Nephron Physiology最新文献

{"title":"Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.","authors":"Graciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, Mickael Quentric, Nina Himmerkus, Toshiyasu Koike, James Poulter, Enriko Klootwijk, Steven L Robinette, Alexander J Howie, Vaksha Patel, Marie-Lucile Figueres, Horia C Stanescu, Naomi Issler, Jeremy K Nicholson, Detlef Bockenhauer, Christopher Laing, Stephen B Walsh, David A McCredie, Sue Povey, Audrey Asselin, Arnaud Picard, Aurore Coulomb, Alan J Medlar, Isabelle Bailleul-Forestier, Alain Verloes, Cedric Le Caignec, Gwenaelle Roussey, Julien Guiol, Bertrand Isidor, Clare Logan, Roger Shore, Colin Johnson, Christopher Inglehearn, Suhaila Al-Bahlani, Matthieu Schmittbuhl, François Clauss, Mathilde Huckert, Virginie Laugel, Emmanuelle Ginglinger, Sandra Pajarola, Giuseppina Spartà, Deborah Bartholdi, Anita Rauch, Marie-Claude Addor, Paulo M Yamaguti, Heloisa P Safatle, Ana Carolina Acevedo, Hercílio Martelli-Júnior, Pedro E dos Santos Netos, Ricardo D Coletta, Sandra Gruessel, Carolin Sandmann, Denise Ruehmann, Craig B Langman, Steven J Scheinman, Didem Ozdemir-Ozenen, Thomas C Hart, P Suzanne Hart, Ute Neugebauer, Eberhard Schlatter, Pascal Houillier, William A Gahl, Miikka Vikkula, Agnès Bloch-Zupan, Markus Bleich, Hiroshi Kitagawa, Robert J Unwin, Alan Mighell, Ariane Berdal, Robert Kleta","doi":"10.1159/000349989","DOIUrl":"10.1159/000349989","url":null,"abstract":"<p><strong>Background/aims: </strong>Calcium homeostasis requires regulated cellular and interstitial systems interacting to modulate the activity and movement of this ion. Disruption of these systems in the kidney results in nephrocalcinosis and nephrolithiasis, important medical problems whose pathogenesis is incompletely understood.</p><p><strong>Methods: </strong>We investigated 25 patients from 16 families with unexplained nephrocalcinosis and characteristic dental defects (amelogenesis imperfecta, gingival hyperplasia, impaired tooth eruption). To identify the causative gene, we performed genome-wide linkage analysis, exome capture, next-generation sequencing, and Sanger sequencing.</p><p><strong>Results: </strong>All patients had bi-allelic FAM20A mutations segregating with the disease; 20 different mutations were identified.</p><p><strong>Conclusions: </strong>This autosomal recessive disorder, also known as enamel renal syndrome, of FAM20A causes nephrocalcinosis and amelogenesis imperfecta. We speculate that all individuals with biallelic FAM20A mutations will eventually show nephrocalcinosis.</p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"122 1-2","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782194/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31260113","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Electrolyte-free water clearance versus modified electrolyte-free water clearance: do the results justify the effort?","authors":"Gregor Lindner,&nbsp;Christoph Schwarz","doi":"10.1159/000336550","DOIUrl":"https://doi.org/10.1159/000336550","url":null,"abstract":"<p><strong>Background: </strong>Calculation of electrolyte-free water clearance (EFWC) allows for quantification of renal losses of free water and was shown to be helpful in the differential diagnosis of dysnatremias and might help in the correction of the electrolyte disorders. A modified EFWC formula (MEFWC) was described to be more accurate than the conventional one; however, it has never been evaluated clinically.</p><p><strong>Methods: </strong>In order to evaluate the performance of MEFWC compared to EFWC under clinical circumstances, we gathered data from a total of 912 patient days of 138 critically ill patients. EFWC and MEFWC were calculated on the basis of these data. Additionally, from data of critically ill patients, we calculated a prediction of serum sodium based on the Edelman equation using either EFWC or MEFWC and compared results.</p><p><strong>Results: </strong>Altogether, 343 normonatremic, 124 hyponatremic and 445 hypernatremic days were analyzed. Results for EFWC and MEFWC correlated significantly (R = 0.98). In patients with hyponatremia, the absolute difference between EFWC and MEFWC was significantly larger than in patients with normonatremia (437 vs. 256 ml, p < 0.01). The absolute difference between EFWC and MEFWC correlated significantly with the level of serum sodium (R = -0.41). The mean difference in the prediction of serum sodium change as calculated based on the Edelman equation between the formula using EFWC and the formula using MEFWC was 0.7 mmol/l (SD 0.68) and was highest in hyponatremia and lowest in hypernatremia.