Maintenance of potassium excretion despite reduction of glomerular filtration during sodium diuresis.
نویسندگان
چکیده
It has been clearly established that mammalian renal tubules can secrete potassium. However, it has not been shown in mammals under physiologic conditions what proportion of the urinary potassium is derived from the filtered potassium and what proportion from secreted potassium. In experiments designed to study the various factors which influence potassium excretion it has sometimes been assumed that the reabsorption of the filtered potassium is essentially complete, and that these factors exert their effects on the secretory mechanism. However, evidence for the completeness of reabsorption of filtered potassium is limited and not conclusive. The proposed tubular mechanism for the secretion of potassium is an ion exchange process in the distal tubule (1), where cellular potassium ions are exchanged for sodium ions derived from the glomerular filtrate. It is implicit in this mechanism that potassium secretion will depend in part on the availability of sodium ions for exchange. If the proximal reabsorption of filtered potassium is complete, the rate of excretion of potassium will be independent of the filtered load of potassium, providing an adequate distal load of sodium is maintained. To test this hypothesis, the glomerular filtration rate was reduced in one kidney and the rate of excretion of potassium from this kidney was compared to that of the control kidney, during both high and low rates of sodium excretion.
منابع مشابه
Blood levels and renal effects of atrial natriuretic peptide in normal man.
Since mammalian atria were recently found to contain vasoactive and natriuretic peptides, we investigated the following in normal humans: plasma human atrial natriuretic peptide concentrations, effective renal plasma flow (ERPF), glomerular filtration rate (GFR), urinary water and electrolyte excretion, blood pressure (BP), and catecholamine, antidiuretic hormone (ADH), angiotensin II, and aldo...
متن کاملThe effect of inhibition of prostaglandin synthesis on urinary sodium excretion in the conscious dog.
Studies were performed to determine the effect of decreased endogenous release of renal prostaglandins on urinary sodium excretion. Two structurally dissimilar inhibitors of prostaglandin synthesis were employed, and studies were performed in conscious dogs allowed to recover from prior surgical instrumentation. Either meclofenamate (2 mg/kg) or the competitive prostaglandin inhibitor RO 20-572...
متن کاملRenal haemodynamic and tubular actions of urotensin II in the rat.
Urotensin II (UTS) is a potent vasoactive peptide that was originally identified in teleost fish. Mammalian orthologues of UTS and its receptor (UTSR) have been described in several species, including humans and rats. We have shown previously that bolus injections of UTS caused a decrease in urine flow and sodium excretion rates in parallel with marked reductions in renal blood flow (RBF) and g...
متن کاملRole of endogenous prostaglandins in volume expansion and during furosemide infusion in conscious dogs.
The renal effects of two structurally dissimilar inhibitors of prostaglandin synthesis (Meclofenamate and RO-20-5720) were studied in conscious, chronically instrumented dogs during mild volume expansion and during a constant infusion of furosemide. When either inhibitor was administered following volume expansion, urinary excretion of PGE2 and urine flow rate were reduced by more than 50%. In ...
متن کاملDiurnal variation in the diuretic response to ingested water.
In normal individuals the renal excretion of water, sodium, potassium, and uric acid is less at night than during the day. This diurnal variation persists when no food or fluids are taken as well as when identical quantities of food, fluid, and electrolyte are ingested at regular intervals throughout the 24-hour period and is not easily altered by changes in the cycle of sleep and activity (1-1...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of clinical investigation
دوره 37 4 شماره
صفحات -
تاریخ انتشار 1958