1,5-Bis(4-amidinophenoxy) pentane (pentamidine) is a potent inhibitor of [3H]idazoxan binding to imidazoline I2 binding sites

• Published in: European journal of pharmacology 1998-07, Vol.353 (1), p.97-103
• Main Authors: WOOD, D. H, HALL, J. E, ROSE, B. G, TIDWELL, R. R
• Format: Article
• Language: English
• Subjects: Animals; Antibacterial agents; Antibiotics. Antiinfectious agents. Antiparasitic agents; Antifungal Agents - chemistry; Antifungal Agents - pharmacology; Binding, Competitive; Biological and medical sciences; Drug Evaluation, Preclinical; Idazoxan - metabolism; Imidazoles - antagonists & inhibitors; Imidazoles - metabolism; Imidazoline Receptors; Ligands; Liver - drug effects; Liver - metabolism; Male; Medical sciences; Membranes; Pentamidine - analogs & derivatives; Pentamidine - chemistry; Pentamidine - pharmacology; Pharmacology. Drug treatments; Pneumonia, Pneumocystis - drug therapy; Radioligand Assay; Rats; Rats, Sprague-Dawley; Receptors, Drug - drug effects; Receptors, Drug - metabolism; Structure-Activity Relationship
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/S0014-2999(98)00386-0

The aromatic diamidine 1,5-bis(4-amidinophenoxy)pentane (pentamidine) is used for treatment and prophylaxis of Pneumocystis carinii pneumonia in patients with Acquired Immune Deficiency Syndrome. Clinical use of pentamidine has been restricted by significant toxicity, that includes hypotension, and hypoglycemia. Although clinical toxicity is well described, the mechanisms are still poorly understood. Competitive binding analyses using [3H]idazoxan as the radioligand, and cirazoline to define non-specific binding, demonstrate that pentamidine binds to an imidazoline I2 binding site on rat liver membranes with a Ki of 1.4+/-0.22 nM. The Ki indicates that pentamidine inhibits radioligand binding at imidazoline I2 sites with an affinity approximating the most potent known ligands and may be related to pentamidine toxicity. Moreover, pentamidine analogs inhibit radioligand binding with a range of affinities that vary according to their structure. Two candidate drugs, Compounds 5 and 6, are more active than pentamidine in the corticosteroid-suppressed rat model of P. carinii pneumonia, yet have different affinities for the imidazoline I2 site (Ki 5 = 50.1+/-1.06 nM and Ki 6 = approximately 3500 nM). Affinity for this site does not correlate with antimicrobial activity (r = 0.60; p = 0.09) or the calculated log of the octanol:water partition coefficient (ClogP) (r = -0.38; p = 0.22).