Cavernous Nerve Injury by Radiation Therapy May Potentiate Erectile Dysfunction in Rats

Javed Mahmood, Caroline Q. Connors, Allen A. Alexander, Radmila Pavlovic, Santanu Samanta, Sandrine Soman, Hotaka Matsui, Nikolai A. Sopko, Trinity J. Bivalacqua, Daniel Weinreich, Cheng Ying Ho, John Eley, Amit Sawant, Isabel L. Jackson, Zeljko Vujaskovic

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Abstract

Purpose/Objectives Radiation-induced erectile-dysfunction (RiED) is one of the most common side effects of radiation therapy (RT) and significantly reduces the quality of life (QoL) of cancer patients. Approximately 50% of prostate cancer patients experience RiED within 3 to 5 years after completion of RT. A series of vascular, muscular, and neurogenic injuries after prostate RT lead to RiED; however, the precise role of RT-induced neurogenic injury in RiED has not been fully established. The cavernous nerves (CN) are postganglionic parasympathetic nerves located beside the prostate gland that assist in penile erection. This study was designed to investigate the role of CN injury, tissue damage, and altered signaling pathways in an RiED rat model. Methods and Materials Male rats were exposed to a single dose of 25 Gy prostate-confined RT. Erectile function was evaluated by intracavernous pressure (ICP) measurements conducted both 9 and 14 weeks after RT. Neuronal injury was evaluated in the CN using quantitative polymerase chain reaction, conduction studies, transmission electron microscopy, and immunoblotting. Masson trichrome staining was performed to elucidate fibrosis level in penile tissues. Results There were significant alterations in the ICP (P<.0001) of RT rats versus non-RT rats. TEM analysis showed decreased myelination, increased microvascular damage, and progressive axonal atrophy of the CN fibers after RT. Electrophysiologic analysis showed significant impairment of the CN conduction velocity after RT. RT also significantly increased RhoA/Rho-associated protein kinase 1 (ROCK1) mRNA and protein expression. In addition, penile tissue showed increased apoptosis and fibrosis 14 weeks after RT. Conclusions RT-induced CN injury may contribute to RiED; this is therefore a rationale for developing novel therapeutic strategies to mitigate CN and tissue damage. Moreover, further investigation of the RhoA/ROCK pathway's role in mitigating RiED is necessary.

Original languageEnglish (US)
Pages (from-to)680-688
Number of pages9
JournalInternational Journal of Radiation Oncology Biology Physics
Volume99
Issue number3
DOIs
StatePublished - Nov 1 2017

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ASJC Scopus subject areas

  • Radiation
  • Oncology
  • Radiology Nuclear Medicine and imaging
  • Cancer Research

Cite this

Mahmood, J., Connors, C. Q., Alexander, A. A., Pavlovic, R., Samanta, S., Soman, S., Matsui, H., Sopko, N. A., Bivalacqua, T. J., Weinreich, D., Ho, C. Y., Eley, J., Sawant, A., Jackson, I. L., & Vujaskovic, Z. (2017). Cavernous Nerve Injury by Radiation Therapy May Potentiate Erectile Dysfunction in Rats. International Journal of Radiation Oncology Biology Physics, 99(3), 680-688. https://doi.org/10.1016/j.ijrobp.2017.06.2449