Toth Peter, Tarantini Stefano, Springo Zsolt, Tucsek Zsuzsanna, Gautam Tripti, Giles Cory B, Wren Jonathan D, Koller Akos, Sonntag William E, Csiszar Anna, Ungvari Zoltan
Reynolds Oklahoma Center on Aging, Department of Geriatric Medicine, University of Oklahoma Health Sciences Center, 975 NE 10th Street, Oklahoma City, OK, 73104, USA; Department of Pathophysiology and Gerontology and Szentagothai Research Center, University of Pecs, Szigeti Street 12, 7624, Pecs, Hungary.
Aging Cell. 2015 Jun;14(3):400-8. doi: 10.1111/acel.12315. Epub 2015 Feb 9.
Recent studies demonstrate that aging exacerbates hypertension-induced cognitive decline, but the specific age-related mechanisms remain elusive. Cerebral microhemorrhages (CMHs) are associated with rupture of small intracerebral vessels and are thought to progressively impair neuronal function. To determine whether aging exacerbates hypertension-induced CMHs young (3 months) and aged (24 months) mice were treated with angiotensin II plus L-NAME. We found that the same level of hypertension leads to significantly earlier onset and increased incidence of CMHs in aged mice than in young mice, as shown by neurological examination, gait analysis, and histological assessment of CMHs in serial brain sections. Hypertension-induced cerebrovascular oxidative stress and redox-sensitive activation of matrix metalloproteinases (MMPs) were increased in aging. Treatment of aged mice with resveratrol significantly attenuated hypertension-induced oxidative stress, inhibited vascular MMP activation, significantly delayed the onset, and reduced the incidence of CMHs. Collectively, aging promotes CMHs in mice likely by exacerbating hypertension-induced oxidative stress and MMP activation. Therapeutic strategies that reduce microvascular oxidative stress and MMP activation may be useful for the prevention of CMHs, protecting neurocognitive function in high-risk elderly patients.
近期研究表明,衰老会加剧高血压所致的认知衰退,但具体的年龄相关机制仍不清楚。脑微出血(CMHs)与脑内小血管破裂有关,被认为会逐渐损害神经元功能。为了确定衰老是否会加剧高血压诱导的CMHs,对年轻(3个月)和老年(24个月)小鼠注射血管紧张素II加L-精氨酸甲酯(L-NAME)进行处理。我们发现,通过神经学检查、步态分析以及对连续脑切片中CMHs的组织学评估显示,相同程度的高血压在老年小鼠中导致CMHs的发病明显更早且发病率更高。衰老过程中,高血压诱导的脑血管氧化应激和基质金属蛋白酶(MMPs)的氧化还原敏感激活增加。用白藜芦醇治疗老年小鼠可显著减轻高血压诱导的氧化应激,抑制血管MMP激活,显著延迟发病并降低CMHs的发病率。总体而言,衰老可能通过加剧高血压诱导的氧化应激和MMP激活来促进小鼠发生CMHs。减少微血管氧化应激和MMP激活的治疗策略可能有助于预防CMHs,保护高危老年患者的神经认知功能。