There is growing evidence that
circular RNAs (
circRNAs) play a vital role in many kinds of diseases, including
erectile dysfunction (ED). Nevertheless, the role of
circRNAs in cavernous nerve-damaging ED (CNI-ED) is unknown. Here, we aimed to discover novel
circRNAs, probed their potential role in the CNI-ED, and construct a
ceRNA network of
circRNAs. Twelve male Sprague Dawley rats were randomly divided into 2 groups by us: bilateral cavernous
nerve crush (BCNC) and control groups. Four weeks after surgery, the spongy smooth muscle tissue of the rat penis was sequenced using high-throughput full transcriptome sequencing. We analyzed the expression of
circRNAs,
miRNAs, and mRNAs in the two groups. Twenty
circRNAs with significantly different expressions were selected for RT-qPCR.
CeRNA network of
circRNAs was established using Cytoscape. GO and KEGG analysis was done by R package. Sequencing showed that 4,587
circRNAs, 762
miRNAs, and 21,661 mRNAs were dysregulated in the BCNC group. The top 20 differentially expressed
circRNAs were further verified via RT-qPCR. The
ceRNA network contained ten
circRNAs, six
miRNAs, and 227 mRNAs, including 23
circRNA-
miRNA pairs and 227
miRNA-
mRNA pairs. GO and KEGG analysis suggested that these ten
circRNAs could main regulate energy metabolism processes. A protein-protein interaction network was constructed with the mRNAs in
ceRNA network, and five hub genes were identified. Our study revealed a potential link between
circRNAs,
miRNAs, and mRNAs in CNI-ED, suggesting that
circRNAs may contribute to the occurrence of ED by regulating the cellular energy metabolism in CNI-ED.