Abstract
The III(a) and III(b) electrophoretic variants of arylsulfatase A (EC 3.1.6.8) are 12 times more prevalent in alcoholic than in nonalcoholic populations. These variant enzymes, found in a subset of alcoholics, possess the pseudodeficient Asn360-Ser mutation of arylsulfatase A and, consequently, lack an N-linked glycan unit. These genetically determined variants of arylsulfatase A show reduced intracellular half-life, and cells from such individuals possess reduced enzymic activity. We propose that this polymorphism is an underlying genetic and biochemical factor contributing to the neuropathology and/or addiction pathway of this disease.
Original language | English (US) |
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Pages (from-to) | 228-233 |
Number of pages | 6 |
Journal | Alcoholism: Clinical and Experimental Research |
Volume | 20 |
Issue number | 2 |
DOIs | |
State | Published - 1996 |
All Science Journal Classification (ASJC) codes
- Medicine (miscellaneous)
- Toxicology
- Psychiatry and Mental health
Keywords
- Alcoholism
- Arylsulfatase A
- Metachromatic Leukodystrophy
- Pseudodeficiency