TY - JOUR
T1 - Nitric oxide/redox-based signalling as a therapeutic target for penile disorders
AU - Burnett, Arthur L.
AU - Musicki, Biljana
AU - Jin, Liming
AU - Bivalacqua, Trinity J.
N1 - Funding Information:
This work is gratefully supported by the National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Diseases Grants DK-02568 and DK-67223 (to AL Burnett), the National Kidney Foundation–Maryland Professional Development Award (to B Musicki) and the American Heart Association National Center Grant 0530007N (to L Jin).
PY - 2006/6
Y1 - 2006/6
N2 - Oxidative and/or nitrosative stress is implicated in the pathogeneses of assorted penile disorders of clinical significance, notably erectile dysfunction, priapism and penile fibrosis. It is becoming increasingly recognised that the generation and activity of reactive oxygen and nitrogen species in the penis influence vascular homeostasis of this organ, with adverse effects exerted at cellular and molecular levels. Furthermore, these elements may interact with molecular signalling pathways operating in the penis, modulating their functional roles. This interaction in particular suggests that by accessing molecular targets associated with oxidative/nitrosative stress in the penis, new pharmacotherapeutic approaches may be developed to promote normal erectile ability and preserve erectile tissue health. This notion pertains to, but also extends beyond, interventions which predictably target components of the nitric oxide-based signal transduction pathway for the on-demand treatment of erectile dysfunction. The next line of pharmaceuticals for disorders of the penis, in general, may well spawn from an integrative understanding of the complex regulatory interactions influenced by, as well as influencing nitric oxide signalling in this organ.
AB - Oxidative and/or nitrosative stress is implicated in the pathogeneses of assorted penile disorders of clinical significance, notably erectile dysfunction, priapism and penile fibrosis. It is becoming increasingly recognised that the generation and activity of reactive oxygen and nitrogen species in the penis influence vascular homeostasis of this organ, with adverse effects exerted at cellular and molecular levels. Furthermore, these elements may interact with molecular signalling pathways operating in the penis, modulating their functional roles. This interaction in particular suggests that by accessing molecular targets associated with oxidative/nitrosative stress in the penis, new pharmacotherapeutic approaches may be developed to promote normal erectile ability and preserve erectile tissue health. This notion pertains to, but also extends beyond, interventions which predictably target components of the nitric oxide-based signal transduction pathway for the on-demand treatment of erectile dysfunction. The next line of pharmaceuticals for disorders of the penis, in general, may well spawn from an integrative understanding of the complex regulatory interactions influenced by, as well as influencing nitric oxide signalling in this organ.
KW - Erectile dysfunction
KW - Guanylate cyclase activator
KW - Nitric oxide synthase (NOS)
KW - Nitrosative stress
KW - Oxidative stress
KW - Penile fibrosis
KW - Phosphodiesterase type 5 inhibitor (PDE-5)
KW - Priapism
KW - Reactive nitrogen species (RNS)
KW - Reactive oxygen species (ROS)
KW - Signal transduction
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U2 - 10.1517/14728222.10.3.445
DO - 10.1517/14728222.10.3.445
M3 - Review article
C2 - 16706684
AN - SCOPUS:33745479208
SN - 1472-8222
VL - 10
SP - 445
EP - 457
JO - Expert Opinion on Therapeutic Targets
JF - Expert Opinion on Therapeutic Targets
IS - 3
ER -