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肾脏的降压功能。卡托普利加解除夹闭对其的阐明。

The antihypertensive function of the kidney. Its elucidation by captopril plus unclipping.

作者信息

Muirhead E E, Pitcock J A, Nasjletti A, Brown P, Brooks B

出版信息

Hypertension. 1985 May-Jun;7(3 Pt 2):I127-35. doi: 10.1161/01.hyp.7.3_pt_2.i127.

DOI:10.1161/01.hyp.7.3_pt_2.i127
PMID:2581897
Abstract

Unclipping the one-kidney, one-clip hypertensive rat during a free flow of urine caused the blood pressure to return to normal levels within about 3 hours. We found that administration of captopril plus unclipping caused the blood pressure to return to normal in minutes (17 +/- 4). Ureterocaval anastomosis plus captopril plus unclipping also caused the blood pressure to return to normal in minutes (8.8 +/- 2). Thus, the potentiation of the drop in blood pressure does not seem to be due to a volume effect. Administration of indomethacin and aprotinin did not prevent a rapid decline of the blood pressure after unclipping, but the decline was less rapid than that occurring after captopril and unclipping, which suggests that prostaglandin may have some effect on this mechanism. Saralasin administration did not potentiate the antihypertensive action of captopril plus unclipping. Chemical papillectomy prevented the drop in blood pressure after unclipping. The bolus dose of captopril to the hypertensive rat often caused a transient depressor effect resembling that due to the antihypertensive neutral renomedullary lipid, which suggests secretion of this lipid into the blood. The renomedullary interstitial cells accumulated large lipid granules after captopril administration. These cells also degranulated after unclipping. These findings are consistent with the hypothesis that the renal papilla secretes an antihypertensive hormone after unclipping. At present, antihypertensive neutral renomedullary lipid is the main putative hormone.

摘要

在自由排尿过程中解除单肾单夹高血压大鼠的夹闭,血压在约3小时内恢复至正常水平。我们发现,给予卡托普利并解除夹闭可使血压在数分钟内(17±4)恢复正常。输尿管腔静脉吻合术联合卡托普利并解除夹闭也可使血压在数分钟内(8.8±2)恢复正常。因此,血压下降的增强似乎并非由于容量效应。给予吲哚美辛和抑肽酶并不能阻止解除夹闭后血压的快速下降,但下降速度比卡托普利与解除夹闭后要慢,这表明前列腺素可能对该机制有一定作用。给予沙拉新并不能增强卡托普利与解除夹闭的降压作用。化学性肾乳头切除可防止解除夹闭后血压下降。给高血压大鼠静脉注射大剂量卡托普利常引起短暂的降压效应,类似于抗高血压中性肾髓质脂质所致的效应,这提示该脂质分泌入血。给予卡托普利后,肾髓质间质细胞积累了大量脂质颗粒。解除夹闭后这些细胞也出现脱颗粒现象。这些发现与肾乳头在解除夹闭后分泌一种降压激素的假说相符。目前,抗高血压中性肾髓质脂质是主要的假定激素。

相似文献

1
The antihypertensive function of the kidney. Its elucidation by captopril plus unclipping.肾脏的降压功能。卡托普利加解除夹闭对其的阐明。
Hypertension. 1985 May-Jun;7(3 Pt 2):I127-35. doi: 10.1161/01.hyp.7.3_pt_2.i127.
2
Different mechanisms maintaining high blood pressure in chronic one-kidney, one-clip, and two-kidney, one-clip hypertensive rats.维持慢性单肾单夹和双肾单夹高血压大鼠高血压的不同机制。
Clin Exp Hypertens A. 1983;5(3):429-45. doi: 10.3109/10641968309069498.
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The reno-hepatic axis of blood pressure control: further studies.血压控制的肾肝轴:进一步研究
Am J Med Sci. 1987 Mar;293(3):177-81. doi: 10.1097/00000441-198703000-00006.
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Effect of 12-hour infusions of saralasin or captopril on blood pressure in hypertensive conscious rats. Relationship to plasma renin, duration of hypertension, and effect of unclipping.在清醒高血压大鼠中,静脉输注沙拉新或卡托普利12小时对血压的影响。与血浆肾素、高血压病程以及解除夹闭的效应的关系。
J Lab Clin Med. 1981 Aug;98(2):302-10.
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The renal antihypertensive endocrine function: its relation to cytochrome P-450.肾脏的降压内分泌功能:及其与细胞色素P-450的关系。
J Hypertens. 1989 May;7(5):361-9. doi: 10.1097/00004872-198905000-00003.
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The liver converts the antihypertensive hormone of the kidney. The renohepatic axis.肝脏可转化肾脏的降压激素。肾肝轴。
Hypertension. 1986 Jun;8(6 Pt 2):II117-22. doi: 10.1161/01.hyp.8.6_pt_2.ii117.
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Derivation of neutral antihypertensive lipid from renal venous effluent in rats.大鼠肾静脉流出液中中性抗高血压脂质的提取
Clin Sci (Lond). 1981 Dec;61 Suppl 7:331s-333s. doi: 10.1042/cs061331s.
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Hypertension. 1983 Nov-Dec;5(6 Pt 3):V61-5. doi: 10.1161/01.hyp.5.6_pt_3.v61.
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Degranulation of renomedullary interstitial cells during reversal of hypertension.高血压逆转过程中肾髓质间质细胞的脱颗粒现象。
Hypertension. 1981 Nov-Dec;3(6 Pt 2):II-75-80. doi: 10.1161/01.hyp.3.6_pt_2.ii-75.
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Surgical reversal of two-kidney one clip hypertension during inhibition of the renin-angiotensin system.在肾素-血管紧张素系统受抑制期间对两肾一夹型高血压进行手术逆转。
Hypertension. 1982 Jan-Feb;4(1):69-76. doi: 10.1161/01.hyp.4.1.69.

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