Alteration in Oxidative/nitrosative imbalance, histochemical expression of osteopontin and antiurolithiatic efficacy of Xanthium strumarium (L.) in ethylene glycol induced urolithiasis

Abstract Xanthium strumarium has traditionally been used in the treatment of urolitiasis especially by the rural people in India, but its antiurolithiatic efficacy was not explored scientifically till now. Therefore, the present study was designed to validate the ethnic practice scientifically, and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biomedicine & pharmacotherapy 2016-12, Vol.84, p.1524-1532
Hauptverfasser: Panigrahi, Padma Nibash, Dey, Sahadeb, Sahoo, Monalisa, Choudhary, Shyam Sundar, Mahajan, Sumit
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1532
container_issue
container_start_page 1524
container_title Biomedicine & pharmacotherapy
container_volume 84
creator Panigrahi, Padma Nibash
Dey, Sahadeb
Sahoo, Monalisa
Choudhary, Shyam Sundar
Mahajan, Sumit
description Abstract Xanthium strumarium has traditionally been used in the treatment of urolitiasis especially by the rural people in India, but its antiurolithiatic efficacy was not explored scientifically till now. Therefore, the present study was designed to validate the ethnic practice scientifically, and explore the possible antiurolithiatic effect to rationalize its medicinal use. Urolitiasis was induced in hyperoxaluric rat model by giving 0.75% ethylene glycol (EG) for 28 days along with 1% ammonium chloride (AC) for first 14 days. Antiurolithiatic effect of aqueous-ethanol extract of Xanthium strumarium bur (xanthium) was evaluated based on urine and serum biochemistry, oxidative/nitrosative stress indices, histopathology, kidney calcium and calcium oxalate content and immunohistochemical expression of matrix glycoprotein, osteopontin (OPN). Administration of EG and AC resulted in hyperoxaluria, crystalluria, hypocalciuria, polyurea, raised serum urea, creatinine, erythrocytic lipid peroxidise and nitric oxide, kidney calcium content as well as crystal deposition in kidney section in lithiatic group rats. However, xanthium treatment significantly restored the impairment in above kidney function test as that of standard treatment, cystone. The up-regulation of OPN was also significantly decreased after xanthium treatment. The present findings demonstrate the curative efficacy of xanthium in ethylene glycol induced urolithiasis, possibly mediated through inhibition of various pathways involved in renal calcium oxalate formation, antioxidant property and down regulation of matrix glycoprotein, OPN. Therefore, future studies may be established to evaluate its efficacy and safety for clinical use.
doi_str_mv 10.1016/j.biopha.2016.11.029
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1843912935</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0753332216316663</els_id><sourcerecordid>1843912935</sourcerecordid><originalsourceid>FETCH-LOGICAL-c417t-4806eee6375aae5f9b035775e91e3259a2f650f6d5fff2877380aabcbac3f1b43</originalsourceid><addsrcrecordid>eNqFUstu1TAQjRCIXgp_gJCXRSKpH7GTbJCqipd0pS4AiZ3lOGPiixNfbKdq_ozPw-GWLtiwsDxjn3PGM8dF8ZLgimAiLg9Vb_1xVBXNWUVIhWn3qNiRjuNSYNw8Lna44axkjNKz4lmMB4wxF6x9WpzRpm0EJXRX_LpyCYJK1s_Izujmzg45uYXL2abg458Y2alXTs0a3qDRxuT1CJPVyiG4OwaIcSN7g3xM4I9-TllIzUNeyS7BO5tGm4U0AmMyTa8b-Fu-He0yoZjCMqmwhRf76vX2Ckjj6mAG9N2t2rt8NCwaBvQgFm18XjwxykV4cb-fF1_fv_ty_bHc33z4dH21L3VNmlTWLRYAIFjDlQJuuh4z3jQcOgKM8k5RIzg2YuDGGNo2DWuxUr3ulWaG9DU7Ly5Ousfgfy4Qk5xs1ODyPMAvUZK2Zh2hHeMZWp-gOk8uBjDyGGxubZUEy80zeZAnz-TmmSREZs8y7dV9haWfYHgg_TUpA96eAJD7vLUQZNQWsh2DDaCTHLz9X4V_BbSz8-bgD1ghHvwS5jxDSWSkEsvP27_Zvg0RjAghGPsNvk_EsA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1843912935</pqid></control><display><type>article</type><title>Alteration in Oxidative/nitrosative imbalance, histochemical expression of osteopontin and antiurolithiatic efficacy of Xanthium strumarium (L.) in ethylene glycol induced urolithiasis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Panigrahi, Padma Nibash ; Dey, Sahadeb ; Sahoo, Monalisa ; Choudhary, Shyam Sundar ; Mahajan, Sumit</creator><creatorcontrib>Panigrahi, Padma Nibash ; Dey, Sahadeb ; Sahoo, Monalisa ; Choudhary, Shyam Sundar ; Mahajan, Sumit</creatorcontrib><description>Abstract Xanthium strumarium has traditionally been used