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Am J Physiol Renal Physiol 291: F495-F502, 2006. First published April 11, 2006; doi:10.1152/ajprenal.00521.2005
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INNOVATIVE METHODOLOGY

Quantitative imaging of basic functions in renal (patho)physiology

Jung Julie Kang, Ildiko Toma, Arnold Sipos, Fiona McCulloch, and Janos Peti-Peterdi

Departments of Physiology and Biophysics and Medicine, Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, California

Submitted 30 December 2005 ; accepted in final form 22 March 2006

Multiphoton fluorescence microscopy offers the advantages of deep optical sectioning of living tissue with minimal phototoxicity and high optical resolution. More importantly, dynamic processes and multiple functions of an intact organ can be visualized in real time using noninvasive methods, and quantified. These studies aimed to extend existing methods of multiphoton fluorescence imaging to directly observe and quantify basic physiological parameters of the kidney including glomerular filtration rate (GFR) and permeability, blood flow, urinary concentration/dilution, renin content and release, as well as more integrated and complex functions like the tubuloglomerular feedback (TGF)-mediated oscillations in glomerular filtration and tubular flow. Streptozotocin-induced diabetes significantly increased single-nephron GFR (SNGFR) from 32.4 ± 0.4 to 59.5 ± 2.5 nl/min and glomerular permeability to a 70-kDa fluorophore approximately eightfold. The loop diuretic furosemide 2-fold diluted and increased ~10-fold the volume of distal tubular fluid, while also causing the release of 20% of juxtaglomerular renin content. Significantly higher speeds of individual red blood cells were measured in intraglomerular capillaries (16.7 ± 0.4 mm/s) compared with peritubular vessels (4.7 ± 0.2 mm/s). Regular periods of glomerular contraction-relaxation were observed, resulting in oscillations of filtration and tubular flow rate. Oscillations in proximal and distal tubular flow showed similar cycle times (~45 s) to glomerular filtration, with a delay of ~5–10 and 25–30 s, respectively. These innovative technologies provide the most complex, immediate, and dynamic portrayal of renal function, clearly depicting the components and mechanisms involved in normal physiology and pathophysiology.

intravital microscopy; diabetic nephropathy; single-nephron glomerular filtration rate; red blood cell velocity; quinacrine; rhodamine; lucifer yellow; proteinuria



Address for reprint requests and other correspondence: J. Peti-Peterdi, Univ. of Southern California, Zilkha Neurogenetic Institute, 1501 San Pablo St., ZNI 335, Los Angeles, CA 90033 (e-mail: petipete{at}usc.edu)




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