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https://hdl.handle.net/11499/5317
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bolaman, Z. | - |
dc.contributor.author | Akalin, N. | - |
dc.contributor.author | Koseoglu, M.H. | - |
dc.contributor.author | Demir, S. | - |
dc.contributor.author | Kadikoylu, G. | - |
dc.contributor.author | Atalay, H. | - |
dc.contributor.author | Aslan, D. | - |
dc.date.accessioned | 2019-08-16T11:44:39Z | - |
dc.date.available | 2019-08-16T11:44:39Z | - |
dc.date.issued | 2003 | - |
dc.identifier.issn | 1108-2682 | - |
dc.identifier.uri | https://hdl.handle.net/11499/5317 | - |
dc.description.abstract | To investigate the effect of amifostine (AMI, WR-2721) against lipid peroxidation caused by adriamycin in rat heart tissue, male Wistar rats, weighing 190-220 g, were divided into three groups and treated as follows: 1) vehicle (saline) control (n = 6); 2) Adriamycin (10 mg/kg, intraperitoneally) (n = 6); 3) Adriamycin plus amifostine (200 mg/kg) (n = 6). Amifostine was applicated to rats 30 minutes previously from Adriamycin application. Rats were sacrificed on third day after drug application and hearts were removed. The hearts were washed with cold saline solution and were stored at -20°C until analysed. The tissues were thawed and homogenised with an Ultra Turrax. Lipid peroxidation was assayed as the malondialdehyde (MDA) levels reacting with thiobarbituric acid, according to the method of Ohkawa. Tissue MDA levels were significantly increased by adriamycin (p<0.05). MDA levels were 168±15 nmol/g wt in the control group. Adriamycin increased the MDA levels to 212±34 nmol/g wt. In the adriamycin plus AMI group, the heart tissue MDA levels were not different from the control levels (156±31 nmol/g wt). This study showed that the MDA levels were not increased if AMI were given previously Adriamycin in rats. AMI can reduce adriamycin induced cardiotoxicity and may be protective for adriamycin induced free radical damage in the heart tissues. So we suggest that the protective effect of AMI pretreatment on ADR heart toxicity should be evaluated extensively. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | HAEMA | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Adriamycine | en_US |
dc.subject | Amifostine | en_US |
dc.subject | Cardiotoxicity | en_US |
dc.subject | Lipidperoxidation | en_US |
dc.subject | amifostine | en_US |
dc.subject | doxorubicin | en_US |
dc.subject | free radical | en_US |
dc.subject | malonaldehyde | en_US |
dc.subject | thiobarbituric acid | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal tissue | en_US |
dc.subject | article | en_US |
dc.subject | cardiotoxicity | en_US |
dc.subject | controlled study | en_US |
dc.subject | drug effect | en_US |
dc.subject | drug mechanism | en_US |
dc.subject | enzyme activity | en_US |
dc.subject | heart protection | en_US |
dc.subject | histopathology | en_US |
dc.subject | lipid peroxidation | en_US |
dc.subject | male | en_US |
dc.subject | nonhuman | en_US |
dc.subject | rat | en_US |
dc.title | Effect of amifostine pre-treatment against adriamycin-induced lipid peroxidation in rat heart | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 6 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 61 | |
dc.identifier.startpage | 61 | en_US |
dc.identifier.endpage | 64 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopus | 2-s2.0-0037835972 | en_US |
dc.identifier.scopusquality | - | - |
dc.owner | Pamukkale_University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
Appears in Collections: | Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu |
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