Abstract
1. The effects of different energy substrates, of low temperature, of urea, and of ouabain and ethacrynic acid were studied on the rate of renin release from viable juxtaglomerular cells during superfusion of isolated rat glomeruli. 2. Neither lactate nor glutamate altered renin release rate from that observed using glucose as the sole energy substrate. Succinate 10 mM elevated release transiently but did not influence the release caused by reductions in osmolality through lowering sucrose concentration. 3. Peak renin release was more prolonged and returned more slowly to control following reductions in osmolality in phosphate-Ringer than in bicarbonate-Ringer. 4. At 37 degrees C, the peak of renin released induced by hypo-osmolality was smaller and delayed, and returned earlier to control than at 30 degrees C. Reduction in temperature from 30 to 4 degrees C resulted in a 32-fold increase in basal release rate. At 4 degrees C a 20 m-osmole/kg reduction in tonicity caused an additional 2-5-fold increase in release rate. 6. Increasing superfusate osmolality with urea did not affect basal renin release but 100 mM urea suppressed the releasing effect of a 15 mM reduction in NaCl concentration. 7. Ouabain (10(-4) M) caused a small (33 +/- 9%, P less than 0-025) transient increase in renin release. Ethacrynic acid (10(-3) M) provoked a progressive increase in release reaching 100 +/- 15% above control within 50 min. In the presence of both inhibitors the release provoked by hyposmolality was prolonged. 8. It is concluded that renin release in vitro is a function of actively regulated cell volume and it is proposed that a similar mechanism could underline both barorecptor and macula densa controls of renin secretion in vivo.
Full text
PDF













Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Blackard W. G., Kikuchi M., Rabinovitch A., Renold A. E. An effect of hyposmolarity on insulin release in vitro. Am J Physiol. 1975 Mar;228(3):706–713. doi: 10.1152/ajplegacy.1975.228.3.706. [DOI] [PubMed] [Google Scholar]
- Blendstrup K., Leyssac P. P., Poulsen K., Skinner S. L. Characteristics of renin release from isolated superfused glomeruli in vitro. J Physiol. 1975 Apr;246(3):653–672. doi: 10.1113/jphysiol.1975.sp010909. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brendel K., Meezan E. Properties of a pure metabolically active glomerular preparation from rat kidneys. II. Metabolism. J Pharmacol Exp Ther. 1973 Nov;187(2):342–351. [PubMed] [Google Scholar]
- COOK W. F., PICKERING G. W. The location of renin in the rabbit kidney. J Physiol. 1959 Dec;149:526–536. doi: 10.1113/jphysiol.1959.sp006359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Corsini W. A., Crosslan K. L., Bailie M. D. Renin secretion by rat kidney slices in vitro. Proc Soc Exp Biol Med. 1974 Feb;145(2):403–406. doi: 10.3181/00379727-145-37819. [DOI] [PubMed] [Google Scholar]
- Daniel E. E., Robinson K. Effects of inhibitors of active transport on 22 Na and 42 K movements and on nucleotide levels in rat uteri at 25 degrees C. Can J Physiol Pharmacol. 1971 Mar;49(3):178–204. doi: 10.1139/y71-025. [DOI] [PubMed] [Google Scholar]
- De Vito E., Gordon S. B., Cabrera R. R., Fasciolo J. C. Release of renin by rat kidney slices. Am J Physiol. 1970 Oct;219(4):1036–1041. doi: 10.1152/ajplegacy.1970.219.4.1036. [DOI] [PubMed] [Google Scholar]
