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芸香苷对实验性急性胰腺炎多器官损伤的保护作用 被引量:2

Protective effect of Rutoside on multi-organ injury during experimental acute pancreatitis
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摘要 目的探讨芸香苷(Ru)对实验性急性胰腺炎(AP)胰外多器官损伤的影响。方法牛磺胆酸钠(STC)逆行胆胰管注射诱发大鼠AP模型后,立即按Ru15、30、60mg/kg3个剂量持续静脉输注6h,观察AP大鼠多器官功能性指标,包括血清淀粉酶(AMS)、尿素氮(BUN)、肌酐(Cr)、谷丙转氨酶(ALT)、谷草转氨酶(AST)和乳酸脱氢酶(LDH)、动脉血气分析的变化。结果Ru15、30、60mg/kg3个给药剂量组可不同程度降低AP大鼠升高的AMS、BUN、Cr、ALT、AST、LDH。60mg/kg剂量组可升高AP大鼠降低的动脉PO2。结论静脉输注Ru对实验性AP胰外多器官功能损伤具有一定的保护作用。 Objective To investigate the effects of Rutoside (Ru) on multi-organ injury during experimental acute panereatitis (AP). Methods The model of AP was induced by retrograde injection of Sodium Tauroeholate (STC) into bilipanereatie duct of rat. Ru (15,30,60mg/kg)was administered with intravenous infusion for 6 h immediately after the induction of AP. Some indicators which reflected the function of multi-organ of AP rats were observed, they were amylase ( AMS), blood urea nitrogen ( BUN ), ereatinine ( Cr), alanine aminotransferase ( ALT), aspartare aminotransferase (AST) ,lactic dehydrogenase (LDH) and indexes of blood gas analysis. Results Ru ( 15, 30, 60mg/kg)deereased AMS, BUN, Cr, ALT, AST and LDH, which had increased in AP rats. Ru (60 mg/kg) increased arterial PO2 in AP rats. Conclusion The study indicates that Ru administered by intravenous infusion exerts certain protective effects on multi-organ function injury in experimental AP rats.
出处 《安徽医科大学学报》 CAS 北大核心 2006年第2期150-153,共4页 Acta Universitatis Medicinalis Anhui
基金 安徽省自然科学基金资助项目(编号:01043907)
关键词 胰腺炎/药物疗法 胰腺炎/酶学 胰腺炎/血液 pancreatitis/drug therapy pancreatitis/enzymology pancreatitis/blood
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  • 1杨春明.重症急性胰腺炎的发病机理[J].普外临床,1994,9(5):260-262. 被引量:21
  • 2雷文章,韦靖江,沈文律,金立人.实验性坏死性胰腺炎多器官损害与内毒素血症的关系[J].中华实验外科杂志,1995,12(3):131-132. 被引量:117
  • 3王广义,刘铜军,谭毓铨,杨春光.实验性急性胰腺炎模型的改进[J].白求恩医科大学学报,1995,21(6):605-606. 被引量:4
  • 4陈志武,宋必卫,方明,张于江,马传庚,徐叔云.芸香甙抗氧化作用的初步研究[J].中国药理学通报,1995,11(1):75-77. 被引量:36
  • 5[1]Lindahl M, Tagesson C. Flavonoids as phospholipase A2 inhibitors: importance of their structure for selective inhibition of group II phospholipase A2 [ J ]. Inflammation, 1997; 21 ( 3 ): 347- 56
  • 6[3]Uhl W, Schrag HJ, Schmitter N, Nevalainen TJ, Aufenanger J, Wheatley AM, et al Pathophysiological role of secretory type Ⅰ and Ⅱ phospholipase A2 in acute pancreatitis: an experimental study in rats[ J ]. Gut, 1997; 40(3): 386 - 92
  • 7[6]Aho HJ, Koskensala SML, Nevalainen TJ. Experimental pancreatitis in the rat: taurocholate-induced acute hemorrhagic pancreatitis[J]. Scand J Gastroenterol, 1980; 15(3) :411 - 6
  • 8[8]Toma H, Winston J, Micci MA, Shenoy M, Pasricha PJ. Nerve grouth factor expression up-regulated in the rat model of L-Arginine-induced acute pancreatitis[J]. Gastroenterology, 2000; 119(5): 1373 - 81
  • 9[9]Kim YM, Son K. A nitric oxide production bioassary for interferon-γ[J]. J Immuno Method, 1996; 198(2) :203 - 9
  • 10[10]Gavino VC, Miller JC. Effect of polyunsaturated fatty acide and antioxidants on lipid peroxidation in tissue culture[J]. J Lipid Res, 1981 ;22(5) :763 - 9

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