Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model

Sodium salt of deoxyribonucleic acid (DNA), Derinat, isolated from the soft roes of Russian sturgeon, has been utilized as an immunomodulator for the treatment of reactive oxygen species (ROS)-associated diseases in clinics. Here we show that treatment with Derinat has an anti-inflammatory and anti-...

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Main Authors: Jiadai Liu, Elena G. Rybakina, Eelena A. Korneva, Mami Noda
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Journal of Pharmacological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1347861318301804
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author Jiadai Liu
Elena G. Rybakina
Eelena A. Korneva
Mami Noda
author_facet Jiadai Liu
Elena G. Rybakina
Eelena A. Korneva
Mami Noda
author_sort Jiadai Liu
collection DOAJ
description Sodium salt of deoxyribonucleic acid (DNA), Derinat, isolated from the soft roes of Russian sturgeon, has been utilized as an immunomodulator for the treatment of reactive oxygen species (ROS)-associated diseases in clinics. Here we show that treatment with Derinat has an anti-inflammatory and anti-oxidative effects on cutaneous ischemia-reperfusion (IR) injury in pressure ulcer (PU) model mice. Dorsal skin damage and dermal edema in mild PU model mice were attenuated by treatment with Derinat. Immunohistochemical and biochemical analyses showed that Derinat suppressed IR-induced oxidative damage, i.e. accumulation of 8-hydroxy-2′-deoxyguanosine (8-OHdG), and related inflammatory factors such as cyclooxygenase 2 (COX-2) and IL-6 receptor (IL-6R) in dorsal skin from PU model mice. We also verified that phospholyated/non-phosphorylated ratio of extracellular signal-regulated kinase (Erk) and p38 mitogen-activated protein kinase (MAPK) increased after IR, which were attenuated by Derinat. We then compared the effect of Derinat with that of salmon DNA and other PU therapeutic agents, prostaglandin E1 (PGE1) and basic fibroblast growth factor (bFGF), by using severe PU model mice. The effects of Derinat and salmon-DNA were compatible with those of PGE1 and bFGF. These results suggest that Derinat other fish-derived DNA formulation could be effective enough and become intriguing new therapeutic options. Keywords: Pressure ulcer, Sodium salt of DNA, Oxidative damage, Inflammation, Mice
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spelling doaj.art-bf5fc47450c444578e16270a565f7be82022-12-22T00:44:02ZengElsevierJournal of Pharmacological Sciences1347-86132018-10-011382123130Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse modelJiadai Liu0Elena G. Rybakina1Eelena A. Korneva2Mami Noda3Laboratory of Pathophysiology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, JapanDepartment of General Pathology and Pathophysiology, Federal State Budgetary Scientific Institution, Institute of Experimental Medicine, Str. Acad. Pavlova 12, Saint Petersburg 197376, Russia; Department of Pathology, Faculty of Medicine, Saint Petersburg State University, RussiaDepartment of General Pathology and Pathophysiology, Federal State Budgetary Scientific Institution, Institute of Experimental Medicine, Str. Acad. Pavlova 12, Saint Petersburg 197376, Russia; Department of Pathology, Faculty of Medicine, Saint Petersburg State University, RussiaLaboratory of Pathophysiology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan; Corresponding author. Fax: +81 92 642 6554.Sodium salt of deoxyribonucleic acid (DNA), Derinat, isolated from the soft roes of Russian sturgeon, has been utilized as an immunomodulator for the treatment of reactive oxygen species (ROS)-associated diseases in clinics. Here we show that treatment with Derinat has an anti-inflammatory and anti-oxidative effects on cutaneous ischemia-reperfusion (IR) injury in pressure ulcer (PU) model mice. Dorsal skin damage and dermal edema in mild PU model mice were attenuated by treatment with Derinat. Immunohistochemical and biochemical analyses showed that Derinat suppressed IR-induced oxidative damage, i.e. accumulation of 8-hydroxy-2′-deoxyguanosine (8-OHdG), and related inflammatory factors such as cyclooxygenase 2 (COX-2) and IL-6 receptor (IL-6R) in dorsal skin from PU model mice. We also verified that phospholyated/non-phosphorylated ratio of extracellular signal-regulated kinase (Erk) and p38 mitogen-activated protein kinase (MAPK) increased after IR, which were attenuated by Derinat. We then compared the effect of Derinat with that of salmon DNA and other PU therapeutic agents, prostaglandin E1 (PGE1) and basic fibroblast growth factor (bFGF), by using severe PU model mice. The effects of Derinat and salmon-DNA were compatible with those of PGE1 and bFGF. These results suggest that Derinat other fish-derived DNA formulation could be effective enough and become intriguing new therapeutic options. Keywords: Pressure ulcer, Sodium salt of DNA, Oxidative damage, Inflammation, Micehttp://www.sciencedirect.com/science/article/pii/S1347861318301804
spellingShingle Jiadai Liu
Elena G. Rybakina
Eelena A. Korneva
Mami Noda
Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model
Journal of Pharmacological Sciences
title Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model
title_full Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model
title_fullStr Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model
title_full_unstemmed Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model
title_short Effects of Derinat on ischemia-reperfusion-induced pressure ulcer mouse model
title_sort effects of derinat on ischemia reperfusion induced pressure ulcer mouse model
url http://www.sciencedirect.com/science/article/pii/S1347861318301804
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