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1.
Pediatr Neonatol ; 52(2): 66-72, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21524625

ABSTRACT

BACKGROUND: Nitric oxide (NO) deficiency contributes to chronic kidney disease progression. NO deficiency could occur for many reasons, one of which is decreased NO synthase (NOS) abundance and/or activity. METHODS: In these experiments, we studied two groups of male Sprague Dawley rats given sham or surgical excision of both poles of the left kidney (at 2 days of age) followed by sham or surgical removal of the right kidney at 10 days. Rats were sacrificed at 9 weeks of age and the kidneys examined for abundance of neuronal NOS (nNOS)-α and -ß, endothelial NOS, arginase II, argininosuccinate synthase and lysate, protein arginine methyltransferase 1, dimethylarginine dimethylamino-hydrolase 1 and 2, as well as renal pathology. RESULTS: The 5/6 nephrectomy (NX) group showed renal dysfunction, severe rapidly progressing glomerulosclerosis, and hypertension. Renal cortical nNOSα abundance was significantly reduced, whereas nNOSß abundance was increased in the 5/6 NX group versus sham. Renal endothelial NOS was unchanged. Next, renal protein arginine methyltransferase 1 abundance was higher, whereas dimethylarginine dimethylamino-hydrolase 2 expression was lower in the 5/6 NX group versus sham. Renal arginase II, argininosuccinate synthase, and argininosuccinate lysate abundances were significantly decreased in 5/6 NX rats than those in sham. CONCLUSION: The neonatal kidney is very susceptible to 5/6 NX-induced injury, and, as in adults, reciprocal changes in the nNOSα and nNOSß in renal cortex occur during progression of chronic kidney disease and may contribute to the injury.


Subject(s)
Kidney/enzymology , Nitric Oxide Synthase/metabolism , Animals , Kidney Diseases/metabolism , Male , Models, Animal , Nephrectomy , Rats , Rats, Sprague-Dawley
2.
J Chromatogr B Analyt Technol Biomed Life Sci ; 826(1-2): 267-72, 2005 Nov 05.
Article in English | MEDLINE | ID: mdl-16169291

ABSTRACT

A simple high-performance liquid chromatographic (HPLC) method was developed for the simultaneous determination of iohexol, iothalamate, p-aminohippuric acid (PAH) and n-acetyl-p-aminohippuric acid (n-acetyl-PAH) in human plasma and urine. A C(18) column at a flow rate of 1 ml/min with an aqueous mobile phase of trifluoroacetic acid (0.1% TFA in deionized water (pH 2.2), v/v) and methanol gradient was used for component separation. The plasma and urine assay demonstrated linearity from 10 to 50 microg/ml for iohexol and iothalamate, 5 to 40 microg/ml for PAH and 2.5 to 40 microg/ml for n-acetyl-PAH. The HPLC plasma and urine results obtained for PAH were used to calculate the subject kidney effective renal plasma flow (ERPF) and the iohexol results were used to calculate the subject kidney glomerular filtration rate (GFR). The HPLC results for PAH were then compared to an alternative colorimetric method for analyzing PAH to determine if subject metabolism (acetylation) of PAH affected the ERPF results obtained using the colorimetric method, the subsequent ERPF/GFR ratio and clinical impression of subject patient kidney function. The method was utilized in several different clinical studies evaluating the effect of kidney function from medications (phase IV evaluations) marketed for patients with cardiovascular disease.


Subject(s)
Aminohippuric Acids/analysis , Glomerular Filtration Rate/physiology , Iohexol/analysis , Iothalamic Acid/analysis , Renal Plasma Flow, Effective/physiology , p-Aminohippuric Acid/analysis , Aminohippuric Acids/blood , Aminohippuric Acids/urine , Chromatography, High Pressure Liquid/methods , Colorimetry/methods , Humans , Reproducibility of Results , Sensitivity and Specificity , Ultraviolet Rays , p-Aminohippuric Acid/blood , p-Aminohippuric Acid/urine
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