@article{RailaSchweigertKohn2014,
  author    = {Raila, Jens and Schweigert, Florian J. and Kohn, Barbara},
  title     = {Relationship between urinary Tamm-Horsfall protein excretion and renal function in dogs with naturally occurring renal disease},
  series = {Veterinary clinical pathology},
  volume    = {43},
  journal   = {Veterinary clinical pathology},
  number    = {2},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0275-6382},
  doi       = {10.1111/vcp.12143},
  pages     = {261 -- 265},
  year      = {2014},
  abstract  = {Background Tamm-Horsfall protein (THP) is physiologically excreted in urine, but little is known about the role of THP in the diagnosis of renal disease in dogs. Objective The aim of this study was to evaluate to which extent naturally occurring renal disease affects the urinary excretion of THP. Methods Dogs were divided into 5 groups according to plasma creatinine concentration, urinary protein-to-creatinine ratio (UP/UC), and exogenous plasma creatinine clearance (P-ClCr) rates: Group A (healthy control dogs; n=8), nonazotemic and nonproteinuric dogs, with P-ClCr rates > 90mL/min/m2; group B (n=25), nonazotemic and nonproteinuric dogs with reduced P-ClCr rates (51-89mL/min/m2); group C (n=7), nonazotemic but proteinuric dogs with P-ClCr rates 53-98mL/min/m2; group D (n=8), azotemic and borderline proteinuric dogs (P-ClCr rates: 22-45mL/min/m2); and group E (n=15), azotemic and proteinuric dogs (not tested for P-ClCr). THP was measured by quantitative Western blot analysis, and the ratio of THP-to-urinary creatinine (THP/UC) was calculated. Results The THP/UC concentrations were not different among dogs of groups A-D, but were reduced in dogs of group E (P<.001). THP/UC correlated negatively with serum creatinine (P<.01) and UP/UC (P<.01), but was not significantly associated with P-ClCr. Conclusions Decreased levels of THP/UC were present in moderately to severely azotemic and proteinuric dogs. This suggests tubular injury in these dogs and that THP might be useful as urinary marker to study the pathogenesis of renal disease.},
  language  = {en}
}
@misc{RailaSchweigertKohn2017,
  author    = {Raila, Jens and Schweigert, Florian J. and Kohn, Barbara},
  title     = {C-reactive protein concentrations in serum of dogs with naturally occurring renal disease},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-402942},
  pages     = {6},
  year      = {2017},
  abstract  = {The current study was undertaken to investigate the relation between serum C-reactive protein (CRP) concentrations and parameters of renal function in dogs with naturally occurring renal disease. Dogs were assigned to groups according to plasma creatinine concentration, urinary protein-to-creatinine ratio (UP/UC), and exogenous plasma creatinine clearance (P-Cl(Cr)) rates. Group A (healthy control dogs; n = 8): non-azotemic (plasma creatinine <125 mu mol/l) and nonproteinuric (UP/UC <0.2), with P-Cl(Cr) rates >90 ml/min/m(2); group B (n = 11): non-azotemic, nonproteinuric dogs with reduced P-Cl(Cr) rates (50-89 ml/min/m(2)); group C (n = 7): azotemic, borderline proteinuric dogs (P-Cl(Cr) rates: 22-67 ml/min/m(2)); and group D (n = 6): uremic, proteinuric dogs (not tested for P-Cl(Cr)). The serum CRP concentrations were measured via commercial enzyme-linked immunosorbent assay. The CRP concentrations in the clinically healthy dogs (group A) ranged from 2.09 mg/l to 8.60 mg/l (median: 3.21 mg/l). In comparison with dogs of group A, median CRP concentrations were significantly (P < 0.01) elevated in dogs of group B (17.6 mg/l, range: 17.0-19.2 mg/l), group C (24.8 mg/l, range: 18.0-32.5 mg/l), and group D (59.7 mg/l, range: 17.7-123 mg/l). Serum CRP was significantly related to P-Cl(Cr) (r = -0.83; P < 0.001), plasma creatinine (r = 0.81; P < 0.001), UP/UC (r = 0.70; P < 0.001), and leukocytes (r = 0.49; P < 0.01). The significant relations between serum CRP concentrations and biochemical parameters of kidney function in plasma and urine suggest that a stimulation of the acute phase response is implicated in the pathogenesis of canine renal disease.},