</p><p><strong>Conclusion: </strong>Results of EFWC and MEFWC were comparable in critically ill patients. Under normal circumstances, the use of the more complicated MEFWC is not justified. In hyponatremia, the difference between EFWC and MEFWC is larger and thus might justify the use of the more complicated formula.</p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"120 1","pages":"p1-5"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000336550","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40148254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Variations of dietary salt and fluid modulate calcium and magnesium transport in the renal distal tubule.","authors":"Chien-Te Lee,&nbsp;Yeong-Hau H Lien,&nbsp;Li-Wen Lai,&nbsp;Hwee-Yeong Ng,&nbsp;Terry Ting-Yu Chiou,&nbsp;Hung-Chun Chen","doi":"10.1159/000353199","DOIUrl":"https://doi.org/10.1159/000353199","url":null,"abstract":"<p><strong>Background: </strong>The renal distal tubule fine-tunes renal epithelial calcium transport. Dietary intake of salt and fluid varies day-to-day and the kidney adapts accordingly to maintain homeostasis. The alternations in salt and fluid balance affect calcium and magnesium transport in the distal tubule, but the mechanisms are not fully understood.</p><p><strong>Methods: </strong>Sprague-Dawley rats were grouped into high-salt, low-salt and dehydration treatment. Daily intake, water consumption and urine output were recorded. At the end of the experiment, blood and urine samples were collected for hormonal and biochemical tests. Genetic analysis, immunoblotting and immunofluorescence studies were then performed to assess the alterations of calcium and magnesium transport-related molecules.</p><p><strong>Results: </strong>High-salt treatment increased urinary sodium, calcium and magnesium excretion. Low-salt treatment and dehydration were associated with decreased urinary excretion of all electrolytes. High-salt treatment was associated with increased intact parathyroid hormone levels. A significant increase in gene expression of TRPV5, TRPV6, calbindin-D28k and TRPM6 was found during high-salt treatment, while low salt and dehydration diminished expression. These findings were confirmed with immunofluorescence studies. High-salt and low-salt intake or dehydration did not cause any significant changes in WNK1, WNK3 and WNK4.</p><p><strong>Conclusions: </strong>Alternations in salt and water intake affect renal calcium and magnesium handling. High-salt intake increases the distal delivery of the divalent cations which upregulates distal tubule calcium and magnesium transport molecules, while the opposite effects are associated with low-salt intake or dehydration.</p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"122 3-4","pages":"19-27"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000353199","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31605601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Assessment of the effect of 24-hour aldosterone administration on protein abundance in fluorescence-sorted mouse distal renal tubules by mass spectrometry.","authors":"Thomas B Jensen, Trairak Pisitkun, Jason D Hoffert, Uffe B Jensen, Robert A Fenton, Helle A Praetorius, Mark A Knepper, Jeppe Praetorius","doi":"10.1159/000346832","DOIUrl":"10.1159/000346832","url":null,"abstract":"<p><strong>Background/aims: </strong>Aldosterone exerts multiple long-term effects on the distal renal tubules. The aim of this study was to establish a method for identifying proteins in these tubules that change in abundance by only 24-hour aldosterone administration.</p><p><strong>Methods: </strong>Mice endogenously expressing green fluorescent protein (eGFP) in the connecting tubule and cortical collecting ducts were treated with a subcutaneous injection of 2.0 mg/kg aldosterone or vehicle (n = 5), and sacrificed 24 h later. Suspensions of single cells were obtained enzymatically, and eGFP-positive cells were isolated by fluorescence-activated cell sorting (FACS). Samples of 100 µg of proteins were digested with trypsin and labeled with 8-plex isobaric tags for relative and absolute quantitation reagents and processed for liquid chromatography-tandem mass spectrometry (LC-MS/MS).</p><p><strong>Results: </strong>FACS yielded 1.4 million cells per mouse. The LC-MS/MS spectra were matched to peptides by the SEQUEST search algorithm, which identified 3,002 peptides corresponding to 506 unique proteins, of which 20 significantly changed abundance 24 h after aldosterone injection.