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Sex-based differences in phagocyte metabolic profile in rats with monosodium glutamate-induced obesity

机译:谷氨酸钠诱发的肥胖大鼠吞噬细胞代谢特征的性别差异

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摘要

The important component of obesity pathogenesis is inflammatory activation of innate immune cells within adipose tissue and in other body locations. Both the course of obesity and innate immune reactivity are characterized by sex-associated differences. The aim of the work was a comparative investigation of metabolic profiles of phagocytes from different locations in male and female rats with MSG-induced obesity. The administration of monosodium glutamate (MSG) caused obesity, with sex-associated differences, that was more severe in male rats. Obesity was associated with pro-inflammatory activation of CD14+ phagocytes from adipose tissue in female, but not in male rats, which was demonstrated by decreased phagocytosis activity along with increased ROS generation. Phagocytes from the peritoneal cavity and peripheral blood of obese female rats exhibited neutral metabolic profile, whereas those cells from obese male rats displayed a pro-inflammatory metabolic profile. Thus, the manifestation of obesity-induced inflammation was characterized by different patterns of metabolic profile of phagocytes in male and female rats. Identified immune cell characteristics expand our knowledge of obesity immunobiology and may help to develop more effective preventive and therapeutic interventions for obese patients of different sexes.
机译:肥胖病发病机制的重要组成部分是脂肪组织内和其他身体部位的先天免疫细胞的炎症激活。肥胖的过程和先天性免疫反应性均以性别相关差异为特征。这项工作的目的是对雄性和雌性MSG肥胖大鼠不同部位吞噬细胞的代谢谱进行比较研究。施用谷氨酸钠(MSG)会导致肥胖,并且存在与性别相关的差异,这种肥胖在雄性大鼠中更为严重。肥胖与雌性大鼠脂肪组织中CD14 +吞噬细胞的促炎性激活有关,而雄性大鼠则不如此,这通过吞噬作用活性降低和ROS生成增加来证明。肥胖雌性大鼠腹膜腔和外周血的吞噬细胞表现出中性代谢特征,而肥胖雄性大鼠的那些细胞表现出促炎性代谢特征。因此,肥胖引起的炎症表现的特征是在雄性和雌性大鼠中吞噬细胞的代谢模式不同。鉴定出的免疫细胞特征扩展了我们对肥胖症免疫生物学的知识,并可能有助于为不同性别的肥胖患者开发更有效的预防和治疗干预措施。

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