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Obesity, metabolic syndrome, adipocytes and vascular function: A holistic viewpoint

机译:肥胖,代谢综合征,脂肪细胞和血管功能:整体观点

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Summary: 1. Obesity is a metabolic disease of pandemic proportions largely arising from positive energy balance, a consequence of sedentary lifestyle, conditioned by environmental and genetic factors. Several central and peripheral neurohumoral factors (the major ones being the anorectic adipokines leptin and adiponecin and the orexigenic gut hormone ghrelin) acting on the anorectic (pro-opiomelanocortin and cocaine- and amphetamine-regulated transcript) and orexigenic (neuropeptide Y and agouti gene-related protein) neurons regulate energy balance. These neurons, mainly in the arcuate nucleus of the hypothalamus, project to parts of the brain modulating functions such as wakefulness, autonomic function and learning. A tilt in the anorectic-orexigenic balance, perhaps determined genetically, leads to obesity.2. Excess fat deposition requires space, created by adipocyte (hypertrophy and hyperplasia) and extracellular matrix (ECM) remodelling. This process is regulated by several factors, including several adipocyte-derived Matrix metalloproteinases and the adipokine cathepsin, which degrades fibronectin, a key ECM protein. Excess fat, also deposited in visceral organs, generates chronic low-grade inflammation that eventually triggers insulin resistance and the associated comorbidities of metabolic syndrome (hypertension, atherosclerosis, dyslipidaemia and diabetes mellitus).3. The perivascular adipose tissue (PVAT) has conventionally been considered non-physiological structural tissue, but has recently been shown to serve a paracrine function, including the release of adipose-derived relaxant and contractile factors, akin to the role of the vascular endothelium. Thus, PVAT regulates vascular function in vivo and in vitro, contributing to the cardiovascular pathophysiology of the metabolic syndrome. Defining the mechanism of PVAT regulation of vascular reactivity requires more and better controlled investigations than currently seen in the literature.
机译:总结:1。肥胖是大流行性比例的代谢疾病,主要来自积极的能量平衡,久坐不动的生活方式,由环境和遗传因素调节。几种中枢和外周神经胃部因子(主要是患有症状脂肪因子瘦素和己二烯素的脂肪蛋白和甲己酮肠道旋风素),作用于肛肠酸(Pro-Omiomelanocortin和可卡因和疗法调节的转录物)和orexigenic(神经肽Y和Agouti基因 - 相关蛋白质)神经元调节能量平衡。这些神经元主要在下丘脑的弧形核,项目到部分脑调制功能,如醒来,自主功能和学习。在肛交 - 甲虫平衡中的倾斜,也许在遗传上确定,导致肥胖症。过量的脂肪沉积需要空间,由脂肪细胞(肥大和增生)和细胞外基质(ECM)重塑产生。该方法由几个因素调节,包括几种脂肪细胞衍生的基质金属蛋白酶和己酮组成蛋白酶,其降低纤连蛋白,一种关键的ECM蛋白。过量的脂肪,也沉积在内脏器官中,产生慢性低级炎症,最终触发胰岛素抵抗和代谢综合征(高血压,动脉粥样硬化,血脂血症和糖尿病患者)的相关性抗性.3。血管外脂肪组织(PVAT)通常被认为是非生理结构组织,但最近已被证明为帕拉卡碱功能,包括释放脂肪衍生的弛缓性和收缩因子,类似于血管内皮的作用。因此,PVAT调节体内和体外血管功能,有助于代谢综合征的心血管病理学生理学。定义PVAT调节的机制血管反应性需要越来越好控制的调查,而不是文献中的目前。

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