Abstract
The renin—angiotensin—aldosterone cascade plays an important role in the blood pressure, electrolyte, and fluid homeostasis of the organism. The activity of the renin—angiotensin system in the circulation is mainly dependent on the activity of the protease renin, which is considered the key regulator of the system. Renin found in the circulation comes predominantly from the kidneys, where renin is produced primarily by the so-called juxtaglomerular epitheloid (JGE) cells. These cells are located in the media layer of the afferent arterioles adjacent to the vascular poles of the glomeruli [12]. JGE cells develop from vascular smooth cells by a reversible metaplastic transformation [12]. This differentiation is associated by a marked change of cell morphology in a way that numerous granular (renin storage) vesicles of various size and shape appear while the number of myofilaments disappear [1]. The morphologic appearance of the cells becomes more epitheloid rather than smooth muscle cell-like. Which intracellular events trigger and control the shift of smooth muscle cells into JGE cells and back is not yet known. The JGE cells are directly neighbored to four cell types: smooth muscle cells of the afferent arterioles, endothelial cells covering the interior of the afferent arterioles, mesangial cells of the glomeruli, and the macula densa cells. It is conceivable, therefore, that the functions of JGE cells, namely renin synthesis and renin secretion, are essentially modulated by these neighboring cells. In fact, it is known that the macula densa cells exert influence on JGE cells by a yet undefined “macula densa signal” which acts inhibitorily on renin secretion and renin synthesis [3].
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Taugner, R., Bührle, C.P., Hackenthal, E., Mannek, E., and Nobiling, R. Morphology of the juxtaglomerular apparatus.Contr. Nephrol. 4376–101 (1984).
Barajas, L. Anatomy of the juxtaglomerular apparatus.Am. J. Physiol. 236F240–F246 (1979).
Briggs, J.P. and Schnermann, J. Macula densa control of renin secretion and glomerular vascular tone: evidence for common cellular mechanisms.Renal Physiol. 9193–203 (1986).
Skott, O. and Briggs, J.P. Direct demonstration of macula densa mediated renin release.Science 2371618–1620 (1987).
Hackenthal, E., Paul, M., Ganten, D., Taugner, R. Morphology, physiology, and molecular biology of renin secretion.Physiol. Rev. 701067–1116 (1990).
Tufro-McReddie, A., Chevalier, R.L., Everett, A.D., and Gomez, R.A. Decreased perfusion pressure modulates renin and ANGII type 1 receptor gene expression in the rat kidney. Am.J. Physiol. 264R696–R702 (1993).
Atlas, D., Melamend, E., and Lahav, M. Beta-adrenergic receptors in rats kidney.Lab. Invest. 36464–468 (1977).
Kurtz, A., Kaissling, B., Busse, R., and Baier, W. Endothelial cells modulate renin secretion from isolated juxtaglomerular cells.J. Clin. Invest. 881147–1154 (1991).
Bachmann, S., Bosse, H.M., and Mundel, P. Topography of nitric oxide synthesis by localizing constitutive NO synthases in mammalian kidney.Am. J. Physiol. 268F885–F898 (1995).
Wilcox, C.S., Welch, W.J., Murad, F., Gross, S.S., Taylor, G., Levi, R., Schmidt, H.H.H.W. Nitric oxide synthase in macula densa regulates glomerular capillary pressure.Proc. Natl. Acad. Sci. USA 8911993–11997 (1992).
Mundel, P., Bachmann, S., Bader, M., Fischer, A., Kummer, W., Mayer, B., and Kriz, W. Expression of nitric oxide synthase in kidney macula densa cells.Kidney Int. 421017–1019 (1992).
Shultz, P.J., Archer, S.L., and Rosenberg, M.E. Inducible nitric oxide synthase mRNA and activity in glomerular mesangial cells.Kidney Int. 46683–689 (1994).
Ahn, K.Y., Mohaupt, M.G., Madsden, K.M., and Kone, B.C. In situ hybridization of mRNA encoding inducible nitric oxide synthase in rat kidney.Am.J. Physiol. 267F748–F757 (1994).
Morrissey, J.J., McCracken, R., Kaneto, H., Vehaskari, M., Montani, D., and Klahr, S. Location of an inducible nitric oxide synthase mRNA in the normal kidney.Kidney Int. 45998–1005 (1994).
