Literature DB >> 9617493

Impairment of methylamine clearance in uremic patients and its nephropathological implications.

P H Yu1, R F Dyck.   

Abstract

The urinary levels of methylamine were analyzed by an HPLC/fluorometric method following derivatization of the amine with O-phthaldialdehyde (OPA). The excretion of methylamine in the uremic patients was found to be dramatically reduced. The impairment of clearance of methylamine explains why this amine was substantially increased in the serum of uremic patients. Increased deamination of methylamine would enhance formaldehyde and oxidative stresses, i.e. in the blood vessels, and cause vascular damage. This may be related to the increased risk of angiopathy associated with renal failure, and accelerate the progression of renal failure.

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Year:  1998        PMID: 9617493

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  2 in total

1.  Methylamine, but not ammonia, is hypophagic in mouse by interaction with brain Kv1.6 channel subtype.

Authors:  Renato Pirisino; Carla Ghelardini; Alessandra Pacini; Nicoletta Galeotti; Laura Raimondi
Journal:  Br J Pharmacol       Date:  2004-04-20       Impact factor: 8.739

Review 2.  Hepatic consequences of vascular adhesion protein-1 expression.

Authors:  Chris J Weston; David H Adams
Journal:  J Neural Transm (Vienna)       Date:  2011-04-22       Impact factor: 3.575

  2 in total

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