Cargando…

Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites

PURPOSE: Calcium oxalate urolithiasis is one of the most common urinary tract diseases and is of high prevalence. The present study proposes to evaluate the antilithiatic property of hydrogen sulfide and its metabolites like thiosulfate & sulfate in an in vitro model. MATERIALS AND METHODS: The...

Descripción completa

Detalles Bibliográficos
Autores principales: Vaitheeswari, S., Sriram, R., Brindha, P., Kurian, Gino A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Urologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752143/
https://www.ncbi.nlm.nih.gov/pubmed/26200543
http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0193
_version_ 1782415682822995968
author Vaitheeswari, S.
Sriram, R.
Brindha, P.
Kurian, Gino A.
author_facet Vaitheeswari, S.
Sriram, R.
Brindha, P.
Kurian, Gino A.
author_sort Vaitheeswari, S.
collection PubMed
description PURPOSE: Calcium oxalate urolithiasis is one of the most common urinary tract diseases and is of high prevalence. The present study proposes to evaluate the antilithiatic property of hydrogen sulfide and its metabolites like thiosulfate & sulfate in an in vitro model. MATERIALS AND METHODS: The antilithiatic activity of sodium hydrogen sulfide (NaSH), sodium thiosulfate (Na(2)S(2)O(3)) and sodium sulfate (Na(2)SO(4)) on the kinetics of calcium oxalate crystal formation was investigated both in physiological buffer and in urine from normal and recurrent stone forming volunteers. The stones were characterized by optical and spectroscopic techniques. RESULTS: The stones were characterized to be monoclinic, prismatic and bipyramidal habit which is of calcium monohydrate and dihydrate nature. The FTIR displayed fingerprint corresponding to calcium oxalate in the control while in NaSH treated, S=O vibrations were visible in the spectrum. The order of percentage inhibition was NaSH>Na(2)S(2)O(3)>Na(2)SO(4). CONCLUSION: Our study indicates that sodium hydrogen sulfide and its metabolite thiosulfate are inhibitors of calcium oxalate stone agglomeration which makes them unstable both in physiological buffer and in urine. This effect is attributed to pH changes and complexing of calcium by S(2)O(3) (2)-and SO(4) (2)- moiety produced by the test compounds.
format Online
Article
Text
id pubmed-4752143
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Sociedade Brasileira de Urologia
record_format MEDLINE/PubMed
spelling pubmed-47521432016-05-09 Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites Vaitheeswari, S. Sriram, R. Brindha, P. Kurian, Gino A. Int Braz J Urol Original Article PURPOSE: Calcium oxalate urolithiasis is one of the most common urinary tract diseases and is of high prevalence. The present study proposes to evaluate the antilithiatic property of hydrogen sulfide and its metabolites like thiosulfate & sulfate in an in vitro model. MATERIALS AND METHODS: The antilithiatic activity of sodium hydrogen sulfide (NaSH), sodium thiosulfate (Na(2)S(2)O(3)) and sodium sulfate (Na(2)SO(4)) on the kinetics of calcium oxalate crystal formation was investigated both in physiological buffer and in urine from normal and recurrent stone forming volunteers. The stones were characterized by optical and spectroscopic techniques. RESULTS: The stones were characterized to be monoclinic, prismatic and bipyramidal habit which is of calcium monohydrate and dihydrate nature. The FTIR displayed fingerprint corresponding to calcium oxalate in the control while in NaSH treated, S=O vibrations were visible in the spectrum. The order of percentage inhibition was NaSH>Na(2)S(2)O(3)>Na(2)SO(4). CONCLUSION: Our study indicates that sodium hydrogen sulfide and its metabolite thiosulfate are inhibitors of calcium oxalate stone agglomeration which makes them unstable both in physiological buffer and in urine. This effect is attributed to pH changes and complexing of calcium by S(2)O(3) (2)-and SO(4) (2)- moiety produced by the test compounds. Sociedade Brasileira de Urologia 2015-05-01 /pmc/articles/PMC4752143/ /pubmed/26200543 http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0193 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Vaitheeswari, S.
Sriram, R.
Brindha, P.
Kurian, Gino A.
Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
title Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
title_full Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
title_fullStr Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
title_full_unstemmed Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
title_short Studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
title_sort studying inhibition of calcium oxalate stone formation: an in vitro approach for screening hydrogen sulfide and its metabolites
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752143/
https://www.ncbi.nlm.nih.gov/pubmed/26200543
http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0193
work_keys_str_mv AT vaitheeswaris studyinginhibitionofcalciumoxalatestoneformationaninvitroapproachforscreeninghydrogensulfideanditsmetabolites
AT sriramr studyinginhibitionofcalciumoxalatestoneformationaninvitroapproachforscreeninghydrogensulfideanditsmetabolites
AT brindhap studyinginhibitionofcalciumoxalatestoneformationaninvitroapproachforscreeninghydrogensulfideanditsmetabolites
AT kurianginoa studyinginhibitionofcalciumoxalatestoneformationaninvitroapproachforscreeninghydrogensulfideanditsmetabolites