E184 M2 macrophages phagocytose renal calcium oxalate crystals and suppress crystal formation in a colony-stimulating factor-1-dependent manner

2013 ◽  
Vol 12 (3) ◽  
pp. 94
Author(s):  
K. Taguchi ◽  
A. Okada ◽  
T. Yasui ◽  
Y. Hirose ◽  
K. Niimi ◽  
...  
Author(s):  
Sathish R ◽  
Jeyabalan G

 Objective: The present study was to demonstrate the in vitro anti-lithiatic effect of Ipomoea batatas (Convolvulaceae) leaves and tuberous roots.Methods: The obtained ethanolic extract of I. batatas leaves and tuberous roots (EIBL and EIBR) and aqueous extract of I. batatas leaves and roots (AIBL and AIBR) were used for this in vitro study. The dissolution method of calcium oxalate by titrimetry method and calcium phosphate by colorimetric method was studied. Nucleation and aggregation of calcium oxalate crystals were determined by a spectrophotometric assay.Results: In the estimation of calcium oxalate by titrimetry method, the I. batatas leaves and roots have very significant (p<0.01) capability to dissolve calcium oxalate. Percentage dissolution of calcium oxalate crystals was found to be 37.53%, 22.74%, 39.74%, and 24.28% for EIBL, AIBL, EIBR, and AIBR, respectively. In the estimation of calcium phosphate by colorimetric method, the percentage dissolution of calcium phosphate crystals by EIBL, AIBL, EIBR, and AIBR was found to be 67.15%, 43.17%, 76.74%, and 47.96%, respectively. The I. batatas leaves and roots were significantly (p<0.01) dissolved calcium phosphate also. The results were clearly shown that I. batatas extracts significantly (p<0.01) inhibited both nucleation and aggregation of calcium oxalate crystals by concentration-dependent manner. The maximum percent inhibition of calcium oxalate nucleation by EIBL, AIBL, EIBR, and AIBR was found to be 59.09%, 50.0%, 84.09%, and 47.73%, respectively, at 1000 μg/ml. The EIBL, AIBL, EIBR, and AIBR were inhibited calcium oxalate aggregation by 63.46%, 36.54%, 84.61%, and 42.3%, respectively, at 1000 μg/ml.Conclusions: The results clearly indicate that I. batatas leaves and tuberous roots were found to express in vitro anti-lithiatic potential.


1982 ◽  
Vol 62 (4) ◽  
pp. 421-425 ◽  
Author(s):  
P. C. Hallson ◽  
G. A. Rose ◽  
S. Sulaiman

1. Samples of fresh human urine were treated with immobilized uricase to lower urate concentration. Urate was added to yield low, normal and high urate samples. 2. Each sample was rapidly evaporated at pH 5.3 to standard osmolality and the yield of calcium oxalate crystals measured either by semi-quantitative microscopy or fully quantitative radioisotope techniques. 3. Increase of urinary urate did not increase the calcium oxalate crystals formed and may even have had an opposite effect. 4. Allantoin was without significant effect upon calcium oxalate crystal formation. 5. These data provide no support for the suggestion that reducing urate concentrations in the urine may be of value in treatment of patients with calcium oxalate stones.


Author(s):  
H. J. Arnott ◽  
K. D. Whitney

Calcium oxalate crystals are often found in association with fungal hyphae. In examining leaf litter samples with the use of scanning electron microscopy, Graustein et al. demonstrated that hyphae of some basidiomycetes are often encrusted with conspicuous calcium oxalate deposits and postulated that these crystals were formed when oxalate released by the fungus precipitated with free calcium ions in the environment. Studies by Arnott and Arnott and Webb, however, showed that at least some calcium oxalate crystals produced by these fungi arose within the fungal cell wall. These studies revealed that the crystals were enclosed within a thin layer of wall material during development, and it was hypothesized that the growth of the crystals is under direct control of the fungal cell.


