Repository logo
Communities & Collections
All of DSpace
  • English
  • العربية
  • বাংলা
  • Català
  • Čeština
  • Deutsch
  • Ελληνικά
  • Español
  • Suomi
  • Français
  • Gàidhlig
  • हिंदी
  • Magyar
  • Italiano
  • Қазақ
  • Latviešu
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Srpski (lat)
  • Српски
  • Svenska
  • Türkçe
  • Yкраї́нська
  • Tiếng Việt
Log In
New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Aydingoz, Selda Emre"

Filter results by typing the first few letters
Now showing 1 - 4 of 4
  • Results Per Page
  • Sort Options
  • No Thumbnail Available
    Item
    Effects of Algan Hemostatic Agent on bleeding time in a rat tail hemorrhage model
    (2020) Totuk, Ozgan Melike Gedar; Guzel, Sevket Ergun; Ekici, Husamettin; Kumandas, Ali; Aydingoz, Selda Emre; Yilmaz, Enis Cagatay; Kirdan, Taylan; Midi, Ahmet; 0000-0001-7823-7620; 33107963; ABA-4291-2020
    BACKGROUND: Algan Hemostatic Agent (AHA) is a multi-herbal extract containing a standardized amount of Achillea millefolium, Juglans regia, Lycopodium clavatum, Rubus caesius or Rubis fruciosus, Viscum album, and Vitis vinifera, each of which is effective in hemostasis. In this study, we aimed to investigate the effects of AHA on bleeding time in a rat tail hemorrhage model. METHODS: Forty-eight Sprague Dawley rats (5-7 weeks old, 180-210 g) were randomly and equally allocated to six groups as follows: heparin plus saline (heparinized control), heparin plus AHA-soaked sponge, heparin plus liquid form of AHA, saline (non-heparinized control), AHA-soaked sponge and liquid form of AHA. Heparin (640 IU/kg) was administered intraperitoneally three times a day for three days in heparinized groups. For the bleeding model, the tail of rats was transected. According to the study group, either saline- or AHA-soaked sponge or liquid form of AHA was applied over the hemorrhage area. In AHA- or saline-soaked sponge groups, once the bleeding time had started, it was checked every 10 seconds. If the bleeding did not stop after 40 seconds, it was accepted as a failure. In liquid AHA group, the duration of bleeding was measured using a chronometer and defined as the time (seconds) from wounding until the bleeding stopped. RESULTS: Bleeding time in the heparinized and non-heparinized control groups was over 40 seconds. After applying the sponge form of AHA on the wound area, bleeding time was significantly shortened to less than 20 seconds in both heparinized and non-heparinized rats (p<0.001 for both). The liquid form of AHA stopped bleeding in 5.0 +/- 1.2 seconds and 8.0 +/- 1.3 seconds in heparinized and non-heparinized groups, respectively. CONCLUSION: AHA is a highly effective topical hemostatic agent in a rat tail hemorrhage model, thus may provide for a unique clinically effective option for control of bleeding during surgical operations or other emergencies.
  • No Thumbnail Available
    Item
    Effects of Hypoxia Versus Ischaemia on Vascular Functions of Isolated Rat Thoracic Aorta: Revisiting the in Vitro Vascular Ischaemia/Reperfusion Model
    (2023) Orhan, Halit Guner; Teimoori, Ariyan; Demirtas, Elif; Zeynalova, Nargiz; Efe, Oguzhan Ekin; Aydingoz, Selda Emre; 37937174
    Introduction The in vitro rat vascular ischaemia and reperfusion model is used to evaluate the molecular and functional effects of potential agents against ischaemia and reperfusion injury of autologous graft veins. However, there is no consensus on whether hypoxia, rather than ischaemia, is sufficient to induce vascular dysfunction. Aim To compare the effects of hypoxia and ischaemia, with or without reperfusion, on the vascular functions of isolated thoracic aortic rings of rats. Material and methods Thoracic aortas of 12 male Sprague-Dawley rats (350-500 g, 18-24 months old) were isolated and divided into rings that were randomly allocated to control, ischaemia, hypoxia, ischaemia-reperfusion, and hypoxia-reperfusion groups. Aortic rings other than those of the control group were stored at 4 degrees C for 24 h in saline. For ischaemia, saline was gassed with nitrogen. After 24 h, aortic rings in the ischaemia-reperfusion and hypoxia-reperfusion groups were incubated with 200 mu M sodium hypochlorite for 30 min. Vascular and endothelial functions were tested in an organ bath set-up. Results Vascular response to potassium chloride (80 mM) decreased in all experimental groups compared to the control group (p = 0.007), but phenylephrine-induced contraction (10-5 M) increased only in the ischaemia-reperfusion group (p < 0.0001). Acetylcholine (10-11-10-5 M)-induced endothelium-dependent vasorelaxations were impaired in all groups - particularly in the ischaemia-reperfusion group (p = 0.0011). Sodium nitroprusside (10-12-10-7 M)-induced endothelium-independent vasorelaxations were similar across all groups (p = 0.1258). Conclusions Ischaemia followed by reperfusion should be implanted to achieve maximum endothelial and contractile dysfunction in vitro, and to replicate ischaemia and reperfusion injury of autologous graft veins.