</p><p><strong>Conclusion: </strong>We find the method suitable and useful for studying hormonal effects on protein abundance in distal tubular segments.</p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"121 3-4","pages":"p9-15"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648998/pdf/nihms459048.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31254706","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Weight, age and coefficients of variation in renal solute excretion.","authors":"Guy M L Perry,&nbsp;Steven J Scheinman,&nbsp;John R Asplin","doi":"10.1159/000346148","DOIUrl":"https://doi.org/10.1159/000346148","url":null,"abstract":"<p><strong>Background: </strong>Homoscedasticity (constant variance over axes or among statistical factors) is an integral assumption of most statistical analyses. However, a number of empirical studies in model organisms and humans demonstrate significant differences in residual variance (that component of phenotype unexplained by known factors) or intra-individual variation among genotypes. Our work suggests that renal traits may be particularly susceptible to randomization by genetic and non-genetic factors, including endogenous variables like age and weight.</p><p><strong>Methods: </strong>We tested associations between age, weight and intra-individual variation in urinary calcium, citrate, chloride, creatinine, potassium, magnesium, sodium, ammonium, oxalate, phosphorus, sulfate, uric acid and urea nitrogen in 9,024 male and 6,758 female kidney stone patients. Coefficients of variation (CVs) were calculated for each individual for each solute from paired 24-hour urines. Analysis of CVs was corrected for inter-measurement collection variance in creatinine and urine volume. CVs for sodium and urea nitrogen were included to correct for dietary salt and protein.</p><p><strong>Results: </strong>Age was positively associated with individual CVs for calcium and negatively associated with CVs for potassium, ammonium and phosphorus (p(FDR) < 0.01). Weight was associated with CVs for creatinine, magnesium and uric acid, and negatively associated with CVs for calcium, potassium and oxalate (p(FDR) < 0.05).</p><p><strong>Conclusion: </strong>Intra-individual variation changes over age and weight axes for numerous urinary solutes. Changing residual variance over age and weight could cause bias in the detection or estimation of genetic or environmental effects. New methodologies may need to account for such residual unpredictability, especially in diverse collections.</p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"122 1-2","pages":"13-8"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000346148","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31365825","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Response of the renal inner medulla to hypoxia: possible defense mechanisms.","authors":"Namhee Kim,&nbsp;Laura Voicu,&nbsp;Gregory M T Hare,&nbsp;Surinder Cheema-Dhadli,&nbsp;Chee Kiong Chong,&nbsp;Stephen K W Chan,&nbsp;Daniel G Bichet,&nbsp;Mitchell L Halperin,&nbsp;C David Mazer","doi":"10.1159/000345516","DOIUrl":"https://doi.org/10.1159/000345516","url":null,"abstract":"<p><strong>Background/aims: </strong>Owing to the precarious blood supply to the renal medulla and the high metabolic requirement of the medullary thick ascending limb of Henle's loop, this nephron segment should be especially vulnerable when its supply of O(2) declines.</p><p><strong>Methods: </strong>Rats were exposed to 8 or 21% O(2) at different time points up to 5 h, and samples were collected for urine flow rate, urine (U(osm)) and renal papillary (RP(osm)) osmolality, urinary excretion of Na(+), Cl(-), K(+) and Mg(2+), blood gases, erythropoietin and vasopressinase activity in plasma. Other groups of rats were pretreated with desmopressin acetate (dDAVP) or underwent bilateral nephrectomy (BNX) 1 h prior to the exposure.</p><p><strong>Results: </strong>Hypoxic rats had water diuresis (WD) within 2.5 h, as evidenced by lower U(osm) (333 ± 42 mosm/l) and RP(osm) (869 ± 57 mosm/l), thus suggesting that hypoxia led to a failure to achieve osmotic equilibrium within the renal papilla. Circulating vasopressinase activity increased, which was partially renal in origin because it was lower after BNX. The renal concentrating ability during hypoxia was maintained with dDAVP pretreatment, suggesting that dDAVP may have improved O(2) delivery and the active reabsorption of Na(+) in the renal medullary region.</p><p><strong>Conclusions: </strong>WD or high vasopressinase activity may be valuable diagnostic tools to assess renal medullary hypoxia. Pretreatment with dDAVP may prevent these changes during hypoxia.