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多发性对称性脂肪瘤病:肾上腺素能刺激的脂肪分解缺陷。

Multiple symmetric lipomatosis: a defect in adrenergic-stimulated lipolysis.

作者信息

Enzi G, Inelmen E M, Baritussio A, Dorigo P, Prosdocimi M, Mazzoleni F

出版信息

J Clin Invest. 1977 Dec;60(6):1221-9. doi: 10.1172/JCI108881.

Abstract

The cellularity of normal and lipomatous adipose tissue and its response to different lipolytic agents have been studied in a group of 10 patients with multiple symmetric lipomatosis (MSL). In MSL patients, fat cells from lipomatous tissue are smaller than normal, uninvolved adipocytes. Fat cells from lipomata show minimal variations in size following conspicuous increase of lipomatous masses. These findings suggest that the growth of lipomata can be attributed to the neoformation of adipocytes rather than to an enlargement in the single fat cells. The incidence of reduced glucose tolerance and of hyperlipoproteinemia is similar in MSL patients and in controls. A significant reduction in plasma free fatty acids was observed in MSL patients after a 24-h fast as well as after noradrenaline infusion. A specific insensitivity of lipomatous tissue to the lipolytic effect of noradrenaline and isoprenaline was observed in vitro, as indicated by glycerol release in the medium, whereas response to theophylline and to dibutyryl cyclic AMP was retained. The lipolytic response to catecholamines was retained. The lipolytic response to catecholamines was normal in the nonlipomatous adipose tissue of MSL patients. In basal conditions ATP concentrations were similar in normal and in lipomatous adipose tissue. However, incubation with noradrenaline induced a significant fall in intracellular ATP levels in normal tissue, whereas no variations were observed in lipomatous tissue. Theophylline, instead, induced a prompt and significant decrease in intracellular ATP levels in lipomatous tissue. These observations indicate that the block in catecholamine-stimulated lipolysis in lipomatous tissue of MSL patients can be localized at a level preceding the formation of cyclic AMP.

摘要

在一组10例多发性对称性脂肪瘤病(MSL)患者中,研究了正常脂肪组织和脂肪瘤样脂肪组织的细胞构成及其对不同脂解剂的反应。在MSL患者中,脂肪瘤样组织中的脂肪细胞比正常未受累的脂肪细胞小。脂肪瘤中的脂肪细胞在脂肪瘤块明显增大后,大小变化极小。这些发现表明,脂肪瘤的生长可归因于脂肪细胞的新形成,而非单个脂肪细胞的增大。MSL患者和对照组中糖耐量降低和高脂蛋白血症的发生率相似。在MSL患者中,禁食24小时以及输注去甲肾上腺素后,血浆游离脂肪酸显著降低。体外实验观察到,脂肪瘤样组织对去甲肾上腺素和异丙肾上腺素的脂解作用具有特异性不敏感性,这可通过培养基中甘油的释放来表明,而对茶碱和二丁酰环磷酸腺苷的反应则得以保留。对儿茶酚胺的脂解反应得以保留。MSL患者非脂肪瘤样脂肪组织对儿茶酚胺的脂解反应正常。在基础条件下,正常脂肪组织和脂肪瘤样脂肪组织中的ATP浓度相似。然而,与去甲肾上腺素一起孵育会导致正常组织中细胞内ATP水平显著下降,而脂肪瘤样组织中未观察到变化。相反,茶碱会导致脂肪瘤样组织中细胞内ATP水平迅速且显著下降。这些观察结果表明,MSL患者脂肪瘤样组织中儿茶酚胺刺激的脂解受阻可能发生在环磷酸腺苷形成之前的水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ae/372478/e3ca2473fd6b/jcinvest00660-0002-a.jpg

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