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黏附分子在腹膜硬化进展中的作用。

Role of adhesion molecules in the progression of peritoneal sclerosis.

作者信息

Imai Hiroe, Nakamoto Hidetomo, Fukushima Rie, Ishida Yuji, Yamanouchi Yasuhiro, Suzuki Hiromichi

机构信息

Department of Nephrology, Saitama Medical School, Saitama, Japan.

出版信息

Adv Perit Dial. 2003;19:180-5.

Abstract

To investigate the role of adhesion molecules [intracellular adhesion molecule 1 (ICAM-1), vascular cell adhesion molecule 1 (VCAM-1), and integrin alpha 5 beta 1] in the progression of encapsulating peritoneal sclerosis (EPS) under peritoneal dialysis, we examined changes in the expression of those adhesion molecules in Wistar-Kyoto (WKY) rats treated with acidic dialysis solution with or without angiotensin II type 1a receptor blocker (ARB). We divided 48 WKY rats into 4 groups and dialyzed them with various solutions as follows: (1) pH 7 1.5% glucose dialysis solution (control group, n = 12); (2) pH 3.5 1.5% glucose dialysis solution (EPS group, n = 12); (3) pH 3.5 1.5% glucose dialysis solution, plus oral administration of CS866 5 mg/kg daily (ARB group, n = 12); and (4) pH 3.5 1.5% glucose dialysis solution, plus oral administration of amlodipine (CA group, n = 12). We injected the dialysis solutions into the abdominal cavity and administered the ARB and CA daily for 42 days. On days 3, 7, 14, and 42, three rats in each group were humanely killed by decapitation, and we studied the expression of adhesion molecules in peritoneum by the immunofluorescence method. In the EPS rats, expression of adhesion molecules was observed in peritoneum on day 3 after start of acidic solution treatment, in conjunction with an increment of interleukin 6 (IL-6) in the dialysate. The peritoneum of EPS rats showed peritoneal fibrosis with interstitial cell infiltration. Treatment with ARB significantly suppressed expression of adhesion molecules in the peritoneum and suppressed peritoneal fibrosis. Treatment with a neutral solution induced no peritoneal fibrosis nor expression of adhesion molecules in the peritoneum. Our results suggest that adhesion molecules play an important role in the progression of peritoneal fibrosis and resultant EPS. Treatment with ARB prevents the progression of peritoneal fibrosis and suppresses expression of adhesion molecules in the peritoneum.

摘要

为研究黏附分子[细胞间黏附分子1(ICAM-1)、血管细胞黏附分子1(VCAM-1)和整合素α5β1]在腹膜透析下包裹性腹膜硬化(EPS)进展中的作用,我们检测了给予或未给予1a型血管紧张素II受体阻滞剂(ARB)的酸性透析液处理的Wistar-Kyoto(WKY)大鼠中这些黏附分子表达的变化。我们将48只WKY大鼠分为4组,并用不同溶液进行透析,如下:(1)pH 7的1.5%葡萄糖透析液(对照组,n = 12);(2)pH 3.5的1.5%葡萄糖透析液(EPS组,n = 12);(3)pH 3.5的1.5%葡萄糖透析液,加每日口服CS866 5 mg/kg(ARB组,n = 12);(4)pH 3.5的1.5%葡萄糖透析液,加每日口服氨氯地平(CA组,n = 12)。我们将透析液注入腹腔,并每日给予ARB和CA,持续42天。在第3、7、14和42天,每组处死3只大鼠,通过免疫荧光法研究腹膜中黏附分子的表达。在EPS大鼠中,酸性溶液处理开始后第3天,腹膜中观察到黏附分子的表达,同时透析液中白细胞介素6(IL-6)增加。EPS大鼠的腹膜显示腹膜纤维化伴间质细胞浸润。ARB治疗显著抑制腹膜中黏附分子的表达并抑制腹膜纤维化。用中性溶液处理未诱导腹膜纤维化,腹膜中也未出现黏附分子的表达。我们的结果表明,黏附分子在腹膜纤维化及由此导致的EPS进展中起重要作用。ARB治疗可预防腹膜纤维化的进展并抑制腹膜中黏附分子的表达。

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