  language  = {en}
}
@article{RailaSchweigert2001,
  author    = {Raila, Jens and Schweigert, Florian J.},
  title     = {Zur Bedeutung der Nieren im Vitamin-Stoffwechsel},
  year      = {2001},
  language  = {de}
}
@article{RailaRohnSchweigertetal.2011,
  author    = {Raila, Jens and Rohn, Sascha and Schweigert, Florian J. and Abraham, Getu},
  title     = {Increased antioxidant capacity in the plasma of dogs after a single oral dosage of tocotrienols},
  series = {The British journal of nutrition : an international journal devoted to the science of human and animal nutrition},
  volume    = {106},
  journal   = {The British journal of nutrition : an international journal devoted to the science of human and animal nutrition},
  number    = {7},
  publisher = {Cambridge Univ. Press},
  address   = {Cambridge},
  issn      = {0007-1145},
  doi       = {10.1017/S0007114511000511},
  pages     = {S116 -- S119},
  year      = {2011},
  abstract  = {The intestinal absorption of tocotrienols (TCT) in dogs is, to our knowledge, so far unknown. Adult Beagle dogs (n 8) were administered a single oral dosage of a TCT-rich fraction (TRF; 40 mg/kg body weight) containing 32\% alpha-TCT, 2\% beta-TCT, 27\% gamma-TCT, 14\% delta-TCT and 25\% alpha-tocopherol (alpha-TCP). Blood was sampled at baseline (fasted), 1, 2, 3, 4, 5, 6, 8 and 12 h after supplementation. Plasma and chylomicron concentrations of TCT and alpha-TCP were measured at each time point. Plasma TAG were measured enzymatically, and plasma antioxidant capacity was assessed by the Trolox equivalent antioxidant capacity assay. In fasted dogs, levels of TCT were 0.07 (SD 0.03) mu mol/l. Following the administration of the TRF, total plasma TCT peaked at 2 h (7.16 (SD 3.88) mu mol/l; P<0.01) and remained above baseline levels (0.67 (SD 0.44) mu mol/l; P, 0.01) at 12 h. The TCT response in chylomicrons paralleled the increase in TCT in plasma with a maximum peak (3.49 (SD 2.06) mu mol/l; P, 0.01) at 2 h post-dosage. alpha-TCP was the major vitamin E detected in plasma and unaffected by TRF supplementation. The Trolox equivalent values increased from 2 h (776 (SD 51.2) mu mol/l) to a maximum at 12 h (1130 (SD 7.72) mmol/l; P<0.01). The results show that TCT are detected in postprandial plasma of dogs. The increase in antioxidant capacity suggests a potential beneficial role of TCT supplementation in the prevention or treatment of several diseases in dogs.},
  language  = {en}
}
@article{RailaNeumannSchweigert2003,
  author    = {Raila, Jens and Neumann, U. and Schweigert, Florian J.},
  title     = {Immunochemical Localization of Megalin, Retinol-binding protein and Tamm-Horsfall Glycoprotein in the Kidneys of Dogs},
  year      = {2003},
  language  = {en}
}
@article{RailaMathewsSchweigert2001,
  author    = {Raila, Jens and Mathews, U. and Schweigert, Florian J.},
  title     = {Plasma transport and tissue distribution of ß-carotene, vitamin A and retinol-binding protein in domestic cats},
  year      = {2001},
  language  = {en}
}
@misc{RailaKawashimaSauerweinetal.2017,
  author    = {Raila, Jens and Kawashima, Chiho and Sauerwein, Helga and H{\"u}lsmann, Nadine and Knorr, Christoph and Myamoto, Akio and Schweigert, Florian J.},
  title     = {Validation of blood vitamin A concentrations in cattle: comparison of a new cow-side test (iCheck™ FLUORO) with high-performance liquid chromatography (HPLC)},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-401978},
