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新型二氢吡啶类钙通道阻滞剂CS-905对大鼠动脉血压、肾脏排泄功能及肾髓质血流量的影响。

Effects of CS-905, a novel dihydropyridine calcium channel blocker, on arterial pressure, renal excretory function, and inner medullary blood flow in the rat.

作者信息

Yagil Y, Miyamoto M, Frasier L, Oizumi K, Koike H

机构信息

University of Rochester School of Medicine and Dentistry, New York.

出版信息

Am J Hypertens. 1994 Jul;7(7 Pt 1):637-46.

PMID:7946166
Abstract

CS-905 is a dihydropyridine calcium channel antagonist which stands out for its prolonged hypotensive effect, and which is currently under investigation for the treatment of hypertension. The aim of the current series of studies was to investigate the effects of CS-905 on renal function in relation to its effects on arterial pressure. In anesthetized spontaneously hypertensive rats (SHR), intravenous bolus injection of CS-905 reduced mean arterial pressure (MAP) in a dose-dependent fashion. In parallel, there was a dose-related increase in urine flow (V), sodium excretion (UNaV), renal plasma flow (RPF), and glomerular filtration rate (GFR). In chronically cannulated unanesthetized SHR, single-dose CS-905 by gavage produced a sustained reduction in MAP, a significant increase in V and UNaV, no effect on RPF, and an increase in GFR. Continuous intrarenal infusion of CS-905 in anesthetized normotensive Munich Wistar rats at doses that did not affect MAP caused a marked diuresis and natriuresis, without affecting RPF or GFR. To determine whether the diuretic and natriuretic effects of CS-905 were mediated by changes in inner medullary blood flow, the effect of CS-905 on vasa recta blood flow (Qvr) was studied by fluorescent videomicroscopy in anesthetized normotensive Munich Wistar rats during continuous intrarenal infusion. At low infusion rates, CS-905 was diuretic and natriuretic while increasing Qvr. With a high infusion rate, although the diuretic and natriuretic effects of CS-905 were maximal, Qvr decreased. These findings suggest that the diuretic and natriuretic effects of CS-905 are dissociated from and cannot be accounted for by changes in RPF, GRF, or Qvr, and are most likely secondary to a direct action of CS-905 on renal tubule handling of sodium and water.

摘要

CS - 905是一种二氢吡啶类钙通道拮抗剂,以其持久的降压作用而突出,目前正在进行治疗高血压的研究。本系列研究的目的是探讨CS - 905对肾功能的影响及其与动脉压的关系。在麻醉的自发性高血压大鼠(SHR)中,静脉推注CS - 905可使平均动脉压(MAP)呈剂量依赖性降低。同时,尿流量(V)、钠排泄量(UNaV)、肾血浆流量(RPF)和肾小球滤过率(GFR)呈剂量相关增加。在长期插管的未麻醉SHR中,经口灌胃单剂量CS - 905可使MAP持续降低,V和UNaV显著增加,对RPF无影响,GFR增加。在麻醉的正常血压慕尼黑Wistar大鼠中,以不影响MAP的剂量持续肾内输注CS - 905可引起明显的利尿和利钠作用,而不影响RPF或GFR。为了确定CS - 905的利尿和利钠作用是否由髓质内血流变化介导,在麻醉的正常血压慕尼黑Wistar大鼠中,通过荧光视频显微镜研究了持续肾内输注期间CS - 905对直小血管血流(Qvr)的影响。在低输注速率下,CS - 905具有利尿和利钠作用,同时增加Qvr。在高输注速率下,尽管CS - 905的利尿和利钠作用最大,但Qvr降低。这些发现表明,CS - 905的利尿和利钠作用与RPF、GRF或Qvr的变化无关,也不能用这些变化来解释,很可能是CS - 905对肾小管钠和水处理的直接作用所致。

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