- Frederiksen O., Leyssac P. P., Skinner S. L. Sensitive osmometer function of juxtaglomerular cells in vitro. J Physiol. 1975 Nov;252(3):669–679. doi: 10.1113/jphysiol.1975.sp011164. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frederiksen O., Leyssac P. P. Transcellular transport of isosmotic volumes by the rabbit gall-bladder in vitro. J Physiol. 1969 Mar;201(1):201–224. doi: 10.1113/jphysiol.1969.sp008751. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KLEINZELLER A., KNOTKOVA A. THE EFFECT OF OUABAIN ON THE ELECTROLYTE AND WATER TRANSPORT IN KIDNEY CORTEX AND LIVER SLICES. J Physiol. 1964 Dec;175:172–192. doi: 10.1113/jphysiol.1964.sp007510. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lund-Andersen H., Hertz L. Effects of potassium content in brain-cortex slices from adult rats. Exp Brain Res. 1970;11(2):199–212. doi: 10.1007/BF00234323. [DOI] [PubMed] [Google Scholar]
- Lyons H. J., Chruchhill P. C. Renin secretion from rat renal cortical cell suspensions. Am J Physiol. 1975 Jun;228(6):1835–1839. doi: 10.1152/ajplegacy.1975.228.6.1835. [DOI] [PubMed] [Google Scholar]
- Macknight A. D., Pilgrim J. P., Robinson B. A. The regulation of cellular volume in liver slices. J Physiol. 1974 Apr;238(2):279–294. doi: 10.1113/jphysiol.1974.sp010524. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Macknight A. D. Water and electrolyte contents of rat renal cortical slices incubated in potassium-free media and media containing ouabain. Biochim Biophys Acta. 1968 Mar 1;150(2):263–270. doi: 10.1016/0005-2736(68)90169-7. [DOI] [PubMed] [Google Scholar]
- Maude D. L. Effects of K and ouabain on fluid transport and cell Na in proximal tubule in vitro. Am J Physiol. 1969 May;216(5):1199–1206. doi: 10.1152/ajplegacy.1969.216.5.1199. [DOI] [PubMed] [Google Scholar]
- Minai K. Circadian variations of plasma renin activity and plasma osmolality in various physiological and pathological states. Tohoku J Exp Med. 1974 Oct;114(2):159–170. doi: 10.1620/tjem.114.159. [DOI] [PubMed] [Google Scholar]
- Naughton R. J., Bertoncello I., Skinner S. L. Abolition of the renin-releasing action of frusemide by acute renal denervation in dogs. Clin Exp Pharmacol Physiol. 1975 May-Jun;2(3):213–227. doi: 10.1111/j.1440-1681.1975.tb03027.x. [DOI] [PubMed] [Google Scholar]
- Ochs H. G., Lamberts B., Saleh M., Heintz R. Reninsekretion in vitro. Vergleich von Nierenschnitten und isolierten Glomeruli. Res Exp Med (Berl) 1973 May 21;160(3):206–212. doi: 10.1007/BF01856784. [DOI] [PubMed] [Google Scholar]
- Oelkers W., Molzahn M., Samwer K. F., Kreiser H., Kutschke H. Reninabgabe aus Nierenschnitten in Abhängigkeit von der Elektrolytzusammensetzung des Mediums. Pflugers Arch. 1970;321(1):67–82. doi: 10.1007/BF00594123. [DOI] [PubMed] [Google Scholar]
- Petersen O. H. Formation of saliva and potassium transport in the perfused cat submandibular gland. J Physiol. 1971 Jul;216(1):129–142. doi: 10.1113/jphysiol.1971.sp009513. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rangachari P. K., Daniel E. E., Paton D. M. Regulation of cellular volume in rat myometrium. Biochim Biophys Acta. 1973 Oct 11;323(2):297–308. doi: 10.1016/0005-2736(73)90153-3. [DOI] [PubMed] [Google Scholar]
- Whittembury G., Fishman J. Relation between cell Na extrusion and transtubular absorption in the perfused toad kidney: the effect of K, ouabain and ethacrynic acid. Pflugers Arch. 1969;307(3):138–153. doi: 10.1007/BF00592080. [DOI] [PubMed] [Google Scholar]
- Whittembury G., Proverbio F. Two modes of Na extrusion in cells from guinea pig kidney cortex slices. Pflugers Arch. 1970;316(1):1–25. doi: 10.1007/BF00587893. [DOI] [PubMed] [Google Scholar]
- Yamamoto K., Tanaka H., Horiuchi K., Ueda J. Release of renin from dog kidney cortex slices in vitro. Jpn J Pharmacol. 1967 Dec;17(4):685–686. doi: 10.1254/jjp.17.685. [DOI] [PubMed] [Google Scholar]