in the treatment of urolitiasis especially by the rural people in India, but its antiurolithiatic efficacy was not explored scientifically till now. Therefore, the present study was designed to validate the ethnic practice scientifically, and explore the possible antiurolithiatic effect to rationalize its medicinal use. Urolitiasis was induced in hyperoxaluric rat model by giving 0.75% ethylene glycol (EG) for 28 days along with 1% ammonium chloride (AC) for first 14 days. Antiurolithiatic effect of aqueous-ethanol extract of Xanthium strumarium bur (xanthium) was evaluated based on urine and serum biochemistry, oxidative/nitrosative stress indices, histopathology, kidney calcium and calcium oxalate content and immunohistochemical expression of matrix glycoprotein, osteopontin (OPN). Administration of EG and AC resulted in hyperoxaluria, crystalluria, hypocalciuria, polyurea, raised serum urea, creatinine, erythrocytic lipid peroxidise and nitric oxide, kidney calcium content as well as crystal deposition in kidney section in lithiatic group rats. However, xanthium treatment significantly restored the impairment in above kidney function test as that of standard treatment, cystone. The up-regulation of OPN was also significantly decreased after xanthium treatment. The present findings demonstrate the curative efficacy of xanthium in ethylene glycol induced urolithiasis, possibly mediated through inhibition of various pathways involved in renal calcium oxalate formation, antioxidant property and down regulation of matrix glycoprotein, OPN. Therefore, future studies may be established to evaluate its efficacy and safety for clinical use.</description><identifier>ISSN: 0753-3322</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2016.11.029</identifier><identifier>PMID: 27876212</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; Ethylene Glycol - toxicity ; Immunohistochemistry ; Internal Medicine ; Male ; Medical Education ; Nitrosation - drug effects ; Nitrosation - physiology ; Osteopontin ; Osteopontin - biosynthesis ; Osteopontin - chemistry ; Oxidative Stress - drug effects ; Oxidative Stress - physiology ; Oxidative/Nitrosative stress ; Plant Extracts - isolation &amp; purification ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Rat ; Rats ; Rats, Wistar ; Urolithiasis ; Urolithiasis - chemically induced ; Urolithiasis - drug therapy ; Urolithiasis - metabolism ; Xanthium ; Xanthium strumarium</subject><ispartof>Biomedicine &amp; pharmacotherapy, 2016-12, Vol.84, p.1524-1532</ispartof><rights>Elsevier Masson SAS</rights><rights>2016 Elsevier Masson SAS</rights><rights>Copyright © 2016 Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-4806eee6375aae5f9b035775e91e3259a2f650f6d5fff2877380aabcbac3f1b43</citedby><cites>FETCH-LOGICAL-c417t-4806eee6375aae5f9b035775e91e3259a2f650f6d5fff2877380aabcbac3f1b43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0753332216316663$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27876212$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Panigrahi, Padma Nibash</creatorcontrib><creatorcontrib>Dey, Sahadeb</creatorcontrib><creatorcontrib>Sahoo, Monalisa</creatorcontrib><creatorcontrib>Choudhary, Shyam Sundar</creatorcontrib><creatorcontrib>Mahajan, Sumit</creatorcontrib><title>Alteration in Oxidative/nitrosative imbalance, histochemical expression of osteopontin and antiurolithiatic efficacy of Xanthium strumarium (L.) in ethylene glycol induced urolithiasis</title><title>Biomedicine &amp; pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>Abstract Xanthium strumarium has traditionally been used in the treatment of urolitiasis especially by the rural people in India, but its antiurolithiatic efficacy was not explored scientifically till now. Therefore, the present study was designed to validate the ethnic practice scientifically, and explore the possible antiurolithiatic effect to rationalize its medicinal use. Urolitiasis was induced in hyperoxaluric rat model by giving 0.75% ethylene glycol (EG) for 28 days along with 1% ammonium chloride (AC) for first 14 days. Antiurolithiatic effect of aqueous-ethanol extract of Xanthium strumarium bur (xanthium) was evaluated based on urine and serum biochemistry, oxidative/nitrosative stress indices, histopathology, kidney calcium