J Marton, G Farkas, T Takacs, Z Nagy, Z Szasz, J Varga, K Jarmay, A Balogh, J Lonovics
{"title":"己酮茶碱治疗大鼠实验性急性胰腺炎的有益作用。","authors":"J Marton, G Farkas, T Takacs, Z Nagy, Z Szasz, J Varga, K Jarmay, A Balogh, J Lonovics","doi":"10.1007/s004330050078","DOIUrl":null,"url":null,"abstract":"<p><strong>Unlabelled: </strong>The purposes of this study were to determine the tumor necrosis factor (TNF) and interleukin-6 (IL-6) levels after the induction of acute necrotizing pancreatitis, and to establish the effects of pentoxifylline on cytokine production.</p><p><strong>Methods: </strong>acute pancreatitis was induced by the retrograde injection of 200 microliters taurocholic acid into the pancreatic duct in male Wistar rats. The serum amylase activity, the wet pancreatic weight/body weight ratio, and the TNF and IL-6 levels were measured. Seven mg/kg pentoxifylline were administered intraperitoneally at the time of operation 6, 12 or 24 h later. Rats were killed 6, 24, 48 or 72 h after the operation.</p><p><strong>Results: </strong>the TNF bioassay revealed high levels of TNF (30.2 +/- 5.4 U/ml, 35.0 +/- 5.0 U/ml and 36.6 +/- 6.0 U/ml) in the control group at 6, 24 and 48 h and (54.1 +/- 20 U/ml and 10.9 +/- 4.2 U/ml) in the pentoxifylline-treated group at 6 and 24 h, respectively, whereas the level had decreased to zero in the pentoxifylline-treated group at 48 h. The IL-6 bioassay likewise demonstrated high levels of IL-6 in the control group at 48 h and in the pentoxifylline-treated group at 6 and 24 h, and markedly decreased levels in the pentoxifylline-treated group at 48 h (7083 +/- 2844 pg/ml, 6463 +/- 1307 pg/ml, 10,329 +/- 5571 pg/ml vs 137.5 +/- 85.5 pg/ml, respectively, P < 0.05). The high mortality observed in the pancreatitis group (43%) was decreased by pentoxifylline administration to 11%.</p><p><strong>Conclusion: </strong>these results demonstrate that pentoxifylline very effectively inhibits cytokine production in acute pancreatitis.</p>","PeriodicalId":76421,"journal":{"name":"Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie","volume":"197 5","pages":"293-9"},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s004330050078","citationCount":"24","resultStr":"{\"title\":\"Beneficial effects of pentoxifylline treatment of experimental acute pancreatitis in rats.\",\"authors\":\"J Marton, G Farkas, T Takacs, Z Nagy, Z Szasz, J Varga, K Jarmay, A Balogh, J Lonovics\",\"doi\":\"10.1007/s004330050078\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Unlabelled: </strong>The purposes of this study were to determine the tumor necrosis factor (TNF) and interleukin-6 (IL-6) levels after the induction of acute necrotizing pancreatitis, and to establish the effects of pentoxifylline on cytokine production.</p><p><strong>Methods: </strong>acute pancreatitis was induced by the retrograde injection of 200 microliters taurocholic acid into the pancreatic duct in male Wistar rats. The serum amylase activity, the wet pancreatic weight/body weight ratio, and the TNF and IL-6 levels were measured. Seven mg/kg pentoxifylline were administered intraperitoneally at the time of operation 6, 12 or 24 h later. Rats were killed 6, 24, 48 or 72 h after the operation.