Sonic Hedgehog Is Neuroprotective in the Cavernous Nerve with Crush Injury

Nicholas Angeloni, Christopher W. Bond, Daniel Harrington, Samuel I Stupp, Carol A. Podlasek

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Introduction. The cavernous nerve (CN) is commonly injured during prostatectomy, resulting in erectile dysfunction (ED). Although peripheral nerves have a limited ability to regenerate, a return of function typically does not occur due to irreversible down stream morphological changes in the penis that result from CN injury. We have shown in previous studies that sonic hedgehog (SHH) is critical for CN regeneration and improves erectile function after crush injury. Aims. Examine a new direction, to determine if SHH is neuroprotective to the pelvic ganglia (PG)/CN after crush injury. A secondary focus is to examine if SHH signaling decreases with age in the PG/CN. Methods. Sprague-Dawley rats underwent bilateral CN crush and SHH and glial fibrillary acidic protein were quantified by western analysis of the PG/CN (N=6 rats at each time point) at 1, 2, 4, 7, and 14days, and the apoptotic index was measured in the penis. SHH was quantified by western in the PG/CN with blockade of anterograde transport (N=4 rats) in comparison to mouse IgG (N=4 rats). If SHH is neuroprotective was examined at 4 (N=14 rats) and 7days (N=16 rats) of treatment after CN crush. SHH protein was quantified in aging (P200-300, N=5 rats) PG/CN in comparison to normal adult (P115-120, N=3 rats) PG/CN. Main Outcome Measures. SHH pathway was examined in PG via immunohistochemistry, in situ, western, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL). Results. SHH is neuroprotective in the PG/CN with injury. SHH localization in the PG/CN suggests SHH interaction in neuronal/glial signaling. SHH protein is significantly decreased in the PG/CN after crush injury and in the aged PG/CN. Signals from the PG are required to maintain SHH in the CN. Conclusions. There is a window of opportunity immediately after nerve insult in which manipulation of SHH signaling in the nerve microenvironment can affect long-term regeneration outcome.

Original languageEnglish
Pages (from-to)1240-1250
Number of pages11
JournalJournal of Sexual Medicine
Volume10
Issue number5
DOIs
Publication statusPublished - May 2013

Fingerprint

Nerve Crush
Hedgehogs
Ganglia
Hedgehog Proteins
Penis
Crush Injuries
Nerve Regeneration
Aptitude
DNA Nucleotidylexotransferase
Nerve Block
Glial Fibrillary Acidic Protein
Wounds and Injuries
Erectile Dysfunction
Prostatectomy
Peripheral Nerves
Neuroglia
Sprague Dawley Rats
Regeneration

Keywords

  • Aging
  • Cavernous Nerve
  • Neuroprotective
  • Regeneration
  • Sonic Hedgehog
  • Transport

ASJC Scopus subject areas

  • Urology
  • Obstetrics and Gynaecology
  • Reproductive Medicine

Cite this

Sonic Hedgehog Is Neuroprotective in the Cavernous Nerve with Crush Injury. / Angeloni, Nicholas; Bond, Christopher W.; Harrington, Daniel; Stupp, Samuel I; Podlasek, Carol A.

In: Journal of Sexual Medicine, Vol. 10, No. 5, 05.2013, p. 1240-1250.

Research output: Contribution to journalArticle

Angeloni, Nicholas ; Bond, Christopher W. ; Harrington, Daniel ; Stupp, Samuel I ; Podlasek, Carol A. / Sonic Hedgehog Is Neuroprotective in the Cavernous Nerve with Crush Injury. In: Journal of Sexual Medicine. 2013 ; Vol. 10, No. 5. pp. 1240-1250.
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N2 - Introduction. The cavernous nerve (CN) is commonly injured during prostatectomy, resulting in erectile dysfunction (ED). Although peripheral nerves have a limited ability to regenerate, a return of function typically does not occur due to irreversible down stream morphological changes in the penis that result from CN injury. We have shown in previous studies that sonic hedgehog (SHH) is critical for CN regeneration and improves erectile function after crush injury. Aims. Examine a new direction, to determine if SHH is neuroprotective to the pelvic ganglia (PG)/CN after crush injury. A secondary focus is to examine if SHH signaling decreases with age in the PG/CN. Methods. Sprague-Dawley rats underwent bilateral CN crush and SHH and glial fibrillary acidic protein were quantified by western analysis of the PG/CN (N=6 rats at each time point) at 1, 2, 4, 7, and 14days, and the apoptotic index was measured in the penis. SHH was quantified by western in the PG/CN with blockade of anterograde transport (N=4 rats) in comparison to mouse IgG (N=4 rats). If SHH is neuroprotective was examined at 4 (N=14 rats) and 7days (N=16 rats) of treatment after CN crush. SHH protein was quantified in aging (P200-300, N=5 rats) PG/CN in comparison to normal adult (P115-120, N=3 rats) PG/CN. Main Outcome Measures. SHH pathway was examined in PG via immunohistochemistry, in situ, western, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL). Results. SHH is neuroprotective in the PG/CN with injury. SHH localization in the PG/CN suggests SHH interaction in neuronal/glial signaling. SHH protein is significantly decreased in the PG/CN after crush injury and in the aged PG/CN. Signals from the PG are required to maintain SHH in the CN. Conclusions. There is a window of opportunity immediately after nerve insult in which manipulation of SHH signaling in the nerve microenvironment can affect long-term regeneration outcome.

AB - Introduction. The cavernous nerve (CN) is commonly injured during prostatectomy, resulting in erectile dysfunction (ED). Although peripheral nerves have a limited ability to regenerate, a return of function typically does not occur due to irreversible down stream morphological changes in the penis that result from CN injury. We have shown in previous studies that sonic hedgehog (SHH) is critical for CN regeneration and improves erectile function after crush injury. Aims. Examine a new direction, to determine if SHH is neuroprotective to the pelvic ganglia (PG)/CN after crush injury. A secondary focus is to examine if SHH signaling decreases with age in the PG/CN. Methods. Sprague-Dawley rats underwent bilateral CN crush and SHH and glial fibrillary acidic protein were quantified by western analysis of the PG/CN (N=6 rats at each time point) at 1, 2, 4, 7, and 14days, and the apoptotic index was measured in the penis. SHH was quantified by western in the PG/CN with blockade of anterograde transport (N=4 rats) in comparison to mouse IgG (N=4 rats). If SHH is neuroprotective was examined at 4 (N=14 rats) and 7days (N=16 rats) of treatment after CN crush. SHH protein was quantified in aging (P200-300, N=5 rats) PG/CN in comparison to normal adult (P115-120, N=3 rats) PG/CN. Main Outcome Measures. SHH pathway was examined in PG via immunohistochemistry, in situ, western, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL). Results. SHH is neuroprotective in the PG/CN with injury. SHH localization in the PG/CN suggests SHH interaction in neuronal/glial signaling. SHH protein is significantly decreased in the PG/CN after crush injury and in the aged PG/CN. Signals from the PG are required to maintain SHH in the CN. Conclusions. There is a window of opportunity immediately after nerve insult in which manipulation of SHH signaling in the nerve microenvironment can affect long-term regeneration outcome.

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