Noller Crystal M, Mendez Armando J, Szeto Angela, Boulina Marcia, Llabre Maria M, Zaias Julia, Schneiderman Neil, McCabe Philip M
From the Department of Psychology (Noller, Szeto, Llabre, Schneiderman, McCabe), University of Miami, Coral Gables, Florida; Diabetes Research Institute (Mendez, Boulina) and Departments of Medicine and Pathology (Zaias), University of Miami Miller School of Medicine, Miami, Florida.
Psychosom Med. 2017 Jan;79(1):59-70. doi: 10.1097/PSY.0000000000000360.
The sympathetic nervous system (SNS) can undergo dramatic structural plasticity in response to behavioral factors and/or the presence of disease, leading to SNS hyperinnervation of peripheral tissues. The SNS has been proposed as an important mediator between stressful behavior and the progression of atherosclerosis in the vasculature. The present study examined whether structural remodeling of the SNS occurs in the vasculature in a genetically hyperlipidemic animal model of atherosclerosis, the Watanabe heritable hyperlipidemic rabbit (WHHL; relative to normolipidemic New Zealand white rabbits [NZW]), and whether SNS plasticity is driven by the progression of disease and/or by stressful social behavior.
WHHL and NZW rabbits were assigned to an unstable or stable social environment for 4 months. Aortic atherosclerosis was assessed and SNS aortic innervation quantified using immunofluorescent microscopy.
Numerous SNS varicosities were observed throughout the aorta in WHHLs and NZWs, extending into the vascular media and intima, an innervation pattern not previously reported. WHHLs exhibited significantly greater innervation than NZWs (F(1,41) = 55.3, p < .001), with extensive innervation of the atherosclerotic neointima. The innervation density was highly correlated with the extent of disease in the WHHLs (r(21) = 0.855, p < .001). Social environment did not influence innervation in NZWs (aortic arch: p = .078, thoracic aorta: p = .34) or WHHLs (arch: p = .97, thoracic: p = .61).
The findings suggest that hyperinnervation is driven largely by the progression of disease rather than social environment. SNS innervation patterns observed in atherosclerotic human and mouse aortas were consistent with the rabbit, suggesting that SNS hyperinnervation of the diseased vessel wall is a general feature across mammalian species.
交感神经系统(SNS)可因行为因素和/或疾病的存在而发生显著的结构可塑性变化,导致外周组织的SNS神经支配过度。SNS被认为是应激行为与血管中动脉粥样硬化进展之间的重要介导因素。本研究探讨了在动脉粥样硬化的遗传性高脂血症动物模型——渡边遗传性高脂血症兔(WHHL;相对于正常血脂的新西兰白兔 [NZW])的血管中,SNS是否发生结构重塑,以及SNS可塑性是否由疾病进展和/或应激性社会行为驱动。
将WHHL兔和NZW兔置于不稳定或稳定的社会环境中4个月。评估主动脉粥样硬化情况,并使用免疫荧光显微镜对SNS主动脉神经支配进行定量分析。
在WHHL兔和NZW兔的整个主动脉中均观察到大量SNS曲张,延伸至血管中膜和内膜,这种神经支配模式此前未见报道。与NZW兔相比,WHHL兔的神经支配显著增加(F(1,41) = 55.3,p < .001),动脉粥样硬化新生内膜有广泛的神经支配。在WHHL兔中,神经支配密度与疾病程度高度相关(r(21) = 0.855,p < .001)。社会环境对NZW兔(主动脉弓:p = .078,胸主动脉:p = .34)或WHHL兔(主动脉弓:p = .97,胸段:p = .61)的神经支配均无影响。
研究结果表明,神经支配过度主要由疾病进展而非社会环境驱动。在动脉粥样硬化的人类和小鼠主动脉中观察到的SNS神经支配模式与兔一致,表明患病血管壁的SNS神经支配过度是所有哺乳动物物种的普遍特征。