PT  - JOURNAL ARTICLE
AU  - Jerzy Barankiewicz
AU  - Anne M. Danks
AU  - Elie Abushanab
AU  - Lewis Makings
AU  - Torsten Wiemann
AU  - Roi Ann Wallis
AU  - Palle V. P. Pragnacharyulu
AU  - Anthony Fox
AU  - Paul J. Marangos
TI  - Regulation of Adenosine Concentration and Cytoprotective Effects of Novel Reversible Adenosine Deaminase Inhibitors
DP  - 1997 Dec 01
TA  - Journal of Pharmacology and Experimental Therapeutics
PG  - 1230--1238
VI  - 283
IP  - 3
4099  - http://jpet.aspetjournals.org/content/283/3/1230.short
4100  - http://jpet.aspetjournals.org/content/283/3/1230.full
SO  - J Pharmacol Exp Ther1997 Dec 01; 283
AB  - The physiological role of adenosine (Ado) is well known. Although a number of pharmacological attempts have been made to manipulate Ado concentrations in ischemic conditions in different tissues, none have been clinically accepted up to now, mostly due to insufficient elevation of Ado concentrations or unacceptable toxicity. In this study, we evaluated the biochemical and pharmacological actions of several novel erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA) analogs to identify new reversible adenosine deaminase (ADA) inhibitors with potential clinical utility. In cell culture experiments, these compounds elevate cellular Ado concentrations under conditions of simulated ischemic stress but very little, if any, under normoxic conditions. Two compounds were selected for study: 9′-chloro-EHNA (CPC-405) and 9′-phthalimido-EHNA (CPC-406), which specifically inhibit ADA in cell-free preparations as well as in intact cells. CPC-405 and CPC-406 do not affect adenosine kinase activity, and they do not affect adenosine transport (influx). CPC-405 and CPC-406 are also more potent than EHNA in elevating adenosine release from human astrocytoma cells and bovine heart microvascular endothelial cells in 2-deoxyglucose-simulated ischemia or under anaerobic conditions. Inhibition of adenosine deaminase by CPC-405 or CPC-406, as well as the 2′-deoxyadenosine toxicity expressed in the presence of these ADA inhibitors, is reversed when the inhibitors are removed by washing the cells. In the isolated rat heart model of ischemia, these novel ADA inhibitors showed enhanced recovery of left ventricular end-diastolic pressure, left ventricular developed pressure, +dP/dtmaxand −dP/dtmax. In the rat hippocampal slice model of hypoxia, these compounds also showed neuroprotective effects on CA1 hypoxic injury. In conclusion, these novel ADA inhibitors may represent clinically useful Ado elevating compounds that show cardioprotective, as well as neuroprotective, effects. Also, their potential for immunotoxicity, if any, appears to be transient in nature, representing an important clinical advantage compared with tight-binding ADA inhibitors such as deoxycoformycin. The American Society for Pharmacology and Experimental Therapeutics