Alexander Marcalee Sipski, Marson Lesley
Birmingham Veterans Affairs Medical Center, 700 South 19th Street, Birmingham, AL 35242, United States; Dept. Physical Medicine and Rehabilitation, University of Alabama at Birmingham School of Medicine, United States; Dept. Physical Medicine and Rehabilitation, Harvard School of Medicine, United States.
Dignify Therapeutics, Research Triangle Park, NC 27709, United States; Dept. Urology, School of Medicine and MOPH Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, United States.
Auton Neurosci. 2018 Jan;209:90-99. doi: 10.1016/j.autneu.2017.01.005. Epub 2017 Jan 25.
Preclinical research in animal models is important for understanding the neural pathways and pathophysiology underlying changes in sexual function after SCI. In vivo animal models, primarily rodents, have provided valuable information on the central pathways regulating sexual arousal and orgasm; however, further research is required in females and preclinical modeling of SCI that can be better translated to men and women. Translation of the autonomic and somatic regulation of sexual responses from preclinical models through clinical research correlates well with respect to the peripheral-spinal systems involved. However, due to the nature of sexual responses, parallel studies are necessary in animals and humans. Human studies of individuals with SCIs have provided information about the neurologic control of arousal and orgasm. Psychogenic arousal is related to the preservation of sensation at T11-L2 whereas orgasm requires the presence of an intact sacral reflex arc. Studies point to evidence of a spinal pattern generator at L3-5. Because of the exact nature of SCIs, further research using neuroimaging will be beneficial, not only to elucidate the neurological control of sexual responses after SCI, but also in able-bodied individuals. Understanding and ameliorating the effects of SCI on sexual function is important to the well-being and quality of life of individuals with SCIs and their partners, thus future research should focus more on this important topic.
动物模型的临床前研究对于理解脊髓损伤后性功能变化背后的神经通路和病理生理学至关重要。体内动物模型,主要是啮齿动物,已经提供了关于调节性唤起和性高潮的中枢通路的有价值信息;然而,在雌性动物以及能够更好地转化应用于男性和女性的脊髓损伤临床前模型方面,仍需要进一步研究。从临床前模型到临床研究,性反应的自主神经和躯体调节的转化在涉及的外周 - 脊髓系统方面相关性良好。然而,由于性反应的性质,在动物和人类中进行平行研究是必要的。对脊髓损伤个体的人体研究已经提供了关于性唤起和性高潮的神经控制的信息。心理性唤起与胸11至腰2节段感觉的保留有关,而性高潮需要完整的骶反射弧的存在。研究指出在腰3至腰5节段存在脊髓模式发生器的证据。由于脊髓损伤的确切性质,使用神经影像学的进一步研究将是有益的,这不仅有助于阐明脊髓损伤后性反应的神经控制,也有助于对健全个体的研究。理解并改善脊髓损伤对性功能的影响对于脊髓损伤个体及其伴侣的幸福感和生活质量很重要,因此未来的研究应更多地关注这个重要课题。