Phosphorylated Endothelial Nitric Oxide Synthase Mediates Vascular Endothelial Growth Factor-Induced Penile Erection

Biljana Musicki, Michael A. Palese, Julie K. Crone, Arthur Burnett

Research output: Contribution to journalArticle

Abstract

The objective of the present study was to evaluate whether vascular endothelial growth factor (VEGF)-induced penile erection is mediated by activation of endothelial nitric oxide synthase (eNOS) through its phosphorylation. We assessed the role of constitutively activated eNOS in VEGF-induced penile erection using wild-type (WT) and eNOS-knockout (eNOS -/-) mice with and without vasculogenic erectile dysfunction. Adult WT and eNOS-/- mice were subjected to sham operation or bilateral castration to induce vasculogenic erectile dysfunction. At the time of surgery, animals were injected intracavernosally with a replication-deficient adenovirus expressing human VEGF145 (109 particle units) or with empty virus (Ad.Null). After 7 days, erectile function was assessed in response to cavernous nerve electrical stimulation. Total and phosphorylated protein kinase B (Akt) as well as total and phosphorylated eNOS were quantitatively assessed in mice penes using Western immunoblot and immunohistochemistry. In intact WT mice, VEGF145 significantly increased erectile responses, and in WT mice after castration, it completely recovered penile erection. However, VEGF145 failed to increase erectile responses in intact eNOS-/- mice and only partially recovered erectile function in castrated eNOS-/- mice. In addition, VEGF145 significantly increased phosphorylation of eNOS at Serine 1177 by approximately 2-fold in penes of both intact and castrated WT mice. The data provide a molecular explanation for VEGF stimulatory effect on penile erection, which involves phosphorylated eNOS (Serine 1177) mediation.

Original languageEnglish (US)
Pages (from-to)282-289
Number of pages8
JournalBiology of Reproduction
Volume70
Issue number2
DOIs
StatePublished - Feb 2004

Fingerprint

Penile Erection
Nitric Oxide Synthase Type III
Vascular Endothelial Growth Factor A
Castration
Erectile Dysfunction
Serine
Phosphorylation
Human Adenoviruses
Proto-Oncogene Proteins c-akt
Knockout Mice
Electric Stimulation
Western Blotting
Immunohistochemistry
Viruses

Keywords

  • Growth factors
  • Male reproductive tract
  • Nitric oxide
  • Penis
  • Signal transduction

ASJC Scopus subject areas

  • Cell Biology
  • Developmental Biology
  • Embryology

Cite this

Phosphorylated Endothelial Nitric Oxide Synthase Mediates Vascular Endothelial Growth Factor-Induced Penile Erection. / Musicki, Biljana; Palese, Michael A.; Crone, Julie K.; Burnett, Arthur.

In: Biology of Reproduction, Vol. 70, No. 2, 02.2004, p. 282-289.

Research output: Contribution to journalArticle

@article{5622f4ed530d47b2b0fe1856ba29d4d8,
title = "Phosphorylated Endothelial Nitric Oxide Synthase Mediates Vascular Endothelial Growth Factor-Induced Penile Erection",
abstract = "The objective of the present study was to evaluate whether vascular endothelial growth factor (VEGF)-induced penile erection is mediated by activation of endothelial nitric oxide synthase (eNOS) through its phosphorylation. We assessed the role of constitutively activated eNOS in VEGF-induced penile erection using wild-type (WT) and eNOS-knockout (eNOS -/-) mice with and without vasculogenic erectile dysfunction. Adult WT and eNOS-/- mice were subjected to sham operation or bilateral castration to induce vasculogenic erectile dysfunction. At the time of surgery, animals were injected intracavernosally with a replication-deficient adenovirus expressing human VEGF145 (109 particle units) or with empty virus (Ad.Null). After 7 days, erectile function was assessed in response to cavernous nerve electrical stimulation. Total and phosphorylated protein kinase B (Akt) as well as total and phosphorylated eNOS were quantitatively assessed in mice penes using Western immunoblot and immunohistochemistry. In intact WT mice, VEGF145 significantly increased erectile responses, and in WT mice after castration, it completely recovered penile erection. However, VEGF145 failed to increase erectile responses in intact eNOS-/- mice and only partially recovered erectile function in castrated eNOS-/- mice. In addition, VEGF145 significantly increased phosphorylation of eNOS at Serine 1177 by approximately 2-fold in penes of both intact and castrated WT mice. The data provide a molecular explanation for VEGF stimulatory effect on penile erection, which involves phosphorylated eNOS (Serine 1177) mediation.",
keywords = "Growth factors, Male reproductive tract, Nitric oxide, Penis, Signal transduction",
author = "Biljana Musicki and Palese, {Michael A.} and Crone, {Julie K.} and Arthur Burnett",
year = "2004",
month = "2",
doi = "10.1095/biolreprod.103.021113",
language = "English (US)",
volume = "70",
pages = "282--289",
journal = "Biology of Reproduction",
issn = "0006-3363",
publisher = "Society for the Study of Reproduction",
number = "2",

