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Increased Expression of Pyloric ERβ Is Associated With Diabetic Gastroparesis in Streptozotocin-Induced Male Diabetic Rats

机译:链脲佐菌素诱导的雄性糖尿病大鼠中幽门ERβ表达增加与糖尿病性胃轻瘫相关。

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Background: Gastroparesis is a significant co-morbidity affecting up to 50% of patients with diabetes and is disproportionately found in women. Prior studies have suggested that loss of interstitial cells of Cajal, hyperglycemia, and nitric oxide dysfunction are potential causes of gastroparesis. Since diabetic gastroparesis affects more women than men, we performed an exploratory study with a diabetic rat model to determine if sex hormone signaling is altered in those where gastroparesis develops.Methods: We injected male rats with streptozotocin (STZ) to model type I diabetes, as confirmed by blood glucose levels. Gastroparesis was determined by acetaminophen gavage and serum acetaminophen levels. Rats were grouped based on acetaminophen and blood glucose data: diabetic (DM), diabetic and gastroparetic (DM + GP), and control (CM). Serum levels of testosterone, estrogen, and insulin were determined as well as aromatase expression in pyloric tissue and serum. Androgen receptor and estrogen receptor α (ERα) and β (ERβ) were also measured in the pylorus.Results: Compared to CM, estrogen increased and testosterone decreased in both DM and DM + GP rats. Sex hormone levels were not different between DM and DM + GP. Serum aromatase was increased in DM and DM + GP rats; however, pyloric tissue levels were not significantly different from controls. ERα was unchanged and androgen receptor decreased in DM and DM + GP. ERβ was increased only in DM + GP animals.Conclusion: Our study implicates increased pyloric ERβ in the development of gastroparesis in STZ-induced male diabetic rats. Increased serum aromatase is likely responsible for altered sex hormone levels. Our study supports the implication of sex hormone signaling in diabetic development and demonstrates a potential unique role for pyloric ERβ in male diabetic gastroparesis.Gastroenterol Res. 2016;9(2-3):39-46doi: http://dx.doi.org/10.14740/gr701w
机译:背景:胃轻瘫是一种严重的合并症,可影响多达50%的糖尿病患者,而且女性比例不高。先前的研究表明,Cajal间质细胞的丢失,高血糖症和一氧化氮功能障碍是胃轻瘫的潜在原因。由于糖尿病性胃轻瘫影响的女性多于男性,因此我们对糖尿病大鼠模型进行了探索性研究,以确定在发生胃轻瘫的人群中性激素信号传导是否发生了改变。方法:我们给雄性大鼠注射链脲佐菌素(STZ)来模拟I型糖尿病,如血糖水平所证实。通过对乙酰氨基酚管饲和血清对乙酰氨基酚水平测定胃轻瘫。根据对乙酰氨基酚和血糖数据对大鼠分组:糖尿病(DM),糖尿病和胃轻瘫(DM + GP)和对照组(CM)。测定血清中睾丸激素,雌激素和胰岛素的水平,以及幽门组织和血清中芳香化酶的表达。结果:与DM相比,DM和DM + GP大鼠的雌激素水平升高,睾丸激素水平下降。与幽门螺杆菌相比,雄激素受体和雌激素受体α(ERα)和β(ERβ)水平均升高。 DM和DM + GP之间的性激素水平没有差异。 DM和DM + GP大鼠血清芳香化酶升高;然而,幽门组织水平与对照组无显着差异。 DM和DM + GP中ERα不变,雄激素受体减少。 ERβ仅在DM + GP动物中增加。结论:我们的研究提示幽门ERβ增加与STZ诱导的雄性糖尿病大鼠胃轻瘫的发展有关。血清芳香化酶升高可能是性激素水平改变的原因。我们的研究支持性激素信号传导在糖尿病发展中的意义,并证明幽门ERβ在男性糖尿病性胃轻瘫中具有潜在的独特作用。 2016; 9(2-3):39-46doi:http://dx.doi.org/10.14740/gr701w

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