Plasma Renin Activity and Sodium, Potassium and Water Excretion during Reversal of Hypertension in the One-Clip, Two-Kidney Hypertensive Rat

1979 ◽  
Vol 57 (1) ◽  
pp. 47-52 ◽  
Author(s):  
R. G. M. Ten Berg ◽  
F. H. H. Leenen ◽  
W. De Jong

1. The effect of removal of the clip on blood pressure, plasma renin activity and the excretion of water, sodium and potassium was studied in renal hypertensive rats. Hypertension was induced by application of a clip with an internal diameter of 0·20 mm, which was removed after 1, 2 or 3 weeks, and by using a clip with an internal diameter of 0·25 mm, which was removed after 2 weeks. The contralateral kidney remained undisturbed. 2. Blood pressure was almost normal 24 h after the removal of the clip; 70–90% of the total decrease in blood pressure occurred within 2–5 h. 3. The increased plasma renin activity, which was observed 2 and 3 weeks after application of a 0·20 mm clip, had returned to control values 24 h after removal of the clip. One week after application of a 0·20 mm clip, and 2 weeks after a 0·25 mm clip, plasma renin activity did not differ significantly from control values, before as well as after unclipping. 4. No significant differences were found between unclipped and sham-operated renal hypertensive rats, nor between the latter and the sham-operated normotensive control rats for water, sodium and potassium excretion, and for change in body weight, during the 24 h after the removal of the clip. 5. It is concluded that urinary loss of water and/or sodium does not play an important role in the acute decrease of blood pressure which occurs after the removal of a renal artery clip in one-clip, two-kidney hypertensive rats. A decrease in peripheral plasma renin activity can only partly explain the reversal of the hypertension.

1982 ◽  
Vol 63 (s8) ◽  
pp. 211s-213s
Author(s):  
Yutaka Takata ◽  
Austin E. Doyle ◽  
Margherita Veroni ◽  
Stuart G. Duffy

1. The aim of this study was to determine whether the urinary excretory function of the contralateral kidney is essential for angiotensin dependency in two-kidney, one-clip renal hypertensive rats. Ureteric ligation was used to abolish excretion from the contralateral kidney. 2. Plasma renin activity (PRA), renal renin content (RRC) and the response of blood pressure to captopril were examined. 3. The increase of blood pressure produced by the application of a clip to one renal artery was slightly accelerated by the ureteral ligation of the contralateral kidney. 4. Ureteral ligation of the contralateral kidney did not alter the response to a single oral administration of captopril. PRA and RRC of both kidneys were not different between the ureteral ligated group and the group without ureteric ligation. The falls in blood pressure produced by captopril correlated with PRA in the two groups. 5. These results suggest that the excretory function of the contralateral kidney is not essential for angiotensin dependency in the two-kidney, one-clip hypertensive rat model.


1975 ◽  
Vol 48 (1) ◽  
pp. 17-26 ◽  
Author(s):  
F. H. H. Leenen ◽  
J. W. Scheeren ◽  
D. Omylanowski ◽  
J. D. Elema ◽  
B. Van Der Wal ◽  
...  

1. The relationships between the renin-angiotensin-aldosterone system, sodium and potassium balance and systolic blood pressure were studied during development of moderate (160–180 mmHg; clip i.d. 0.25 mm) and severe (200–230 mmHg; clip i.d. 0.20 mm) renal hypertension in rats with an undisturbed contralateral kidney. 2. In severely hypertensive rats renin activity in the peripheral plasma increased from day 9, by which time the systolic blood pressure was elevated to 160–180 mmHg. The rate of total corticosteroid and aldosterone production in vitro increased from day 14 and plasma renin substrate concentration increased from day 24. In moderately hypertensive rats, none of these changes occurred. 3. During the first 10 days after the application of 0.25 and 0.20 mm clips, sodium and potassium retention/g gain in body weight were higher than in sham-operated controls. During the next 10 days, the positive balance stabilized in animals with a 0.25 mm clip whereas, in animals with a 0.20 mm clip, sodium and potassium balance returned to the level of the sham-operated controls through increased renal losses. Despite these changes the systolic pressure rose further in animals with a 0.20 mm clip. 4. The initial sodium retention could be a factor in the early rise of blood pressure and could account for the delay in the rise of peripheral plasma renin activity. The subsequent loss of the retained sodium and potassium during the development of severe hypertension could have facilitated the rise in peripheral plasma renin activity, but did not initiate this rise.


