Effect of dexmedetomidine on acute kidney injury in endotoxemic rats
Huijuan Cao, Dongmei Yu, Tiezheng Zhang, Keyan Chen
Abstract
Huijuan Cao, Dongmei Yu, Tiezheng Zhang, Keyan Chen
Abstract
Objective To investigate the effect of dexmedetomidine on acute kidney injury in endotoxemic rats. Methods Thirty adult male Sprague-Dawley rats, aged 4-6 months, weighing 180-220 g, were randomly divided into 3 groups (n= 10 each) using a random number table: control group (group C), lipopolysaccharide group (group L), and dexmedetomidine (group D). Lipopolysaccharide (LPS) 5 mg/kg was injected slowly into the femoral vein to establish the model of endotoxemic in rats anesthetized with chloral hydrate.In group D, after LPS injection, a loading dose of dexmedetomidine 7 μg/kg was injected intravenously, and 15 min later dexmedetomidine was infused for 6 h at 5 μg·kg-1·h-1, while the equal volume of normal saline was given in L and C groups.At 6 h after the end of LPS administration, blood samples were collected from the femoral vein for determination of serum creatinine (Cr), blood urea nitrogen (BUN), tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) concentrations.At 24 h after the end of LPS administration, the animals were sacrificed and kidneys were removed for microscopic examination and for determination of the expression of tight junction proteins ZO-1 and occludin in renal tissues by Western blot. Results Compared with group C, the serum Cr, BUN, TNF-α and IL-6 concentrations were significantly increased, and the expression of ZO-1 and occluding was down-regulated in L and D groups.Compared with group L, the serum Cr, BUN, TNF-α and IL-6 concentrations were significantly decreased, the expression of ZO-1 and occluding was up-regulated, and the pathological changes of kidneys were mitigated in D group. Conclusion Dexmedetomidine can alleviate acute kidney injury in endotoxemic rats. Key words: Dexmedetomidine; Endotoxemia; Kidney
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Objective To investigate the effect of dexmedetomidine on acute kidney injury in endotoxemic rats. Methods Thirty adult male Sprague-Dawley rats, aged 4-6 months, weighing 180-220 g, were randomly divided into 3 groups (n= 10 each) using a random number table: control group (group C), lipopolysaccharide group (group L), and dexmedetomidine (group D). Lipopolysaccharide (LPS) 5 mg/kg was injected slowly into the femoral vein to establish the model of endotoxemic in rats anesthetized with chloral hydrate.In group D, after LPS injection, a loading dose of dexmedetomidine 7 μg/kg was injected intravenously, and 15 min later dexmedetomidine was infused for 6 h at 5 μg·kg-1·h-1, while the equal volume of normal saline was given in L and C groups.At 6 h after the end of LPS administration, blood samples were collected from the femoral vein for determination of serum creatinine (Cr), blood urea nitrogen (BUN), tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) concentrations.At 24 h after the end of LPS administration, the animals were sacrificed and kidneys were removed for microscopic examination and for determination of the expression of tight junction proteins ZO-1 and occludin in renal tissues by Western blot. Results Compared with group C, the serum Cr, BUN, TNF-α and IL-6 concentrations were significantly increased, and the expression of ZO-1 and occluding was down-regulated in L and D groups.Compared with group L, the serum Cr, BUN, TNF-α and IL-6 concentrations were significantly decreased, the expression of ZO-1 and occluding was up-regulated, and the pathological changes of kidneys were mitigated in D group. Conclusion Dexmedetomidine can alleviate acute kidney injury in endotoxemic rats. Key words: Dexmedetomidine; Endotoxemia; Kidney
Key concepts: Dexmedetomidine, Occludin, Saline, Blood urea nitrogen, Creatinine, Lipopolysaccharide, Kidney, Chloral hydrate