</p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"121 1-2","pages":"p1-7"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000345516","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31094804","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Extracellular pyrophosphate in the kidney: how does it get there and what does it do?.","authors":"Shabbir H Moochhala","doi":"10.1159/000341597","DOIUrl":"https://doi.org/10.1159/000341597","url":null,"abstract":"<p><p>Pyrophosphate (PPi) is well known as a regulator of calcification, and the ANKH (ANK in mouse) protein has a role in the membrane transport of PPi. Earlier work concentrated on bones and joints, but ANKH is also likely to have important roles in the kidney, with newer studies focusing on vascular calcification in renal failure. Renal calcification can occur due to a naturally occurring ANK mouse mutation, yet other ANK mutations do not cause a renal phenotype. Despite evidence over 10 years of ANKH's involvement in PPi transport, efflux of PPi via ANKH has never been demonstrated. Rather than physically moving PPi, the ANKH protein may assist its membrane transport in other ways such as by hydrolysis and compartmentalisation. Protein complexes may account for effects of ANKH that are specific to particular tissues. In the kidney, recent localisation data may be helpful in suggesting physiological roles for ANKH, such as its co-localisation with aquaporin-2 and cilial proteins. Such diverse functions would reflect the ubiquitous nature of ANKH in tissues and its profound evolutionary conservation. </p>","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"120 4","pages":"p33-8"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000341597","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30982301","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Title Page / Table of Contents","authors":"","doi":"10.1159/000330593","DOIUrl":"https://doi.org/10.1159/000330593","url":null,"abstract":"","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"119 1","pages":"pI - pIV"},"PeriodicalIF":0.0,"publicationDate":"2011-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000330593","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64544935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Contents Vol. 118, 2011","authors":"S. Bucharles, S. Barberato, A. E. Stinghen, B. Gruber, H. Meister, A. Mehl, Luciana Piekala, A. Dambiski, A. Souza, M. Olandoski, Usama Elewa, A. M. Sandri, S. Rizza, F. Fervenza, A. Fujimori, Shioko Okada, M. Sakai, K. Tome, M. Fukagawa, T. Ellam, M. Noordzij, F. Dekker, C. Zoccali, K. Jager, C. Cruz, R. Pecoits-Filho, D. Packham, Sara E. Ivory, A. Reutens, R. Wolfe, R. Rohde, H. Heerspink, J. Dwyer, R. Atkins, J. Lewis, H. J. Nye, W. Herrington, M. A. Graaf, G. Tripepi, V. Stel, C. Moura, C. Mangueira, L. S. Cruz, J. Heaf, L. S. Mortensen, A. A. Kutlugun, M. Arıcı, T. Yıldırım, D. Turgut, R. Yılmaz, M. Altındal, B. Altun, Y. Erdem, Ü. Yasavul, Ç. Turgan, M. Nagai, K. Hirayama, I. Ebihara, H. Shimohata, Masaki Kobayashi, A. Koyama, M. Onuigbo, B. Agarwal, F. Kovari, R. Saha, S. Shaw, A. Davenport, Satz Mengensatzproduktion, D. R. Basel","doi":"10.1159/000330662","DOIUrl":"https://doi.org/10.1159/000330662","url":null,"abstract":"Clinical Nephrology Guidelines J. Cunningham, London G. Eknoyan, Houston, Tex. A. Khwaja, Sheffield Clinical Appraisal/Evidence Based Nephrology A.K. El-Sherif, Ismailia R.J. Glassock, Laguna Niguel, Calif. A. Meyrier, Paris Global CKD G. Remuzzi, Bergamo N. Perico, Bergamo R. Atkins, Melbourne, Vic. Clinical Trials D. de Zeeuw, Groningen F. Locatelli, Lecco D. Wheeler, London Continuing Nephrology Education R. Barsoum, Cairo M. Field, Sydney, N.S.W. C. Zoccali, Reggio Calabria Clinico-Pathological Conferences T.H. Jafar, Karachi Editor-in-Chief","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"118 1","pages":"I - VI"},"PeriodicalIF":0.0,"publicationDate":"2011-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64545839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Author and Subject Index Vol. 117, 2011","authors":"","doi":"10.1159/000326826","DOIUrl":"https://doi.org/10.1159/000326826","url":null,"abstract":"","PeriodicalId":18996,"journal":{"name":"Nephron Physiology","volume":"102 1","pages":"p37 - p37"},"PeriodicalIF":0.0,"publicationDate":"2011-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000326826","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64508843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}