Key result
Adenosine A1 receptor (A1AR) knockout mice showed markedly enhanced stimulation of Ren-1 mRNA expression and renal renin content by salt restriction compared with wild-type mice.
The adenosine A1 receptor exerts a tonic inhibitory role in the renin system but is not indispensable for macula densa control of renin secretion.
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Supports tonic A1AR inhibition of renin; extends animal mechanistic data but leaves open human relevance.
Recent studies demonstrated that the influence of the macula densa on glomerular filtration is abolished in adenosine A(1) receptor (A(1)AR) knockout mice. Inasmuch as the macula densa not only regulates glomerular filtration but also controls the activity of the renin system, the present study aimed to determine the role of the A(1)AR in macula densa control of renin synthesis and secretion. Although a high-salt diet over 1 wk suppressed renin mRNA expression and renal renin content to similar degrees in A(1)AR(+/+), A(1)AR(+/-), and A(1)AR(-/-) mice, stimulation of Ren-1 mRNA expression and renal renin content by salt restriction was markedly enhanced in A(1)AR(-/-) compared with wild-type mice. Pharmacological blockade of macula densa salt transport with loop diuretics stimulated renin expression in vivo (treatment with furosemide at 1.2 mg/day for 6 days) and renin secretion in isolated perfused mouse kidneys (treatment with 100 microM bumetanide) in all three genotypes to the same extent. Taken together, our data are consistent with the concept of a tonic inhibitory role of the A(1)AR in the renin system, whereas they indicate that the A(1)AR is not indispensable in macula densa control of the renin system.
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Schweda et al. (2003) studied this question. Adenosine A1 receptor (A1AR) knockout vs. Wild-type mice was evaluated on Renin mRNA expression and renal renin content. Adenosine A1 receptor (A1AR) knockout mice showed markedly enhanced stimulation of Ren-1 mRNA expression and renal renin content by salt restriction compared with wild-type mice.
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