1991 ◽  
Vol 37 (9) ◽  
pp. 1589-1594 ◽  
Author(s):  
I R Doyle ◽  
R L Ryall ◽  
V R Marshall

Abstract The abundance of protein in the matrix of calcium oxalate uroliths has fueled speculation regarding its role in stone genesis. In this study, we wanted to characterize the composition of the proteins associated with early stages of calcium oxalate crystallization in urine. Calcium oxalate crystallization was induced in urine from healthy men and women by the addition of an oxalate load. The crystals were harvested and demineralized, and the proteins remaining were separated and characterized by polyacrylamide gel electrophoresis and Western blotting. Most urinary proteins were not detected in the crystals or were present in only small quantities. The most abundant urinary macromolecule, Tamm-Horsfall glycoprotein, was notably absent from the crystal extracts. The predominant protein associated with the crystals, a previously unknown urinary constituent that we call crystal matrix protein (CMP; molecular mass, 30,000 Da), was more prevalent in the crystals derived from female urine. We conclude that most urinary proteins play no direct role in calcium oxalate crystal formation. However, the protein CMP exhibits a remarkable affinity for calcium oxalate crystals and may be important in stone pathogenesis.


2015 ◽  
Vol 3 (01) ◽  
pp. 77-81
Author(s):  
Asheesh Kumar Gupta ◽  
Preeti Kothiyal

Objectives: The plant Kigelia africana (Lam.) Benth. Family: Bignoniaceae is used in traditional medical practices of Africa and India to treat various diseases including renal disorders. The present study is designed to evaluate the effect of K. africana fruit extract (KAFE) for in-vitro anti-urolithic activity on generated calcium-oxalate crystals. Method: The aqueous and alcoholic (ethanolic) extracts of fruits were tested for anti-urolithiatic potential on generated calcium-oxalate crystals by homogenous precipitation method and simultaneously a supporting two step vice-versa reactions were assessed (New method). The activity was assessed by studying the crystal dissolution by microscopy and quantitative alimental ions analysis for calcium and oxalates. Result: They exhibited significant activity when compared to standard drug Cystone- a poly herbal formulation. The aqueous and alcoholic extracts significantly decreased (p 0.001) crystal size and increased calcium and oxalate concentration in reaction setup of all tested groups as compared to normal control. Simultaneously a supporting two step vice-versa reaction was assessed that have shown significant inhibition of crystal formation. Conclusion: All the interpretations of various result outcomes direct the use of this drug for urolithiasis prophylaxis and treatments.


2021 ◽  
Vol 2021 ◽  
pp. 1-19
Author(s):  
Wei-Bo Huang ◽  
Guo-Jun Zou ◽  
Gu-Hua Tang ◽  
Xin-Yuan Sun ◽  
Jian-Ming Ouyang

The original Laminaria polysaccharide (LP0) was sulfated using the sulfur trioxide-pyridine method, and four sulfated Laminaria polysaccharides (SLPs) were obtained, namely, SLP1, SLP2, SLP3, and SLP4. The sulfated (–OSO3–) contents were 8.58%, 15.1%, 22.8%, and 31.3%, respectively. The structures of the polysaccharides were characterized using a Fourier transform infrared (FT-IR) spectrometer and nuclear magnetic resonance (NMR) techniques. SLPs showed better antioxidant activity than LP0, increased the concentration of soluble Ca2+ in the solution, reduced the amount of CaOx precipitation and degree of CaOx crystal aggregation, induced COD crystal formation, and protected HK-2 cells from damage caused by nanometer calcium oxalate crystals. These effects can inhibit the formation of CaOx kidney stones. The biological activity of the polysaccharides increased with the content of –OSO3−, that is, the biological activities of the polysaccharides had the following order: LP0 < SLP1 < SLP2 < SLP3 < SLP4. These results reveal that SLPs with high –OSO3− contents are potential drugs for effectively inhibiting the formation of CaOx stones.


Author(s):  
H. J. Arnott ◽  
M. A. Webb ◽  
L. E. Lopez

Many papers have been published on the structure of calcium oxalate crystals in plants, however, few deal with the early development of crystals. Large numbers of idioblastic calcium oxalate crystal cells are found in the leaves of Vitis mustangensis, V. labrusca and V. vulpina. A crystal idioblast, or raphide cell, will produce 150-300 needle-like calcium oxalate crystals within a central vacuole. Each raphide crystal is autonomous, having been produced in a separate membrane-defined crystal chamber; the idioblast''s crystal complement is collectively embedded in a water soluble glycoprotein matrix which fills the vacuole. The crystals are twins, each having a pointed and a bidentate end (Fig 1); when mature they are about 0.5-1.2 μn in diameter and 30-70 μm in length. Crystal bundles, i.e., crystals and their matrix, can be isolated from leaves using 100% ETOH. If the bundles are treated with H2O the matrix surrounding the crystals rapidly disperses.


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