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降钙素基因相关肽受体拮抗剂对清醒大鼠中机制不同的血管调节剂引起的全身血压反应的影响。

Effect of calcitonin gene-related peptide receptor antagonism on the systemic blood pressure responses to mechanistically diverse vasomodulators in conscious rats.

机构信息

Department of Central Pharmacology, Merck Research Laboratories, West Point, PA 19486, USA.

出版信息

J Cardiovasc Pharmacol. 2010 Nov;56(5):518-25. doi: 10.1097/FJC.0b013e3181f5d414.

Abstract

The effects of calcitonin gene-related peptide (CGRP) receptor antagonism with CGRP 8-37 on blood pressure changes evoked by the intravenous administration of the vasoactive modulators angiotensin II, phenylephrine, adenosine, nitroglycerine, and sodium nitroprusside were assessed in conscious rats. The effects of sumatriptan and dihydroergotamine on the blood pressure responses evoked by these vasomodulators also were assessed. The intravenous test dose of CGRP 8-37 was validated through block of depressor responses to intravenous CGRP in conscious rats, whereas the intravenous test doses of sumatriptan and dihydroergotamine were validated by reductions in carotid blood flow in anesthetized rats. CGRP 8-37 had no significant effects on blood pressure dose-response profiles and individual dose blood pressure responses to any of the vasomodulators tested. In contrast, sumatriptan altered the blood pressure dose-response profiles to angiotensin II and sodium nitroprusside (P < 0.03) and dihydroergotamine altered the blood pressure dose-response profile to sodium nitroprusside (P < 0.02) and tended to alter that of phenylephrine (P = 0.06). Both sumatriptan and dihydroergotamine displayed frequent alterations of individual dose blood pressure responses to all vasomodulators. These findings are consistent with concerns for sumatriptan and dihydroergotamine to alter systemic hemodynamics, whereas CGRP receptor antagonism did not display the same hemodynamic liability.

摘要

在清醒大鼠中评估了降钙素基因相关肽 (CGRP) 受体拮抗剂 CGRP 8-37 对血管活性调节剂血管紧张素 II、苯肾上腺素、腺苷、硝酸甘油和亚硝基铁氰化钠静脉给药引起的血压变化的影响。还评估了舒马曲坦和二氢麦角胺对这些血管调节剂引起的血压反应的影响。通过阻断 CGRP 8-37 在清醒大鼠中对静脉内 CGRP 的降压反应来验证静脉内 CGRP 8-37 的测试剂量,而舒马曲坦和二氢麦角胺的静脉内测试剂量则通过麻醉大鼠颈动脉血流量的减少来验证。CGRP 8-37 对血压剂量-反应曲线和对任何测试的血管调节剂的单个剂量血压反应均无显著影响。相比之下,舒马曲坦改变了血管紧张素 II 和亚硝基铁氰化钠的血压剂量-反应曲线 (P < 0.03),二氢麦角胺改变了亚硝基铁氰化钠的血压剂量-反应曲线 (P < 0.02),并倾向于改变苯肾上腺素的血压剂量-反应曲线 (P = 0.06)。舒马曲坦和二氢麦角胺都经常改变所有血管调节剂的单个剂量血压反应。这些发现与舒马曲坦和二氢麦角胺改变全身血液动力学的担忧一致,而 CGRP 受体拮抗剂则没有显示出相同的血液动力学风险。

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