Effects of ulinastatin on global ischemia via brain pro-inflammation signal

Ulinastatin [urinary trypsin inhibitor (UTI)] plays an important role in the protection of organs against ischemic injury during severe inflammation. The purposes of this study were to examine the effects of UTI on the levels of pro-inflammatory cytokines (PICs) and protein expression of PIC recepto...

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Autores principales: Jiang Xiao-Ming, Hu Jing-Hai, Wang Lu-Lu, Ma Chi, Wang Xu, Liu Xiao-Liang
Formato: article
Lenguaje:EN
Publicado: De Gruyter 2016
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Acceso en línea:https://doaj.org/article/79e39bfcbb764dedb1273578e052b80a
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spelling oai:doaj.org-article:79e39bfcbb764dedb1273578e052b80a2021-12-05T14:11:04ZEffects of ulinastatin on global ischemia via brain pro-inflammation signal2081-693610.1515/tnsci-2016-0023https://doaj.org/article/79e39bfcbb764dedb1273578e052b80a2016-01-01T00:00:00Zhttps://doi.org/10.1515/tnsci-2016-0023https://doaj.org/toc/2081-6936Ulinastatin [urinary trypsin inhibitor (UTI)] plays an important role in the protection of organs against ischemic injury during severe inflammation. The purposes of this study were to examine the effects of UTI on the levels of pro-inflammatory cytokines (PICs) and protein expression of PIC receptors in the neocortex and hippocampus CA1 region of rats after transient global ischemia induced via cardiac arrest (CA). Specifcally, interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) were analyzed. CA was induced by asphyxia followed by cardiopulmonary resuscitation in rats. ELISA and western blot analysis were employed to determine PICs and their receptors in the neocortex and hippocampus. Our results show that IL-1β, IL-6 and TNF-α were significantly elevated in the neocortex and hippocampal CA1 field after CA. This was accompanied with an increase in PIC receptors, namely IL-1R, IL-6R and TNFR1. Systemic injection of UTI attenuated the amplification of PIC signal pathways in these brain regions. UTI also improved the modified Neurological Severity Score and brain tissue edema in CA rats. Notably, UTI resulted in an increase in survival of CA rats as compared to CA rats without treatment. In conclusion, UTI plays a beneficial role in modulating transient global ischemia induced by CA by altering PIC signal mechanisms, but further studies are needed to draw more firm conclusions.Jiang Xiao-MingHu Jing-HaiWang Lu-LuMa ChiWang XuLiu Xiao-LiangDe Gruyterarticlecardiac arrestcardiopulmonary resuscitationcortexcytokineshippocampusulinastatinNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571ENTranslational Neuroscience, Vol 7, Iss 1, Pp 158-163 (2016)
institution DOAJ
collection DOAJ
language EN
topic cardiac arrest
cardiopulmonary resuscitation
cortex
cytokines
hippocampus
ulinastatin
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
spellingShingle cardiac arrest
cardiopulmonary resuscitation
cortex
cytokines
hippocampus
ulinastatin
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Jiang Xiao-Ming
Hu Jing-Hai
Wang Lu-Lu
Ma Chi
Wang Xu
Liu Xiao-Liang
Effects of ulinastatin on global ischemia via brain pro-inflammation signal
description Ulinastatin [urinary trypsin inhibitor (UTI)] plays an important role in the protection of organs against ischemic injury during severe inflammation. The purposes of this study were to examine the effects of UTI on the levels of pro-inflammatory cytokines (PICs) and protein expression of PIC receptors in the neocortex and hippocampus CA1 region of rats after transient global ischemia induced via cardiac arrest (CA). Specifcally, interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) were analyzed. CA was induced by asphyxia followed by cardiopulmonary resuscitation in rats. ELISA and western blot analysis were employed to determine PICs and their receptors in the neocortex and hippocampus. Our results show that IL-1β, IL-6 and TNF-α were significantly elevated in the neocortex and hippocampal CA1 field after CA. This was accompanied with an increase in PIC receptors, namely IL-1R, IL-6R and TNFR1. Systemic injection of UTI attenuated the amplification of PIC signal pathways in these brain regions. UTI also improved the modified Neurological Severity Score and brain tissue edema in CA rats. Notably, UTI resulted in an increase in survival of CA rats as compared to CA rats without treatment. In conclusion, UTI plays a beneficial role in modulating transient global ischemia induced by CA by altering PIC signal mechanisms, but further studies are needed to draw more firm conclusions.
format article
author Jiang Xiao-Ming
Hu Jing-Hai
Wang Lu-Lu
Ma Chi
Wang Xu
Liu Xiao-Liang
author_facet Jiang Xiao-Ming
Hu Jing-Hai
Wang Lu-Lu
Ma Chi
Wang Xu
Liu Xiao-Liang
author_sort Jiang Xiao-Ming
title Effects of ulinastatin on global ischemia via brain pro-inflammation signal
title_short Effects of ulinastatin on global ischemia via brain pro-inflammation signal
title_full Effects of ulinastatin on global ischemia via brain pro-inflammation signal
title_fullStr Effects of ulinastatin on global ischemia via brain pro-inflammation signal
title_full_unstemmed Effects of ulinastatin on global ischemia via brain pro-inflammation signal
title_sort effects of ulinastatin on global ischemia via brain pro-inflammation signal
publisher De Gruyter
publishDate 2016
url https://doaj.org/article/79e39bfcbb764dedb1273578e052b80a
work_keys_str_mv AT jiangxiaoming effectsofulinastatinonglobalischemiaviabrainproinflammationsignal
AT hujinghai effectsofulinastatinonglobalischemiaviabrainproinflammationsignal
AT wanglulu effectsofulinastatinonglobalischemiaviabrainproinflammationsignal
AT machi effectsofulinastatinonglobalischemiaviabrainproinflammationsignal
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