</p><p><strong>Results: </strong>the TNF bioassay revealed high levels of TNF (30.2 +/- 5.4 U/ml, 35.0 +/- 5.0 U/ml and 36.6 +/- 6.0 U/ml) in the control group at 6, 24 and 48 h and (54.1 +/- 20 U/ml and 10.9 +/- 4.2 U/ml) in the pentoxifylline-treated group at 6 and 24 h, respectively, whereas the level had decreased to zero in the pentoxifylline-treated group at 48 h. The IL-6 bioassay likewise demonstrated high levels of IL-6 in the control group at 48 h and in the pentoxifylline-treated group at 6 and 24 h, and markedly decreased levels in the pentoxifylline-treated group at 48 h (7083 +/- 2844 pg/ml, 6463 +/- 1307 pg/ml, 10,329 +/- 5571 pg/ml vs 137.5 +/- 85.5 pg/ml, respectively, P < 0.05). The high mortality observed in the pancreatitis group (43%) was decreased by pentoxifylline administration to 11%.</p><p><strong>Conclusion: </strong>these results demonstrate that pentoxifylline very effectively inhibits cytokine production in acute pancreatitis.</p>\",\"PeriodicalId\":76421,\"journal\":{\"name\":\"Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie\",\"volume\":\"197 5\",\"pages\":\"293-9\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s004330050078\",\"citationCount\":\"24\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Research in experimental medicine. 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引用次数: 24
摘要
未标记:本研究的目的是测定急性坏死性胰腺炎诱导后的肿瘤坏死因子(TNF)和白细胞介素-6 (IL-6)水平,并确定己酮茶碱对细胞因子产生的影响。方法:雄性Wistar大鼠胰管逆行注射200微升牛磺胆酸诱导急性胰腺炎。测定血清淀粉酶活性、胰腺湿重/体重比及TNF、IL-6水平。术后6、12、24 h腹腔注射己酮茶碱7 mg/kg。分别于术后6、24、48、72 h处死大鼠。结果:TNF生物测定显示高水平的肿瘤坏死因子(30.2 + / - 5.4 U / ml, 35.0 + / - 5.0 U /毫升和36.6 + / - 6.0 U /毫升)在对照组6,24和48 h和20 U /毫升(54.1 + / - 10.9 + / - 4.2 U /毫升)pentoxifylline-treated组在6 - 24小时,分别而水平已经下降到零pentoxifylline-treated组48 h。il - 6生物测定同样表现出高水平的il - 6在对照组48 h和pentoxifylline-treated组在6 - 24小时,且在48 h时己酮茶碱处理组显著降低(7083 +/- 2844 pg/ml, 6463 +/- 1307 pg/ml, 10329 +/- 5571 pg/ml vs 137.5 +/- 85.5 pg/ml, P < 0.05)。胰腺炎组的高死亡率(43%)经己酮茶碱治疗降至11%。结论:己酮茶碱能有效抑制急性胰腺炎细胞因子的产生。
Beneficial effects of pentoxifylline treatment of experimental acute pancreatitis in rats.
Unlabelled: The purposes of this study were to determine the tumor necrosis factor (TNF) and interleukin-6 (IL-6) levels after the induction of acute necrotizing pancreatitis, and to establish the effects of pentoxifylline on cytokine production.
Methods: acute pancreatitis was induced by the retrograde injection of 200 microliters taurocholic acid into the pancreatic duct in male Wistar rats. The serum amylase activity, the wet pancreatic weight/body weight ratio, and the TNF and IL-6 levels were measured. Seven mg/kg pentoxifylline were administered intraperitoneally at the time of operation 6, 12 or 24 h later. Rats were killed 6, 24, 48 or 72 h after the operation.
Results: the TNF bioassay revealed high levels of TNF (30.2 +/- 5.4 U/ml, 35.0 +/- 5.0 U/ml and 36.6 +/- 6.0 U/ml) in the control group at 6, 24 and 48 h and (54.1 +/- 20 U/ml and 10.9 +/- 4.2 U/ml) in the pentoxifylline-treated group at 6 and 24 h, respectively, whereas the level had decreased to zero in the pentoxifylline-treated group at 48 h. The IL-6 bioassay likewise demonstrated high levels of IL-6 in the control group at 48 h and in the pentoxifylline-treated group at 6 and 24 h, and markedly decreased levels in the pentoxifylline-treated group at 48 h (7083 +/- 2844 pg/ml, 6463 +/- 1307 pg/ml, 10,329 +/- 5571 pg/ml vs 137.5 +/- 85.5 pg/ml, respectively, P < 0.05). The high mortality observed in the pancreatitis group (43%) was decreased by pentoxifylline administration to 11%.
Conclusion: these results demonstrate that pentoxifylline very effectively inhibits cytokine production in acute pancreatitis.