Measurement and Distribution of Zinc, Cadmium, and Mercury in Human Kidney Tissue

1972 ◽  
Vol 18 (1) ◽  
pp. 67-72 ◽  
Author(s):  
Hugh D Livingston
Keyword(s):  
Neutron Activation ◽  
Gamma Spectrometry ◽  
Kidney Tissue ◽  
Germanium Detector ◽  
Human Kidney ◽  
Kidney Cortex ◽  
Outer Cortex ◽  
Tissue Slices ◽  
Outer Medulla ◽  
Zinc Cadmium

Abstract Simultaneous analyses of human kidney cortex tissues for zinc, cadmium, and mercury were made by neutron activation combined with either radiochemical separation prior to counting or direct germanium detector gamma spectrometry. For some samples from adults and infants, analyses were made on successive tissue slices from the outer cortex to the inner medulla. Zinc and cadmium show a concentration gradient, with the highest concentrations at the outer medulla. Mercury was preferentially concentrated deeper in the cortex. All three metals, and especially cadmium, are found in higher concentrations in adult than in infant kidneys. A mechanism for the rapid increase in renal cadmium is proposed. The heterogeneous renal distribution of the elements indicates that careful sampling is necessary in any comparative study of their occurrence in human kidney tissue.

17-Oxidoreduction of 17β-Estradiol, Estrone and Their 3-Sulfates by Kidney Slices from Guinea Pig and Human

1975 ◽  
Vol 53 (12) ◽  
pp. 1333-1336 ◽  
Author(s):  
R. Hobkirk ◽  
Mona Nilsen ◽  
Barbara Jennings
Keyword(s):  
Guinea Pig ◽  
Marked Reduction ◽  
Human Kidney ◽  
Kidney Cortex ◽  
Limited Extent ◽  
Tissue Slices ◽  
Ample Evidence ◽  
Sulfatase Activity ◽  
17Β Estradiol ◽  
Dehydrogenation Reactions

Slices of whole kidney and kidney cortex from the female guinea pig catalyzed a marked reduction of estrone 3-sulfate (E13S) and estrone (E1) to 17β-estradiol 3-sulfate (E23S) and 17β-estradiol (E2), respectively, as well as the reverse (dehydrogenation) reactions. Slices of medulla did not appear active in E23S–E13S interconversion but did possess the ability to interconvert E2 and E1, besides possessing considerable sulfatase activity. The use of [3H-35S]E13S and [3H-35S]E23S as substrates, together with a demonstrated lack of estrogen sulfate synthesis by the tissue slices, provided ample evidence that the intact sulfates were involved in direct oxidoreduction. Slices of human kidney cortex catalyzed the reduction of E13S to a very limited extent. Slices of whole kidney and of cortex from guinea pig formed small amounts of estrogen glucuronide(s).

Abstract 089: Dopamine D 2 Receptor is Associated with Inverse Salt Sensitivity

Hypertension ◽  
2016 ◽  
Vol 68 (suppl_1) ◽  
Author(s):  
Peng Xu ◽  
John J Gildea ◽  
Pedro A Jose ◽  
Robert M Carey ◽  
Robin A Felder
Keyword(s):  
Blood Pressure ◽  
Kidney Tissue ◽  
Human Kidney ◽  
Salt Sensitivity ◽  
T Test ◽  
Receptor Expression ◽  
Nucleotide Polymorphisms ◽  
Wild Type ◽  
Tissue Slices ◽  
Type D

Our previous studies of salt sensitivity of blood pressure have demonstrated that approximately 11% of study participants have a paradoxical increase in blood pressure (> or = to 7-mm Hg) on a low NaCl diet (defined as inverse salt sensitivity (ISS)). However the mechanisms responsible for this effect are not known. We demonstrated that single nucleotide polymorphisms (SNPs) in the dopamine type 2 receptor (D 2 R) (RS6276 and 6267) are highly associated with ISS ( P values of 1.0х10 –2 and 3.8х10 –2 with odds ratios of 0.32 and 0.48 in unadjusted regression models, respectively). The C allele at both sites confers protection. The D 2 R is strongly expressed throughout the cytoplasm of proximal tubule cells in human kidney tissue slices. We also cultured RPTC from the urine from 4 salt resistant (SR) and 3 ISS participants enrolled in our clinical salt sensitivity studies. We hypothesize that D 2 R containing SNPs have altered receptor expression, and altered signaling compared to wild type controls. ISS participants were homozygous variant for the two D 2 R alleles and showed more D 2 R expression than SR RPTC heterozygous variant (HV) for the two alleles (ISS: 1.166±0.059 n=3 vs SR: 0.969±0.024 n=4, P<0.05, t-test). D 2 R expression was increased when the ISS cells were stimulated by a non-selective D 2 R agonist bromocriptine to a greater extent in the D 2 R SNP cell lines (ISS: VEH 1.166±0.059, vs bromocriptine 1.474 ± 0.040, n=3, P<0.05, t-test). Using the ROS reagent assay, dihydroethidium, there was found to be more ROS products in ISS cells than SR cells when stimulated under low salt (ISS: 1.145 ± 0.053, n=3 vs SR: 0.722 ± 0.101, n=4, P<0.05, t-test). We used a highly selective D 2 R agonist (sumanirole) to stimulate wild-type and SNPed cells, and the results demonstrated no effect in the cells with wild type D 2 R but an increase in ROS in cells heterozygous for the D 2 R SNPs (SNP: VEH 38,364±1,266, sumanirole 50,926 ± 3,310, VS WT: VEH 34,562±1,831 sumanirole 34,435 ± 1,614 RFU n=12, P<0.05, t-test) consistent with the higher expression of D 2 R found in ISS urine cells. We hypothesize that SNPs in the D 2 R lead to increased reactive oxygen species which has previously been associated with renal fibrosis and hypertension.

