Effect of bevacizumab and everolimus combination treatment on peritoneal sclerosis in an experimental rat model

被引:1
作者
Mert, Gizem Sultan Acikgoz [1 ]
Ceri, Mevlut [2 ]
Demirkan, Nese Calli [3 ]
Sahin, Barbaros [4 ]
Mert, Mehmet [1 ]
Dursun, Belda [2 ]
机构
[1] Pamukkale Univ, Dept Internal Med, Fac Med, Denizli, Turkey
[2] Pamukkale Univ, Dept Nephrol, Fac Med, Denizli, Turkey
[3] Pamukkale Univ, Dept Pathol, Fac Med, Denizli, Turkey
[4] Pamukkale Univ, Dept Expt Surg Applicat & Res, Fac Med, Denizli, Turkey
关键词
bevacizumab; everolimus; MMP-2; peritoneal dialysis; peritoneal thickness; sclerosis; ENCAPSULATING PERITONITIS; MORPHOLOGIC CHANGES; DIALYSIS; INHIBITORS;
D O I
10.1111/1744-9987.13565
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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-beta 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.
引用
收藏
页码:323 / 330
页数:8
相关论文
共 50 条
  • [41] Effect of everolimus treatment for regrown renal angiomyolipoma associated with tuberous sclerosis complex after transcatheter arterial embolization
    Takashi Hatano
    Taishi Matsu-ura
    Kei-ichiro Mori
    Hiroyuki Inaba
    Katsuhisa Endo
    Mayumi Tamari
    Shin Egawa
    International Journal of Clinical Oncology, 2018, 23 : 1134 - 1139
  • [42] Bevacizumab, a vascular endothelial growth factor inhibitor, promotes orthodontic tooth movement in an experimental rat model
    Abuohashish, Hatem
    Alamri, Abdulaziz
    Shahin, Suliman
    Almazrou, Dalal
    Alkhamis, Taleb
    Omar, Omar
    HELIYON, 2023, 9 (05)
  • [43] Comparison of the inhibitory effect of different doses of subconjunctival bevacizumab application in an experimental model of corneal neovascularization
    Ulas, Burak
    Altan-Yaycioglu, Rana
    Bal, Nebil
    INTERNATIONAL JOURNAL OF OPHTHALMOLOGY, 2018, 11 (07) : 1090 - 1095
  • [44] EFFECT OF NATALIZUMAB TREATMENT ON METALLOPROTEINASES AND THEIR INHIBITORS IN A MOUSE MODEL OF MULTIPLE SCLEROSIS
    Pyka-Fosciak, G.
    Lis, G. J.
    Litwin, J. A.
    JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2020, 71 (02): : 265 - 273
  • [45] Combination therapy of oncolytic herpes simplex virus HF10 and bevacizumab against experimental model of human breast carcinoma xenograft
    Tan, Gewen
    Kasuya, Hideki
    Sahin, Tevfik Tolga
    Yamamura, Kazuo
    Wu, Zhiwen
    Koide, Yusuke
    Hotta, Yoshihiro
    Shikano, Toshio
    Yamada, Suguru
    Kanzaki, Akiyuki
    Fujii, Tsutomu
    Sugimoto, Hiroyuki
    Nomoto, Shuji
    Nishikawa, Yoko
    Tanaka, Maki
    Tsurumaru, Naoko
    Kuwahara, Toshie
    Fukuda, Saori
    Ichinose, Toru
    Kikumori, Toyone
    Takeda, Shin
    Nakao, Akimasa
    Kodera, Yasuhiro
    INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (07) : 1718 - 1730
  • [46] Donor pre-treatment with everolimus or cyclosporine does not reduce ischaemia-reperfusion injury in a rat kidney transplant model
    Martinez-Palli, Graciela
    Hirose, Ryutaro
    Liu, Tao
    Xu, Fengyun
    Dang, Kim
    Feiner, John
    Serkova, Natalie J.
    Niemann, Claus U.
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2011, 26 (06) : 1813 - 1820
  • [47] Anti-PD-L1 treatment enhances antitumor effect of everolimus in a mouse model of renal cell carcinoma
    Hirayama, Yukiyoshi
    Gi, Min
    Yamano, Shotaro
    Tachibana, Hirokazu
    Okuno, Takahiro
    Tamada, Satoshi
    Nakatani, Tatsuya
    Wanibuchi, Hideki
    CANCER SCIENCE, 2016, 107 (12): : 1736 - 1744
  • [48] Comparison of the effect of intravitreal bevacizumab and intravitreal fasudil on retinal VEGF, TNFα, and caspase 3 levels in an experimental diabetes model
    Celik, Fatih
    Ulas, Fatih
    Ozunal, Zeynep Gunes
    Firat, Tulin
    Celebi, Serdal
    Dogan, Umit
    INTERNATIONAL JOURNAL OF OPHTHALMOLOGY, 2014, 7 (01) : 57 - 61
  • [49] Comparison of the effect of intravitreal bevacizumab and intravitreal fasudil on retinal VEGF,TNFα,and caspase 3 levels in an experimental diabetes model
    Fatih elik
    Fatih Ulas
    Zeynep Günes zünal
    Tülin F|rat
    Serdal elebi
    mit Dogan
    International Journal of Ophthalmology, 2014, (01) : 57 - 61
  • [50] Adoptive transfer of DMSO-induced regulatory T cells exhibits a similar preventive effect compared to an in vivo DMSO treatment for chemical-induced experimental encapsulating peritoneal sclerosis in mice
    Lin, Gu-Jiun
    Wu, Chih-Hsiung
    Yu, Chiao-Chi
    Lin, Jeng-Rong
    Liu, Xiao-Dong
    Chen, Yuan-Wu
    Chang, Hao-Ming
    Hong, Zhi-Jie
    Cheng, Chia-Pi
    Sytwu, Huey-Kang
    Huang, Shing-Hwa
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2019, 378