Protter A A, Wallace A M, Ferraris V A, Weishaar R E
Scios Inc., Mountain View, California 94043, USA.
Am J Hypertens. 1996 May;9(5):432-6. doi: 10.1016/0895-7061(95)00435-1.
Brain natriuretic peptide (BNP) is a cardiac-derived peptide hormone with cardiovascular and renal actions that is structurally and functionally related to atrial natriuretic peptide (ANP). Previous studies using rat vascular tissue have demonstrated a direct vasorelaxant effect of BNP. However, species-specific potency issues have precluded an accurate measurement of the effect of human BNP. This report demonstrates the vasorelaxant effects of human BNP on human vascular tissue prepared from internal mammary artery and saphenous vein samples. The vasorelaxant effect of human BNP is compared to the other members of the natriuretic peptide family, human ANP and C-type natriuretic peptide (CNP). With regard to potency and magnitude of effect, human BNP and human ANP were similar in relaxing arterial tissue preconstricted with endothelin-1 (BNP ED50 = 1.9 nmol/L and ANP ED50 = 1.8 nmol/L) or phenylephrine (BNP ED50 = 10 nmol/L and ANP ED50 = 19 nmol/L), while CNP was significantly less effective. All three natriuretic peptides exhibited weak venodilating action. These data demonstrate that human BNP is a potent inhibitor of the vasoconstrictive actions of endothelin-1 and the alpha-adrenergic agonist phenylephrine on isolated human artery tissue preparations.
脑钠肽(BNP)是一种源自心脏的肽类激素,具有心血管和肾脏作用,在结构和功能上与心房钠尿肽(ANP)相关。先前使用大鼠血管组织的研究已证明BNP具有直接的血管舒张作用。然而,物种特异性效力问题妨碍了对人BNP作用的准确测量。本报告证明了人BNP对从乳内动脉和大隐静脉样本制备的人血管组织的血管舒张作用。将人BNP的血管舒张作用与钠尿肽家族的其他成员,即人ANP和C型钠尿肽(CNP)进行了比较。就效力和作用强度而言,人BNP和人ANP在舒张用内皮素-1预收缩的动脉组织(BNP的半数有效浓度[ED50] = 1.9 nmol/L,ANP的ED50 = 1.8 nmol/L)或去氧肾上腺素(BNP的ED50 = 10 nmol/L,ANP的ED50 = 19 nmol/L)方面相似,而CNP的效果明显较差。所有三种钠尿肽均表现出较弱的静脉舒张作用。这些数据表明,人BNP是内皮素-1和α-肾上腺素能激动剂去氧肾上腺素对分离的人动脉组织制剂的血管收缩作用的有效抑制剂。