Oxidative stress associated with middle aging leads to sympathetic hyperactivity and downregulation of soluble guanylyl cyclase in corpus cavernosum.

Impairment of nitric oxide (NO)-mediated cavernosal relaxations in middle age contributes to erectile dysfunction. However, little information is available about the alterations of sympathetic neurotransmission and contraction in erectile tissue at middle age. This study aimed to evaluate the alterations of the contractile machinery associated with tyrosine hydroxylase (TH) in rat corpus cavernosum (RCC) at middle age, focusing on the role of superoxide anion. Male Wistar young (3.5-mo) and middle-aged (10-mo) rats were used. Electrical-field stimulation (EFS)- and phenylephrine-induced contractions were obtained in RCC strips. Levels of reactive-oxygen species (ROS) and TH mRNA expression, as well as protein expressions for α₁/β₁-subunits of soluble guanylyl cyclase (sGC), in RCC were evaluated. The neurogenic contractile responses elicited by EFS (4-32 Hz) were greater in RCC from the middle-aged group that was accompanied by elevated TH mRNA expression (P < 0.01). Phenylephrine-induced contractions were also greater in the middle-aged group. A 62% increase in ROS generation in RCC from middle-aged rats was observed. The mRNA expression for the α₁A-adrenoceptor remained unchanged among groups. Protein levels of α₁/β₁-sGC subunits were decreased in RCC from the middle-aged compared with young group. The NADPH oxidase inhibitor apocynin (85 mg·rat(-1)·day(-1), 4 wk) fully restored the enhanced ROS production, TH mRNA expressions, and α₁/β₁-subunit sGC expression, indicating that excess of superoxide anion plays a major role in the sympathetic hyperactivity and hypercontractility in erectile tissue at middle age. Reduction of oxidative stress by dietary antioxidants may be an interesting approach to treat erectile dysfunction in aging population.

[1]  Kaiyu Wang,et al.  Improvement of Pharmacokinetics Behavior of Apocynin by Nitrone Derivatization: Comparative Pharmacokinetics of Nitrone-Apocynin and its Parent Apocynin in Rats , 2013, PloS one.

[2]  P. Kadowitz,et al.  The sGC activator BAY 60-2770 has potent erectile activity in the rat. , 2013, American journal of physiology. Heart and circulatory physiology.

[3]  F. Priviero,et al.  Superoxide anion production by NADPH oxidase plays a major role in erectile dysfunction in middle-aged rats: prevention by antioxidant therapy. , 2013, The journal of sexual medicine.

[4]  Z. Ye,et al.  Apocynin improves erectile function in diabetic rats through regulation of NADPH oxidase expression. , 2012, The journal of sexual medicine.

[5]  A. Papapetropoulos,et al.  Soluble guanylyl cyclase is a target of angiotensin II-induced nitrosative stress in a hypertensive rat model. , 2012, American journal of physiology. Heart and circulatory physiology.

[6]  P. Brum,et al.  Increased Vascular Contractility and Oxidative Stress in β2-Adrenoceptor Knockout Mice: The Role of NADPH Oxidase , 2012, Journal of Vascular Research.

[7]  A. Senbel,et al.  Evaluation of vitamin E in the treatment of erectile dysfunction in aged rats. , 2012, Life sciences.

[8]  J. Stasch,et al.  Cinaciguat, a novel activator of soluble guanylate cyclase, protects against ischemia/reperfusion injury: role of hydrogen sulfide. , 2012, American journal of physiology. Heart and circulatory physiology.

[9]  K. Andersson Mechanisms of Penile Erection and Basis for Pharmacological Treatment of Erectile Dysfunction , 2011, Pharmacological Reviews.

[10]  H. Macarthur,et al.  Neuronal and non‐neuronal modulation of sympathetic neurovascular transmission , 2011, Acta physiologica.

[11]  M. Saad,et al.  High‐fat diet associated with obesity induces impairment of mouse corpus cavernosum responses , 2011, BJU international.

[12]  A. Burnett,et al.  eNOS-uncoupling in age-related erectile dysfunction , 2011, International Journal of Impotence Research.

[13]  S. N. Murthy,et al.  Pulmonary and systemic vasodilator responses to the soluble guanylyl cyclase activator, BAY 60-2770, are not dependent on endogenous nitric oxide or reduced heme. , 2011, American journal of physiology. Heart and circulatory physiology.

[14]  A. S. Alves,et al.  Tyrosine hydroxylase immunoreactivity as indicator of sympathetic activity: simultaneous evaluation in different tissues of hypertensive rats. , 2011, American journal of physiology. Regulatory, integrative and comparative physiology.

[15]  A. Burnett,et al.  Hypercholesterolemia-induced erectile dysfunction: endothelial nitric oxide synthase (eNOS) uncoupling in the mouse penis by NAD(P)H oxidase. , 2010, The journal of sexual medicine.

[16]  Y. Kitamura,et al.  Altered function of nitrergic nerves inhibiting sympathetic neurotransmission in mesenteric vascular beds of renovascular hypertensive rats , 2010, Hypertension Research.

[17]  J. Galligan,et al.  Localization of NADPH oxidase in sympathetic and sensory ganglion neurons and perivascular nerve fibers , 2009, Autonomic Neuroscience.

[18]  N. Villalba,et al.  Differential structural and functional changes in penile and coronary arteries from obese Zucker rats. , 2009, American journal of physiology. Heart and circulatory physiology.

[19]  J. Stasch,et al.  Nitric oxide-independent vasodilator rescues heme-oxidized soluble guanylate cyclase from proteosomal degradation , 2009, Circulation research.

[20]  N. Hayashi,et al.  Role of N-terminus of tyrosine hydroxylase in the biosynthesis of catecholamines , 2009, Journal of Neural Transmission.