CORTICOSTEROIDS IN HUMAN KIDNEY TISSUE

1969 ◽  
Vol 61 (1_Suppl) ◽  
pp. S66
Author(s):  
A. T. A. Fazekas ◽  
I. Gy. Fazekas
Keyword(s):  
Kidney Tissue ◽  
Human Kidney

Multielement neutron activation analysis of fresh water using lithium-doped germanium gamma spectrometry

1975 ◽  
Vol 47 (7) ◽  
pp. 1011-1016 ◽  
Author(s):  
Brit. Salbu ◽  
Eiliv. Steinnes ◽  
Alexis C. Pappas
Keyword(s):  
Neutron Activation Analysis ◽  
Activation Analysis ◽  
Neutron Activation ◽  
Fresh Water ◽  
Gamma Spectrometry

Investigation of the Thermal and Injury Behavior During Microwave Thermal Therapy of Porcine Kidney

2002 ◽  
Author(s):  
Xiaoming He ◽  
Shawn Mcgee ◽  
James E. Coad ◽  
Paul A. Iaizzo ◽  
David J. Swanlund ◽  
...  
Keyword(s):  
Thermal Model ◽  
Histological Study ◽  
Kidney Cortex ◽  
Cellular Injury ◽  
Bioheat Equation ◽  
Tissue Slices ◽  
Thermal Histories ◽  
Microwave Probe

In this paper, we report on the characterization of microwave therapy of normal porcine kidneys both in vitro and in vivo. This technology is being developed for eventual use in the treatment of small renal cell carcinoma (RCC) by minimally invasive procedures. During experiments, microwave energy was applied through an interstitial microwave probe (Urologix, Plymouth, MN) to the kidney cortex with occasional involvement of the kidney medulla. The thermal histories at several locations were recorded. After treatment, the kidneys were bisected and small tissue slices were cut out at approximately the same depth as the thermal probes. The tissue slices were further processed for histological study. Both cellular injury and the area of microvascular stasis were quantitatively evaluated by histology. Absolute rate kinetic models of cellular injury and vascular stasis were developed and fit to this data. A 3-D finite element thermal model based on the Pennes Bioheat equation was developed and solved using a commercial software package (ANSYS, V5.7). The Specific Absorption Rate (SAR) of the microwave probe was measured experimentally in tissue equivalent gel-like solution. The thermal model was first validated by the measured in vitro thermal histories. It was then used to determine the blood perfusion term in vivo.

scholarly journals The tight junction protein ZO-1 is concentrated along slit diaphragms of the glomerular epithelium.

1990 ◽  
Vol 111 (3) ◽  
pp. 1255-1263 ◽  
Author(s):  
E Schnabel ◽  
J M Anderson ◽  
M G Farquhar
Keyword(s):  
Tight Junction ◽  
Rat Kidney ◽  
Freeze Fracture ◽  
Kidney Tissue ◽  
Slit Diaphragm ◽  
Kidney Cortex ◽  
Adult Rats ◽  
Junction Protein ◽  
Collecting Tubules ◽  
Lateral Cell

The foot processes of glomerular epithelial cells of the mammalian kidney are firmly attached to one another by shallow intercellular junctions or slit diaphragms of unknown composition. We have investigated the molecular nature of these junctions using an antibody that recognizes ZO-1, a protein that is specific for the tight junction or zonula occludens. By immunoblotting the affinity purified anti-ZO-1 IgG recognizes a single 225-kD band in kidney cortex and in slit diaphragm-enriched fractions as in other tissues. When ZO-1 was localized by immunofluorescence in kidney tissue of adult rats, the protein was detected in epithelia of all segments of the nephron, but the glomerular epithelium was much more intensely stained than any other epithelium. Among tubule epithelia the signal for ZO-1 correlated with the known fibril content and physiologic tightness of the junctions, i.e., it was highest in distal and collecting tubules and lowest in the proximal tubule. By immunoelectron microscopy ZO-1 was found to be concentrated on the cytoplasmic surface of the tight junctional membrane. Within the glomerulus ZO-1 was localized predominantly in the epithelial foot processes where it was concentrated precisely at the points of insertion of the slit diaphragms into the lateral cell membrane. Its distribution appeared to be continuous along the continuous slit membrane junction. When ZO-1 was localized in differentiating glomeruli in the newborn rat kidney, it was present early in development when the apical junctional complexes between presumptive podocytes are composed of typical tight and adhering junctions. It remained associated with these junctions during the time they migrate down the lateral cell surface, disappear and are replaced by slit diaphragms. The distribution of ZO-1 and the close developmental relationship between the two junctions suggest that the slit diaphragm is a variant of the tight junction that shares with it at least one structural protein and the functional property of defining distinctive plasmalemmal domains. The glomerular epithelium is unique among renal epithelia in that ZO-1 is present, but the intercellular spaces are wide open and no fibrils are seen by freeze fracture. The presence of ZO-1 along slit membranes indicates that expression of ZO-1 alone does not lead to tight junction assembly.

