Laboratory of Genetic Metabolic Diseases, Academic Medical Center at the University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
J Lipid Res. 2009 Nov;50(11):2139-47. doi: 10.1194/jlr.R900009-JLR200. Epub 2009 Apr 8.
It is well established that peroxisomes play a crucial role in de novo bile acid synthesis. Studies in patients with a peroxisomal disorder have been indispensable for the elucidation of the precise role of peroxisomes. Several peroxisomal disorders are associated with distinct bile acid abnormalities and each disorder has a characteristic pattern of abnormal bile acids that accumulate, which is often used for diagnostic purposes. The patients have also been important for determining the pathophysiological consequences of defects in bile acid biosynthesis. In this review, we will discuss all the peroxisomal steps involved in bile acid synthesis and the bile acid abnormalities in patients with peroxisomal disorders. We will show the results of bile acid measurements in several tissues from patients, including brain, and we will discuss the toxicity and the pathological effects of the abnormal bile acids.
众所周知,过氧化物酶体在从头合成胆汁酸中起着至关重要的作用。过氧化物酶体疾病患者的研究对于阐明过氧化物酶体的确切作用是不可或缺的。几种过氧化物酶体疾病与明显的胆汁酸异常有关,每种疾病都有其特征性的异常胆汁酸堆积模式,常用于诊断目的。这些患者对于确定胆汁酸生物合成缺陷的病理生理后果也很重要。在这篇综述中,我们将讨论参与胆汁酸合成的所有过氧化物酶体步骤以及过氧化物酶体疾病患者的胆汁酸异常。我们将展示来自患者包括大脑在内的几种组织中的胆汁酸测量结果,并讨论异常胆汁酸的毒性和病理影响。