| Literature DB >> 30958362 |
Xiaowen Shi1, Yasuyuki Ohta1, Xia Liu1, Jingwei Shang1, Ryuta Morihara1, Yumiko Nakano1, Tian Feng1, Yong Huang1, Kota Sato1, Mami Takemoto1, Nozomi Hishikawa1, Toru Yamashita1, Koji Abe1.
Abstract
Alzheimer's disease (AD) is the most common dementia and a progressive neurodegenerative disorder aggravated by chronic hypoperfusion (HP). Since numerous evidence suggests that inflammation is related with AD pathology, we investigated the expression change of two anti-inflammatory markers, inter-alpha-trypsin inhibitor heavy chain H4 (ITIH4) and alpha-2-HS-glycoprotein (AHSG), in a novel AD model (APP23) with HP at 12 month of age. As compared with wild type (WT, n = 10), immunohistochemical analysis showed a higher ITIH4 and a lower AHSG expressions in the cerebral cortex, hippocampus, and thalamus of the APP23 + HP group (n = 12) than the simple APP23 (n = 10) group (*p < 0.05 and **p < 0.01 versus WT; #p < 0.05 and # #p < 0.01 versus APP23). The present study provides an upregulation of anti-inflammatory ITIH4 and a downregulation of pro-inflammatory TNFα-dependent AHSG in a novel AD plus HP mice model.Entities:
Keywords: AHSG; APP23 mice; ITIH4; alzheimer’s disease; hypoperfusion; inflammation
Year: 2019 PMID: 30958362 DOI: 10.3233/JAD-181218
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472