Angiotensin receptor blocker use is associated with upregulation of the memory-protective angiotensin type 4 receptor (AT(4)R) in the postmortem brains of individuals without cognitive impairment

Cosarderelioglu C., Nidadavolu L. S., George C. J., Marx-Rattner R., Powell L., Xue Q., ...Daha Fazla

GEROSCIENCE, cilt.45, sa.1, ss.371-384, 2023 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45 Sayı: 1
  • Basım Tarihi: 2023
  • Doi Numarası: 10.1007/s11357-022-00639-8
  • Dergi Adı: GEROSCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, ABI/INFORM, BIOSIS, CAB Abstracts, EMBASE, MEDLINE, Veterinary Science Database
  • Sayfa Sayıları: ss.371-384
  • Anahtar Kelimeler: Angiotensin receptor blocker, AT(4)R, Alzheimer's disease, Oxidative stress, Inflammation, Brain, OXIDATIVE STRESS, CONVERTING ENZYME, RUSH MEMORY, MOUSE MODEL, TELMISARTAN, AMINOPEPTIDASE, IDENTIFICATION, DYSFUNCTION, INHIBITION, ACTIVATION
  • Hacettepe Üniversitesi Adresli: Evet

Özet

The reported primary dementia-protective benefits of angiotensin II type 1 receptor (AT(1)R) blockers (ARB) are believed, at least in part, to arise from systemic effects on blood pressure. However, there is a specific and independently regulated brain renin-angiotensin system (RAS). Brain RAS acts mainly through three receptor subtypes; AT(1)R, AT(2)R, and AT(4)R. The AT(1)R promotes inflammation and mitochondrial reactive oxygen species generation. AT(2)R increases nitric oxide. AT(4)R is essential for dopamine and acetylcholine release. It is unknown whether ARB use is associated with changes in the brain RAS. Here, we compared the impact of treatment with ARB on not cognitively impaired individuals and individuals with Alzheimer's dementia using postmortem frontal-cortex samples of age- and sex-matched participants (70-90 years old, n = 30 in each group). We show that ARB use is associated with higher brain AT(4)R, lower oxidative stress, and amyloid-beta burden in NCI participants. In AD, ARB use was associated with lower brain AT(1)R but had no impact on inflammation, oxidative stress, or amyloid-beta burden. Our results may suggest a potential role for AT(4)R in the salutary effects for ARB on the brains of not cognitively impaired older adults.