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The Role of Magnesium Supplementation in Cisplatin-induced Nephrotoxicity in a Rat Model: No Nephroprotectant Effect
Cisplatin (CP) is used as the commonest drug to treat solid tumors. It is accompanied by a nephrotoxicity side effect. The main objective of this study is to investigate the protective role of magnesium (Mg) supplementation in CP-induced nephrotoxicity in a rat model. Twenty-nine Wistar rats were ra...
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Published in: | International journal of preventive medicine 2012-09, Vol.3 (9), p.637-643 |
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description | Cisplatin (CP) is used as the commonest drug to treat solid tumors. It is accompanied by a nephrotoxicity side effect. The main objective of this study is to investigate the protective role of magnesium (Mg) supplementation in CP-induced nephrotoxicity in a rat model.
Twenty-nine Wistar rats were randomly assigned to four groups (1-4). Groups 1-3 received 20, 80, and 200 mg/kg magnesium sulfate respectively, for 10 days, but on day 3, a single dose of CP (7 mg/kg, i.p.) was also injected. Group 4 (positive control group) received the same regimen of Groups 1-3 except saline instead magnesium sulfate. One week after CP administration, blood samples were obtained and all animals were killed for kidney histopathological investigations.
All CP-treated animals lost weight, and the percentage of weight loss in Group 1 (low dose Mg sulfate treated) was significantly higher compared with the positive control group (Group 4, P < 0.05). The increase in blood urea nitrogen (BUN) and creatinine (Cr) levels in serum in Group 1 were more than those in other groups (P < 0.05). No statistical differences were observed in serum magnesium, nitrite, and total protein levels among the groups. The kidney tissue damage in Groups 1-3 was not significantly different when compared with Group 4. Moreover, the kidney and testis weights in Group 1 were significantly greater than those in the positive control group (P < 0.05).
Regarding the BUN and Cr levels in the serum, kidneys weight, and the histopathological study, the low dose of Mg supplementation intensifies kidney toxicity and renal dysfunction in CP-induced nephrotoxicity in the rat model. However, the protective role of Mg with moderate and high doses is not certain. |
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Twenty-nine Wistar rats were randomly assigned to four groups (1-4). Groups 1-3 received 20, 80, and 200 mg/kg magnesium sulfate respectively, for 10 days, but on day 3, a single dose of CP (7 mg/kg, i.p.) was also injected. Group 4 (positive control group) received the same regimen of Groups 1-3 except saline instead magnesium sulfate. One week after CP administration, blood samples were obtained and all animals were killed for kidney histopathological investigations.
All CP-treated animals lost weight, and the percentage of weight loss in Group 1 (low dose Mg sulfate treated) was significantly higher compared with the positive control group (Group 4, P < 0.05). The increase in blood urea nitrogen (BUN) and creatinine (Cr) levels in serum in Group 1 were more than those in other groups (P < 0.05). No statistical differences were observed in serum magnesium, nitrite, and total protein levels among the groups. The kidney tissue damage in Groups 1-3 was not significantly different when compared with Group 4. Moreover, the kidney and testis weights in Group 1 were significantly greater than those in the positive control group (P < 0.05).
Regarding the BUN and Cr levels in the serum, kidneys weight, and the histopathological study, the low dose of Mg supplementation intensifies kidney toxicity and renal dysfunction in CP-induced nephrotoxicity in the rat model. However, the protective role of Mg with moderate and high doses is not certain.</description><identifier>ISSN: 2008-7802</identifier><identifier>EISSN: 2008-8213</identifier><identifier>PMID: 23024853</identifier><language>eng</language><publisher>Iran: Medknow Publications & Media Pvt. Ltd</publisher><subject>Cancer ; Chemotherapy ; Cisplatin ; Dietary supplements ; Magnesium ; nephrotoxicity ; Original ; rat ; Rodents ; Toxicity</subject><ispartof>International journal of preventive medicine, 2012-09, Vol.3 (9), p.637-643</ispartof><rights>Copyright International Journal of Preventive Medicine (IJPM) Sep 2012</rights><rights>Copyright: © International Journal of Preventive Medicine 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445280/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1287517446?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,37012,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23024853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ashrafi, Farzaneh</creatorcontrib><creatorcontrib>Haghshenas, Sara</creatorcontrib><creatorcontrib>Nematbakhsh, Mehdi</creatorcontrib><creatorcontrib>Nasri, Hamid</creatorcontrib><creatorcontrib>Talebi, Ardeshir</creatorcontrib><creatorcontrib>Eshraghi-Jazi, Fatemeh</creatorcontrib><creatorcontrib>Pezeshki, Zahra</creatorcontrib><creatorcontrib>Safari, Tahereh</creatorcontrib><title>The Role of Magnesium Supplementation in Cisplatin-induced Nephrotoxicity in a Rat Model: No Nephroprotectant Effect</title><title>International journal of preventive medicine</title><addtitle>Int J Prev Med</addtitle><description>Cisplatin (CP) is used as the commonest drug to treat solid tumors. It is accompanied by a nephrotoxicity side effect. The main objective of this study is to investigate the protective role of magnesium (Mg) supplementation in CP-induced nephrotoxicity in a rat model.
