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维生素D合成与代谢缺陷。

Defects in the synthesis and metabolism of vitamin D.

作者信息

Holick M F

机构信息

Vitamin D, Skin and Bone Research Laboratory, Boston University Medical Center, MA 02118, USA.

出版信息

Exp Clin Endocrinol Diabetes. 1995;103(4):219-27. doi: 10.1055/s-0029-1211354.

Abstract

It is now recognized that it is casual exposure to sunlight that provides most humans with their vitamin D requirement. During exposure to sunlight, the high energy ultraviolet B photons (290-315 mm) photolyzes cutaneous stores of 7-dehydrocholesterol to previtamin D3. Once formed, previtamin D3 undergoes a thermal isomerization that results in the formation of vitamin D3. Vitamin D3 is biologically inert and requires successive hydroxylations in the liver and kidney to form its biologically active hormone 1,25-dihydroxyvitamin D3. The major physiologic function of 1,25-dihydroxy-vitamin D3 is to maintain blood calcium in the normal range. It accomplishes this by increasing the efficiency of intestinal calcium absorption and mobilizing stem cells to become osteoclasts which, in turn, remove calcium from the bone. It is now recognized that there are a variety of calcium metabolic disorders that are related to defects in the synthesis and metabolism of vitamin D. Chronic granulomatous disorders are often associated with hypercalciuria and hypercalcemia. The mechanism by which this occurs is that activated macrophages within granulomatous tissue, in an unregulated manner, convert 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D. Besides its calcemic activity 1,25-dihydroxyvitamin D3 is a potent antiproliferative factor for cells and tissues that possess its vitamin D receptor. This has clinical utility in that 1,25-dihydroxyvitamin D3 and its analogs have been successfully used for the treatment of the hyperproliferative skin disease psoriasis.

摘要

现在人们认识到,正是偶尔暴露在阳光下满足了大多数人对维生素D的需求。在阳光照射期间,高能紫外线B光子(290 - 315纳米)将皮肤中的7 - 脱氢胆固醇储存光解为前维生素D3。一旦形成,前维生素D3会发生热异构化,从而形成维生素D3。维生素D3在生物学上是无活性的,需要在肝脏和肾脏中连续羟化才能形成其具有生物活性的激素1,25 - 二羟基维生素D3。1,25 - 二羟基维生素D3的主要生理功能是将血钙维持在正常范围内。它通过提高肠道对钙的吸收效率并动员干细胞成为破骨细胞来实现这一点,而破骨细胞反过来又从骨骼中去除钙。现在人们认识到,有多种钙代谢紊乱与维生素D的合成和代谢缺陷有关。慢性肉芽肿性疾病常与高钙尿症和高钙血症相关。其发生机制是肉芽肿组织内活化的巨噬细胞以不受调控的方式将25 - 羟基维生素D转化为1,25 - 二羟基维生素D。除了其血钙活性外,1,25 - 二羟基维生素D3对具有其维生素D受体的细胞和组织是一种有效的抗增殖因子。这在临床上具有实用性,因为1,25 - 二羟基维生素D3及其类似物已成功用于治疗增殖性皮肤病银屑病。

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