Characterization and Clinical Significance of Membrane Bound Proteases from Human Kidney Cortex

1984 ◽  
pp. 179-190 ◽  
Author(s):  
J. Scherberich ◽  
C. Gauhl ◽  
G. Heinert ◽  
W. Mondorf ◽  
W. Schoeppe
Keyword(s):  
Clinical Significance ◽  
Human Kidney ◽  
Kidney Cortex ◽  
Membrane Bound

scholarly journals Test spectra experimental construction for evaluating gamma-spectrometry computer codes for the 235U determination

2014 ◽  
Vol 29 (suppl.) ◽  
pp. 1-7 ◽  
Author(s):  
Konstantinos Karfopoulos ◽  
Dimitrios Karangelos ◽  
Marios Anagnostakis ◽  
Simos Simopoulos
Keyword(s):  
Gamma Spectrometry ◽  
Energy Region ◽  
Environmental Samples ◽  
Activity Concentration ◽  
Germanium Detector ◽  
Computer Code ◽  
High Background ◽  
Spectrometry Analysis ◽  
Background Continuum ◽  
Concentration Levels

The determination of 235U in environmental samples from its 185.72 keV photons may require the deconvolution of the multiplet photopeak at ~186 keV, due to the co-existence of the 186.25 keV photons of 226Ra in the spectrum. Successful deconvolution depends on many parameters, such as the detector characteristics, the activity concentration of the 235U and 226Ra in the sample, the background continuum in the 186 keV energy region and the gamma-spectrometry computer code used. In this work two sets of experimental test spectra were constructed for examining the deconvolution of the multiplet photopeak performed by different codes. For the construction of the test spectra, a high-resolution low energy germanium detector was used. The first series consists of 140 spectra and simulates environmental samples containing various activity concentration levels of 235U and 226Ra. The second series consists of 280 spectra and has been derived by adding 137Cs, corresponding to various activity concentration levels, to specific first series test spectra. As the 137Cs backscatter edge is detected in the energy region of the multiplet photopeak at ~186 keV, this second series of test spectra tests the analysis of the multiplet photopeak in high background continuum conditions. The analysis of the test spectra is performed by two different g-spectrometry analysis codes: (a) spectrum unix analysis code, a computer code developed in-house and (b) analysis of germanium detector spectra, a program freely available from the IAEA. The results obtained by the two programs are compared in terms of photopeak detection and photopeak area determination.

scholarly journals Autofluorescence microscopy as a label-free tool for renal histology and glomerular segmentation

2021 ◽  
Author(s):  
Nathan Heath Patterson ◽  
Elizabeth K Neumann ◽  
Kavya Sharman ◽  
Jamie L Allen ◽  
Raymond C Harris ◽  
...  
Keyword(s):  
Recognition Performance ◽  
Periodic Acid ◽  
Kidney Tissue ◽  
Human Kidney ◽  
True Positive Rate ◽  
Label Free ◽  
Periodic Acid Schiff ◽  
Renal Histology ◽  
Fresh Frozen ◽  
Histological Staining

Functional tissue units (FTUs) composed of multiple cells like the glomerulus in the kidney nephron play important roles in health and disease. Histological staining is often used for annotation or segmentation of FTUs, but chemical stains can introduce artefacts through experimental factors that influence analysis. Secondly, many molecular -omics techniques are incompatible with common histological stains. To enable FTU segmentation and annotation in human kidney without the need for histological staining, we detail here the use of widefield autofluorescence (AF) microscopy as a simple, label-free modality that provides detailed renal morphology comparable to periodic acid-Schiff (PAS) stained tissue in both formalin-fixed paraffin-embedded (FFPE) and fresh frozen samples and with no tissue processing beyond sectioning. We demonstrate automated deep learning-based glomerular unit recognition and segmentation on PAS and AF images of the same tissue section from 9 fresh frozen samples and 9 FFPE samples. All training comparisons were carried out using registered AF microscopy and PAS stained whole slide images originating from the same section, and the recognition models were built with the exact same training and test examples. Measures of recognition performance, such as the Dice-Sorensen coefficient, the true positive rate, and the positive predictive value differed less than 2% between standard PAS and AF microscopy for both preservation methods. These results demonstrate that AF is a potentially powerful tool to study human kidney tissue, that it can serve as a label-free source for automated and manual annotation of tissue structures.

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