  pages     = {6},
  year      = {2017},
  abstract  = {Background: Plasma concentration of retinol is an accepted indicator to assess the vitamin A (retinol) status in cattle. However, the determination of vitamin A requires a time consuming multi-step procedure, which needs specific equipment to perform extraction, centrifugation or saponification prior to high-performance liquid chromatography (HPLC). Methods: The concentrations of retinol in whole blood (n = 10), plasma (n = 132) and serum (n = 61) were measured by a new rapid cow-side test (iCheck™ FLUORO) and compared with those by HPLC in two independent laboratories in Germany (DE) and Japan (JP). Results: Retinol concentrations in plasma ranged from 0.033 to 0.532 mg/L, and in serum from 0.043 to 0.360 mg/L (HPLC method). No significant differences in retinol levels were observed between the new rapid cow-side test and HPLC performed in different laboratories (HPLC vs. iCheck™ FLUORO: 0.320 ± 0.047 mg/L vs. 0.333 ± 0.044 mg/L, and 0.240 ± 0.096 mg/L vs. 0.241 ± 0.069 mg/L, lab DE and lab JP, respectively). A similar comparability was observed when whole blood was used (HPLC vs. iCheck™ FLUORO: 0.353 ± 0.084 mg/L vs. 0.341 ± 0.064 mg/L). Results showed a good agreement between both methods based on correlation coefficients of r2 = 0.87 (P < 0.001) and Bland-Altman blots revealed no significant bias for all comparison. Conclusions: With the new rapid cow-side test (iCheck™ FLUORO) retinol concentrations in cattle can be reliably assessed within a few minutes and directly in the barn using even whole blood without the necessity of prior centrifugation. The ease of the application of the new rapid cow-side test and its portability can improve the diagnostic of vitamin A status and will help to control vitamin A supplementation in specific vitamin A feeding regimes such as used to optimize health status in calves or meat marbling in Japanese Black cattle.},
  language  = {en}
}
@article{RailaKawashimaSauerweinetal.2017,
  author    = {Raila, Jens and Kawashima, Chiho and Sauerwein, Helga and H{\"u}lsmann, Nadine and Knorr, Christoph and Myamoto, Akio and Schweigert, Florian J.},
  title     = {Validation of blood vitamin A concentrations in cattle: comparison of a new cow-side test (iCheck™ FLUORO) with high-performance liquid chromatography (HPLC)},
  series = {BMC veterinary research},
  volume    = {13},
  journal   = {BMC veterinary research},
  publisher = {BioMed Central},
  address   = {London},
  doi       = {10.1186/s12917-017-1042-3},
  year      = {2017},
  abstract  = {Background: Plasma concentration of retinol is an accepted indicator to assess the vitamin A (retinol) status in cattle. However, the determination of vitamin A requires a time consuming multi-step procedure, which needs specific equipment to perform extraction, centrifugation or saponification prior to high-performance liquid chromatography (HPLC). Methods: The concentrations of retinol in whole blood (n = 10), plasma (n = 132) and serum (n = 61) were measured by a new rapid cow-side test (iCheck™ FLUORO) and compared with those by HPLC in two independent laboratories in Germany (DE) and Japan (JP). Results: Retinol concentrations in plasma ranged from 0.033 to 0.532 mg/L, and in serum from 0.043 to 0.360 mg/L (HPLC method). No significant differences in retinol levels were observed between the new rapid cow-side test and HPLC performed in different laboratories (HPLC vs. iCheck™ FLUORO: 0.320 ± 0.047 mg/L vs. 0.333 ± 0.044 mg/L, and 0.240 ± 0.096 mg/L vs. 0.241 ± 0.069 mg/L, lab DE and lab JP, respectively). A similar comparability was observed when whole blood was used (HPLC