Beyond erectile dysfunction: cGMP-specific phosphodiesterase 5 inhibitors for other clinical disorders

A Samidurai, L Xi, A Das… - Annual review of …, 2023 - annualreviews.org
Cyclic guanosine monophosphate (cGMP), an important intracellular second messenger,
mediates cellular functional responses in all vital organs. Phosphodiesterase 5 (PDE5) is …

Mammalian cyclic nucleotide phosphodiesterases: molecular mechanisms and physiological functions

SH Francis, MA Blount, JD Corbin - Physiological reviews, 2011 - journals.physiology.org
The superfamily of cyclic nucleotide (cN) phosphodiesterases (PDEs) is comprised of 11
families of enzymes. PDEs break down cAMP and/or cGMP and are major determinants of …

Tissue injury and hypoxia promote malignant progression of prostate cancer by inducing CXCL13 expression in tumor myofibroblasts

M Ammirante, S Shalapour, Y Kang… - Proceedings of the …, 2014 - National Acad Sciences
Prostate cancer (PC) is a slowly progressing malignancy that often responds to androgen
ablation or chemotherapy by becoming more aggressive, acquiring a neuroendocrine …

Molecular control of luteal secretion of progesterone

GD Niswender - Reproduction, 2002 - rep.bioscientifica.com
Cholesterol provided by low-or high-density lipoprotein is the precursor for biosynthesis of
progesterone. Once inside the cell, cholesterol can be used for steroidogenesis or esterified …

[HTML][HTML] Anti-fibrotic effects of soluble guanylate cyclase stimulators and activators: A review of the preclinical evidence

P Sandner, JP Stasch - Respiratory medicine, 2017 - Elsevier
It is now well established that the NO-sGC-cGMP signal transduction system mediates many
different physiological functions in almost every conceivable organ system; this has been …

Latest evidence on the use of phosphodiesterase type 5 inhibitors for the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia

M Gacci, KE Andersson, C Chapple, M Maggi… - European urology, 2016 - Elsevier
Context Several preclinical reports, randomized controlled trials, systematic reviews, and
posthoc analyses corroborate the role of phosphodiesterase type 5 inhibitors (PDE5-Is) in …

Stimulation of the soluble guanylate cyclase (sGC) inhibits fibrosis by blocking non-canonical TGFβ signalling

C Beyer, C Zenzmaier, K Palumbo-Zerr… - Annals of the …, 2015 - ard.bmj.com
Objectives We have previously described the antifibrotic role of the soluble guanylate
cyclase (sGC). The mode of action, however, remained elusive. In the present study, we …

Novel drug targets for the pharmacotherapy of benign prostatic hyperplasia (BPH)

S Ventura, VL Oliver, CW White, JH Xie… - British journal of …, 2011 - Wiley Online Library
Benign prostatic hyperplasia (BPH) is the major cause of lower urinary tract symptoms in
men aged 50 or older. Symptoms are not normally life threatening, but often drastically affect …

Tadalafil for the treatment of benign prostatic hyperplasia

FZ Mónica, G De Nucci - Expert opinion on pharmacotherapy, 2019 - Taylor & Francis
Introduction: In men, lower urinary tract symptoms (LUTS) are primarily attributed to benign
prostatic hyperplasia (BPH). Therapeutic options are targeted to relax prostate smooth …

Mechanism of action of phosphodiesterase type 5 inhibition in metabolic syndrome‐associated prostate alterations: An experimental study in the rabbit

A Morelli, P Comeglio, S Filippi, E Sarchielli… - The …, 2013 - Wiley Online Library
Abstract BACKGROUND Phosphodiesterase type 5 (PDE5) inhibitors improve benign
prostatic hyperplasia (BPH)‐related lower urinary tract symptoms (LUTS), often associated …