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Effect of genistein on basal jejunal chloride secretion in R117H CF mice is sex and route specific

机译:金雀异黄素对R117H CF小鼠基础空肠氯化物分泌的影响是性别和途径特异性的

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摘要

Cystic fibrosis (CF) results from the loss or reduction in function of the CFTR (cystic fibrosis transmembrane conductance regulatory protein) chloride channel. The third most common CFTR mutation seen clinically is R117H. Genistein, a naturally occurring phytoestrogen, is known to stimulate CFTR function in vitro. We aimed to determine whether route of administration of genistein could mediate differential effects in R117H male and female CF mice. Mice were fed (4 weeks) or injected subcutaneously (1 week) with the following: genistein 600 mg/kg diet (600Gd); genistein-free diet (0Gd); genistein injection 600 mg/kg body weight (600Gi); dimethyl sulfoxide control (0Gi). In male R117H mice fed 600Gd, basal short circuit current (Isc) was unchanged. In 600Gd-fed female mice, there was a subgroup that demonstrated a significant increase in basal Isc (53.14±7.92 μA/cm2, n=6, P<0.05) and a subgroup of nonresponders (12.05±6.59 μA/cm2, n=4), compared to 0Gd controls (29.3±6.5 μA/cm2, n=7). In R117H mice injected with 600Gi, basal Isc was unchanged in both male and female mice compared to 0Gi controls. Isc was measured in response to the following: the adenylate cyclase activator forskolin (10 μM, bilateral), bumetanide (100 μM, basolateral) to indicate the Cl secretory component, and acetazolamide (100 μM, bilateral) to indicate the HCO3 secretory component; however, there was no effect of genistein (diet or injection) on any of these parameters. Jejunal morphology (ie, villi length, number of goblet cells per villus, crypt depth, and number of goblet cells per crypt) in R117H mice suggested no genistein-mediated difference among the groups. Serum levels of genistein were significantly elevated, compared to respective controls, by either 600Gd (equally elevated in males and females) or 600Gi (elevated more in females versus males). These data suggest a sex-dependent increase in basal Isc of R117H mice and that the increase is also specific for route of administration.
机译:囊性纤维化(CF)是由CFTR(囊性纤维化跨膜电导调节蛋白)氯化物通道功能的丧失或减少导致的。临床上常见的第三大CFTR突变是R117H。金雀异黄素是一种天然存在的植物雌激素,已知可在体外刺激CFTR功能。我们旨在确定染料木黄酮的给药途径是否可以介导R117H雄性和雌性CF小鼠的差异作用。给小鼠喂食(4周)或皮下注射(1周)以下药物:染料木黄酮600 mg / kg饮食(600Gd);无染料木素饮食(0Gd);金雀异黄素注射液600 mg / kg体重(600Gi);二甲基亚砜对照(0Gi)。在饲喂600Gd的雄性R117H小鼠中,基础短路电流(Isc)不变。在600Gd喂养的雌性小鼠中,有一个亚组显示基础Isc显着增加(53.14±7.92μA/ cm 2 ,n = 6,P <0.05),一个无响应的亚组(12.05)。与0Gd对照(29.3±6.5μA/ cm 2 ,n = 7)相比,±6.59μA/ cm 2 ,n = 4)。在注射600Gi的R117H小鼠中,与0Gi对照相比,雄性和雌性小鼠的基础Isc均未改变。测量Isc的反应如下:腺苷酸环化酶激活剂福司可林(10μM,双侧),布美他尼(100μM,基底侧)表示Cl -分泌成分,以及乙酰唑胺(100μM,双侧) )表示HCO3 -分泌成分;但是,染料木黄酮(饮食或注射)对这些参数均无影响。 R117H小鼠的空肠形态(即绒毛长度,每个绒毛的杯状细胞数量,隐窝深度和每个隐窝的杯状细胞数量)表明各组之间没有染料木素介导的差异。与相应对照组相比,金雀异黄素的血清水平显着升高了600Gd(男性和女性均升高)或600Gi(女性与男性相比升高了更多)。这些数据表明R117H小鼠基础Isc的性别依赖性增加,并且该增加也对给药途径具有特异性。

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