vs. iCheck™ FLUORO: 0.353 ± 0.084 mg/L vs. 0.341 ± 0.064 mg/L). Results showed a good agreement between both methods based on correlation coefficients of r2 = 0.87 (P < 0.001) and Bland-Altman blots revealed no significant bias for all comparison. Conclusions: With the new rapid cow-side test (iCheck™ FLUORO) retinol concentrations in cattle can be reliably assessed within a few minutes and directly in the barn using even whole blood without the necessity of prior centrifugation. The ease of the application of the new rapid cow-side test and its portability can improve the diagnostic of vitamin A status and will help to control vitamin A supplementation in specific vitamin A feeding regimes such as used to optimize health status in calves or meat marbling in Japanese Black cattle.},
  language  = {en}
}
@article{RailaForterreSchweigert2005,
  author    = {Raila, Jens and Forterre, Simone and Schweigert, Florian J.},
  title     = {Markerproteine im Harn von Hunden},
  isbn      = {3-8304-1051-4},
  year      = {2005},
  language  = {de}
}
@article{RailaForterreSchweigert2005,
  author    = {Raila, Jens and Forterre, Simone and Schweigert, Florian J.},
  title     = {Physiologische und pathophysiologische Grundlagen der Proteinurie : eine {\"U}bersicht},
  year      = {2005},
  language  = {de}
}
@article{RailaForterreSchweigert2005,
  author    = {Raila, Jens and Forterre, Simone and Schweigert, Florian J.},
  title     = {Physiology and pathophysiology of proteinuria : a review},
  issn      = {0005-9366},
  year      = {2005},
  abstract  = {The term proteinuria is taken to mean abnormally high protein excretion in the urine. Proteinuria is the consequence of glomerular filtration of plasma proteins, their subsequent reabsorption by the proximal tubular cells and secretion of protein by the tubular cells and distal urinary tract. In physiological conditions, the structural integry of the glomerular filtration barrier prevents the abnormal passage of albumin (molecular mass 66 kDa) and high-molecular- weight proteins (> 66 kDa),whereas the passage of low-molecular-weight proteins (< 66 kDa) is almost completely unrestricted. Proteins that arrive the tubular lumen are reabsorbed by endocytosis after binding to the megalin-cubilin complex. An increased load of proteins in the tubular lumen leads to the saturation of the reabsorptive mechanism and higher urinary protein excretion. Proteinuria can originate from prerenal, renal and postrenal causes. Elevated tubular protein concentrations have been recognized to be toxic to tubular cells and associated with the progression of chronic renal disease. Therefore, the quantitative and qualitative evaluation of proteinuria is important for the diagnosis of renal disease},
  language  = {en}
}
@article{RailaForterreSchweigert2003,
  author    = {Raila, Jens and Forterre, Simone and Schweigert, Florian J.},
  title     = {Die Bedeutung von Megalin in der Pathogenese der tubul{\"a}ren Proteinurie des Hundes},
  isbn      = {3-936815-65-8},
  year      = {2003},
  language  = {de}
}
@article{RailaForterreSchweigert2003,
  author    = {Raila, Jens and Forterre, Simone and Schweigert, Florian J.},
  title     = {Levels of retinol and retinyl esters in plasma and urine of dogs with urolithiasis},
  year      = {2003},
  language  = {en}
}
@article{RailaEnjalbertMothesetal.2012,
  author    = {Raila, Jens and Enjalbert, Francis and Mothes, Ralf and Hurtienne, Andrea and Schweigert, Florian J.},
  title     = {Validation of a new point-of-care assay for determination of ss-carotene concentration in bovine whole blood and plasma},
  series = {Veterinary clinical pathology},
  volume    = {41},
  journal   = {Veterinary clinical pathology},
  number    = {1},
