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在中年Cyp1a1-Ren2转基因大鼠中逐渐诱导高血压会导致空间学习能力显著受损。

Gradual hypertension induction in middle-aged Cyp1a1-Ren2 transgenic rats produces significant impairments in spatial learning.

作者信息

Willeman Mari N, Chawla Monica K, Zempare Marc A, Biwer Lauren A, Hoang Lan T, Uprety Ajay R, Fitzhugh Megan C, De Both Matthew, Coleman Paul D, Trouard Theodore P, Alexander Gene E, Mitchell Kenneth D, Barnes Carol A, Hale Taben M, Huentelman Matthew

机构信息

Evelyn F. McKnight Brain Institute, University of Arizona, Tucson, Arizona.

Neurogenomics Division, The Translational Genomics Research Institute (TGen), Phoenix, Arizona.

出版信息

Physiol Rep. 2019 Mar;7(6):e14010. doi: 10.14814/phy2.14010.

DOI:10.14814/phy2.14010
PMID:30916484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6436186/
Abstract

Hypertension is a major health concern in the developed world, and its prevalence increases with advancing age. The impact of hypertension on the function of the renal and cardiovascular systems is well studied; however, its influence on the brain regions important for cognition has garnered less attention. We utilized the Cyp1a1-Ren2 xenobiotic-inducible transgenic rat model to mimic both the age of onset and rate of induction of hypertension observed in humans. Male, 15-month-old transgenic rats were fed 0.15% indole-3-carbinol (I3C) chow to slowly induce renin-dependent hypertension over a 6-week period. Systolic blood pressure significantly increased, eventually reaching 200 mmHg by the end of the study period. In contrast, transgenic rats fed a control diet without I3C did not show significant changes in blood pressure (145 mmHg at the end of study). Hypertension was associated with cardiac, aortic, and renal hypertrophy as well as increased collagen deposition in the left ventricle and kidney of the I3C-treated rats. Additionally, rats with hypertension showed reduced savings from prior spatial memory training when tested on the hippocampus-dependent Morris swim task. Motor and sensory functions were found to be unaffected by induction of hypertension. Taken together, these data indicate a profound effect of hypertension not only on the cardiovascular-renal axis but also on brain systems critically important for learning and memory. Future use of this model and approach may empower a more accurate investigation of the influence of aging on the systems responsible for cardiovascular, renal, and neurological health.

摘要

高血压是发达国家主要的健康问题,其患病率随年龄增长而增加。高血压对肾脏和心血管系统功能的影响已得到充分研究;然而,其对认知重要脑区的影响却较少受到关注。我们利用Cyp1a1-Ren2外源性诱导转基因大鼠模型来模拟人类高血压的发病年龄和诱导率。给15个月大的雄性转基因大鼠喂食0.15%的吲哚-3-甲醇(I3C)饲料,在6周内缓慢诱导肾素依赖性高血压。收缩压显著升高,在研究期末最终达到200 mmHg。相比之下,喂食不含I3C对照饲料的转基因大鼠血压没有显著变化(研究结束时为145 mmHg)。高血压与I3C处理大鼠的心脏、主动脉和肾脏肥大以及左心室和肾脏中胶原蛋白沉积增加有关。此外,高血压大鼠在依赖海马体的莫里斯游泳任务测试中,先前空间记忆训练的记忆保持能力下降。运动和感觉功能未受高血压诱导的影响。综上所述,这些数据表明高血压不仅对心血管-肾脏轴有深远影响,而且对学习和记忆至关重要的脑系统也有深远影响。未来使用该模型和方法可能有助于更准确地研究衰老对负责心血管、肾脏和神经健康系统的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/18fe1ecaafc2/PHY2-7-e14010-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/f9df6682cdf2/PHY2-7-e14010-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/4e45932e8db4/PHY2-7-e14010-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/9f3f864edb81/PHY2-7-e14010-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/ffe500fb2dc3/PHY2-7-e14010-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/0be08846f286/PHY2-7-e14010-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/e8c5c5db2f31/PHY2-7-e14010-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/d5649b8775f3/PHY2-7-e14010-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/18fe1ecaafc2/PHY2-7-e14010-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/f9df6682cdf2/PHY2-7-e14010-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/4e45932e8db4/PHY2-7-e14010-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/9f3f864edb81/PHY2-7-e14010-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/ffe500fb2dc3/PHY2-7-e14010-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/0be08846f286/PHY2-7-e14010-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/e8c5c5db2f31/PHY2-7-e14010-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/d5649b8775f3/PHY2-7-e14010-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb6/6436186/18fe1ecaafc2/PHY2-7-e14010-g008.jpg

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