Effects of Vitamin D On Cisplatin Induced Heart and Lung Toxicity in Albino Rat
Background: While Cisplatin (CP) is a powerful DNA alkylating agent used to treat many malignancies, its clinical use is linked to a number of negative side effects. It has been proposed that vitamin D can shield biological systems against harm caused by CP. The current study's objective was to...
Gespeichert in:
Veröffentlicht in: | International journal of anatomy and research 2022-12, Vol.10 (4), p.8512-8522 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 8522 |
---|---|
container_issue | 4 |
container_start_page | 8512 |
container_title | International journal of anatomy and research |
container_volume | 10 |
creator | Hussein Omar, Sally Mahmoud Mohamed El Aziz Ahmed, Marwa Mohamed Abd Mohamed Khalil, Ola Abd El-Samie Mahmoud Mady, Marwa |
description | Background: While Cisplatin (CP) is a powerful DNA alkylating agent used to treat many malignancies, its clinical use is linked to a number of negative side effects. It has been proposed that vitamin D can shield biological systems against harm caused by CP. The current study's objective was to look into how vitamin D protects the rat heart and lung against cisplatin-induced damage. Material and methods: Thirty adult male Albino rats; 180–220 g body weight were allocated into 3 groups; Group I (n=10) receiving saline, Group II (n=10); rats receiving CP (single dose of 6.5 mg/kg intraperitoneal) and Group III (n=10); receiving CP and 50 ng/kg/day alfacalcidol. Results: Alterations included a significant increase in malondialdehyde (MDA) level in the CP group compared with the other groups (p value for comparing between control and each other group, statistically significant at p ≤ 0.05). Histopathologically, CP induced severe changes were observed. However, the CP-induced disturbances significantly improved by treatment with Vitamin D. Conclusion: According to this study, CP treatment significantly harmed rats' hearts and lungs; however, treatment with vitamin D significantly lessened these harms. Keywords: Cisplatin, Immunohistochemical, Vitamin D, Malondialdehyde, Oxidative stress. |
doi_str_mv | 10.16965/ijar.2022.252 |
format | Article |
fullrecord | <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_16965_ijar_2022_252</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_16965_ijar_2022_252</sourcerecordid><originalsourceid>FETCH-LOGICAL-c792-dc3e421fc34534c55dac2b87abf1ad88d892b4d30c63fb26d83b972fc2ffb2753</originalsourceid><addsrcrecordid>eNotkMtqwzAUREVpoSHNtmv9gF3pSrLlZUjTJmAwBNOt0MMqCo4cLAeav6_TZjVzYJjFQeiVkpwWVSHewlGPORCAHAQ8oAUwoBkHWT7eu6yK8hmtUjoSQijjHIRYoGbrfWenhAePv8KkTyHid9xEvAnp3Otpxn10F9s5vOv0OGEdHa4v8Ru3w0-wYbriebLuTYgDPujpBT153adudc8laj-27WaX1c3nfrOuM1tWkDnLOg7UW8YF41YIpy0YWWrjqXZSOlmB4Y4RWzBvoHCSmaoEb8HPWAq2RPn_rR2HlMbOq_MYTnq8KkrUnxB1E6JuQtQshP0CavhToQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effects of Vitamin D On Cisplatin Induced Heart and Lung Toxicity in Albino Rat</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>Hussein Omar, Sally Mahmoud Mohamed ; El Aziz Ahmed, Marwa Mohamed Abd ; Mohamed Khalil, Ola Abd El-Samie ; Mahmoud Mady, Marwa</creator><creatorcontrib>Hussein Omar, Sally Mahmoud Mohamed ; El Aziz Ahmed, Marwa Mohamed Abd ; Mohamed Khalil, Ola Abd El-Samie ; Mahmoud Mady, Marwa ; Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt ; Assistant Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt ; Lecturer, Pathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><description>Background: While Cisplatin (CP) is a powerful DNA alkylating agent used to treat many malignancies, its clinical use is linked to a number of negative side effects. It has been proposed that vitamin D can shield biological systems against harm caused by CP. The current study's objective was to look into how vitamin D protects the rat heart and lung against cisplatin-induced damage. Material and methods: Thirty adult male Albino rats; 180–220 g body weight were allocated into 3 groups; Group I (n=10) receiving saline, Group II (n=10); rats receiving CP (single dose of 6.5 mg/kg intraperitoneal) and Group III (n=10); receiving CP and 50 ng/kg/day alfacalcidol. Results: Alterations included a significant increase in malondialdehyde (MDA) level in the CP group compared with the other groups (p value for comparing between control and each other group, statistically significant at p ≤ 0.05). Histopathologically, CP induced severe changes were observed. However, the CP-induced disturbances significantly improved by treatment with Vitamin D. Conclusion: According to this study, CP treatment significantly harmed rats' hearts and lungs; however, treatment with vitamin D significantly lessened these harms. Keywords: Cisplatin, Immunohistochemical, Vitamin D, Malondialdehyde, Oxidative stress.