1984 ◽  
Vol 246 (4) ◽  
pp. H573-H578
Author(s):  
B. Waeber ◽  
J. Nussberger ◽  
H. R. Brunner

A total of 75 male Wistar rats with one-kidney, one-clip renal hypertension was maintained on either a regular (RNa) or a low-salt (LNa) diet for 3 wk after clipping. Blood pressure in the unanesthetized rats was equally elevated independent of sodium intake. Plasma renin activity was higher in LNa animals, and blood pressure was renin dependent only in this group, as evidenced by the blood pressure response to 10 mg/kg captopril iv. There was no significant difference in plasma catecholamines between RNa and LNa rats, although in the former the sympathetic nervous system is believed to play a major role in sustaining high blood pressure. The acute intravenous administration of 0.5 mg/kg prazosin did not induce a more pronounced blood pressure fall in the RNa rats. Prazosin enhanced plasma norepinephrine levels similarly in both groups, but epinephrine levels only rose in the LNa animals. Prazosin also markedly stimulated plasma renin activity rendering blood pressure renin dependent even in RNa rats. Thus, using alpha 1-adrenoceptor blockade, it has not been possible to demonstrate that the blood pressure elevation of salt-repleted one-kidney, one-clip renal hypertensive rats is due to an enhanced sympathetic nerve activity. Data obtained with sympatholytic agents must be interpreted with great caution if renin activity cannot be kept unchanged.


1983 ◽  
Vol 64 (5) ◽  
pp. 463-470
Author(s):  
Y. Takata ◽  
A. E. Doyle ◽  
M. Veroni ◽  
S. G. Duffy

1. Blood pressure, the hypotensive effect of captopril, plasma renin activity, renal renin content and kidney weight were measured in the two-kidney—one-clip model, the one-kidney—one-clip model and the two-kidney—one-clip model with the ureter of the contralateral kidney ligated in rats. The ureteric ligation was performed to abolish urinary excretion from the contralateral kidney in the two-kidney—one-clip model. 2. The development of hypertension after renal artery constriction was earlier and greater in the one-kidney—one-clip model and the two-kidney—one-clip model with ureter of the contralateral kidney ligated than in the two-kidney—one-clip model. A single oral dose of captopril produced a greater fall in blood pressure in both the two-kidney models than in the one-kidney—one-clip group. 3. Plasma renin activity and renal renin content of the clipped kidney were higher in the two-kidney model rats, whether or not the ureter had been ligated, than in the one-kidney—one-clip model animals, although more than half the rats from the two-kidney model had normal values. There was a significant correlation between plasma renin activity and the response to captopril in all groups, whereas in none of the three groups was the correlation between plasma renin activity and blood pressure significant. 4. The clipped kidney had a higher renin content than did the contralateral kidney, and the weight of the ischaemic kidney was decreased compared with the contralateral kidney whether it was untouched or had its ureter ligated. The weight of the clipped kidney was in the order one-kidney—one-clip model > two-kidney—one-clip model with ureter of the contralateral kidney ligated > two-kidney—one-clip model. 5. It was concluded that the renin-angiotensin system was stimulated to the similar degree in some animals for the two-kidney—one-clip models, whether or not the ureter of the contralateral kidney had been ligated, compared with the one-kidney—one-clip animals. This finding suggests that the contralateral kidney can stimulate renin secretion and synthesis in the clipped kidney independently of Na+ excretion.


1982 ◽  
Vol 32 (4) ◽  
pp. 742-745 ◽  
Author(s):  
Yukio HASEGAWA ◽  
Takushi X. WATANABE ◽  
Koichiro KAWASHIMA ◽  
Hirofumi SOKABE ◽  
Ken SAITO

1992 ◽  
Vol 82 (4) ◽  
pp. 389-395 ◽  
Author(s):  
C. Stonier ◽  
J. Bennett ◽  
E. A. Messenger ◽  
G. M. Aber

