg) that lasted for many hours. We showed in that study that endorphin and serotonin systems were involved. In the present study drugs with selective affinity for the serotonin (5-HT) receptors were used to analyse further the involvement of different serotonin systems. In one group of SHR, a prestimulatory dose of metitepine maleate (a 5-HT1 and 5-HT2 receptor antagonist) completely abolished the post-stimulatory depressor response. The long-lasting depressor response was still present, although less pronounced, after a bolus dose of the 5-HT2 blocking agent ritanserin (R 55667) at the start of stimulation. The 5-HT3 receptor antagonist ICS 205-930 did not influence the response at all, nor did the selective 5-HT1a receptor agonist 8-OH-DPAT enhance the depressor response. These results indicate that the reduction in blood pressure after muscle stimulation is mainly mediated by the 5-HT1 receptor.
在先前的一项研究中,已表明对自发性高血压大鼠(SHR)后肢进行长时间的低频肌肉刺激可导致血压降低(约15 mmHg),且这种降低可持续数小时。我们在该研究中表明,内啡肽和血清素系统参与其中。在本研究中,使用对血清素(5-HT)受体具有选择性亲和力的药物来进一步分析不同血清素系统的参与情况。在一组SHR中,刺激前剂量的马来酸甲噻平(一种5-HT1和5-HT2受体拮抗剂)完全消除了刺激后的降压反应。在刺激开始时给予大剂量的5-HT2阻断剂利坦色林(R 55667)后,持久的降压反应仍然存在,尽管不太明显。5-HT3受体拮抗剂ICS 205-930对反应没有任何影响,选择性5-HT1a受体激动剂8-OH-DPAT也没有增强降压反应。这些结果表明,肌肉刺激后血压的降低主要由5-HT1受体介导。