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  • 1
    ISSN: 1432-2013
    Keywords: Antidiuretic hormone ; Glucagon ; Brattleboro rats ; Adenylate-cyclase ; Na−K-ATPase ; Single tubule ; Thick ascending limb ; Collecting tubule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The medullary thick ascending limb (MAL), but not the medullary collecting tubule (MCT), has been shown to have an impaired adenylate cyclase (AC) responsiveness to ADH and a selective hypoplasia in Brattleboro diabetes insipidus (DI) rats. Since chronic ADH administration has been found to increase epithelium volume and basolateral membrane surface area in MAL but not in MCT, we investigated whether chronic ADH infusion would affect the hormone-sensitive AC and the Na−K-ATPase activity — two markers of the basolateral membrane — in single microdissected portions of thick ascending limb and collecting tubule in DI rats. Results indicate that 1. in MAL of ADH-treated rats, AC resposes to in vitro AVP and glucagon and Na−K-ATPase activity increased to the same extent as did epithelium volume (60–80%); 2. changes in the other segments were independent of any morphological alteration. In the cortical thick ascending limb, AVP and glucagonsensitive AC decreased by 30–40% whereas Na−K-ATPase activity did not change. In the collecting tubule, AC response to in vitro AVP was not altered by ADH-treatment but glucagon-sensitive AC dropped by 50% and Na−K-ATPase activity doubled, independently of any variation in plasma aldosterone and glucagon levels. These results show that, in the MAL, the ADH-induced variations in enzyme activity are a reflection of the enlargement of the basolateral membrane surface area. Further studies are needed to clarify the origin of enzymatic alterations in the other segments.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 399 (1983), S. 139-146 
    ISSN: 1432-2013
    Keywords: Adrenalectomized rats ; Sodium clearance ; Nephron microdissection ; Mineralocorticoids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The short-term effect of one single injection of aldosterone on the renal sodium transport on one hand, and the Na−K-ATPase activity on the other hand, was studied in chronic adrenalectomized rats. Sodium transport was estimated by clearances, and Na−K-ATPase was measured in microdissected fragments of the nephron, according to our microtechnique previously described. Five to eight days after adrenalectomy, only 30% of the initial enzyme activity was recovered in the cortical collecting tubule (CCT). Administration of aldosterone completely restored the ATP-ase activity within three hours. Adrenalectomy also curtailed by 20–45% the activity of other nephron segments but aldosterone had no stimulatory effect on them. Sodium-reabsorption also increased after the hormone injection, following the same time (0.5〈t 1/2〈1 h) and dose dependencies (0.8〈K 1/2〈0.9 μg/kg) as those observed for the enzyme activity in the CCT. It is concluded that the short-term stimulation of Na−K-ATPase in the collecting tubule, after an acute administration of aldosterone, may be responsible for the simultaneous increase in sodium transport.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 399 (1983), S. 147-151 
    ISSN: 1432-2013
    Keywords: Adrenalectomized rabbits ; Kidney microdissection ; Mineralocorticoid and glucocorticoid effects ; Spironolactone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Both glucocorticoids and mineralcorticoids stimulate the renal Na−K-ATPase. However, the exact site of their respective action is not precisely determined and it is still unknown wheter these effects are cumulative or not. We studied the effects of dexamethasone and aldosterone on Na−K-ATPase activity in microdissected nephron segments from adrenalectomized rabbits. In proximal convoluted tubule (PCT) the enzyme activity was altered neither by adrenalectomy nor by any steroid replacement. In the medullary thick ascending limb of the loop of Henle (MAL) and the distal convoluted tubule (DCT), Na−K-ATPase activity decreased by 40% after adrenalectomy, and was restored to control level three hours after administration of dexamethasone (100 μg/kg) but not by aldosterone (up to 10 μg/kg). In the cortical (CCT) and medullary (MCT) collecting tubule the enzyme activity decreased by 75% after adrenalcetomy but in contrast with the MAL and the DCT, these two segments were sensitive to both dexamethasone (100 μg/kg) and aldosterone (10 μg/kg) and recovered their activities within 3 h after the hormone injection. These effects were not additive. Spironolactone (100 μg/kg) abolished the action of each of the two hormones on the CCT and MCT. In contrast, spironolactone did not curtail the effect of dexamethasone on MAL and DCT. These results indicate that whereas glucocorticoid action is localized in MAL, DCT, CCT and MCT, the mineralocorticoid effect is restricted to the CCT and MCT exclusively. They also suggest that, in the CCT and MCT, the two types of hormones share the same receptors.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 402 (1984), S. 258-263 
    ISSN: 1432-2013
    Keywords: Adrenalectomized rabbit ; Kidney microdissection ; Mineralocorticoid and glucocorticoid effects ; 3H ouabain binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Both aldosterone and dexamethasone are known to stimulate renal Na−K-ATPase activity although their action is restricted to specific nephron segments: the collecting tubule, the target site for mineralocorticoids, and the thick ascending limb and distal convoluted tubule, the target sites for glucocorticoids. As this stimulation by corticosteroids is very fast, we attempted to establish whether it occurs through de novo synthesis of new Na−K-ATPase units or by increasing the specific activity of the Na−K-ATPase units already present. For this purpose we studied the effects of aldosterone and dexamethasone on Na−K-ATPase specific activity in microdissected nephron segments from adrenalectomized rabbits. This specific activity was determined by the ratio of ATPase activity over the apparent number of catalytic units, as measured by specific3H ouabain binding. In the proximal tubule, neither adrenalectomy nor steroid replacement altered Na−K-ATPase activity or the apparent number of catalytic sites. In other nephron segments, adrenalectomy reduced Na−K-ATPase activity and specific3H ouabain binding concomitantly, and therefore left this enzyme's specific activity unaltered. In the cortical and outer medullary collecting tubules, 10 μg/kg aldosterone simultaneously restored both the activity and apparent number of catalytic units of Na−K-ATPase to their control levels, and therefore did not modify the specific activity of the pump. Conversely, 100 μg/kg dexamethasone increased Na−K-ATPase activity in the thick ascending limb and distal convoluted tubule without changing the apparent number of catalytic units. These results indicate that both mineraloand glucocorticoids control kidney Na−K-ATPase activity, but at different sites and by different mechanisms: Aldosterone induces appearance of new catalytic units in the collecting tubule, whereas dexamethasone increases the specific activity of pre-existing units in the thick ascending limb and distal convoluted tubule.
    Type of Medium: Electronic Resource
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