1. The effect of oestradiol alone and in combination with indomethacin on blood pressure, erythrocyte cation concentration and Na+−K+ flux has been studied in adult female normotensive and spontaneously hypertensive rats. 2. Oestradiol alone resulted in a significant decrease in blood pressure in spontaneously hypertensive rats (from 165.3 ± 3.9 to 146.4 ± 2.7 mmHg, P < 0.001), whereas it induced a significant increase in normotensive rats (from 111.8 ± 1.8 to 124.1 ± 3.6 mmHg, P < 0.001). When indomethacin and oestradiol were administered simultaneously or when indomethacin was given alone, no change in blood pressure occurred in spontaneously hypertensive rats (158.6 ± 6.9 and 159.8 ± 6.2 mmHg, respectively). 3. The fall in blood pressure induced by oestradiol in spontaneously hypertensive rats was associated with significant reductions in erythrocyte K+ concentration (from 127.4 ± 1.2 to 116.9 ± 1.7 mmol/l of cells, P < 0.001), in erythrocyte Na+ concentration (from 14.3 ± 0.8 to 13.0 ± 0.6 mmol/l of cells, P < 0.02), in ouabain-sensitive erythrocyte Na+ flux (from 17.8 ± 0.3 to 16.0 ± 0.4 mmol h−1 (1 of cells)−1, P < 0.01) and in ouabain-sensitive erythrocyte K+ flux (from 11.4 ± 0.2 to 10.4 ± 0.2 mmol h−1 (1 of cells)−1, P < 0.01). No change in blood pressure, erythrocyte cation concentration or Na+−K+ flux occurred when oestradiol and indomethacin were given together or when indomethacin was administered alone. 4. The hypertensive influence of oestradiol in normotensive rats was unaccompanied by any changes in erythrocyte K+ concentration, erythrocyte Na+ concentration and total, ouabain-sensitive and ouabain-resistant Na+−K+ flux. 5. The divergent changes in blood pressure noted in the two strains occurred despite comparable changes in plasma renin activity after oestradiol, with significant increases in plasma renin activity in normotensive rats (from 16.4 ± 4.2 to 28.4 ± 6.6 ng of angiotensin I h−1 ml−1, P < 0.05) and in spontaneously hypertensive rats (from 28.3 ± 2.7 to 39.5 ± 5.7 ng of angiotensin I h−1 ml−1, P < 0.01). The plasma renin activity in spontaneously hypertensive rats receiving oestradiol or indomethacin and oestradiol were similar with values of 39.5 ± 5.7 and 40.6 ± 5.7 ng of angiotensin I h−1 ml−1, respectively, but were significantly higher than that seen in control animals (28.3 ± 2.7 ng of angiotensin I h−1 ml−1, P < 0.01). Similarly, indomethacin alone induced a significant increase in plasma renin activity in spontaneously hypertensive rats to 35.8 ± 7.6 ng of angiotensin I h−1 ml−1 (P < 0.05). 6. The contrasting effects of oestradiol on blood pressure in the two rat strains occurred without any change in packed cell volume. Likewise, the changes in blood pressure in spontaneously hypertensive rats with either oestradiol alone or in combination with indomethacin occurred without any change in packed cell volume, although indomethacin alone resulted in a significant reduction in packed cell volume (from 30.9 ± 1.6 to 26.8 ± 2.0, P < 0.01). 7. The results suggest that the hypotensive action of oestradiol in spontaneously hypertensive rats might be mediated through its influence on erythrocyte cation concentration and/or the modulation of Na+−K+ flux either directly or via the action of prostanoids.


1973 ◽  
Vol 45 (s1) ◽  
pp. 251s-255s ◽  
Author(s):  
G. Dauda ◽  
J. Möhring ◽  
K. G. Hofbauer ◽  
E. Homsy ◽  
Ulrike Miksche ◽  
...  

1. In renal hypertensive rats, increase in blood pressure above 180 mmHg may induce sodium and water loss, reduced growth rate, elevated haematocrit, a marked rise in plasma renin concentration, an increase in renin extractable from the clamped and the contralateral kidney and malignant nephrosclerosis of the contralateral kidney. These symptoms characterize the malignant phase of renal hypertension in rats. 2. When water was given as drinking fluid, ten of eighteen rats developed signs of malignant hypertension and malignant nephrosclerosis within 3–4 weeks. Administration of 0.9% saline instead of water induced higher blood-pressure levels, but only five of eighteen rats showed malignant nephrosclerosis. When drinking fluid was changed from water to saline shortly before or shortly after the onset of malignant hypertension, the condition improved, and in only one of twelve rats was malignant nephrosclerosis observed. 3. It is concluded that in renal hypertensive rats sodium supplements may improve or prevent signs of malignant hypertension and the development of malignant nephrosclerosis.


1980 ◽  
Vol 33 (2) ◽  
pp. 87-94 ◽  
Author(s):  
C.E. Grim ◽  
F.C. Luft ◽  
J.Z. Miller ◽  
G.R. Meneely ◽  
H.D. Battarbee ◽  
...  

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