Prolonged Therapy with the Soluble Guanylyl Cyclase Activator BAY 60-2770 Restores the Erectile Function in Obese Mice

Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60-2770 reactivate the heme-oxidized sGC in vascular diseases. This study aimed to evaluate the effec...

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Published in:Journal of sexual medicine Vol. 11; no. 11; pp. 2661 - 2670
Main Authors: Silva, Fábio H., Leiria, Luiz O., Alexandre, Eduardo C., Davel, Ana Paula C., Mónica, Fabíola Z., De Nucci, Gilberto, Antunes, Edson
Format: Journal Article
Language:English
Published: Netherlands Elsevier Inc 01-11-2014
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Abstract Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60-2770 reactivate the heme-oxidized sGC in vascular diseases. This study aimed to evaluate the effects of 2-week oral intake with BAY 60-2270 on a murine model of obesity-associated ED. C57BL/6 male mice were fed for 12 weeks with standard chow or high-fat diet. Lean and obese mice were treated with BAY 60-2770 (1 mg/kg/day, 2 weeks). Measurements of intracavernosal pressure (ICP), along with acetylcholine (10−9 to 10−5 M) and electrical field stimulation (EFS; 4–10 Hz)-induced corpus cavernosum relaxations in vitro, were obtained. Levels of cyclic guanosine monophosphate (cGMP), reactive oxygen species (ROS), and sGC protein expressions in cavernosal tissues were measured. Cavernous nerve stimulation caused frequency-dependent ICP increases, which were significantly lower in obese compared with lean mice (P < 0.05). Two-week therapy with BAY 60-2770 fully reversed the decreased ICP in obese group. Acetylcholine-induced cavernosal relaxations were 45% lower (P < 0.001) in obese mice, which were fully restored by BAY 60-2770 treatment. Likewise, the EFS-induced relaxations in obese mice were restored by BAY 60-2770. Basal cGMP content in erectile tissue was 68% lower (P < 0.05) in obese mice, an effect normalized by BAY 60-2770. Levels of ROS were 52% higher (P < 0.05) whereas protein expression of α1 sGC subunit was reduced in cavernosal tissue of obese mice, both of which were normalized by BAY 60-2770. In lean group, BAY 60-2770 did not significantly affect any functional, biochemical, or molecular parameter analyzed. Two-week therapy with BAY 60-2770 restores the erectile function in obese mice that is associated with reduced ROS levels, up-regulation of α1 sGC subunit, and increased cGMP levels in the erectile tissue. Silva FH, Leiria LO, Alexandre EC, Davel APC, Mónica FZ, De Nucci G, and Antunes E. Prolonged therapy with the soluble guanylyl cyclase activator BAY 60-2770 restores the erectile function in obese mice. J Sex Med 2014;11:2661–2670.
AbstractList Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60-2770 reactivate the heme-oxidized sGC in vascular diseases. This study aimed to evaluate the effects of 2-week oral intake with BAY 60-2270 on a murine model of obesity-associated ED. C57BL/6 male mice were fed for 12 weeks with standard chow or high-fat diet. Lean and obese mice were treated with BAY 60-2770 (1 mg/kg/day, 2 weeks). Measurements of intracavernosal pressure (ICP), along with acetylcholine (10−9 to 10−5 M) and electrical field stimulation (EFS; 4–10 Hz)-induced corpus cavernosum relaxations in vitro, were obtained. Levels of cyclic guanosine monophosphate (cGMP), reactive oxygen species (ROS), and sGC protein expressions in cavernosal tissues were measured. Cavernous nerve stimulation caused frequency-dependent ICP increases, which were significantly lower in obese compared with lean mice (P < 0.05). Two-week therapy with BAY 60-2770 fully reversed the decreased ICP in obese group. Acetylcholine-induced cavernosal relaxations were 45% lower (P < 0.001) in obese mice, which were fully restored by BAY 60-2770 treatment. Likewise, the EFS-induced relaxations in obese mice were restored by BAY 60-2770. Basal cGMP content in erectile tissue was 68% lower (P < 0.05) in obese mice, an effect normalized by BAY 60-2770. Levels of ROS were 52% higher (P < 0.05) whereas protein expression of α1 sGC subunit was reduced in cavernosal tissue of obese mice, both of which were normalized by BAY 60-2770. In lean group, BAY 60-2770 did not significantly affect any functional, biochemical, or molecular parameter analyzed. Two-week therapy with BAY 60-2770 restores the erectile function in obese mice that is associated with reduced ROS levels, up-regulation of α1 sGC subunit, and increased cGMP levels in the erectile tissue. Silva FH, Leiria LO, Alexandre EC, Davel APC, Mónica FZ, De Nucci G, and Antunes E. Prolonged therapy with the soluble guanylyl cyclase activator BAY 60-2770 restores the erectile function in obese mice. J Sex Med 2014;11:2661–2670.
