Premium
Studies on the mechanism of renin release from isolated superfused rat glomeruli: effects of calcium, calcium ionophore and lanthanum
Author(s) -
Baumbach L.,
Leyssac P. P.
Publication year - 1977
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1977.sp012121
Subject(s) - calcium , egta , ionophore , chemistry , endocrinology , medicine , lanthanum , renin–angiotensin system , incubation , biophysics , biochemistry , biology , inorganic chemistry , organic chemistry , blood pressure
1. The effects of external medium calcium concentration, the ionophore A 23187 and lanthanum on the rate of renin release in vitro were studied with particular emphasis on results obtained from isolated superfused glomeruli of rat kidneys. 2. The response to reduction in superfusate calcium concentration from 2 m M was a graded and reversible increase in the rate of renin release. An increase in release was detectable at 0.2 m M calcium; a threefold increase was found 36 min after a change from 2 m M calcium to calcium‐free superfusate. A similar relative increase in release resulted from reductions from 0.1 m M to zero calcium, but the absolute amounts of renin released were greater in this latter series. Renin release from kidney cortical slices similarly increased in response to calcium‐free incubation medium. 3. The effects of A 23187 on renin release were modest. Changing from 2 m M calcium during control periods to calcium‐free Ringer with A 23187 added caused an attenuated and more delayed increase in release than the change to calcium‐free Ringer without ionophore. This difference in response was abolished when glomeruli were superfused with 0.1 m M calcium during the preceding 1 hr control period. There was no significant difference in renin release from glomeruli exposed to calcium‐free EGTA‐Ringer with and without A 23187 in the 2 m M calcium series; in the 0.1 m M calcium series the increase in release following a shift to calcium‐free EGTA‐containing superfusate with A 23187 added was significantly greater than in the absence of the ionophore. 4. Addition of lanthanum (1 or 0.05 m M ) to calcium‐containing as well as calcium‐free superfusate resulted in a significant depression of renin release. Subsequent removal of the lanthanum did not restore the rate of release unless EGTA was added; in the latter case a massive increase in renin release occurred resulting in a marked depletion of the remaining renin content of the glomeruli. 5. It is concluded that calcium influences renin release by a direct action on the juxtaglomerular cells. The data support the previous suggestion that basal renin release is a function of active, calcium‐dependent cell volume regulation — swelling causing an increase in the release; and further suggest that membrane‐bound calcium has a direct effect on the cell membrane permeability to renin. 6. The results exclude that calcium‐stimulated exocytosis is responsible for basal renin release from the juxtaglomerular cells adhering to isolated glomeruli.