Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats

Abstract Microcirculatory dysfunction plays a crucial role in renal ischemia/reperfusion (IR)-induced injury. Dexmedetomidine was reported to ameliorate IR-induced acute kidney injury. This study investigated the effects of dexmedetomidine on renal microcirculation after IR-induced acute kidney inju...

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Autores principales: Szu-Jen Yang, Chia-Ning Fan, Ming-Jiuh Wang, Shou-Zen Fan, Jui-Chang Tsai, Wei-Zen Sun, Wing-Sum Chan, Yu-Chang Yeh, NTUH Center of Microcirculation Medical Research (NCMMR)
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3502e6b27c25449facf02462e92e7a6a
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spelling oai:doaj.org-article:3502e6b27c25449facf02462e92e7a6a2021-12-02T10:49:29ZEffects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats10.1038/s41598-021-81288-32045-2322https://doaj.org/article/3502e6b27c25449facf02462e92e7a6a2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-81288-3https://doaj.org/toc/2045-2322Abstract Microcirculatory dysfunction plays a crucial role in renal ischemia/reperfusion (IR)-induced injury. Dexmedetomidine was reported to ameliorate IR-induced acute kidney injury. This study investigated the effects of dexmedetomidine on renal microcirculation after IR-induced acute kidney injury in rats. In total, 50 rats were randomly allocated to the following five groups (10 in each group): Sham, Control‒IR, Dex (dexmedetomidine) ‒Sham, Dex‒IR, and IR‒Dex group. The microcirculation parameters included total small vessel density, perfused small vessel density (PSVD), proportion of perfused small vessels, microvascular flow index, and tissue oxygen saturation (StO2) were recorded. The repeated measures analysis showed that PSVD on renal surface was higher in the Dex‒IR group than in the Control‒IR group (3.5 mm/mm2, 95% confidence interval [CI] 0.6 to 6.4 mm/mm2, P = 0.01). At 240 min, StO2 on renal surface was lower in the Control‒IR group than in the Sham group (– 7%, 95% CI − 13 to − 1%, P = 0.021), but StO2 did not differ significantly among the Sham, Dex‒IR, and IR‒Dex groups. Our results showed that pretreatment with dexmedetomidine improved renal microcirculation in rats with IR-induced acute kidney injury. However, the adverse effects of low mean arterial pressure and heart rate might offset the protective effect of dexmedetomidine on organ injury.Szu-Jen YangChia-Ning FanMing-Jiuh WangShou-Zen FanJui-Chang TsaiWei-Zen SunWing-Sum ChanYu-Chang YehNTUH Center of Microcirculation Medical Research (NCMMR)Nature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Szu-Jen Yang
Chia-Ning Fan
Ming-Jiuh Wang
Shou-Zen Fan
Jui-Chang Tsai
Wei-Zen Sun
Wing-Sum Chan
Yu-Chang Yeh
NTUH Center of Microcirculation Medical Research (NCMMR)
Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
description Abstract Microcirculatory dysfunction plays a crucial role in renal ischemia/reperfusion (IR)-induced injury. Dexmedetomidine was reported to ameliorate IR-induced acute kidney injury. This study investigated the effects of dexmedetomidine on renal microcirculation after IR-induced acute kidney injury in rats. In total, 50 rats were randomly allocated to the following five groups (10 in each group): Sham, Control‒IR, Dex (dexmedetomidine) ‒Sham, Dex‒IR, and IR‒Dex group. The microcirculation parameters included total small vessel density, perfused small vessel density (PSVD), proportion of perfused small vessels, microvascular flow index, and tissue oxygen saturation (StO2) were recorded. The repeated measures analysis showed that PSVD on renal surface was higher in the Dex‒IR group than in the Control‒IR group (3.5 mm/mm2, 95% confidence interval [CI] 0.6 to 6.4 mm/mm2, P = 0.01). At 240 min, StO2 on renal surface was lower in the Control‒IR group than in the Sham group (– 7%, 95% CI − 13 to − 1%, P = 0.021), but StO2 did not differ significantly among the Sham, Dex‒IR, and IR‒Dex groups. Our results showed that pretreatment with dexmedetomidine improved renal microcirculation in rats with IR-induced acute kidney injury. However, the adverse effects of low mean arterial pressure and heart rate might offset the protective effect of dexmedetomidine on organ injury.
format article
author Szu-Jen Yang
Chia-Ning Fan
Ming-Jiuh Wang
Shou-Zen Fan
Jui-Chang Tsai
Wei-Zen Sun
Wing-Sum Chan
Yu-Chang Yeh
NTUH Center of Microcirculation Medical Research (NCMMR)
author_facet Szu-Jen Yang
Chia-Ning Fan
Ming-Jiuh Wang
Shou-Zen Fan
Jui-Chang Tsai
Wei-Zen Sun
Wing-Sum Chan
Yu-Chang Yeh
NTUH Center of Microcirculation Medical Research (NCMMR)
author_sort Szu-Jen Yang
title Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
title_short Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
title_full Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
title_fullStr Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
title_full_unstemmed Effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
title_sort effects of dexmedetomidine on renal microcirculation in ischemia/reperfusion-induced acute kidney injury in rats
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3502e6b27c25449facf02462e92e7a6a
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