近红外光生物调节治疗与年龄相关的勃起功能障碍:小鼠模型的分子和生理恢复。

IF 2.7
Zhong-Jie Zheng, Yan Chen, Qian-Xi Chen, Wen-Hao Tang, Eric Chung, Kai Hong, Shu-Dong Zhang, Hao-Cheng Lin
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引用次数: 0

摘要

摘要:年龄相关性勃起功能障碍(ARED)是一项重大的临床挑战,因为慢性合并症与年龄相关性生理衰退之间存在相互作用。本研究探讨了近红外光生物调节疗法(NIR-PBMT)对急性勃起功能障碍小鼠的治疗潜力,重点探讨了其复杂勃起功能恢复的分子和生理机制。老龄小鼠每48 h接受NIR-PBMT (4 J cm-2)治疗,持续2周。使用海绵体神经刺激后的最大海绵体内压/平均动脉压(ICPmax/MAP)比值评估勃起功能。组织学分析和western blotting显示,阴茎组织结构显著改善,包括平滑肌含量增加,胶原沉积减少,衰老标志物(p21和磷酸化H2A组蛋白家族成员X [γ-H2A.X])和内皮型一氧化氮合酶(eNOS)的表达改变。体外研究表明,NIR-PBMT可以减少细胞衰老(通过SA-β-半乳糖苷酶染色进行评估),增强一氧化氮(NO)的产生,并改善线粒体网络的完整性。血管生成实验进一步证实了NIR-PBMT的促血管生成作用。总的来说,这些发现强调了NIR-PBMT作为一种有前途的非侵入性治疗方法,通过多种途径逆转病理性重塑和恢复内皮功能。需要进一步的转化研究来验证其临床疗效并优化治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Near-infrared photobiomodulation therapy for age-related erectile dysfunction: molecular and physiological restoration in a mouse model.

Abstract: Age-related erectile dysfunction (ARED) represents a significant clinical challenge due to the interplay between chronic comorbidities and age-related physiological decline. This study investigated the therapeutic potential of near-infrared photobiomodulation therapy (NIR-PBMT) in ARED mice, focusing on molecular and physiological mechanisms of complex erectile function restoration. Aged mice received NIR-PBMT (4 J cm-2) every 48 h for 2 weeks. Erectile function was evaluated using the maximum intracavernosal pressure/mean arterial pressure (ICPmax/MAP) ratio following cavernous nerve stimulation. Histological analysis and western blotting revealed significant improvements in penile tissue architecture, including increased smooth muscle content, reduced collagen deposition, and altered expression of senescence markers (p21 and phosphorylated H2A histone family member X [γ-H2A.X]) and endothelial nitric oxide synthase (eNOS). In vitro studies using human corpus cavernous endothelial cells (HCCECs) demonstrated that NIR-PBMT reduced cellular senescence (assessed via SA-β-galactosidase staining), enhanced nitric oxide (NO) production, and improved mitochondrial network integrity. Angiogenesis assays further confirmed the pro-angiogenic effects of NIR-PBMT. Collectively, these findings highlight NIR-PBMT as a promising non-invasive therapy for ARED, acting through multiple pathways to reverse pathological remodeling and restore endothelial function. Future translational research is necessary to validate its clinical efficacy and optimize treatment protocols.

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