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在一种古老的全骨鱼类雀鳝(Amia calva)中血管紧张素I、血管紧张素II和去甲肾上腺素介导的升压反应。

Angiotensin I- and II- and norepinephrine-mediated pressor responses in an ancient holostean fish, the bowfin (Amia calva).

作者信息

Butler D G, Oudit G Y, Cadinouche M Z

机构信息

Department of Zoology, University of Toronto, Ontario, Canada.

出版信息

Gen Comp Endocrinol. 1995 Jun;98(3):289-302. doi: 10.1006/gcen.1995.1071.

Abstract

Dorsal aortic blood pressure (PSYS, systolic; PDIAS, diastolic; and PDA, mean) and heart rate (HR) were measured in resting freshwater bowfins (n = 6), Amia calva L., before and after i.v. injections of 50, 100, 200, 500, and 1000 ng.kg-1 of synthetic [Asn1, Val5]-angiotensin II (ANG II). Baseline PSYS, PDIAS, and PDA were 27.7 +/- 2.8, 22.4 +/- 1.8, and 24.5 +/- 2 mm Hg, respectively. Bowfins were only moderately responsive to ANG II in a stepwise manner and the increase in blood pressure became significant only at the two highest doses; lower doses tended only to increase arterial pressure. Pressor responses due to 200 and 500 ng.kg-1 decayed over a greater time period compared with other doses. alpha-Adrenergic blockade abolished 70% of the ANG II-mediated pressor responses. Eel, salmon, and goosefish angiotensin I (ANG I; 500 ng.kg-1) elicited similar vasopressor responses (magnitude and time course) which were eliminated by prior angiotensin converting enzyme inhibition (captopril; 2-10 mg.kg-1). Bullfrog ANG I evoked a pressor effect, only at a higher dose (5000 ng.kg-1). Consecutive norepinephrine (NE) injections (100, 200, 500, and 1000 ng.kg-1) increased PSYS, PDIAS, and PDA in a dose-dependent manner which was dependent on alpha-adrenoceptors since phentolamine (1-3 mg.kg-1) abolished 80% of the pressor action of NE. PSYS was elevated by 100 ng.kg-1 of NE but PDIAS and PDA were significantly increased only at 200 ng.kg-1 ANG II and NE had no measurable chronotropic effect and resting HR (27.2 +/- 0.8 beats.min-1) was unchanged. Captopril and phentolamine treatments produced rapid hypotension and bradycardia (25-30%) which lasted from 15 to 30 and 20 to 40 min, respectively. The rising and decreasing phases of the NE-mediated pressor responses had shorter durations than ANG II effects. Tachyphylaxis occurred with the high doses of ANG II and NE. The data show that in the ancient bowfin, which evidently lacks renal juxtaglomerular cells, the cardiovascular system can be regulated by the renin-angiotensin system and NE.

摘要

在静息状态下,对6条淡水雀鳝(Amia calva L.)静脉注射50、100、200、500和1000 ng·kg-1的合成[天冬酰胺1,缬氨酸5]-血管紧张素II(ANG II)前后,测量其背主动脉血压(收缩压PSYS、舒张压PDIAS和平均压PDA)及心率(HR)。基线PSYS、PDIAS和PDA分别为27.7±2.8、22.4±1.8和24.5±2 mmHg。雀鳝对ANG II仅呈中度的逐步反应,仅在两个最高剂量时血压升高才显著;较低剂量仅倾向于升高动脉压。与其他剂量相比,200和500 ng·kg-1剂量的ANG II引起的升压反应在更长时间内衰减。α-肾上腺素能阻断消除了70%的ANG II介导的升压反应。鳗鱼、鲑鱼和海鲶的血管紧张素I(ANG I;500 ng·kg-1)引起相似的血管升压反应(幅度和时程),在预先给予血管紧张素转换酶抑制剂(卡托普利;2 - 10 mg·kg-1)后反应消失。牛蛙ANG I仅在较高剂量(5000 ng·kg-1)时引起升压作用。连续注射去甲肾上腺素(NE)(100、200、500和1000 ng·kg-1)以剂量依赖方式升高PSYS、PDIAS和PDA,这依赖于α-肾上腺素能受体,因为酚妥拉明(1 - 3 mg·kg-1)消除了80%的NE升压作用。100 ng·kg-1的NE使PSYS升高,但仅在200 ng·kg-1时PDIAS和PDA才显著升高,NE对心率无明显影响,静息心率(27.2±0.8次/分钟)不变。卡托普利和酚妥拉明治疗产生快速低血压和心动过缓(25 - 30%),分别持续15至30分钟和20至40分钟。NE介导的升压反应的上升和下降阶段持续时间比ANG II的作用短。高剂量的ANG II和NE会出现快速耐受性。数据表明,在明显缺乏肾球旁细胞的古老雀鳝中,心血管系统可由肾素 - 血管紧张素系统和NE调节。

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