and calcium oxalate content and immunohistochemical expression of matrix glycoprotein, osteopontin (OPN). Administration of EG and AC resulted in hyperoxaluria, crystalluria, hypocalciuria, polyurea, raised serum urea, creatinine, erythrocytic lipid peroxidise and nitric oxide, kidney calcium content as well as crystal deposition in kidney section in lithiatic group rats. However, xanthium treatment significantly restored the impairment in above kidney function test as that of standard treatment, cystone. The up-regulation of OPN was also significantly decreased after xanthium treatment. The present findings demonstrate the curative efficacy of xanthium in ethylene glycol induced urolithiasis, possibly mediated through inhibition of various pathways involved in renal calcium oxalate formation, antioxidant property and down regulation of matrix glycoprotein, OPN. Therefore, future studies may be established to evaluate its efficacy and safety for clinical use.</description><subject>Animals</subject><subject>Ethylene Glycol - toxicity</subject><subject>Immunohistochemistry</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medical Education</subject><subject>Nitrosation - drug effects</subject><subject>Nitrosation - physiology</subject><subject>Osteopontin</subject><subject>Osteopontin - biosynthesis</subject><subject>Osteopontin - chemistry</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - physiology</subject><subject>Oxidative/Nitrosative stress</subject><subject>Plant Extracts - isolation &amp; purification</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Urolithiasis</subject><subject>Urolithiasis - chemically induced</subject><subject>Urolithiasis - drug therapy</subject><subject>Urolithiasis - metabolism</subject><subject>Xanthium</subject><subject>Xanthium strumarium</subject><issn>0753-3322</issn><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUstu1TAQjRCIXgp_gJCXRSKpH7GTbJCqipd0pS4AiZ3lOGPiixNfbKdq_ozPw-GWLtiwsDxjn3PGM8dF8ZLgimAiLg9Vb_1xVBXNWUVIhWn3qNiRjuNSYNw8Lna44axkjNKz4lmMB4wxF6x9WpzRpm0EJXRX_LpyCYJK1s_Izujmzg45uYXL2abg458Y2alXTs0a3qDRxuT1CJPVyiG4OwaIcSN7g3xM4I9-TllIzUNeyS7BO5tGm4U0AmMyTa8b-Fu-He0yoZjCMqmwhRf76vX2Ckjj6mAG9N2t2rt8NCwaBvQgFm18XjwxykV4cb-fF1_fv_ty_bHc33z4dH21L3VNmlTWLRYAIFjDlQJuuh4z3jQcOgKM8k5RIzg2YuDGGNo2DWuxUr3ulWaG9DU7Ly5Ousfgfy4Qk5xs1ODyPMAvUZK2Zh2hHeMZWp-gOk8uBjDyGGxubZUEy80zeZAnz-TmmSREZs8y7dV9haWfYHgg_TUpA96eAJD7vLUQZNQWsh2DDaCTHLz9X4V_BbSz8-bgD1ghHvwS5jxDSWSkEsvP27_Zvg0RjAghGPsNvk_EsA</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Panigrahi, Padma Nibash</creator><creator>Dey, Sahadeb</creator><creator>Sahoo, Monalisa</creator><creator>Choudhary, Shyam Sundar</creator><creator>Mahajan, Sumit</creator><general>Elsevier Masson SAS</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20161201</creationdate><title>Alteration in Oxidative/nitrosative imbalance, histochemical expression of osteopontin and antiurolithiatic efficacy of Xanthium strumarium (L.) in ethylene glycol induced urolithiasis</title><author>Panigrahi, Padma Nibash ; Dey, Sahadeb ; Sahoo, Monalisa ; Choudhary, Shyam Sundar ; Mahajan, Sumit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-4806eee6375aae5f9b035775e91e3259a2f650f6d5fff2877380aabcbac3f1b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Ethylene Glycol - toxicity</topic><topic>Immunohistochemistry</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medical Education</topic><topic>Nitrosation - drug effects</topic><topic>Nitrosation - physiology</topic><topic>Osteopontin</topic><topic>Osteopontin - biosynthesis</topic><topic>Osteopontin - chemistry</topic><topic>Oxidative Stress - drug effects</topic><topic>Oxidative Stress - physiology</topic><topic>Oxidative/Nitrosative stress</topic><topic>Plant Extracts - isolation &amp; purification</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Urolithiasis</topic><topic>Urolithiasis - chemically induced</topic><topic>Urolithiasis - drug therapy</topic><topic>Urolithiasis - metabolism</topic><topic>Xanthium</topic><topic>Xanthium strumarium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panigrahi, Padma Nibash</creatorcontrib><creatorcontrib>Dey, Sahadeb</creatorcontrib><creatorcontrib>Sahoo, Monalisa</creatorcontrib><creatorcontrib>Choudhary, Shyam