Metabolites | |
Clinically Important Features of Porphyrin and Heme Metabolism and the Porphyrias | |
Siddesh Besur2  Weihong Hou1  Paul Schmeltzer2  Herbert L. Bonkovsky3  | |
[1] Department of Research and the Liver, Digestive, and Metabolic Disorders Laboratory, Carolinas HealthCare System, Charlotte, NC 28203, USA; E-Mail:;Department of Medicine and Center for Liver Disease, Carolinas HealthCare System, Charlotte, NC 28204, USA; E-Mail:;Department of Medicine, Universities of CT, Farmington, CT 06030 and North Carolina, Chapel Hill, NC 27599, USA; E-Mail: | |
关键词: 5-aminolevulinic acid; heme; iron; metalloporphyrins; mitochondria; porphobilinogen; porphyrias; porphyrins; | |
DOI : 10.3390/metabo4040977 | |
来源: mdpi | |
【 摘 要 】
Heme, like chlorophyll, is a primordial molecule and is one of the fundamental pigments of life. Disorders of normal heme synthesis may cause human diseases, including certain anemias (X-linked sideroblastic anemias) and porphyrias. Porphyrias are classified as hepatic and erythropoietic porphyrias based on the organ system in which heme precursors (5-aminolevulinic acid (ALA), porphobilinogen and porphyrins) are chiefly overproduced. The hepatic porphyrias are further subdivided into acute porphyrias and chronic hepatic porphyrias. The acute porphyrias include acute intermittent, hereditary copro-, variegate and ALA dehydratase deficiency porphyria. Chronic hepatic porphyrias include porphyria cutanea tarda and hepatoerythropoietic porphyria. The erythropoietic porphyrias include congenital erythropoietic porphyria (Gűnther’s disease) and erythropoietic protoporphyria. In this review, we summarize the key features of normal heme synthesis and its differing regulation in liver
【 授权许可】
CC BY
© 2014 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
Files | Size | Format | View |
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RO202003190020074ZK.pdf | 336KB | download |