Cockcroft J R, Noon J P, Gardner-Medwin J, Bennett T
Department of Medicine and Therapeutics, University Hospital, Queen's Medical Centre, Nottingham, UK.
Br J Clin Pharmacol. 1997 Jul;44(1):57-60. doi: 10.1046/j.1365-2125.1997.00622.x.
The haemodynamic effects of adrenomedullin and calcitonin gene-related peptide (CGRP) were studied in resistance and capacitance vessels of healthy volunteers.
Adrenomedullin and CGRP were infused into the brachial artery of eight healthy subjects on two separate occasions at doses between 0.3-30 pmol min(-1). Forearm blood flow was measured using venous occlusion plethysmography. Venodilatation to adrenomedullin and CGRP was assessed in a further eight subjects by infusing the peptides at doses between 0.3-10 pmol min(-1) into a dorsal hand vein preconstricted with noradrenaline. Venodilator responses were measured as percentage reduction in noradrenaline preconstriction.
Adrenomedullin and CGRP at a dose of 30 pmol min(-1), produced an increase in forearm blood flow of 288 +/- 42% and 252 +/- 30% respectively (mean +/- s.e. mean, P<0.001). At doses between 3 and 10 pmol min(-1) adrenomedullin was significantly more potent than CGRP. The vasodilatation to both peptides was of similar duration with a biological half-life of approximately 18 min. Adrenomedullin reversed constriction in dorsal hand veins by 84 +/- 2% (P<0.001) at a dose of 10 pmol min(-1). CGRP produced a similar effect reversing constriction by 72 +/- 12% at the same dose (P<0.01). In veins, adrenomedullin was also more potent than CGRP at doses between 0.3 and 3 pmol min(-1).
The lowest dose of adrenomedullin producing significant arteriolar dilatation was calculated to produce plasma levels similar to those found in heart failure. These findings suggest that in pathophysiological conditions such as heart failure circulating levels of adrenomedullin may be within a range capable of influencing vascular resistance directly.
研究肾上腺髓质素和降钙素基因相关肽(CGRP)对健康志愿者阻力血管和容量血管的血流动力学影响。
在两个不同时间段,以0.3 - 30 pmol min⁻¹的剂量将肾上腺髓质素和CGRP注入8名健康受试者的肱动脉。使用静脉阻断体积描记法测量前臂血流量。通过以0.3 - 10 pmol min⁻¹的剂量将肽类物质注入预先用去甲肾上腺素收缩的手背静脉,在另外8名受试者中评估肾上腺髓质素和CGRP引起的静脉扩张。静脉扩张反应以去甲肾上腺素预收缩减少的百分比来衡量。
剂量为30 pmol min⁻¹时,肾上腺髓质素和CGRP分别使前臂血流量增加288±42%和252±30%(平均值±标准误平均值,P<0.001)。在3至10 pmol min⁻¹的剂量范围内,肾上腺髓质素比CGRP显著更有效。两种肽类物质引起的血管扩张持续时间相似,生物半衰期约为18分钟。剂量为10 pmol min⁻¹时,肾上腺髓质素使手背静脉收缩逆转84±2%(P<0.001)。相同剂量下,CGRP产生类似效果,使收缩逆转72±12%(P<0.01)。在静脉中,剂量在0.3至3 pmol min⁻¹之间时,肾上腺髓质素也比CGRP更有效。
产生显著小动脉扩张的肾上腺髓质素最低剂量经计算可产生与心力衰竭患者中发现的血浆水平相似的水平。这些发现表明,在诸如心力衰竭等病理生理状况下,肾上腺髓质素的循环水平可能处于能够直接影响血管阻力的范围内。