Tojo, A., Gross, S.S., Zhang, L., Tisher, C.C., Schmidt, H.H.H.W., Wilcox, C.S., and Madsden, K.M. Immunocytochemical localization of distinct isoforms of nitric oxide synthase in the juxtaglomerular apparatus of normal rat kidney.J. Am. Soc. Nephrol. 4S1438–S1447 (1994).
Hof, R.P., Evenou, J.P., and Hof-Miyashita, A. Similar increases in circulating renin after equihypotensive doses of nitroprusside, diihydralazine or isradipine in conscious rabbits.Eur. J. Pharmacol. 136251–254 (1987).
Johnson, R.A., and Freeman, R.H. 1994. Renin release in rats during blockade of nitric oxide synthesis.Am. J. Physiol. 266R1723–R1729 (1994).
Shultz, P.J. and Tolins, J.P. Adaptation to increased dietary salt intake in the rat.J. Clin. Invest. 91642–650 (1993).
Dewan, S., Majid, A., and Navar, G.L. Suppression of blood flow autoregulation plateau during nitric oxide blockade in canine kidney.Am. J. Physiol. 262F40–F46 (1992).
Sigmon, D.H., Carretero, O.A., and Beierwaltes, W.H. Endothelium-derived relaxing factor regulates renin release in vivo.Am. J. Physiol. 263F256–F261 (1992).
Schricker, K., Della Bruna, R., Hamann, M., and Kurtz, A. Endothelium derived relaxing factor is involved in the pressure control of renin gene expression in the kidney.Pflügers Arch. 428261–268 (1994).
Bosse, H.M., Böhm, R., Resch, S., and Bachmann, S. Parallel regulation of constitutive nitric oxide synthase and renin at the juxtaglomerular apparatus of rat kidney under various stimuli.Am. J. Physiol. 269F793–F805.
Johnson, R.A. and Freeman, R.H. Sustained hypertension in the rat induced by chronic blockade of nitric oxide production.Am. J. Hyperten. 5919–922 (1992).
Naess, P.A., Christensen, G., Kirkeboen, K.A., and Kiil, F. Effect on renin release of inhibiting renal nitric oxide synthsis in anaesthetized dogs.Acta Physiol. Scand. 148137–142 (1993).
Beierwaltes, W.H. Selective neuronal nitric oxide synthase inhibition blocks furosemide-stimulated renin secretion in vivo.Am. J. Physiol. 269F134–F139 (1995).
Persson, P.B., Baumann, J.E., Ehmke, H., Hackenthal, E., Kirchheim, H.R., and Nafz, B. Endothelium-derived NO stimulates pressure-dependent renin release in conscious dogs.Am. J. Physiol. 264F943–F947 (1993).
Delacretaz, E., Zanchi, A., Nussberger, J., Hayoz, D., Aubert, J.F., Brunner, H.R., and Waeber, B. Chronic nitric oxide synthase inhibition and carotid artery distensability in renal hypertensive rats.26332–336 (1995).
Schricker, K., Hegyi, I., Hamann, M., Kaissling, B., and Kurtz, A. Tonic stimulation of renin gene expression by nitric oxide is counteracted by tonic inhibition through angiotensin II.Proc. Natl. Acad. Sci. USA 928006–8010 (1995).
Schricker, K., Hamann, M., and Kurtz, A. Nitric oxide and prostaglandins are involved in the macula densa control of the renin system.Am. J. Physiol. 269F825–F830.
Schricker, K. and Kurtz, A. Blockade of nitric oxide formation inhibits the stimulation of the renin system by low salt intake.Pflügers Arch. 432187–189.
Furchgott, R.E. Role of endothelium in responses of vascular smooth muscle cells.Circ. Res. 53557–573 (1983).
Scholz, H. and Kurtz, A. Endothelium derived relaxing factor is involved in the pressure control of renin secretion from the kidneys.J. Clin. Invest. 911088–1094 (1993).
Münter, K. and Hackenthal, E. The participation of the endothelium in the control of renin release.J. Hyperten. 9S236–S237 (1991).