  publisher = {Wiley-Blackwell},
  address   = {Malden},
  issn      = {0275-6382},
  doi       = {10.1111/j.1939-165X.2012.00400.x},
  pages     = {119 -- 122},
  year      = {2012},
  abstract  = {Background: beta-Carotene is an important precursor of vitamin A, and is associated with bovine fertility. beta-Carotene concentrations in plasma are used to optimize beta-carotene supplementation in cattle, but measurement requires specialized equipment to separate plasma and extract and measure beta-carotene, either using spectrophotometry or high performance liquid chromatography (HPLC). Objective: The objective of this study was to validate a new 2-step point-of-care (POC) assay for measuring beta-carotene in whole blood and plasma. Methods: beta-carotene concentrations in plasma from 166 cows were measured using HPLC and compared with results obtained using a POC assay, the iCheck-iEx-Carotene test kit. Whole blood samples from 23 of these cattle were also evaluated using the POC assay and compared with HPLC-plasma results from the same 23 animals. The POC assay includes an extraction vial (iEx Carotene) and hand-held photometer (iCheck Carotene). Results: Concentrations of beta-carotene in plasma measured using the POC assay ranged from 0.40 to 15.84 mg/L (n = 166). No differences were observed between methods for assay of plasma (mean +/- SD; n = 166): HPLC-plasma 4.23 +/- 2.35 mg/L; POC-plasma 4.49 +/- 2.36 mg/L. Similar good agreement was found when plasma analyzed using HPLC was compared with whole blood analyzed using the POC system (n = 23): HPLC-plasma 3.46 +/- 2.12 mg/L; POC-whole blood 3.67 +/- 2.29 mg/L. Conclusions: Concentrations of beta-carotene can be measured in blood and plasma from cattle easily and rapidly using a POC assay, and results are comparable to those obtained by the highly sophisticated HPLC method. Immediate feedback regarding beta-carotene deficiency facilitates rapid and appropriate optimization of beta-carotene supplementation in feed.},
  language  = {en}
}
@article{RailaEisenachBuchholzetal.1997,
  author    = {Raila, Jens and Eisenach, C. and Buchholz, Ingeborg and Schweigert, Florian J.},
  title     = {Verteilung von Vitamin A und Retinol-Bindungs-Protein (RBP) in verschiedenen Geweben von Caniden},
  year      = {1997},
  language  = {de}
}
@article{RailaEisenachBuchholzetal.1997,
  author    = {Raila, Jens and Eisenach, C. and Buchholz, Ingeborg and Schweigert, Florian J.},
  title     = {Distribution of vitamin A and retinol-binding-protein (RBP) in various tissue of dogs and reccoon dogs},
  year      = {1997},
  language  = {en}
}
@article{RailaBuchholzSchweigert1997,
  author    = {Raila, Jens and Buchholz, Ingeborg and Schweigert, Florian J.},
  title     = {Untersuchungen zur Vitamin-A-Bindung im Harn von Hunden},
  year      = {1997},
  language  = {de}
}
@article{RailaBuchholzAupperleetal.2000,
  author    = {Raila, Jens and Buchholz, Ingeborg and Aupperle, Heike and Raila, Jens and Schoon, Heinz-Adolf and Schweigert, Florian J.},
  title     = {The distribution of vitamin A and retinol-binding protein (RBP) in the blood plasma, urine, liver and kidney of carnivores},
  year      = {2000},
  language  = {en}
}
@article{RailaBokBuchholzetal.1997,
  author    = {Raila, Jens and Bok, V. and Buchholz, Ingeborg and Schweigert, Florian J.},
  title     = {Untersuchungen zum Vitamin-A-Stoffwechsel der Niere des Hundes},
  year      = {1997},
  language  = {de}
}
@article{RailaBokBuchholzetal.1997,
  author    = {Raila, Jens and Bok, V. and Buchholz, Ingeborg and Schweigert, Florian J.},
  title     = {Investigations on the excretion of vitamin A as retinol and retinyl esters bound to a high molecular complex},
  year      = {1997},
  language  = {en}
}