Physiopathological effects of entrance versus distal spread-out Bragg peak on mouse spinal cord neurons

• Published in: Scientific reports 2025-01, Vol.15 (1), p.2134-11, Article 2134
• Main Authors: Torrisi, Filippo, Cammarata, Francesco Paolo, Bravatà, Valentina, Calvaruso, Marco, Alberghina, Cristiana, Pavone, Anna Maria, Petringa, Giada, Cirrone, Giuseppe Antonio Pablo, Denaro, Simona, Gervasi, Anna, D’Aprile, Simona, Vicario, Nunzio, Scifoni, Emanuele, Pisciotta, Pietro, Russo, Giorgio, Parenti, Rosalba
• Format: Article
• Language: English
• Subjects: 631/378; 631/443; 631/57; Animals; Bragg peak; Central nervous system diseases; Humanities and Social Sciences; Irradiation; Mice; multidisciplinary; Neurons - physiology; Neurons - radiation effects; Neuroplasticity; Population studies; Presynaptic plasticity; Proton therapy; Proton Therapy - adverse effects; Radiation; Radiation-induced off-target effects; RBE; Science; Science (multidisciplinary); Spinal cord; Spinal Cord - radiation effects; Spinal plasticity; Synaptic plasticity; Synaptophysin; Synaptophysin - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-84902-2

Recent investigations into radiation-induced side effects have focused on understanding the physiopathological consequences of irradiation on late-responding tissues like the spinal cord, which can lead to chronic progressive myelopathy. Proton therapy, an advanced radiation treatment, aims to minimize damage to healthy tissues through precise dose deposition. However, challenges remain, particularly regarding the variation in dose distribution, characterized by maximum deposition at the end of the proton range, known as the distal fall-off of a spread-out Bragg peak. This variation is critical for nearby organs at risk. In this preliminary study, we evaluated the effects of proton irradiation on the neuronal cell population in mouse spinal cord by comparing two positions of the particle range dose deposition profile. We irradiated the spinal cords at the entrance and the distal edge of the spread-out Bragg peak with a single proton dose. Results showed changes in the expression of synaptophysin, a presynaptic protein crucial for synaptic plasticity. Our findings suggest that examining early radiation-induced physiopathological effects on late-responding tissues can provide valuable insights into neuronal plasticity, informing clinical treatment planning for proton beam positioning.