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肾上腺升压素的血管活性及其与肾上腺髓质素的相互作用 被引量:3

Vasoactive effects of adrenotensin and iflteractions between adrenotensin and adrenomedullin
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摘要 本研究发现10和100nmol/L肾上腺升压素(adrenotensin,AT)呈剂量依赖性增加大鼠主动脉环张力(P<001);2.5nmol/kg AT静脉推注可使麻醉大鼠平均动脉压升高28%(P<0.01);100nmol/L可使培养的大鼠血管平滑肌细胞的3H-胸腺嘧啶核苷参入量增加55%(P<0.01);肾上腺髓质素(adrenomedullin,AM)则在不同程度上抑制AT的上述活性;1、10和100nmol/LAT可分别抑制AM的释放率达19%、35%和46%(P<0.05或0.01),而10nmol/LAM也是一种新的缩血管、升血压和促进血管平滑肌增殖的多肽;AT与AM之间在血管活性上相互拮抗,在释放上交互抑制,这些相互作用可能是肾上腺髓质素原的分子内调节的体现。 Our study found that: 10 and 100 nmol/L adrenotensin (ADT ) augmented rat aortic tension in a dosedependent manner (P<0.01 ): an intravenous bolus injection of ADT (2.5nmol/kg) increased mean arterial pressure (MAP) offanesthetized rat by 28% (p<0.01 ); 100 nmol/L ADY increased 3H-thymidine incorporation in cultured rat vascular smooth muscle cell (VSMC ) by 55% (P<0.01 ): adrenomedullin (ADM ) inhibited these activities of ADT in different degrees: ADT at dose of decreased 1, 10 and 100 nmol/L ADM release rate by 19% 35% and 46%, respectively (P<0.05 or 0.01 ) and 10 nmol/L ADM also inhibited ADT release by 45% from rat aorta (P<0.01). These data suggested that ADT might be a novel peptide that have the activities ofvasoconstriction, pressor and inducing VSMC proliferation: there are antagonistic effects in vascular activities and reciprocal inhibition in release regulation between ADT and ADM; and these interactions may be the manifestations of intramolecular regulation of proadrenomedullin.
出处 《基础医学与临床》 CSCD 2000年第1期63-65,共3页 Basic and Clinical Medicine
关键词 肾上腺升压素 肾上腺髓质素 血管活性 adrenotensin, adrenomedullin, vascular activities, release regulation
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