Benign prostatic hyperplasia (BPH) is characterized by stromal cell proliferation and contraction of the periurethral smooth muscle, causing lower urinary tract symptoms. Current BPH treatment, based on monotherapy with α1A-adrenoceptor antagonists, is helpful for many patients but insufficient for others, and recent reports suggest that stimulation of α1D-adrenoceptors and 5-HT1A receptors contribute to cell proliferation.
Here, we investigated the potential of three N-phenylpiperazine derivatives - LDT3, LDT5 and LDT8 - as multi-target antagonists of BPH-associated receptors. The affinity and efficacy of LDTs were estimated in isometric contraction and competition binding assays using tissues (prostate and aorta) and brain membrane samples enriched in specific on- or off-target receptors. LDTs potency was estimated in intracellular Ca(2+) elevation assays using cells overexpressing human α1-adrenoceptors subtypes. The anti-proliferative effect of LDTs on prostate cells from BPH patients was evaluated by viable cell counting and MTT assays. We also determined LDTs effects on rat intraurethral and arterial pressure. LDT3 and LDT5 are potent antagonists of α1A-, α1D-adrenoceptors and 5-HT1A receptors (Ki values in the nanomolar range), and fully inhibited phenylephrine- and 5-HT-induced proliferation of BPH cells. In vivo, LDT3 and LDT5 fully blocked the increase of intraurethral pressure induced by phenylephrine at doses (ED50 of 0. 15 and 0. 09 µg. kg(-1), respectively) without effect on basal mean blood pressure. LDT3 and LDT5 are multi-target antagonists of key receptors in BPH, and are capable of triggering both prostate muscle relaxation and human hyperplastic prostate cell growth inhibition in vitro. Thus, LDT3 and LDT5 represent potential new lead compounds for BPH treatment.
The Journal of pharmacology and experimental therapeutics. 2015 Oct 22 [Epub ahead of print]
Jessica B Nascimento-Viana, Aline R Carvalho, Luiz Eurico Nasciutti, Rocio Alcantara-Hernandez, Fernanda Chagas-Silva, Pedro A R de Souza, Luiz A Romeiro, J Adolfo Garcia-Sainz, Francois Noel, Claudia L M Silva
Federal University of Rio de Janeiro;, Federal University of Rio de Janeiro;, Federal University of Rio de Janeiro;, Universidad Nacional Autonoma de Mexico;, Federal University of Rio de Janeiro;, Federal University of Rio de Janeiro;, Brasilia University;, Univerdidad Nacional Autonoma de Mexico. , Federal University of Rio de Janeiro;, Federal University of Rio de Janeiro;