Sundar</creatorcontrib><creatorcontrib>Mahajan, Sumit</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedicine &amp; pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panigrahi, Padma Nibash</au><au>Dey, Sahadeb</au><au>Sahoo, Monalisa</au><au>Choudhary, Shyam Sundar</au><au>Mahajan, Sumit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alteration in Oxidative/nitrosative imbalance, histochemical expression of osteopontin and antiurolithiatic efficacy of Xanthium strumarium (L.) in ethylene glycol induced urolithiasis</atitle><jtitle>Biomedicine &amp; pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>84</volume><spage>1524</spage><epage>1532</epage><pages>1524-1532</pages><issn>0753-3322</issn><eissn>1950-6007</eissn><abstract>Abstract Xanthium strumarium has traditionally been used in the treatment of urolitiasis especially by the rural people in India, but its antiurolithiatic efficacy was not explored scientifically till now. Therefore, the present study was designed to validate the ethnic practice scientifically, and explore the possible antiurolithiatic effect to rationalize its medicinal use. Urolitiasis was induced in hyperoxaluric rat model by giving 0.75% ethylene glycol (EG) for 28 days along with 1% ammonium chloride (AC) for first 14 days. Antiurolithiatic effect of aqueous-ethanol extract of Xanthium strumarium bur (xanthium) was evaluated based on urine and serum biochemistry, oxidative/nitrosative stress indices, histopathology, kidney calcium and calcium oxalate content and immunohistochemical expression of matrix glycoprotein, osteopontin (OPN). Administration of EG and AC resulted in hyperoxaluria, crystalluria, hypocalciuria, polyurea, raised serum urea, creatinine, erythrocytic lipid peroxidise and nitric oxide, kidney calcium content as well as crystal deposition in kidney section in lithiatic group rats. However, xanthium treatment significantly restored the impairment in above kidney function test as that of standard treatment, cystone. The up-regulation of OPN was also significantly decreased after xanthium treatment. The present findings demonstrate the curative efficacy of xanthium in ethylene glycol induced urolithiasis, possibly mediated through inhibition of various pathways involved in renal calcium oxalate formation, antioxidant property and down regulation of matrix glycoprotein, OPN. Therefore, future studies may be established to evaluate its efficacy and safety for clinical use.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>27876212</pmid><doi>10.1016/j.biopha.2016.11.029</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0753-3322
ispartof Biomedicine & pharmacotherapy, 2016-12, Vol.84, p.1524-1532
issn 0753-3322
1950-6007
language eng
recordid cdi_proquest_miscellaneous_1843912935
source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Ethylene Glycol - toxicity
Immunohistochemistry
Internal Medicine
Male
Medical Education
Nitrosation - drug effects
Nitrosation - physiology
Osteopontin
Osteopontin - biosynthesis
Osteopontin - chemistry
Oxidative Stress - drug effects
Oxidative Stress - physiology
Oxidative/Nitrosative stress
Plant Extracts - isolation & purification
Plant Extracts - pharmacology
Plant Extracts - therapeutic use
Rat
Rats
Rats, Wistar
Urolithiasis
Urolithiasis - chemically induced
Urolithiasis - drug therapy
Urolithiasis - metabolism
Xanthium
Xanthium strumarium
title Alteration in Oxidative/nitrosative imbalance, histochemical expression of osteopontin and antiurolithiatic efficacy of Xanthium strumarium (L.) in ethylene glycol induced urolithiasis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T22%3A42%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Alteration%20in%20Oxidative/nitrosative%20imbalance,%20histochemical%20expression%20of%20osteopontin%20and%20antiurolithiatic%20efficacy%20of%20Xanthium%20strumarium%20(L.)%20in%20ethylene%20glycol%20induced%20urolithiasis&rft.jtitle=Biomedicine%20&%20pharmacotherapy&rft.au=Panigrahi,%20Padma%20Nibash&rft.date=2016-12-01&rft.volume=84&rft.spage=1524&rft.epage=1532&rft.pages=1524-1532&rft.issn=0753-3322&rft.eissn=1950-6007&rft_id=info:doi/10.1016/j.biopha.2016.11.029&rft_dat=%3Cproquest_cross%3E1843912935%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1843912935&rft_id=info:pmid/27876212&rft_els_id=S0753332216316663&rfr_iscdi=true