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https://hdl.handle.net/11499/37284
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DC Field | Value | Language |
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dc.contributor.author | Açıkgöz Mert, Gizem Sultan | - |
dc.contributor.author | Çeri, Mevlüt | - |
dc.contributor.author | Çalli Demirkan, Neşe | - |
dc.contributor.author | Şahin, Barbaros | - |
dc.contributor.author | Mert, Mehmet | - |
dc.contributor.author | Dursun, Belda | - |
dc.date.accessioned | 2021-02-02T09:24:58Z | |
dc.date.available | 2021-02-02T09:24:58Z | |
dc.date.issued | 2020 | - |
dc.identifier.issn | 1744-9979 | - |
dc.identifier.uri | https://hdl.handle.net/11499/37284 | - |
dc.identifier.uri | https://doi.org/10.1111/1744-9987.13565 | - |
dc.description.abstract | The aim of this study was to investigate whether bevacizumab and everolimus combination therapy is superior to bevacizumab treatment alone as a treatment for peritoneal sclerosis. Forty Wistar albino rats were divided into five equal groups. The control group received isotonic saline solution (2 mL/day) intraperitoneal (IP) daily for 3 weeks. The CG group received 2 mL 0.1% chlorhexidine gluconate (CG) and 15% ethanol dissolved in saline IP daily for 3 weeks. Peritoneal tissue samples were taken at the end of 3 weeks. The resting group received CG (weeks 0-3), plus isotonic saline solution (2 mL/day) IP daily and tap water (2 mL/day) via a feeding tube daily (weeks 3-6).The bevacizumab group received CG (weeks 1-3) plus bevacizumab at 2.5 mg/kg/day (2 mL) IP daily and tap water (2 mL/day) via a feeding tube daily (weeks 3-6). The bevacizumab+everolimus group received CG (weeks 1-3) plus bevacizumab at 2.5 mg/kg/day (2 mL) IP daily and everolimus at 0.3 mg/kg/day (2 mL) via a feeding tube daily (weeks 3-6). Peritoneal tissue samples were taken from these three groups at the end of 6 weeks and were examined after staining with hematoxylin-eosin and Masson's trichrome. Inflammation, vasculopathy, fibrosis, and peritoneal thickness were evaluated under light microscopy. The samples were also stained with anti-TGF-ß and anti-MMP-2. Inflammation and vasculopathy scores were significantly decreased in the VEGF-i group compared to the CG group. The addition of everolimus to VEGF-i showed significantly lower inflammation, vasculopathy, fibrosis scores, and an evident decrease in peritoneal thickening (respectively, 2.29 ± 0.76 vs 0.57 ± 0.53, P =.003; 2.71 ± 0.76 vs 1.43 ± 0.53, P =.008; 2.57 ± 0.79 vs 1.57 ± 0.79, P =.04; 247.5 ± 136.1 vs 84.5 ± 48.6, P =.048). MMP-2 levels were lower in the combination group compared to the resting group (2.63 ± 0.74 vs 1.86 ± 0.38, P =.019). The study results demonstrated that bevacizumab and everolimus combination therapy was more effective than bevacizumab therapy alone. © 2020 International Society for Apheresis, Japanese Society for Apheresis, and Japanese Society for Dialysis Therapy | en_US |
dc.language.iso | en | en_US |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.relation.ispartof | Therapeutic Apheresis and Dialysis | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | bevacizumab | en_US |
dc.subject | everolimus | en_US |
dc.subject | MMP-2 | en_US |
dc.subject | peritoneal dialysis | en_US |
dc.subject | peritoneal thickness, sclerosis | en_US |
dc.title | Effect of bevacizumab and everolimus combination treatment on peritoneal sclerosis in an experimental rat model | en_US |
dc.type | Article | en_US |
dc.authorid | 0000-0002-2276-5157 | - |
dc.identifier.doi | 10.1111/1744-9987.13565 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 33439548 | en_US |
dc.identifier.scopus | 2-s2.0-85089494892 | en_US |
dc.identifier.wos | WOS:000560369600001 | en_US |
dc.identifier.scopusquality | Q3 | - |
dc.owner | Pamukkale University | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 01.01. Experimental Surgical Application and Research Center | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | Acıpayam Meslek Yüksekokulu Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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