Journal
BRAIN RESEARCH
Volume 1596, Issue -, Pages 48-57Publisher
ELSEVIER
DOI: 10.1016/j.brainres.2014.11.035
Keywords
Chronic intermittent hypoxia; Apoptosis; Hippocampus; Telmisartan; NO synthases; Inflammation
Categories
Funding
- National Natural Science Foundation of PR China [81370185, 81070067]
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Obstructive sleep apnea syndrome (OSAS) plays a critical role in the initiation and progression of Alzheimer's disease (AD), but little is known about the precise mechanism of OSAS-induced AD. Nitric oxide synthase (NOS) and nitric oxide (NO) are known to play key roles in the development of AD. Several studies have confirmed that an angiotensin II type 1 receptor blocker, telmisartan, beneficially regulates NOS and NO. Here, we examined the neuroprotective effects of telmisartan against hippocampal apoptosis induced by chronic intermittent hypoxia (CIH), the most characteristic pathophysiological change of OSAS. Adult male Sprague Dawley rats were subjected to 8 h of intermittent hypoxia per day with or without telmisartan for eight weeks. Neuronal apoptosis in the hippocampal CA1 region, NOS activity, NO content, and the presence of inflammatory agents and radical oxygen species in the hippocampus were determined. The results showed that CIH activated inducible nitric oxide synthase (iNOS), increased NO content, and enhanced lipid peroxidation and inflammatory responses in the hippocampus. Treatment with telmisartan inhibited excessive iNOS and NO generation and reduced lipid peroxidation and inflammatory responses. In addition, telmisartan significantly ameliorated the hippocampal apoptosis induced by CIH. In conclusion, Pre-CIH telmisartan administration attenuated CIH-induced hippocampal apoptosis partly by regulating NOS activity, inhibiting excessive NO generation, and reducing lipid peroxidation and inflammatory responses. (C) 2014 Elsevier B.V. All rights reserved.
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