Twenty-nine Wistar rats were randomly assigned to four groups (1-4). Groups 1-3 received 20, 80, and 200 mg/kg magnesium sulfate respectively, for 10 days, but on day 3, a single dose of CP (7 mg/kg, i.p.) was also injected. Group 4 (positive control group) received the same regimen of Groups 1-3 except saline instead magnesium sulfate. One week after CP administration, blood samples were obtained and all animals were killed for kidney histopathological investigations.
All CP-treated animals lost weight, and the percentage of weight loss in Group 1 (low dose Mg sulfate treated) was significantly higher compared with the positive control group (Group 4, P < 0.05). The increase in blood urea nitrogen (BUN) and creatinine (Cr) levels in serum in Group 1 were more than those in other groups (P < 0.05). No statistical differences were observed in serum magnesium, nitrite, and total protein levels among the groups. The kidney tissue damage in Groups 1-3 was not significantly different when compared with Group 4. Moreover, the kidney and testis weights in Group 1 were significantly greater than those in the positive control group (P < 0.05).
Regarding the BUN and Cr levels in the serum, kidneys weight, and the histopathological study, the low dose of Mg supplementation intensifies kidney toxicity and renal dysfunction in CP-induced nephrotoxicity in the rat model. However, the protective role of Mg with moderate and high doses is not certain.</description><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Dietary supplements</subject><subject>Magnesium</subject><subject>nephrotoxicity</subject><subject>Original</subject><subject>rat</subject><subject>Rodents</subject><subject>Toxicity</subject><issn>2008-7802</issn><issn>2008-8213</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVkVtLHTEQx5fSUsX6FUrA54XcdjfxQSgH2wpeQO1zmE0m5-SwJ1l3s0W_faOeis7L3P78hpn5VB1ySlWtOBOf93GnKD-ojud5S4sJ3ba8-VodcEG5VI04rPL9BsltGpAkT65gHXEOy47cLeM44A5jhhxSJCGSVZjHoWSxDtEtFh25xnEzpZwegw356VkD5BYyuUoOh1NynfaKsYjQZoiZnHtfom_VFw_DjMd7f1T9-Xl-v_pdX978ulj9uKydaGmuJXjWCk2VYL32vkX01HVUW-AMuPUehGeaMt070SAK9J3VwJ0SDWubcoWj6uKV6xJszTiFHUxPJkEwL4U0rQ1MOdgBDZcFK1vOneykpQoE7cvQRjuhe6a6wjp7ZY1Lv0Nny2kmGD5AP3Zi2Jh1-muElA1XtABO9oApPSw4Z7NNyxTL_oZx1TWsk7Itqu_vx7zx_39M_ANlPpVU</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Ashrafi, Farzaneh</creator><creator>Haghshenas, Sara</creator><creator>Nematbakhsh, Mehdi</creator><creator>Nasri, Hamid</creator><creator>Talebi, Ardeshir</creator><creator>Eshraghi-Jazi, Fatemeh</creator><creator>Pezeshki, Zahra</creator><creator>Safari, Tahereh</creator><general>Medknow Publications & Media Pvt. 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It is accompanied by a nephrotoxicity side effect. The main objective of this study is to investigate the protective role of magnesium (Mg) supplementation in CP-induced nephrotoxicity in a rat model.
Twenty-nine Wistar rats were randomly assigned to four groups (1-4). Groups 1-3 received 20, 80, and 200 mg/kg magnesium sulfate respectively, for 10 days, but on day 3, a single dose of CP (7 mg/kg, i.p.) was also injected. Group 4 (positive control group) received the same regimen of Groups 1-3 except saline instead magnesium sulfate. One week after CP administration, blood samples were obtained and all animals were killed for kidney histopathological investigations.
All CP-treated animals lost weight, and the percentage of weight loss in Group 1 (low dose Mg sulfate treated) was significantly higher compared with the positive control group (Group 4, P < 0.05). The increase in blood urea nitrogen (BUN) and creatinine (Cr) levels in serum in Group 1 were more than those in other groups (P < 0.05). No statistical differences were observed in serum magnesium, nitrite, and total protein levels among the groups. The kidney tissue damage in Groups 1-3 was not significantly different when compared with Group 4. Moreover, the kidney and testis weights in Group 1 were significantly greater than those in the positive control group (P < 0.05).
Regarding the BUN and Cr levels in the serum, kidneys weight, and the histopathological study, the low dose of Mg supplementation intensifies kidney toxicity and renal dysfunction in CP-induced nephrotoxicity in the rat model. However, the protective role of Mg with moderate and high doses is not certain.</abstract><cop>Iran</cop><pub>Medknow Publications & Media Pvt. Ltd</pub><pmid>23024853</pmid><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cancer Chemotherapy Cisplatin Dietary supplements Magnesium nephrotoxicity Original rat Rodents Toxicity |
title | The Role of Magnesium Supplementation in Cisplatin-induced Nephrotoxicity in a Rat Model: No Nephroprotectant Effect |
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