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角质细胞生长因子基因治疗改善大鼠溃疡性结肠炎。

Keratinocyte growth factor gene therapy ameliorates ulcerative colitis in rats.

机构信息

Department of Pharmaceutical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.

出版信息

World J Gastroenterol. 2011 Jun 7;17(21):2632-40. doi: 10.3748/wjg.v17.i21.2632.

Abstract

AIM

To investigate the effect of keratinocyte growth factor (KGF) gene therapy in acetic acid-induced ulcerative colitis in rat model.

METHODS

The colitis of Sprague-Dawley rats was induced by intrarectal infusion of 1 mL 5% (v/v) acetic acid. Twenty-four hours after exposed to acetic acid, rats were divided into three experimental groups: control group, attenuated Salmonella typhimurium Ty21a strain (SP) group and SP strain carrying human KGF gene (SPK) group, and they were separately administered orally with 10% NaHCO(3), SP or SPK. Animals were sacrificed and colonic tissues were harvested respectively on day 3, 5, 7 and 10 after administration. Weights of rats, colonic weight/length ratio and stool score were evaluated. Histological changes of colonic tissues were examined by hematoxylin and eosin (HE) staining method. The expression of KGF, KGF receptor (KGFR) and TNF-α were measured either by enzyme-linked immunosorbent assay or Western blotting. Immunohistochemistry was used to detect the cellular localization of KGFR and Ki67. In addition, superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in the homogenate were measured.

RESULTS

Body weight and colonic weight/length ratio were declined in SPK group compared with SP and control groups (body weight: 272.78 ± 17.92 g vs 243.72 ± 14.02 g and 240.68 ± 12.63 g, P < 0.01; colonic weight/length ratio: 115.76 ± 7.47 vs 150.32 ± 5.99 and 153.67 ± 5.50 mg/cm, P < 0.01). Moreover, pathological changes of damaged colon were improved in SPK group as well. After administration of SPK strain, KGF expression increased markedly from the 3rd d, and remained at a high level till the 10th d. Furthermore, KGFR expression and Ki67 expression elevated, whereas TNF-α expression was inhibited in SPK group. In the group administered with SPK, SOD activity increased significantly (d 5: 26.18 ± 5.84 vs 18.12 ± 3.30 and 18.79 ± 4.74 U/mg, P < 0.01; d 7: 35.48 ± 3.35 vs 22.57 ± 3.44 and 21.69 ± 3.94 U/mg, P < 0.01; d 10: 46.10 ± 6.23 vs 25.35 ± 4.76 and 27.82 ± 6.42 U/mg, P < 0.01) and MDA contents decreased accordingly (d 7: 7.40 ± 0.88 vs 9.81 ± 1.21 and 10.45 ± 1.40 nmol/mg, P < 0.01; d 10: 4.36 ± 0.62 vs 8.41 ± 0.92 and 8.71 ± 1.27 nmol/mg, P < 0.01), compared with SP and control groups.

CONCLUSION

KGF gene therapy mediated by attenuated Salmonella ameliorates ulcerative colitis induced by acetic acids, and it may be a safe and effective treatment for ulcerative colitis.

摘要

目的

研究角质细胞生长因子(KGF)基因治疗对乙酸诱导的溃疡性结肠炎大鼠模型的影响。

方法

通过直肠内输注 1ml 5%(v/v)乙酸诱导 Sprague-Dawley 大鼠结肠炎。在暴露于乙酸 24 小时后,大鼠被分为三组:对照组、减毒鼠伤寒沙门氏菌 Ty21a 株(SP)组和携带人 KGF 基因的 SP 株(SPK)组,分别口服 10%碳酸氢钠、SP 或 SPK。在给药后第 3、5、7 和 10 天分别处死动物并采集结肠组织。评估大鼠体重、结肠重/长比和粪便评分。通过苏木精和伊红(HE)染色法观察结肠组织的组织学变化。通过酶联免疫吸附试验或 Western blot 法测定 KGF、KGF 受体(KGFR)和 TNF-α的表达。免疫组化法检测 KGFR 和 Ki67 的细胞定位。此外,还测量了匀浆中超氧化物歧化酶(SOD)活性和丙二醛(MDA)含量。

结果

与 SP 和对照组相比,SPK 组大鼠体重和结肠重/长比下降(体重:272.78±17.92 g 比 243.72±14.02 g 和 240.68±12.63 g,P<0.01;结肠重/长比:115.76±7.47 vs 150.32±5.99 和 153.67±5.50 mg/cm,P<0.01)。此外,SPK 组受损结肠的病理变化也有所改善。SPK 菌株给药后,KGF 表达明显增加,第 3 天开始,一直保持在较高水平,直至第 10 天。此外,KGFR 表达和 Ki67 表达升高,而 TNF-α表达受到抑制。在给予 SPK 组中,SOD 活性显著增加(第 5 天:26.18±5.84 vs 18.12±3.30 和 18.79±4.74 U/mg,P<0.01;第 7 天:35.48±3.35 vs 22.57±3.44 和 21.69±3.94 U/mg,P<0.01;第 10 天:46.10±6.23 vs 25.35±4.76 和 27.82±6.42 U/mg,P<0.01),MDA 含量相应降低(第 7 天:7.40±0.88 vs 9.81±1.21 和 10.45±1.40 nmol/mg,P<0.01;第 10 天:4.36±0.62 vs 8.41±0.92 和 8.71±1.27 nmol/mg,P<0.01),与 SP 和对照组相比。

结论

减毒鼠伤寒沙门氏菌介导的 KGF 基因治疗可改善乙酸诱导的溃疡性结肠炎,可能是溃疡性结肠炎安全有效的治疗方法。

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