Hypertension, Vol 7, 855-859, Copyright © 1985 by American Heart Association
N Nakamura, F Soubrier, J Menard, JJ Panthier, F Rougeon and P Corvol
The expression of the renin gene in rat kidneys was studied using mouse
submaxillary gland renin complementary DNA. The length of rat renin
messenger RNA (mRNA) was approximately 1600 nucleotides, similar to that of
mouse submaxillary gland and kidney renin mRNA. Rat renin mRNA was
quantified by a radiodensitometric complementary DNA hybridization assay.
The effects of intense long-term stimulation and short-term inhibition of
renin secretion on plasma renin concentration, renal renin concentration,
and renin mRNA content were compared with those of controls. After 15 days
of sodium depletion and captopril treatment, plasma renin concentration
increased 46-fold, renal renin concentration only 1.5-fold, and renin mRNA
content increased about threefold. Following a 1-hour infusion of
angiotensin II in sodium-depleted and captopril-treated rats, plasma renin
concentration decreased by 84% whereas no significant changes in either
renal renin concentration or renin mRNA content were observed. These
results show that sodium depletion and captopril treatment increase the
level of renin gene transcription and renin biosynthesis. However, there
are nonproportional changes in plasma renin levels, renal renin content,
and its mRNA. These results suggest that newly synthesized renin is not
stored in the kidney but is rapidly secreted into the blood. Short-term
inhibition of plasma renin concentration by angiotensin II is most likely
mediated by posttranslational mechanisms.
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Nonproportional changes in plasma renin concentration, renal renin content, and rat renin messenger RNA
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