Gardes, J., Poux, J.M., Gonzales, M.F., Alhenc-Gelas, F., and Menard, J. Decreased renin release and constant kallikrein secretion after injection of L-Name in isolated perfused rat kidney.Life Sci. 50987–993 (1992).
Gardes, J., Gonzales, M.F., Alhenc-Gelas, F., and Menard, J. Influence of sodium diet on L-Name effects on renin release and renal vasoconstriction. Am.J. Physiol. 267F798–F804 (1994).
Vidal, M.J., Romero, J.C., and Vanhoutte, P.M. Endothelium-derived relaxing factor inhibits renin release.Eur. J. Pharmacol. 149401–402 (1988).
Beierwaltes, W.H. and Carretero, O.A. Nonprostanoid endothelium-derived factors inhibit renin release.Hypertension 19II68–II73 (1992).
Schricker, K., Ritthaler, T., Krämer, B.K., and Kurtz, A. Effect of endothelium-derived relaxing factor on renin secretion from isolated mouse renal juxtaglomerular cells. Acta Physiol. Scand. 140347–354 (1993).
Schricker, K. and Kurtz, A. Liberators of NO exert a dual effect on renin secretion from isolated mouse renal juxtaglomerular cells.Am. J. Physiol. 265F180–F186 (1993).
Greenberg, S.G., He, X.-R., Schnermann, J.B., and Briggs, J.P. Effect of nitric oxide on renin secretion. I. Studies in isolated juxtaglomerular granular cells.Am. J. Physiol. 268F948–F952 (1995).
Della Bruna, R., Pinet, F., Corvol, P., and Kurtz, A. Opposite regulation of renin gene expression by cyclic AMP and calcium in isolated mouse juxtaglomerular cells.Kidney Int. 471266–1273 (1995).
He, X.-R., Greenberg, S.G., Briggs, J.P., and Schnermann, J.B. Effect of nitric oxide on renin secretion. II. Studies in the perfused juxtaglomerular apparatus.Am.J. Physiol. 268F953–F959 (1995).
Gnarro, L.J. Endothelium-derived nitrix oxide: actions and properties.FASEB J. 331–36 (1989).
Kurtz, A., Della Bruna, R., Pfeilschifter, J., Taugner, R., and Bauer, C. Atrial natriuretic peptide inhibits renin release from isolated renal juxtaglomerular cells by a cGMP mediated process.Proc. Natl. Acad. Sci. USA 834769–4773 (1986).
Laffranchi, R., Gogvadze, V., Richter, C., and Spinas, G.A. Nitrix oxide stimulates insulin secretion by inducing calcium release from mitochondria.Biochem. Biophys. Res. Commun. 217584–591 (1995).
Schmidt, H.H.H.W., Warner, T.D., Ishii, K., Sheng, H., and Murad, F. Insulin secretion from pancreatic B cells caused by L-arginine-derived nitriogen oxide.Science 255721–723 (1992).
Schmidt, H.H.H.W., Lohmann, S.M., and Walter, U. The nitric oxide and cGMP signal transduction system: regulation and mechanismen of action.Biochem. Biophys. Acta 1178153–175 (1993).
Gambarian, S., Lohmann, S., and Walter, S. Personal communication.
Singh, I.J., Graham, M., Wang, W.H., Young, T., Killen, P., Smart, A., Schnermann, J., Briggs, J.P. 1996. Coordinate regulation of renal expression of nitric oxide synthase, renin, and angiotensinogen oxide mRNA by dietary salt.Am. J. Physiol. 270F1027—F1037.
Fischer, E., Schnermann, J., Briggs, J.P., Kriz, W., Ronco, P.M., and Bachmann, S. Ontogeny of NO synthase and renin in juxtaglomerular apparatus of rat kidneys.Am. J. Physiol. 268F1164–F1176 (1995).
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1997 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Kurtz, A., Schricker, K. (1997). NO and The Renin System. In: Goligorsky, M.S., Gross, S.S. (eds) Nitric Oxide and the Kidney. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-6039-5_12
Download citation
DOI: https://doi.org/10.1007/978-1-4615-6039-5_12
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4613-7768-9
Online ISBN: 978-1-4615-6039-5
eBook Packages: Springer Book Archive