  • No Thumbnail Available
    Item
    Mechanism of acitretin-induced relaxations in isolated rat thoracic aorta preparations
    (2022) Efe, Oguzhan Ekin; Aydos, Tolga Resat; Aydingoz, Selda Emre; 0000-0002-3243-7843; 0000-0001-7823-7620; 34411501; W-7908-2019; ABA-4291-2020
    Acitretin is a member of vitamin A-derived retinoids, and its effect on vascular smooth muscle had not yet been studied. The aim of this study is to investigate the effect of acitretin, a retinoid, on vascular smooth muscle contractility. Thoracic aorta preparations obtained from 34 male Sprague-Dawley rats (355 +/- 15 g) were studied in isolated organ baths containing Krebs-Henseleit solution. The relaxation responses were obtained with acitretin (10-12-10-4 M) in endotheliumpreserved and endothelium-denuded aorta preparations precontracted with submaximal concentration of phenylephrine (10-6 M). The role of retinoic acid receptors (RARs), nitric oxide, adenylyl, and guanylyl cyclase enzymes, and potassium channels in these relaxation responses were investigated. Acitretin produced concentration-dependent relaxations, which were independent of its solvent dimethylsulfoxide (DMSO), in endothelium-denuded phenylephrine-precontracted thoracic aorta preparations. While incubation with the RAR antagonist (AGN193109, 10-5 M) had no effect on these relaxations; nitric oxide synthase inhibitor (L-NG-Nitro arginine methyl ester (L-NAME), 10-4 M), adenylyl cyclase inhibitor (SQ2253, 10-5 M), guanylyl cyclase inhibitor (oxadiazolo [4,3-a] quinoxalin-1-one (ODQ), 10-6 M), and potassium channel blocker (tetraethylammonium (TEA), 10-2 M) significantly eliminated the relaxation responses induced by acitretin. Acitretin induces relaxation in rat isolated thoracic aorta preparations without endothelium, which may be mediated by nitric oxide, cyclic adenosine monophosphate, and cyclic guanosine monophosphate-dependent kinases and potassium channels.
  • No Thumbnail Available
    Item
    Reporting quality of animal studies published in journals listed in ULAKBIM TR index: a systematic review on compliance to the ARRIVE guidelines
    (2022) Aydingoz, Selda Emre; Efe, Oguzhan Ekin; Caliskan, Gokce; 0000-0001-7823-7620; 0000-0002-3243-7843; ABA-4291-2020; W-7908-2019
    Transparent reporting of animal studies is key to ensure reproducibility. The primary guideline for reporting animal studies is the ARRIVE (Animal Research: Reporting of In Vivo Experiments). We aimed to evaluate the compliance to the updated ARRIVE guidelines (version 2.0, date 2020) in animal studies published in journals indexed by the Turkish Academic Network and Information Centre (ULAKBIM TR Index). This was a retrospective analysis of reporting quality of animal studies published in journals listed in ULAKBIM TR Index between January 2010 and August 2021. The percentage of articles that fully reported each " of the ARRIVE Essential 10: Compliance Questionnaire was calculated, and effects of journal- and article-related factors were evaluated. Totally, 235 articles published in 89 journals were included into the analysis. The mean percentage of fully reported items was 59.1%+/- 10.9%, the least reported items being those related with bias - "blinding", "allocation to study groups", "assessment of statistical assumptions", "excluded animals", and "sample size calculation" (0.9%-10.6%). The journal's publisher, frequency, language, being indexed in the Science Citation Index Expanded, and the ratio of animal studies had no significant effect on this percentage (p>0.05). However, journals supporting the ARRIVE guidelines had significantly and higher compliance (62.1 %+/- 10.1% vs. 58.2%+/- 11.0% for supporters and non-supporters, respectively; p=0.017, 95%CI -7.0 to-0.7). Articles published after 2015 had higher compliance to the ARRIVE guidelines than those published previously (60.9%+/- 10.4% vs. 57.9%+/- 11.1%, respectively; p=0.037, 95%CI -5.8 to -0.2). Although progress has been made, compliance to the ARRIVE guidelines is still low in animal studies published in journals listed in ULAKBIM TR Index-Turkey's scientific journal database that covers over 800 peer-review journals. In order to increase the reporting quality and reproducibility of animal studies, it is imperative to raise awareness among researchers and journals, and to enforce the ARRIVE guidelines in editorial policy of journals.

| Başkent Üniversitesi | Kütüphane | Açık Bilim Politikası | Açık Erişim Politikası | Rehber |

DSpace software copyright © 2002-2026 LYRASIS

  • Privacy policy
  • End User Agreement
  • Send Feedback
Repository logo COAR Notify