4.5 Article

Pharmacology and Clinical Pharmacology of Methylarginines Used as Inhibitors of Nitric Oxide Synthases

Journal

CURRENT PHARMACEUTICAL DESIGN
Volume 20, Issue 22, Pages 3530-3547

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/13816128113196660750

Keywords

Asymmetric dimethylarginine (ADMA); Symmetric dimethylarginine (SDMA); Monomethylarginine (L-NMMA); Nitric oxide synthase (NOS); Dimethylarginine dimethylaminohydrolase (DDAH); Alanine-glyoxylate aminotransferase 2 (AGXT2)

Funding

  1. Interdisciplinary Center for Clinical Research [IZKF] of the Universitatsklinikum Erlangen [TP F02]

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The methylarginines asymmetric dimethylarginine (ADMA) and monomethylarginine (L-NMMA) are endogenously formed inhibitors of nitric oxide synthases (NOS), which have extensively been investigated as risk markers and used as pharmacological tools to study the L-arginine-nitric oxide (NO) pathway in vitro and in vivo. It is the aim of the present review to summarize the clinical and experimental data on the pharmacological properties that are of relevance when planning and conducting experiments and clinical studies involving methylarginines. Key pharmacodynamic and pharmacokinetic data including IC50 values of ADMA and L-NMMA for NOS isoforms and transport proteins, as well as metabolism by dimethylarginine dimethylaminohydrolases (DDAH1 and DDAH2) and alanine-glyoxylate aminotransferase 2 (AGXT2) are discussed.

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