Champion H C, Santiago J A, Murphy W A, Coy D H, Kadowitz P J
Department of Pharmacology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Am J Physiol. 1997 Jan;272(1 Pt 2):R234-42. doi: 10.1152/ajpregu.1997.272.1.R234.
The effects of adrenomedullin (ADM)-(22-52), a putative ADM receptor antagonist, on vasodilator responses to ADM and the structurally related peptide, calcitonin gene-related peptide (CGRP), were investigated in the hindlimb vascular bed of the cat under constant-flow conditions. ADM-(22-52) had no significant effect on hindlimb perfusion pressure when injected in doses up to 120 nmol; after administration of ADM-(22-52), vasodilator responses to ADM were unchanged, whereas vasodilator responses to CGRP were inhibited. The inhibitory effects of ADM-(22-52) on responses to CGRP were selective and reversible and were similar to the inhibitory effects of the CGRP antagonist CGRP-(8-37). Hindlimb vasodilator responses to CGRP and to ADM were increased in duration by the adenosine 3',5'-cyclic monophosphate (cAMP) phosphodiesterase inhibitor rolipram but were not altered by inhibitors of guanosine 3',5'-cyclic monophosphate phosphodiesterase, nitric oxide synthetase, K(+)-ATP channels, the cyclooxygenase pathway, or the adrenergic nervous system. These results demonstrate that ADM-(22-52) is a selective CGRP receptor antagonist in the hindlimb vascular bed of the cat. The present data suggest that vasodilator responses to CGRP and ADM are mediated by different receptors but that these peptides dilate the hindlimb vascular bed of the cat by a similar cAMP-dependent mechanism.
在恒流条件下,研究了一种假定的肾上腺髓质素(ADM)受体拮抗剂肾上腺髓质素(ADM)-(22 - 52) 对猫后肢血管床中ADM和结构相关肽降钙素基因相关肽(CGRP)血管舒张反应的影响。注射剂量高达120 nmol的ADM-(22 - 52) 对后肢灌注压无显著影响;给予ADM-(22 - 52) 后,对ADM的血管舒张反应未改变,而对CGRP的血管舒张反应受到抑制。ADM-(22 - 52) 对CGRP反应的抑制作用具有选择性和可逆性,且与CGRP拮抗剂CGRP-(8 - 37) 的抑制作用相似。腺苷3',5'-环磷酸单酯(cAMP)磷酸二酯酶抑制剂咯利普兰可延长后肢对CGRP和ADM的血管舒张反应持续时间,但鸟苷3',5'-环磷酸单酯磷酸二酯酶抑制剂、一氧化氮合酶抑制剂、K(+) - ATP通道抑制剂、环氧化酶途径抑制剂或肾上腺素能神经系统抑制剂对此无影响。这些结果表明,ADM-(22 - 52) 是猫后肢血管床中的一种选择性CGRP受体拮抗剂。目前的数据表明,对CGRP和ADM的血管舒张反应由不同受体介导,但这些肽通过类似的cAMP依赖性机制使猫的后肢血管床舒张。