The vasopressin-sensitive adenylate cyclase of the rat kidney. Effect of adrenalectomy and corticosteroids on hormonal receptor-enzyme coupling.

نویسندگان

  • R Rajerison
  • J Marchetti
  • C Roy
  • J Bockaert
  • S Jard
چکیده

A subcellular fraction prepared from rat kidney medulla contained vasopressin-sensitive adenylate cyclase and vasopressin binding sites. Vasopressin stimulation resulted in an increase in the maximal velocity of the reaction with no change in the apparent K, for ATP. A maximum activation ratio (5 to 10) was obtained at low Mg2+ concentration (0.75 mM) and pH 7.4. The apparent Km for vasopressin was (1 to 7 X fOB8 M). Vasopressin binding sites (0.3 pmole per mg of protein) can be identified with the hormonal receptors involved in adenylate cyclase activation on the basis of the two following criteria: (a) saturation of receptor sites and adenylate cyclase activation occurred in the same range of hormone concentrations and (b) a good correlation was observed between the relative potencies of unlabeled [8-a@ninelvasopressin, [Wysinelvasopressin, and oxytocin as inhibitors of [3H]vasopressin binding and as activators of the adenylate cyclase. Adrenalectomy reduced the adenylate cyclase stimulation that was induced by vasopressin. It did not modify the basal enzyme activity or its activation by parathyroid hormone and sodium fluoride. The small reduction in vasopressinbinding capacity observed after adrenalectomy cannot account for the reduction in enzyme activation, an observation which suggests an impairment in the efficacy of receptor-enzyme coupling. Aldosterone treatment of adrenalectomized rats restored the hormone-binding capacity to control level but did not correct the receptor-enzyme coupling defect. Dexamethasone enhanced coupling efficiency in adrenalectomized rats and to a lesser extent in control animals. Dexamethasone was as active as aldosterone in restoring the hormone-binding capacity of adrenalectomized rats but had no effect in normal animals. Corticosterone was inactive under our experimental conditions. Neither adrenalectomy nor corticosteroid treatment modified the apparent Km of vasopressin for its receptor. Aldosterone and dexamethasone were ineffective when added in vifro to the membrane preparation. It is suggested that adrenal steroids exert a dual action on the vasopressin-sensitive adenylate cyclase of the kidney: (a)

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The Vasopressimsensitive Adenylate Cyclase of the Rat Kidney EFFECT OF ADRENALECTOMY AND CORTICOSTEROIDS ON HORMONAL RECEPTOR-ENZYME COUPLING*

A subcellular fraction prepared from rat kidney medulla contained vasopressin-sensitive adenylate cyclase and vasopressin binding sites. Vasopressin stimulation resulted in an increase in the maximal velocity of the reaction with no change in the apparent K, for ATP. A maximum activation ratio (5 to 10) was obtained at low Mg2+ concentration (0.75 mM) and pH 7.4. The apparent Km for vasopressin...

متن کامل

Specific binding of (3H) lysine-vasopressin to pig kidney plasma membranes. Relationship of receptor occupancy to adenylate cyclase activation.

A plasma membrane fraction was prepared from pig kidney medulla. It contained lysine-vasopressin-sensitive adenylate cyclase activity (maximum activation: 4to 6fold, apparent Km value for the hormone: about 5 X 1OV M). Lysine-vasopressin was not inactivated by the membrane preparation even at low hormonal concentrations. The specific [3H]lysine-vasopressin (vasopressin) binding sites found are ...

متن کامل

The Effect of Aspartate-Lysine-Isoleucine and Aspartate-Arginine-Tyrosine Mutations on the Expression and Activity of Vasopressin V2 Receptor Gene

Background: Vasopressin type 2 receptor (V2R) plays an important role in the water reabsorption in the kidney collecting ducts. V2R is a G protein coupled receptor (GPCR) and the triplet of amino acids aspartate-arginine-histidine (DRH) in this receptor might significantly influence its activity similar to other GPCR. However, the role of this motif has not been fully confirmed. Therefore, the ...

متن کامل

Sites of hormone action in the mammalian nephron.

Hormone-dependent adenylate cyclase activity was measured separately in the different nephron portions by combining the microdissection of collagenase-treated rabbit kidneys and the use of a single tubule enzyme microassay. The results obtained in the rabbit for vasopressin, parathyroid hormone, calcitonin, and isoproterenol are given and discussed. Each hormone stimulated adenylate cyclase act...

متن کامل

Neurohypophyseal hormone-responsive adenylate cyclase from mammalian kidney.

The investigation was undertaken to evaluate the direct stimulatory effects of neurohypophyseal hormones upon adenylate cyclase activity in a cell-free, particulate fraction derived from the kidney medulla of various mammalian species. The relative affinity of neurohypophyseal hormones for the receptor component of the adenylate cyclase system (as defined by the concentration of hormone require...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • The Journal of biological chemistry

دوره 249 20  شماره 

صفحات  -

تاریخ انتشار 1974