SESSION TITLE: Cytokines/Cellular Interactions Posters
SESSION TYPE: Original Investigation Poster
PRESENTED ON: Wednesday, October 30, 2013 at 01:30 PM - 02:30 PM
PURPOSE: The enzyme myeloperoxidase is very well known to participate in the fibrotic pathway with inflammatory and apoptotic actions. EPO is a multiple functional cytokine with anti-oxidative, anti-inflammatory and anti-apoptotic properties. Aim of this study was to investigate the role of EPO on the expression of MPO in bleomycin-induced pulmonary fibrosis in rats.
METHODS: Fifty Wistar rats (average weight 300gr) were divided into five groups of 10 animals each. Group 1: control animals, Group 2: intratracheal (i.t) and intraperitoneal (i.p) injection of saline (0.5ml/kg), Group 3: intratracheal injection of BLM hydrochloride (7.5mg/kg), Group 4: intratracheal injection of BLM hydrochloride (7.5mg/kg) followed by intraperitoneal injection of EPO (2000 iu/kg), Group 5: intratracheal injection of saline (0.5ml/kg) followed by intraperitoneal injection of EPO (2000 iu/kg). All rats were sacrified after 14 days. The expression of MPO was immunohistochemically measured and a scale of 4 grades was used to evaluate it (grade A: 0 - 25%, grade B: 25 - 50%, grade C: 50 - 75% and grade D: 75 - 100%) .
RESULTS: In groups 1,2 and 5 (control groups), MPO was expressed mainly in the grade A (80%) and fairly in the grade B (20%). In group 3, MPO was expressed in the high grades C (20%) and D (80%). Finally, in group 4, MPO was expressed only in the low grades A (80%) and B (20%). It is obvious that the expression of the enzyme took place in the high grades for group 3 (BLM group) and in the lower grades for group 4 (BLM+EPO group) (p<0.001 and p<0.005 respectively).
CONCLUSIONS: Administration of EPO after the BLM intratracheal injection (group 4) resulted in significant lower expression of MPO in comparison with the BLM group (group 3). Additional studies are required to clarify the underlying mechanisms of the protective action of EPO on pulmonary fibrosis.
CLINICAL IMPLICATIONS: These findings suggest that EPO may serve as a novel potential target for the therapeutic treatment of PF.
DISCLOSURE: The following authors have nothing to disclose: Drosos Tsavlis, Anna Tzoumaka, Georgia Kokaraki, Kokona kouzi-Koliakos, Anastasia Tektonidou, Evangelia Spandou
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