Photobiomodulation therapy for diabetic erectile dysfunction targeting neuroinflammation and neurovascular regeneration

Sci Rep. 2025 Jul 1;15(1):20513. doi: 10.1038/s41598-025-04873-w.

Abstract

Erectile dysfunction (ED) in diabetes often resists phosphodiesterase type 5 inhibitors due to neuropathy and vasculopathy, both worsened by neuroinflammation. This study evaluated light-emitting diode (LED) therapy's effects on diabetes-induced neurovascular damage using a diabetic mouse model. Diabetes was induced in C57BL/6 mice with streptozotocin, followed by treatment with RED (660 nm) and near-infrared (NIR; 830 nm) LED light, separately and combined, for ten days over two weeks. Functional and molecular analyses assessed neurovascular regeneration. LED therapy significantly improved intra-cavernous pressure (ICP), with combined RED and NIR wavelengths restoring ICP to 90% of normal levels, indicating enhanced nerve and vascular function. Histological analyses showed increased endothelial cell density, angiogenesis, pericyte recruitment, and neural regeneration. Molecular findings revealed upregulation of neurotrophic factors (NGF, NT-3, BDNF), angiogenic markers (VEGF, eNOS), and phosphorylated PI3K, alongside reduced apoptosis and increased cell proliferation. These results demonstrate that LED therapy mitigates diabetes-induced neuropathy and vasculopathy by enhancing neurovascular repair and modulating neuroinflammatory pathways. The study highlights the potential of combined RED and NIR LED therapy as a non-invasive treatment for diabetic ED and related neurovascular complications, offering a promising approach to improving patient outcomes.

MeSH terms

  • Animals
  • Diabetes Mellitus, Experimental* / complications
  • Erectile Dysfunction* / etiology
  • Erectile Dysfunction* / metabolism
  • Erectile Dysfunction* / pathology
  • Erectile Dysfunction* / radiotherapy
  • Erectile Dysfunction* / therapy
  • Low-Level Light Therapy* / methods
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nerve Regeneration* / radiation effects
  • Neuroinflammatory Diseases*