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胰岛素通过细胞间黏附分子-1的表面表达增强视网膜微循环中白细胞与内皮细胞的黏附。

Insulin enhances leukocyte-endothelial cell adhesion in the retinal microcirculation through surface expression of intercellular adhesion molecule-1.

作者信息

Hirata Fumisato, Yoshida Munenori, Niwa Yuji, Okouchi Masahiro, Okayama Naotsuka, Takeuchi Yoshiyuki, Itoh Makoto, Ogura Yuichiro

机构信息

Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Mizuho-ku, Nagoya, Aichi 4678601, Japan.

出版信息

Microvasc Res. 2005 May;69(3):135-41. doi: 10.1016/j.mvr.2005.03.002.

Abstract

The purpose of this study was to evaluate the effects of insulin on leukocyte-endothelial cell adhesion in the retinal microcirculation in vitro and in vivo. Human retinal endothelial cells (HRECs) were cultured in medium with or without insulin, and neutrophils allowed to adhere. Adherent neutrophils were quantified by measuring myeloperoxidase activity. Surface expression of endothelial adhesion molecules were studied with the use of an enzyme immunoassay. Insulin at concentrations of 50 and 100 microU/ml significantly increased neutrophil adhesion to HRECs compared with the control cells (P < 0.01, respectively). Surface expression of intercellular adhesion molecule-1 (ICAM-1) significantly increased when HRECs were exposed to 100 microU/ml insulin, as compared with the control cells (P < 0.05). Anti-ICAM-1 antibody significantly inhibited neutrophils adhesion to HRECs (P < 0.0001). Brown-Norway rats received subcutaneous injection of 0.2 U per 100 g body weight insulin three times. Control rats received the same amount of phosphate-buffered saline. Leukocyte entrapment in the retina was evaluated using acridine orange leukocyte fluorography. The number of leukocytes trapped in the retina of insulin-treated rats was significantly elevated compared with that in the control animals (P < 0.0001). These results suggested that insulin enhances leukostasis in retinal microcirculation. Hyperinsulinemia may be a risk factor of retinal microcirculatory disturbances.

摘要

本研究的目的是评估胰岛素在体外和体内对视网膜微循环中白细胞 - 内皮细胞黏附的影响。将人视网膜内皮细胞(HRECs)培养于含或不含胰岛素的培养基中,并使中性粒细胞黏附。通过测量髓过氧化物酶活性对黏附的中性粒细胞进行定量。使用酶免疫测定法研究内皮黏附分子的表面表达。与对照细胞相比,浓度为50和100微单位/毫升的胰岛素显著增加了中性粒细胞对HRECs的黏附(P分别<0.01)。与对照细胞相比,当HRECs暴露于100微单位/毫升胰岛素时,细胞间黏附分子-1(ICAM-1)的表面表达显著增加(P<0.05)。抗ICAM-1抗体显著抑制中性粒细胞对HRECs的黏附(P<0.0001)。将Brown-Norway大鼠按每100克体重皮下注射0.2单位胰岛素,共注射三次。对照大鼠注射等量的磷酸盐缓冲盐水。使用吖啶橙白细胞荧光造影术评估视网膜中的白细胞滞留情况。与对照动物相比,胰岛素处理大鼠视网膜中滞留的白细胞数量显著增加(P<0.0001)。这些结果表明胰岛素增强了视网膜微循环中的白细胞淤滞。高胰岛素血症可能是视网膜微循环障碍的一个危险因素。

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