Introduction Cardiovascular and endocrine‐metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60‐2770 reactivate the heme‐oxidized sGC in vascular diseases. Aim This study aimed to evaluate the effects of 2‐week oral intake with BAY 60‐2270 on a murine model of obesity‐associated ED. Methods C57BL/6 male mice were fed for 12 weeks with standard chow or high‐fat diet. Lean and obese mice were treated with BAY 60‐2770 (1 mg/kg/day, 2 weeks). Main Outcome Measures Measurements of intracavernosal pressure (ICP), along with acetylcholine (10−9 to 10−5 M) and electrical field stimulation (EFS; 4–10 Hz)‐induced corpus cavernosum relaxations in vitro, were obtained. Levels of cyclic guanosine monophosphate (cGMP), reactive oxygen species (ROS), and sGC protein expressions in cavernosal tissues were measured. Results Cavernous nerve stimulation caused frequency‐dependent ICP increases, which were significantly lower in obese compared with lean mice (P < 0.05). Two‐week therapy with BAY 60‐2770 fully reversed the decreased ICP in obese group. Acetylcholine‐induced cavernosal relaxations were 45% lower (P < 0.001) in obese mice, which were fully restored by BAY 60‐2770 treatment. Likewise, the EFS‐induced relaxations in obese mice were restored by BAY 60‐2770. Basal cGMP content in erectile tissue was 68% lower (P < 0.05) in obese mice, an effect normalized by BAY 60‐2770. Levels of ROS were 52% higher (P < 0.05) whereas protein expression of α1 sGC subunit was reduced in cavernosal tissue of obese mice, both of which were normalized by BAY 60‐2770. In lean group, BAY 60‐2770 did not significantly affect any functional, biochemical, or molecular parameter analyzed. Conclusions Two‐week therapy with BAY 60‐2770 restores the erectile function in obese mice that is associated with reduced ROS levels, up‐regulation of α1 sGC subunit, and increased cGMP levels in the erectile tissue. Silva FH, Leiria LO, Alexandre EC, Davel APC, Mónica FZ, De Nucci G, and Antunes E. Prolonged therapy with the soluble guanylyl cyclase activator BAY 60‐2770 restores the erectile function in obese mice. J Sex Med 2014;11:2661–2670.
INTRODUCTIONCardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60-2770 reactivate the heme-oxidized sGC in vascular diseases.AIMThis study aimed to evaluate the effects of 2-week oral intake with BAY 60-2270 on a murine model of obesity-associated ED.METHODSC57BL/6 male mice were fed for 12 weeks with standard chow or high-fat diet. Lean and obese mice were treated with BAY 60-2770 (1 mg/kg/day, 2 weeks).MAIN OUTCOME MEASURESMeasurements of intracavernosal pressure (ICP), along with acetylcholine (10(-9) to 10(-5)  M) and electrical field stimulation (EFS; 4-10 Hz)-induced corpus cavernosum relaxations in vitro, were obtained. Levels of cyclic guanosine monophosphate (cGMP), reactive oxygen species (ROS), and sGC protein expressions in cavernosal tissues were measured.RESULTSCavernous nerve stimulation caused frequency-dependent ICP increases, which were significantly lower in obese compared with lean mice (P < 0.05). Two-week therapy with BAY 60-2770 fully reversed the decreased ICP in obese group. Acetylcholine-induced cavernosal relaxations were 45% lower (P < 0.001) in obese mice, which were fully restored by BAY 60-2770 treatment. Likewise, the EFS-induced relaxations in obese mice were restored by BAY 60-2770. Basal cGMP content in erectile tissue was 68% lower (P < 0.05) in obese mice, an effect normalized by BAY 60-2770. Levels of ROS were 52% higher (P < 0.05) whereas protein expression of α1 sGC subunit was reduced in cavernosal tissue of obese mice, both of which were normalized by BAY 60-2770. In lean group, BAY 60-2770 did not significantly affect any functional, biochemical, or molecular parameter analyzed.CONCLUSIONSTwo-week therapy with BAY 60-2770 restores the erectile function in obese mice that is associated with reduced ROS levels, up-regulation of α1 sGC subunit, and increased cGMP levels in the erectile tissue.
Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60-2770 reactivate the heme-oxidized sGC in vascular diseases. This study aimed to evaluate the effects of 2-week oral intake with BAY 60-2270 on a murine model of obesity-associated ED. C57BL/6 male mice were fed for 12 weeks with standard chow or high-fat diet. Lean and obese mice were treated with BAY 60-2770 (1 mg/kg/day, 2 weeks). Measurements of intracavernosal pressure (ICP), along with acetylcholine (10(-9) to 10(-5)  M) and electrical field stimulation (EFS; 4-10 Hz)-induced corpus cavernosum relaxations in vitro, were obtained. Levels of cyclic guanosine monophosphate (cGMP), reactive oxygen species (ROS), and sGC protein expressions in cavernosal tissues were measured. Cavernous nerve stimulation caused frequency-dependent ICP increases, which were significantly lower in obese compared with lean mice (P < 0.05). Two-week therapy with BAY 60-2770 fully reversed the decreased ICP in obese group. Acetylcholine-induced cavernosal relaxations were 45% lower (P < 0.001) in obese mice, which were fully restored by BAY 60-2770 treatment. Likewise, the EFS-induced relaxations in obese mice were restored by BAY 60-2770. Basal cGMP content in erectile tissue was 68% lower (P < 0.05) in obese mice, an effect normalized by BAY 60-2770. Levels of ROS were 52% higher (P < 0.05) whereas protein expression of α1 sGC subunit was reduced in cavernosal tissue of obese mice, both of which were normalized by BAY 60-2770. In lean group, BAY 60-2770 did not significantly affect any functional, biochemical, or molecular parameter analyzed. Two-week therapy with BAY 60-2770 restores the erectile function in obese mice that is associated with reduced ROS levels, up-regulation of α1 sGC subunit, and increased cGMP levels in the erectile tissue.
Abstract Introduction Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of soluble guanylyl cyclase (sGC) such as BAY 60-2770 reactivate the heme-oxidized sGC in vascular diseases. Aim This study aimed to evaluate the effects of 2-week oral intake with BAY 60-2270 on a murine model of obesity-associated ED. Methods C57BL/6 male mice were fed for 12 weeks with standard chow or high-fat diet. Lean and obese mice were treated with BAY 60-2770 (1 mg/kg/day, 2 weeks). Main Outcome Measures Measurements of intracavernosal pressure (ICP), along with acetylcholine (10−9 to 10−5 M) and electrical field stimulation (EFS; 4–10 Hz)-induced corpus cavernosum relaxations in vitro, were obtained. Levels of cyclic guanosine monophosphate (cGMP), reactive oxygen species (ROS), and sGC protein expressions in cavernosal tissues were measured. Results Cavernous nerve stimulation caused frequency-dependent ICP increases, which were significantly lower in obese compared with lean mice (P < 0.05). Two-week therapy with BAY 60-2770 fully reversed the decreased ICP in obese group. Acetylcholine-induced cavernosal relaxations were 45% lower (P < 0.001) in obese mice, which were fully restored by BAY 60-2770 treatment. Likewise, the EFS-induced relaxations in obese mice were restored by BAY 60-2770. Basal cGMP content in erectile tissue was 68% lower (P < 0.05) in obese mice, an effect normalized by BAY 60-2770. Levels of ROS were 52% higher (P < 0.05) whereas protein expression of α1 sGC subunit was reduced in cavernosal tissue of obese mice, both of which were normalized by BAY 60-2770. In lean group, BAY 60-2770 did not significantly affect any functional, biochemical, or molecular parameter analyzed. Conclusions Two-week therapy with BAY 60-2770 restores the erectile function in obese mice that is associated with reduced ROS levels, up-regulation of α1 sGC subunit, and increased cGMP levels in the erectile tissue.
