Nephrology Dialysis Transplantation, Vol 12, Issue 3 404-417, Copyright © 1997 by Oxford University Press
GH Neild, PJ Foxall, JC Lindon, EC Holmes and JK Nicholson
From the experiments described, it can be seen that there are different
research approaches that can be taken and these are summarized in Table 1.
Whereas much scientific research is principally hypothesis led, there
remains, nevertheless, an important place for exploratory research. High
resolution NMR can measure, directly and simultaneously, a wide range of
endogenous metabolites in biological fluids and has the unique capability
of providing structural information on the metabolites detected. It has
proved to be a powerful research tool with which to study inherited
metabolic diseases, renal disease, drug metabolism, and toxicity, and can
be used to monitor the effects of drug therapy. For instance, by using a
library of experimental toxins one can map the metabolic profile of
site-specific nephron injury. With this approach in man one could
eventually take an unknown disease such as Balkan nephropathy and predict
the initial site of tubular injury, the mode of injury and therefore the
kind of toxin capable of producing that injury. NMR spectroscopic
techniques are still advancing rapidly, with ever increasing sensitivity
and sophistication of NMR pulse sequences to enhance structural elucidation
in complex mixtures. Given the advances in directly coupled HPLC-NMR and
even HPLC-NMR-mass spectroscopy it is likely that these technologies in
conjunction with pattern recognition will make major contribution to our
understanding of renal processes and provide new diagnostic insights in the
21st century.
REVIEWS
Uroscopy in the 21st century: high-field NMR spectroscopy
Institute of Urology and Nephrology, University College London Medical School, UK.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
J. P. Faure, C. Jayle, D. Dutheil, M. Eugene, K. Zhang, J. M. Goujon, I. Petit-Paris, J. P. Tillement, G. Touchard, R. Robert, et al. Evidence for protective roles of polyethylene glycol plus high sodium solution and trimetazidine against consequences of renal medulla ischaemia during cold preservation and reperfusion in a pig kidney model Nephrol. Dial. Transplant., July 1, 2004; 19(7): 1742 - 1751. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Jayle, P. Corbi, M. Eugene, M. Carretier, W. Hebrard, E. Menet, and T. Hauet Beneficial effect of polyethylene glycol in lung preservation: early evaluation by proton nuclear magnetic resonance spectroscopy Ann. Thorac. Surg., September 1, 2003; 76(3): 896 - 902. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Faure, T. Hauet, Z. Han, J. M. Goujon, I. Petit, G. Mauco, M. Eugene, M. Carretier, and V. Papadopoulos Polyethylene Glycol Reduces Early and Long-Term Cold Ischemia-Reperfusion and Renal Medulla Injury J. Pharmacol. Exp. Ther., September 1, 2002; 302(3): 861 - 870. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Bairaktari, K. Seferiadis, G. Liamis, N. Psihogios, O. Tsolas, and M. Elisaf Rhabdomyolysis-related Renal Tubular Damage Studied by Proton Nuclear Magnetic Resonance Spectroscopy of Urine Clin. Chem., July 1, 2002; 48(7): 1106 - 1109. [Full Text] [PDF] |
||||
![]() |
T. Hauet, H. Baumert, I. B. Amor, H. Gibelin, C. Tallineau, M. Eugene, J. P. Tillement, and M. Carretier Pharmacological Limitation of Damage to Renal Medulla after Cold Storage and Transplantation by Trimetazidine J. Pharmacol. Exp. Ther., January 1, 2000; 292(1): 254 - 260. [Abstract] [Full Text] |
||||
![]() |
S. H. Moolenaar, J. Poggi-Bach, U. F.H. Engelke, J. M.B. Corstiaensen, A. Heerschap, J. G.N. de Jong, B. A. Binzak, J. Vockley, and R. A. Wevers Defect in Dimethylglycine Dehydrogenase, a New Inborn Error of Metabolism: NMR Spectroscopy Study Clin. Chem., April 1, 1999; 45(4): 459 - 464. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Bairaktari, K. Katopodis, K. C. Siamopoulos, and O. Tsolas Paraquat-induced renal injury studied by 1H nuclear magnetic resonance spectroscopy of urine Clin. Chem., June 1, 1998; 44(6): 1256 - 1261. [Abstract] [Full Text] [PDF] |
||||



