{"title":"氨基类固醇U74389G在炎症性肠病大鼠模型中的作用","authors":"P. Krastev, A. Blazhev, G. Stavreva","doi":"10.2478/jbcr-2021-0018","DOIUrl":null,"url":null,"abstract":"Summary Lazaroid U-74389G is a synthetic 21-aminosteroid with free radical-scavenging and anti-inflammatory effects. This study was designed to evaluate the anti-inflammatory activity of U-74389G on experimental 2,4-dinitrobenzene sulfonic acid hydrate (DNBS)-induced colitis in Wistar rats. Five experimental groups were formed: a sham control group, a control group, treated with 0.25 ml of 50% ethanol intrarectally (n=8), a group treated with DNBS (30 mg in 0.25 ml of 50% ethanol administered intrarectally, (n=8), a group treated with DNBS and U-74389G at a daily dose of 15 mg/kg i.p. (n=8), and a group treated with DNBS and sulfasalazine, orally, at a dose of 300 mg/kg. During the experiment, the bodyweight of the rats, food intake, stool consistency, and presence of blood in the stool were recorded as markers of clinical condition. On day 6, colonic tissues were excised and scored for macroscopic and histological damage. Blood samples were taken to measure levels of cytokines by ELISA methods. DNBS decreased significantly body weight (from 237.00±2.52 g to 212.50±6.25 g, p=0.04). The rats treated with U-74389G showed greater food intake and weight gain. U-74389G reduced ulceration index: the U-74389G score was 1.25±0.25, and the DNBS score –3.87±0.61; p<0.05. All other macroscopic parametersassessed were significantly improved in rats treated with U-74389G. The levels of inflammatory cytokines IL-1, IL-6, and TNF-α, were significantly lower than those of the DNBS group, while U-74389G significantly elevated the level of anti-inflammatory IL-10. These findings indicate that U-74389G significantly inhibits colonic inflammatory damages in a rat model of inflammatory bowel disease.","PeriodicalId":15099,"journal":{"name":"Journal of Biomedical and Clinical Research","volume":"27 1","pages":"131 - 139"},"PeriodicalIF":0.0000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of Aminosteroid U74389G in a Model of Inflammatory Bowel Disease in Rats\",\"authors\":\"P. Krastev, A. Blazhev, G. Stavreva\",\"doi\":\"10.2478/jbcr-2021-0018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Summary Lazaroid U-74389G is a synthetic 21-aminosteroid with free radical-scavenging and anti-inflammatory effects. This study was designed to evaluate the anti-inflammatory activity of U-74389G on experimental 2,4-dinitrobenzene sulfonic acid hydrate (DNBS)-induced colitis in Wistar rats. Five experimental groups were formed: a sham control group, a control group, treated with 0.25 ml of 50% ethanol intrarectally (n=8), a group treated with DNBS (30 mg in 0.25 ml of 50% ethanol administered intrarectally, (n=8), a group treated with DNBS and U-74389G at a daily dose of 15 mg/kg i.p. (n=8), and a group treated with DNBS and sulfasalazine, orally, at a dose of 300 mg/kg. During the experiment, the bodyweight of the rats, food intake, stool consistency, and presence of blood in the stool were recorded as markers of clinical condition. On day 6, colonic tissues were excised and scored for macroscopic and histological damage. Blood samples were taken to measure levels of cytokines by ELISA methods. DNBS decreased significantly body weight (from 237.00±2.52 g to 212.50±6.25 g, p=0.04). The rats treated with U-74389G showed greater food intake and weight gain. U-74389G reduced ulceration index: the U-74389G score was 1.25±0.25, and the DNBS score –3.87±0.61; p<0.05. All other macroscopic parametersassessed were significantly improved in rats treated with U-74389G. The levels of inflammatory cytokines IL-1, IL-6, and TNF-α, were significantly lower than those of the DNBS group, while U-74389G significantly elevated the level of anti-inflammatory IL-10. 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引用次数: 0
摘要
Lazaroid U-74389G是一种具有清除自由基和抗炎作用的合成21-氨基类固醇。本研究旨在评价U-74389G对实验性2,4-二硝基苯磺酸水合(DNBS)诱导的Wistar大鼠结肠炎的抗炎作用。实验分为5组:假对照组、对照组(0.25 ml 50%乙醇)直肠内给药(n=8)、DNBS (30 mg,加入0.25 ml 50%乙醇)直肠内给药(n=8)、DNBS和U-74389G(每日15 mg/kg i.p)治疗组(n=8)、DNBS和柳氮磺胺嘧啶(300 mg/kg)口服治疗组(n=8)。在实验过程中,记录大鼠的体重、食物摄入量、粪便稠度和粪便中是否有血作为临床状况的标志。第6天,切除结肠组织并进行宏观和组织学损伤评分。采用ELISA法测定血清细胞因子水平。DNBS显著降低体重(由237.00±2.52 g降至212.50±6.25 g, p=0.04)。用U-74389G治疗的大鼠表现出更大的食物摄入量和体重增加。U-74389G降低溃疡指数:U-74389G评分为1.25±0.25,DNBS评分为-3.87±0.61;p < 0.05。U-74389G对大鼠的其他宏观指标均有显著改善。炎症因子IL-1、IL-6、TNF-α水平显著低于DNBS组,而抗炎因子IL-10水平则显著升高。这些结果表明,U-74389G显著抑制炎症性肠病大鼠模型的结肠炎症损伤。
Effect of Aminosteroid U74389G in a Model of Inflammatory Bowel Disease in Rats
Summary Lazaroid U-74389G is a synthetic 21-aminosteroid with free radical-scavenging and anti-inflammatory effects. This study was designed to evaluate the anti-inflammatory activity of U-74389G on experimental 2,4-dinitrobenzene sulfonic acid hydrate (DNBS)-induced colitis in Wistar rats. Five experimental groups were formed: a sham control group, a control group, treated with 0.25 ml of 50% ethanol intrarectally (n=8), a group treated with DNBS (30 mg in 0.25 ml of 50% ethanol administered intrarectally, (n=8), a group treated with DNBS and U-74389G at a daily dose of 15 mg/kg i.p. (n=8), and a group treated with DNBS and sulfasalazine, orally, at a dose of 300 mg/kg. During the experiment, the bodyweight of the rats, food intake, stool consistency, and presence of blood in the stool were recorded as markers of clinical condition. On day 6, colonic tissues were excised and scored for macroscopic and histological damage. Blood samples were taken to measure levels of cytokines by ELISA methods. DNBS decreased significantly body weight (from 237.00±2.52 g to 212.50±6.25 g, p=0.04). The rats treated with U-74389G showed greater food intake and weight gain. U-74389G reduced ulceration index: the U-74389G score was 1.25±0.25, and the DNBS score –3.87±0.61; p<0.05. All other macroscopic parametersassessed were significantly improved in rats treated with U-74389G. The levels of inflammatory cytokines IL-1, IL-6, and TNF-α, were significantly lower than those of the DNBS group, while U-74389G significantly elevated the level of anti-inflammatory IL-10. These findings indicate that U-74389G significantly inhibits colonic inflammatory damages in a rat model of inflammatory bowel disease.