Author Leiria, Luiz O.
Davel, Ana Paula C.
Silva, Fábio H.
De Nucci, Gilberto
Alexandre, Eduardo C.
Mónica, Fabíola Z.
Antunes, Edson
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  surname: Silva
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  givenname: Luiz O.
  surname: Leiria
  fullname: Leiria, Luiz O.
  organization: Department of Pharmacology, Faculty of Medical Sciences, University of Campinas, Campinas, Brazil
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  givenname: Eduardo C.
  surname: Alexandre
  fullname: Alexandre, Eduardo C.
  organization: Department of Pharmacology, Faculty of Medical Sciences, University of Campinas, Campinas, Brazil
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  givenname: Ana Paula C.
  surname: Davel
  fullname: Davel, Ana Paula C.
  organization: Department of Anatomy, Cellular Biology, Physiology and Biophysics, Institute of Biology, University of Campinas, Campinas, Brazil
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  givenname: Fabíola Z.
  surname: Mónica
  fullname: Mónica, Fabíola Z.
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  organization: Department of Pharmacology, Faculty of Medical Sciences, University of Campinas, Campinas, Brazil
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  givenname: Edson
  surname: Antunes
  fullname: Antunes, Edson
  email: edson.antunes@uol.com.br, antunes@fcm.unicamp.br
  organization: Department of Pharmacology, Faculty of Medical Sciences, University of Campinas, Campinas, Brazil
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Issue 11
Keywords Erectile Dysfunction
Obesity
Reactive Oxygen Species
Oxidative Stress
Corpus Cavernosum
Cyclic GMP
Intracavernous Pressure
Language English
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SSID ssj0033332
Score 2.2526813
Snippet Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED). Activators of...
Introduction Cardiovascular and endocrine‐metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED)....
Abstract Introduction Cardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction...
INTRODUCTIONCardiovascular and endocrine-metabolic diseases associated with increased oxidative stress such as obesity lead to erectile dysfunction (ED)....
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SubjectTerms Animals
Benzoates - administration & dosage
Biphenyl Compounds - administration & dosage
Corpus Cavernosum
Cyclic GMP
Cyclic GMP - metabolism
Diet, High-Fat - adverse effects
Enzyme Activators - administration & dosage
Erectile Dysfunction
Erectile Dysfunction - drug therapy
Erectile Dysfunction - enzymology
Erectile Dysfunction - etiology
Erectile Dysfunction - physiopathology
Guanylate Cyclase - genetics
Guanylate Cyclase - metabolism
Humans
Hydrocarbons, Fluorinated - administration & dosage
Intracavernous Pressure
Male
Mice
Mice, Inbred C57BL
Mice, Obese
Obesity
Obesity - complications
Oxidative Stress
Penile Erection - drug effects
Penis - blood supply
Reactive Oxygen Species
Reactive Oxygen Species - metabolism
Receptors, Cytoplasmic and Nuclear - agonists
Receptors, Cytoplasmic and Nuclear - genetics
Receptors, Cytoplasmic and Nuclear - metabolism
Soluble Guanylyl Cyclase
Up-Regulation
Title Prolonged Therapy with the Soluble Guanylyl Cyclase Activator BAY 60-2770 Restores the Erectile Function in Obese Mice
URI https://dx.doi.org/10.1111/jsm.12682
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjsm.12682
https://www.ncbi.nlm.nih.gov/pubmed/25196910
https://search.proquest.com/docview/1618139710
Volume 11
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