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丹吉尔病:脂质储存的一种解释。

Tangier disease: one explanation of lipid storage.

作者信息

Herbert P N, Forte T, Heinen R J, Fredrickson D S

出版信息

N Engl J Med. 1978 Sep 7;299(10):519-21. doi: 10.1056/NEJM197809072991005.

Abstract

Normal high-density lipoproteins are absent from plasma in Tangier disease, and the disorder is characterized by accumulation of cholesteryl esters in several tissues, particularly those of the reticuloendothelial system. Electron microscopy of the abnormal high-density lipoproteins in the plasma of three patients with Tangier diseases revealed large (68-nm), flattened, translucent particles in all cases. These particles were most abundant in the plasma of the splenectomized patient. Restriction of dietary fat eliminated or drastically reduced the numbers of these particles among the Tangier high-density lipoproteins. Thus abnormal products of chylomicron metabolism that appear to occur in plasma in this disorder may be targets for phagocytosis and may be at least one source of the cholesteryl esters that accumulate in reticuloendothelial tissues in Tangier disease.

摘要

丹吉尔病患者的血浆中不存在正常的高密度脂蛋白,该病症的特征是胆固醇酯在多个组织中蓄积,尤其是网状内皮系统的组织。对三名丹吉尔病患者血浆中异常高密度脂蛋白进行电子显微镜检查发现,所有病例中均有大的(68纳米)、扁平的、半透明颗粒。这些颗粒在脾切除患者的血浆中最为丰富。限制饮食中的脂肪可消除或大幅减少丹吉尔高密度脂蛋白中这些颗粒的数量。因此,在这种病症中似乎出现在血浆中的乳糜微粒代谢异常产物可能是吞噬作用的靶点,并且可能至少是丹吉尔病网状内皮组织中蓄积的胆固醇酯的一个来源。

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