[21]  D. Paterson,et al.  l-arginine supplementation reduces cardiac noradrenergic neurotransmission in spontaneously hypertensive rats , 2008, Journal of molecular and cellular cardiology.

[22]  A. Ergul,et al.  DOCA-salt treatment enhances responses to endothelin-1 in murine corpus cavernosum. , 2008, Canadian journal of physiology and pharmacology.

[23]  A. Burnett,et al.  NADPH oxidase activation: a mechanism of hypertension-associated erectile dysfunction. , 2008, The journal of sexual medicine.

[24]  R. Busse,et al.  Apocynin Is Not an Inhibitor of Vascular NADPH Oxidases but an Antioxidant , 2008, Hypertension.

[25]  E. Inscho,et al.  Adenosine actions are preserved in corpus cavernosum from obese and type II diabetic db/db mouse. , 2005, The journal of sexual medicine.

[26]  W. Woodward,et al.  Postinfarct sympathetic hyperactivity differentially stimulates expression of tyrosine hydroxylase and norepinephrine transporter. , 2008, American journal of physiology. Heart and circulatory physiology.

[27]  H. Macarthur,et al.  Oxidative stress attenuates NO-induced modulation of sympathetic neurotransmission in the mesenteric arterial bed of spontaneously hypertensive rats. , 2008, American journal of physiology. Heart and circulatory physiology.

[28]  G. Angelini,et al.  Reactive oxygen species and erectile dysfunction: possible role of NADPH oxidase , 2007, International Journal of Impotence Research.

[29]  C. Roussos,et al.  Regulation of the expression of soluble guanylyl cyclase by reactive oxygen species , 2007 .

[30]  C. Roussos,et al.  Regulation of the expression of soluble guanylyl cyclase by reactive oxygen species , 2007, British journal of pharmacology.

[31]  O. V. Evgenov,et al.  NO-independent stimulators and activators of soluble guanylate cyclase: discovery and therapeutic potential , 2006, Nature Reviews Drug Discovery.

[32]  J. Stasch,et al.  Targeting the heme-oxidized nitric oxide receptor for selective vasodilatation of diseased blood vessels. , 2006, The Journal of clinical investigation.

[33]  Ferdinando Fusco,et al.  Pharmacology of erectile dysfunction in man. , 2006, Pharmacology & therapeutics.

[34]  Cleber E Teixeira,et al.  Vasorelaxing Effect of BAY 41-2272 in Rat Basilar Artery: Involvement of cGMP-Dependent and Independent Mechanisms , 2006, Hypertension.

[35]  J. Morrison,et al.  The effects of age and streptozotocin diabetes on the sympathetic innervation in the rat penis , 2006, Molecular and Cellular Biochemistry.

[36]  F. Priviero,et al.  MECHANISMS UNDERLYING RELAXATION OF RABBIT AORTA BY BAY 41‐2272, A NITRIC OXIDE‐INDEPENDENT SOLUBLE GUANYLATE CYCLASE ACTIVATOR , 2005, Clinical and experimental pharmacology & physiology.

[37]  U. Zabel,et al.  Reduced cGMP signaling associated with neointimal proliferation and vascular dysfunction in late-stage atherosclerosis. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[38]  R. Pickard,et al.  Physiology of erectile function. , 2004, The journal of sexual medicine.

[39]  H. Macarthur,et al.  Nitric oxide decreases the biological activity of norepinephrine resulting in altered vascular tone in the rat mesenteric arterial bed. , 2004, American journal of physiology. Heart and circulatory physiology.

[40]  J. Stasch,et al.  BAY 41-2272: A stimulator of soluble guanylyl cyclase induces NO-dependent penile erection in vivo , 2003 .

[41]  W. Hellstrom,et al.  Gene transfer of extracellular SOD to the penis reduces O2-* and improves erectile function in aged rats. , 2003, American journal of physiology. Heart and circulatory physiology.

[42]  S. Moncada,et al.  BAY41-2272, a novel nitric oxide independent soluble guanylate cyclase activator, relaxes human and rabbit corpus cavernosum in vitro. , 2003, The Journal of urology.

[43]  C. Stief,et al.  Cavernous and systemic plasma levels of norepinephrine and epinephrine during different penile conditions in healthy men and patients with erectile dysfunction. , 2002, Urology.

[44]  J. Jeremy,et al.  The effect of superoxide dismutase on nitric oxide‐mediated and electrical field‐stimulated diabetic rabbit cavernosal smooth muscle relaxation , 2001, BJU international.

[45]  S. Klöss,et al.  Aging and chronic hypertension decrease expression of rat aortic soluble guanylyl cyclase. , 2000, Hypertension.

[46]  M. Shores,et al.  Tyrosine hydroxylase mRNA is increased in old age and norepinephrine uptake transporter mRNA is decreased in middle age in locus coeruleus of Brown–Norway rats , 1999, Brain Research.

[47]  A. Matsumoto,et al.  Daily melatonin administration at middle age suppresses male rat visceral fat, plasma leptin, and plasma insulin to youthful levels. , 1999, Endocrinology.

[48]  S. Moncada,et al.  Nitrergic control of peripheral sympathetic responses in the human corpus cavernosum: a comparison with other species. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[49]  U. Förstermann,et al.  Endogenous and exogenous nitric oxide inhibits norepinephrine release from rat heart sympathetic nerves. , 1995, Circulation research.

[50]  G. Christ,et al.  Pharmacological studies of human erectile tissue: characteristics of spontaneous contractions and alterations in α‐adrenoceptor responsiveness with age and disease in isolated tissues , 1990, British journal of pharmacology.

[51]  R. Bahnson,et al.  Effect of local alpha-adrenergic blockade on human penile erection. , 1985, Journal of Urology.