</description><identifier>ISSN: 2321-8967</identifier><identifier>EISSN: 2321-4287</identifier><identifier>DOI: 10.16965/ijar.2022.252</identifier><language>eng</language><ispartof>International journal of anatomy and research, 2022-12, Vol.10 (4), p.8512-8522</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-0728-5761 ; 0000-0003-2318-7368 ; 0000-0003-4230-7775 ; 0000-0001-6601-4243</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Hussein Omar, Sally Mahmoud Mohamed</creatorcontrib><creatorcontrib>El Aziz Ahmed, Marwa Mohamed Abd</creatorcontrib><creatorcontrib>Mohamed Khalil, Ola Abd El-Samie</creatorcontrib><creatorcontrib>Mahmoud Mady, Marwa</creatorcontrib><creatorcontrib>Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><creatorcontrib>Assistant Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><creatorcontrib>Lecturer, Pathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><title>Effects of Vitamin D On Cisplatin Induced Heart and Lung Toxicity in Albino Rat</title><title>International journal of anatomy and research</title><description>Background: While Cisplatin (CP) is a powerful DNA alkylating agent used to treat many malignancies, its clinical use is linked to a number of negative side effects. It has been proposed that vitamin D can shield biological systems against harm caused by CP. The current study's objective was to look into how vitamin D protects the rat heart and lung against cisplatin-induced damage. Material and methods: Thirty adult male Albino rats; 180–220 g body weight were allocated into 3 groups; Group I (n=10) receiving saline, Group II (n=10); rats receiving CP (single dose of 6.5 mg/kg intraperitoneal) and Group III (n=10); receiving CP and 50 ng/kg/day alfacalcidol. Results: Alterations included a significant increase in malondialdehyde (MDA) level in the CP group compared with the other groups (p value for comparing between control and each other group, statistically significant at p ≤ 0.05). Histopathologically, CP induced severe changes were observed. However, the CP-induced disturbances significantly improved by treatment with Vitamin D. Conclusion: According to this study, CP treatment significantly harmed rats' hearts and lungs; however, treatment with vitamin D significantly lessened these harms. Keywords: Cisplatin, Immunohistochemical, Vitamin D, Malondialdehyde, Oxidative stress.</description><issn>2321-8967</issn><issn>2321-4287</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNotkMtqwzAUREVpoSHNtmv9gF3pSrLlZUjTJmAwBNOt0MMqCo4cLAeav6_TZjVzYJjFQeiVkpwWVSHewlGPORCAHAQ8oAUwoBkHWT7eu6yK8hmtUjoSQijjHIRYoGbrfWenhAePv8KkTyHid9xEvAnp3Otpxn10F9s5vOv0OGEdHa4v8Ru3w0-wYbriebLuTYgDPujpBT153adudc8laj-27WaX1c3nfrOuM1tWkDnLOg7UW8YF41YIpy0YWWrjqXZSOlmB4Y4RWzBvoHCSmaoEb8HPWAq2RPn_rR2HlMbOq_MYTnq8KkrUnxB1E6JuQtQshP0CavhToQ</recordid><startdate>20221205</startdate><enddate>20221205</enddate><creator>Hussein Omar, Sally Mahmoud Mohamed</creator><creator>El Aziz Ahmed, Marwa Mohamed Abd</creator><creator>Mohamed Khalil, Ola Abd El-Samie</creator><creator>Mahmoud Mady, Marwa</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-0728-5761</orcidid><orcidid>https://orcid.org/0000-0003-2318-7368</orcidid><orcidid>https://orcid.org/0000-0003-4230-7775</orcidid><orcidid>https://orcid.org/0000-0001-6601-4243</orcidid></search><sort><creationdate>20221205</creationdate><title>Effects of Vitamin D On Cisplatin Induced Heart and Lung Toxicity in Albino Rat</title><author>Hussein Omar, Sally Mahmoud Mohamed ; El Aziz Ahmed, Marwa Mohamed Abd ; Mohamed Khalil, Ola Abd El-Samie ; Mahmoud