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七氟醚预先给药对大鼠肾缺血再灌注时炎性反应的影响 被引量:3

Effect of sevoflurane pretreatment on inflammatory response during renal ischemia-reperfusion in rats
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摘要 目的 评价七氟醚预先给药对大鼠肾缺血再灌注时炎性反应的影响.方法 清洁级健康雄性SD大鼠30只,12~ 14周龄,体重220 ~ 260 g,采用随机数字表法,将其分为3组(n=10):假手术组(S组)、肾缺血再灌注组(I/R组)和七氟醚预先给药组(SP组).I/R组和SP组采用夹闭左肾蒂45min后恢复灌注的方法制备大鼠肾缺血再灌注损伤模型,S组腹部正中切口,右肾切除,左肾蒂游离后,缝合腹腔;SP组模型制备前30 min开始吸入3%七氟醚和氧气的混合气体.于再灌注3h时采集下腔静脉血样5 ml,测定血清BUN和Cr的浓度,光镜下观察肾组织病理学结果,测定肾组织TNF-α、IL-6和细胞间黏附分子-1(ICAM-1)的含量.结果 与S组比较,I/R组和SP组血清BUN和Cr浓度、肾脏近曲小管坏死程度分级、肾组织TNF-α、IL-6和ICAM-1含量升高(P<0.05);与I/R组比较,SP组血清BUN和Cr浓度、肾脏近曲小管坏死程度分级、肾组织TNF-α、IL-6和ICAM-1含量降低(P<0.05).结论 七氟醚预先给药通过抑制肾组织炎性反应减轻大鼠肾缺血再灌注损伤. Objective To evaluate the effect of sevoflurane pretreatment on the inflammatory response during renal ischemia-reperfusion (I/R) in rats.Methods Thirty pathogen-free male Sprague-Dawley rats,aged 12-14 weeks,weighing 220-260 g,were randomized into 3 groups (n =10 each) using a random number table:sham operation group (group S),I/R group and sevoflurane pretreatment group (group SP).Renal I/R was induced by clamping the left renal pedicle for 45 min followed by reperfusion in I/R and SP groups.In group S inhalation of 3% sevoflurane in O2 was started at 30 min before I/R and maintained throughout the experiment.Venous blood samples were taken at 3 h of reperfusion for determination of serum blood urea nitrogen (BUN) and creatinine (Cr) concentrations.The animals were then sacrificed and the left kidneys were removed for microscopic examination and for measurement of the content of tumor necrosis factor-apha (TNF-α),interleukin-6 (IL-6) and intercellular cell adhesion molecule-1 (ICAM-1) in renal tissues (by ELISA).Results Compared with group S,the serum BUN and Cr concentrations,severity of necrosis of renal proximal convoluted tubules (0 =normal,4 =necrosis of whole segment of proximal convoluted tubules),and contents of TNF-α,IL-6 and ICAM-1 were significantly increased in I/R and SP groups (P 〈 0.05).Compared with group I/R,the serum BUN and Cr concentrations,severity of necrosis of renal proximal convoluted tubules,and contents of TNF-α,IL-6 and ICAM-1 were significantly decreased in SP group (P 〈 0.05).Conclusion Sevoflurane pretreatment can protect kidney against I/R injury by inhibiting the inflammatory responses in the renal tissues of rats.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2014年第1期120-122,共3页 Chinese Journal of Anesthesiology
关键词 麻醉药 吸入 再灌注损伤 炎症 Anesthetics,inhalation Reperfusion injury Kidney Inflammation
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  • 1Onem Y, Ipcioglu OM, Haholu A, et al. Posttreatment with amino- guanidine attenuates renal ischemia/reperfusion injury in rats [ J]. Ren Fail, 2009,31 ( 1 ) : 50-53.
  • 2Lee HT, Ota-Setlik A, Fu Y, et al. Differential protective effects of volatile anesthetics against renal ischemia-reperfusion injury in vivo [J], Anesthesiology, 2004,101 (6) : 1313-1324.
  • 3Ranganathan PV, Jayakumar C, Ramesh G. Netrin-l-treated macro- phages protect the kidney against ischemia-reperfusion injury and suppress inflammation by inducing M2 polarization[ J ]. Am J Physiol Renal Physiol, 2013,304 (7) : F948- F957.
  • 4Jablonskl P, Howden BO, Rae DA, et al. An experimental model for assessment of renal recovery from warm ischemia[ J]. Transplantation, 1983,35(3) : 198-204.
  • 5Obal D, Dettwiler S, Favoceia C, et al. Effect of sevotlurane preco- nditioning on ischaemia/reperfusion injury in the rat kidney in vivo [J]. Eur J Anaesth,2006,23(4) :319-332.
  • 6Bomsztyk K, Flanagin S, Mar D, et al. Synchronous recruitment of epigenetic modifiem to endotoxin synergistically activated Tnf-a gene in acute kidney injury[J]. PLoS One, 2013,8(7) :36-40.
  • 7Miklos Z, Kurthy M, Degrell P, et al. Ischaemic postconditioning reduces serum and tubular TNF-α expression in ischaemic-reperfused kidney in healthy rats[ J]. Clin Hemorheol Microcirc, 2012,50(3) : 167-178.
  • 8Phull H, Lien YH, Salkini MW. Delivery of intercellular adhesion molecule-1 antisense oligonucleotides using a topical hydrogel tissue sealant in a murine partial nephrectomy/ischemia model[J]. Urology, 2008,72(3) : 690-695.
  • 9Kelly KJ, Williams WW Jr, Coluin RB, et al. Intercellular adhesion molecule-1 deficient mice are protected against ischemic renal injury [J]. J Clin Invest, 1996,97(4) : 1056-1063.
  • 10Gan X, Su G, Zhao W, et al. The mechanism of sevoflurane preconditioning-induced protections against small intestinal ischemia reperfusion injury is independent of mast cell in rats[J]. Mediators Inflamm,2013,20(8) : 12-16.

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