}

TY - JOUR

T1 - Phosphorylated Endothelial Nitric Oxide Synthase Mediates Vascular Endothelial Growth Factor-Induced Penile Erection

AU - Musicki, Biljana

AU - Palese, Michael A.

AU - Crone, Julie K.

AU - Burnett, Arthur

PY - 2004/2

Y1 - 2004/2

N2 - The objective of the present study was to evaluate whether vascular endothelial growth factor (VEGF)-induced penile erection is mediated by activation of endothelial nitric oxide synthase (eNOS) through its phosphorylation. We assessed the role of constitutively activated eNOS in VEGF-induced penile erection using wild-type (WT) and eNOS-knockout (eNOS -/-) mice with and without vasculogenic erectile dysfunction. Adult WT and eNOS-/- mice were subjected to sham operation or bilateral castration to induce vasculogenic erectile dysfunction. At the time of surgery, animals were injected intracavernosally with a replication-deficient adenovirus expressing human VEGF145 (109 particle units) or with empty virus (Ad.Null). After 7 days, erectile function was assessed in response to cavernous nerve electrical stimulation. Total and phosphorylated protein kinase B (Akt) as well as total and phosphorylated eNOS were quantitatively assessed in mice penes using Western immunoblot and immunohistochemistry. In intact WT mice, VEGF145 significantly increased erectile responses, and in WT mice after castration, it completely recovered penile erection. However, VEGF145 failed to increase erectile responses in intact eNOS-/- mice and only partially recovered erectile function in castrated eNOS-/- mice. In addition, VEGF145 significantly increased phosphorylation of eNOS at Serine 1177 by approximately 2-fold in penes of both intact and castrated WT mice. The data provide a molecular explanation for VEGF stimulatory effect on penile erection, which involves phosphorylated eNOS (Serine 1177) mediation.

AB - The objective of the present study was to evaluate whether vascular endothelial growth factor (VEGF)-induced penile erection is mediated by activation of endothelial nitric oxide synthase (eNOS) through its phosphorylation. We assessed the role of constitutively activated eNOS in VEGF-induced penile erection using wild-type (WT) and eNOS-knockout (eNOS -/-) mice with and without vasculogenic erectile dysfunction. Adult WT and eNOS-/- mice were subjected to sham operation or bilateral castration to induce vasculogenic erectile dysfunction. At the time of surgery, animals were injected intracavernosally with a replication-deficient adenovirus expressing human VEGF145 (109 particle units) or with empty virus (Ad.Null). After 7 days, erectile function was assessed in response to cavernous nerve electrical stimulation. Total and phosphorylated protein kinase B (Akt) as well as total and phosphorylated eNOS were quantitatively assessed in mice penes using Western immunoblot and immunohistochemistry. In intact WT mice, VEGF145 significantly increased erectile responses, and in WT mice after castration, it completely recovered penile erection. However, VEGF145 failed to increase erectile responses in intact eNOS-/- mice and only partially recovered erectile function in castrated eNOS-/- mice. In addition, VEGF145 significantly increased phosphorylation of eNOS at Serine 1177 by approximately 2-fold in penes of both intact and castrated WT mice. The data provide a molecular explanation for VEGF stimulatory effect on penile erection, which involves phosphorylated eNOS (Serine 1177) mediation.

KW - Growth factors

KW - Male reproductive tract

KW - Nitric oxide

KW - Penis

KW - Signal transduction

UR - http://www.scopus.com/inward/record.url?scp=0742271502&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0742271502&partnerID=8YFLogxK

U2 - 10.1095/biolreprod.103.021113

DO - 10.1095/biolreprod.103.021113

M3 - Article

C2 - 14522830

AN - SCOPUS:0742271502

VL - 70

SP - 282

EP - 289

JO - Biology of Reproduction

JF - Biology of Reproduction

SN - 0006-3363

IS - 2

ER -