Mady, Marwa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c792-dc3e421fc34534c55dac2b87abf1ad88d892b4d30c63fb26d83b972fc2ffb2753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Hussein Omar, Sally Mahmoud Mohamed</creatorcontrib><creatorcontrib>El Aziz Ahmed, Marwa Mohamed Abd</creatorcontrib><creatorcontrib>Mohamed Khalil, Ola Abd El-Samie</creatorcontrib><creatorcontrib>Mahmoud Mady, Marwa</creatorcontrib><creatorcontrib>Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><creatorcontrib>Assistant Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><creatorcontrib>Lecturer, Pathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt</creatorcontrib><collection>CrossRef</collection><jtitle>International journal of anatomy and research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hussein Omar, Sally Mahmoud Mohamed</au><au>El Aziz Ahmed, Marwa Mohamed Abd</au><au>Mohamed Khalil, Ola Abd El-Samie</au><au>Mahmoud Mady, Marwa</au><aucorp>Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</aucorp><aucorp>Assistant Lecturer, Department of Anatomy and Embryology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</aucorp><aucorp>Lecturer, Pathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Vitamin D On Cisplatin Induced Heart and Lung Toxicity in Albino Rat</atitle><jtitle>International journal of anatomy and research</jtitle><date>2022-12-05</date><risdate>2022</risdate><volume>10</volume><issue>4</issue><spage>8512</spage><epage>8522</epage><pages>8512-8522</pages><issn>2321-8967</issn><eissn>2321-4287</eissn><abstract>Background: While Cisplatin (CP) is a powerful DNA alkylating agent used to treat many malignancies, its clinical use is linked to a number of negative side effects. It has been proposed that vitamin D can shield biological systems against harm caused by CP. The current study's objective was to look into how vitamin D protects the rat heart and lung against cisplatin-induced damage. Material and methods: Thirty adult male Albino rats; 180–220 g body weight were allocated into 3 groups; Group I (n=10) receiving saline, Group II (n=10); rats receiving CP (single dose of 6.5 mg/kg intraperitoneal) and Group III (n=10); receiving CP and 50 ng/kg/day alfacalcidol. Results: Alterations included a significant increase in malondialdehyde (MDA) level in the CP group compared with the other groups (p value for comparing between control and each other group, statistically significant at p ≤ 0.05). Histopathologically, CP induced severe changes were observed. However, the CP-induced disturbances significantly improved by treatment with Vitamin D. Conclusion: According to this study, CP treatment significantly harmed rats' hearts and lungs; however, treatment with vitamin D significantly lessened these harms. Keywords: Cisplatin, Immunohistochemical, Vitamin D, Malondialdehyde, Oxidative stress.</abstract><doi>10.16965/ijar.2022.252</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-0728-5761</orcidid><orcidid>https://orcid.org/0000-0003-2318-7368</orcidid><orcidid>https://orcid.org/0000-0003-4230-7775</orcidid><orcidid>https://orcid.org/0000-0001-6601-4243</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2321-8967 |
ispartof | International journal of anatomy and research, 2022-12, Vol.10 (4), p.8512-8522 |
issn | 2321-8967 2321-4287 |
language | eng |
recordid | cdi_crossref_primary_10_16965_ijar_2022_252 |
source | EZB-FREE-00999 freely available EZB journals |
title | Effects of Vitamin D On Cisplatin Induced Heart and Lung Toxicity in Albino Rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T07%3A10%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20Vitamin%20D%20On%20Cisplatin%20Induced%20Heart%20and%20Lung%20Toxicity%20in%20Albino%20Rat&rft.jtitle=International%20journal%20of%20anatomy%20and%20research&rft.au=Hussein%20Omar,%20Sally%20Mahmoud%20Mohamed&rft.aucorp=Lecturer,%20Department%20of%20Anatomy%20and%20Embryology,%20Faculty%20of%20Medicine,%20Alexandria%20University,%20Alexandria,%20Egypt&rft.date=2022-12-05&rft.volume=10&rft.issue=4&rft.spage=8512&rft.epage=8522&rft.pages=8512-8522&rft.issn=2321-8967&rft.eissn=2321-4287&rft_id=info:doi/10.16965/ijar.2022.252&rft_dat=%3Ccrossref%3E10_16965_ijar_2022_252%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |