Publications by authors named "Alia O Alia"

Article Synopsis
  • ACE1 plays a crucial role in regulating blood pressure and is important for cognitive functions like learning and memory, primarily expressed in the excitatory neurons of the hippocampus.
  • Research conducted with ACE1 conditional knockout (cKO) mice revealed significant memory impairments and dysregulation of the renin-angiotensin system in the hippocampus, even when total ACE1 levels were reduced in both hippocampus and cortex.
  • The findings highlight a specific vulnerability in the hippocampal microvasculature and suggest a connection between neuronal ACE1 and cerebrovascular health in that region of the brain.
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Current scientific research is driven by the ability to manipulate gene expression by utilizing the Cre/loxP system in transgenic mouse models. However, artifacts in Cre-driver mouse lines that introduce undesired effects and confound results are increasingly being reported. Here, we show aberrant neuroinflammation and synaptic changes in two widely used Cre-driver mouse models.

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Background: Amyloid plaque deposition and axonal degeneration are early events in AD pathogenesis. Aβ disrupts microtubules in presynaptic dystrophic neurites, resulting in the accumulation of impaired endolysosomal and autophagic organelles transporting β-site amyloid precursor protein cleaving enzyme (BACE1). Consequently, dystrophic neurites generate Aβ42 and significantly contribute to plaque deposition.

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The current study investigated the independent and combined effects of caffeine and taurine on anxiety-like behavior and neuroendocrine responses in adult zebrafish (). Caffeine (1,3,7-trimethylpurine-2,6-dione), the world's most commonly used psychoactive drug, acts as an adenosine receptor blocker and a mild central nervous system stimulant. However, excessive use of caffeine is associated with heightened anxiety levels.

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